ECO BOT THE ttamafptiat Jjaitwal, AND AND transactions. THIRD SERIES. VOLUME X. 1879-80. ♦ LONDON : J. & A. CHURCHILL, NEW BURLINGTON STREET; Edinburgh, MACLACHLAN & STEWART ; Dublin, FANNIN & Co. ; Leipzig, TWIETMEYER. 1 880. ■ - v> r »* -• y ■ ; • - . • ' * m * *• * . ■ .. - . .. . X . -I ■ . . ■c ■ ■ - - . . . • .V- • ' - •* ■ ' 5'- - ' ' .'••• ‘ ■" •• - , i. / •>- ■ - . . >. • • • e , * ■ \ i ] • ;r - . ; * * . ' . ? ’* , ...... * : • •> ; “*■ • « ■ •• - • - • • . . . • * ... • - • • • . •' • • ■ • •• > " • . ■ ... ' . • . . • • • . . ■ . •. - • ■ ■ • • . f . • • • • - - - ! : : • * .* •— • • • • * ■, ** >■ ... - ■ 'v: • • • , ^ * > /* > - '• V . - • u • if . • ■ •/' v. ; r. •: 1 . ■ •* • X ■ ■ :• ■ • \ rRINTED BY STEVENS AND RICHARDSON, . 5, great queen street, Lincoln’s inn fields, London, vt.c. ✓ Che o Itarmaceutical Journal AND Sfranaattiirna. YOL. X.— JULY 5, 1 87 9. NOTES OF SOME OBSERVATIONS ON NITRIFICATION." BY EDMUND W. DAVY, A.M., M.D., M.R.I.A. Professor of Forensic Medicine , in the Royal College of Surgeons, Ireland. A good deal of attention on the part of chemists has of late been given to the subject of nitrification, nr the formation of nitrites and nitrates under dif¬ ferent circumstances. This has arisen, in a great measure, from the observations of MM. Schloesing and Muntz, f which were laid before the Academy of France about two years ago. From the researches of those gentlemen, they arrived at the conclusion, that nitrification was due to an organized ferment, and that it was probably the office of some of the low forms of vegetable life, to produce those oxides of nitrogen under different circumstances. And the subsequent investigations of Warrington, Storer and of other chemists, would appear to go far to ■confirm the correctness of their theory of nitrifica¬ tion, at least, under the conditions in which their experiments were made. Though there exists, no doubt in many cases, an intimate relation between the formation of nitrites and nitrates, and the development of certain organized germs, still, as far as my observations go, I do not -think that there is sufficient proof to show that their development in such instances is the cause of nitrification, and not, rather, one of the circumstances •attendant on that process. My experiments, however, were made not with a view to determine that question, but in reference to the detection of animal impurities in potable waters, and to ascertain the circumstances which were favourable or otherwise, to the formation of nitrites and nitrates in waters which were so polluted, as the presence of such salts is generally regarded as indicating previous sewage contamination ; and the drinking of water with such pollution is not only injurious to the health of those who thus employ it, but there exist strong grounds for the opinion which is now very generally entertained, that such water frequently becomes the means of conveying the germs of certain formidable diseases, especially those of typhoid fever and cholera, from its contain¬ ing the fecal and other emanations of individuals suffering under those maladies, and thus disease and death are often insidiously brought into many homes, when such diseases are prevalent in different localities. Besides, as the formation or production of nitrates is one of great industrial and agricultural * Read before the Royal Irish Academy, May 12, 1879. f Comptes Rendus, lxxxiv., 301. Third Series, No. 471. importance, any facts which might directly or indirectly enable us to facilitate or hasten that process, would be of much practical value. As human urine and feculent matters may justly be regarded as the most offensive and dangerous ingredients of sewage in general, my experiments have been confined to those matters, and were principally made on urine, which from its containing different nitrogenous substances readily susceptible of decomposition, is peculiarly suited for the study of the nitrification of animal matters. By mixing this liquid with various proportions of water, and placing the mixtures under different circumstances, I have endeavoured to ascertain those that were favourable or otherwise to their nitrification, and to determine some points connected with that process which required further investigation. I should here observe, that in detecting the occurrence of nitrification, I have principally used the well known test of Price for nitrites, which consists in adding to the water or mixture, a thin solution of starch containing a little iodide of potas¬ sium and acidifying with diluted sulphuric acid, when a blue reaction from the liberated iodine will be immediately produced, should a very minute quantity even, of a nitrite be present. And as there is every reason to suppose that the production of nitrites precedes that of nitrates in the nitrification of organic matters in solution, and the detection of the former is much more easily effected than the latter, at least under the conditions existing in my experiments, I was satisfied in most cases to obtain the evidence of the formation of nitrites by the employment of the test to which I have just referred. The experiments of Warrington* have led him to conclude, that darkness is an essential condition to the development of those low forms of vegetable life, which are supposed in many instances to give rise to nitrification. This is a question which it is difficult to determine decisively, one way or the other, owing to the impossibility of having with us continuous daylight to operate with. Still I think we may arrive at an approximate conclusion on this point, by making comparative experiments on similar mixtures kept altogether excluded from the light, and on those exposed to its full influence, and then deter¬ mining the amount of nitrification which had taken place in each after a given time ; and if darkness be so essential to that process, we should naturally ex¬ pect that in the mixtures exposed to its continuous influence, there would be an earlier and a greater development of nitrification, than in those which had been placed under it, for about one-third or one-half * Journal of the Chemical Society , January, 1878. 2 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 5, 1879, the time each day of twenty-four hours. From the re¬ sults of several comparative experiments made in this way, I have come to the conclusion, that the conditions of light or darkness exercise but little influence one way or the other in this process, at least under the circumstances existing in my experiments, which consisted in placing different portions ot the same mixture in similar bottles, some of which were sur¬ rounded with black cloth or velvet to exclude light, whilst others were left uncovered, and all of them were suffered to remain open or uncorked. On ex¬ amination after a few days, there was but little difference as to the amount* of nitrification that had taken place in each — indeed in some of my experi¬ ments, it had progressed to a greater extent in the uncovered than in the covered bottles ; and in all made on this subject (except those to determine this point as to the necessity or not of darkness) the mixtures were left exposed to the light, and some to the full influence of strong sunshine, yet still a con¬ siderable amount of nitrification took place in each ; besides in nature much of the nitrates which occur in the surface soils of different localities, must have been formed under the influence of more or less day¬ light, all of which facts, I conceive, are more or less opposed to the necessity of darkness in this process. Another point which has not, I believe, been clearly established, at least as regards nitrification occurring in water containing organic matters, is the necessity of having a certain amount of air or of free oxygen to carry on the process ; this I have proved in the following very simple manner : — To water which had been kept boiling for some time to expel its contained air, I added a small quantity of freshly voided urine (the proportion employed being about one part of urine to sixteen parts of water, such a mixture having been found to be very suitable for nitrification), and then repeated the boiling to en¬ sure the removal as far as possible of any dissolved air. Several bottles which had been kept immersed in the boiling mixture, were then filled completely with it, corked and sealed with sealing wax to pre¬ vent the access of air. Some, however, of them containing this mixture were left open for compari son. After leaving the bottles for a day or two in the same place, I first examined the open ones for nitrites, and when the test indicated the abundant formation of those salts, I opened one of those sealed, when not a trace of nitrites was discoverable in its contents ; the remaining sealed ones were opened at different periods subsequently with the same results. Other comparative experiments were made, where the temperature of the mixtures was artificially kept at a heat very favourable to nitrification, but in every instance where the access of air had been ex¬ cluded no trace of nitrites could be detected, clearly proving the necessity of more or less air or free oxygen for their formation. But the amount neces¬ sary to commence at least, the process is small, for I found that where the mixture had not been boiled previous to the complete filling, corking and sealing of the bottle, that the air dissolved in the liquid was * In ascertaining the amount of nitrification, the indigo process, as described by Sutton in his ‘ Volumetric An¬ alysis/ was employed, which served f-^r the determination of the nitrites and nitrates collectively, and though it may not be quite so accurate as some other methods, was suffi¬ ciently so for this purpose, as it was only the comparative amount of nitrites and nitrates formed under the different circumstances of the experiments that I wanted to de¬ termine. sufficient to cause the production of nitrites to some extent. The quantity of animal matter which is held in solution in the water, I find exercises a considerable influence over nitrification, for where it occurs in very large proportion, there the process either does not take place at all, or is carried on much slower than in the more dilute solutions. This I have proved by comparative experiments with water mixed with different proportions of the same sample of urine, or of solution of excrementitious matter, where 1 found that nitrification occurred first in the more dilute mixtures ; and that where there was much organic matter present, that the nitrites which might ultimately be formed soon afterwards dis¬ appeared again, by their subsequent change or de¬ composition ; whereas those that had been produced in more dilute solutions, have remained unchanged for a considerable time. But the circumstance which I have found to exer¬ cise the greatest influence over nitrification is that of temperature, for 1 have observed that in cold weather it is very slow in taking place, whilst in warm it is much quicker, and that by the application of artificial heat the process can be greatly acce¬ lerated. The correctness of this observation is borne out by the well-known fact, that it is from the soils of different hot climates that we obtain our chief supply of nitrates. As to what may be the most favourable temperature for this process, I have not yet been able to determine, owing to the difficulty, as I am circumstanced, in maintaining continuously the same degree of artificial heat ; but I have found that where the mixtures were placed where they were kept at a temperature which varied from about 70° to 80° F. , that there the process was carried on very quickly and that nitrites were soon abundantly formed, whereas in similar mixtures maintained at lower degrees of heat or at the ordinary temperature not a trace of those salts could be detected in the same time, and that their presence was not discover¬ able till after a much longer period. The foregoing observations have, I conceive, some important bearings as regards the contamination of water with sewage, and the evidence of such derivable from the occurrence in it of nitrites and nitrates. For though the presence of those salts is undoubtedly, in many instances, an indication of previous sewage pollution, still their absence, taken by itself, cannot be relied on as a sure indication of the freedom of the water from such contamination. F or the circum¬ stances present may have either been unfavourable to the formation of nitrites and nitrates, or have produced their subsequent rapid disappearance : thus, for instance, the lowness of the temperature of the water may have prevented their formation, or the quantity of organic matter present may have inter¬ fered with their development, or have led to their subsequent change and disappearance. Such, amongst other circumstances influencing the presence of those salts in water containing animal matters, it will at once be evident, that their absence, unless accompanied by other indications of purity, cannot be relied on as a proof of the freedom from such contamination. Before I conclude, I wish to call attention to another fact which I have noticed in connection with this subject, viz., the rapidity with which nitrites are sometimes formed in waters contamin¬ ated with sewage impurities. This is a subject of considerable importance in an analytical point of July 5, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 3 view, as I shall endeavour briefly to explain. It is well known "by those who have analysed potable waters, that the method which chemists now princi¬ pally employ, to ascertain their purity or otherwise, is to determine the quantity of ammonia a given amount of the water will yield on distillation, both before and after the addition of a strongly alkaline solution of permanganate of potash. The first obtained is termed the free, and the second the albu¬ minoid ammonia. The former is regarded as the representative of the nitrogenous organic matters previously existing in the water, which have under¬ gone more or less decomposition ; whilst the latter is produced by the action of the alkaline perman¬ ganate or those substances still present in the water. Consequently, the less of each that is furnished by a sample of water when so treated, the purer organi¬ cally is it regarded, and the safer, other circum¬ stances being similar, would it be for potable purposes. When lately analysing a sample of water that had been contaminated with sewage, to ascertain the amount of such pollution, which was afterwards the subject of an important legal inquiry, in my first trial, I found that the water yielded a quantity of free ammonia, which was equivalent to 0-970 parts of a grain per gallon, but on repeating the deter¬ mination a few days afterwards, it was discovered that it had fallen to 0T86 parts of a grain for the same quantity of water, or to less than one-fifth of the former amount ; whereas the quantity of albu¬ minoid ammonia yielded had slightly increased. This result as to the great decrease of free ammonia, which at first rather surprised me, I ascertained was due to the formation of nitrites, which had been de¬ veloped to a large extent, in so short a time, at the expense of the free ammonia. Such being the case, if the water had not been examined till the date of the second analysis, and if the nitrites had not been taken into account, this water would have been regarded as containing much less free ammonia than it did, and consequently that the previous sewage contamination was less than it really was ; this point, is therefore, one of some analytical importance. It is right for me to observe in connection with this latter fact of the decrease of free ammonia in waters by keeping, that long after I had made that observation, I came across in the Chemical News for March 2, 1877, a letter written by Professor Pattison Muir, of Owens College, in which he calls the atten¬ tion of chemists to some observations his brother had just made in the laboratory of the University at Sydney, in which he had noticed that the amount of free and of albuminoid ammonia, as determined by Wanklyn’s process, varied very considerably with the time the sample of water had been kept ; but neither of those gentlemen have offered (in the letter referred to) any explanation of the fact further than that Professor P. Muir throws out the suggestion, in the case of the increase by keeping of the albuminoid ammonia, that possibly it might have been owing to the “ germs ” which have escaped decomposition by the permanganate, undergoing a gradual decomposition in the water, and that ammonia is one of the products of this process. Be this as it may, I have satisfied myself that the loss of free ammonia is often due to the formation of nitrites or nitrates, which are very rapidly formed from it under different circumstances. And as regards albuminoid ammonia, the very slight ncrease which I observed in my experiment, was, I thought, very easily accounted for by my having in the second determination, carried on the process of distillation somewhat further than in the first trial, and in this way the amount might be very naturally increased. Finally, my observations that nitrification is greatly promoted by warmth might, I conceive, admit of some practical application in the manu¬ facture of the nitrate of potash in the artificial nitre beds, especially in those of cold countries, and I am not aware that heat has hitherto been anywhere artificially applied to hasten or promote that im¬ portant manufacture. NOTES ON SOME JAPANESE DRUGS. BY E. M. HOLMES, F.L.S., Curator of the Museum of the Pharmaceutical Society. The Japanese are perhaps the most enterprising and progressive of Eastern nations, and have already made vast strides in the science and education of the West. In Japanese medicine a similar improvement seems to have taken place, for it was remarked at the Centennial Exhibition at Philadelphia, that although 300 specimens representing the advanced materia medica of Japan were exhibited, none of the specimens belonged to the animal kingdom, the various disgusting remedies of that class still used by the Chinese being conspicuous by their absence. Yet comparatively little is known in English- speaking countries of the drugs used by the Japanese. Beyond an enumeration of thirty well-known drugs used in other countries, no description that I can discover has been published in the English language of the 300 specimens above mentioned. In New Remedies for January, 1877, a short ac¬ count is given of Japanese medicine,* and the names and uses of a few drugs, and some analyses of a few others have been published in the American Journal of Pharmacy, January, 1879, p. 25. The large quantity of Japanese aconite that has during the last few years been imported into this country, has in some measure drawn attention to the drugs of Japan . Messrs. Wright and Luff have recently obtained from this aconite an alkaloid which they call Japaconitine. Another alkaloid has been discovered in an unnamed Japanese plant by M. A. Petit. These results have led me to examine the collection which was recently presented to the museum, with a view to ascertain whether any of them appeared to merit chemical examination or could be turned to any practical account in this country. Among those which seem most promising may be mentioned the root of Coptis anemoncefolia, containing a quantity of berberine ; the fruits of Gardenia radicans and G. florida, in which a colouring matter supposed to be identical with that of saffron has been found ; kuh- sing root, containing the very bitter alkaloid dis¬ covered by M. Petit, and a valerian root, which seems to be more powerful than the English drug. The thoroughness with which the drugs have been dried, their freedom from admixture and their ex¬ cellent quality, seem to indicate that it may be pos¬ sible in the future for drugs from Japan to compete successfully with less carefully prepared products nearer home. The specimens hereafter described were all met with in the London market, where for some months * Pharm. Journ., vol. vii., p. 674. 4 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 5, 1879. tliey found no purchaser, nothing being known of their names or uses, all the names being in Japanese characters. In the following notes the drugs have been arranged for convenience of reference under the heads of Roots, Herbs and Leaves, Flowers, Fruits and Seeds, and the Japanese names have been placed in alphabetical order, as being those in which Japanese drugs are most likely to be met with in English commerce on future occasions. The Japanese names hung, soli, yoh , hah, she, nine/, which are of frequent occurrence in the follow¬ ing list of drugs mean respectively, root, herb, leaves, flowers, seeds and kernels, and must therefore not be looked upon as part of the name of the plant which yields them. When presented to the museum of the Pharmaceu¬ tical Society by Mr. Christy, the specimens had merely numbers and the names in Japanese charac¬ ters attached to each parcel ; these numbers are here placed in parentheses after each Japanese name, to enable others to whom similar -specimens have been distributed to easily identify them by this means. I have to acknowledge the great assistance kindly afforded me by Mr. K. Takemura, a Japanese gen¬ tleman studying in the Society’s laboratory, in translating the Japanese labels of the specimens, and also portions of the So mokou Zoussetz, a valuable Japanese work recently presented to the North British Branch of the Society. Without Mr. Takemura’s assistance the botanical sources of many of the specimens could not probably have been so satisfactorily determined . The works to which abbreviated reference is made, and from which the synonyms for the various drugs have been taken, are as follows : — Kcempfer, ‘ Amoenitates Exotica?,’ 1712. Thunberg, ‘Flora Japonica,’ 1786. Siebold and Zuccarini, ‘Flora Japonica,’ 1835. Smith, Dr. F. Porter, ‘Chinese Materia Medica,’ 1871. Miquel, ‘ Prolusio Florae Japonicse,’ 1866-7. Franchet and Sava tier, ‘Enumeratio Plantarum Japoni- carum,’ 1875. Hanbury ‘ Science Papers,’ 1876. ROOTS. Bai-mo (30) : — Fritillaria Thunbergii, Miq. Prol. p. 321 ; Fr. et Sav. vol. ii. pt. 1, p. 61 ; So mokou Zoussetz, vol. v. fig. 79; Uvularia cirrhosa, Thunb. FI. Jap. p. 136. Syn. Faru juri, Amisa juri, Fr. et Sav. The drug consists of a white starchy corm varying in size from a hazel nut to a filbert, and consisting of two halves which seem to be respectively the old and young corm, and which enclose between them very young flower buds. They have a bitter taste but no odour, and appear to correspond with the description of the bitter hermodactyle mentioned in the ‘ Pharmacopoeia of India,’ p. 246. This plant is often found cultivated in gardens in Japan, and flowers in June. The corm is the part used in medicine. The corms have some resemblance to those of the hermodactyle formerly used in medicine in this country, and, indeed, closely re¬ semble in appearance the hermodactyle described by Dr. Porter Smith in his work on ‘ The Materia Medica of China.’ The Chinese character is also identical with the Japanese one, but in Chinese is pronounced Pei-mu instead of Bai-mo. Pei-mu is used in China for rheumatism and aching joints. Whether it is used similarly in Japan I have no certain knowledge. Biakoo-boo rung (34) : — Roxburghia sessilifolia Miq. Prol. p. 143; Stemone sessilifolia, Fr. et Sav. vol. ii. pt. 1, p. 92. Syn. Hiyakubu, So mokou Zoussetz, vol. ii. fig. 55; Shia-kou-bou, Phonzou Zoufou, vol. xxviii. p. 6. The roots occur in the form of pale shrunken pieces from two to five inches long and internally present a horny appearance. They are tough' and flexible. The taste is sweetish at first and afterwards slightly bitter. In China it is credited with expectorant, antiphlo¬ gistic and vulnerary properties. This liliaceous plant grows in the islant of Kiusiu, and has ovate leaves in whorls of four, flowering in May. It is furnished with numerous tubercular roots, which form the drug used in medicine. The Japanese name is probably given in allusion to the number of these tubercul.es, Biakoo meaning a hun¬ dred, boo, parts, and hung, root. The Japanese character for the name is the same as the Chinese character translated Peh-pu by Dr. Porter Smith in his ‘ Chinese Materia Medica,’ and referred by him to Melanthium {]). The specimen in his collection is also identical in appearance with the Japanese drug. Biak-yitz (12) : —Atractylis ovata, Thunb. FI. Jap. p. 306. Syn. Biyaku jutsu, So mokou Zoussetz, vol. xv. fig. 49 ; Biakou sitsou, Phonzou Zoufou, vol. iv. p. 25, 26; Ikera, Fr. et Sav., vol. i. p. 256. The root of Biak-yitz occurs in pale brown knotty pieces, irregular in shape and slightly bent or twisted, about one inch long and half an inch in diameter. Internally it is whitish and speckled with yellowish brown dots, which under a lens are seen to contain an oily and resinous looking matter, which in another species (. A . lancea, Thunb.), according to Hanbury (‘ Science Papers,’ p. 255), is not removed by water, alcohol or ether. According to a writer in New Remedies, January 1877, and quoted in the Pharmaceutical Journal ,* “ Biaku juszu” is much used, as well as the root of Sad juzu or So jutsu ( Atractylis lancea), as an anti¬ febrile remedy in Japan. In China it is used as a tonic, stimulant, diaphoretic and diuretic. The Japanese name signifies, biak, white, yitz or jutsu, atractylis, and is possibly given in allusion to the pale under-surface of the leaves, since the flowers are red. The plant appears to have somewhat the habit of the Serratula tinctoria of this country. It grows in damp places by waysides, and flowers in October. The root is the part used in medicine. The drug mentioned under Atractylodes alba, in Dr. Porter Smith’s ‘ Chinese Materia Medica ’ has the same written character for which Peh-shuh (white shuh) is given as the equivalent sound. His specimens of the root are evidently those of a nearly allied, but different species, being almost globular, and of a more fragrant and slightly different odour. Several species of this genus appear to be used in China under the name of “ Shuh.” Boo rung (42) -.— Eulalia Japonica, Tim. ; To eiwa, Ito raja, raja, Miq. Prol. p. 177 ; Obanna, Sussuri, Thunb. FI. Jap. p. 42; Fuku, Tsirusits, Tsirube, Sasadsitz, Sasa. Syn. Meguri, Koempf. Amcen. p. 899, Fr. et Sav. vol. ii. p. 182. Boo kung consists of very small pieces, much re- * Yol. vii., [3], p. 675. July 5, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 5 sembling in general appearance the Triticum repens of English pharmacies, but the pieces rarely exceed a quarter of an inch in length. The taste is slightly sweet; the odour scarcely any. According to Dr. Porter Smith, Boo kung, or as the Chinese pronounce it Mau-ken — for the written character is the same in both languages — is a generic name for the roots of grasses and sedges. He refers the Chinese drug to Saccharum spicatum, which is also known in Japan under the name of Boo and Tsubanna according to Thunberg. This grass is not unfrequent in damp copses in various parts of Japan, and flowers in August. Biak-mong-dau . Ker.). (28) : — ( Ophiopogon J aponicus, Syn. Jano hige, So mokou Zoussetz, vol. vi, fig. 45, under Fluggea Japonica , Kunth., Jamma sob, Jawrang; Thunb. FI. Jap. p. 139; under Convallaria Japonica, L.; Mondo, Biakfmondo, Riuno Fige, Kcempf. Amoen. Exot. p. 823 and fig. p. 824 ; Mih-mun'-tung, Hanbury ‘ Science Papers/ p. 256, with fig. of tubercules ; Djia- no-shige, Fr. et Sav. vol. ii. pt. 1, p. 85. The tubercules which form the drug are about two- thirds of an inch in length and one-eighth of an inch in diameter, of a yellowish- white colour and have a central thread running through them. They evi¬ dently consist of dilatations of the cortieal portion of the rootlets, the central thread being the meditullium. The taste is sweetish. In China the drug is considered to be a pectoral and probably answers the same purpose in Japan. The plant yielding these tubercules is common in uncultivated places in Japan, flowering in October or November. There are several varieties of the plant, var. genuinus being small, and vars. umbrosus and Wallichianus larger plants. Kcempfer also alludes to another species growing near Satsuma, which has larger roots and is called Temondo. In the S6 mokou Zoussetz, both Ophiopogon spicatus and 0. Japonicus, (Fluggea Japonica ) are described as “Mong dau” according to Mr. Takemura, but 0. spicatus is Called large and 0. Japonicus small “Mong- dau.” The Chinese character for Men-tung is exactly the same as the Japanese for Mong-dau. The Japanese specimens are, however, smaller than those from China. The name mong-dau means literally mong, gate, dau , winter, probably on account of the plant flowering at the commencement of winter, and biak, white, in allusion to the white flowers. Tsiku-setz nin-jin (27) : — Aralia edulis, Sieb.(?) Syn. Udo, Do-tooki, Sieb. et Zucc. p. 57 ; Doku quatz, Dosjen, Koempf. Amoen. p. 826 ; Aralia cordata , Thunb. (p. 127) F. et Sav. vol. i. p. 191. In external appearance and size this drug bears a strong resemblance to the rhizome of Polygonatum officinale (Solomon’s Seal) ; the disc-like scars left by the aerial stems are, however, arranged in a some¬ what spiral manner, and are rarely more than half an inch apart. The transverse section of the root is of a dirty white colour, horny consistence, and is marked near the circumference with a ring of linear, loosely packed, radiating, vascular bundles. The taste is bitter. The rhizome has no distinctive odour. The Japanese name, according to Mr. Takemura, means bamboo-knotted-ginseng, tsiku meaning bamboo, setz a knot or joint, and nin-jin ginseng, or in other words a root similar to ginseng, but having scars like those of the bamboo rhizome. The above identification is given with uncertainty, as I have not been able to obtain either authenticated specimens of the root of Aralia edulis or a description of it. It is said to be often cultivated in Japan, and is also found wild, flowering in October. When young it is called sika, when older udo, and when mature dosjen, according to Koempf er. (To be continued). COPAIBIC ACID.* BY WARREN B. RUSH, PH. G. In preparing copaibic acid the volatile oil must first be removed, which is usually done by distillation with steam. The oil is, however, much more readily separated on a small scale by one of the following processes : First, by dissolving ten parts of copaiba in ten parts of benzin, adding an equal part of caustic soda solution, sp. gr. T30, and agitating well ; or, secondly, by mixing ten parts of copaiba, ten parts of alcohol and four parts of soda solution, when the mixture will separate into three layers. A third and most economical way for separating the volatile oil is to shake together three parts of the soda solution with one of the copaiba. After separation, pour off the volatile oil, decant the alkali solution, pass a stream of water over the resin, to wash off adhering particles of alkali, and let it dry. Next, dissolve the resins in benzin, and agitate the solution with very diluted hydrochloric acid until the aqueous liquid remains slightly acid to litmus. Let the mixture rest until the resin and water have separated, decant the water and evaporate the benzin solution to a thick syrupy mass, and let cool. The same resins are thus obtained which are left on the distillation of the volatile oil. I have observed that if the percentage of oil is below 55 then the oil does not separate, there being sufficient resin to hold the volatile oil combined, and in this con¬ dition some of the later is oxidized or altered. It may be separated from the resin by dissolving in benzin or alcohol and treating as above. The resinous residue left after the separation of the oil contains an acid, a neutral and a soft resin. The following are among the processes for the isol%tion of the different resins of copaiba : Liquefy the resins by the heat of a water-bath, pour into about twice the weight of petroleum benzin, stir until dissolved, filter, and let evaporate spontaneously. A few particles will remain on the filter, consisting of the usual impurities. Warm the residue left by evaporation over a water-bath and pour it into three times its quantity of alcohol ; or heat the alcohol to boiling, mix thoroughly, and while hot filter. The portion left on the filter is the neutral resin. Set the filtrate aside for several days to crystallize. Treat a portion of the neutral resin with hot alcohol, and if it colours the alcohol there is left behind some of the acid resin, and this maybe obtained by treatment with hot al¬ cohol and adding the filtrate to the first. The neutral resin is a yellowish powder, without taste or odour, neutral to test paper; it softens in alcohol and is soluble in ten times its weight of hot chloroform. After crystals have formed in the alcoholic liquid, filter, and dry on the filter paper under glass. On distill¬ ing off the alcohol from the filtrate, the soft resin is left behind. Copaibic acid may also be obtained from the resin by dissolving it in benzin, filtering and evaporating. The residue is heated to 200° F., dissolved in pure naphtha, filtered while warm and set asid to crystallize, after which the crystals are dried under glass. Of the other processes which have been tried, the following deserve to be briefly mentioned. Dissolve the oleo-resin in caustic ammonia (sp. gr. 95), * From the American Journal of Pharma June, 1879 G THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 5, 1ST?. and expose this in a shallow dish at a temperature below 63° F., until hardened ; then dissolve in wood naphtha, crystallize and filter. Expose copaiva to the air in shallow dishes until it has become hard and brittle, dissolve it in ammonia water and leave to evaporate in a cool place ; then dissolve in hot alcohol, filter and set aside to crystal¬ lize. Dissolve the resins left after the distillation of volatile oil in caustic ammonia, let evaporate, disssolve in hot alcohol, filter and set aside to crystallize. The alcohol may be partly recovered in these different processes by distillation. The crystals cannot be easily obtained without the previous separation of the volatile oil, the acid being soluble in fixed and volatile oils. Doubtless the copaiva yielding the largest amount of resins will produce the most acid. Copaibic acid forms soft prismatic crystals, which are soluble in strong alcohol, ether, fixed and volatile oils. Its alcoholic solution reddens litmus, is not precipitated by potasia or soda, yields 'with an alcoholic solution of acetate of lead a crystalline precipitate ; but, on adding it to an alcoholic solution of nitrate of silver, no pre¬ cipitate is occasioned until a little ammonia is added. A white crystalline powder falls, which is with difficulty soluble in alcohol but readily soluble in ammonia. THE ALKALOID OF MIO-MIO (BACCHAEIS CORIDIFOLIA).* BY PEDRO N. ARATA. The Mio-Mio ( Bacchciris coridifolia , Lam.) is a Com¬ posite plant abundant in the Banda Oriental del Uruguay, the Argentine Republic and Brazil. The notoriety which this plant has acquired in these countries is due to the toxic action which it exercises upon the animal organism, it being the cause of considerable losses of sheep and cattle to the farmers, and it is the more dreaded because the animals confound it with the healthy pasture among which it grows. The author reports that he has obtained from this plant an alkaloid in sufficient quantity to allow of the following description. The dry powdered plant was boiled with distilled water in a porcelain capsule and the water separated by decantation, the operation being repeated until the material was completely exhausted. The united liquors were filtered and evaporated, at first over a fire, and afterwards in a water-bath, to the consistence of an ex¬ tract, which was mixed with double its weight of a mixture of caustic lime and magnesia and the evaporation was then continued to dryness. The product was pul¬ verized and digested for forty-eight hours with amylic alcohol in a closed vessel with frequent agitation, then thrown on a filter ; the filtrate of amylic alcohol upon evaporation left the alkaloid in a crystalline form. Amylic alcohol is preferable to ether in this operation as it dissolves the alkaloid very readily, especially with heat, and a saturated solution deposits a very voluminous crystalline mass. Under the microscope the crystals appear as long delicate needles, sometimes united and radiating from a common centre so as to form stars. Water dissolves the alkaloid sparingly ; ether and alcohol dissolve it with more facility, but it is not very soluble in them ; the best solvent is amylic alcohol. Dissolved in water the alkaloid gives neither an alkaline nor an acid reaction, it showing no change of colour with vegetable reagents. It dissolves with greater facility in boiling water to which some drops of acetic acid have been added. The acetate that results is fairly soluble in boiling water, but upon cooling the liquid becomes turbid as if concentrated, the turbidity disappearing upon the addition of more water. The solution of the acetate gave the following re- * Abstract of a paper in the ‘ Annales de la Sociedad Cientifica Argentina,’ vol. iv., p. 34. actions With sodium phosphomolybdate or phospho- molybdic acid a greenish yellow precipitate, disappearing when heated and reappearing on cooling ; with potassium iodohydrargyrate, a yellowish white precipitate ; with the double iodide of cadmium and potassium, a light crystalline precipitate ; with potassium platinocyanide, a very marked turbidity ; with platinum chloride, a light yellow precipitate, disappearing when heated and reap¬ pearing on cooling ; with gold chloride or picric acid, a yellowish precipitate ; with potassium iodoiodide or sodium phosphoantimoniate, a reddish yellow precipitate ; with phosphotungstic acid or mercury bichloride, a white precipitate; with potassium ferrocyanide, an abundant white precipitate ; with potassium ferricyanide, a dark green coloration when heated ; with sodium nitro- prussiate, a coloration, and with sodium phosphoanti¬ moniate, potassium sulphocyanide or potassium bichromate, no change. The author considers that the foregoing reactions demonstrate that this substance is an alkaloid and he has named it “ baccarina.” Some physiological experiments made upon a sparrow have proved that baccarina exercises a toxic action, and further investigation in this direction has been undertaken by Professor Pirovano. Senor Arato promises to study the elementary composition of the alkaloid and its salts with a fresh quantity of material. THE DISCOVERY OF MINERAL WAX, OZOCERITE, IN UTAH.* BY PROFESSOR J. S. NEWBERRY. I have obtained some of the recently-discovered ozocerite in Salt Lake City from Professor J. E. Clayton, to whom also I am chiefly indebted for such information as I have in regard to its place and manner of occurrence. He writes me as follows : — “ The geographical position of the ozocerite deposits is in the Wahsatch Range, on the head waters of the Spanish Fork, east from the South End of Utah Lake. The material has been found saturating beds of brown and bluish shales, probably of Tertiary age, and in masses of various dimensions, more or less mingled with clay. These shales extend from the San Pete valley in a north-north-east direction for a distance of fifty or sixty miles, and the width of the area or basin which they occupy is at the middle point about twenty miles. The shale beds richest in paraffin vary in thickness from twenty to sixty feet, but there is no considerable accumulation of that substance on the surface, nor would this be possible, as it would be destroyed by the autumnal fires which sweep the country. I examined portions of this region two years ago for coal, and found in the oil shales a few thin seams, and saw the wax-like exudation in several places, but only in small quantity.” Other parties in Salt Lake informed me that the paraffin itself is sometimes twenty feet thick, and that the quantity is enormous ; but Professor Clayton says that such statements are not authorized by any facts which have come under his observation. In the above remarks I have called the earth wax of Utah ozocerite. As it has been stated to be zietrisikite, I may s ty that on my return from the West, my son and assistant, Spencer B. Newberry, made a series of careful experiments in my laboratory of these hydrocarbons, and with authentic specimens which I have received directly from Gallicia. He found that it had a melting point of 6U5° C., that it was completely soluble in a large volume of boiling ether, and that boiling alcohol extracted from it twenty per cent, of a white wax-like substance. It seems, therefore, to be certainly ozocerite and not zietri¬ sikite, the latter melting at 90° C., and being insoluble in ether. From t ne a mencan Journal of /Science and Art, April, 1879, p. 340. Reprinted from the American Journal of Pharmacy, June, 1879. July 5, 1879. ] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 7 Sfa jhanmaqulual Jaapal. - » . . SATURDAY, JULY 5, 1879. Communications for the Editorial department of this Journal , books for review , etc., should be addressed to the Editor, 17, Bloomsbury Square. Instructions from Members and Associates respecting the transmission of the Journal should be sent to Mr. Elias Bremridge, Secretary , 17, Bloomsbury Square, W.C. A dvertisements , and payments for Copies of the Journal, Messrs. Churchill, New Burlington Street , London , W. Envelopes indorsed “ Pharm. JournP THE CONFERENCE MEETING. Within a few weeks the British Pharmaceutical Conference — guided as usual by the British Asso¬ ciation in the selection of a locality for the annual gathering — will again visit Yorkshire, as our readers will be reminded by the report which appears in the present number of the Journal of the proceedings of the Executive Committee last Wednesday. Those who have experience of the cordial reception the members of the Conference met with in Bradford will not need to be assured an equally hearty welcome probably awaits them in Sheffield, and those who have not had the experience will have heard quite enough of the agreeable nature of the first meeting in York¬ shire to make them anxious to participate in the enjoyment of the one now about to be held. For these reasons we anticipate that the desire to attend the Conference will be very general, and con¬ sidering the central situation of Sheffield, as well as the marked prominence of Yorkshire pharmacists in the endeavour to advance the interests of the body to which they belong, we venture to think these com¬ bined inducements and the prospect of being able to combine benefit with pleasure, will outweigh even the depressing influence of “ bad times ” and 11 bad weather” with such effect as to make the meeting at Sheffield one the most largely attended that has been known since the Conference has been in existence. There is one circumstance of no small moment to the attendants at such a gathering as the Pharma- maceutical Conference which seemed, up to within the last few days, to furnish ground for apprehension. It is a somewhat exasperating thing to find, after having responded to the kindly invitation of friends to pay a visit to their town, that the local Boniface, in the shape either of an over keen individual, or of an imposing Board of limited liability organization, intervenes between host and guest, holding out his cap with exorbitant demands for the payment of black mail as the sole condition upon which oppor¬ tunity for friendly intercourse will be allowed. But such things do happen sometimes, and we regret having to remember that a notable instance of the kind was furnished when the Conference last met in Yorkshire. Hotel charges multiplied fourfold to those known to be visitors, and kept at the ordinary rate for chance comers., is a form of purse- cutting that under any conditions would require more than ordinary meekness and pecuniosity to be endured, and that is, we think, especially impolitic at a time when the hotelkeepers have no reason to complain of lack of business. There was some reason to apprehend that this eminently vicious system of taking undue advantage of a full demand for hotel accommodation would be put in practice at Sheffield and that it would have had the effect of deterring many from going there. But we are glad to learn that arrangements have been made to prevent the rapacity of hotelkeepers being an obstacle to intending visitors. According to a communication just received from Mr. Maleham, the local secretary of the Committee for the Sheffield meeting, a reasonable scale of charges has been fixed at one or two of the hotels where a number of rooms have already been secured, and where Mr. Maleham offers to secure accommodation for members of the Conference if they will only make early application to him stating what they require. We think, therefore, this notification holds out the certainty of being able to secure a comfortable pied d terre and that we can without any risk urge upon those who are already habitues of the Con¬ ference gatherings not to omit taking advantage ot this opportunity for scientific and social intercourse, while at the same time we recommend those who have not hitherto done so to make the experiment under the favourable auspices now presented and with such fair prospect of realizing the pleasurable as well as profitable results which the President of the Sheffield Pharmaceutical and Chemical Associa¬ tion spoke of at the last annual meeting of that Association as having been experienced by himself on the occasion of his visit to Dublin last year. Sheffield is a town which is of interest in various ways in a pharmaceutical point of view. It has always taken a prominent position in pharmaceutical as well as in general politics. For some years it sent a member to 1 the Council of the Pharmaceutical Society who, though less aggressive than one of the members of Parliament who represents the borough, on a subsequent occasion led the van of the band of malcontents that came down with a stern front upon the Council to remonstrate against its supposed disregard of trade interests. It cannot, however, be said that even in that position he excited any less kindly feeling towards himself than he did while holding the position of member of the Council. But at the British Pharmaceutical Conference discussion of political questions is not permitted, and whatever may be the individual differences of opinion on such subjects between those who meet at Sheffield, we feel sure they will in no way interfere on that occasion with that friendly intercourse amongst the followers of pharmacy which it is the object of the Conference to promote. On the contrary we antici¬ pate that political war paint of all colours will be washed off for the time and that even timid conser- 8 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 5, 1879 vatives and uncompromising Tories will have no occasion to fear being subjected to the vengeance of the peculiar institution for which Sheffield is famous. Sheffield itself has but little claim to beauty, though occupying a very fine situation upon a natural amphitheatre of hills ; but it is surrounded by some of the most lovely scenery in the Kingdom, partly in Derbyshire and partly in Nottinghamshire. The tovrn is the centre of the steel trade, formerly the cutlery ware was the chief article of manufacture ; but since the introduction of the Bessemer method of producing steel, this material has been applied for armour plating of ships and other heavy purposes, and the manufacture of these products has been carried out extensively in Sheffield. In other respects the situation of Sheffield is one calculated to induce every one who can spare the time to spend a few days in visiting the immediate neighbourhood. On the east lies the district of Sherwood Forest formerly the resort “Of Robin Hood and Little John; Of Scarlet, George k Green and Much the Miller’s Son, Of Tuck the merry Friar, which many a sermon made In praise of Robin Hood, his outlaws and their trade.” Here, between Mansfield and Worksop, is the famous “ Dukery,” including Clumber and Welbeck Abbey, the seats of the Dukes of Newcastle and Portland, where interesting traces of the ancient forest are still preserved. Close by is Newstead Abbey, one of the most beautiful buildings of the kind in the country. On the west, within a few miles of Sheffield, is Chatsworth, “ the palace of the Peak,” and seat of the Duke of Devonshire, sur¬ rounded by scenery which in its way is quite unrivalled. Somewhat further west is Buxton, near the rise of the Derbyshire Wye, with the famous mineral springs that have made it a celebrated watering place, one yielding water having a tempe¬ rature of 82° F., and the other yielding cold water at a distance of not more than a foot apart. “ Unto St. Anne the fountain sacred is ; With waters hot and cold its sources rise, And in its sulphur veins there medicine lies. This cures the palsied members of the old, And cherishes the nerves grown stiff and cold. Crutches the lame unto to its brink convey, Returning, the ingrates fling them away.” This water is in both instances remarkable for its purity, clearness and transparency, and it is used both for drinking and for baths. The use of it for these purposes dates back to a very remote period. Remains of a Roman bath have been discovered, and in the middle ages the chapel of St. Anne was the re¬ sort of numerous devotees in search of health. This practice was interfered with at the time of the Re¬ formation, but in the reign of Elizabeth the Buxton waters again came into repute and caused the place tp be the resort of great numbers of nobility and gentry, who were crowded into low wooden sheds and regaled with oat cake and a viand which the hosts called mutton, but the guests suspected to be dog. The accommodation for visitors has improved since then, however, and it may be ventured upon without fear of the dog. Matlock Bath further south has in its neighbour¬ hood some of the most striking scenery in Derby¬ shire, which was described by Lord Byron as equal to anything in Greece or Switzerland. The lime¬ stone caverns and the several tors near Matlock are objects of considerable interest. The mineral springs of Matlock are less celebrated than those of Buxton and the water is chiefly used for bathing ; it is highly impregnated with carbonic acid and carbonate of lime, which is deposited when the gas escapes. Owing to this circumstance any object over which the water passes continuously in a thin layer becomes coated or incrusted with the deposited calcareous materials which are locally called petrifactions. The limestone districts of Derbyshire abound in ferns and fossil remains, as well as minerals, that afford scope for the exercise of botanical and mineral- ogical skill, and to the geologist the country presents numerous features of interest. FLOWER FARMING IN SOUTH AUSTRALIA. In a report on the Botanic Garden and Govern¬ ment Plantations of Adelaide, South Australia, for the year 1878, Dr. Schomburgk speaks favourably of the introduction of flower farming for the purposes of perfumery, but he thinks the further application of the produce in the manufacture of perfumes would be better done elsewhere than in the colony. Dr Schomburgk illustrates the importance of the matter by reference to the quantities of perfume consumed. According to him, British India and Europe consume about 150,000 gallons of handkerchief perfume yearly, and the English revenue from eau de Cologne alone is about ,£8000 a year, while the total revenue from imported perfumes is estimated at about £40,000 a year. One great perfume distillery at Cannes is said to use annually some 100,000 lbs. of acacia flowers, Acacia farnesiana, 140,000 lbs. of rose flower leaves, 32,000 lbs. of jasmine blossoms, 20,000 lbs. of tuberose, besides a great many other sweet herbs. These data will serve to show that the quantity of material used as perfume is immense, and that in the genial climate of South Australia the production of the raw material for extracting the fragrant essential oils is likely to be a successful enterprise. A MARK OF BARBARISM. According to a writer in the Chicago Pharmacist , the United States Government having recently applied to the German Government for information as to the number of patent medicines and the extent to which they were sold in Germany, a polite reply ' was sent that as that country was now civilized patent medicines had no existence in it. July 5, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 9 Stations 0j[ tlje ||arntaptical MEETING OE THE COUNCIL. Wednesday, July 2, 1879. MR. GEORGE WEBB SANDFORD, PRESIDENT. MR. GEORGE FREDERICK SCHACHT, VICE-PRESIDENT. Present — Messrs. Atkins, Bottle, Churchill, Frazer, Gostling, Greenish, Hainpson, Hills, Richardson, Rim- mington, Robbins, Savage, Shaw, Sjmes, Williams and Woolley. The minutes of the previous meeting were read and confirmed. Weights and Measures Act. The President in reference to the Weights and Measures Act, said it had occurred to him whether the half-scruple had not been intended to be recognized under the half-drachm. Looking at the table adopted, it would be found that the words used were 1J scruple or half- drachm and he thought probably the half-scruple was intended to be authorized. The Inaugural Address in October. The President read a letter from Dr. Tilden, agreeing to deliver the Inaugural Address to the students in Octo¬ ber next, in accordance with a resolution of Council passed last month. The name of Mr. Rimmington was added to the Benevolent Fund Committee, having been accidentally omitted. The Sale of Food and Drugs Bill. The President drew attention to this Bill now before the House of Lords, where it had been read a first time. He said there was nothing in it specially affecting chemists and druggists, but he found a provision that prosecutions should in all cases be instituted within a reasonable time, in the cases of perishable articles not exceeding twenty-eight days. Who was to be the judge of what was a reasonable time, he did not know. Mr. Woolley asked if it would not be possible to in¬ troduce a clause providing that a reasonable time should be allowed for the return of summonses under this Act. He had known of a case where a summons was served on Saturday and heard in court on the Monday. If assist¬ ance had not been at hand, and great efforts used ta get evidence, the defendant would probably have been con¬ victed. The President said if it was considered desirable, an effort might be made to insert some provision of the kind referred to . Mr. Rimmington said it would be easy in such cases to obtain an adjournment. Mr. Robbins said it must be the fault of the summon¬ ing officer. Mr. Savage said no doubt in such a case an adjourn¬ ment would be obtained on asking, but it might entail expense on the defendant. After some further conversation it was unanimously resolved, on the motion of Mr. Woolley, that an en¬ deavour be made to obtain the insertion of a clause providing that no summons under the Act should be returnable in less than three days. At a subsequent stage of the proceedings — The President said he found that the discussion on this point might have been saved if the Bill had been looked at more carefully, for the last line stated that no summons should be returnable in less than seven days. The New Bye-Laws. A communication was read from the Privy Council signifying that the Privy Council had approved the new bye-laws recently passed by the Society. The following being duly registered as Pharmaceutical Chemists were respectively granted a diploma stamped with the seal of the Society : — Gibbs, Robert Darton. Howard, George William. Hoyle, Richard Ashworth. Mann, George Frederick. Elections. MEMBERS. Pharmaceutical Chemists. The following, having passed the Major examination and tendered their subscriptions for the current year, were elected “ Members ” of the Society: — Gibbs, Robert Darton . Wednesbury. Howard, George William ...Tunbridge Wells. Hoyle, Richard Ashworth ...Rawtenstall. Mann, George Frederick . Wells, Norfolk. Chemists and Druggists. Butterfield, William . . Blackburn. Fox, Alfred Russell . Sheffield. ASSOCIATES IN BUSINESS. The following, having passed the respective examina¬ tions, being in business on their own account, and having tendered their subscriptions for the current year, were elected “ Associates in Business ” of the Society : — Minor. Rouse, Fi-ederick William ...Clapliam. Modified. Evelyn, William Francis . Truro. ASSOCIATES. The following, having passed the Minor examination and tendered their subscriptions for the current year, or paid as Apprentices or Students, were elected “Asso¬ ciates” of the Society : — Bucher, William Henry . Crediton. Cherrington, Geo. WiddowsonLondon. Dobson, George Turner . Holsworth}^. Gamble, Arthur Gompertz ...Grantham. Gordelier, Frank Heward ...Sittingbourne. Holmes, William Albert . Kendal. Hugill, Arthur Major . London. Isaac, John Percy . London. Jelley, George William . Coventry. Jenner, William Edward ...Sandgate. Kirk, William Peele . Retford. Milner, Thomas . Thirsk. Richardson, William Henry. .Boston Spa. Scammell, Luther Robert ...Adelaide. Smith, Frederick Adolphus... Macclesfield. Thomas, John . Aberystwith. Williams, James Edward ...Louth. Williams, Thomas Henry ...Plymouth. APPRENTICES OR STUDENTS. The following, having passed the Preliminary examina¬ tion and tendered their subscriptions for the current year, were elected “ Apprentices or Students ” of the Society : — Barber, William . Shefford. Barton, Francis . Guernsey. Cooper, William Ecklee . Upton-on-Severn. Cox, Frederick John . Newark. Harrison, Peter Webster ...St. Helens. Hope, Arthur Peach . Uppingham. Lewis, Jonas Henry . London. Mackenzie, Donald . Dingwall. Pope, Albert Harry . Southport. Robinson, George Duncan R.York. Taylor, James . Bayswater. Watson, William Malcolm ...Southport. Willis, Joseph Danin gton ...Northampton. . 10 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS [iuly 5, 1879. Several persons were restored to their former status in the Society upon payment of the current year’s subscrip¬ tion and a fine. The names of the following persons, who have severally made the required declarations and paid a fine of one guinea were restored to the Register of Chemists and Druggists : William Henry Fisher, 37, Beresford Road, London, N. Alexander Scott Hill, 68, Devonshire Road, Hollo¬ way, London, N. Charles Edward Mitchell, 31, Cottenham Road, Holloway, London, N. Charles Wilkinson, 4, Raglan Street, Coventry. Additions to the Register. The Secretary reported that Charles Robert Fenn, 83, Regency Street, London, S.W. and Augustus Thomas Isaac, Orange, New South Wales, having made statutory declarations that they were in business before the passing of the Pharmacy Act, 1868, and these declarations having been duly supported by medical practitioners, their names had been placed on the Register. Payment of Subscriptions. Mr. Greenish drew attention to the case of a member who had handed his subscription to a traveller in April last, but the latter forgot to tender it to the Secretary until May 1, when the Secretary said he was unable to receive it, as the gentleman’s name had been struck off the list of members. The President said such cases sometimes occurred in the country, where the subscriptions were paid to the local secretaries in time, but were not forwarded to the office. In such cases he apprehended, the local secre¬ taries being representatives of the Society, the members were entitled to be retained on the list. Mr. Bottle said in the case before the Council the traveller was not its agent and he could not see how the bye-law could be departed from. The only thing that could be done would be to restore the member on pay¬ ment of the minimum fine. Mr. Greenish said he believed the traveller through whose forgetfulness the difficulty arose was willing to pay the fine himself, but the member would not allow it. Mr. Symes suggested that in the case of country mem¬ bers it would be much better that they should forward their subscriptions direct to the office, and be entitled to deduct the cost of the post office order. Mr. Atkins thought the gentleman in question had a grievance. He had complied in spirit, if not in letter, with the regulations. Mr. Schacht asked if a post office order received on May 1 would be taken. The Secretary said if the envelope 'bore the postmark of April 30, it would be received, being taken as a pay¬ ment in April. It was stated continually in the Journal that April 30 was the last day on which subscriptions could be received. Mr. Hampson thought the Secretary had cut the ground from under his own feet. If he received a post office order on May 1, why should not he receive cash, which was better? Mr. Churchill thought the office was made for the convenience of subscribers, not the subscribers for the convenience of the office. He would move that the gen¬ tleman’s name be restored without a fine. The Secretary said he would rather pay the fine himself. Mr. Robbins thought this case should be dealt with the same as that of a person who sent a post office order. The Secretary read the resolution under which he had acted for several years past, under which all sub* criptions not paid in March were applied for directly by himself, notice thereof being sent to the local secre¬ taries. Mr. Richardson thought the Council must support the authority of its officers. The line must be drawn somewhere. Mr. Williams said the officers must act according to the bye-laws. The Assistant Secretary explained that subscrip¬ tions that came to hand after the office was opened on the 1st of May were not received. Remittances found in the letter-box before the office opened on that day were received. Mr. Frazer said as soon as a post office order was issued, the money became virtually the property of the Society. There was a wide difference between that and paying money to an outsider who might do anything he liked with it. Mr. Bottle suggested that a half -guinea, which the gentlemen in question had sent at the same time as a sub¬ scription to the Benvolent Fund, be received as the fine. The bye-laws did not say to what the fine should be applied. This recommendation did not meet with any approval. Mr. Greenish said the gentleman felt he had a griev¬ ance, and he himself did think it was a pity that, under the circumstances, the money had not been received. The Vice-President also thought the rules had been carried out with greater strictness than necessary. He understood that cheques were received and he did not see that the agency of a banker was different to that of any other person. The President said there was no doubt that this case was clearly within the rules, but he did not think the good of the Society was promoted by over strictness in such a matter. With regard to the question of local secretaries receiving subscriptions he hoped the Council would agree to a resolution proposed by M r. Greenish : — “That the regulations regarding the closing of the Registrar’s accounts with local secretaries, so far as regards annual subscriptions being paid before the 1st of JMay, be referred to the Finance Committee for consideration and report.” Mr. Williams suggested that the resolution should be enlarged, and that the Committee should consider the whole question of local secretaries collecting subscrip¬ tions at all. Mr. Rimmington thought it would be a great incon¬ venience to country members if local secretaries were not empowered to collect subscriptions. Mr. Savage said he should not object to the scope of the inquiry being enlarged, but he agreed with Mr. Rim¬ mington that it would be a disadvantage to the Society to alter the regulation. The President said the mover had consented to the addition of the words “ and to consider the desirability of relieving local secretaries from the duty of receiving subscriptions.” The motion was carried unanimously. Reports of Committees. FINANCE. The report of this Committee was received and adopted, and various accounts ordered to be paid. The Vice-President drew attention to the increase in the gas account as compared with the same quarter last year. The Committee was unable to explain how it occurred, and he should like to know if any experiment had been made with a view to test if any leak existed ; for instance, if the state of the meter had been carefully taken at night and in the morning, all burners having been carefully turned out in the meantime. The Secretary said that Professor Redwood, himself, and the gasfitter were now carefully investigating the matter, and he hoped to be able to place some statistics before the next meeting of the Committee. Several other suggestions were made with regard to the mode of examining and checking the accounts. July 5, 1679.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 11 BENEVOLENT FUND. The report of this Committee included recommenda¬ tions of the following grants : — £15 to a member of the Society, in business for fifteen years, but latterly suffering from sickness. £10 to a member of the Society, aged 69, having failed in business and being unable to obtain a situation. £5 to a registered chemist and druggist (female), who has had three previous grants of £10 each. £10 to the widow of a late member. Applicant has had five previous grants. £15 to the widow of a registered chemist and druggist, having three children dependent on her. £10 to the widow of a registered chemist and druggist. £10 to a former associate of the Society suffering fi'om ill-health. £10 to the orphan boys of a registered chemist and druggist. £5 to the widow of a registered chemist and druggist. £5 to the widow of a late member who had £10 in October last. In two other cases the Committee made no recom¬ mendations, in one instance a grant having been made very recently. Another grant had also been recommended, but the Secretary stated that he had that morning re¬ ceived information of the death of applicant. An application had been received from the managers of the establishment in Belgium, where an orphan child had been placed, for some years past, asking if the annual payment would be renewed, as otherwise the child must be returned to her mother. The Secretary was desired to make further inquiries. Mr. Robbins moved that in the case of the applicant who had died, the amount of the grant should be handed over to the widow. The President thought the Council should wait and see if application were made. It was not competent to the Council to make a grant to persons on whose behalf no application had been made. The report and recommendations of the Committee were received and adopted. LIBRART, MUSEUM AND LABORATORY. The report of this Committee included the usua^ report from the Librarian, to the following effect : — Attendance during the day : highest, 29, lowest, 9, average, 21; Evening, highest, 19, lowest, 8, average, 12. Circulation of books : town, 150 ; country, 66 ; carriage paid, £1 7s. 7\d. He had also reported the following donations to the Library : — Analytical Index to the Records known as the Remembrancia, 1579-1664 ; London, 1878. From the Corporation of the City of London. Institute of Chemistry of Great Britain and Ireland, Register of Fellow's and Associates, 1879. From the Institute. Berzelius (I. J.), Traite de Chimie, trad, par A. J. L. Jourdan [et M. Esslinger], 1829-33, 8 vols. Whitlaw (C.), New Medical Discoveries, with a Defence of the Linnean Doctrine, and a Trans¬ lation of his Vegetable Materia Medica, 1829, 2 vols. New London Dispensatory, containing a translation of the Pharmacopoeia Londinensis, etc., 2 ed. ; also a translation of Magendie’s Formulary, by T. Cox and C. W. Gregory, 1835, 2 vols. Liebig (J. v.), Organic Chemistry in its Applications to Agriculture and Physiology, edited by L. Play¬ fair, 1840. Journal de Pharmacie, 1835-6, sundry numbers. From the Rev. C. E. Drew. Muter (J.), Introduction to Pharmaceutical and Medical Chemistry, 2 ed., 1879 ; Introduction to Analytical Chemistry, 2 ed., 1878. From the Author. Tommasi (D.), Riduzione del Cloruro di Argento e del Cloruro Ferrico, 1878; Riduzione del Cloralio, 1878 ; Azione dei Raggi Solari sui Composti Aloidi d’ Argento, 1878. Frtm the Author. Victorian Chemists’ Assistants’ Association, Sixth Annual Report, Rules, Catalogue of Library and Museum, etc., 1879. From the Association. Squibb (E. R.), Notes on the Estimation of Urea, and on the Revision of the United States Pharma¬ copoeia in 1880, 1879 ; Fluid Extracts by Reper¬ colation, 1879; Proposed Legislation on the Adulteration of Food and Medicine, etc., 1879. From the Author. The Committee recommended that the usual letters of thanks be forwarded. The Committee recommended the purchase of the following books for the library ; — General Fund Wurtz (Ad.), Dictionnaire de Chimie, latest ed. Buchoz (P.), Herbier de la Chine, 1788-9. Hanbury Fund Bentham (G.), Flora Hongkongensis, 1861. Griesbach (A.), Flora of the British West India Islands, 1864. The Curator had reported the attendance in the Museum to have been as follows : — During the day, average, 10 ; evening, average, 6. He had also reported the following donations to the Museum : — Fresh Specimens of Biennial Henbane, from Mr. A. P. Balk will. Specimens of the Seed of Psoralea corylifolia, from India, from Messrs. Corbyn, Stacey and Co. A dried Ostrich Stomach, as used by the South American Iudiansfor indigestion, from Dr. Symes. Specimens of Queensland Sassafras Bark, Queens¬ land Sandal Wood (Eremophila Mitchclli), the Stem of Piper Novce-Hollanclice, the bark of a species of Achras, known as sweet bark from Queensland, and a fine Fruit of the Trinidad Cocoa Tree, from Mr. Thomas Christy. Three remarkably fine crystals of Codeia, from Messrs. T. and H. Smith and Co. A new variety of Salep, the root of West Indian Ipecacuanha (Asclepias Ourassavica), false Sarsa¬ parilla from St. Vincent, and specimens of natur¬ ally crystallized Realgar, from Mons. C. Chantre. The last specimen was obtained from a crack in the earth which served as a vent to a burning coal mine called Ricamarie, near St. Etienne. The Curator had also reported that he had received from Dr. O. Hesse, specimens of the alkaloids to illustrate his recent paper in the Pharmaceutical Journal. The Committee recommended that the usual letters of thanks be forwarded. The Curator had reported that he had forwarded nine duplicate specimens to the Society’s Museum in Edin¬ burgh. He had also reported that nineteen duplicate specimens bad been forwarded to the Leeds Chemists’ Associa¬ tion. Professors Redwood, Bentley and Attfield had reported that the progress of their respective classses was satis¬ factory. Professor Bentley had reported that his class had in¬ creased 25 per cent, over 1878. The Committee recommended the purchase of the collection of Malayan specimens of materia medica offered by Mr. Collins. The report and recommendations of the Committee were received and adopted. Mr. Shaw said the Association at Liverpool wras now I’e-arranging the museum, and wTould be very much obliged by the Council granting a set of labels, which he understood were in possession of the Society. The President said he had no doubt that if Mr. Shaw would specify what was wanted, and send an application 12 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 5, 1879. to the Committee, which met next week, it would be acceded to. HOUSE. This Committee recommended that a memorial be addressed to the Board of Works Avith a \Tiew to getting the roadway in Great Russell Street relaid with Avood. Also some other minor matters in connection with the house. Mr. Hills asked if any reply had been received to the memorial. The President said it had been ascertained that it Avould be useless to make any application of the sort before Michaelmas; but if one Avere sent in then, there might be a chance of its being acceded to. The report and recommendations Avere received and adopted. GENERAL PURPOSES. The report of this Committee included the usual letter from the Solicitor giving information as to the progress of cases A\Thich had been placed in his hands. In one case, the defendant, Mr. Mumby, had paid the penalty of £5 and costs. The appeal in the „case of the Society v. The London and Provincial Supply Association, Limited, A\ras not likely to come on before No\rember. A communication Avas read from Mr. James GalloAvay, Great Horton, authorizing the erasure of his name from the register. In tAVo cases it Avas recommended that the Solicitor be instructed to commence proceedings, one of the cases having been a long time under consideration, and with regard to which a great deal of correspondence has taken place. The President moved “ That the Council go into Committee to consider the various items in the report.” Mr. Symes had no objection, but thought it would be well if some reference Avere made in the report to the subjects on which the Council Avent into Committee, so that members might see that the matters referred to Avere being considered. After some further conversation on this subject, it Avas unanimously resolved to go into Committee to consider certain cases of alleged breaches of the Pharmacy Act. The various cases having been discussed in detail, the Council resumed, and the report and recommendations of the Committee Avere adopted unanimously. It Avas moved by Mr. Williams, seconded by Mr. Gostling, and carried unanimously, that a certain firm of solicitors, Avho had made inquiry as to the form of appeal from a decision of the Registrar, be informed that any such appeal must be made in writing. Appointment op Professors and Curator for the ensuing Year. Professor Redwood was reappointed Professor of Chemistry and Pharmacy for the ensuing year. Professor Bentley Avas reappointed Professor of Botany and Materia Medica for the ensuing year. Professor Attfield was reappointed Professor of Prac¬ tical Chemistry for the ensuing year. Mr. Holmes Avas reappointed Curator of the Society’s Museum for the ensuing year. List of Local Secretaries, 1879-80.* The following Avere proposed as Local Secretaries for the ensuing year : — Towns eligible. Names of persons appointed. Aberdare . Thomas, Watkin Jones. Aberdeen . . Davidson, Charles. Abergele . . Hannah, John. Aberystwith . Davies, John Hugh. Abingdon . Smith, William. '* Local Secretaries are apj minted in all toAvns in Great Britain which return a Member or Members to Parliament, and in such other towns as contain not less than three Members of the Society or Associates in Business. Towns eligible. Accrington . Altrincham . . Andover . Arbroath . Ashbourne . Ashby-de-la-Zouch . . Ashton-under-Lyne .. Aylesbury . Ayr . Banbury . Banff . Bangor . . . . Barnsley . Barnstaple . Barrow-in-Eurness .. Bath . Beaumaris . Bedford . Belper . Berwick . Beverley . Bewdley . Birkenhead . Birmingham . Bishop Auckland . Blackburn . Blackpool . . . Blandford . Bodmin . Bolton . Boston . Bournemouth . Bradford (Yorkshire) Brecon . Bridgnorth . Bridlington . Bridport . Brighton . Bristol . Buckingham . Burnley . Burslem . Bury . Bury St. Edmunds .. Buxton . . Caine . Cambridge . Canterbury . Cardiff . Cardigan . Carlisle . Carmarthen . . . Carnarvon Chatham . Chelmsford . . Cheltenham . Chester . Chesterfield . Chichester . Chippenham . Christchurch . Cirencester . . Clitheroe . . Coclcermouth . Colchester . . Congleton . Coventry . Crewe . , Cricklade . Croydon . . Darlington . Deal . . Denbigh . Derby . Devizes . . . Names of persons appointed. .Sprake, David Lewis. .Hughes, EdAvard. .Gould, Robert George. .Shield, George. .Bradley, Edwin Silvester. .Johnson, Edvvin Eli. .Bostock, William. .Turner, John. Ball, George Vincent. Ellis, Bartlett. Baker, Henry Villars. Badger, Alfred. Goss, Samuel. Steel, Thomas. Connnans, Robert Dyer. Cuthbert, John M. Ashton, John. Carr, William Graham. Hobson, Charles. Nicholson, Henry. Southall, William. .Leigh, John James. Pickup, Thomas Hartley. .Harrison, John. Bird, Matthew Mitchell. Williams, Joel Drew. Dutton, George. Duncan, Alexander. Rimmington, Felix W. E. Meredith, John. Deighton, Thomas Milner Forge, Christopher. Tucker, Charles. G watkin, James Thomas, Stroud, J ohn. Sirett, George. Thomas, Richard. BlackshaAV, Thomas. .Youngman, Edward. .Barnett, Alexander. .Deck, Arthur. .Bing, Edwin. .Hollway, Alfred Brown. .Jones, John EdAvard. Thompson, AndreAV. .Davies, Richard M. .Lloyd, William. .Crofts, Holmes Cheney. .Baker, Charles Patrick. .Smith, Nathaniel. .Baxter, Geoige. .Greaves, Abraham. .Long, William Elliott. .Coles, John Coles. .Green, John. .Mason, Joseph Wright. Bowerbank, Joseph. Cordley, William Bain?. Goode, Charles. Wyley, John. McNeil, James Norton. Barritt, George. Robinson, James. Green, John. EdAvards, William. Stevenson, Richard. Evans, John. July 5, 1879. J THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS 13 Towns eligible. Davonport . Dewsbury . Diss . Doncaster . Dorchester . Dorking . Dover . Droitwich . Dudley . Dumfries . Dundee . Dunfermline . Durham . Eastbourne . Edinburgh . Elgin . Ely .., . Evesham . Exeter . Eye . Ealltirk . Falmouth . F areham . Faversham . Flint . Folkestone . Forfar . Frome . Gainsborough . Gateshead . Glasgow . Gloucester . Gosport . Grantham . . Gravesend . Greenock . Grimsby, Great . . Guernsey . Guildford . . Haddington . •. . Halifax . Harrogate . Hartlepool . Harwich . Hastings and St. Leonards Haverfordwest . Hawick . . . Helensburgh . Helston . Hereford . . Hertford . Hexham . Heywood . Hitchin . Horncastle . Horsham . Huddersfield . Hull . . Huntingdon . Huntly . Hyde . Hythe . Inverness . Ipswich . Jersey . Kendal . Kidderminster . Kilmarnock . . King’s Lynn . Kingston-on-Thames . Kirkcaldy . Knaresborough . Knutsford . Lancaster . Launceston . Names of persons appointed. ..Codd, Francis. ..Matterson, Edward H. . .Gostling, Thomas Preston. ..Howorth, James. ..Evans, Alfred John. ..Clift, Joseph. ..Bottle, Alexander. ..Taylor, Edmund. ..Gare, Charles Hazard. ..Allan, William. ..Hardie, James. ..Stiell, Gavin. ..Sarsfield, William. ...Gibbs, Joseph. ..Mackay, John. ..Robertson, William. ..Pate, Henry Thomas. ..Dingley, Richard Loxley. ..Delves, George. ..Bishop, Robert. ..Murdoch, David. . .Newman, Walter Francis. ...Batchelor, Charles. ..Underdown, Fredk. W. ..Jones, Michael. . . Goodliff e, George. ..Ranken, James A. Spouncer, Henry Thomas. Elliott, Robert. Kinninmont, Alexander. Meadows, Henry. Hunter, John. Cox, John. Clarke, Richard Feavei’. Fraser, Charles. Botterill, George Thomas. Arnold, Adolphus. Martin, Edward W. Watt, James. Dyer, William. Davis, R. Hayton. Jackson, William G-. Bevan, Charles F. Jameson, William E. Williams, William. .Harvie, George. .Troalce, Marler H. .Jennings, Reginald. .Lines, George. .Gibson, John Pattison. .Beckett, William. .Ransom, William. .Kemp, William. .Williams, Philip. .King, William. .Bell, Charles Bains. .Provost, John Pullen. .Chalmers, George. .Wild, Joseph. Lemmon, Robei't Alee. .Galloway, George Ross. Anness, Samuel Richard. Ereaut, John, jun. • Severs, Joseph. Hewitt, George. Borland, John. • Palmer, Wm. Jos. Walmsley, Samuel. • Storrar, David. • Potter, Charles. Silvester, Henry Thomas. Bagnall, Wm. Henry. Eyre, Jonathan Symes. Names of persons appointed. Davis, Henry. Reynolds, Richard. Johnson, William. Clark, Walter Beales. Readman, William. Finlayson, Thomas. Davis, David Frederick. Martin, Thomas. Perkins, John Jaquest. Maltby, Joseph. Young, Richard. Abraham, Thomas Fell. Williams, Thomas. Prince, Arthur G. Paget, John. Hurst, John B. Sale, Thomas J. Woodhouse, George. Thornton, Edward. Allen, Adam U. Bates, William Isaac. Henry, James Hay. Walton, Ralph. Rowcroft, Albert Edward. \Y allworth, David. Brown, Francis James. Hardy, George. Metcalfe, Edmund Henry. Wilkinson, William. Davies, Peter Hughes. Candler, Joseph Thomas. Smyth, Walter. Robson, James Crosby. Key, Hobson. Burrell, George. Birkett, John. Marshall, George T. Hibbert, Walter. March, William. Hickman, Frederick. Cartwright, William. Martin, Nicholas H. Orchard, Herbert Joseph. Seys, James Ancas. Poulton, John. Owen, Edward. Warrior, William. Bingley, John. .Sutton, Francis. Fitzhugh, Richard. Iliffe, George. .Hargraves, H. Lister. Saunders, George James. Hargreaves, Wm. Henry. Prior, George Thomas. Hatrick, William. John, David W. ..Kirkbride, William. Cornish, Henry Robert. Towns eligible. Leamington Leeds Leek Leicester Leith Leominster Lewes Lichfield Lincoln Liskeard Liverpool Llandudno Longton Loughborough Louth Lowestoft Ludlow Lyme Regis Lymington Macclesfield Macduff Maidenhead . Maidstone . Maldon . Malmesbury . Malton . M alvern . Manchester’, etc. March . Margate . Marlborough Marlow Merthyr Tydvil Middlesborough Midhurst . Monmouth . Montgomery .... Montrose . Morecambe .... Morpeth . Neath . . Newark . Newbury . Newcastle-under-Lyme Newcastle-on-Tyne . Newport (I. of Wight) Newport (Mon.) New Radnor Newton Abbot Newtown Northallerton Northampton Norwich Nottingham Nuneaton Oldham Oswestry Over Darwen Oxford . Paisley . Pembroke .... Pembroke Dock Penrith . Penzance . Perth . Peterborough . . Petersfield . Plymouth . Pontefract . Poole . Portsmouth, etc. Preston . Ramsgate . Reading . Heanley, Marshall. Edgeler, William B. Balkwill, Alfred P. Bratley, William. Penney, William. Rastrick, Joseph L. Barnes, James. Morton, Henry. Hayward, Wm. Griffith. 14 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 5, 1*79 Towns eligible. Redditch . Retford . Richmond (Yorks) . . . . Ripon . Rochdale . Rochester . Rothesay . Runcorn . Rugby . Ruthin . Ryde (Isle of Wight) . Rye . St. Albans . St. Andrews . St. Austell . St. Ives (Cornwall) .... Salisbury . Sandwich . Scarborough . Seacombe . Selby . . Shaftesbury . Sheerness . Sheffield . Shields, South . Shipley . Shoreham . . Shrewsbury . Slough . Southampton . Southport . Spalding . Stafford . . Stalvbridge . Stamford . Stirling . . Stockport . . Stockton-on-Tees . Stoke-on-Trent . Stourbridge . Stratford-on-Avon Stroud . . Sudbury . Sunderland . . . Sutton-in-Ashfield . . . Swansea . Tamworth . Taunton . Tavistock . Teignmouth . Tenby . . Tewkesbury . Thirsk . Tiverton . Torquay . Totnes . . Truro . Tunbridge Wells . Tynemouth . Uttoxeter . . Wakefield . Wallingford . Walsall . Wareham . Warrington . Warwick . Watford . Wednesbury . . Wellington (Somerset) WeDlock . Westbury . West Bromwich . Weston-super-Mare Weymouth . Whitby . . Names of persons appointed. .Mousley, William. .Clater, Francis. Thompson, John Thoma®. .Judson, Thomas. .Taylor, Edward. .Harris, Henry William. .Duncan, William. .Whittaker, William. . Chamberlain, Arthur G-. .Bancroft, John James. Pollard, Henry Hindes. .Waters, William Allen. Ekins, Arthur Edward. , Go van, Alexander. .Hern, William Henry. .Young, Tonkin. . Atkins, Samuel Ralph. Baker, Frank. . Whitfield , J ohn. .Walker, John Henry. .Cutting, Thomas John. .Powell, John. .Bray, John. .Ward, William. .Mays, Robert J. J. .Dunn, Henry. Towns eligible. Names of persons appointed. Whitehaven . Wick . Wigan . Wigton . Wilton . Winchester . Windsor . . Wolverhampton . Woodbridge . Woodstock . . Worcester . Worthing . . . Cortis, Arthur Brownhill. Wrexham . Wycombe . Yarmouth, Great . Yeovil . York . Previous to the vote being taken, Mr. Williams said he wished to make a few observa¬ tions on the appointment of one of these local secretaries, but it being a personal matter, he must ask the Council to go into Committee. This having been done, and the Council having resumed, the list was put to the vote and adopted unanimously. Cross, William Gowen. Griffith, Richard. Dawson, Oliver R. Ashton, William. Shadford, Major. Averill, John. Brierley, Richard. Duncanson, William. Kay, Samuel. Brayshay, Thomas. Adams, Jonathan Henry. Bland, Thomas Frederick. Hawkes, Richard. .Blake, William F. .Harding, James John. .Nicholson, John Joseph. .Buckland, E. .Griffiths, William. Alikins, Thomas Boulton. Prince, Henry. .Gill, William. .Cornelius, Joseph. Davies, Moses Prosser. Allis, Francis. Thompson, John. Havill, Paul. Smith, Edward. Keen, Benjamin. .Percy, Thomas Bickle. Howard, Richard. Superintendents of Written Examinations. It was unanimously resolved that the superintendence of the written examinations be offered to the local secretaries at the centres where those examinations are held. Mr. Churchill asked how the new plan worked. There had been complaints of the number of centres not being sufficient. The President said there was a feeling in some quarters to reduce the number still further. The Vice-President said there was also a feeling in many quarters that the number should be enlarged. Mr. Shaw asked why Worcester had been continued as a local centre, when the Committee had recommended that it should be omitted ? The President presumed the Council must have ordered it. At any rate that was not the question before the Council then. Mr. Atkins said he still believed that individual cases of hardship had occurred from the present scheme of local centres, though on the whole the reduction in number might have been an advantage. He hoped that another year the Committee would take careful account of geographical considerations and railway facilities in deciding on these centres. He also hoped that the Pre¬ liminary examinations were still in a transition state. He should not be satisfied until this examination, which was purely a scholastic one, was removed from the Society altogether. Nothing in the world could be easier than to demand a certificate from the College of Preceptors or from a university local examination. Johnson, John Borwell. Wice, Jonathan H. Payne, Sidney. Elliott, George. Randall, Thomas. Woods, Joseph Henry. Pratt, Henry. Chater, Edward Mitchell. Gittoes, Samuel James. .Langford, John Brown. Taylor, Stephen. Council Examination Prizes. Messrs. Southall and Moss were appointed to conduct the examinations in the present month for the Council prizes. Mr. Greenish proposed an alteration in the regula¬ tions providing that candidates should be required to give five days’ notice of their intention to compete for these prizes, instead of ten as at present. The Assistant Secretary explained that five days would be sufficient, and, in fact, more convenient than ten. The motion was carried unanimously. .Gibbons, George. .Groves, Thomas Bennett. Mr. Churchill asked who fixed the dates for the .Stevenson, John. Major examination. July 5, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 15 Mr. Williams said the Council fixed the months. The exact days were fixed by the office, according to the number of candidates. He had proposed formerly that the examinations should take place every month instead of every alternate month, a change which, he thought, would have proved more convenient ; this suggested al¬ teration, however, did not meet with the approval of the Board of Examiners. This month there were L2 can¬ didates coming up. Report of Examinations. June, 1879. ENGLAND AND WALES. Candidates. - — - _ Examined. Passed. Failed. Major, 18th ..... 7 4 3 Minor, 18 th . 16 8 8 „ 19th . 25—41 15-23 10-18 Modified . 2 1 1 50 28 22 Preliminary Examination. Seven certificates were received in lieu of the Society’s examination : — 3 College of Preceptors. 4 University of Cambridge. Sales of Poisons by Co-operative Stores. Mr. Williams was next called upon by the President to move a resolution of which he had given notice with re¬ gard to co-operative societies selling or dispensing poisons. The President asked if the question should be discussed in Committee. Mr. Williams said he had no objection to what he had to say being published. Mr. Shaw thought it was not desirable to show their hand, and on the question being put to the vote it was resolved to go into Committee. The motion was discussed at considerable length, but on being put to the vote it was not carried. Sale of Patent Medicines. Mr, Hampson then moved the following resolution, of which he had given notice : — “That the General Purposes Committee take into con¬ sideration the largely increasing sale of ‘patent medicines ’ containing scheduled poisons, by grocers, general dealers, and other unregistered persons, and report thereon, more especially with regard to the advisability of endeavouring to restrict the sale of such ‘patent medicines' to persons registered under the Pharmacy Act of 1868.” He said he was very desirous that this Committee should take this subject into earnest consideration. It was evident to all that the sale of poisons under the cover of the patent medicine stamp was a growing evil. He heard the other day that a grocer’s as¬ sistant was asked what was the dose of chlorodyne, and replied a tea-spoonful. When the Pharmacy Act of 1868 was obtained, it was to all intents and purposes an Act for regulating the sale of poisons, but if anyone were able to sell poison upon affixing a patent medicine stamp to it, evidently the Act was of little or no use. He was told that in the country wholesale houses sent out two-ounce bottles of laudanum by the gross with a stamp on, and that opium itself was also sold in this way. Tincture of aconite was sold by grocers under a stamp, and in fact if any adventurous quack chose to put up the dilute hydro¬ cyanic acid of the Pharmacopoeia, under a stamp, and say that 2 or 3 drops were to be taken in water in case of sickness, it might be done with impunity. The time had come when this matter should be considered, for it was never intended that grocers, tailors and others should become the vendors of poisons. If the spirit of the Act were to be carried out, those who knew something about medicines should alone sell these things. The very fact that a person had to go into a special shop in order to purchase a poison was to a certain extent a safeguard ; but if people were able to get it at any ordinary shop, the use of poisons would become so indiscriminate that a parliamentary com- misssion or inquiry would be the probable result. He did not ask the Council to come to any decision at present, but simply to refer the matter to the Committee. Mr. Savage seconded the motion. Mr. Hills asked if it would not be better to refer the subject to the Committee for considering amendments to the Pharmacy Act. Mr. Hampson thought not ; that was a special Com¬ mittee for a particular purpose. Mr. Williams said that Committee had considered that any change of the law in this direction was unneces¬ sary. The President said the great point of the motion was patent medicines. He did not recognize a bottle of laudanum as a patent medicine simply because it had a stamp affixed to it, and he believed that if a prosecution were instituted in such a case it would be found that the law did not protect it. With regard to patent medicines he did not see that it mattered who sold them. If any one came to him for a bottle of chlorodyne, and asked him what was the nature of it, he said he did not know what it contained. In fact, he never recommended patent medicines at all, but rather discouraged the sale of them. Mr. Greenish suggested an alteration of the wording of the motion to the effect that the Committee take into consideration the largely increasing sale of scheduled poisons by grocers and others under the guise of patent medicines. Mr. Frazer said if patent medicines were within the law this motion was not required, and if they were not he did not think it was desirable to bring them within it for reasons which he had frequently stated. It was contrary to his notions of trade, and he did not think it would be wise, because it was very doubtful, if chemists would obtain what they asked, whilst they might most probably lose some of the privileges they at present pos¬ sessed. Mr. Rimmington thought Mr. Greenish’s suggestion would be an improvement. The Vice-President, on the contrary, thought Mr. Hampson’s original form was better. Mr. Hampson also said he preferred the original word¬ ing. He demurred to the statement of the President that it did not matter who sold a bottle of chlorodyne, because it contained several scheduled poisons, and in the interest of the public as well as in justice to themselves, it was desirable that only registered persons should be allowed to sell patent medicines containing poisons. He equally demurred to Mr. Frazer’s view that a change was not necessary or desirable. Putting aside the interest of the public, which was of course paramount, it was the privilege of registered persons to deal in poisons. The President remarked that Parliament fully con¬ sidered the question when the Pharmacy Act was passed, and said that nothing in the Act should interfere with the making or selling of patent medicines. Mr. Frazer said his point was that if patent medicines were included in the Act there was no need of further legislation. Mr. Hampson said he did not assume that the Council had the power to restrict the sale of patent medicines, he simply asked that the Committee should consider the matter. Mr. Williams thought the Council was now doing the work of the Committee in discussing the merits of the question. The motion was simply that the Committee consider it and report. The resolution was then put and carried nem. con, 16 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 5, 1879. PRELIMINARY EXAMINATION. List of Centres and Table of Attendances of Candidates at each Centre. 187S. Oct. 1879. Jan. 1879. April. 1879. July. Total num¬ ber of at¬ tendances at each Centre. ENGLAND AND WALES. Birmingham . 12 20 23 21 76 Brighton . 3 5 4 1 13 Bristol . 6 6 9 12 33 Cambridge . 5 9 7 4 25 Canterbury . — 1 4 2 -T / Cardiff . 3 5 7 7 22 Carlisle . 6 7 2 10 25 Carmarthen . 7 10 11 8 36 Carnarvon . 2 1 9 9 21 Cheltenham . 2 2 3 7 Darlington . 3 7 6 6 22 Exeter . 2 8 8 8 26 Hull . — 16 13 5 34 Lancaster . 1 5 2 6 14 Leeds . 7 14 16 17 54 Lincoln . 3 10 8 7 28 Liverpool . ... 7 16 24 13 60 London . 33 59 46 52 190 Manchester . 18 26 32 20 96 Newcastle . 5 9 5 10 29 Northampton . — 8 9 6 23 Norwich . 2 14 7 14 37 Nottingham . 8 14 11 12 45 Oxford . 1 3 2 1 7 Peterborough . 2 3 5 15 25 Sheffield . 8 12 8 7 35 Shrewsbury . 2 5 7 4 18 Southampton . 5 4 19 15 43 Truro . 1 4 4 4 13 Worcester . 2 5 2 2 11 York . 2 9 12 11 34 SCOTLAND. Aberdeen . . 13 8 11 16 48 Dundee . 7 6 2 7 22 Edinburgh . 11 14 14 16 55 Glasgow . 3 12 ■ 11 12 38 Inverness . 2 3 2 7 Douglas, I. of Man ... 2 2 Guernsey . 1 — — 1 • 2 Jersey . 0 1 mmUtqjs of Jijientijiit Societies. BRITISH PHARMACEUTICAL CONFERENCE. Meeting of Executive Committee. Wednesday, July 2, 1879. Present — G-. F. Schacht, President, in the chair ; Messrs. Greenish, Ellinor, Carteighe, Symes, Williams and Attfield. The minutes of the previous meeting were read and confirmed. Professor Attfield, Honorary General Secretary, re¬ ported the work done since the previous meeting of Committee, including matters relating to the editing, printing, publishing and delivery to members of the Year-Book ; the grants in aid of research ; correspondence respecting improper use of the membership of the Con¬ ference ; correspondence respecting the Bell and Hills Fund books ; compilation and distribution of the list of subjects for research ; collection of subscriptions ; or¬ ganization of the approaching meeting at Sheffield ; cor¬ respondence with members likely to work on the Executive Committee in 1879-80 ; and, arrangements for inviting all registered chemists and druggists not already members to join the Conference. A letter was read from Mr. Siebold, editor of the Year-Book, reporting that the manuscript of the volume for 1879 would be completed a fortnight before the annual meeting. A meeting of the Committee of Pub¬ lication was ordered to be convened as soon as the manu¬ script was received, with power to make all arrangements for the issue of the volume. Mr. Ellinor, from Sheffield, stated that he was authorized by the Vice-President, Mr. Ward, the Local Secretary, Mr. Maleham, and the members of the Local Committee in Sheffield, to explain that rooms for the general meetings of the Conference on August 19 and 20 had been secured, that a considerable amount of interest and enthusiasm existed locally respecting the meetings, that permission had been obtained for members after the meeting to inspect some of the interesting factories of Sheffield, and that on Thursday, the 21st of August, the local members would invite their visitors to accompany them on a drive through some of the scenery of Derby¬ shire, visiting “ Chatsworth ” and “ Haddon ” en route. He ventured to think that their friends would not be disapjiointed with the welcome they would receive, even although in accordance with annually stated requests, strongly renewed this year, the idea of holding a formal banquet in honour of their guests would not be carried out. SOCIETY OF ARTS. The History of Alizarin and Allied Colouring Matters, and their Production from Coal Tar.'* BY IV. H. PERKIN, F.R.S. Lecture I. — Delivered May 8. In December, 1868, I had the honour of delivering three lectures before this society on the “Aniline or Coal Tar Colours.” In these I commenced with mauveine, or the mauve dye, the first discovered of this remarkable series of compounds, and then gave briefly the history of all the other important colouring matters which had been discovered up to that date. Last year, Mr. Wills, who always arranged the busi¬ ness of this Section so assiduously, wished me to give a further account of these colouring matters, but I was unable to do so then. He, however, asked me again this year, and I was glad to be able to accede t chis request, little thinking then, and still less only a few weeks since when I met him full of activity and enthusiasm, that he would so soon be called from our midst, and his career here, so full of promise, ended. When I promised to bring a paper before you, I thought that I would continue the history of the coal tar colours, from the time I gave the lectures just referred to up to the present time. However, on considering the subject in detail, I found the amount of matter far too large, owing to the great number of discoveries which had been made in this field since then ; I therefore thought it best to confine myself to the consideration of the most im¬ portant of the products which have been obtained, and selected alizarin and allied colouring matters. In giving you a somewhat brief account of this subject, I think it best first to refer to madder, the dye-stuff which, until 1869, was the only source of alizarin. Up to the date just mentioned madder root was one of the most important dye-stuffs known, the annual value of the im¬ ports into the United Kingdom being about £1,000,000 sterling. * From the Journal of the Society of Arts. July 5, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 17 The plant that gives this root belongs to the natural order Rubiacece. It is nearly allied botanically, and in appearance, to the ordinary G-aliums, or bedstraws. It is a perennial, with herbaceous stem, which dies down every year, the stalk is square and jointed, and this and the leaves are rough with prickles. The flower is very small, and of a greenish yellow colour. The root is cylindrical and fleshy, and of a reddish yellow colour ; this, when dried, constitutes madder. It is one of the oldest known dye-stuffs, and is referred to by Pliny. The principal varieties in cultivation are — Rubia tinctorum, Rubia pere- grina, and Rubia cardifolia. It is grown in Holland, South of Germany, France, Italy, Turkey and India. It has been cultivated also in this country, but not with permanent success. It is propagated from suckers, and the time from planting until the roots are drawn is from eighteen to thirty months, and sometimes longer. When dried the roots lose their reddish yellow colour and become of a pale red shade. The process of drying is conducted in the air, or in kilns. When dry the roots are beaten to remove sand, clay and loose skin. They are sent into the market either in this condition or in a ground state. There are also various preparations of madder made, the principal ones being Fleur de gar ance, or flowers of madder, and garancine. Their preparation is briefly as follows : — Fleur de gar ance is made by soaking ground madder in water, with the addition of a small quantity of sulphuric acid ; it is then drained in a filter and well washed. The washings contain a considerable amount of glucose, besides other products, and when fermented yield alcohol, which is suitable for a variety of purposes, but is not fit for drinking unless purified. The washed madder is then pressed and dried, and constitutes fleur de gar ance. Oa account of the products which have been removed this substance is considerably richer in colouring matter than madder. Garancine is prepared by first washing ground madder much in the same way as for the preparation of fleur de garance, and after being pressed it is mixed with concen¬ trated sulphuric acid, in quantity equal to about half the weight of the madder originally taken. After being thoroughly incorporated with this it is heated with steam for three or four hours, placed on filters, and thoroughly washed, pressed and dried. Tinctorially it is about three and a half times as strong as madder. Madder will not dye unprepared fabrics ; they require to be what is called mordanted. In this case the mordants consist of metallic oxides, those of aluminum and iron being the chief ones. With alumina mordants it produces shades of red and pink, with iron mordants shades of black and purple. These mordants may likewise be mixed, and then produce various kinds of chocolate colour. The value of madder and its preparations is determined by taking weighed quantities and dyeing pieces of mordanted cloth with them, the size of the cloth being always the same ; after dyeing the patterns are cleared by treatment with soap, and are then dried ; and, of course, according to the depth of the colour, so is the value. Standard specimens are used at the same time for the sake of comparison. In mordanting cotton goods, the mordants, which are chiefly the acetates of iron and aluminum, are thickened and printed on, either with a machine or blocks. They are “aged,” as it is called. This used to be performed by hanging the goods in a moist atmosphere for some days, but now they are passed through properly constructed rooms, kept at the requisite temperature and degree of moisture by steam, and then laid in bundles for a time. The next process is called “dunging.” Its object is to remove the thickening which has been used with the mor¬ dants, and also to thoroughly neutralize them, at the same time removing any that has not combined with the fibre. This is accomplished by passing the goods through warm water containing cow dung, but now more commonly con¬ taining certain salts, as phosphates, arseniates, etc. ; these are called dung substitutes. When this operation has been finished the goods are washed, and are then ready for dyeing. Dyeing with madder is an operation requiring consider¬ able care, especially as the temperature of the dye-bath must be raised only very slowly, otherwise a loss of colour¬ ing matter occurs. This makes the operation take some con¬ siderable time, often two hours. If garancin is used the dyeing can be conducted more quickly. In this operation the ground madder, or the garancin, is mixed with the water in the dye-bath. A little chalk is also sometimes added. As^the colouring matter of the dye-stuff gradually dissolves in the water, the mordants on the goods take it up. It is important in this process that the mordants should be thoroughly saturated with colouring matter, otherwise they do not resist the after-clearing process so well. When dyed the goods are washed with water and then cleared, as most of the colours are very impure, especially the reds, which have a rusty look. The methods of clearing vary according to the class of goods, madder pinks receiving the greatest amount of treatment and care. In this process soap is largely used, but it will not be necessary to enter into further details, as it would occupy too much time, and I only wish to convey to you a general impression of the application of madder to calico printing. Before leaving this subject I must refer to another most important application of madder, namely, Turkey red dyeing. This mode of dyeing was introduced into Europe from the East, and is undoubtedly of Indian origin ; from India it came to the Levant, and was afterwards intro¬ duced into France about 1747. The first Turkey red works in the United Kingdom were established about the end of the last century. Turkey red is remarkable for its brilliancy of colour and permanence, and also for the peculiar nature of the processes employed in its produc¬ tion. For dyeing Turkey red the cotton is first prepared by treatment with olive oil, which is afterwards oxidized by exposure to the air. The oil is usually employed in the form of an emulsion, made by agitating the oil with a solution of carbonate of soda or potash. The goods are passed through this and then exposed to the air, after which they are treated several times in the same manner. When sufficiently charged with oxidized olive oil they are mordanted with an alumina salt, galls, shumach, or other tannin matter. Cotton thus prepared for dyeing is of a buff or yellowish shade. In the next operation the dye-bath is charged with madder or garancin, a little shumach, and a quantity of blood. The prepared goods are entered into this bath, and heat gradually applied, until it reaches the boiling point, at which temperature it is kept until the dyeing is complete. The goods are then washed in water, and present a dark, heavy, dull red colour. They are next subjected to the clearing processes, which are two in number. These are performed in large copper boilers, with moveable covers, as the clearing has to be done under pressure. The dyed goods are placed in these, with a mixture of common soda crystals and soap, and boiled under pressure for about six hours. They are then removed, washed in hot water, and again placed in boilers, with a solution of soap, to which chloride of tin (tin crystals) has been added. They are boiled in this, under pressure, for about four hours, and then removed, washed and finished. The first clearing considerably improves the colour, but the last one gives that remarkable brilliancy peculiar to good Turkey red. After all this treatment with soap, we can understand that Turkey red is a very fast colour. No satisfactory process for printing Turkey red has yet been found. Some time since I made a few experiments on the subject. The cloth prepared ready for dyeing was used, and then printed with the colouring matter ; it was then steamed, washed and cleared as above. The colours were very good indeed, but the parts which should be white were still of the yellowish colour of the prepared cloth. When a Turkey red is wanted in a pattern the cloth is 18 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [Ju1)’ S, 187P. first dyed all over with this colour. If white is required in the pattern, those parts are printed with thickened tar¬ taric acid ; if yellow, with tartaric acid and a lead salt ; if blue, with tartaric acid and Prussian blue. On passing cloth printed in this manner into a solution of chloride of lime, the parts printed with acid, as they come in contact with this solution, cause chlorine to be evolved and the Turkey red destroyed, thus white is produced. If blue has been printed on with the acid, the red being discharged, blue remains. If a lead salt has been printed on, white is obtained ; but when passed through a solution of bichromate of potash, yellow chromate of lead is formed. Of course green can be obtained by combining the last two processes. Black is printed on direct. Most beauti¬ ful results are obtained in this manner. Madder is also employed for woollen goods. It is generally used in combination with other dye-stuffs for the purpose of producing brown, buff, or chocolate colours. But I must pass on, the application of madder being a subject on which books have been written, my remarks are therefore necessarily of only a very general character, though I hope sufficient to give some idea of the pro¬ cesses. Having seen the importance of madder as a dye-stuff and the methods of applying it to fabrics, it will next be desirable to consider the colouring matters it contains, which render it so valuable. Scarcely anything was know of these until 1827. At this date, two chemists, Colin and Robiquet, obtained the principal colouring matter in a state of tolerable purity. They extracted ground madder with hot water, and, after treating this extract in various ways, obtained a product which, when heated carefully in a glass tube, gave off a yellowish vapour, condensing into brilliant bright red needles. They named this substance Alizarin, from the Levant name of madder, Alizari. But the method they adopted for its preparation, viz.r sublimation, rendered it a matter of uncertainty whethe alizarin pre-existed in madder pr was a product of decom' position of some other body. Dr. Schunck, however’ afterwards succeeded in obtaining it without having recourse to sublimation. If further proof were needed it was found in the fact that thist colouring matter was capable of dyeing mordanted cloth just in the same way as madder. It exists in madder in only very small quantities, not more than to the extent of one per cent. Alizarin is nearly insoluble in cold water, and 1000 parts of boiling water dissolve only about three parts of the colouring matter. It is more soluble in alcohol, and from high boiling naphtha it may be crystallized in red needles. When crystallized from alcohol it is obtained in orange -coloured needles. One of the characteristic properties of alizarin is the beautiful blue violet solution it produces on being dissolved in caustic alkalies. This solution, when viewed by the spectroscope, shows two strong absorption bands, one near to C, and the other at D, and a very faint one near to E. Alizarin also dissolves in ammonia with a purple colour. It forms a red lake with alumina, and a black one with oxide of iron. Curiously, alizarin is not found in the growing madder root. This is easily seen by expressing some of its juice and treating it with caustic potash. In this way a red- coloured solution is produced, and not a violet one, as would be the case if alizarin were present. This colora¬ tion is due to the presence of a substance called rubianic acid. This body is a glucoside of alizarin, and when decomposed yields ali sarin and glucose. This can be easily effected by boiling it with hydrochloric acid, when alizarin separates as a yellow precipitate. Rubianic acid does not possess dyeing properties. The decomposition of this glucoside in the madder root occurs partly during the process of drying, but not entirely until it is gently heated with water in the dye-bath. This decomposition is caused by a peculiar ferment called Erythrozyme, a product which is destroyed if heated with water to 100° C. This is one reason why the madder dyers have to gently raise the temperature of their dye-bath so that this glucoside may entirely decompose, and all the alizarin be liberated and rendered useful. The importance of this may be easily seen by taking two equal parts of growing madder root, and, after bruising them in a mor¬ tar, to throw one into boiling water and the other into cold water. On placing a piece of mordanted cloth in each, keeping the one with boiling water still boiling, and gradually raising the temperature of the other, it will be found that the one in boiling water will have scarcely coloured the mordants, whilst the one in cold water and gently warmed up will have dyed them tho¬ roughly. There is only one other colouring matter in madder that I need refer to, and that is purpurin. This substance was discovered by Colin and Robiquet, and called by them Mature colorante rose. It was afterwards obtained in a somewhat purer state by Debus, and by Wolff and Strecker. This substance is separated from madder by boiling it with a solution of alum; munjeet, however, is its best source. It is precipitated from the alum solution with hydrochloric acid and then further purified. When pure purpurin crystallizes in red or orange-red needles, it differs from alizarin in the way it behaves with a'kalies; solutions of these yielding with it beautiful cherry-red colours. It also dissolves in alumina salts with formation of pink solutions, which are fluorescent. The spectrum is also very different from that 6f alizarin. It dyes mordanted cloth, forming with alumina mor¬ dants a yellowish scarlet. The colours it produces with iron mordants, however, are not at all good. The pur¬ purin colours do not resist soaping well, so that madder prints, in the process of clearing, lose all the purpurin taken on in the dye-bath. It is retained, however, to some extent in the cheaper class, such as garancine styles. From this it will be seen that it is a substance of but little value. It exists in the growing madder-root as a glucoside. A great deal of controversy has taken place respecting the chemical formula of alizarin. Dr. Schunck proposed CI4H504, which, according to the present notation, would be C7H502, whilst Strecker believed it to be C10H6O3, and related to chloroxynaphthalic acid, a derivative of naphthalene, so that it has long been supposed that it was possible to obtain alizarin from a coal-tar product, though not from the right one. Still there was a good deal of reason to believe that it was a naphthalene deri¬ vative, from the fact that, when oxidized it yields the same acid as naphthalene, namely, phthalic acid. Strecker’s formula was the one generally believed in. It is right to mention that Strecker changed his views of this subject afterwards. The chloroxynaphthalic acid above referred to was sup¬ posed to be a chlorine derivative of alizarin, the two bodies being thus related : — Ci„h„o3 c10h5ci o3 Alizarin. Chlorinated Alizarin. And many attempts were made to remove this chlorine and replace it by hydrogen, so as to form alizarin ; and eventually Martius and Greiss obtained the substance, C10H6O3, when investigating some amido derivatives of naphtbal, but it was not alizarin. They assumed it, how¬ ever, to be an isomer of that body. Some time after the experiments of Martius and Greiss, Graebe commenced some researches on quinone (a body related to benzene). At that time no analogous sub¬ stance to quinone, related to any other hydrocarbon than benzene, was recognized. However, he was induced to consider chloroxynaphthalic acid as a derivative of a naph¬ thalene quinone, which has since been obtained, and also discovered a chlorinated derivative of a quinone of toluene. {To be continued.) July 5, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 19 JOHN THOMPSON. On Friday, June 20, John Thompson, one of the Founders of the Pharmaceutical Society, and one of its earliest local secretaries, died in the seventy-seventh year of his age. John Thompson was born at Laversdale, in Cumber¬ land, on January 23, 1803. He was apprenticed to a chemist in Hull — Mr. Foster, of Lowgate — and subse¬ quently engaged as assistant to Mr. Fouracre, of Gloucester. He returned to Hxill to the late Mr. Edward Smeeton, with whom, in the capacity of assist¬ ant, he removed to Leeds when that gentleman opened his establishment there. By Mr. Smeeton he was very highly esteemed, and at his suggestion, and by his help, he commenced business in Thirsk, in the year 1828, where he greatly prospered. The business then established is now carried on by one of his sons, four of whom are connected with the Pharmaceutical Society. He was inferred at Thirsk on Tuesday, the 24th of June, amid signs of universal respect. Notice has also been received of the death of the fol¬ lowing : — On the 2nd of May, 1879, Mr. Frederick Whiteman, Chemist and Druggist, Vernon Street, Ipswich. Aged 38 years. On the 2nd of June, 1879, Mr. Richard John Hinsley, Chemist and Druggist, Manchester Road, Bradford. Aged 42 years. On the 6th of June, 1879, Mr. Benjamin Alfred Eyre, Pharmaceutical Chemist, Tacket Street, Ipswich. Aged 67 years. Mr. Eyre had been a Member ot the Pharma¬ ceutical Society since 1842. On the loth of June, 1879, Mr. James Sellick Hicks, Pharmaceutical Chemist, Fore Street, Looe. Aged 40 years. Mr. Hicks had been a Member of the Pharma¬ ceutical Society since 1864. Dispijnsiiiijg Hftmottmutit. In order to assist as much as possible our younger brethren, for whose salce partly this column was established, considerable latitude is alloived, according to promise, in the propounding of supposed difficxdties. But the right will be exercised of excluding too trivial questions, or re¬ petitions of those that have been previously discussed in principle. And we would suggest that those ivho meet U'ith difficxdties should before sending them search previous numbers of the Journal to see if they can obtain the re¬ quired information. Replies . [315] . Considering the solubility of ammon. chloride in spirit (1 in 50) it would be impossible to obtain a perfect solution from this recipe. The salt should be used in powder, and the insoluble portion shaken up before the “volatile liniment” be applied. Hastings. D. H. [316] . A very presentable “jelly” might be made of this, only it should be sent out for convenience in a galli¬ pot with a china or glass spoon. If this did not meet with the intention of the prescriber, it would teach him a lesson on “Incompatibles” and enable him in future to order a mixture that would pour out of a bottle. Hastings. D. H. [319]. I should also be glad, of a little information about this prescription. Some time ago the following recipe was brought to be dispensed : — R Litharge . ^x. 01. Olivae . gv. 01. Lavand . ill 40. Ft. ung. My directions were more vague than A. Y.’s; but as boiling with water was the only way of forming an ointment, except by using wax, the litharge and oil were boiled with water until combination had taken place. The resulting product, though stiff, might still be called an ointment. Shortly after our customer complained of its being darker and harder than what he had got in London. He obtained some more from the same source, which was nearly but not quite white, soft, contained moisture, and had a cooling effect on the skin. The spirit of emulation being aroused the greater portion of Whit Monday and part of another day were devoted to preparing a fresh lot. The litharge was found to be contaminated with per¬ oxide, so some fresh, light-yellow protoxide was made by heating carbonate of lead in an iron vessel, from which a much lighter coloured ointment was produced; but still the consistence was too stiff, the colour not quite white enough, and the ointment did not contain sufficient moisture. The best result was obtained with Litharge . 3v. Ol. Amygd . 5iij. Aq . 3iss. the water being replaced as it evaporated. I have not had an opportunity of learning whether this retained its appearance and consistence. The prescription was from the pen of a well-known skin doctor. W. [321]. This presents a mixture that undergoes chemical decomposition after standing a few hours. The acid carbonate of soda acting upon the liq. bismuthi displaces ammonia and inevitably precipitates carbonate of bismuth. (This may be proved by filtering the mix¬ ture, and washing until it ceases to make lime water turbid. Nitric acid added dissolves the precipitate with effer¬ vescence, giving a solution blackened by AmHS.) Unless the liq. bismuthi had been omitted it would be impossible not to have a deposit. Hastings. D. H. [321]. The precipitate was caused by the loss of ammonia. All the bright samples of liq. bismuthi have a slight odour of ammonia. If that was hardly per¬ ceptible I should doubt the stability of the compound, particularly if the weather was warm and the customer were to leave the cork out. In such cases I should be disposed to add a few di-ops of liq. ammon. This addition to the stock bottle, or a mixture, will redissolve the precqjitate. The ammonia should be added in small quantities, and the bottle shaken and allowed to stand after each addition. I should tell the customer the cause of the change, and show how the supplying what has been lost restores the mixture. It should be remembei'ed the addition of ammonia only supplies what has escaped from the bottle, and is quite different to adulterating or sophisticating. H. G. C. Queries. [322]. Here is a puzzle to solve ; how to make a usable preparation of these ingredients ? I had it as an orthodox physician’s prescription to prepare. R Tr. Lyttse . • • • 3j- Acid. Sulph. Dil . . • • 3ij. Tr. Lavand. Co . • • • 3«j Vaseline or Prepared Lard . . • ad gij. M. “for external use.” W. B. 20 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 5, 1879. [-323]. How should the following be dispensed ? — Sod* Siccatas ......... gtt. 2. Ex. Nucis V . gr. Ex. Gentianae . q.s. Ut fiat pilula. Mitte 24. I enclose a tracing of the prescription from which it ■will be seen that the gtt. in the first line is very different from the gr. in the second. The prescription is from a well-known and experienced M.D., who could not be consulted at the time. W. S. [324]. Can any readers of the Pharmaceutical Journal throw light on the following? — R. Morphise (the alkaloid) . . . . gr. 8. Chloroformi . ill 60. Lin. Belladonnae . ad fl. dr. 4. Ft. linimentum. As dispensed by me the greater portion of the morphia, as I expected, remained undissolved, and a “shake the bottle ” label was attached. The patient, however, in¬ forms me that he has had it before perfectly bright and clear, cf a brownish tint (he compared it 4in colour to tinct. camph. comp.), and about twice as much in bulk as I had sent. I fail to see how this could be done without departing from the formula. Gulielmus. [325]. I should be glad to have the opinion of the readers of the Pharmaceutical Journal as to the proper .salt of bismuth to use in dispensing the following : — R Bismuthi . Adipis . 3vj. Creosoti . H v. M. ft. ung. I used the subnitrate as being that probably intended, although I must admit that the prescription might as reasonably have been dispensed with either carbonate or •oxide. Gulielmus. Jtotys and faeries. [610]. FURNITURE CREAM.— In reply to A. P. S. the following is an excellent recipe for furniture paste : — Bees’ Wax . 1| pounds. Spirit of Turpentine .... 4 pints. Dissolve by means of a water-bath in a closed vessel, then add common soap, % pound, previously dissolved in 4 pints of water, and stir well together until nearly cold. A. W. Postans. [610]. FURNITURE CREAM.— I would recommend the following receipt for furniture cream : — R Yellow Wax . 5v. Turps . . . Oj. Castille Soap . §iss. Cut the bees’ wax in small pieces, and dissolve in the turpentine by a gentle heat; when nearly cool add the soap (first powdered, rubbed up with §ij of water), gradu¬ ally stirring continually until it becomes thick. Ferri Cit. [610]. FURNITURE CREAM.— I think A. P. S. •will find the following to suit his purpose : — R Cerse Flav . 2^ ozs. Cerse Alb . 1 oz. Sapo. Cast . 1 dram. 01. Terebinth. Aq. Bull . ana 10 ozs. Potass. Garb . 1 dram. Melt the wax and turpentine together, dissolve the soap and potass, carb. in the water and mix while warm, stirring till cold. Cambridge. G. J. Bull. [611]. MOORE’S OINTMENT.— I beg to ask through the medium of your Journal, can any of the readers kindly give me a recipe for Moore’s or Old Moore’s Ointment, much used in Golden Square, West district? Unguentum. dDnftjssfuwIpq. Lin. Potassii Iodid. o. Sapone, B.P. Sir, — Apropos of a new edition of the British Pharma¬ copoeia may I be allowed to suggest that the directions for making the above liniment be made more definite, and also be supplemented by a note as to the appearance it is in¬ tended to have when finished. Ought it to be a solid or a liquid ? Is it meant to be dispensed in a pot or in a bottle ? A s it is possible for such questions as these to be asked, I think none can deny that there are grounds for the above suggestion. The directions say, “mix the two solutions together.” Is it intended to add the iodide of potassium solution to the soap solution or vice versa, for the first process results in a solid substance, whilst by adding the soap solution to the iodide of potassium solution a liquid is produced. There are other difficulties, however, for I have made several experiments, but have had no two results alike, although the same kind of material and the same quantities were used in each case. There seems to be a difficulty about the soap most ad¬ vantageous for the purpose ; but the experience above recorded would suggest that hard soap is evidently not an “ advantageous soap.” I should feel greatly obliged if those who had the framing of the last British Pharmacopoeia will come forward and state what this liniment should be like, or rather what they intended it to be like, for, as far as I know the profes¬ sion, medical men prefer it in liquid form. However, when lin. potassii iodid. c. sapone, B.P., is pre¬ scribed it ought to be dispensed. Here then comes the query. Is it a liquid or a solid or is it both (for it will readily sepa¬ rate into two parts representing each of those conditions), or ought a substance with a jelly-like appearance to be dis¬ pensed for it ? An answer that will remove any cause for doubt will be heartily welcomed by W. H. de B. “ Qucero.” — (1) Trapogon porrifolius, in flower. (2) Fungus ( Ustilago receptaculorum ) destroying flowers of goat’s beard. (See Cooke, ‘Microscopic Fungi,’ pi. v., fig. 92-94. Mr. J. R. Thompson is thanked for his communication. “Nux.” — (1) Eriophorumpolystachyon. (2) Rhinanthus Crista-Galli. (3) St ellaria graminea. (4) Crepis setosa. (5) Sedum acre. G. R. Y. — Several formulae for syr. ferri lactophosphatis have already been given in the present series of this Journal. Among others, see that sanctioned by the Paris Society, vol. vii., p. 1041. E. K. C. — We shall be glad to hear the result of the further experiments you propose to make. W. C. 8. (Luton). — The information will be found in the “ Students’ Numbers ” of the medical journals which are issued previous to the opening of the medical schools. C. J. Bennett. — We know of no better work for the pur- pose than the one mentioned. “ Gulielmus.” — (1). Trifolium minus. (2). Car ex, vul- pinus. (3 ). Arrenatherum elatior. (4b Trifolium repens. (5). Lychnis Flo s-Cuculi. (6). Cardamine pratensis. Cyprus. — (1). Cynoglossum officinale. (2). Anthyllis Vulneraria. (3). Honckenya peploides. “ OrchisP — (1). Orchis maculata. (2). Gymnadenia Conopsea. (3). Hahenaria bifolia. R. Roberts. — (1). Orchis maculata. (8). Send specimen with leaves. (6). Ceteracli ojficinarum. Nos. 2, 4 and 5 are correctly named. G. Stevens. — Recipes for “Nervine Balsam” will be found in the Journal for March 30, 1878, vol. viii., pp. 773 and 782. _ _ _ Communications, Letters, etc., have been received from Messrs. Maleham, Nemo, Strachan, J. B. P., G. R.yY., W. C. S., Hirudo, Quaero. July 12, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 21 SWEET SPIRIT OF NITRE -WHAT IT WAS, IS, AND OUGHT TO BE. BY W. SMEETON. Under the above comprehensive title appeared a paper, written by Mr. Rimmington, of Bradford, in the November number of the Journal for 1877. It provoked a discussion and the facts that ap¬ peared to come out were that the ethereal liquid which is produced when alcohol and nitric acid are distilled together by the B.P. process is a compound of alcohol, nitrite of ethyl, aldehyde, and perhaps ■other unknown substances, and that the B.P. process would always yield an article containing the same proportion of the same ingredients. But at the outset, Mr. Rimmington condemned the B.P. process as being unnecessarily complex, and one that probably did not meet with universal adoption. Of ■course this might be said of any process, and the quantity to be operated upon will also be a modify¬ ing agent. Mr. Rimmington’s remarks respecting the directions to allow the still to cool before adding more acid were quite to the point; but if, on the other hand, the whole of the acid is added to start . with the action is very violent, and if the quantities dealt with are large, it is almost sure to lead to loss of ether. If the acid is added later on without waiting for the cooling, red fumes are apt to come over. In this dilemma we are left, and we should have been under obligation had Mr. Rimmington pointed out a more excellent way. Mr. Umney lias also stated that nitre made by the B.P. process was unfavourably received, and I suppose most manu¬ facturers must occasionally have lound the result unsatisfactory. J ust before the British Pharmacopoeia came out, Professor Redwood read a very exhaustive article on spirit of nitre, explaining the B. P. process, and briefly reviewing other processes. The Edinburgh and Dublin forms of making hy- ponitrous ether first, were dismissed as not being applicable for large quantities and expensive. There may be something in this, for whatever Professor Redwood states is so well considered that it may always be taken as correct. Still, after trying several processes, I have come to the conclusion that with the quantities with which I deal, none is so satisfactory as the Edinburgh plan. It is as easy and takes less time, but what is of much more moment, it makes a nitre that is very pleasant and uniform in character. I am not sure it is the best plan, but it is the best I know, and I do not find it very difficult to manipulate. I take twelve pints of alcohol and add to it care¬ fully three pints of nitric acid either at once or in successive portions. This is placed in a still having a capacity of eight gallons, connected with a stone worm and Woulfe’s bottles to catch what escapes the first condenser and receiver. Action will sometimes commence without artificial heat; if it does not I turn on steam till it does, but before the temperature reaches 140°, distillation commences, rapidly at first, and requires very careful condensa¬ tion. The distillate is in appearance and quantity about the same as that obtained by the B.P. process, but I think it is more ethereal and certainly more acid. It is now neutralized with milk of lime and solution of chloride of calcium added. The nearly pure ether separates, floats on the surface, the heavy liquid below contains the alcohol of the dis- Third Series, No. 472. tillate, and certainly most if not all the aldehyde and possibly other products. With the hope of utilizing the washings and recovering alcohol or ether, I have redistilled them with lime and filtered through charcoal, but it is bad smelling, ultimately goes yellow, and is certainly best out of good spt. nitre, though not worse than much that is sold. The main difficulty of this process is the volatile charac¬ ter of the ether, rendering the separation by a syphon a somewhat risky process, and giving, if inhaled, a most cadaverous hue to the operator. Great care has also to be taken wb^n the water and lime are added to keep all very Cuid, as the mixture with the spirituous liquid generates heat enough to make the ether boil. With these precautions the process is not more than ordinarily difficult. One ounce of the ether with a pint of sptirit makes nitre of 5 per cent, strength ; two ounces 10 per cent, or B.P. strength, as Mr. Rimmington has pointed out. The 5 per cent, is, I think, strong enough for medicinal purposes, and would generally be pre¬ ferred. In conclusion, I beg to say that whether this is the spt. nitre that is to be, or not, it has much to recommend it. It has a beautiful sweet flavour, something like chloroform, and I believe is free from aldehyde and other noxious products. NOTES ON SOME JAPANESE DRUGS. BY E. M. HOLMES, F.L.S. , Curator of the Museum of the Pharmaceutical Society. ROOTS. ( Continued from 'page 5.) Dee-oh (53) : — Rehmannia lutea, Max. Syn. Ti-hwang, Porter Smith, p. 184; Sas-hime, So mokou Zoussetz, vol. xi. fig. 62 ; Dziwo, Fr. et Sav. vol. i. p. 328; Sao hime, Goma tome sao, Phonzou Zoufou, vol. xvii. fol. 23. This root occurs in pieces one or two inches long and about one-quarter to one-third of an inch in diameter, soft and flexible, and very much wrinkled externally, internally soft and moist, of a deep brownish-black colour, with a darker line marking the juncture of the bark and meditullium. Taste earthy and slightly sweet. Several species of this Gesneraceous genus are largely used in China as alteratives and tonics, and are supposed to possess cooling and purifying properties. The Japanese character for this drug is identical with that translated Ti-hwang, under Rehmannia Chinensis , in Dr. Porter Smith’s ‘ Chinese Materia Medica,’ “dee ” or “ ti” being the name of the plant and “ oli,” like the Chinese “ hwang,” meaning yellow, in allusion to the yellow colour of the flowers. The plant is cultivated in Japanese gardens and flowers in May, and was in the first place probably brought from China. Gah-ditz (23) : — Curcuma Zerumbet, Roxb. This root corresponds exactly in shape and taste and odour with specimens of zedoary or zerumbet root in the museum of this Society ; most of the pieces are, however, of a rather more horny con¬ sistence than the zedoary root seen in commerce. Mixed with this rhizome are a few specimens of cassumunar root ( Curcuma Zedoaria, Roxb.), which are easily distinguishable by their yellow colour when cut or scraped. 22 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 12 Gah-ditz comprises both the long and short zedoary’ or in other words, both the central and lateral rhi¬ zomes. This plant is probably not wild in Japan, as it is not mentioned either in the ‘So mokou Zoussetz ’ or in ‘Franchet and Savatier’s Flora’; it is probably cultivated in Japan like several other medicinal plants belonging to the Scitaminese. Hak-tau-au (48) : — Anemone cernua, Th. Syn. Neko bana, Fr. et Sav. vol. i. p. 4 ; Hokina g’za, Phonzou Zoufou, vol. vi. fol. 23 ; Okina gusa, Shaguma saiko, So mokou Zoussetz, vol. x. fig. 34; Ollina gusa, Thunb. FI. Jap. p. 238 ; Kawara saiko, Sieb. et Zucc. FI. Jap. p. 14. This is an unbranclied, cylindrical, hard and brittle root, three to five inches long, or more, about the size of a goose quill, coarsely furrowed longitu¬ dinally, and crowned with the silky bases of the leaves. The transverse section ds brown and horny, and shows a small central cavity lined with white fibres ; this cavity appears to run through nearly the whole length of the root. The taste is sweet and slightly acrid. It probably possesses similar pro¬ perties to the common Anemone Pulsatilla, to which plant it is nearly allied. The Japanese name literally translated means white-headed old man, and is probably given in allusion to the white silky appearance of the tufts of young leaves. The Chinese name Hak-too-woo, is very similar in pronunciation. The plant, like Anemone Pulsatilla, grows in J apan on dry hilly places at an altitude of 500 to 2000 feet, and flowers in March or April. It is said to be used as a bitter medicine in China and Japan. Han-Ge (47) : — Pinellia tuberifera, Ten. Syn. Karasubishaku, So mokou Zouss. vol. xix. fig. 1 ; Phonzou Zoufou, vol. xvii. p. 23; Sang- pwan-hea, Hanbury ‘ Science Papers,’ p. 262, with fig. of root ; Midsummer Root, Pwan- hia, Porter Smith, ‘ Chinese Materia Medica,’ p. 149. Too hange, Fr. et Sav. vol. ii. pi. 1, p. 3; Fanke so, Kras no Fisiaku, Thunb. FI. Jap. p. 233. This drug consists of small white starchy corms, varying in size from a pea to that of a small marble. They are usually slightly flattened, and have a small depression on one side surrounded by a num¬ ber of little pits, which are apparently the scars of the radical fibres. They appear to have but little taste, but a powerful pungency is perceptible after the drug is chewed, as in many other plants of the arum family. According to Dr. Porter Smith the powdered drug has an action like colchicum and has been used for a long time in the Hankow Mission Hospital as a substitute for the sulphate of potash in Dover’s powders. Although containing a quantity of starch this drug is never attacked by insects. The plant is found in uncultivated places and in fallow fields, flowering in May and June. It pro¬ bably derives its name from the time of flowering, “ lian” meaning middle and “ge ” summer. Kai (56) : — Dioscorea quinqueloba, Thunb. Syn. Ktkuba-dokoro, So mokou Zouss. vol. xx. fig. 54; Kai, Tokoro, Koempf. Amoen. p. 827. - ... , - - 1 ~ — i. Kassuda Fanna dakka, Karasuno Sent,, Thunb. FI. Jap. p. 150. This is a sliced tuber, the slices being one inch or more broad, about half an inch thick, or rather less, and two or three inches long. The cortical portion consists of a wrinkled pale brown skin, marked here and there with the scars of rootlets. Internally it is yellowish-white and shows a few scattered vascular bundles. The substance is moderately hard and tough. The taste is slightly but not persistently bitter. It has very little odour. Of its medicinal properties I have no knowledge. The root is edible, according to Koempfer, who describes it as similar in appearance to ginger. Thunberg states that the name “■fanna dakka means nose higher, and is given because children put the winged capsules on their noses to make their nose& look larger, while “karasuno seni” means crow-berry. The plant has much the habit of the black bryony of this country, but the leaves are larger and have five shallow lobes. It flowers from June to Sep¬ tember. Kas-hi-yu (43). This is a large tuberous root, varying in size from two to four inches long and one to two inches in diameter. Externally it is of a blackish-brown colour, with one or two deep furrows, or in some pieces it exhibits a slightly wrinkled surface, while in others it presents transverse scar3 or ridges which by friction have become pale. Internally the root presents a nut-brown colour and a shining resinous fracture ; the structure appears uniform. The root is extremely hard, requiring a blow from a hammer to fracture it. The taste is slightly astringent and the odour earthy. I have not been able to identify it. Kesso : — Patrinia scabiosafolia, Link. (Valerianacese. Syn. Omina-meshi, So mokou Zoussetz, vol. ii. p. 21 ; Womina mesi, Jama njan kusoo, Uro amisi, Oro ami, Fr. et Sav. vol. i. p. 216. This root was not presented with the others, but was offered in the London market under the name of “kesso” and was imported from Japan ; as a product of that country it seems to demand notice here.. The root resembles that of Valeriana officinalis in general appearance and odour, but differs in the central portion to which the rootlets are attached, being very small and short, rarely exceeding one- third of an inch in diameter; the rootlets form a compact tuft from two to three inches long, are of a dark brown colour, and have a slightly scaly surface, by which and by the colour they are easily distinguished 1 10m valerian root. The odour of the root is even more powerful than that of Valeriana officinalis. The taste is bitter and aromatic. It grows in stony mountainous places and blossoms in July. Ki-KYo (33) : — Platycodon grandijlorum, A.DC. (Campanulacece), So mokou Zoussetz, vol. iii. fig. 3; Phonzou Zoufou, vol. iv. p. 14, 15. Syn. Campanula glauca, Tliunb.. FI. Jap. p. 88 ; Kekko, Kir jo, Kirakoo, Koempf. Amoen. p„ 822. This root is white, about three or four inches long, strongly but sparingly furrowed longitudinally, taper- July 12, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 23 ing from just below the part where the stem arises, -simple, or once forked, and giving off from the shoulder or thickened portion near the top of the root one or two short often horizontally-spreading lateral branches. Internally it is tough, white, and slightly spongy, with a yellowish-white horny ring surrounding the meditullium. The taste is at first sweet and mucilaginous, but afterwards faintly bitter. The juice is milky in the fresh root, according to Koempfer. These specimens do not in any way correspond with those described under the name of Platycodon grandiflorum by Dr. Porter Smith (p. 173). The Chinese character there translated kih-kang is, however, identical with the Japanese character ldkyo. The Japanese root was, however, recognized at sight by Mr. Takemura, who told me the plant yielding it had a large blue flower, and on showing him the figure of the plant in the So mokou Zoussetz, he at once identified it as the one yielding the root. Dr. Porter Smith’s specimen in the museum of the Phar¬ maceutical Society is therefore probably incorrect. According to Koempfer, this root is considered only second in medicinal value to the celebrated ..ginseng, which is not surprising, since it has a -stronger resemblance to the outline of a human body than even that famous root. Kikyo grows commonly on the borders of culti¬ vated fields, and flowers in July and August. Kin-kee (55) : — Mcdva sylvestris, L., Fr. and Sav. vol. i. p. 62. Syn. Zeni-aoi, So mokou Zoussetz, vol. xii. fig. 54. This root resembles in every respect that obtain¬ able in England, except that it is whiter and evi¬ dently carefully washed and rubbed before drying. It is probably cultivated in J apan, and not really wild, according to Franchet and Savatier. Kuh-shing (14). This drug is very similar in appearance to decor¬ ticated marshmallow root, but of a more yellowish tint. It occurs in angular pieces four or six inches long and one- third to three-quarters of an inch in diameter, and is very fibrous; the meditullium occupies the greater portion of the root and is marked where it joins the cortical portion by a ring of faint brown radiating dotted lines. The dotted appearance under a lens is seen to be due to the presence of porous vessels. The taste is intensely bitter. Examined by Mons. A. Petit, of Paris, it was found to contain a new alkaloid, to which its bitterness is due. Thunberg refers “ krism,’’ a name similar in sound but different in meaning, to Sophora lieptaphylla , L., but the root of that plant does not appear to be bitter.. The Japanese character for “shing” means bitter. I have not yet been able to identify this drug. Oh-ren (58) : — Coptis anemonoefolia , Sieb. et Zucc. (Ranunculacese) ; So mokou Zouss. vol. x. fig. 36. Syn. Kakouma G’za, Fr. et Sav. vol. i. p. 10; Phonzou Zoufou, vol. vii. p. 2. This drug closely resembles in appearance that of i to this is that the loss resulting from reduction of fees would be more than covered by the fees received for a larger number of visits. The other questions do not involve so much diffi¬ culty ; thus, for instance, in the obtaining of medicine upon Sundays and at night there is little reason to fear chemists and druggists would not be able to satisfy all requirements. As to the security that good drugs and preparations would be supplied by chemists and druggists, it may fairly be taken for granted that, at the present day, medical men need not be under any apprehension. Apart from the influence exercised by the provisions of the Food and Drugs Act, the improved education of the phar¬ maceutical body may be trusted to as ensuring proper regard to this point and due consideration that the intention of the prescribe!’ should be properly carried out both by the use of pure drugs and accuracy in compounding. Another question of some importance has reference to the scale upon which the poorer class of patients would be charged for their medicines. It is sugges¬ ted that to meet this difficulty a standard scale of charges for medicine should be adopted, and that exceptional reductions of charge should be made in accordance with the recommendation of the prescri¬ bes, to be made known by marking the prescriptions with the letters P. or V.P., in those cases where the medical man thought the patients entitled to this consideration on the grounds of being poor or very poor. A further provision for such cases is suggested, according to which an arrangement is to be made with the guardians of the poor to pay one half or some proportion of the dispenser’s charge. These suggestions are worthy of consideration by pharmacists generally as being calculated to pave the way towards a very considerable modification of the mode in which the dispensing of medicine is carried out, and as there is no branch of the chemist and druggist’s business which is more in need of such a change for the better, we commend to the attention of our readers the work that has been done in this direction by the Rochdale Association . It is emi¬ nently desirable that the attempt thus made to provide for the transfer of dispensing to the hands of chemists and druggists should receive general and earnest support from every member of the body, and we are disposed to believe that by such means it may eventually be possible to secure a very much larger share of this business. The feeling on the part of medical practitioners is in many instances very decidedly in favour of giving up the practice of dispensing, and we would urge upon every member of the trade the importance of taking all possible advantage of this disposition by offering facilities which will remove some of the difficulties attending such a change of procedure, and by giving every assurance to medical men that the dispensing of their prescriptions would be carried out in all respects so as to command the satisfaction of themselves and their patients. STRANGE CASE OF ARSENICAL POISONING Another extraordinary case of poisoning with arsenic is reported as having occurred at Hudders¬ field which recalls to mind the cases of poisoning, resulting from the use of “ violet powder ” contain¬ ing an admixture of arsenic. A woman who had been in the habit of taking prepared chalk to relieve heart-burn was attacked after taking a dose with sickness and pains, for which a medical man adminis¬ tered a sedative. Two days afterwards the woman died and a post mortem examination revealed appear¬ ances of arsenical poisoning. It was then found that she had been supplied with powdered “French chalk ” by mistake, instead of prepared chalk, and that this “French chalk” contained as much as 40 per¬ cent. of arsenic. It is stated that the French chalk had been supplied by a Manchester firm and the- coroner requested the chief constable to communicate with the Manchester police on the subject. CHEMICAL SOCIETY’S RESEARCH FUND. According to the Chemical News the following O’ grants have just been made from the Research Fund of the Chemical Society : — £30 to Mr. W. Whiteley Williams, for experiments on an Improved Method of Organic Analysis. £25 to Mr. M. M. Pattison Muir, of Caius College,, Cambridge, for Determining the Physical Constants and Chemical Habitudes of certain Bismuth Compounds. £15 to Mr. J. M. Thomson, for experiments on the- Action of Isomorphous Bodies in Exciting the Crystal¬ lization of Supersaturated Solutions. £50 to Dr. Wright, for continuing his Researches o Chemical Dynamics. £25 to Mr. F. D. Brown, for continuing his Researches- on the Theory of Fractional Distillation. £30 to Mr. Bolas, for an Investigation of certain Chro¬ mium Compounds. £20 to Mr. F. R. Japp, for an Investigation of the- Action of Organo-zine Compounds on Quinons. £100 (the De la Rue donation) to Dr. H. E. Armstrong,, for the Determination of certain Physical Properties, especially Refraction Indices, of Typical Chemical Com¬ pounds. SCHOOL OF PHARMACY STUDENTS’ ASSOCIATION. The Annual Meeting of the above Association will be held on Thursday, the 17th inst., at 8.30 p.m. precisely, when the President, Professor Attfield, will take the chair, and the Annual Report of the Committee will be read. July 12, 1879. J THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 33 fltkpattufkal fonctir of IJrelnnl MEETING OF THE COUNCIL. Wednesday, July 2, 1879. Present — Charles R. C. Tichborne, LL.D., Ph.D., Pre¬ sident ; Dr. Collins, Messrs. Brunker, Goodwin, Hayes, Hodgson, Holmes, Oldham, Pring (Belfast). The minutes of the meeting held on June 4 were read and signed. The President announced the death of Mr. James Whitla, licentiate of Apothecaries’ Hall, of Monaghan, a member of the Council ; and stated that in accordance with clause 11 of the Pharmacy Act it was necessary to fill up the vacancy thus created within ten days after its notification to him. Proposed by Mr. Pring, seconded by Dr. Collins, and resolved, “ That this Council have heard with extreme regret of the death of Mr. James Whitla, of Monaghan, and desires to offer to his widow and family their condo¬ lence and sympathy in their great affliction ; and to express to them the Council’s appreciation of the late Mr. Whitla’s valuable services as a member of this Board.” Mr. Alexander E. Doran, member of the Society, of Goldsmith Terrace, Bray, Co. Wicklow, was proposed by Mr. E. M. Hodgson, and seconded by Mr. J. L. Holmes, for election to the vacant seat on the Council. The President having put the motion, Mr. Doran was elected unanimously. William Whitla, M.D., licentiate of Apothecaries’ Hall, Dublin, of Victoria Place, Belfast, was registered as a pharmaceutical chemist. He was also proposed by Mr. R. W. Pring, and seconded by Mr. E. M. Hodgson, as a candidate for membership. Mr. James Wells, 52, Upper Sackville Street, Dublin, who was proposed by Mr. W. Hayes at the June meeting and seconded by the President, was now elected a member of the Society. The above business, which did not admit of postpone¬ ment, having been transacted, it was Proposed by Mr. Holmes, seconded by Mr. Hayes, and resolved, “ That the Council do now adjourn, in respect to the memory of the late Mr. Whitla, of Monaghan, member of the Council.” The examination for the pharmaceutical chemists’ li¬ cense was held on the same day, but had not concluded when the Council rose. Five candidates presented them¬ selves for the examination. provincial transactions. SUNDERLAND CHEMISTS’ ASSISTANTS AND APPRENTICES’ ASSOCIATION. The general meeting of the Sunderland Chemists’ Assistants and Apprentices’ Association was held at the rooms, corner of William Street, on Monday evening last, the 7th inst. The President, Mr. R. H. Mushens, occupied the chair. The President gave a brief resume •of the past session, saying that he had been much pleased by the manner in which every department of the work had been carried out ; that the success of the Association, which had just now closed its first session, had exceeded bis highest expectations, which he ascribed to the great interest taken in it by every individual member, as shown by their regular attendance at the meetings, etc. He then stated how the Association had first originated, and how frhe attempt of the assistants and apprentices in this matter had been ably supported by the chemists, who had rendered very great service to it. The pro¬ gramme drawn up at the commencement of the session had been carried out almost in its entirety, several of the papers reflecting great credit upon their authors. A very fair library also had been raised for the use of the members, which, together with the splendid materia medica collection sent by Messrs. Wright, Layman and Umney and Messrs. Burgoyne, Burbidges, Cyriax and Farries, would be of great value to the Association. Besides these donations, Messrs. Clarke, Bleasdale, Bell and Tollington gave £3 3s., at the same time promising £2 2s. annually; Messrs. Hearon, Squire and Francis, £2 2s.; Messrs. Maw, Son and Thompson, £1 Is.; Messrs. Sanger and Son, 10s.; Messrs. Southall, Brothers and Barclay, one of their cabinets of materia medica ; Att- field’s ‘ Chemistry,’ had also been received from Pro¬ fessor Attfield ; several books from Mr. George S. V. Wills, and others from chemists in the town. The President then tendered his hearty thanks to the members for their valuable assistance, and also for the harmony and goodwill which had characterized the past session, rendering his position as much a pleasure as a duty, and expressed a wish that this Association might prosper in the future as it had done in the past ; that it might prove useful to every individual member in some way or other and become ultimately second to none in the kingdom. The Secretary (Mr. R. Thompson) then read his re¬ port, in which he stated the number of honorary members was 26, of members 27, and that the average attendance had been 15. The Treasurer (Mr. A. Harding) read the financial statement, showing the income for the session to be £17 19s. 3 d., the expenditure £6 5s. Id., leaving a balance of £11 14s. 2 d. The reports, as read, were unanimously adopted, and a hearty vote of thanks having been accorded to the offi¬ cers and committee for their services, to the donors to the library and materia medica collection and to the authors of papers, the meeting proceeded to elect the officers for the ensuing session, with the following re¬ sults : — President, Mr. A. Harding ; Vice-Presidents, Messrs. Robert H. Mushens and R. Leithead ; Secretary, Mr. R. Thompson ; Treasurer, Mr. G. C. W. Wright ; Librarian, Mr. J. Johnson ; Committee, Messrs. W. Fowler, J. J. Browell, G. Proctor, J. W. Robinson, C. Rankin and A. H. Rhymer. ABERDEEN SOCIETY OF CHEMISTS AND DRUGGISTS. The members of this society held their annual dinner in the Huntley Arms Hotel, Aboyne, last week. Among those present were Mr. D. Reid, (in the chair), Dr. Moir, Baillie Sangster, Messrs Coutts, Cruickshank, Giles, Gordon, Gordon, jun., Presslie, Ritchie, Shepherd, Sinclair, Strachan and J. J. Petrie, Aboyne. After dinner the following toast-list was gone over. “The Queen and the Royal Family,” and “The Aberdeen Society of Chemists and Druggists,” by the Chairman ; The Pharma¬ ceutical Society,” proposed by Mr. Presslie, and replied to by Baillie Sangster; “The Medical Profession,” by Mr. Cruickshank, acknowledged by Dr. Moir; “The Town and Trade of Aberdeen,” proposed by Mr. Strachan, responded to by Mr. Sinclair ; “ The Aberdeen School of Pharmacy,” by Mr. D. Ritchie, replied to by Messrs. Strachan and Gordon; “The Ladies,” by Mr. Gordon, jun., responded to by Mr. Giles; “Aboyne and District,” by Mr. Shepherd, replied to by Mr. J. J. Petrie; and “The Chairman,” by Baillie Sangster. The party returned to Aberdeen in the evening, having enjoyed themselves thoroughly. 34 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 12, 1879 SOCIETY OF ARTS. The History of Alizarin and Allied Colouring Matters, and their Production from Coal Tar.* BY W. H. PERKIN, F.R.S. (Continued from page 18). The attention of Graebe, in conjunction with Lieber- mann, was then turned to alizarin, which they thought probably might belong to the quinone series ; but it was important that they should first know to what hydrocar¬ bon it was related. To obtain that information, alizarin prepared from madder was taken and heated with pow¬ dered zinc, according to Baeyer’s method of reducing aromatic compounds, and in this manner they obtained a crystalline hydrocarbon, having the composition CUH10. This was shown to be anthracene, a hydrocarbon contained in coal tar. Reasoning from the information which they had thus obtained, they assumed alizarin to be a dioxy- quinone acid of anthracene — c14h 10 c14h8o2 Anthracene. Anthraquinone. Alizarin. But to prove this to be the case it was necessary to pro¬ duce alizarin from anthracene. This hydrocarbon was discovered by Dumas and Laurent in 1 832. They obtained it from the product which comes over towards the end of the distillation of coal tar. They gave it the formula C15H12, and as this was one and a-half times the molecular weight of naphthalene they called it paranaphthalene. It was further examined by Laurent, who changed its name to anthracene. He also obtained from it a body which he called anthracenuse, by oxidizing it with nitric acid ; to this he gave the formula Q15H-8O4 and C15H705. In 1854-55, when studying under Dr. Hofmann, at his suggestion I took up the subject of anthracene for my first investigation. I prepared the hydrocarbon by dis¬ tilling pitch. Dr. Hofmann afterwards kindly obtained for me, from Messrs. Bethel, several pounds of a product rich in anthracene. On oxidizing anthracene I obtained a product to which I assigned the formula C]4H10O2, and not doubting Laurent’s formula for the hydrocarbon anthracene, believed this oxygenated product to be de¬ rived from it by loss of carbon and hydrogen. These results were not published, and I only mention them here because it was through the experiments I then made that I obtained much information, which afterwards proved to be of great value to me ; and, moreover, the products I then made served for the experiments to which I shall have to refer presently. In 1857, Fritsche examined a hydrocarbon from coal tar, to which he gave the formula C14H10, and showed that it had many properties in common with anthracene. In 1862, Dr. Anderson published an account of his investigations on anthracene. He found it to possess the formula C]4H10, and to be identical with Fritsche’s hydro¬ carbon. Dr. Anderson also prepared the oxidation pro¬ duct, and found it to contain C14H802. He called it oxanthracene ; it is identical with Laurent’s anthracenuse, and with the product I obtained. Graebe and Liebermann at once recognized this as the quinone of anthracene. It, therefore, only remained for them to convert this into the quinone acid by replacing two atoms of hydrogen by hydroxyl, and thus settle the question as to whether alizarin be a quinonic acid of anthracene or not. The process they adopted has long been used by che¬ mists ; it consists in first replacing the hydrogen of the compound with bromine or other halogen, and then * From the Journal of the Society of Arts. treating the resulting body with sodic, potassic or other metallic hydrate, and according as one, two or more atoms of hydrogen have been replaced by bromine, so on its removal by the metal of the hydrate, a compound con¬ taining a corresponding number of atoms of hydrogen replaced by hydroxyl is obtained. Acting upon this principle, Graebe and Liebermann heated anthraquinone in sealed tubes, with bromine, in the proper proportions, to obtain a dibromanthraquinone-, Cj4H6Br202. And this substance, when fused with caustic^ potash, yielded alizarin in combination with the alkali, from which it was separated by means of an acid. They also proposed a second method for preparing dibroman¬ thraquinone, viz., by oxidizing tetrabromanthracene — C14HBBr4 + 02 = Ci4H6Br202 + Br2. The great importance of alizarin, as a dyeing agent,, induced Graebe and Liebermann to patent their process,, but it was of no commercial value. They had, however, solved the question of its relationship to anthracene and anthraquinone, and also established its formula — Strecker, in 1866, had given the correct formula for alizarin, but did not publish it in the ordinary way results of research are usually published, but adopted it in his * Traits de Chimie Organique.’ And it was not until he drew my attention to the fact, that I became aware of it. He also states that he instituted experiments in 1855, in conjunction with Staedel, to establish the relationship between alizarin and anthracene. Graebe and Lieber¬ mann appear to have had no knowledge of this. On distilling purpurin, the other colouring matter of madder previously referred to, Graebe and Liebermann also obtained anthracene, and this confirmed the formula Strecker had assigned to this substance, viz., Cx4H805. Purpurin is anthraquinone, with three atoms of hydro¬ gen replaced by hydroxyl. C14H5 I OH | 02 Graebe and Liebermann’s process for the preparation of alizarin being found to be impracticable, it was desir¬ able, if possible, to find a new method which would render their discovery of commercial value. It has been known for a very long time that sulphuric acid acts upon many organic bodies, producing sub¬ stances called sulpho-acids. In composition these repre¬ sent the body acted upon plus sulphuric anhydride, the basicity of the product (if derived from a neutral body) increasing with the number of molecules of sulphuric anhydride used in its formation. These so-called sulpho- acids have been found, however, to be nothing more than acid sulphites ; thus the acid produced by the combination of benzol with one molecule of sulphuric anhydride is an. acid sulphite of phenyl, or phenyl-sulphurous acid : — CsHeSO^ = CgHsSOgH Sulphobenzjlic Phenylsulphurous acid. acid. And that obtained by combining naphthalin with two- molecules of sulphuric anhydride is an acid disulphite : — C.0H8(SO3)2=Cl0H6 j * 3 Disulphonaphthalic Naphthylene-sulphur- acid. ous acid. The experiments of Wiirtz and Kekul6, in 1867, cor.t- firmed this view of the constitution of these acids. They found that sulpho-benzolic acid, when heated with caustic potash, produced a phenate and sulphite, thus : — - CfiHgSOgH + 3 K HO = Sulpho-beuzolic acid. C..H.OK + SO0K0 + 2 OH., Potassic phenate. July 12, 1879.3 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 35 In the same year Dusart also found that disulphonaph- thalic acid yielded in the same way a naphthylenate and a. sulphite. °»H«iio^6KHO= Disulphonaphthalic acid. OK OK + 2 S03lL + 4 OH2 Potassic naphthylenate By the addition of an acid to the products of these reactions they obtained, first from benzol, by means of the sulpho acid, hydrate of phenyl, phenol of carbolic sicid, and from naphthylene, the dihydrate of naphthy- lene. c6h6 Benzol. c10h8 c6h5oh Hydrate of phenyl. fi it j OH viori6 j OH Naphthylene. Dihydrate of naphthylene. In this second example it will be seen that we have obtained a body standing to naphthylene as alizarin does to anthraquinone. In other words, two atoms of hydro¬ gen have been replaced by two hydroxyls. It therefore appeared probable to me that, if a disulpho acid of anthraquinone could be produced, alizarin might possibly be obtained by a similar process. From my previous knowledge of the remarkable stability of anthraquinone, and that it might be dissolved in strong hot sulphuric acid, and would then crystallize out unchanged on cooling, it did not appear very probable that a sulpho acid could be formed ; nevertheless, experi¬ ments were made, varying temperatures being employed, when eventually it was found that by heating a mixture of sulphuric acid and anthraquinone very strongly, com¬ bination actually took place, the mixture becoming perfectly soluble in water. After removing the excess of sulphuric acid from the new product it was mixed with caustic potash and heated to about 180° C. ; it soon became coloured, and then black. When the reaction was considered complete, the black alkaline mass was dissolved in water, and formed a rich purple solution. On acidifying this it became yellow, from the separation of a copious precipitate, which, on examination, proved to be artificial alizarin. This product, when collected on a filter and thoroughly washed, was found to dye madder mordants with the greatest readiness. The great obstacle to the preparation of alizarin, viz., the use of bromine, was thus removed, and, as the result has proved, a process had been obtained by which this colouring matter could be manufactured in quantity. I may here mention that, while these experiments were in progress, Caro, Graebe, and Liebermann were investi¬ gating the same reaction in Germany.* * * * * § * Graebe and Liebermann, in a paper published in the Moniteur Scientifique, April, 1879, p. 399, state that “ Caro was the first to observe that anthraquinone, when heated with sulphuric acid above 200°, formed sulphoconjugated acids, which, like the brominated compound, gave alizarin on fusion with potassium hydrate ; soon afterwards, or almost at the same time, Perkin made the same observa¬ tion.” Again, at pp. 400 — 401, they state “The patent of Caro, Graebe, and Liebermann is dated a day before that of Perkin. If any particular importance is attached to dates, the advantages rests without dispute with Caro, for tho filing of the patent of the German chemist was delayed through irregularity ( vice de forme). The signatures had already been given in to the Patent Office, Berlin, on the 15th June.” I may remark, in reference to the first state¬ ment, that Graebe and Liebermann neither give or adduoe any evidence to substantiate their claim to priority. Their remark that I had soon afterwards, or almost at the same time, made the same observation, also goes to show that they have none. And in reference to the statement that their | A short time after I had discovered this method of making artificial alizarin, I found an entirely new process, in which anthraquinone is not required at all.* Anthracene forms with chlorine a beautifully crystalline body, called dichloranthracene, having the formula, C14H8CL>. This substance combines with Nordhausen sulphuric acid, forming a bright green solution, which consists of a sulpho acid of dichloranthracene. This compound undergoes a remarkable change when heated with sulphuric acid, hydrochloric acid and sulphurous anhydride being evolved, and a sulpho acid of anthra¬ quinone formed. This process has proved to be of great value, as will be seen further on. When artificial alizarin was first manufactured it was noticed that the colours produced by it differed, to some extent, from those produced with madder or alizarin. The red shades were more brilliant and more scarlet, and the purples bluer ; the blacks were also more intense, and some persons went the length of saying that alizarin had not been produced artificially at all. This I refuted in a paper read before the Chemical Society in May, 1870,+ when I showed that alizarin could be readily separated from the commercial product, and then possessed all the properties of natural alizarin, both as regards its dyeing power and in its other characteristics. As no doubt now exists on this point, I think I need not further discuss it. In a foot note+ in the paper just referred to I stated that “ when purifying artificial alizarin by converting it into an alumina lake, I found that, upon digestion with carbonate of potash, this lake gave a red coloured solution, containing a colouring matter dyeing mordants very similarly to alizarin, with the difference that the reds were more scarlet, and the purples bluer or more slaty. I have not obtained this body in a perfectly pure state as yet, but it appears to be crystalline. It gives two faint black bands when examined in alkaline solution with the prism, but these may perhaps be due to the presence of traces of alizarin.” Some time after this, I made a complete examination of this substance, § and my analytical results showed it to have the same composition as natural pur- purin, viz : — \ °H ) C14H5 OH 02 (oh! though it differs from it in properties, in fact, it is an isomeride of that substance. Being a derivative of anthracene, I therefore named it anthrapurpurin. Auer¬ bach, || in 1872, separated a colouring matter from artificial alizarin. He named it isopurpurin. It is, how¬ ever, identical with anthrapurpurin. The name isopur¬ purin is now mostly used for this substance on the Continent. The importance of anthrapurpurin as a colouring matter can scarcely be overrated. I believe I may truly say it is of as great importance as alizarin itself, and its existence in artificial alizarin has been the cause of its marvellously rapid success, as it gives a brilliancy to the reds which cannot be obtained with madder. Anthrapurpurin differs from alizarin in many particulars. When heated it is mostly decomposed, only a little subliming in orange-red vapours, and condensing a3 yellowish red leaves. If a mixture of anthrapurpurin and alizarin be sublimed, the signatures had been given in to the Patent Office, Berlin, on the 15th June, I find that on May 20th I wrote to Mr. Robert Hogg, of Glasgow, enclosing patterns dyed with artificial alizarin, which I had prepared by fusing the sulphoconjugated acids of anthraquinone with potassium hydrate, and my patent might then have been secured, but was delayed. Therefore, their conclusions, from the argu¬ ment as to dates, should be reversed. * Patented November, 1869, No. 3318. + Journal of the Chemical Society , 18/0, p. 133. X Journal of the Chemical Society, 1870, p. 143. § Journal of the Chemical Society, 1872, p. 659 ; 1873, p. 425. |J Moniteur Scientifique, 1872, p. 686. 36 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. (July 1?, 187*. sublimate will consist almost entirely of alizarin, as this substance is not so easily decomposed by heat. Anthrapurpurin dissolves in caustic alkalies with a more purple colour than alizarin. It also differs in its behaviour with alumina. A solution of anthrapurpurin in sodic carbonate, when mixed with freshly precipitated alumina, is not absorbed by it, whereas alizarin under the same conditions is perfectly absorbed. It crystallizes in orange yellow needles, from alcohol or glacial acetic acid. By heating it with acetic anhydride I obtained a triacetyl derivative, and by using benzoyl chloride, a tribenzoyl one, thus showing it to contain three replaceable hydrogens. Its alkaline solutions give two faint absorption bands when viewed with the spectroscope, these bands being in the same region of the spectrum as those produced with alkaline solutions of alizarin. When oxidized with nitric acid it does not yield phthalic acid. On heating anthrapurpurin with ammonia to a tempera¬ ture of 160° — 180°C., in a closed tube, I found it changed into an amidated compound, which has been named anthrapurpuramide. This substance does not dye mordants. Its solution in alcohol is of a clear dark orange- red colour. It dissolves in alkalies with a purple colour. Anthrapurpuramide is isomeric with amido alizarin. Its formula is — ( NH.2 ) C14H5 OH 02 ( °H ) . In my paper on anthrapurpurin it is mentioned that there is a colouring matter in artificial alizarin dyeing alumina mordants of an orange colour.* * * * § This was afterwards obtained in a crystalline condition, and was under investigation for some time, but the research was laid aside on account of more pressing subjects. This substance, however, proves to be flavopurpurin, a colouring matter lately described by Schunck and Roemer,f and obtained by them from anthraflavic acid. It has the formula — ( 0H ) C14H5 \ OH } 0o ( OH ) and is therefore isomeric with anthrapurpurin. The amount of it contained in artificial alizarin is not very large. It is much more freely soluble in alcohol than anthrapurpurin, and crystallizes from that solvent in orange coloured silky needles. Its alcoholic solution, when poured into water, forms a yellow precipitate ; this, however, has a satiny aspect, owing to the crystalline character of the precipitate ; it dissolves in caustic alkali with a purple colour, redder than that produced with anthrapurpurin, and in ammonia it forms a brownish red colour, anthrapurpurin forming a purple solution. Flavopurpurin dyes mordants, but the colours on those of alumina are of an orange red colour, the pinks being somewhat of a salmon shade. The purples are more like those of alizarin, but very dull in comparison with them. In artificial alizarin I believe there is yet another colouring matter not investigated, dyeing alumina mordants a still yellower shade than flavopurpurin. It is apparently present in very small quantities. We now see that the product at first made and called “artificial alizarin,” contained at least three colouring matters, viz., alizarin, anthrapurpurin, and flavopurpurin ; as I think it will be convenient to retain this name at present, for simplicity sake, it will be understood that, when I use it, I do not refer to pure alizarin, but to commercial products known by that name. Before proceeding to speak of some of the products found in artificial alizarin, I wish to draw attention to a soluble intermediate substance which is obtained in its preparation if the process of heating with caustic soda be not carried on sufficiently long. In this case, although the alkaline product dissolved with a strong violet colour, I noticed that, when acidified, no colouring matter, or * Journal of the Chemical Society, 1873, p. 425. f Deut. Chem. Ges. Ber., 1876, p. 679. only a small quantity, was precipitated, a strong dark yellow solution being obtained. On isolating this body it was found to be crystalline, forming orange -coloured needles, easily soluble in water, but insoluble in ether. With alkalies it forms a blue violet-coloured solution ; it does not dye mordants. When fused with caustic aklali it is converted into anthrapurpurin. From the mode of its formation and from its decomposition with alkalies I gave it the formula : — c14h6 i OH \ S03H o„ and named it sulphoxanthraquinonic acid.* Some time afterwards Graebe and Liebermannf further investigated! this compound and confirmed this formula. With the alkaline earths it forms two sets of salts — acid and neutral ones — the former being of a yellow colour ; the latter violet. These probably could be used as pigments. The artificial alizarin, as first made, contained not only three colouring matters, but also other products not possessing dyeing powers. These are of considerable interest, as will be seen further on. Amongst these are anthracene, anthraquinone, and hydroanthraquinone, pro¬ ducts which are the result of a peculiar reverse action, or process of reduction, which takes place in the preparation of artificial alizarin during the operation of heating with caustic alkali. The first, viz., anthracene, was only formed in the early experiments, and resulted from over¬ heating. But the two other substances are always obtained if caustic alkalies alone are used. Of anthra¬ quinone I have already spoken, but I have not referred to the action of reducing agents upon it. If anthraquinone be mixed with a solution of caustic potash and ziuc dust, the liquid quickly becomes red, especially if heated, the anthraquinone dissolving. Tnis liquid may be filtered ; but as the oxygen of the air quickly acts upon it, films of anthraquinone are formed ; if the air be excluded, a clear red-coloured fluid is obtained, and on the addition of an acid, a yellow precipitate is formed. This substance is hydroanthraquinone, produced from anthraquinone by its union with hydrogen. Its formation may be represented thus : — C14H802+H2 = Ci4H10Oa Anthraquinone. Hydroanthraquinone The other bddies I have to speak of are not due to any reverse chemical action, but are the products of direct changes, and were regarded as secondary products. On boiling up artificial alizarin with dilute caustic soda, and adding milk of lime, it was found that the colouring, matter was precipitated, leaving a yellow or orange coloured solution. On filtering this off, and adding an acid to the filtrate, a pale yellow precipitate was obtained. A quantity of this was prepared, washed and dried, and from some of it Dr. SchunckJ succeeded in isolating a beautiful yellow crystalline product. This he called anthraflavic acid, and assigned to it the formula, C15H10O4. Not being satisfied with this: ormula, I afterwards sub¬ mitted it to investigation^ and showed it to have the composition C14H804, which has since been confirmed by others. I his formula is the same as that of alizarin, and therefore, anthraflavic acid is an isomeride of that substance. It is prepared from its barium salt, which is somewhat difficultly soluble in water. Anthraflavic acid is a beautiful substance, crystallizing- in bright yellow silky needles, and, when heated, gives a* sublimate of golden yellow crystals in the form of leaves or plates, a certain amount being, at the same time, carbonized. It does not dye mordants. It combines with alkalies, forming compounds dissolving in water with an orange red colour. The barium salt, already referred to, crystallizes in needles of a brownish red * Jou/rnal of the Chemical Society, 1870, p. 139. f ‘ Jahresberioht,’ 1871, p. 685. t ‘ Broc. Lit. and Phil. Soc./ Manchester, vol. x., p. 13$. § Journal of the Chemical Society, 1871, p. 1109. July 12, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS 37 colour, and its cold aqueous solution is somewhat similar in appearance to that of potassic bichromate. Dr. Schunck found that anthraflavic acid when fused with caustic potash was converted into a colouring matter, which he thought to be alizarin. I also believed this to be the case until some time afterwards, when I prepared a sufficient quantity of the colouring matter to dye a pattern with. I then found it produced orange red colours with alumina mordants.* Schunck and Roemerf have since investigated this reaction, and found that the colouring matter is an isomer of anthrapurpurin ; in fact, it is flavopurpurin, which has already been described. Its formation may be ex¬ pressed thus — C14H804 + 3 OKH = C14H5K305+H2 + 20H2 Anthraflavic acid. Potassic fiavopurpurate. To effect this change in small experiments, a temperature over 200° C. is necessary. Dr. Schunck and H. RoemerJ have published an account of another substance which accompanies anthra¬ flavic acid. They have named it isoanthraflavic acid. I had also succeeded in obtaining this substance, and also in preparing it without the formation of colouring matter, except in small quantities.^ To this I shall refer presently. Isoanthraflavic acid crystallizes from glacial acetic acid, in which it is difficultly soluble, in yellow needles. These lose their lustre on being dried at 100° C. When strongly heated it sublimes in leaves of a golden or orange colour. This substance has the formula — OH c14h6 OH O, and is, therefore, another isomer of alizarin. It differs from anthraflavic acid, in forming a barium derivative, which is easily soluble in cold water with a dark red colour. Heated with acetic anhydride it forms a pale yellow crystalline body, having the formula- OCoH.O CUH, 6 1 OC0H3O 0„ Diacetoisoanthraflavic acid. When heated to about 180° C. with caustic potash it undergoes a very interesting change. The mixture gives a black-looking product, which dissolves in water with a beautiful purple colour. On acidifying this with an acid a yellow precipitate is formed, which is found to consist of anthrapurpurin. This change is similar to that which takes place when anthraflavic acid is treated with caustic alkalies, but occurs at a much lower temperature. This reaction is as follows : — C14H804 + 3 OKH = C14H5K305 + H2 + 2 OH, Is >antbrafl»vic acid. Potassic Anthrapu rpurate. Isoanthraflavic acid does not dye mordants. Another substance was found in artificial alizarin, as a bye-product, by Caro and Glaser. It was first examined in 1871 by Liebermann,|| who found it to have the for¬ mula: — Cl4H7 (OH) 02 and named it monoxanthraquinone. It crystallizes from alcohol in fine yellow needles. It does not dye mor¬ dants. Monoxanthraquinone, when fused with alkalies, also undergoes an interesting change. It becomes a nearly black mass, which dissolves in water with a blue- violet colour, and this solution, on being acidified, gives a yellow precipitate, which is nothing but pure alizarin. * Journal of the Chemical Society , 1873, p. 20. t Deut. Chem. Ges. Ber., 1876, p. 679. X Deut. Chem. Ges. Ber., 18/5, p. 1628, and 1876, p. 379. § Journal of the Chemical Society, 1876, i, 851. || Deut. Chem. Ges. Ber., 1871, p. 108. C14H7 (OH) 0,-f 2 0KH = Monoxanthraquinone. C!4Hg I Q]£ I °2 "k Ho “k 0H2 Potassic Alizarate. Now, how can the presence of monoxanthraquinone, anthraflavic, and isoanthraflavic acid in artificial alizarin be accounted for ? When sulphuric acid acts upon anthraquinone, two kinds of sulpho acids are formed, namely, a mono and a di. C14H7 (S03H) o2 Monosulphanthraquinonic acid. C»H« i SOgH i O. V. _ / Disulphanthraquinonic acid. After the manufacture of alizarin had been commenced, Graebe and Liebermann published an account of these bodies.* They found that monosulphanthraquinonic acid, when heated carefully with alkali, yields monoxanthra¬ quinone. C14H7 (S03H) 02 4- 3 OKH = C14H7 (OK) 0, + S03K2 + 2 0H, Potassic monoxanthraquinonate. And this, when further heated, yielded alizarin as pre¬ viously stated. The disulpho acid, when heated with alkali, they said, formed alizarin. CuHejJgg j 02 + 6KHO = 02 + 2 S03K2 + 4 OH2 This, as we shall see presently, was a mistake, prob¬ ably from the fact that the need of a disulpho acid for the preparation of alizarin had never been doubted, the process being supposed to be analogous to that originally described with dibromanthraquinone. But it was gradually found, when manufacturing artificial alizarin on the large scale, that the smaller the amount of sulphuric acid used to convert the anthra¬ quinone into sulpho acids, the temperature being also kept as low as practicable, that the colouring matter made from such a product yielded with mordants shades of colour more nearly approaching those produced with madder, until eventually the unexpected result was arrived at, that it was necessary to have a monosulpho acid of anthraquinone for the preparation of pure alizarin, and that the disulpho acid does not yield this substance at all, so that, in the preparation of pure alizarin, the following reactions take place, monosul¬ phanthraquinonic acid is first decomposed into monoxan¬ thraquinone ; and this, when further In ated with alkali, is oxidized into alizarin. We thus see that this formation of alizarin differs entirely from that originally discovered by Graebe and Liebermann, both as regards the chemicals employed and the chemical changes which take place. We also see that monoxanthraquinone is an intermediate product and not a secondary one. Disulphanthraquinonic acid, although it does not yield alizarin when heated with alkalies, yields anthrapurpurin. But how is this to be accounted for ? It has been shown that the first action of caustic alkali on this acid results in the formation of sulphoxanthraquinonic acid : — C, ,H Uu6 OH S03H O., This, when further treated with the same reagent, changes into anthrapurpurin : — OH OH J. 0., OH C'i4H5 * ‘Jahresbericht,’ 1871, 683-684. 38 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 12, 1879. When I became fully acquainted with this fact, I was under the impression that an intermediate body must be formed, standing to anthrapurpurin as monoxanthra- quinone does to alizarin, and formed simply by the replacement of the SOoH group in sulphoxanthraquinonic acid by HO. Such a substance was found in artificial alizarin, and I have already described it ; it is isoanthraflavic acid. In proof of its being always formed previously to anthra- purpurin, I succeeded in obtaining it directly by heating a salt of disulphanthraquinonic acid with a dilute solution of caustic potaslb. I employed a 5 per cent, solution of this alkali, and only little more than a sufficient amount to effect the decomposition indicated by theory, thus : — Cl4H6 j J 03 + 60KH = Disulphanthraquinonic acid. C14H8 j | 02 + 2S03K;! + 40H;, Potassic Isoanthra- fiavate. The mixture was heated in a closed iron vessel to 180°- 190° C. for six or seven hours. In this manner scarcely any anthrapurpurin was formed, and the alkaline solu¬ tion, when acidified, gave a precipitate consisting chiefly of isoanthraflavic acid. So that in the formation of anthrapurpurin from disulphoanthraquinonic acid we get the following changes : — First, the formation of sulphox¬ anthraquinonic acid ; second, the formation of isoanthra¬ flavic acid ; third, the formation, of anthrapurpurin ; and we see that isoanthraflavic acid is also an intermediate product in the formation of anthrapurpurin, and not a secondary one. The formation of anthraflavic acid has now to be accounted for. When sulphuric acid acts upon anthraquinone, it is found to form two isomeric disulpho acids, one forming an easily soluble sodium salt, the other a less soluble one. The former is known as the @ sodic ‘disulphanthraquinonate, the latter as the a. This less soluble, or a salt, when treated with alkalies, undergoes analogous changes to the (3 salt, but, instead of forming isoanthraflavic acid, yields anthraflavic acid, and this, as previously stated, when heated strongly with alkalies yields flavopurpurin. Anthraflavic acid is, therefore, an intermediate body and not a secondary one. We see, then, how these various bodies are formed, and as they are proved to be intermediate products, their presence shows imperfection in the process of manufac¬ turing, because, if perfect, these substances should not have been left, but have been converted into colouring matter. There are two other substances whose presence has not as yet been accounted for, and these are anthra- ■quinone and hydroanthraquinone. Monexanthraquinone, isoanthraflavic acid, and anthra¬ flavic acid, when being converted into colouring matter by treating with caustic alkali, cause nascent hydrogen to be liberated, as we have seen. This, acting upon other portions of these same substances, reduces them thus: — cuh8o3 + h2 = c14h8o2 + oh2 Oxanthraquinone. Ci^HsOi + H4 = C14H802 + 20H2 Isoanthraflavic and anthraflavic acid. And part of the anthraquinone thus formed also unites with hydrogen, forming hydroanthraquinone. The presence of these two substances, then, represents a certain amount of reverse action, and, consequently, iloss to the manufacturer. Fortunately, means have been found of almost entirely preventing their formation, and .also of ensuring the intermediate products being con¬ verted into colouring matter. I shall have to speak of this further on. (To be continued.) arttameittarg and San ^rocfertiitgs. The Prosecution under the Apothecaries Act at Birmingham. Mr. Motteram, Q.C., judge of the Birmingham County Court, gave judgment on Friday, the 4th inst., in the case of the Apothecaries’ Company of the city of London against James Harrison, chemist, Stafford Street, Birmingham. The action, which has been several times before the Court, was brought to recover £20 damages, by way of penalty, under 55 Geo. III., cap. 194, sec. 20, against the defendant for prescribing medicine to one Julia Caddick, who was suffering from weakness sub¬ sequent to confinement, in November, 1876. The case had been postponed pending the decision of a higher Court in what is known as “Shepperley’s case,” of Nottingham. The plaintiffs contended that in prescribing medicine for the woman Caddick the defendant infringed the rights of an apothecary. The defendant took refuge under a proviso of the 28th section of the same Act, and counsel on his behalf contended that he had a right to prescribe medicine in a case like that under the notice of the Court. In giving judgment, Mr. Motteram said that if the language of the 28 th section were carefully considered, he was afraid it would be found not to have the effect contended for on the part of the defendant. He found from the evidence that the defendant had clearly and unmistakably acted as an apothecary, and Jhe proviso relied upon afforded, in his opinion, no defence in such a case as that. The verdict, therefore, would be for the plaintiffs for £20 damages and costs. — Times. Notice has been received of the death of the fol¬ lowing : — On the 24th of May, 1879, at Newark, Mr. John Hanson Gibson. Aged 21 years. Mr. Gibson was a Registered Apprentice of the Society. On the 12th of June, 1879, Mr. James Briggs, Phar¬ maceutical Chemist, Tipton. Aged 64 years. Mr. Briggs had been a Member of the Pharmaceutical Society since 1842. On the 28th of June, 1879, Mr. William Henry Moon, Pharmaceutical Chemist, High Street, Ilfracombe. Aged 43 years. Mr. Moon had been a Member of the Phar¬ maceutical Society since 1863. On the 1st of July, 1879, Mr. Stephen Cox, Chemist and Druggist, Fore Street, Hatfield. Aged 75 years. Stspensittg Jftentoitanda. In order to assist as much as possible our younger brethren, for whose sahe partly this column was established , considerable latitude is alloived, according to promise, in the propounding of supposed difficulties. But the right will be exercised of excluding too trivial questions, or re • petitions of those that have been previously discussed in principle. And toe would suggest that those ivho meet ivith difficulties should before sending them search previous numbers of the Journal to see if they can obta/in the re¬ quired information. Replies. [315]. Sal Ammonise. Spt. Nitre. Sp. Wine. Opodeldoc. In this recipe “ sal ammonise ” means liq. ammon., B.P., and if “A Norfolk Man” tries it he will get a clear solution. In many districts liq. ammon. is well-know n by the name of sal ammonise or spirit of sal ammoni se (just as uly 12, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 39 liq. vol. c.c. is called Hartshorn), and recipes similar to the one in question are so commonly met with that I am surprised there should be any doubt or difficulty in the matter. Manchester. W. Wilkinson. [319]. I think W. took an entirely mistaken \iew of the prescription in question. In my opinion, he should simply have triturated the litharge and olive oil in a mortar till a liniment was formed. The late Professor Hamilton, professor of midwifery in Edinburgh, used to prescribe the following as a nipple liniment : — ■* R Plumb. Oxy. Sem. Yit. Acetum . a a oij. 01. Olivae . ‘ 3vj. Rub together till a flesh colour is obtained. H. C. B. [322], What is meant by W. B. in regard to the puzzle to solve, in the admixture of tr. lyttae, acid, sulph. dil., tr. lavand. co. and vaseline or lard ? I have made a very nice ointment, almost similar in appearance to pink shaving cream, with the proportions given. I find no difficulty; but I was rather interested in the prescription, owing to the addition of tr. lavand. co., as I have employed a somewhat similar ointment for ringworm. In regard to the compatibility or incompa¬ tibility I have nothing to say. It is sometimes very useful as an application. Northallerton. Henry Brown. [323]. The gtt. 2 after sod. siccat. was evidently a slip of the pen ; grs. 2 was clearly meant. Northallerton. Henry Brown. [324]. The prescription of “ Gulielmus ” is one of those which a pharmacist is often at a loss to understand, and if he be thoroughly orthodox and will adhere to the exact written order of a physician or surgeon, it certainly is sufficient to raise not only discussion but much doubt as to what is meant by morphia when ordered in the proportion of eight grains to half an ounce of a mixture of chloroform and liniment of belladonna. I observe “ Gulielmus ” adds after morphia “ the alkaloid,” so as to italicise, as it were. Now morphia is very sparingly soluble in chloroform ; so also are the acetate and hydrochlorate. Cold alcohol dissolves one in fifty of morphia, the hydrochlorate is soluble in about sixty parts of cold alcohol, the acetate in a little less, and the sulphate in still less. I have often used the liniment, although not in exactly the same proportions as given by “Gulielmus,” in painful neuralgias of the face. The practical point is, How can a complete solution be obtained ? I am sure in “ The Month ” this question will occupy, as it deserves, some consideration. As an old compounder, I saw at once the difficulty. The fact was that the person who first dispensed the prescription fully understood the insolubility of morphia in the menstruum ordered. Was a departure of only a slight degree justifiable, so as to have morphia in perfect solution, although that must necessarily be a salt of morphia, under the circumstances ? I at once say it was. In my opinion the medical man intended perfect solu¬ tion. How, then, is a perfect solution to be obtained ? It cannot be obtained by using hydrochlorate or acetate of morphia. Sulphate, if well prepared, will dissolve, but the easiest mode is to add a small quantity of dilute sul¬ phuric acid, and all trouble vanishes, to either morphia, or hydrochlorate or acetate. Some one may say this is unjustifiable meddling with a prescription. I say no. The intention is to have morphia in solution, and if the prescriber is unaware of the insolubility of such a large quantity in a given quantity of menstruum, but yet intends a strong solu¬ tion, surely it is the business of the pharmacist to carry out his intention. I look upon this question as one of the most important and interesting that has yet been asked. Not one medical man in a hundred, and not one pharmacist in fifty, has any idea of such exact proportions as given by “Gulielmus.” Northallerton. Henry Brown. Queries . [326]. I shall be glad if any reader can inform me if the following prescription can be dispensed so as to form a mixture of a presentable appearance : — R Tinct. Gelsemin. Semper. . . . . 3iv. Ferri et Quiniae Cit . . . 3iss. Croton Chloral Hyclrat. . . • • 3j- Potass. Bromidi . Potass. Iodid . . . 3ss. Aquae Chloroformi .... . ad gviii. M. Sign, sss 4tis horis ex aqua. Sub Umbra Floresco. [327]. What is the best method of dispensing the following to obtain a presentable mixture : — R Sodae Salicylat . . . [)iv. Croton Chloral . . . 5 iv. Quiniae Sulphat . • • Bj Aq . M. Ft. mist. 5j ter in die sd. [328]. R Ammon. Bromid. ....... 3^* Tinct. Hyoscyami, Tinct. Humuli . a a 3^v< Aquae . ad gviij. M. Ft. mist. Can any of your readers inform me how the above may be dispensed so that the mixture should be of a clear bright sherry colour — not at all opaque ? I had the prescription brought by a customer, who assured me it was made up in one of the well known leading city establishments, and it was sent out as thus described. It was afterwards dispensed by respectable chemists in the country and by myself. All the mixtures obtained in the country corresponded with the one I mixed. How is it that the London one was an exception, and how can the compound result in a clear bright mixture ? C. B. [329]. Will you kindly inform me through the Journal how I can make a clear mixture of “ dandelion and quinine,” on mixing the tr. quiniae with liq. tarax. ? Luton. W. C. S. [330]. Will some of your readers kindly inform me how the enclosed prescriptions should be dispensed ? No. 1. R Quinae Sulph . gr. xx. Sodae Salicylatis . 3iss* Acidi Sulph. Dil . 3j* Aquae Piment . ad §viij. Misce et signe — A tablespoonful to be taken three times a day. No. 2. R Feni Perchlor. . 3’ss* Acidi Hydrochlor . gtt. viij. Aquae . ad §vj. Misce et signe — A tablespoonful to be taken three times a day. J. S. Nemo. 40 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 12, 1879. Jjtotys and [609]. A good ruby colour for bottle lenses is formed by adding a solution of iodine made the same as lin. iodi, B.P. (omitting the camphor), to glycerine slightly diluted. It should be added gradually until the required shade is obtained. Stands well. Cortex. [610]. FURNITURE CREAM.— The following is a good formula : — r>f Yellow Wax . . . 1 lb. Yellow Soap . 2 ozs. Spirit of Turpentine . 2 pints. Boiling Water . 2 „ Melt the wax and soap over a slow fire, add the tur¬ pentine, and lastly, stir in the water gently until it is quite cold. Sub Umbra Floresco. [611] . MOORE’S OINTMENT. — It is doubtful whether “Unguentum” can obtain an authentic formula for Moore’s ointment. Moore was a quack with a cart who treated bad legs, etc., coram populo. Leather Lane on Sunday morning was a favoui ite “ pitch.” He died a short time ago. W. J. R. [612] . SYRUP OF SCAMMONY.- Would' some reader kindly oblige me with a good formula for pre¬ paring syrup, scammonii, dose 3j> ad 3ij? ' i Sub Umbra Floresco. [613]. DANDELION COFFEE.— Could any^eader oblige me with a good foi’m for making dandelion coffee? Ferri Cit [614]. “PULV. SALINI EFFERYESC. APERI- ENTIS.” — Information is required respecting the com¬ position of the above, occurring in a prescription snmed j. p. [615]. DENTIFRICE WATER.— Could any one ob¬ lige me with a recipe for a good dentifrice water. Qujero. [616]. SILVER PLATING LIQUID.— Will some one kindly furnish me with a formula for a silver plating liquid suitable for coating steel ? VfATOR. [617], CHERRY TOOTH PASTE.— D. A. would be greatly obliged for a recipe for cherry tooth paste. He has tried several published in receipt books and journals, but cannot obtain either a good consistency or that bright transparent cherry colour which is so attractive in good tooth paste. SULPHO-TARTRATE OF QUTNIA.— Dr. Pren- geber recommends for hypodermic use the following solutions : — 1. Quinia Sulphate . . 2*00 gm. or 30 grs. Tartaric Acid . . . 0’60 gm. or 9 grs. Distilled Water. . . 6’00 gm. or 100 min. To be dissolved by gently heating. 2. Quinia Sulphate . . 2*00 gm. or 30 grs. Morphia (alkaloid). . 0‘006 gm. or gr. Tartaric Acid . . . 065 gm. or 10 grs. Cherry-laurel Water . 6‘00 gm. or 100 min. Both of these injections are very rarely followed by abscess. — Rep. de Pharm ., 1879, 99. CINNABAR-PLASTER. — Dr. Yidal uses with good success, in the treatment of scrofulous ulcerations and of ecthyma, the following plaster, spread upon silk in the usual manner : — Red Oxide of Lead . 2*50 gm. or 40 grs. Cinnabar . 1*50 gm. or 25 grs. Lead-plaster .... 26’00 gm. or 400 grs. Melt the lead-plaster, add the red lead and cinnabar, mix well and spread. — Rep. de Pharm., 1879, 99. SUMMER DRINKS:— Milk Lemonade. — Loaf sugar, one and a half pounds, dissolved in a quart of boiling water, with half a pint of lemon juice, and one and a half pints of milk ; this makes a capital summer beverage. A half-pint of sherry added is a great improvement. Still Lemonade. — The juice of three lemons, the peel of one, quarter of a pound of lump sugar, and a quart of cold water. Mix, digest for five hours, and strain. Lemon Whey.- — One pint of boiling milk, half a pint of lemon juice, sugar to taste. Mix and strain. Lemon Shrub. — The juice of twelve lemons, the thin rind of two, one pound of sugar, the whites of two eggs well whisked, one pint of water, half a pint of rum, and half a pint of brandy. Mix and strain. — Monthly Maga¬ zine of Pharm. *,* No notice can be taken of anonymous communica¬ tions. Whatever is intended for insertion must be authenti¬ cated by the name and address of the uniter; not necessarily for publication, but as a guarantee of good faith. Lin. Potass. Iodid. c. Sapone, B.P. Sir, — In answer to W. H. de B.’s inquiry as to the above preparation, we have much pleasure in giving him the infor. mation he requires. The liniment was, we believe, originally introduced to the Medical Council by the late Dr. Rumsey, of Chelten¬ ham, where it was very largely used. It was always intended to be made with white curd soap dissolved in the whole of the glycerine and water, mixed in a water-bath ; then,~having powdered the iodide of potassium in a large mortar previously warmed, pour the hot solution on the iodide in the mortar, and stir a few minutes until cold ; •lastly, add the oil of lemon. You will then have a white solid preparation which does not separate. It was sent out in covered pots as an oint¬ ment, although some London houses send it in wide-mouthed bottles. South Kensington. Plaister and Hillen. “ Beta.” — Cotyledon Umbilicus. R. G. Bumpstead. — The practice of pharmacy in France is limited to persons possessing diplomas as pharmaciens. Ricini. — We do not consider that an article answering fairly to the name, or that can be sold without danger of prosecution under the Sale of Food and Drugs Act, can be prepared. R. Roberts. — (1), Not complete enough to identify; calyx absent. (2) Cor nust sang uinea. (3) Vicia Cracca. (4) Stellaria graminea. (5) Tamus communis. (6) Veronica officinalis. C. T. — (l) Lgsimachia nemorum. (2) Potentilla Tor¬ ment ilia. (3) Orchis maculata. (4) Erysimum cheiran- thoides. (5) Galium saxatile. (6) Lycopus europceus. (7) Hieracium umbellatum. G. Morgan , j'in. — (1) Centaurea nigra. (2) Geum urbanum. (3) Stachys sylvatica. (4) Alliaria officinalis. A. H. Cleland. — We should be glad if you would watch the growth and communicate the result at a future time. F. N. — Ganot’s ‘ Elementary Treatise on Physics,’ pub¬ lished by Longmans. W. Reynolds. — We believe not, but recommend you to apply to the Registrar. W. B. Stonham. — We are not acquainted with such a work. “ Owen.” — A number of papers upon the composition of chlorodyne will be found in vol. xi. of the second series of thia Journal. _ _ _ _ "Communications, Letters, etc., have been received from Messrs. J. H. Dingle, H. Long, Audio, Alpha. July IP, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 41 SPIRITUS .ZETHERIS NITROSI: ITS COMPOSITION AND ANALYSIS. BY F. M. RIMMINGTON, F.C.S. ij The nature, substance and quality of spiritus •setheris nitrosi has long been a problem asking for solution ; and as I have given a good deal of atten¬ tion to it for a long time, and feel myself under a pledge to contribute another paper on the question raised some time ago as to the actual existence of nitrite of ethyl in this compound, I now purpose fulfilling that promise. Perhaps some discriminating minds will draw a distinction between sweet spirit of nitre and spiritus setheris nitrosi. I make no such distinction, and all that is said in this paper has reference to a spirit that corresponds with that described in the British Pharmacopoeia, in nature, substance and quality. I think all who have attempted the analytical examination of this preparation, will admit it is surrounded with some difficulty. There is first, an ethereal fluid, so designated ; secondly, an ethereal oil or hydrocarbon ; thirdly, .aldehyde ; fourthly, nitrous acid, uncombined ; fifthly, acetic acid uncombinecl ; sixthly, alcohol and water. The presence of nitrite of ethyl in the spirit of the Pharmacopoeia has been denied ; and I am willing to admit it may be possibly true, but if true, it is culpably wrong, and is the result of mismanage¬ ment. If no nitrite of ethyl be formed, what be¬ comes of the nitric acid used in the operation, and what are the products of the chemical action that takes place? It does not distil over, it does not pass away as gas, but it is nevertheless consumed. After many attempts to investigate this matter, and trying all the methods that suggested themselves to me, or that I could find described for the estima¬ tion of the nitrites, I found none that gave satis¬ factory results until I adopted the following scheme, by which not only the nitrite of ethyl, but all the other constituents, may be accurately estimated. The following table, at all events, shows the results in two analyses (out of a great many others) of a typical sample, agreeing with the B.P. tests, otc.: — (0- Oh- Water .... . . 7*96 7-93 Aldehyde . . . . . 1T9 1-19 Alcohol . . . . . 88-10 88-10 Acetic Acid . . . . -47 •50 Nitrous Acid . . -59 •56 Nitrite of Ethyl . . 1-69 1-72 100-00 100-00 The method of analysis is as follows : — The nitrite of ethyl is to be estimated by the con¬ version of its nitrogen into ammonia, first by decomposing it with pure potash into KN02, and distilling this with a zinc and copper couple some¬ what after the method recommended by Thorpe, but modified by Dr. Cornelius Fox, and titrating the result with standard acid (process in detail given below). The amount of nitrous and acetic acids are esti¬ mated volumetrically. The two acids are afterwards separately estimated. Aldehyde is estimated by conversion into acetic acid by peroxide of hydrogen, and titrated. Water and alcohol by difference. Third Series, No. 473. Estimation of Nitrite of Ethyl. 5 c. c. of the spirit are added to 1 gram of pure potash (free from nitre) dissolved in 40 c.c. of pure water in a 50 c.c. graduated, flask, stoppered and capped with leather, digest in a warm place at a temperature of 150° — 200° F. for three hours. Allow the flask to cool and then dilute with water to 50 c.c., shake and then take out with a pipette 10 c.c. of the liquid and run it into a platinum dish, and add to it 40 c.c. of water, evaporate on a water-bath to 20 c.c. to get rid of the alcohol, etc. This residue is now to be washed into a flask of 16 ounces (or 450 c.c.) capacity, containing 10 grams of zinc foil coated with copper, and the volume of liquid made up to about 350 c.c. with water, and connected with a condenser; heat is now to be applied and the distillation carried on as usual. Most of the ammonia comes over in the first 100 c.c. of distillate, but it is necessary to distil another 50 c.c. to ensure perfect exhaustion. The ammonia thus obtained is now to be estimated with a standard sulphuric acid, 1 c.c. equal to -001 gram ammonia. The amount of NH3 found is to be multiplied by 100 x *824 which will equal the total nitrogen in the spirit ; and this, minus the nitrogen present in the free nitrous acid, when multiplied by 5-357 will give the nitrite of ethyl contained in the spirit. Estimation of Nitrous and Acetic Acids. The amounts of these two acids are necessary to be known in order to judge of the quality of the preparation, and for correctly estimating the nitrite of ethyl. 10 c.c. are to be measured with a pipette and run into a platinum dish, and diluted with an equal volume of pure water, and ’5 gram carbonate of potash added, and stirred until dissolved ; the solution is then evaporated on a water-batli to dry¬ ness. This saline residue is now to be treated with 5 c.c. of pure alcohol for the separation of the po¬ tassium acetate, from the potassium nitrite, and again repeated, and the mixed solutions filtered through a very small Swedish filter ; this filtrate evaporated in a tared capsule to dryness, and rapidly weighed. The weight minus *021 gram (the weight of KN02 which is dissolved by 10 c.c. of alcohol) and the amount multiplied by ’6122 gives the quantity of acetic acid present in the spirit. The amount of acetic acid thus found, multiplied by ’7666 gives the equivalent of N02 to which it is equal, and this product deducted from the total acidity, (previously determined alkalimetrically,) leaves the nett amount of N02 present. Estimation of the Aldehyde. Into a 25 or 50 c.c. flask run 10 c.c. of the spirit, and add 10 c.c. of peroxide of hydrogen, and let it stand two or three hours ; by this time the aldehyde will have become converted into acetic acid, and may be estimated by decinormal alkali; the amount thus determined, less the number of c.c. required by the free acids previously determined, multiplied by •0044 will give the amount of aldehyde. Estimation of Alcohol and Water. The alcohol is estimated by the specific gravity, and the water by difference. The foregoing scheme of analysis probably may look formidable in the eyes of very practical people. It certainly involves some nicety of selection of materials, as to purity, but otherwise it is not diffi¬ cult. 42 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 19, 187 I append the statement of analysis of four samples of spirit of nitrons ether, obtained from different sources and represented as the “best.” No. 1 No. 2. No. 3. No. 4. Water .... 10*55 14-12 16-17 15-49 Aldehyde . . . •75 •21 •26 •00 Alcohol .... 87-5 85-2 82-60 83-6 Acetic Acid . . . •16 •03 •18 •16 Nitrous Acid . . •29 •27 •69 •68 Nitrite of Ethyl . *75 T7 •10 •07 100-00 100-00 100-00 100-00 The nice gradation of 'quality here exhibited, without any design, is very remarkable. THE BOTANICAL SOURCE OF ARAROBA. In a former note on Goa powder, which appeared in this Journal,* it was suggested by Mr. E. M. Holmes that this drug might perhaps be derived from a species of Ccesa Ipinia nearly allied to C. Sappan, L. This opinion was founded partly on a microscopical examination of the structure of fragments of wood found in the araroba of commerce, and partly on the appearance of a single leaf of the araroba plant, which was found to bear a considerable resemblance in habit to those of G. Sappan. This leaf, kindly supplied from the Royal Botanical Gardens at Edinburgh, was ob¬ tained from a slip of the plant brought home from Bahia by Dr. J. L. Paterson. Those who are well acquainted with the plants of the Leguminosre will readily acknowledge the difficulty of judging of the genus from a leaf alone, without flowers and fruit. These have at length been procured, and the true source of the araroba may now be considered to be definitely settled, and the mystery which has so long attended the natural history of the drug to be satis¬ factorily cleared up. This information is supplied by Dr. J. M. de Aguiar, who has just published at Bahiaf a pamphlet containing a very full and detailed description of the plant, with illustrations of the leaves and flowers, a copy of which has recently been placed at our disposal by Mr. T. Christy. According to Dr. de Aguiar the flowers and fruit which have been obtained show that the araroba plant is more nearly allied to Centrolobium than to Ccesalpinia , having truly papilionaceous flowers, and that it belongs to the genus Andira of the sub- t.ribe Geofl'rieeai, which is characterized by having a hard drupaceous one-seeded fruit, sweet-smelling violet or purplish flowers arranged in panicles, a calyx with short teeth, and five distinct petals. From Centrolobium it is distinguished by the fruit, which in that geniis resembles a samara and is furnished with prickles at its base. The araroba plant is therefore nearly allied to Andira inermis , the bark of which was formerly a well known remedy in this country for intestinal parasites, under the name of cabbage-tree bark or worm bark. J The following description is a precis made from the information contained in Dr. J. M. de Aguiar’s pamphlet : — The plant from which araroba is extracted is one of the larger intertropical trees which are met with between 13Q and 15° of latitude, south of Bahia, * Pharmaceutical Journal [3], vol. v., p. 801, note f. f Memoria Sobre a Araroba, pelo Dr. J. M. de Aguiar. Bahia, 1870. X Lewis, ‘Materia Medica,’ p. 320. especially in the forests of Camamu, Igrapiunar Santorem, Taperoa and Valencia, and rivals in height the tree commonly known under the name of Oleo ( Myrocarpus fastigiatusPv Myrospermum erythroxy- lum *), and sometimes attains even greater dimensions. The ordinary height of the tree is 80 to 100 feet ; the trunk is straight, cylindrical, and in the two specimens which were measured in the thickest part one was 31 and the other 48 centimetres in diameter. The tree commences to branch at more than a third of its whole height, and forms a not very leafy head, having the form of a segment of a spheroid. The bark of the tree is not very thick and appears to con¬ tain scarcely any of the active principle of the plant.. The wood has a yellow colour, and is very porous, hav¬ ing numerous longitudinal canals visible to the naked eye, although these are more distinctly seen under a lens. The trunk in a transverse or tangential section presents lacunse, more or less large according to the age of the tree, and in these a pulverulent substance (araroba) is found, which in trees recently cut down and before being dried is of a light or pale tint, clearer than that of the wood. The medullary centre exhibits a canal different in appearance from the lacunsc, having a diameter much more consider¬ able. The young branches are entirely fistulose. So far these particulars seem to correspond exactly with the statement of Dr. Rameiro A. Monteiro, published in the Journal de Therapeutique , vol. vi.,. p. 248. f The following details, however, have not, so far as- is known, been before published in this country. The leaves are alternate, compound and paripinnate. The petiole in two specimens which were measured was in the one 32 and in the other 44 centimetres in length, having a variable number of pairs of stalked leaflets, in one specimen 20, and in another,. 24. The leaflets are alternate and articulated, oblong, obtuse, entire, and emarginate at the apex, measuring from 2|- to 4| centimetres in length, and from 1 to 1^ centimetres in width. The distance between the points of insertion of the leaflets is about 2 centimetres, so that the leaflets only slightly over¬ lap each other. The common petiole or racliis is slender, convex on the under surface, and hollowed above into a small very smooth furrow ; the secondary petioles which, measure about half a centimetre in length are ac¬ companied for a small distance by the rudiments of stipels. The leaflets are feather-veined, of a green colour on the upper surface and of an ashy hue beneath. The inflorescence is centripetal, consisting of a panicle with a variable number of racemes, each of which consists, in the more luxuriant specimens, of about eight flowers or flower buds. The flowers are shortly stalked, alternately arranged, and are each furnished with a bract, which does not develop at the same rate as the flower, and hence the lower bracts appear smaller than the upper ones. The common peduncle is bare of flowers at the base for about a third of its length. The flowers are purple, papilionaceous, measuring to 3 centimetres without the claw, which is about \ centimetre long. The calyx is gamosepalous, 2 centimetres long, covered with rusty- coloured hairs, a little flattened on three faces, like- * Almeida Pinto, ‘Diccionaria de Botanica Brasileira/ p. 335. f Pharm. Journ. [3], vol. viii., p. 1048. July 19, 1679.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 43 a triangular prism with rounded angles, the dorsal angle being the more prominent and corresponding to the middle of the standard. The calyx is five¬ toothed, the two upper teeth being larger and longer Leaf of Andira Araroba , showing venation, natural size. and separated by a more obtuse angle than the other three, which are equal and of which two correspond in position to the wings of the corolla and the central one to the keel. The corolla consists of five clawed petals, the standard being entire, orbicular, about 2 centimetres in diameter, slightly emarginate at the apex, and furnished with a claw about \ centimetre long, and consisting in great part of the thickened middle vein of the standard. The alte or wings are obovate, elongated, about 16 millimetres long by 6 broad, curved towards the base, and forming a longitudinal and oblique sinus* (gotteira) near the top of the claw on the side opposite to the standard, the claw being about 7 millimetres long. The two petals forming the keel are similarly formed, but less curved, and 4 or 5 millimetres broad. The stamens, nine 'in number, are monadelphous and perigynous, about 2 centimetres long, and adherent for about a third ot their length, but having a slit opposite to the middle of the vexillum. The anthers are ovoid with a longitudinal furrow on their inferior surface, in the middle of which the filament is inserted. The upper surface is convex and smooth. The pistil consists of a single carpel, and exceeds the stamens in length by 1 or 2 millimetres. The ovary, which has a stalk about 4 millimetres long, is flattened at the sides, and presents two salient lines or rudimentary wings. The ovary and style (the latter for two-thirds of its length only) are covered with rusty hairs. The ovary is convex on the side opposite to the slit in the androphore, and concave on the side nearest to the two lateral wings. Flower of Andira Araroba. ■ 1. Showing three lower teeth of calyx ; 2. Corolla, lateral view; 3. Pistil; 4. Petal of keel; 5. Petal ©f wing; 0. Standard; 7. Stamens in situ, after removal of corolla; 8. Monadelphous stamens, separated from calyx. The ovary is one-celled and one-seeded. The embryo is curved, and the seed exalbuminous . The arillus is short and tortuous. From the above description it will be seen that the araroba plant belongs to the Leguminosoe, and to the tribe of Dalbergiese. It much resembles in some characters Dalbergia miscolobimn, Benth., and * This is not well shown in the original wood- cut. 44 TIIE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 19, 1879. Andira fraxinifolia, Bentli. Neither of these two plants, nor the Andira inermis, has the obtuse emar- ginate leaflets which characterize the araroha tree. The author believes the plant to have been hitherto un described, and proposes the name of Andira Ara- roba , Aguiar, for it, since the drupaceous fruit, panicled inflorescence, purple flowers and the other characters above mentioned clearly point to its being an Andira. This opinion is further strengthened by the fact that some other Andiras possess parasiticiclal properties, and that the natives, who call the A. anthehnintica “ Angelim de folha grande,” the Andira Fraxinifolia “ Angelim doce,” and the A. stipulacea “Angelim Coco,” also call the A. Araroba “An¬ gelim amargoso/’ thus recognizing a close alliance in the plants. With regard to the production of the araroba, the author gives it as his opinion that it is formed by the oxidation of the resin which exists in great abundance in the tree, the oxidation being facilitated by the canals made by insects. He explains the presence of the larger cavities in the tree by the corrosive action of the araroba on the wood. He lias not, however, as yet confirmed his theory by experiment. The araroba is collected throughout the year, the older trees being selected because the powder occurs in them in greater abundance. The trunk is cut into sections transversely and these are then split longitudinally. The portions containing powder are then chipped or scraped off with an axe, which is done the more easily as the wood in these parts offers but little resistance. The colour when freshly collected varies from that of the flower of the cotton plant (pale primrose colour), becoming by the action of the air darker, to that of rhubarb, and finally dark purple. The commerce of this article is now chiefly developed in Camamu and Taperoa, although the tree exists in abundance in all the southern part of the Province of Bahia and, according to Drs. Bom- fim and Agnello Leite, also in the forest of Sergipe. The tree is not cultivated, but propagates itself spon¬ taneously. LACTUCARIUM FROM LACTUCA CANADENSIS.* BY HILAND FLOWERS, PH.G. The milk-juice, which exudes almost at the commence¬ ment of the plant’s career, is perfectly inert, though a large quantity is produced. As collected up to July 20, the exudation has a strong narcotic odour, while the palate perceives no bitterness, but simply a flat sweetish taste. Up to this time the plant has borne its repro¬ ductive organs, but failed in giving the requisite bitter¬ ness. A change, however, occurs about the 25th of July, when we find that the laticiferous vessels are yielding a large supply of juice with a slightly bitter taste and a stronger and more lasting odour. As the season advances, both the bitter principle and the narcotic odour increase. The milk-juice collected during the latter part of the season dried in irregular masses, crumbling into minute fragments when rubbed between the fingers, and was of a blackish-brown colour, a strong odour and very bitter taste. If kept in a closely-corked bottle it remains soft and is capable of being moulded into cakes. The odour is slightly stronger in the fresh state, and the colour of a greyish-brown. Aubergier, in 1843, experimented upon this plant, while investigating the subject to ascertain from which * From th American Journal of Pharmacy, July, 1879. lactucarium might be most advantageously obtained ; ho stated that the millc-juice of Lactuca canadensis, or don - gata, had a flat, sweetish taste and contained mannit, etc., but no bitter principle. In September, 1867, Professor Maisch commenced a series of experiments upon the plant, and upon the personal observation then made, as well as the reports of Doctors DaCosta and Muller, of this city, rested con¬ vinced that the plant did contain a bitter principle and did possess decidedly medicinal properties, and that Aubergier had perhaps improperly conducted his experi¬ ments, possibly using the expressed juice of the plant, which, according to Professor Maisch (ride American Journal of Pharmacy , 1869, p. 145), has a flat, sweetish taste. Four drachms of the milk- juice collected in September and October were exhausted upon a filter with boiling alcohol. Eight ounces of filtrate were obtained, passed through animal charcoal and concentrated by spontaneous evaporation, when inodorous and tasteless needles were obtained, which melted at about 175° F. and on cooling, congealed to a granular mass. They were evidently* lactucerin. On still further evaporating the mother liquor and adding to it water, a whitish precipitate was produced, from which the aqueous liquor was thoroughly drained. On dissolving the precipitate in boiling alcohol and evaporating the solution spontaneously, more of the tasteless needles were obtained, and pale-brownish bitter scales, which were evidently impure lactucin. The aqueous mother liquor was precipitated by basic acetate of lead, and both the precipitate and the filtrate were freed from lead by sulphuretted hydrogen. On evaporating the solutions, brownish amorphous masses, having a bitter taste, were left, corresponding to the lactacic acid and lactucopicrin of the European lactu¬ carium. Lactucerin is in colourless needle-shaped crystals, either united in stellate groups or crossing and over¬ lapping each other; tasteless, soluble in boiling alcohol, petroleum benzin, ether, chloroform, and slightly soluble in cold alcohol ; insoluble in water. If heated to above its melting point (175° F.), it volatilizes slowly. Sul¬ phuric acid chars it; nitric acid has no effect unless- heated. Lactucin is insoluble, or nearly so, in water; soluble in alcohol and acetic acid. When pure and not exposed to much heat, the lactucin is in scales of a dull- white cast ; under the microscope it presents a rugged surface, slightly tinged with a reddish-brown colour. From my experience, I am inclined to think that if the scales are heated in solution for some time, they will not form again very readily, and are deprived of some of their bitterness. Ammonia will not precipitate it, but rather tends to alter the taste. It is, however, precipitated from alcohol by water, and may thus be purified by repeated precipitation and crystallization. Nitric acid will not dissolve it, nor will the addition of alcohol facilitate this end. The characteristics given by Kromayer, Ludwig and Walz are in accordance with these results. Lactucic acid is precipitated by basic acetate of lead, care being taken that an excess is not used, for it is soluble in that salt when in excess. It changes blue litmus paper to red, proving its acidity; has an acrid, bitter taste; is soluble in alcohol, both hot and cold, insoluble in petroleum benzin, bisulphide of carbon, ether and chloroform, and has a brownish-green colour. Lactucopicrin is a brown amorphous mass, and may be purified by repeated treatment with ether, chloroform or alcohol, filtering and evaporating. It has a strong and purely bitter taste, is soluble in alcohol, chloroform, ether and water, and is not precipitated by lead salts from its solution. The residue of the lactucarium, left after the above principles had been removed by hot alcohol, was treated with bisulphide of carbon, which dissolved a large amount of caoutchouc (gum elastic ), but there yet remained a July 19, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 45 residue, which was treated with ether, removing a pale- yellowish granular powder; with chloroform, removing the remaining caoutchouc and some of the colouring matter, and with alcohol, which yielded, on evaporation, a brownish, bitter, amorphous mass resembling lactuco- picrin. Water extracted a large amount of colouring matter. The residue which was now left defied the solvent powers of carbon bisulphide, ether, chloroform, alcohol, water and acetic acid. The yellowish powder obtained on the evaporation of ether in the above treatment closely resembles lactucerin ; but the identity of the two was not proven. When heated it will melt, and volatilize if the temperature is increased. On cooling it forms a resinous mass. It is soluble in hot alcohol, petroleum benzin and chloroform, insoluble in hot or cold water. Sulphuric acid dissolves it, but does not char it. Nitric acid has little or no effect. Muriatic acid dissolves it slightly. Acetic acid and ammonia have no effect. It is precipitated from the alcoholic solution by water. The statement of Aubergier regarding the worthlessness of this plant is undoubtedly wrong, as there exist, beyond question, several bitter principles with decided physio¬ logical action. It is very likely that he collected the juice before the plants were sufficiently matured and the bitter principles developed. GLYCYRRHIZIN.* * * § BY J. HABERMANN. In a previous communication the author had stated that by the treatment of commercial glycyrrliizin with glacial acetic acid he had obtained a considerable quantity of an almost colourless crystalline body. Since then he has pursued the subject as opportunity offered and now presents the result of his further investigation, first giving a resume of the history of the subject. Our knowledge of the nature of glycyrrhizin is princi¬ pally based upon the work of A. Vogel, jun.,+ T. Lade,^ Gorup-Besanez,§ and, more recently, Z. Roussin. || Vogel prepared glycyrrhizin by precipitating an aqueous extract of liquorice root with lead acetate, carefully wash¬ ing the precipitate, suspending it in water and decomposing it with sulphuretted hydrogen; it was only after re¬ peatedly boiling the mass that he was able to separate the lead sulphide by filtration. Vogel purified the gly¬ cyrrhizin by dissolving it several times in absolute alcohol, and he describes it as a light yellow mass, showing no trace of crystallization when considerably magnified, soluble in water, especially when boiling, readily soluble to a large extent in alcohol, and melting at 200° C. to a transparent dark brown mass. He described also the precipitate obtained with neutral lead acetate, as well as a compound with sulphuric acid, and attributed to glycyrrhizin the formula C16H2406. Lade obtained his glycyrrhizin by extracting liquorice root with cold water, concentrating upon a water-bath, filtering, precipitating with dilute acid, and purification of the viscous pitchy black precipitate by continued kneading in acidulated and pure water, repeatedly dis¬ solving it in absolute alcohol and evaporating the solution on a water-bath. Lade describes his product as a shining translucent, brown mass, forming upon trituration a brownish-yellow powder, slightly soluble in cold water, especially when containing a little acid, but dissolving more readily in boiling water and giving off then a pecu¬ liar odour, recalling that of fusel alcohol. A solution saturated when hot is said to be gelatinous at the ordinary temperature or when perfectly cool to thicken to a clear * Abstract of a paper read before the Vienna Academy of Sciences ( Liebig’s Annalen d. Chemie, vol. cxcvii., p. ]05. t Journ. f. prakt. Chemie , xxviii., 1. X Annalen, lix., 224. § Annalen, cxviii., 236. [1 Pharm. Journal [_3], vi., 53. brown jelly. The taste was extremely sweet, but it was accompanied by a peculiar bitter, and was unpleasant. In absolute alcohol the substance was readily soluble. The yellow colour appeared to Lade to be characteristic of gly¬ cyrrhizin . The solutions had an acid reaction upon litmus paper, and small quantities of alkalies made the glycyrrhizin much more soluble in water and coloured the solution deep yellow-brown. Lade also described two lead com¬ pounds and attributed to glycyrrhizin the formula C18H2407. He appears to have been of opinion (1) that glycyrrhizin exists in the root combined with an organic base like ammonia ; (2) that he did not succeed in obtain¬ ing glycyrrhizin free from nitrogen, although the quantity present amounted to only 0’03 to 0‘06 per cent. ; (3) that the body was a hydrate, represented by the rational formula— C18H2206 + H20. Gorup-Besanez modified Lade’s method by decom¬ posing the alcoholic solution with small quantities of ether, by which a brown resinous mass was separated, whilst a light wine-yellow solution resulted ; this upon evaporation left a light yellow varnish -like residue that yielded a faintly yellowish powder when triturated. Gorup-Besanez expressly states that the product obtained in this way corresponded in properties and composition with the glycyrrhizin of A. Vogel, and differed in analy¬ tical results and especially in containing no nitrogen from that of Lade. He describes the preparation and properties of a lead and a lime compound, the former containing six the latter three equivalents of base. Lastly, he describes the decomposition of glycyrrhizin by dilute acids into glycyrretin and sugar according to the equation — P24H3609 + H20 = C18H2604 + CfiH1206 According to this glycyrrhizin would be a non-nitro- genous glucoside, but Gorup-Besanez does not appear to have effected the [decomposition by emulsin or any other ferment. The glycyrretin he describes as a brown-yellow resin, with a taste at first scarcely but afterwards strongly - bitter, insoluble in water, freely soluble in alcohol, some¬ what less so in ether, and precipitated from its alcoholic solution by water. When decolorized by animal charcoal it formed a nearly white powder that he did not succeed in obtaining in a crystalline form. The sugar was ob¬ tained as a brownish coloured only faintly sweetish tasted syrup, which reduced alkaline cupric solution in the cold, blackened oxide of bismuth in the presence of carbonate of soda, took a brown colour with potash, showed Petten- kofer’s reaction with galls and sulphuric acid, and lastly, upon the addition of yeast, quickly passed into fermenta¬ tion. Roussin, like Lade, looks upon glycyrrhizin as an acid, which he calls glycyrrhizic acid, contained in the liquorice root as an ammonia compound. He states that it forms with ammonia two different compounds, of which one, with an excess of ammonia, forms a dark yell®w solution, the other, with half the quantity of base, forms an amber solution. According to Roussin, glycyrrhizin plays in both compounds the part of an actual acid, and the compounds are actually salts, capable of undergoing double decom¬ position not only with all metallic salts, but also with salts of the alkaloids. Roussin considers glycyrrhizic acid to be intermediate in its principal characters between tannic and pectic acids. Of the above-mentioned ammonia compounds the first is a basic glycyrrhizate of ammonia, the second and more important, since it repre¬ sents the actual sweet principle of liquorice, is glycyrrhi- zate of ammonia, or ammoniacal glycyrrhizin. In its preparation and purification Roussin followed the method of Gorup-Besanez at first, and then precipitated the ethereal-alcoholic solution with a strong alcoholic solution of ammonia, and washed the precipitate with alcohol. Roussin gives no analytical data. The starting point of the present author, Herr Haber- mann, was the glycyrrhizin of commerce, described in the current price lists as “ ammoniacal glycyrrhizin,” and occurring in more or less deep brown coloured shining amorphous scales. From this substance he finds that a 46 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 19, 1879. ^crystalline body may be obtained as follows : — Some of it is placed in a good sized retort with glacial acetic aeid and heated, while carefully swinging the retort, to boiling. Upon the addition of the acetic acid the substance forms at first a black viscous syrup, which becomes thinner as the temperature rises. The syrup is maintained in full ebullition for a few moments and when solution is com¬ plete is filtered through paper as rapidly as possible, preferably by means of a water-bath funnel into a glass or porcelain dish. If sufficient glacial acetic acid has been used solution is not difficult ; but if too small a quantity* be used there is a separation of crystalline matter in the retort and on the filter, and the filtration becomes pro¬ longed and troublesome. Nevertheless too much solvent is a greater disadvantage than too little, the yield of crys¬ tals being smaller. The crystalline mass is separated from the deep brownish black syrupy mother-liquor, pressed, and washed with glacial acetic acid and with absolute alcohol. It still remains contaminated with the dark coloured mother-liquor, and to obtain it perfectly pure and free from ash it requires to be again boiled with glacial acetic acid, filtered rapidly, and the crystalline mass that forms upon cooling recfystallized two or three times from boiling alcohol. The purified substance forms slightly yellowish bright shining crystalline scales, which under the microscope appear to be homogeneous, perfectly transparent and colourless, and which are better formed in proportion as the separation from the alcoholic solution takes place slowly. In water at the ordinary temperature it is really but little soluble, it forming a transparent faintly wine- yellow coloured jelly, in which isolated hard particles remain suspended in the form of small lumps even after some days. Upon mixing 1 gram with 100 c.c. of water the mass acquires after standing several hours a consis¬ tence that will allow an open vessel to be reversed with¬ out it falling out. When the jelly is heated it becomes liquefied, and is quite thin when the water boils. In boiling water the compound is very readily soluble. Sufficiently dilute aqueous solutions are at the ordinary temperature gum-like, viscous and frothy. The com¬ pound is insoluble in ether, slightly soluble in absolute alcohol even when boiling, slightly soluble at the ordinary temperature in alcohol above 90 per cent., but more soluble therein when boiling. The solubility in alcohol increases rapidly with the amount of water it contains. T rom weak alcoholic and aqueous solutions it cannot be obtained crystalline; an aqueous solution when evaporated spontaneously or upon a water-bath only yields an amor¬ phous brittle gum-like slightly coloured mass which when dried is not unlike white of egg. Upon treating the aqueous jelly with a little dilute sulphuric or hydrochloric acid it becomes turbid and of greater consistence. Small quantities of ammonia and caustic alkalies added increase the solubility of glycyrrhizin to an extraordinary extent, the solution so obtained being, if the material is pure, almost colourless, but if not pure it is more or less per¬ ceptibly coloured. In aqueous solutions sugar of lead and other salts of the heavy metals produce voluminous pre¬ cipitates ; the silver precipitate is cheesy, runs together in globules on being heated, and dissolves readily in ammonia. Similar but more compact precipitates are formed in the alcoholic solution by alcoholic solution of sugar of lead, caustic baryta, etc. ; whilst alcoholic solutions of ammonia and caustic potash produce in a strong alco¬ holic solution precipitates which after standing deposit on the bottom of the vessel as a resinous m ass. Fehling’s cupric liquor is reduced by it after prolonged heating. Nitric acid dissolves the substance at the ordinary temperature with considerable production of heat to an almost colour¬ less liquid, from which nothing separates upon dilution with water. Upon heating the hydrochloric acid solution over a spirit lamp a brief but tolerably brisk evolution of gas takes place, the liquid becomes turbid through the separation of resinous flocks, and upon dilution with water there is a much more copious separation of colourless flocks. In concentrated sulphuric acid the substance dis¬ solves to an orange-red liquid, from which colourless flocks are precipitated by water. The substance possesses an intensely sweet taste with an after-flavour faintly resembling liquorice. This after¬ taste appears to be weaker in proportion with the increas¬ ing purity of the product, but in no case in the author’s experience was it quite absent. The substance bears a temperature of 100° C. without change, but turns brown at 110° C. and melts at a higher temperature, decompos¬ ing to a black pitchy mass and diffusing an odour scarcely resembling that of sugar; finally it inflames and bums with a very sooty flame, and leaves a greyish-black coke¬ like residue. Analysis of the crystalline substance was attended at first with considerable difficulty in consequence of ad¬ herent acetic acid, which could not be got rid of in the ordinary drying apparatus without discoloration ; es¬ pecially was this the case when the recrystallization from alcohol had not been repeated several times. The difficulty was overcome by drying in a vacuum. Analy¬ sis was made of specimens of ash-free substance obtained from different preparations of glycyrrhizin, dried at 100°. As the simplest expression of the mean of the analytical data obtained, the author gives the formula C22H33N09, but he does not look upon this as the true representation of the molecular weight. Mean of re- Required for suits obtained. C22H33NO9. C . . . . 58-03 “ 5-8-17 H . . . . 7-25 7*71 N . . . . 3-07 3-05 Upon treating a solution in strong alcohol with an alcoholic solution of platinic chloride, a crystalline forma¬ tion of the platino- ammonium salt was obtained. A further investigation, however, led the author to the conclusion that only a portion of the nitrogen is present in this body in the form of ammonia, whilst the other part is combined in another way. The result corre¬ sponded with the composition of an acid ammonium salt of a nitrogenous acid represented by the formula C44H(;2N01g (NH4), and for this acid the author adopts the name proposed by Roussin, of “ glycyrrhizic acid.” Some other compounds of this acid are also described by the author as follows, the analyses being made after drying at 100° : — Neutral Glycyrrhizate of Ammonium. — C44H60NO18 (NH4)3. — Obtained upon treating an alcoholic solution of the acid salt with excess of ammonia and evaporating to perfect dryness in a vacuum over sulphuric acid. It formed an amorphous, brittle, light yellow-brown, trans¬ parent mass, resembling gum arabic. It was extremely soluble in water and alcohol, but insoluble in absolute alcohol ; its solutions were precipitated by various metallic salts. It possessed a nauseous sweet taste. It was rather hygroscopic and when heated readily un¬ derwent change, apparently giving up part of its am¬ monia Neutral Glycyrrhizate of Potassium — C44H60NO18K3. — Aqueous solution of potash was added in slight excess to a concentrated solution of the acid ammonium salt in weak alcohol. The smell of ammonia was perceptible at the ordinary temperature. The solution was heated for some time, then left to cool, and absolute alcohol added as long as any precipitate was produced. It was then allowed to stand twenty-four hours under a bell glass, at the end of which time the flocculent precipitate had collected into a resinous mass adhering closely to the sides of the vessel. This, after the clear liquor had been poured off, was washed repeatedly and carefully with absolute alcohol and dried at the ordinary temperature over sulphuric acid. It then appealed as a yellowish- white, light, friable mass, very soluble in water and dilute alcohol, butjalmost insoluble in absolute alcohol and ether. July 19, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS.' 47 Acid Glycyrrhizate of Potassium. — C44H62N018K.— If the previous compound be treated in the dry condition with a moderate quantity of acetic acid and heated it dissolves to a clear slightly coloured liquid. From this solution, filtered whilst boiling, the acid compound quickly separates on cooling in colourless microscopically small granular crystals. It has a very persistent intensely sweet taste, exceeding in this respect levulose, cane sugar, and even the acid ammonium salt. The compound swells up in cold water to a jell}’-, but it is soluble in hot water to a considerable extent, such solution gela¬ tinizing as it cools. It is soluble in aqueous alcohol, especially when heated, very slightly soluble in alcohol above 90 per cent., soluble in glacial acetic acid when heated, and scarcely soluble in ether. All the solutions are colourless. The salt can be dried at 100° C., but upon heating it further it swells and eventually burns with a smoky flame giving off a pecu¬ liar odour. Neutral Glycyrrhizate of Barium, (C44H60NO18)2 Ba3, is obtained as a yellowish-white amorphous body by adding baryta water in slight excess to a hot alcoholic solution of acid glycyrrhizate of ammonium. Neutral Glycyrrhizate of Lead. — (C44H60NOj8)2 Pb3. — Upon treating a solution of acid glycyrrhizate of ammo nium with solution of sugar of lead there is produced a very voluminous white transparent mucilaginous precipi¬ tate ; when alcoholic solutions are used the precipitate is more compact and more convenient for filtering and washing. Dried in a vacuum over sulphuric acid it forms a yellow-brown, transparent, brittle and friable gum-like mass, having a sweet taste. It is soluble in glacial acetic acid, slightly soluble in water, insoluble in alcohol and ether. Upon heating to 100° C. it is perceptibly coloured browm. Glycyrrhizic Acid. — C44H63N018. — The lead compound is the most suitable material for the separation of the free acid. The precipitate after being well puri¬ fied by washing and pressing is rubbed up with a little water to a fine mucilage, placed in a beaker in a water-bath and decomposed by a current of sulphu¬ retted hydrogen continued several hours, the mixture being diligently stirred. The finely suspended lead sulphide is removed by boiling and adding to the liquid in small quantities at a time the white of egg beaten to a froth, and when the precipitate appears in large flocks in the colourless liquid filtering while still boiling through coarse paper. The filtrate thickens on cooling to a somewhat turbid jelly, which upon heating in an open dish on a water-bath shrivels up in a remarkable manner, leaving a brown residue resemb¬ ling dried egg-white. It has a persistent pure, but not excessively sweet taste. The acid reddens blue litmus paper and decomposes the carbonates of the alkaline earths gradually by boiling. It swells up in water at the ordinary temperature to a jelly, without actually dissolving, and with boiling water forms a thin viscous solution. It dissolves tolerably freely in weak alcohol, especially when heated, also in boiling glacial acetic acid, and only slightly in absolute alcohol and ether. It turns brown at 100° C., and puffs up and burns upon further heating to a black coal. Glycyrrhizic acid re¬ duces Fehling’s solution upon heating almost as quickly as grape sugar. The results of this investigation may be thus summed up: — (1) In liquorice root there is contained a peculiar nitrogenous acid in the form of .‘alts; (2) The acid is tribasic and forms neutral and acid salts ; (3) Among these salts the acid potassium and ammonium salts are, from their crystallizability and intensely sweet tastes, espeoially important ; (4) It is probably to the ammo¬ nium salts of glycyrrhizic' acid that liquorice root owes its peculiar sweet taste. The author is continuing his investigations upon various decomposition products of glycyrrhizic acid and a second constituent of liquorice root. RECENT CONTRIBUTIONS TO THE HISTORY OF DETONATING AGENTS.* ET PROFESSOR ABEL, C.B. F.R.S. (Continued from paye 29). That the power possessed by different very highly explosive substances, of inducing the detonation of such bodies as gun-cotton and nitro-glycerine, is not solely ascribable to the operation of mechanical force very sud¬ denly developed, is indicated not only by the singular inertness of gun-cotton to the influence of nitro-glycerine as a detonating agent, but also by a comparison of the behaviour of other detonating substances with that of the mercuric fulminate, when applied to the detonation of gun-cotton. Thus the detonation of silver fulminate is very decidedly sharper than that of the mercury com¬ pound, yet it is in no way superior to the latter in its power as an initiative detonating agent ; indeed, a some¬ what larger amount of it appeared to be required than of the mercury salt to induce detonation of gun-cotton with certainty. Again, the iodide and chloride of nitrogen are far more susceptible of sudden detonation than the silver fulminate ; yet while five grains of the latter, confined in a stout metal envelope, suffice to detonate gun-cotton, fifty grains of chloride of nitrogen confined by water appeared to be the minimum amount with which the detonation of gun cotton could be accomplished with certainty, while no success attended the employment of confined iodide of nitrogen in quantities ranging up to 100 grains. The incompatibility of these results with the general conclusion, based upon numerous and greatly varied experiments, that the facility with which the detonation of gun-cotton and nitro glycerine, and bodies of a similar character as explosives, is induced by an initiative detonation, is proportionate to the mechanical force aided by the heat developed by the latter, led the lecturer to the conclusion that a synchronism or similarity in character or quality of the vibrations developed by the detonation of particular substances, operates in favouring the detona¬ tion of one such substance by the initiative detonation of a small quantity of another, while in the absence of such synchronism, a much more powerful detonation, or the application of much greater force, would be needed to effect the detonation of the material operated upon. This view has received considerable support from results since obtained by other experimenters, especially by MM. Champion and Pellet ; but the subject is one which still needs further experimental elucidation. The physical character of explosive substances, as also the mechanical condition of a mass of the particular explosive substance operated on, are of great influence in determining its behaviour when submitted to the action of an initiative detonation. The liquid nitro-glycerine is far more sensitive to detonation than gun-cotton ; one grain of mercuric fulminate, confined in a metal case, suffices to detonate nitro-glycerine when surrounded by it : but, in order to attain this result with any degree of certainty, it is necessary so to confine the nitro-glycerine as to prevent its yielding to the blow developed by the initiative detonation, and thus to some extent escaping from the operation of the sudden concussion to which the particles contiguous to the fulminate charge are sub¬ mitted. If nitro-glycerine be mixed with solid substances in a fine state of division, plastic mixtures may be obtained, and the liquid may thus be presented in something like a solid form to the detonating agent ; if the particles of absorbent material be moreover of porous nature, as is the case with the infusorial earth called Kieselguhr used in the production of dynamite, a solid nitro-glycerine preparation may be obtained which contains a very large proportion of the liquid (75 per cent, by weight). In this condition nitro-glycerine may be detonated without any difficulty when freely exposed to air ; and although it is * Lecture delivered at the Royal Institution of Great Britain, Friday, March 21, 1879. 48 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 19, 1879. diluted with a considerable proportion of absolutely inert material, its sensitiveness to detonation is not in the least diminished. Each particle of the diluent is enveloped in the liquid, so that no portion of the latter becomes iso¬ lated from the remainder by the admixture of inert solid matter ; hence, when the initiative detonator is sur¬ rounded by such a mass, it is in contact at all points with some portion of the nitro-glycerine, and the latter is in continuous connection throughout, though no longer in a mobile condition ; detonation is consequently as readily established and transmitted through the mass as though it consisted entirely of nitro-glycerine. Indeed, while the liquid in its undiluted state, if freely exposed to air in a long layer, transmits detonation with difficulty, and very slowly as compared with compressed gun-cotton (the observed rate of progression being, in several experiments, below 6000 feet per second), detonation is transmitted with ease and certainty through very long trains of a solid preparation of nitro-glycerine, such as dynamite, and the rate of transmission is decidedly more rapid than it is with compressed gun-cotton, a result which is in harmony with the greater sensitiveness to detonation and the greater violence of action of nitro-glycerine. It has already been stated that gun-cotton may be detonated if a confined charge of not less than 2 grains of mercuric fulminate be detonated when closely sur¬ rounded by the substance. But in order to attain this result, the cellulose-product must be presented to the detonating agent in a mechanical condition favourable to its action. Gun-cotton in a loose flocculent condition, or even if in the more compact form of a spun yarn or thread, cannot be detonated through the agency of a large charge of fulminate buried in the material. The light and loose gun-cotton is simply scattered with violence ; portions are sometimes inflamed by the heat developed where the fulminate is detonated, a result which is obtained with greater certainty the less violent the detonation produced by the fulminate-charge. If, however, the gun-cotton be converted into a compact form, either by ramming the wool or thread very tightly into a case, or better still, by reducing the gun-cotton fibre to a very fine state of division, and compressing it, when in that condition, into compact masses, it becomes susceptible of detonation by the initiative action of mercuric fulminate, and the quantity of the latter required to bring about detonation is small (down to the limit which has been named above) in proportion as the compactness or density of the com¬ pressed material is increased. Detonation, when established in compressed gun¬ cotton, is transmitted with great velocity throughout the mass, as already stated, or from one to another of con¬ tiguous masses, laid out in long rows, and even, though at a reduced rate, if small spaces exist between the indi¬ vidual masses. But if a small mass of compressed gun¬ cotton freely exposed to air be detonated when in immediate contact with gun-cotton wool or loosely twisted yarn, the detonation will not be transmitted to these, but they will merely be scattered and perhaps inflamed. The difference in the behaviour of nitro-glycerine and of gun-cotton when presented to the action of a so-called initiative detonation under the different conditions spoken of above, admits of ready explanation. It was established, in the first instance, that the action of an initiative detonation is not ascribable to the heat developed within the detonating material itself, in under¬ going chemical metamorphosis. If it were so, the deto¬ nating mixture known as percussion cap composition and other explosive mixtures, the detonation of which is attended by much greater development of heat than is obtained by the action of pure mercuric fulminate, should detonate gun-cotton more readily tban the latter does, whereas very much larger quantities of such materials are required to attain that result ; moreover, the readi¬ ness with which gun-cotton is detonated should be solely proportionate to the amount of fulminate used, which has been shown not to be the case ; and gun-cotton should be more readily detonated when in the loose and open con¬ dition than in the highly compressed or compact form, because the latter presents it in the condition least favourable, and the former in that most favourable, to ready and rapid transformation by heat. Again, the actual temperature required for the explosion of nitro¬ glycerine is very considerably above the exploding tem¬ perature of gun-cotton, yet a very much smaller charge is required for the detonation of nitro-glycerine than is needed for the detonation of gun-cotton. On the other hand, a quantity of confined percussion cap composition which, if it were pure mercuric fulminate, would be altogether inadequate for the detonation of gun-cotton, suffices for the detonation of nitro-glycerine. The action of an initiative detonation has already been compared to that of a blow from a hammer or falling weight. The readiness and certainty with which gun¬ powder, gun-cotton, and other explosive agents are detonated by the latter agency are regulated by several circumstances ; they are in direct proportion to the weight of the falling body, to the height of its fall, and to the force with which it is impelled downwards ; to the velocity of its motion ; to the mass and rigidity or hard¬ ness of the support upon which the substance to be detonated rests ; lastly, to the quantity and mechanical condition of the explosive agent struck, and to its sensi¬ tiveness. Gunpowder is much more readily detonated by a sharp blow from a small hammer, than by the simple fall of a heavy hammer, or by a comparatively weak blow from the latter. It is very difficult by repeated blows, applied at very brief intervals, to detonate gun-cotton if placed upon a support of wood or lead, both of which materials yield to a blow, the force applied by that blow being transferred through the explosive agent and absorbed in work done upon the material composing the support. But if the latter be of iron, which does not yield per¬ manently to the blow of tbe hammer, the detonation of those substances is easily accomplished. If the quantity of the explosive agent employed be so considerable as to form a thick layer between the hammer and support, the force applied is to so great an extent expended in impart¬ ing motion to the particles of the compressible mass, that there remains little or none by which its detonation can be accomplished, and if the material be in a loose or porous condition (as in the case of a powder or of loose wool), much work has to be accomplished in moving particles of the mass through a comparatively considerable space, in the operation of compressing them, so that a second or even a third blow is required for their detona¬ tion ; whereas if, by blows or pressure previously applied, the explosive material will be presented in the form of a compact mass, the particles of which have little tendency to motion when force is applied to them, detonation will be much more readily developed. It appears therefore that the detonation of an explosive substance by means of a blow is the result of the development of heat suffi¬ cient to bring about most energetic chemical action, or change, by expenditure of force in the compression of the material, or by establishing violent friction between its particles, consequent upon the motion momentarily im¬ parted to them, and that it is brought about with a readiness proportionate to the resistance which they oppose to their motion by the degree of their contiguity to each other. The exceedingly violent motion of particles resulting from the sudden or extremely rapid transformation of a solid or liquid explosive body into highly heated gas or vapour (which is the effect of a detonation), must obvi¬ ously exert force which operates upon a body opposed to it in a manner precisely similar to the force applied by opposing a body in the path of a solid mass which is set into very rapid motion. In other words, a detonation exerts a mechanical effect upon resisting bodies precisely similar to that of a blow from a hammer or from a pro- July 19, 1879. THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 49 jectile propelled from a gun. Just as the force of a sufficiently sudden or powerful blow from a hammer is trans¬ formed into heat by the resistance to the motion of the hammer which the particles of an opposing body offer, and by the consequent friction established between them, so the force or concussive action exerted by the matter set in motion when a solid or liquid is converted into gas or vapour, will also be transformed into heat, the develop¬ ment of which in an opposing body will be proportionate to the resistance to motion which its particles offer, and to the suddenness and violence of the concussion to which it is subjected. The power of accomplishing the detona¬ tion of nitro-glycerine, gun-cotton, or other highly ex¬ plosive substances, freely exposed to the air, through the agency of detonation produced in their vicinity or in close contact with them, appears therefore correctly ascribable to the heat suddenly developed in some portion of the mass by the mechanical effect, or blow exerted by that detonation, and is regulated by the violence and sudden¬ ness (either singly or combined) of the detonation, by the extent to which the particles composing the mass of the explosive material are in a condition to oppose resistance to the force, and by the degree of sensitiveness of the substance to detonation, or to sudden metamorphosis, under the influence of heat thus developed. It will now be evident why the readily yielding nature of the particles of liquid nitro-glycerine tends to coun¬ teract its great sensitiveness to detonation, and why, when the motion of the liquid particles is impeded by their admixture with solid matter, and when they are consequently placed in a position to resist mechanical motion by the force applied through the agency of deto¬ nation, its natural sensitiveness to detonation, and the rapidity with which it can be transmitted from particle to particle became fully developed. Again, the reduction of gun-cotton 'fibre to a fine state of division, which renders the material readily convertible into very compact and dense masses, places the particles in the condition most favourable to resist mechanical motion upon the application of a blow, or of the concus¬ sion resulting from a detonation ; hence, compressed gun¬ cotton is readily susceptible of detonation in proportion to the extent of compression, or to its density and com¬ pactness, while loose gun-cotton wool, or the lightly twisted or compressed material cannot be readily de¬ tonated, because the force applied is expended in imparting motion to the readily yielding particles of the mass. If the force applied through the agency of a detonator to a mass of explosive material just borders upon that required for the development of the detonation, or if the condition of the mass is such as hardly to present the requisite resistance to mechanical motion essential for its detona¬ tion, then, results intermediate between the mechanical dispersion of the ma«s and its violent chemical dispersion or disintegration, i.e., detonation, are obtained. Thus, frequent instances have been observed, especially in the experiments in the transmission of detonation through tubes, in which the initiative detonation has brought about an explosion attended with little, if any, destructive effect, portions of the mass being at the same time dispersed and occasionally inflamed. Not only have such results often been obtained with gun-cotton and dynamite, but even mercuric fulminate, exposed to the concussion of a distant detonation transmitted through a tube, has frequently been exploded in a manner quite distinct from the violent detonation developed in other instances. Silver fulminate, which under ordinary conditions de¬ tonates violently, even when only a particle of the mass is subjected to a sufficient disturbing influence, has been exploded without the usual demonstrations of force, by the transmitted effect of a detonation of mercuric ful¬ minate. In these instances the violence of the concussion produced by the initiative detonation was only just bordering on that required for the development of detona tion, and it appears probable that only some small portion of the mass operated upon was in a condition or position favourable to the action of the initiative blow. The remainder of the mass would then be dispersed by the gases developed from the detonated portion ; in some instances the particles would be inflamed at the moment of their dispersion, in others, they would even escape ignition. The latter appears to be always the case when gun-cotton is exploded by a blow from a hammer or falling weight. However carefully the arrangements are adjusted with a view to distribute such a blow uniformly over the entire mass struck, the concentration of a pre¬ ponderance of the force applied upon some portion or portions of the entire mass appears almost inevitable ; hence, only a small portion is actually detonated, the remainder being instantaneously dispersed by the gases suddenly generated while the weight is still resting upon the support. Some experiments made in firing at masses of com¬ pressed gun-cotton, differently arranged and of different thicknesses, with a Martini-Henry rifle, at short ranges, afforded interesting confirmation of the correctness of the explanation given of the operation of a blow upon masses of explosive material under different conditions. Disks of gun-cotton of the same density and diameter, but differing in thickness, were fired at; they were freely suspended, and their distance from the marksman was in all instances 100 yards. The thinnest disks were simply perforated by the bullets, not a particle of the gun-cotton being ignited. Somewhat thicker disks were inflamed by the impact of the bullet, while still thicker disks, fired at under the same conditions, were exploded, portions being in some instances dispersed in a burning state. No instance of detonation was, however, obtained. These differences in effect, obtained with masses of different thickness and weight, are due to the difference in their power to resist mechanical motion when struck by the bullet, and in the different amount of resistance to pene¬ tration presented by the thin and the thicker disks. It has been explained that nitro-glycerine may be largely diluted with inert solid matters without its sensitiveness to detonation being reduced, while its deto¬ nation in open air becomes very much facilitated, because the mobility of the particles, and their consequent ten¬ dency to yield to the force of a blow or detonation is very greatly diminished. But if a solid explosive agent is diluted with inert solid matter the case is different ; for in such a mixture of the finely divided solid with non¬ explosive solid particles, there must be a partial and sometimes a complete separation of the particles of the explosive by the interposed inert particles with which it is diluted; hence the sensitiveness to detonation is reduced, and its transmission by the particles is retarded or altogether impeded, by a diminution of the extent of contact between the substance to be detonated and the initiative detonation, and by the barrier which the inter¬ posed non-explosive particles oppose to the transmission of detonation. Thus a mixture of mercuric fulminate with more than one-fifth its weight of French chalk could not be detonated by means of one grain of pure fulminate enclosed in a copper capsule, which was inserted into the mixture ; that quantity, similarly confined, sufficed to detonate undiluted fulminate through a tube 8 inches long and 0'5 inch in diameter. In experiments made in this direction with finely divided gun-cotton, it was found that although dilution with an inert solid, applied in the solid form, reduced the sensitiveness of the material to detonation, this was not the case when it was incorpo¬ rated with a salt soluble in water, the mixture being then compressed while in the wet state. The compressed masses thus obtained were, when dried, in a condition of greater rigidity than could be attained by submitting undiluted gun-cotton to considerably more powerful pressure, because the crystallization of the soluble salt used as the diluent upon evaporation of the water, cemented the particles composing the mass more rigidly together. The gun-cotton was therefore presented in a form more capable of resisting the mechanical action of a 50 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 19, 1879 small charge of fulminate than a more highly compressed undiluted gun-cotton, and hence the reduction in sensi¬ tiveness due to the detonation of the explosive compound is nearly counterbalanced by the greater rigidity imparted to the mass. If a soluble oxidizing agent (a nitrate or chlorate) be employed as the diluting material, the pre¬ disposition to chemical reaction between it and the gun¬ cotton (which is susceptible of some additional oxidation), appears to operate in conjunction with the effect of the salt in imparting rigidity to the mixture, thus rendering the latter quite as sensitive to the detonating action of the minimum fulminate charge as undiluted gun-cotton. Moreover, the interesting fact has been conclusively established, that these compressed mixtures of gun-cotton with a nitrate or a chlorate are much less indifferent to the influence of detonating nitro-glycerine than gun-cot¬ ton in its pure state. Chlorated and nitrated gun-cotton are detonated with certainty by means of half-ounce of nitro-glycerine, whereas the detonation of 2 oz. of the latter accomplished the detonation of ordinary compressed gun cotton only once in a large number of experiments. [To be continued.) QUEBRACHO, A PALLIATIVE REMEDY IN DYSPNOEA.* Dr. F. Penzoldt, of Erlangen (Berl. Klin. Wochen- schri/t, No. 19, 1879), narrates some experiments both on man and animals with a new drug, the bark of Aspiclo- spervia quebracho ( Apocynacece ), sent from Brazil, where it is reputed to have antipyretic properties. The form of preparation used throughout was a watery solution of an alcoholic extract of the bark, ten parts of the latter being percolated with one hundred of alcohol for several days, and the liquid filtered, evaporated, dissolved in water, again evaporated to dryness, and the residue dis¬ solved in twenty parts. ,water. The main results obtained in frogs were complete motor paralysis of central origin, respiratory paralysis, and diminished frequency of the pulse, independent of irri¬ tation of the vagus. In rabbits and dogs, motor paralysis and dyspnoea, increasing with the dose administered, were noticed. The dyspnoea in the rabbit, however, appeared to depend on retardation and deepening of the inspira¬ tions ; while in the dog the inspirations were accelerated. In the latter, also, there was salivation. Experiments on animals "with artificial fever, produced by injecting putrid fluids, showed no decided reduction of the temperature, and hence quebracho is probably not, as was supposed, an antipyretic. It should be added that it is not an antiseptic, but only temporarily retards putre¬ faction. The results obtained in actual cases of fever in men were also negative, but Dr. Penzoldt thinks that, considering the close chemical relationship between the alkaloid “ aspidodermine ” which Baeyer has extracted from quebracho-bark, and quinine, the subject requires further working out in this direction. By the accidental observation of a patient with pleurisy and emphysema, on whom the antifebrile effect of que¬ bracho was being tried, Dr. Penzoldt was led to try the bark in various forms of dyspnoea, depending on emphy¬ sema, bronchitis, phthisis, pleurisy, etc., and obtained remarkably good results. A teaspoonful of the above- mentioned solution was given two or three times a day. The most marked objective phenomenon after its exhibition was a reddening of the previously cyanosed or livid tint of the lips and face. In a case of emphysema where the patient was blessed with a nose the seat of acne hypertrophica, the ordinary violet-blue colour of the organ became fiery red, and excited the surprise of the other patients in the ward. The respirations generally became deeper and less frequent, and the patients ex¬ pressed themselves subjectively much relieved. The first feeling after taking the drug was one of warmth in the head ; many said that they had less desire to cough, and * From the Medical Times and Gazette, July 12, 1879. that they found expectoration easier. Occasionally sweat¬ ing occurred, and in some cases abundant salivation. No bad effects were noticed with the dose mentioned. Dr. Penzoldt finds that the addition of quebracho solution to blood, in the presence of oxygen, makes it assume a bright red colour, and he is inclined to think that possibly the blood is rendered capable of taking up more oxygen than usual, and carrying it to the tissues. This is, however, merely a provisional hypothesis, and at present there is no satisfactory explanation of the fact that, while moderate doses of the extract alleviate dyspnoea in man, large doses cause dyspnoea in the lower animals. As yet, quebracho bark is not a commercial product, but the wood is imported in large quantities for tanning purposes. The action of an extract of the wood is similar to that of the bark, but weaker. The alkaloid aspido¬ dermine affects the frog, on the whole, just as the extract of the bark does. ANALYSIS OF EUPATORIUM PERFOLIATUM. * BY PETER COELIER. The author reports the following result of the exami¬ nation of “Boneset,” Eupatorium perfoliatum, Lin. This plant has long had the reputation in domestic medicine of being a good tonic, especially valuable in the spring. Physicians have also attributed to it virtues as a diaphor¬ etic, expectorant, emetic and anti-intermittent. Whether all claimed for it is true must be settled by the physician, but the present chemical examination has been under¬ taken with the hope of throwing some light upon the proximate principles to which are due the medicinal effects of the herb. Partial analyses have been made by W. Peterson (Amer. Jour. Pharm., 1851, xxiii., p. 206), and by M. H. Bickley ( Amer . Jour. Pharm., 1854, xxvi., p. 459). Probably the bitter principle is the only one of medicinal importance. It is a brown uncrystallizable substance, soluble in water and alcohol, insoluble in ether. It was impossible to purify this substance well. Upon evaporation of an alcoholic extract of the drug a few white prismatic crystals were deposited. These crystals were difficultly soluble in hot alcohol and in¬ soluble in ether, water, dilute acids and dilute alkalies. They seem, therefore, to be neither acid nor alkaloid, but rather of an indifferent character. The drug appears to contain very little volatile oil, although its odour may be accounted for by this small amount present. Starch is not abundant. The tannic acid found gave the usual reactions, except that it failed to precipitate tartar emetic from its aqueous solution. The albuminoids were calculated from total nitrogen, multiplied by 6*25. It is impossible to say whether sugar was present in the substance, since the bitter principle would probably give similar reactions. The following analysis is regarded as an approximation only, but care has been taken to eliminate all preventable errors : — Analysis of “ Boneset,'1' Eupatorium Perfoliatum. Water . 917 per cent. Ash . 7*51 Albuminoids . 13*30 „ Resins and Chlorophyll .... 15*15 „ Indifferent Crystalline Substance . 2*87 „ Tannic Acid . 5*04 „ Bitter Extractive . 18*84 „ Gum and Colouring Matter ... 7*23 „ Starch Isomers . 12*47 „ Cellulose . 9*32 „ Humus Substances . traces. Volatile Oil . traces. * From the American Journal of Pharmacy , July, 1879. July 19, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 51 ©ti Jjkpaqntica! Jtruptl. • - ♦ - SATURDAY, JULY 19, 1879. Communications for the Editorial department of this Journal , boohs for review, etc., should be addressed to the Editor, 17, Bloomsbw'p Square. Instructions from Members and A ssociates respecting the transmission of the Journal should be sent to Mr. Elias Bremridge, Secretary, 17, Bloomsbury Square , W.C. Advertisements, and payments for Copies of the Journal, Messrs. Churchill, New Burlington Street, London , W. Envelopes indorsed “ Pharm. Journ .” THE PROSECUTION UNDER THE APOTHECARIES ACT AT BIRMINGHAM. After a delay of about two years, judgment has been given in the case of prosecution for breach of the Apothecaries Act at Birmingham, and as re¬ ported in the Journal last week, that judgment is adverse to the defendant . When the case was tried in the Birmingham County Court in July, 1877, it was believed and expected that the appeal then being made against the decision given in the Shep- perley case would result in causing some light to be thrown upon the questions involved in this prosecution as between medical practitioners and chemists and druggists. Upon that ground the County Court Judge resolved to defer judgment until after a decision had been given in the appeal so as to avoid putting the defendant to the trouble and expense of taking a second case to be decided by a higher tribunal. At the time the Judge expressed himself as being in some perplexity as to the proper intrepretation of the law relating to the case, and as to what might and might not be regarded as coming within the legi¬ timate functions of the chemist^ and druggist as a vendor of drugs. Having regard to the opinion ex¬ pressed by Baron Bramwell shortly before, he con¬ sidered that the recommendation and supply of any medicine or drug for the purpose of relieving some bodily ailment might be technically construed as infringing the terms of the Apothecaries Act, inas¬ much as that would be doing what the apothecary had a right to do in the exercise of his calling and under the licence of the Society of Apothecaries. Whilst recognizing this strict reading of the law as correct from a legal point of view, however, the County Court Judge also concurred with Baron Bramwell in thinking that it would be very un¬ reasonable for the Society of Apothecaries to inter¬ fere in a case so simple as that of a person asking for and receiving a simple remedy for such an ailment as a headache or any similar ordinary complaint. But he also stated that in his own mind he was not prepared to adopt in its entirety the view of Baron Bramwell that in every instance a chemist and druggist furnishing medicine to relieve bodily ail¬ ments would be stepping beyond his province and — by infringing upon that of the medical practitioner — be committing a breach of the Apothecaries Act. The opinion expressed at the time by the Judge was that the Society of Apothecaries never intended to interfere with chemists and druggists supplying remedies in trifling cases. He therefore considered that such an interpretation of the law as Baron Bramwell had adopted was too strict, and he appears to have been led to this opinion by recog¬ nizing the possibility of a distinction being drawn between mere advice or recommendation as to the kind of medicine and its use for certain purposes, as forming part of the business of vending, and the prescribing of medicine as a result of the examina¬ tion of a patient by the ordinary means of ascertain¬ ing symptoms, and with the object of treating disease. From a common sense point of view there is much reason for recognizing this distinction, but unfor¬ tunately the Apothecaries Act does not either define what is meant by acting as an apothecary or specify whether the rights specially reserved to chemists and druggists by the 28th section comprised the right to do as they and apothecaries also had previously done in giving advice as to the use of simple remedies. As a matter of law, therefore, it was difficult, if not impossible, to decide whether or not the recom¬ mendation of medicine or advice as to its use in connection with the vending of it was to be under¬ stood in the meaning of the Act as “ practising as an apothecary.” If this were held to be the case it was equally difficult to decide whether or not the right of giving such recommendation and advice was reserved to chemists and druggists in virtue of usage prior to the Act of 1815. For the sake of gaining from the decision of the Shepperley appeal some information and guidance on these points the Birmingham County Court Judge adjourned the case heard by him in 1877. That appeal has now been disposed of, but the assistance it was expected to furnish towards the settlement of the important questions above men¬ tioned has not been obtained. It is still an open question what is meant by acting as an apothecary within the meaning of the Act of 1815. It is still a question where the line is to be drawn between the recommendation and advice properly appertain¬ ing to the vending of drugs and medicines, as foaming part of the chemist and druggist’s business, and the application of remedies to the treatment and cure of disease, which is the function of. the medical prac¬ titioner holding himself out to the public as specially qualified for that work. It was upon this view that the decision just given by the Birmingham County Court Judge was based. He takes the evidence of Mr. Parsons as showing undoubtedly that before the year 1815 chemists and druggists did something beyond merely selling medi¬ cines ; but he points out that even if they were then 52 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 19, 1879. in the habit of advising patients or prescribing medicine it does not follow that they ever had the legal right to do so, or that at the present day chemists and druggists are protected by the 28th sec¬ tion of the Act in case they do so. The legal right to practise medicine or surgery and to treat disease is given by the registration of the practitioner who holds himself out, in virtue of the special qualification by which he has secured registration, as the proper person for performing those duties. In the case that has now been decided at Bir¬ mingham the defendant had not the legal right to practise medicine, and as the case for which he pre¬ scribed was considered to require medical knowledge and skill, he is held to have “ acted as an apothe¬ cary ” and thus to have come within the provisions of the Apothecaries Act. That this is a just decision of the case we may gather from the resolve of the Executive Committee of the Chemists and Druggists’ Trade Association not to appeal against it. In connection with this matter it will be interest¬ ing to learn that the President of the Nottingham Medical Defence Association also expresses regret that the Shepperley case has not led to a decision of the question as to the legality of counter practice, although affording opportunity for an authoritative exposition of the law. In speaking of the general weakness of the case which has called forth so much comment, he seeks to explain this by stating that it was never intended Death’s evidence should be relied upon, and that even in the original county court proceedings he was not to be put into the box. There were — he goes on to say— other witnesses, who, judging from the statements they made to the solicitors of the Medical Defence Association, were prepared to prove a strong case against the defendant. Those wit¬ nesses entirely failed to support the objects of the prosecutors, who, Mr. Stanger informs us, would have accepted their defeat if the Judge had not unfortunately given a decision in their favour, partly on the evidence of Death, but chiefly on the admissions made by the defendant. It is seldom that litigation is productive of so much satisfaction all round as is claimed to have been the result of the Shepperley case, and though we are inclined to think that the most substantial satisfaction fell to the share of the lawyers, we are not at all disposed to interfere with the happiness of those who find reason to be pleased. A NEW PHARMACY ACT IN THE STATES. The “ People of the State of New York, repre¬ sented in Senate and Assembly,” have just enacted a law “ governing the sale of drugs and poisons in the County of Kings ” in that state. For conveni¬ ence of reference and to illustrate the position which pharmacy is taking in the United States a short abstract will be useful. In accordance with its title this Act makes it illegal for any one not registered under its pro¬ visions, after the first day of October next, to open or conduct any pharmacy or store for retailing or compounding medicines or poisons in the county of Kings ; but it also goes further and makes it illegal for any but a registered pharmacist to prepare phy¬ sicians’ prescriptions except under the supervision of a registered pharmacist. The Act is not wanting in stringency in other directions, for in order to procure the registration necessary a person must (1) be a graduate in phar¬ macy or in medicine, who has had at least four years’' experience in stores where prescriptions of medical practitioners have been compounded and hold a diploma from a legally constituted college; or (2) have had at the time of the passing of the Act ten years’ practical experience in the preparation of phy¬ sicians’ prescriptions ; or (3) have had four years’ similar experience and pass an examination by a Board appointed under the terms of the Act, consisting of three pharmacists and two medical men, or some other recognized Board of Pharmacy. There are two schedules of poisons. Schedule A corresponds to Part 1 of our schedule in containing the poisons that are not to be sold without registra¬ tion. Among these are to be found several that are in Part 2 of the British schedule, such as the white and red precipitates, essential oil of bitter almonds, and opium and its preparations, except paregoric and other preparations of opium containing less than two grains to the ounce. On the other hand aconite, savin, ergot and cantharides are remitted to the second schedule, which also includes henbane, digitalis, croton oil, creosote, sulphate of zinc, mineral acids and carbolic acid. The registers used for recording the sale of poisons in Schedule A are to be preserved for five years and to be open for inspection by the proper authorities, and none of the poisons in either schedule are to be sold without labelling the bottle or other containing vessel, as well as the outside wrapper, with the name and address of the seller and the word “ poison,” or without ascertaining that the buyers are aware of their poisonous nature. Another feature of the Bill is an adulteration section, which provides that the pharmacist shall be held responsible for the quality of his goods, except in the case of original packages and patent medicines. A conviction for fraudulent adulteration is to be punishable by a fine of one hundred dollars and erasure of the offender’s name from the register. The duty of prosecuting for offences under the Act is thrown upon the district attorney upon informa¬ tion laid by the Board of Pharmacy. The Sale of Food and Drugs Act (1875) Amend¬ ment Bill was read a third time in the House of | Lords on Wednesday last. July 19. 1879. J THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS 53 §OTS!U|tiotts of |g barmaqrat teal PRELIMINARY EXAMINATION. At a meeting of the Board of Examiners for England and Wales, held in London, on Wednesday, July 16, 1879, the report of the College of Preceptors on the ex¬ amination held on July 1 was received. Three hundred, and sixty-fire candidates had presented themselves for examination, of whom • one hundred and eighty -one had failed. The following one hundred and eighty-four passed, and the Registrar was authorized to place their names upon the Register of Apprentices or Students : — (Arranged alphabetically). Allen, Ernest Edward . Winchester. Allen, Richard . Ramsey. Angus, Wm. Cockburn . Aberdeen. Armstrong, Charles . Streatham. Bailey, Henry . Chesterfield. Bailey, Walter Thomas . Coventry. Baker, Alfred, jun . March. Barber, William John . Croydon. Barnett, Henry Frederick . Uttoxeter. Baron, Richard Edward . Alderney. Barrass, Arthur . Hingham. Beesly, Charles William . Cambridge. Berry, Walter . Manchester. Betts, George Priest . Norwich. Blair, Thomas, jun . Girvan. Blankley, T. E. B . Sleaford. Bostock, Samuel . Hyde. Bousie, William Hutton . Kirkcaldy. Bradley, Frederick William ...Wisbech. Brice, Ernest . Wirksworth. Briggs, George . .Leeds. Brindle, Edward . Edinburgh. Broad, Arthur Edmund . London. Broumpton, Frederick Richard. London. Brown, Andrew P . Glasgow. Brown, Charles Maltby . York. Bruce, Alexander Gibb . Broughty Ferry. Butterfield, Frederick Victor ...Thirsk. Butler, Ernest F. N. G . London. Callow, Ewan . Douglas. Cameron, John Wallace . Sunderland. Capper, William . Bath. Carruthers, Christopher . Carlisle. Chadwick, Arthur ' . Leeds. Clarke, Walter . Bromley. Clayton, Walter F . . London. Clegg. George . Accrington. Cooper, Harry Stanley . London. Countze, Napoleon W . Bournemouth. Crookes, George Wilkson . Eckington. Cubey, Robert Hewison . South Shields. Cummings, John Dickie . Alloa. Deakin, John William . Leftwich. Deck, Arthur Albert . London. Dibble, Alfred Tom . Bristol. Dickson, James Currie . Dumfries. Dixon, Philip Thomas . King’s Lynn. Dodds, Ernest . Sheffield. Dunn, George M . London. Edwards, Henry . Bootle. Edwards, Llewelyn . Llandyssul. Elliott, Henry . . . London. Ellisson, Charles . Barnsley. Elston, Albert . Long Sutton. England, William . Sheffield. Fairhurst, John James . Grappenhall. Farlow, James Southward . London. Farthing, Thomas William . Devonport. Flower, Edward Ashbrook . Derby. Fooks, Robert Spiller . Bridport. Forster, James . Foster, Henry Simpson . Freshury, John William S. . Gascoyne, Edward . Gaskin, Alfred Charles . Gibson, Matthew Henry .... Glasspole, Lorenzo B . Gooch, Stephen Leeds . Greaves, John Elijah . Green, Charles A. P . Green, Frederick . Green, Joseph H. B . Grey, William . Gourlay, Robert George .... Graham, Frederick Albert . Grant, Daniel .., . Grim wade, Edward Hall _ Haining, Edward . Hankinson, Alfred William. Hall, Ernest Edward . Hart, Edgar Thomas . Hartley, George Thomas _ Hasler, Joseph . Hawley, Arthur . Henderson, David James . Hill, Major . Hocken, James Preston .... Hornby, Robert William.... Horsfall, William . . Hurcomb, Lawrence E . Idenden, Richard Frederick Ingham, William Linnell ., Inman, Thomas Leonard _ Irvine, John C. D . . Jarvis, Joseph Alexander . John, Benjamin . Johnson, Henry Haden . Johnson, Sydney Arthur.... J ones, Eustace Harry . Jones, Maurice Howell . Jones, Thomas John . Joye, Joseph . Keene, Walter F. W . Knox, John . Lawton, Ernest . Levick, George A. M . Llewhelin, Ivor Vaughan . Loudon, John James . Lumby, Walter . Macaulay, Colin McUlloch. Marshall, Henry B. K . Massey, William . McEwan, David . Me Master, Thomas . Matthews, Henry Paget . Melhado, Howard Emanuel Mercer, Frederick Clarke . Middleton, Burton . Milton, Alexander . Mohun, Charles Thomas .... Morgan, Richard . Morgan, William J ohn .... Musse 11 white, William . Naylor, James Louis . Neale, Matthew Henry _ Neech, James Thomas . Oldis, Edward Charles . Owen, Robert Godfrey . Owen, William . Pawson, Frederick Thomas.. Priestly, William . Pugh, Joseph . Pye, Thomas . Rees, Harding . Roberts, Griffith . Robinson, Thomas . ...Musselburgh. ...Rotherham. ...Lincoln. . . .Wolverhampton. . . . W olverhampton . ...Matlock Bath. ...Portsmouth. , ...Reepham. ...London. ...London. ..London. ..Swindon. ...Blyth. ...Lytham. ..Leeds. ..Edinburgh. ..Croydon. ..Dumfries. . . Grange-over-Sands. ..Wednesbury. ..Rochester. ..Bath. ..Blackburn. ..Coventry. ..Dunbar. ..Sleaford. ..Heaton Chapel. ...London. ..York. ..Nottingham. ..Dartford. ..London. ..Batley. ..Aberdeen. ...Devizes. . .Narberth. ..Sedgley. j ..Wisbeach. ..Dartford. ..Machynlleth. ..Cardigan. ..Southport, ..Margate. ..March. ..Barnsley. ..Mansfield. ..Fishguard, ..Glasgow. , . .Tranmere. ...Perth. . .Hardingstone, . .Preston. ..Perth. ..Stranraer. . .Aldershot. . . Ramsgate. . .Coventry. ..Ilkley. ..Aberdeen. . . Herne Bay. ..London. ..St. Clears. ..Basingstoke. ..Brownedge. ..Woolwich. ..Felmingham. ..London. ..Liverpool. ..Towyn. ..Oakham. ..Harrogate. . . Wotton-under-Edge. . .Bennetthorpe. ..South Norwood. ..London. ..Wigton. 54 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 19, 1879. Roper, Joseph Charles . Chesterfield. Rowe, Arthur . Windsor. Rowell, Joseph Elsum . Whittlesea. Rowntree, Alfred Henry . Manchester. Rule, Alexander . Aberdeen. Rushton, Martin . Liverpool. Sant, Esdras . Pontypridd. Sapsed, William George . London. Saunders, Samuel Harry . Oswestry. Scudamore, George William ...Bristol.. Shadwick, Joseph . Wigton. Shepard, William . Newport, I.W. Shepperd, William John . Newport, I.W. Siddall, George Ward . Plymouth. Skoulding, William George . Oakham. Smalley, Arthur William . Stamford. Smedley, Arthur William W.... Northampton. Smedley, Erederic Robert . Northampton. Smith, Corbet Edward . Newport, I.W. Southwell, Charles Bullock . Bridgenorth. Spicer, George William . Cranleigh. Spivey, Fred . Huddersfield. Spurge, Ernest Clements . Ipswich. Staley, Henry . Burton-on-Trent. Strachan, Alexander . . Rothienorman. Stuart, Alexander . Dufftown. Swinburn, Banks . Penrith. Thomas, Thomas . Swansea. Thomas, William Morgan . Glamorgan. Thomason, Henry Williams ...Birmingham. Thompson, Michael John . Hexham. Timm, Edmund . Goole. Valpy, Edmund Renouf . Aylesbury. Vaughan, Edward Edwards ...Rhyl. Vickery, William Henry . Plymouth. Walker, Arthur . London. Walker, Arthur Heesom . Altrincham. Walker, James Henry . Hyde. Watt, George . Aberdeen. Watt, John . Leslie-by-Insch. Whaley, Thomas Cope . Barnsley. White, Cresswell Fitzherbert... Chippenham. Whyte, James . . . Aberdeen. Williams, George Alfred . Shrewsbury. Wilson, John . Kirkcaldy. Wilson, Joseph . Chislehurst. Wing, Arthur Joseph . ....Cambridge. Young, John . Arbroath. The questions for examination were as follows : — First or Preliminary Examination. ls£ July 1879. Time allowed : Three Hours for the three subjects. 1. Translate the following passages into English : — A. Eo concilio dimisso, iidem principes civitatum, qui ante fuerant ad Caesarem, reverterunt, petieruntque, uti sibi secreto de sua omniumque salute cum eo agere liceret. Ea re impetrata, sese omnes flentes Caesari ad pedes pro- jecerunt : “ Non minus se id contendere et laborare, ne ea, quae dixissent, enunciarentur, quam uti ea, quae vellent, impetrarent ; propterea quod, si enunciatum esset, summum in cruciatum se venturos viderent.” B. Caesar loquendi finem fecit, seque ad suos recepit ; suisque imperavit ne quod omnino telum in hostes rej ice- rent. Nam, etsi sine ullo periculo legionis delectae cum equitatu praelium fore videbat, tamen committendum non putabat, ut, pulsis hostibus, dici posset, eos ab se per fidem in colloquio circumventos. 2. Decline throughout principes, re, finem, equitatu, colloquio. 3. Explain the construction known as the “ Ablative Absolute,” by the aid of the examples of it in the above passages. 4. Name the prepositions which occur above, arranging them in a table, according to the case which each takes after it. 5. ' Translate into Latin : — Caesar did not wish the conference to be broken off. They appointed a day for the conference. The Helvetii were defeated by Caesar. The forces of Ariovistus were distant four and twenty miles from our men. II. ARITHMETIC. (The working of these examples, as well as the answers must be written out in full.) 6. Find the value of 1 cwt. 3 qrs. 12 lbs. at £1 2s. 6cL per cwt. 7. Calculate the equivalent, on the metric system, of 10 oz. 5 dr. 2 scr. 8. Divide (f + Ar) by ($ + $). 9. Express as decimals *, -§, 10. What is the income corresponding to an Income Tax of £13 2s. 6d., at the rate of 7d. in the £ ? 11. Compare the measurement of weight in the metric system with the various English standards. Why is the metric system easier to work ? The following is a list of the centres at which the examination was held, showing the number of candidates examined at each centre and the result : — Candidates. Candidates. cS CD O m a> c3 P4 a Aberdeen . ..16 9 7 Birmingham... ..21 10 11 Brighton . .. 1 1 0 Bristol . ...12 7 5 Cambridge ... ... 4 2 2 Canterbury ... ... 2 2 0 Cardiff . ... 7 3 4 Carlisle . ... 9 6 3 Carmarthen ... ... 8 5 3 Carnarvon . . . ... 9 3 6 Cheltenham . . . .. 3 0 3 Darlington . . . ... 6 0 6 Douglas, I. of M. 2 2 0 Dundee . ... 7 4 3 Edinburgh . . . ...16 6 10 Exeter . ... 8 3 5 Glasgow . ...12 5 7 Guernsey . ... 1 0 1 Hull . ... 5 1 4 V T3 *1 Ha OQ 8 Cu CD • H C3 Lancaster . . 6 4 2 Leeds . .17 8 9 Lincoln . . 7 4 3 Liverpool . .13 7 6 London . . . .52 36 16 Manchester .... .20 9 11 Newcastle-on-T. 10 4 6 Northampton . . 6 3 3 Norwich . .14 4 10 Nottingham . .12 4 8 Oxford . . 1 1 0 Peterborough . .15 10 5 Sheffield . . 7 7 0 Shrewsbury .... . 4 3 1 Southampton . .15 6 9 Truro . . 4 1 3 Worcester . . 2 0 2 York . .11 4 7 III. ENGLISH. 12. What parts of speech may an adverb qualify ? 13. Explain, by the help of examples, the correct use of shall and will. 14. In what respects does the Relative agree with its Antecedent? How far is it independent of its Ante¬ cedent ? 15. Parse: — “If the pilot slumber at the helm, The very wind that wafts us towards the port May dash us on the shelves.” 16. Write a short essay on one of the following sub¬ jects : — The Electric Light, the Phonograph, the Tele¬ phone, the War in Zululand, Recreation, Co-operative Stores. |rouim[iai $ransaflttons. CHEMISTS AND DRUGGISTS’ TRADE AS30- CIATION OF GREAT BRITAIN. Meeting of the Executive Committee. A meeting of the Executive Committee of this Associa¬ tion was held at the office of the Association, 23, Bur¬ lington Chambers, New Street, Birmingham, on July 8, 1879, at 1 p.m., Mr. Thomas Barclay (Birmingham), July 19, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 55 President, in the chair. Mr. Robert Hampson (London), Vice-President. Present — Messrs. Andrews (London), Arblaster (Bir¬ mingham), Bell (Hull), Churchill (Birmingham), Cross (Shrewsbury), Davison (Glasgow), Holdsworth (Birming¬ ham), Jones (Leamington), Maltby (Lincoln), Reynolds (Leeds), Southall (Birmingham), Symes (Liverpool), Walker (Coventry), and the Solicitor of the Association. The minutes of the previous meeting of the Executive were read and approved, the appointment of committees and officials for the ensuing year was proceeded with. In reply to a question, the Secretary said the taxed costs of the defendant in the case of the Apothecaries’ Company v. Shepperley, amounting to £165 15s. Sd., had a few days previously been paid to the Association. Mr. J ones directed the attention of the committee to the medical bills before Parliament. The President said he thought it would be undesirable for the Association to take any steps in regard to these bills until the Select Committee which had been ap¬ pointed by the House of Commons had issued their report. Mr. Hampson said it appeared evident that the medical profession were not disposed to allow the ques¬ tion of counter practice to rest. The Apothecaries’ Company had just sustained a case in that town and gentlemen reading the medical journals would find their tendency was to support all the demands of the medical men. If the Select Committee were going into the whole question of medical legislation the question naturally arose as to the desirability of the Association moving in the matter. Mr. Davison said he thought the fact of so many medical men keeping open shops, in very many instances managed by unqualified persons, should be brought under the notice of the chairman of the Select Committee. In Glasgow alone there were about a hundred and twenty such shops. Mr. Symes said the Select Committee would scarcely be likely to accept any dicta from the Association. If the Association attempted to in any way regulate the practice of medical men it would be stepping out of its province. Mr. Reynolds said the Duke of Richmond’s Bill was the only medical bill which stood any chance of passing during the present session of Parliament. It was moved by Mr. Hampson, seconded by Mr. Rey¬ nolds, and unanimously resolved : — “ That the Law and Parliamentary Committee be directed to watch the pro¬ ceedings of the Select Committee sitting to consider the medioal bills in the House of Commons, and to take such action as they may deem necessary.” The President said the gentlemen present would be aware that the Birmingham County Court judge had given his decision a few days previously in the case of the Apothecaries’ Company v. Harrison, tried in the Bir¬ mingham County Court so far back as July 2, 1877, the judgment being withheld pending the decision in the case of the Apothecaries’ Company v. Shepperley. The decision of the judge was in favour of the plaintiffs, and the defendant had been fined £20 and costs. The Secretary would read the judgment. The following judgment was then read : — “ This is an action brought by the plaintiffs against the defendant to recover the sum of £20 by way of penalty under the 20th section of the 55 Geo. III. c. 194, for practising as an apothecary without having first obtained the necessary certificate. It was heard before me as far back as July 2, 1877, and was adjourned in conse¬ quence of the pending of an appeal to the High Court of Justice against the decision of the county court judge at Nottingham, in a case similar to the present and under the same Act of Parliament. That appeal has now been disposed of, and I am sorry not to be able to derive the assistance from it I anticipated. So far as concerns the question of what is meant by ‘acting as an apothecary ’ within the meaning of the Act, or the still more important question whether in virtue of usage prior to the Act in 1815, the right continued for chemists to act as apothe¬ caries in the treatment of simple ailments and the admin¬ istration of simple remedies for their relief, the law is left very much in the same state of doubt as it was before. The facts of the case are really these. The defendant is a chemist and druggist carrying on business at Birming¬ ham, and a young woman named Julia Caddick being unwell was advised to go to the defendant’s shop for medicine. In her evidence she states that she went to the defendant’s shop on November 27, 1876, and saw the defendant and asked him if he would make up some medicine to relieve her from a weakness she was suffering from. She says, ‘ she told him it was a weakness left on her from her last confinement, and that her womb came down.’ She says further, ‘that the defendant felt her pulse, looked at her tongue and asked her to describe her feeling, when she told him she suffered much from pains in the back.’ After this, according to her evidence, the defendant gave her a bottle of medicine which he said would do her good, and told her to take it according to the instructions on the bottle. She says, ‘ she gave the defendant one shilling for the medicine and took some of it at once in the shop.’ A bottle half full of medicine was produced in court at the trial by the witness and she stated that it was the same she obtained from the de¬ fendant at his shop on November 27. The witness was cross-examined at length, but her evidence was not shaken in any respect. The above is all the evidence on the part of the plaintiffs I consider necessary to state at length except that of the medical man, Dr. Suffield, who, in his examination stated, ‘ that he had heard the evi¬ dence given by the woman, and from her description of her suffering, and from what she stated she had told the defendant, he should imagine she was suffering from anaemia, which was a constitutional complaint of a dan¬ gerous character, frequently leading to death, if the patient was not properly treated.’ In diagnosing a com¬ plaint of the nature described, Dr. Suffield observed, ‘ that one would go a little deeper into particulars than seemed to have been done in this case by the defend¬ ant.’ On cross-examination Dr. Suffield said, ‘he did not think feeling the pulse was a sufficient diagnosis of the disease.’ Upon being requested by defendant’s counsel, he examined the medicine in the bottle and said he thought it was a preparation of iron and would be a proper medicine for the case. In opposition to this, defendant himself was called as a witness and the material parts of his evidence were to the effect ‘ that he remembered Julia Caddick visiting his shop in Novem¬ ber in the afternoon. She came and asked him to supply her with a bottle of strengthening medicine for a weak¬ ness after lying in.’ He denies that he examined her at all and states it was not necessary. He says, ‘ he did not feel her pulse, and she did not tell him anything about the womb coming down.’ He admitted, however, ‘ that he did ask her if the weakness had anything to do with her confinement, stating that he did so because he saw she had been recently confined, and had a baby in in her arms which she said was hers.’ The witness then stated, ‘ I said to her, do you mean general weakness of the constitution ; when she said, yes.’ The witness then added, ‘ I mixed her up some stuff which I put into a bottle and put a label upon it. The label on the bottle which had been produced the witness admitted was his label.’ He said, ‘ that the mixture in the bottle was not what the woman had from his shop, that he would swear.’ This, with the exception of the evidence of an aged chemist called by the defendant, to whose evidence he should refer hereafter, is the whole of the evidence on the one side and the other, so far as the real question to be determined in the case is concerned. By the 20th section of the 56 Geo. III., c. 194, under which this action is brought, it is enacted, ‘ that if any person shall after the 1st August, 1815, act or practise as an apothecary in any part of England or Wales without having obtained a 56 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS [July 19, 1879 certificate as mentioned in the preceding section of the Act he shall be liable to forfeit and pay the sum of £20.’ The 28th section of the same Act, the one on which defendant grounds his defence, enacts by way of proviso ‘ nothing in this Act contained shall extend or be construed to extend to prejudice, or in any way to affect the trade or business of a chemist and druggist in the buying, preparing, com¬ pounding, dispensing or vending drugs, medicines or medicinable compounds, wholesale and retail, but all persons using or exercising the said trade or business, or who shall, or may hereafter, use or exercise the same, shall and may use, exercise, and carry on the same trade or business in such manner and as fully and amply to all intents and purposes as the same trade or business was used, exercised or carried on by chemists and druggists before the passing of this Act.’ The first point in this case to be considered is, has the defendant in the instance proved by this evidence acted as an apothecary ? if he has, and is not protected by the pro¬ viso (it being admitted he has not obtained a certificate from the Society of Apothecaries), he is undoubtedly liable to pay the penalty sued for and the verdict must be for the plaintiffs. The defendant, however, raises two questions by way of defence. First, he says in what he did he did not act as an apothecary, and second, that if in strictness it should be held that he did, inasmuch as he was only carrying on his business of a chemist as chemists carried on their business before the passing of the Act in 1815, he is protected by the proviso referred to, which he contends permits chemists and druggists to carry on their business in the same manner as they did before the pass¬ ing of the Act, and that chemists, so he says, the evidence proves were in the habit of advising patients in trifling cases as well as supplying them with medicines, and he argues that the present is a case of that character which a chemist would have treated before the passing of the Act, as the defendant has done since. Now with refer¬ ence to the question raised by the first part of the defence, whether in what the defendant did he acted as an apothe¬ cary, the case of the Apothecaries’ Company v. Lotinga, 2 M. and R., p. 500, decided in 1843, goes perhaps more fu'lly into the question than any other, and in that case, Mr. Justice Cresswell told the jury that, ‘ an apothecary is a person who professes to judge of internal disease by its symptoms and applies himself to cure that disease by medicine,’ and in the same case he tells them that ‘ a chemist is one who sells medicines which are asked for,’ and in effect states, ‘ that if a chemist himself selected the medicines and determined on what he ought to give, he is stepping out of his lawful province as a chemist and entering upon that of an apothecary.’ The definition of a chemist as given by Mr. Justice Cresswell in Lotinga’s case would appear not to be large enough, because the 28th section of the Apothecaries Act referred to clearly shows that the trade of a chemist was not confined to sell¬ ing medicines which were asked for merely, but extended to the preparing, compounding and dispensing them. His lordship’s definition of an apothecary is, however, doubt¬ less perfectly correct, for as recently observed by Mr. Baron Pollock, in Shepperley’s case, it is to be presumed that Mr. Justice Cresswell did not mean internal as opposed to external disease, in the sense of a man having an eruption produced by some diseased condition of the body which the learned Baron observed would not be any less an internal disease, and if anyone proceeded to judge of it by the symptoms and apply medicine for its cure the law would equally apply to him as it would to the man who attempted to cure a persistent difficulty of indigestion, a diseased condition of the lungs or any of the other evils to which flesh is heir and which affect mankind internally. There is another case, The Apothe¬ caries’ Company v. Nottingham (34 L. T. N. S. 76), tried before Lord Justice (then Baron) Bramwell in 1876. In that case it was proved ‘ that the defendant, who was a certified chemist, but not an apothecary, had been in partnership with a duly qualified medical practitioner, but it was also shown that this medical man was not always on the spot. It also appeared in evidence that the defendant had on various occasions been applied to for advice and medicine, both of which he gave to the applicants, but did so as an ordinary shopkeeper from behind the counter. It did not appear that he ever went from his shop to attend on patients, and he was proved in cases of serious illness always to have referred the patients to the doctor with whom he was in partner¬ ship,’ and the learned Judge in addressing the jury said, ‘ I feel some little difficulty in putting the case to you, for on the defendant's own admission he says he pre¬ scribed and that if a person brought a child to him suffering from diarrhoea and asked what was good for it, he gave a medicine ; if, however, the case was serious he sent it to the doctor. Surely,’ said the learned Baron, ‘ that is acting and practising as an apothecary within the meaning of the Act.’ There is also a third case, known as ‘Wiggins’s cp.se,’ tried before Mr. Justice Field, on the 23rd and 24th May, 1878, in the Bail Court at Westminster (but not reported, so far as I know, in any of the recognized legal reports), in which his Lord- ship approves and adopts the definition of Mr. Justice Cresswell in Lotinga’s case with the qualification men¬ tioned by Baron Pollock. Upon these authorities, and there are several others of earlier date, I am bound te find and must hold upon the evidence, which is clear and decisive, that the defendant, in what he did, acted as an apothecary in contravention of the Act of Parliament and has incurred the penalty prescribed by it, for it is distinctly proved by the plaintiffs’ evidence, and that of the defendant cannot be relied on to alter it in any material degree, that the defendant in performing the acts men¬ tioned in the evidence to enable him to form an opinion on the case proceeded, in the language of Mr. Justice Cresswell, to judge (or pretend to judge) of the internal disease from which the young woman was suffering by the symptoms ascertained by his acts, and applied himself to cure it by medicine. If this is not acting as an apothecary, it is really, I believe, impossible to define what acting as an apothecary is. Upon the second part of the defence the defendant called a witness, named Thomas Parsons, who said ‘ he was eighty-four years old, andhad been apprenticed to a chemist and druggist in 1809.’ He said he was apprenticed to Messrs. Blews and Company of Worcester, where one of the partners was an apothecary; and that he (the witness), in the shop, over the counter, and as I understand him, others in the same shop supposed to be competent, though not apothecaries, were in the habit of giving advice as well as medicine in trifling cases, but that if the case were a serious one it would be attended to by the principal, meaning, I suppose, the partner who was an apothecary. This evidence un¬ doubtedly shows that chemists in carrying on their business before the year 1815 did something (lawful or otherwise) beyond selling medicines merely, as stated by Mr. Justice Cresswell, and if the present instead of being a case of a serious character, as I find it from Dr. Suffield’s evidence to have been, had been of the trivial nature of those referred to in the evidence of Mr. Parsons, the second part of the defence would have arisen and would deserve serious consideration ; but the evidence of Mr. Par¬ sons convinces me that though chemists before 1815 might have advised in trivial cases, they were not in the habit of advising and prescribing as the defendant has done in a case of the serious nature of the present, but would have sent such a case to the apothecary. If, however, it be correct, as Mr. Parsons in his evidence states, that before 1815 some chemists were in the habit, in trifling cases, of advising as well as supplying persons with medicines, it does not at least follow that they ever had the legal right to so advise and supply the medicine or are protected by the 28th section of the Act in case they do. If I were at liberty to speculate, I think it is very probable that some chemists, before 1815, did act as Mr. Parsons says they did, and as is well known some do now, July 19 '879.] THE rilARMACEUTICAL JOURNAL AND TRANSACTIONS. 57 but if they did, I believe they had no legal right to do so and were usurping the rights of those who had, just as the surgeon, as shown by Lotinga’s case, usurped and contended for the right to advise and supply medicine as an apothecary, or indeed as the apothecary did when, as is known, he sometimes exercised, though illegally, the right of the physician t ) attend and prescribe for patients, before he possessed the legal right to do so, which at the present time he undoubtedly possesses. If the language of the 28th section is carefully considered I am afraid it will be found not to have the effect contended for by Mr. Herbert on the part of the defendant. He says that the business of chemists before 1815 extended to, or was carried on by them, ‘ in advising or prescribing in the shop, over the counter as it were, in cases of a trifling nature and supplying the persons with medicines for the cure of them, and secondly are protected in what they do now, provided they do no more than they did then ; but the section with regard to the business of a chemist does not say a word about advising or prescribing.’ On the contrary it would seem, from the language used, rather to ignore the fact that to do so formed, at the time of the passing of the Act, any part of the chemist’s business. The words of the section are ‘ that nothing in the Act contained shall extend ’ or be construed to extend, to pre¬ judice, or in any way to affect the trade or business of a chemist or druggist in — be it observed, not the advising or prescribing as stated by Mr. Herbert was the chemist’s business in small matters, but only in ‘the buying, prepar¬ ing, compounding, dispensing, and vending drugs, medi¬ cines and medicinable compounds wholesale and retail.’ The section then proceeds to provide that all persons using or exercising the said trade or business, or who shall or who may thereafter use or exercise the same, shall and may use, exercise, and carry on the same trade or business, in such manner and as fully and amply to all intents and purposes as the same trade or business was used, exercised or carried on by chemists and druggists before the passing of the Act. What business, therefore, the section provides is not to be affected by the Act, and what might be carried on notwithstanding the Act, would appear to be not that trade of a chemist as carried on by him according to Mr. Parsons’s evidence in the ‘advising and selling medicines,’ but only as he carried it on in the buying, pre¬ paring, compounding, dispensing and vending his drugs. So it is this trade or business of a chemist so described, not the enlarged or extended one as contended for by Mr. Herbert, that the Act permits him to carry on (and pro¬ tects him in doing) as fully as he might have done before the passing of the Act. The Legislature would appear not to have known (if indeed it existed) of this extended business of a chemist as now contended for, or if it did, it appears to have ignored it as no part of the legitimate business of the chemist, and declined to protect him in tke exercise of it after the passing of the Act. The words ‘advising and prescribing’ are, as already remarked, not mentioned in the proviso, and there is no word so used in it that could by any ingenuity be construed as including these words unless it be the word ‘dispensing,’ and that word in my opinion does not, for the true meaning of the word dispensing (in pharmacy), according to Bailey’s Dictionary, is, when simples of a composition are set in order lest any of the ingredients should be forgotten ; and according to Rees’s Encyclopaedia, title ‘Dispense’ (in phar¬ macy) means ‘To dispose and arrange several medicines, either simple or compound, by weight in their proper doses or quantities in order to be employed in the making of the composition.’ I have made these few observations for the consideration of the defendant and those associated with him ; they form no part of my judgment, which is in no way founded upon them, for, as I have already said, I find the present case was of a serious if not a dangerous nature, and in that view of it I do not understand that even the defendant’s counsel would contend his client had the right to treat it as he has done. The defendant, I find from the evidence, has clearly and unmistakeably ‘acted as an apothecary,’ and the proviso relied upon, in my opinion, affords him no defence in such a case as this, even though I were to admit it is possible that he might in those trifling cases contended for by Mr. Herbert, which for the l’easons given, however, I very much doubt. The verdict, therefore, will be for the plaintiffs.” Verdict for the plaintiffs, £20, and costs. In reply to a question from the President, the solicitor said there were three courses open, provided the Associa¬ tion desired to carry the case further, namely, appli¬ cation for a new trial, appeal by case or appeal by motion. An application for a new trial would have to be sup¬ ported by one of three grounds, either that the Judge refused evidence that was proposed, that he admitted evidence wrongfully, or that the verdict was against the weight of evidence. Taking the last first, as the Judge acted in the capacity of Judge and jury, he would no doubt say the verdict was not against the weight of evi - dence, and would refuse a new trial if it were applied for. As regarded the admission of evidence wrongfully, if any such course was taken, according to the Judge’s view it was in admitting the testimony of the defendant’s aged witness, as to the mode of conducting a chemist’s business prior to 1815, and in no other respect had evidence been improperly admitted. Then lastly, as to the refusal of evidence, no evidence which was tendered at the trial was refused. An appeal might be had by case or motion ; of these the former was to be preferred as the facts were in such a case stated by the Judge and the matter was brought under review much more easily than was the case where upon motion the Judge’s notes taken at the trial were produced in court. After con¬ sultation with counsel and taking into consideration that the Judge had found as a fact that the defendant had treated a dangerous case, and that this must be admitted in any subsequent appeal, and since the judgment of one County Court would not govern a case in any other court, he (the solicitor) could not advise the Association to pro¬ ceed further in that action. The Executive then went into committee to consider the question of an appeal and after a long and careful discussion on all the points of the case, it was moved by Mr. Churchill, seconded by Mr. Jones, and unanimously resolved: — “ That the finding of the County Court Judge in the case of the Apothecaries’ Company v. Harrison, being as follows : ‘ I find the present case was of a "serious if not a dangerous nature,’ this Committee is of opinion that no further steps should be taken by the Association in this action.” Some considerable discussion took place on the advisa¬ bility of steps being taken by the Association to amend the Pharmacy Act, 1868, when it was moved by Mr. Arblaster, seconded by Mr. Symes, and unanimously resolved : — “ That the Law and Parliamentary Committee be directed to take any steps which they may deem desir¬ able to obtain information to enable them to bring about modifications in the Pharmacy Act, 1868, to restrict the sale of scheduled poisons under cover of the patent medi¬ cine stamp to registered chemists and druggists, and to report to the next meeting of the Executive.” The President said the next question on the agenda paper was the consideration of the advisability of steps being taken by the Association to endeavour to obtain the exemption of all registered chemists and druggists from jury service. He continued to say that he was fre¬ quently receiving letters from chemists and druggists, relative to the extreme hardship which they suffered from being compelled to attend bn juries, and he would move: — “ That the Law and Parliamentary Committee be and are hereby empowered to take such steps as they deem advisable to obtain the exemption of all registered che¬ mists and druggists from jury service.” The resolution was seconded by Mr. Andrews, sup¬ ported by Mr. Arblaster, and carried unanimously. Several letters were read from members of the Associa¬ tion complaining of cases of infringements of the Pharmacy •58 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 19, 1879. Act, when it was moved by Mr. Andrews, seconded by Mr. Symes, and unanimously resolved : — “ That the secretary be instructed to collect evidence of infringe¬ ments of the Pharmacy Act, 1868, and forward particu¬ lars of same to the Secretary and Registrar of the Pharmaceutical Society.” The case of a member of the Association against whom an action had been brought by the Excise authorities for the sale of methylated spirit without a licence was con¬ sidered. It was moved by Mr. Davison, seconded by Mr. Hampson, and unanimously resolved: — “That the secretary be instructed to investigate the case of a member against whom legal proceedings have been taken by the Excise authorities for the sale of methylated .spirit without a licence, and that the solicitor be instructed to defend the action if the case on investigation be found satisfactory.” |ro(t«eilin[p of ^oqietics. SCHOOL OP PHARMACY STUDENTS’ ASSOCIATION. A meeting of the above Association was held on June 26, Mr. C. H. Hutchinson, P.C.S., in the chair. After the reading of the minutes, Mr. R. H. Parker read a paper on “ Myrrh.” This paper will be printed in a future number of the Journal. After a short discussion, Mr. J. G. Sangster read his report on “Pharmacy,” in which he gave an account of the following prepara¬ tions: — Vaseline, oleate of mercury, oleate of zinc and guaiacate or lithia. Oleate of Mercury is made by triturating together for some hours oleicacid and freshly precipitated mercuric oxide till combination is effected. In this process heat must be avoided. The ordinary strengths used are 5 per cent., 10 per cent, and 20 per cent. The first and second are thick liquids, the third having the consistenceof a soft ointment. Oleate of Zinc is usually prepared by mixing together hot solutions of soft soap and sulphate of zinc. The precipitated oleate is washed and dried by hydraulic pressure. It is of the consistence of suet, and possesses a pearly- white colour. To mix it with other fats it must be first melted. Guaiacate of Lithia , introduced by Dr. Garrod, is in the form of dark brown scales. It is prepared by digest¬ ing pure guaiacum resin with a saturated solution of lithium hydrate, decanting the clear solution, evaporating .and scaling. It is usually ordered in the form of pills, for which spirit is the best excipient. Mr. Sangster then noticed the following mixture which •he had dispensed : — R Eerri Am. Cit . 3SS< Quin. Su'.ph . . . . . gr. 12. Acid. Citric . 3j* Sp. Chlorof . 3j. Aquie . . ad ^vj. The quinine was dissolved with the citric acid in a small quantity of water and the scale compound in another portion of water. On mixing the two solutions a reddish-brown precipitate occurred, which in a few days •dissolved in the supernatant liquid, giving a clear green solution. It seemed to him probable therefore that a compound resembling the citrate of iron and quinine of the Pharmacopoeia was formed. After a short discussion the meeting adjourned. SOCIETY OF ARTS. The History of Alizarin and Allied Colouring Matters, and their Production from Coal Tar.* BY W. H. PERKIN, F.R.S. {Continued from page 38). I will now refer to’the process of making artificial alizarin by means of dichloranthracene in place of anthraquinone. * From the Journal of the Society of Arts. Sulphuric acid forms two sulpho acids with dichloran¬ thracene, a mono and a di. To obtain the former, pure dichloranthracene is intimately mixed with concentrated sulphuric acid, warmed up to about 50° C., the mixture being well stirred ; this process is continued for about twenty-four hours. It is then diluted, boiled, and filtered from any undissolved dichloranthracene. This filtrate gelatinizes on cooling, and consists chiefly of monosulphodichloran- thracenic acid ; it is formed thus : — C14H8C12 + S04H2 = C14H7 (S03H) ci2 + oh2. iionosulphodichlorantlii acenic acid. On boiling this with an oxidizing agent, it yields mono¬ sulpha nthraquinonic acid. CuH7 (S03H) C12 + 02 = CuH7 (S03H) 02 + Cl2. And this, when fused with caustic alkali, behaves in the same manner as the acid prepared from anthraquinone, yielding finally, pure alizarin. If the dichloranthracene be heated more strongly with sulphuric acid, it is converted into the disulphodichloran- thracenic acid* thus : — • C14H8C12 + 2 S04H2 = cuh«|!o:hK+2oh* v'" - - * — Disulphodicliloranthracenic acid. An acid remarkable for the fluorescence of its solutions and salts. If the heating with sulphuric acid be in¬ creased after the acid is formed, a very remarkable change takes place, sulphurous anhydride and hydro¬ chloric acid being evolved in abundance, disulphanthra- quinonic acid being at the same time formed: — CwH«js033H!C1= + S°A = c«h«|IoJh|°2+so^+2hci This, of course, when fused with alkali, eventually forms anthrapurpurin ; and, as some of the disulphanthra- quinonate is also formed, a little flavopurpurin is likewise produced. There is also another reaction which takes place. As dichloranthracene combines with sulphuric acid, water is liberated, so that this acid becomes somewhat diluted. This does not readily form a sulpho acid with the di¬ chloranthracene which has not dissolved, but when heated with it, converts it into anthraquinone. ChH8C12 + S04H2 = Cl4H802 + 2 HOI + S02 Dichloranthracene. Anthraquinone. As the temperature rises, the acid becomes concentrated, and then combines Avith it, forming chiefly monosulphan- thraquinonic acid. The process of making monosulphanthraquinonic acid from the monosulphodichloranthracenic acid has not been carried out successfully on the large scale, partly owing to the processes of filtration being very difficult to perform. But the preparation of artificial alizarin from the sulpho acids prepared by heating dichloranthracene strongly with sulphuric acid, is a process of very great importance. As pure alizarin can now be obtained in any quantity, attention has been turned to the preparation of its deriva¬ tives. In 1874, I studied the action of bromine upon it, and obtained monobrom alizarin, having the formula C14H7Br04.+ This compound dyes mordants somewhat similiarly to alizarin, the colours being a little redder in shade, but not sufficiently different to make it of technical interest. In 1875, I also obtained a nitroderivative of alizarin by acting on diaceto alizarin Avith fuming nitric * Journal of the Chemical Society, 1871, p- 15. f Journal of the Chemical Society, 1874 p. 401. July If), 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. GD acid.* * * § This substance crystallizes in beautiful orange needles, and has the formula, C14H7(N0o)04. It produces with mordants colours very different from alizarin, giving with alumina brilliant orange, and with iron mordants reddish purple colours. It would be a valuable deying agent if it could be produced by a more easy process. When treated with reducing agents, such as sodium amalgam, or metallic tin and potash, its blue alkaline solution changes to a clear bright red colour, contain¬ ing another new derivative, namely amidoalizarin, C14H7(NHo)04. This also dyes mordants, the alumina ones of a purple and the iron ones of a bluish or steel-like colour. A second, or @ nitroalizarin, isomeric with that I pro¬ duced, has been obtained by Rosenstiehl,+ and, apparently about the same time, by Caro, if: by submitting dry alizarin to the action of nitrous acid vapours. It is now manu¬ factured in some quantities, and is known as alizarin orange. Like the nitroalizarin previously described, it gives orange colours with alumina mordants. They are, however, much yellower, and not so fine. This nitro¬ alizarin dissolves in dilute alkalies with a purplish crimson colour ; but strong alkaline solutions precipitate it, especially caustic soda, and this property affords a means of purifying it. When boiled with metallic tin and caustic potash, it is reduced, becoming blue and then yellowish green ; but, on exposure to the air, this solution changes back to bluish green. Schunck and Roemer§ have just published an account of this reduction product ; it is an amidoalizarin isomeric with that just described. It crystallizes in deep yellow prismatic needles, and dissolves in potash with a blue colour. It dyes alumina mordants a dull red, and iron mordants a dull grey colour. A very peculiar result has been obtained by M. Prud’ homme|| by heating a mixture of glycerine, /3 nitroalizarin, and concentrated sulphuric acid. By this means a colour¬ ing matter is obtained which dyes alumina, and especially iron mordants, an indigo blue shade. It crystallizes in needles of an almost black colour, but having a coppery reflection. The formula is Cl7H9N04. It is manufactured commercially, but as its colours are fugitive it has not met with much favour. F. de LalandeTfhas made the interesting discovery that purpurin, identical with that found in madder, can be obtained by the oxidation of alizarin. He takes a solution of one part of alizarin in eight or ten parts of sulphuric acid, and adds to it one part of arsenic acid or peroxide of manganese, and heats this mixture to a temperature of 150° to 160° C., until a drop of the fluid mixed with an alkali gives a red coloration. The product is then thrown into water, and the purpurin which precipitates is collected on a filter and well washed. In this paper I have purposely confined my remarks to the colouring matters and other substances obtained in the manufacture of artificial alizarin, and also to some of the more important derivatives of alizarin; a considerable number of products have, however, been obtained, which are related to anthracene, although this hydrocarbon has not been used in their preparation, such, for example, as anthraflavone from oxybenzoic acid, etc. And, although I do not propose to give an account of these bodies, I wish briefly to refer to some very interesting results which have been obtained by Baeyer and Caro. These chemists have observed that, when phenol is heated with phthalic acid or anhydride and an excess of sulphuric acid, that two monoxanthraquinones are pro¬ duced, one identical with that already described, the other being an isomeride of that body. Both of these, however, when fused with caustic alkali, yield alizarin. * Journal of the Chemical Society, 1870, vol. ii., p. 5 78, and Dent. Chem. Ges. Ber., 1875, pi 780. t Deut. Chem. Ges. Ber., 1876, 1003. X Patent No. 1, 229, March 22, 1876. § Deut. Chem. Ges. Ber., 1879, 558. II Bull. Soc. Chem. (2), xxviii, 62— <54. T ‘ Jahresbericht,’ 1874, p. 486. By substituting pyrocatechin for phenol in the above process, they succeeded in obtaining alizarin at once. These results, although at present of no practical value, are of considerable scientific interest, and also show us that anthracene is not the only artificial soi ree of alizarin. From what I have already said it will be seen to what an advanced state the chemistry of my subject has arrived (and yet there is much to be done), and only those who have been interested in the progress of the manufacture can rightly appreciate the great value of all this research in forwarding the successful and enconomical production of these colouring matters. As I have already shown, both of the important colour¬ ing matters of madder have now been obtained from anthracene, and not only so, but new products allied to these have also been produced, the most important one being that valuable colouring matter anthrapurpurin ; we have also flavopurpurin and the derivatives of alizarin. So that, with these colouring matters, dyers and calico printers are not only able to produce all the various madder styles, but to introduce colours of greater beauty and variety than when employing the natural dye-stuff madder. (To he continued.) IRtinoi’aiutd In order to assist as much as possible our younger brethren, for whose sale partly this column ivas established , considerable latitude is allowed, according to promise, in the propounding of supposed difficulties. But the right will be exercised of excluding too trivial questions, or re¬ petitions of those that have been previously discussed in principle. And ive would suggest that those who meet ivith difficulties should before sending them search previous numbers of the Journal to see if they can obtain the re¬ quired information. Replies. [315]. In my reply to this question in last week’s Journal, I am made, by a printer’s error, to say, “ sal ammoniae ” in three instances. It ought in each case to be “ sal ammoniac.” W. Wilkinson. [322]. Will Mr. Brown kindly detail the method of making a stable preparation of this formula ? I can, like him, get a pink creamy ointment; but I fail to induce the components to remain in the combination any suffi¬ cient time for the daily use of the patient, and obviously that is the intention of the prescribes — Anon. [324]. Permit me to correct what I gather from the remarks of Mr. Henry Brown is a misunderstanding rela¬ tive to this prescription. Mr. Brown, to whom I am greatly indebted for his clear and lucid arguments, says : — • “I observe ‘Gulielmus’ adds after morphia, ‘the alkaloid,’ so as to italicize as it were.” The words however were not my addition, but formed part of the prescription, and this being so forced me to the conclusion that the pre- scriber meant what he had written. I cannot think that the pharmacist under those circumstances would be justified in adding anything to convert the morphia into a salt, but having explained my position in relation to this point shall be glad with further expressions of opinion thereon. Gulielmus. [324]. In Mr. H. Brown’s very practical answer to No. 324, he does not explain how the preparation which was first obtained by the patient was (according to the statement by “Gulielmus”) about twice as much in bulk. The addition of a small quantity of acid, sulph. dil. could not cause such a difference. G. H. Weight. [326]. The mixture containing tr. gelsemin., fer. et quime cit., butyl chloral hyd., potass, bromid., potass, iodid. 60 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 10, 1879. .and aq. chloroform., may be made perfectly transparent, and therefore “ presentable,” by adding a little magnesia, and filtei ing through fine filtering paper. The question is, How far is a dispenser justified in thus turning out a slightly opaque mixture as bright and as clear as dark .sherry wine ? In this case, and in many other instances (328, infra), a perfectly bright mixture may be obtained by the simple act of filtration through magnesia, bismuth or orris root, as the case may be. I hold, however, whilst a strong advocate for elegant dispensing, that a mixture like the above, which is only slightly opaque, should not be sent out clear. By filtration, as sug¬ gested, I have convinced myself that no change in con¬ stitution occurs ; but, there is a manifest injustice done to other compounders and other houses, by having resort to the process indicated. I am aware some houses make it a study to send all mixtures out transparent, if such is possible without undue interference. If therefore, a prescription similar to that given by “ Sub Umbra Flortsco ” or C. B., 328, is filtered, and sent out bright by the first house at which it is compounded, and then the patient has it dispensed at another pharmacist’s, will he not naturally wonder why in the one case it was transparent, but in the other opaque? And will he not think that in the first instance it was properly compounded, and look upon the first pharmacist as superior in his art to the second, because from the same ingredients he is able to turn out a bright and pleasing mixture, whilst the second is only able to form a muddy looking compound? I see a great injustice to members of the pharmaceutical body by such pro¬ cedures. If the patient is whimsical, or if the medical man’s wish is understood in such instances, I think in all fairness a note might and ought to be written, such as, ■“ Filter through magnesia,” by the medical man or phar¬ macist who first dispenses the mixture. If such is not done, there is manifest unfairness in thus Heating any such prescription. By what means is a pharmacist, even in the same town, to know exactly how a mixture was at first compounded and its subsequent treatment, if a note be not appended indicative of the mode in which it was dispensed, i. e., provided such a mixture was sent out perfectly trans¬ parent ? Northallerton. Hy. Brown. [327]. I am afraid J. H. cannot, without materially altering the prescription, send out a mixture of sodse salicyl., croton, butyl, and quinse sulph., so as to have the quinine in perfect solution. If the quinine is dissolved by the aid of an acid it is at once precipitated on the addition of the salicylate and, in the form of a resin oid mass, adheres to the sides of the bottle. The best mode is just to powder the quinine very fine and add “ shake the bottle.” The mixture is not unsightly and the quinine will remain long enough in suspension to enable a correct dose to be measured. Hy. Brown. [328]. Is sufficiently answered in my note, vide supra, 326. When filtered the mixture is a beautiful light sherry colour and has its original taste unaltered. The small quantity of the resin of the hop only removed. Hy. Brown. [330]. No. 1 is another example somewhat akin to No. 327. In this case the only way I see out of a diffi¬ culty is to omit the acid, sulph. dil., dissolve the sodae salicyl. and rub up the quinine. The same remarks apply, in the main, as in No. 327, supra. No. 2. “ J. S. Nemo ” should use solid perchloride of iron and add the acid, hydrochlor. after solution. The HC1 is added to obviate oxidation. Hy. Brown. and (funks. [614]. “PULV. SALINI EFFERVESC. APE- RIENTIS.” — The composition of this preparation is published by Messrs. H. and S. Kirby and Co., of 14, Newman Street, W., in their formulae. London, W. Veritas. [618]. NICOTINE. — Will some reader state a process for extracting the nicotine from tobacco, and leaving the tobacco inert for smoking? Fraxinus. [619]. STAMPING INK.— Wanted a formula for a good black ink to use with india-rubber stamps on paper. W. W. ^oimespndqnq. *»* No notice can be taken of anonymous communica¬ tions. Whatever is intended for insertion must be authenti¬ cated by the name and address of the writer; not necessarily for publication, but as a guarantee of good faith. The Supply of Gas. Sir, — No doubt I only express the sentiments of hun¬ dreds of your readers when 1 express my thanks that you have taken up the gas question. I have had my attention drawn to a discussion now going on in The English Mechanic , and to the evident partiality “ and unfairness of that journal to any but one side of the discussion,” and have come to the conclusion that the Me¬ chanic, like a good many other journals connected with trade interests, is probably influenced in favour of the gas companies and the great body of gas engineers up and down the country. This last year, as witnessed by newspapers in every part of the country, has given rise to complaints from every class, but instead of trying to help and trace the cause— and most assuredly there is one — the effort seems to be to try and intimidate and “ burke ” any inquiry. I trust you will exercise patience and give scope in your columns for free ventilation of the subject, and if the ap¬ proaching Conference would add “ Gas Deterioration ” to the list of subjects requiring elucidation, it would be a very legitimate inquiry. Gas engineers and gas officials certainly have net the ability, even if they had the willingness to clear up the present difficulty. The reference to the production of “ marsh gas ” by gas companies in place of olifiant gas, as explained in the letter of your last number, to my mind goes a long way to ex¬ plain matters and 1 should like to ask my brother chemists if they can bring any evidence to prove that consumers uear the works are more often complaining than those at a greater distance away ? My theory is that ordinary coal gas is a “ wonderful ” compound of various gases, and that the lighter and least luminous find their way to the nearest outlets, and those streets nearest the works are the worst lighted. Any evidence pro or con. would tend to clear up a diffi* cult problem. More Light. “ Natura.” — It is a mixture of the light hydrocarbons of petroleum. “ Apprentice." — Boil with nitro-muriatic acid and pre¬ cipitate with ammonia. J. H. Dingle. — (1) Sonchus asper. (2) Festuca ovina. (3) Lolium perenne. (4) Festuca Myurus. (5) Festuca loliacea. (6) Pinus sylvestris. A. P. S. — (1) Fellowship of the Chemical Society is con¬ ferred by election. (2) The other degree is granted by some foreign universities upon conditions varying with the university. C. Marshall. — The seeds of Garcinia purpurea yield the fat known as “ Kokum butter.” A description will be found in ‘ Pharmacographia,’ p. 79. C. Kemp. — (1) Hypericum perforatum. (2) Listera ovata. (3) Lithospermum officinale. Communications, Letters, etc., have been received from Messrs. Berm ingham, Davidson, Roberts, Sawyer, C. II . F. Student. July 26, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 61 “ THE MpNTH.” After the continuous rain of May and June, it might have been expected that St. Swithin would waive his claim to his accustomed sway of forty days, hut since such has not been the case, it is only natural that the long continued rainy weather should give rise to grumbling in agricultural districts ; still there is perhaps some reason to be thankful that the weather has been wet rather than fine. Owing most likely to the heat of last summer and to other conditions, as yet not well understood, the number of insects would probably have amounted to a plague this year, had not the wet weather to a certain extent limited their numbers. In Nature * accounts are given of a swarm of butterflies (appar¬ ently Vanessa Cardui ), being observed on the con¬ tinent, which obscured the light of day and took two hours to pass, proceeding in a north-westerly direction. This or a similar swarm appears to have passed through Turin on June 2nd, through Swit¬ zerland from the 2nd to the 9tli, Alsace, France and Spain from the 5th to the 10th, and through Wur- temberg from the 11th to the 21st. The majority of specimens examined by Professor Eimer, of Tubingen, proved to be females, apparently seeking a place to deposit their eggs, of which they were full. This insect is very common this year in the south of England. Another instance of the abundance of insects this year occurred at Elizabetlipol, in Armenia, where the vegetation has been devasted by grasshoppers and locusts. At this place the locusts were so numerous and settled so thickly on the Russian soldiers’ faces, uniforms and muskets, that the major ordered firing at them for half an hour, to drive them off, but as this produced no effect a march back was ordered. Some results of an interesting series of experiments as to the proportion of carbonic anhydride present in the atmosphere and the extent to which it is affected by various causes are reported by M. Reiset in the current number of the Repertoire de Pharmacie (vol. viii., p. 308). At a station in the open country a few miles outside Dieppe, having the sea on its west and north-east horizon, and at an elevation of 320 feet, which was taken as a standard for comparison, the mean of ninety-two observations gave equal to 2 942 parts, by volume, of C02 to 10,000 of air. The observations at this station were very con¬ cordant, the difference between the maximum and minimum proportion of carbonic anhydride observed not exceeding 3 parts in 100,000. Air taken in a leafy wood gave an average of 2'917 parts of C02 per 10,000, the average in the air taken at the standard station at the same time being 2’902 ; air taken in a fine crop of red clover gave 2-898 parts C02 per 10,000 against 2 915 at the standard station; air taken in a field of barley and lucerne grass in July gave 2-829 parts of C02 per 10,000 against 2'933 at the standard station. These results de¬ monstrate how instantaneously the diffusion of gases takes place. On the other hand the presence of a flock of three hundred sheep at pasture, on a calm day, in the neighbourhood of the apparatus, raised the proportion of carbonic anhydride to 3*178 parts in 10,000 of air. In Paris, in the month ol May, observations extending over three years gave an average of 3 027 parts by volume in 10,000 of air. Comparatively few fresh plants are out in flowei * June 2b, p. 197. Third Series, No. 474. this month in the Botanical Gardens. At Regent’s Park, in the Economic House, the pimento is in blossom, and in the Herbaceous Ground at Kew, Adcea spicata, Delphinium Staphisagria , Nigella saliva , Pyrethrum roseum and P. Parthenium , valerian, coriander, rue, black and white mustard, lavender, alkanet, borage and motherwort are in flower. Of rarer British plants now in blossom at Kew may be mentioned Liparis Loeselii, Stacliys germanica, Verbascum Lychnitis and V. pulverulentum, Echiwm violaceum and a variety of Linncea borealis. In the country the elder may now be seen covered with blossom, and the red poppy and the white mustard already deck the railway embankments and chalky cornfields with their lively hues, while the pretty pink-flowered cent ary, always retiring when a cloud overcasts the sun, scarcely opens its blossoms for more than an hour or two now and then. The digitalis, one of our handsomest wild flowers, is now in perfection. In London it seems coming into fashion again as a garden ornament, cartloads of plants in full blossom being hawked about the streets. A correspondent in the Gardeners’ Chron icle calls attention to the absence of this plant from the Cotswold Hills and attributes it to the fact that it loves a sandy soil, but does not flourish on the Silurian limestones and shales. The Cotswold Hills are almost entirely composed of the cream coloured limestones of the inferior oolite, and to this he attri¬ butes its absence. The writer has, however, seen magnificent specimens of the foxglove on the chalk hills of Kent, and it is probably rather the porous character of the soil that it prefers, than its chemical composition, although digitalis can scarcely be called a plant of the chalk. The flowers of this plant are said to be exclusively fertilized by humble bees, which alone are large enough to fill the corolla, and thus deposit pollen on the stigma. The flowers are proterandrous and appears to be capable of self-fertilization if not visited in time by insects. The anthers at first occupy a transverse position but as they ripen become longitudinal.* Another plant belonging to the Scrophulariacece deserves notice from having been used in former times for the disease known as “burnt holes” in children. A formula for the ointment of Scrap /at- laria may still be found in Cooley’s ‘ Cyclopedia ’ This is the Scrophularia nodosa , a common plant in damp ditches by roadsides, etc. From the other British species it is easily distinguished by its acutely pointed, smooth leaves and tuberous knobby root ; S. aquatica , which grows in similar situations, having obtuse leaves. The flower is interesting on account of the presence of the rudiment of a fifth stamen (staminode) at the base of the upper lip of the flower. This staminode differs slightly in shape in the different species, and in some cases it bears pollen In the genus Pentstemon, which is not uncommon, in gardens, the fifth stamen is furnished with a long filament, but the anther is abortive, and the filament is bent in a curious manner from the upper towards the lower lip of the flower, from which it appears to spring, so as to be out of the way of the pistil. Scro¬ phularia nodosa is proterogynous ; both this species and S. aquatica are fertilized by wasps, and as the * Lubbock, ‘British Wild Flowers in Relation to Insects/ p. 138. 62 THE PHARMACEOTICAL JOURNAL AND TRANSACTIONS. [July 26, 187SK. pistil is l>ent ‘downwards from tlie mouth of the corolla it strikes the pollen-dusted breast of the wasps when they visit the flower. It is rather singular that irregular flowers are hardly ever wind-fertilized. " The leaves of S. nodosa are. said to possess emetic and purgative properties and are sometimes used externally as an application to burns and swellings, being simply bruised before being applied. In olden times this plant was considered an excellent remedy for the scrofula or king’s evil, whence its name. A decoction of the root is sometimes used by farmers for the scab in swine. The juice of the leaves of the water betony, Scrophularia aquatica, formerly had a reputation as a cosmetic for the face, “to take away the redness and deformity of it.” This plant must not be confounded with the wood betony ( Bdonica officinalis), which is quite a different plant, belonging to the Labia tae. Another little plant, common in heathy places and woods, Veronica officinalis, is now in blossom. As its name indicates it was formerly used in medi¬ cine. It was at one time official in the Edinburgh Pharmacopoeia, under the name of Veronica mas or Betonica pauli. At the present day it is sometimes used by homoeopaths. It possesses bitter and astringent properties, although probably in a less degree than the Koromiko ( Veronica salicifolia), which a short time ago was so highly spoken of as a New Zealand remedy for diarrhoea. When the Linnean system of botany was in vogue the plant was comparatively easy to determine, but at the present day the tyro in botany finds it somewhat difficult to assign a place to the plants of this genus, since the ovary when young is difficult to examine, and the plants differ from the majority of the order to which they belong in having only two stamens in the flower, as well as in the corolla being not very obviously irregular, at least to an unpractised observer. The present species is easily distinguished by its small flowers and obovate stalked leaves from V. Chanmdrys , fire most beautiful and consequently the most commonly recognized species, which has sessile leaves, and from V. montana which has ovate stalked leaves. The arrangements for fertilization differ consider¬ ably in the different species of this genus. In V. Chamcedrys the anthers and stigmas ripen at the same time, but the stamens turn outwards, while the stigma projects straight forward, so that self- fertilization is impossible. In V Beccabuncja (whose curious name is supposed to be derived from the German bachlmnge) the flowers are proterogynous, and in V hederaifolia the flowers are minute and fertilize themselves. The Scotch fir (Tinus Sylvestris ) seems to have produced an unusual abundance of male flowers this year, and the paths and roads in plantations are now everywhere strown with the fallen catkins. In a letter to the Times a few weeks ago, a corre¬ spondent wrote, 44 After a heavy rain a thin film of sulphur has been observed at Windsor, Slough, and in the neighbourhood generally, to settle upon the surface of rain water caught in butts and cisterns.” According to a letter on the same subject in Nature, by Mr. P. H. Carpenter, 4 4 it was first observed on the afternoon of Sunday, June 8, after a remarkably heavy shower, and much disturbed the inhabitants of some of the villages around Eton, who fancied that it smelt 4 awful like brimstone,’ of which its f Darwin, ‘ Forms of Flowers,’ p. 147. yellow colour was somewhat suggestive. In some places it gave rise to such a feeling of fright that the people were afraid to go to bed, thinking that the judgment day was at hand.” On investigation the sulphur proved, as might have been supposed, to be pine pollen (probably from Pinus sylvestris) blown from Windsor Forest. A local chemist and druggist is said to have supported the sulphur theory — a statement which it may be hoped is mistaken. The pollen of Conifers is so different in appearance from sulphur, under the microseope, and is so characteristic, that such a mistake could hardly have occurred to any one familiar with the use of a microscope. The compound pollen of theGymnosperms has long been known, but it is only lately that F. Elfiring, of Helsingfors, has proved in Strasburger’s laboratory, at Jena, that the pollen cell of wind-fertilized or self-fertilized angiosperms is also compound, or in other words that each pollen grain becomes divided into two cells, the one of which plays the part of a vegetative cell merely, and the other takes upon itself the growth and functions of the pollen tube. Of these cells the vegetative one is the smaller and is- only separated from the larger by a wall of 44 cortical plasm,” which in particular instances can become transformed into a firmer membrane. The pollen grain may thus be likened to the microspore of a lycopod. This observer does not, how'ever, appear yet to have examined the pollen of cleistogamous flowers, which, as suggested by Dr. E. P. Wright in Nature ,* might reveal some interesting facts. The little pine tortrix moth, Ortholcma turionana,. may now be seen hovering around the fir trees and depositing its eggs on the buds. Later on in October, little turpentine drops may be seen on the buds, underneath which the grub may be found. It is a singular fact that the flowers of the dahlia have a narcotic effect upon the bees which visit them, so much so that the cultivation of the dahlia has been pronounced to be incompatible with the success of bee-keeping. The honey of the oleander is also- avoided by bees and is known to be fatal to Hies. The dahlia is such a common flower in gardens that its insecticidal properties might easily be investigated with regard to other insects. Most persons who live in the country are familiar with the singular botanical monstrosity known as the 44 hen and chicken ” daisy, in -which a number of small stalked capitula arise from the primary one. Such a growth in the water-lily family is, however, a great rarity. An instance of this kind is figured in the Garden, for July 12th, in which secondary stalked flowers are produced from the primary flower, and in another specimen leaves as well as flowers arise from the primary flower.f The extent to which a medicinal preparation may be affected by the soil upon which the plant it is prepared from has grown is illustrated by an ex¬ perience of M. Gerardin, a pliarmacien in the Marne department. Having prepared some extract of bella¬ donna from a defecated juice, he found it after some weeks full of granulations. These were removed by dissolving the extract in distilled water and decant¬ ing. After washing and drying at 100° C., they proved to consist of a mixture of silicate and chloride of potassium equal in weight to 6*8 per cent, of the original extract. It was then remembered that the * June 19, p. 183. f See Journ. Bot., 1877, p. 59. J-aly 26, 1679.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. G 3 belladonna plants used liad been collected from a spot which had long been frecpiented by charcoal burners for their operations and the remainder of the explanation was to be found in the pronounced taste of solanaceous plants for silica and potash. Some time ago an attempt was made in Mozam¬ bique to cultivate the opium poppy. The yield of opium from the first crop only amounted to a few pounds, which upon examination proved to be only of moderate quality ; it had the appearance of a soft ■extract of a clay-brown colour and contained 4 per cent, of morphia, 4 -3 per cent, of narcotine and 40 ’9 per cent, of moisture. A specimen of this Mozambique opium was recently presented to the Society’s Museum by Messrs. T. and H. Smith ; another is included in the case sent by them to the Sydney International Exhibition, and it is noticeable that it has been described by two journals at least, when referring to this case, as the first opium grown in Africa, a state¬ ment that would hardly pass muster in the Board ■schools, notwithstanding the extent to which Egypt has become Europeanized. Messrs. Smith’s case appears to rival in interest and value that sent to Paris by the same firm and described in this Journal last year. Perhaps the most striking objects would be some splendid crystallizations of caffein, aloin, muriate of thebaia, codeia and muriate of papaverine, the •demand for the latter alkaloid on the continent being said to be in excess of the supply. There is also the cryptopia from 10,000 lbs. of opium, as well as specimens of the new bodies gnoscopine and meconoisine. Among the salts of morphia are the muriate in crystalline cubes, the sulphate in woolly needles resembling sulphate of quinine and the tartrate which has been recently recommended by Dr. Erskine Stuart as the best preparation of morphia for hypodermic injection. There are also specimens, several ounces in weight, of muriate of apomorphia in large steel grey crystals and of cantharidin in flue four-sided prisms. M. Carles recently called the attention of the Bor¬ deaux Pharmaceutical Society to the presence in commerce of quinine containing an exaggerated quantity of water. A sample examined lost 17 per cent, of water when dried at 100° C., or 5 per cent, in excess of the normal quantity. The same sample was found to contain a quantity of quinidine. M. Dambier said that he had recognized the same fact •several times in sulphate of quinine obtained from ..good houses. Japanese wax has been the subject of an inves¬ tigation by Dr. E. Buri, of the University of Strasburg. From the results obtained (Archiv d. Pkarm., xiv. 403) he has come to the conclusion that .this substance, like other fats, is a mixture of several glycerides, the mixture of fatty acids yielded upon saponification consisting principally of palmitic acid. Tire palmitic acid is accompanied by one or more acids having a higher melting point, the presence of one having been ascertained which has a melting- point considerably higher than that of stearic acid. There is also a small quantity of oleic acid. According to the Pharniaceutische Zeitung a ■German house is bringing into the market a number of so-called “extra strong essential oils,” obtained by the fractional distillation of the finest and most aromatic parts of the respective oils from the less characteristic and more or less indifferent portions. They have, as a rule, a higher boiling-point, and a higher specific gravity than the unseparated oils, and some of them are more soluble in spirit, but this is not always the case. It is claimed, however, that all these oils are essentially improved in aroma. According to MM. E. Duvillier, and A. Buisine, in the Comptes Rendus , the trimethylamine of French commerce, which is chiefly obtained, as indicated by M. Vincent, by the calcination in a close vessel of the residue after the distillation of spirit from beet¬ root mash, is far from being a pure product, it containing only about 5 — 10 per cent, of trimethyla¬ mine, while dimethylamine is present to the extent of 50 per cent., besides which there are present in the remainder monomethylamine, monopropylamine and monoisobutyl amine in about equal proportions. A new antiseptic agent is reported to have been recently discovered accidentally, during experiments on separating the crystalline sugar from molasses. It is, according to the Scientific American, now sold at twenty-five cents the pound, and is made in large quantities by dissolving in water equal parts of chloride of potassium, nitrate of sodium and boracic acid, filtering and evaporating to dryness. It is easily soluble in water and is deliquescent. It passes under the unscientific name of double borate of potassium and sodium, and its action as an antiseptic is said to be prompt and to continue un- diminished for a long time. Messrs. Paterno and Oglialoro, in the Gazetta Chimica Italiana, state that the limonine of Schmidt, extracted from the seeds of oranges and lemons, is not identical, as that writer supposed, with the calumbin of Wittstock, derived from calumba root. Limonin is obtained in magnificent colourless shining laminae, fusible at 275°, while calumbin crystallizes in colourless prisms, fusible at 182°. Its formula is C21H22Or, while that of limonin is O2gH30O8. In the Practitioner, Dr. T. N. Dolan reports that he has found chloride of barium successful in certain forms of aneurism, and recommends a trial of it in some cases in which the administration of iodide of potassium is inadmissible. The dose given' appears to have been one-fifcli to two-fifths of a grain. Dr. Rutherford in a communication to the British. Medical Journal , referring to the variation in the dose of euonymin required to produce the desired effect, remarks that “ allowing for individual peculiarities, I cannot but suspect that the substance found in the market is not always of the same strength. ” ^ It is highly desirable either that a definite process for the manufacture of this substance or that tests for dis¬ criminating its quality should be sought for and published by those who have introduced these re¬ medies into medicinal use in this country, so that dispensers may know what particular preparation to use. An interesting account of the dugong, the oil of which is used as a substitute for cod liver oil, is given in New Remedies for July. One merchant engaged in the fishery is said to capture as many as six in a day. Unless some protection be afforded it, this interesting cetacean will probably become an extinct animal in the course of years, especially since its flesh makes an excellent substitute for bacon, dugong rashers being easily mistaken for those of pork. The possibility of poisoning by the absorption of an iline through the skin deserves to be known. _ A chemist in Poland was experimenting with aniline, when the bottle burst and part of the contents satu- THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 26, 1879. G4 rated some of liis clothing. A few hours afterwards weakness in the muscles set in, his speech became affected, he forgot a number of words and became comatose. By the use of stimulants he recovered, but the muscular weakness remained during the fol¬ lowing day. The fact of the symptoms not appearing until a few hours afterwards, although a quantity of the aniline had evaporated in the room, seem to show that the aniline acted as a poison by entering the circulation through the skin. M. Battandier, in the Journal de Pharmacie, points out the danger of using gla the ovens, to prevent the action of any “drip,” which might otherwise injure the top of the oven. The top is July '26 >879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 77 strengthened by cross pieces of timber, fastened with leaden straps. The ovens were usually made of 20-lb. Lad. The luting for the end manholes was made of china clay and chlorine oils. When first made, these ovens were supported on solid brickwork, and it was found that by passing a good ourrent of chlorine oves the anthracene, sufficient heat was, by the chemical action, evolved to complete the process ; if, however, the temperature was allowed to fall from an interrupted or slow supply of chlorine, the pro¬ duct partially crystallized, and the temperature could not be got up again sufficiently. The anthracene was, there¬ fore, imperfectly chlorinated. To avoid this, a steam chamber was formed in the brickwork and covered b}7 an iron plate, on which the oven rested, and in this way the temperature was always sufficiently maintained. The hydrochloric acid gas which was formed in this operation, was condensed in coke towers, and the acid used again. The reaction may be written thus : — C14H10 + 4 Cl = C14H8CL + 2 H Cl. Anthracene. Dichloranthracene. It is, however, probably much more complicated. Chlorine when acting upon anthracene first forms a di- cMoride : — C14H10 + C12=C14H10, Cl2. This substance is extremely unstable, and unless the temperature be kept near 0° C., decomposes as quickly as it forms, yielding monochloranthracene : — C14H10C12 = Cl4HyCl + HC1. Monochloranthracene. This substance, when meeting with fresh chlorine, is be'ieved to combine directly, and form a dichloride of monochloranthracene : — - Ct 4HyCl + CL, = C4 4H9C1 CL. Dichloride of monochloranthracene. and, lastly, this, on decomposing, to yield dichloran¬ thracene : — c14h„ci, cl = C14H8CL + H Cl. Dichloranthracene. Towards the end of the operation of chlorinating anthracene the chlorine is not all absorbed, and escapes into the air from the coke towers. This was not only a nuisance but also a loss. To avoid this the ovens were put up in pairs, and connected with a leaden pipe ; both were charged with anthracene, but only one chlorinated. .Any unused chlorine passing away with the hydrochloric acid over the anthracene in the second oven was thus absorbed. The next day the anthracene in the second oven was chlorinated, and the gases passed over the o’htr one, which had been re-charged with anthracene. The charge for each oven was usually about 400 lbs. of anthracene which had been distilled with potash, and of between 45 and 50 per cent, quality. On passing the chlorine gas into the charged ovens, the anthracene gets dark in colour and fuses,* hydrochloric acid being evolved in abundance. After a time, this fluid product begins to deposit crystals, and soon becomes a semi-solid mass. The operation occupies about five or six hours. When finished, the top manholes were removed, and a light wooden flue placed over them, and connected with the opening into the chimney shaft, the end manholes were then opened, and in a short time the excess of hydro¬ chloric acid and chlorine in the ovens was drawn out. The crude dichloranthracene, which covers the bottom of the oven as a crystalline cake, was loosened by a wooden tool, and then drawn out with a wooden hoe into some convenient vessel. When broken up, the pieces of di- chloranthracene appear as a mass of beautiful bright yellow interlaced needles. * This is due to the chlorination of the impurities, the dichloranthracene being formed afterwards. This product was next broken up with a wooden beater in tubs containing dilute caustic soda (it must not be ground, however), to remove adhering hydrochloric acid. It was then separated from the alkaline solution, and pressed between linen cloths in the hydraulic press, when a dark, thick, oily product separated out. This consists, principally of chlorinated phenanthrene, holding in solu¬ tion a little dichloranthracene and anthracene, and was- called “ chlorine oils.” I shall have occasion to refer to these again presently. After pressure, the dichloranthracene was obtained in hard yellow crystalline cakes, but not sufficiently pure for use. It was again broken, and allowed to soak in coal-tar naphtha* for some time, and pressed; this operation was again repeated. The adhering naphtha was then recovered by blowing steam through the pro¬ duct. The dichloranthracene thus purified was afterwards placed on trays, and dried in a drying-room, and was then ready for the next process. It contains about 84 per cent, pure dichloranthracene. The chlorine oils, and also the residue left after dis¬ tilling the naphtha used for washing the dichloranthracene contains a certain amount of dichloranthracene and an¬ thracene. This separates out to a considerable extent if the oils be cooled with ice, but the product is then so thick that it cannot be filtered or pressed. t Experiments were made on distilling them alone, but owing to the copious evolution of hydrochloric acid, and the frothing of the product, it was not found practicable to treat tlnm in this manner; but by previously mixing an excess of ground lime, and then distilling in iron retorts, a considerable amount of solid product came over containing about 25 per cent, anthracene, which only required to be treated with petroleum spirit to fit it for use. It is believed that the anthracene represents that which had not been chlorinated, the dichloranthracene being decomposed by distillation with lime. The next process consists in converting the dichloran¬ thracene into the sulpho acids of anthraquinone by treat¬ ing it with ordinary concentrated sulphuric acid, and the ease with which this is effected was originally one of the advantages of the use of dichloranthracene over anthra¬ quinone. For this process iron pots were used, as they were found to answer nearly as well as glass, and, of course, were more manageable. As hydrochloric and sulphurous- acids are evolved in quantity in the operation, special arrangements had to be made for conducting these away and condensing them. The apparatus used consists of a row of cast iron pots, capable of holding about 30 gallons. These are cast with half-covers, in which there is an opening f<~>r the escape of the acid vapours. Earthenware pipes are luted into these openings and connected with a large main, which leads to arrangements filled with coke and supplied with water for the condensation of the hydrochloric and sulphurous acids. The pots are set in brickwork, and heated by a fire, the upper part being also surrounded by brickwork to prevent loss of heat-, the open part of the pot is covered with a lid made of 20-lb. lead, which can be removed when they are emptied. In the centre of this lid an oblong hole, about 6 in. by 8 in., is cut, for the introduc¬ tion of the dichloranthracene. This is covered by a piece of lead. There are also two small round holes in the lid ; one for the introduction of a thermometer, the other as a testing-hole, and fitted with a wooden plug. These pots were charged with 350 lbs. of sulphuric acid. This was then heated up to about 140° to 1(50% and the dichloranthracene gradually added in small sliovelfulls at a time, hydrochloric and sulphurous acid being evolved after each addition, causing frothing, * Petroleum spirit does not answer well for this purpose. f Perhaps a filter press might be used for this purpose successfully. 78 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 26, 1879. -especially if the dichloranthracene be of a low quality or clamp. The charge used was usually 7 Q lbs. After all the dichloranthracene had been added, the temperature was gradually raised until it reached about 2609 C., and then continued at this until a sample, taken out by a glass rod and diluted with water, formed a nearly clear solution, devoid of fluorescence. The fire was then drawn, and the product left to cool down until the next morning. It was then found to be still warm, of a brown colour, and the consistency of treacle. The lids being lifted off, it was ladled into copper pails, and carried away to be neutralized with lime. In this process the following reactions take place : — First, disulphodichloranthracenic acid is formed by the union of the sulphuric acid with the dichloranthracene ; and, secondly, this product is oxidized by the excess of sulphuric acid forming disulphanthraquinonic acid. These, however, are not the only changes. Anthraquinone is also formed, which becomes converted chiefly into mono- sulphanthraquinonic acid ; some of it also sublimes, and then condenses in the earthenware main, through which the acid vapours pass. When fuming sulphuric acid is used in place of the ordinary, no anthraquinone or monosulphanthraquinonic acids are formed. Pure dichloranthracene, when treated with Nordhausen sulphuric acid, gives the theoretical yield of disulphan- thraquinonic acid. ( To be continued.) j3arliamimt;irj) anti Haiti Inqmtutgs. Alleged Death , by .Opium (?) Poisoning through eating Lettuces. On Friday, July 19, Mr. C. Aspinall, Liverpool borough coroner, held an inquest on the body of John M’George, sixty-nine years of age. The deceased, who was said to have been a strong and healthy man, was seized with what appeared to be a bilious attack on Monday morning and died about two o’clock the same afternoon. On Sunday evening, at tea, the deceased partook of lettuce, of which the other members of the family had a share. After being taken ill on Monday morning he had some1 breakfast, but was found apparently in a fit at nine o’clock and was unable to speak afterwards. Dr. Fisher, Walton Road, Kirkdale, was called to the deceased on Monday morning, about half -past ten, and found him in a comatose state. The pupils of the eyes were much contracted, the face livid, the body cold, the mouth wide open, the limbs relaxed and the breathing difficult, all of which were symptoms of narcotic poisoning. The stomach pump was used and remedies prescribed, but without the desired result. Dr. Fisher said he had made a post¬ mortem examination of the body and found traces of •opium in the stomach and enough of digested lettuce to account for the symptoms of opium poisoning. He was quite certain that the deceased had died from the effects of opium. In reply to a juror, Dr. Fisher said that the stomach would hold much more lettuce than would be sufficient to account for the traces of opium found. Dr. Anderson, who assisted the last witness in the post¬ mortem examination, said that in his opinion the deceased died from apoplexy, induced by narcotic poisoning. He thought it reasonable to attribute the presence of an ■opiate in the system to the lettuce deceased had eaten overnight. A very small dose of narcotic would affect an elderly person. The jury returned a verdict that they were of opinion deceased had died from the effects of poison, but there was not sufficient evidence to show that it was attribut¬ able to eating lettuce. — Liverpool Daily Post. Proceedings of the American Pharmaceutical Asso¬ ciation at the Twenty- Sixth Annual Meeting, held in Atlanta, Ga., November, 1878. Also the Constitution, By-Laws, and Roll of Members. Philadelphia: Sher¬ man and Co. 1879. At an unusually late date the annual volume of the Proceedings of the American Pharmaceutical Association has come to hand. A partial explanation of its retarda¬ tion is to be found in the postponement of the last annual meeting until November, in consequence of the prevalence of yellow fever in the Southern States last summer. The volume is very bulky, as it contains just one thousand pages, upwards of six hundred being occupied by the Report on Pharmacy, by Mr. Louis Diehl, which corre¬ sponds with the Year-Book of the British volume. This report is very copious. It is preceded by an Introduction and is divided into sections of “Pharmacy” (with sub¬ sections of “Apparatus and Manipulations,” which is use¬ fully illustrated, and “Preparations”), “ Materia Medica,” “Inorganic Chemistry” and “Organic Chemistry.” The re¬ porter has evidently spared no trouble to make his resume of the history of pharmacy as complete as possible ; in fact he has almost exceeded proper limits, for some of the authorities, which are carefully placed at the end of each quotation, date as far back as 1876. The Reports of Standing Committees appointed by the Association to deal with special subjects always form an interesting feature of these volumes, and in the present one there are reports on the Drug Market, Legis¬ lation and the Revision of the Pharmacopoeia. The last-named lays down the general principles which the Committee thinks should be followed in constructing the Pharmacopoeia, and on a future occasion it is proposed to refer to them in this Journal in greater detail; it also contains a scheme for co-operative experiments on the fluid extracts. The latter part of the volume is taken up with the papers read at the meeting, the discussions on them and the general business. The papers are many of them of much practical interest. As to the business, we regret that some embarrassment exists in the ways and means, due apparently to the commutation for life membership having been fixed at too low a rate at a time when the volume of proceedings, a copy of which is supplied free to each member, was not nearly so large and expensive as now. Several propositions were made, such as a kind of sliding scale of life subscriptions and a per capita tax, but after discussion the attempt to find a remedy was post¬ poned until the next meeting, which is to commence in the city of Indianapolis, Ind., on the 9th of September. ©biiffitvjT. Notice has been received of the death of the follow¬ ing : — On the 4th of June, 1879, Mr. George Masson, Phar¬ maceutical Chemist, Grenada House, Torquay. Aged 30 years. Mr. Masson had been a Member of the Phar¬ maceutical Society since 1871, and on several occasions contributed papers to this Journal. On the 8th of July, 1879, Mr. William Glencross, Chemist and Druggist, Kidwelly, Carmarthenshire. Aged 47 years. On the 14th of July, 1879, Mr. William Powell, Chemist and Druggist, Bridgend, Glamorganshire. Aged 40 years. July 26, 1*79.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 79 gisj^nsmjg Uftmmputa. In orilei' to assist as much as ’possible our younger brethren, for whose salce partly this column was established, considerable latitude is allowed, according to promise, in the propounding of supposed difficulties. But the right icill be exercised of excluding too trivial questions, or re- petitions of those that have been previously discussed in principle. And we would suggest that those ivho meet with difficulties should before sending them search previous numbers of the Journal to see if they can obtain the re¬ quired information. Replies. [322]. “Anon” asks how I am able to make a “'stable preparation” of tr. lyttse, acid. 3ulph. dil., tr. lavand. co., and vaseline or prepared lard, as given in the formula by W. B., July 5? I enclose you two specimens of the ointment prepared with vaseline and lard. I need hardly say the mixture is mechanical, and the simplest way is to rub the tinctures, acid, and vaseline or lard together on a slab, using an ebonite spatula. The rubbing should be in one direction, as in making “ Cold Cream.” I have experienced no difficulty. Northallerton. Hr. Brown. [324], In further elucidation of the question asked by “ Gulielmus,” and in reply to Mr. G. H. Wright, permit me to say I think the pharmacist is justified in dissolving such an alkaloid as m Drphine. It must be observed eight grains are ordered with one drachm of chloroform and three drachms of liniment of belladonna. Practically morphine is insoluble in chloroform, and cold alcohol dis¬ solves only one in fifty. Now, Mr. Wright call’s attention to the statement that the person who compounded the prescription first sent “ twice the bulk.” I observed that, but I had nothing to do with the fact. My object was to show that eight grains of morphine can be dissolved in three drachms of liniment of belladonna. I purposely leave out the chloroform at present. Sulphate of morphine is a very soluble salt, indeed the most soluble of the morphia series. Its solubility in boiling water is one in two. I must not enter into the molecular weight question, as it might be considered foreign ; but I may observe that in my opinion it is more scientific to use a soluble salt of morphia than to apply morphine to the skin in the form of a fine powder, trusting to the acids of the sweat— formic, butyric, propionic, or sudoric — to combine with it so as to form an absorbable compound. Of course I cannot tell whether or not the prescriber knew the exact solubility of morphine. He evidently intended a strong solution, and one equal to eight grains of the alkaloid in four drachms of menstruum. I have shown how this can be accomplished without in any way interfering with the activity of the liniment, but rather increasing its curative properties. If spirit, or water, or double the quantity of liniment of belladonna was added, so as to accomplish solution, by the first compounder, it is manifest the liniment would only be half the strength intended. I may inform Mr. Wright I did not overlook this point, but I had nothing to say upon it except that it was obviously wrong, and I there¬ fore confined my remarks to “Gulielmus’s” query. Hy. Brown. Queries. [331]. Would some of your readers kindly tell me what should be the colour of the following when correctly dispensed? — R Liq. Hydrarg. Perchlor., B.P. . . . jij. Liq. Arsenici et Hydrarg. Hydriod., (Donovan) . ttlclx. Infusi Gentian . ^ij. Aquas . . ad 5viij. M. [332]. R Acid. Tannic . gr. xx Gelatine . . . . gr. iv. Aq. q. s., Glycerin . itlxvi. M. ft. pess. Will some of your readers kindly inform me if it is at all possible to make up the above as written; if not, how it should be dispensed ? It was written by a well-known London doctor, and has been presented at one of the co-operative stores to be made up. They refused to do it. B. Sawyer. and Entries. [615]. DENTIFRICE WATER.— R Radicis Calami . 5SS. Radicis Pyrethri, Resinse Guaiaci . aa 3vj. Ligni Santalini Rubri . 3’h Corticis Cinnamomi, Caryophyllorum . aa [)iiss. Eoliorum* Cochlearke Recentium . . Jiv. Spiritus Rectificati . wxij. Aquae Destillatse . t^vij. Acidi Acetici Diluti . Jiij. Sepone per dies octo, turn expressione cola. In colla- tura solve — Acidi Salicylici . [)i. Turn filtra. Popp's Anatherine Dentifrice. (Hager’s ‘Manuale Pharmaceuticum.’) R Caryophyllorum, Ligni Santalini Rubri . aa 3iy. Ligni Guaiaci, Corticis Cinnamomi . f.a 7)ij. Myrrhae . . 3V* Bj- Olei Caryophyllorum, Olei Cassiae Cinnamomi . . . . f.a gtt. xx. Spiritus Rectificati . ^lij. Aquas Rosarum . §xxvj. H. W. Langbeck. [616]. SILVER PLATING LIQUID. — The Che- on iker Zeitung gives the following prescription, which I myself have tried with success: — Nitrate of Silver . 55 parts. Solution of Ammonia ... 60 ,, Hyposulphite of Soda, Precipitated Chalk . . of each 100 „ Distilled Water . 1000 „ H. W. Langbeck. [617]. CHERRY TOOTH PASTE.— Cochineal in powder . £iij. Cream of Tartar . ....... ^j. Honey . 21bs. Radix Ireos subtile pulverat. . . . §iv. Mix in a stone mortar and allow to ferment in a warm place. After fermentation has ceased, add — Glycerine . ,^vj. Tragacanth . ^ss. Burnt Alum . 3iij. Dried Carbonate of Soda ..... 31- Precipitated chalk sufficient to make a suitable paste,, which may be perfumed with — 01. Gaultherise . 7)j. 01. Caryophyllorum . >)iv. 01. Geranii . 3iss* H. W. Langbeck. W. R. Roberts. * The leaves ought to be bruised in a stone mortar. 80 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [July 16 1879. [618]. NICOTINE. — It is impossible to extract nico¬ tine from tobacco without injuring more or less its quality. The tobacco should be either treated with dilute sul¬ phuric acid or distilled in a current of hydrogen. H. W. Langbeck. [619]. STAMPING- INK. — One part of nigrosine {aniline black) dissolved in ten parts of rectified spirit, and mixed with eight parts of distilled water and two parts of glycerine (sp. gr. 1*260), gives a good black ink to use with india-rubber stamp on paper H. W. Langbeck. (^otftesptulqtq. The Confusion of Medicine with Pharmacy. Sir, — “ The confusion of pharmacy with medicine which has come to the medical practitioners and the pharmacies of to-day is an inheritance from the apothecaries of last century . Therefore gratitude is due to any in¬ dividuals or association that strive by any means to show the desirability of effecting, as far as possible, a separa¬ tion of the duties of the dispenser from those of the pre- scriber.” The above quotation from your temperate and sensible “ leader” in the Journal, July 12, cannot fail to arrest the attention of every one who sincerely desires to see the long vexed question set at rest, viz., shall chemists continue to be perpetually dragged into County Courts for an infringe¬ ment of the Apothecaries Act of 1815 ? The genus “ homo,” species “ John Bull,” is notoriously a physic-loving mammal. He has always preferred, and ever will prefer, to call at a “ doctor’s shop,” no matter to him whether that establishment is under the jurisdiction of a L.A.S. of Blackfriars, or a M.P.S. of Bloomsbury Square, London, for help, advice and mediciue in every little malaise that may befall him. No one can blame the man, and no sober minded person can find fault with the chemist who listens to a tale of suffeiing, proposes this or that dose, then makes it up and receives the money for his goods. If this is prescribing and violating the Apothe¬ caries Act of 1815, the sooner such a condemnatory power is expunged from the statute book the better, for it is violated every hour of the year. A more unjust clause affecting the lower millions of our population could not •exist. As a veteran apothecary let me claim your gratitude if I point out briefly a ready method by which this frequent .collision between the authorities at Blackfriars and the respectable chemists can be fully prevented in future. The great increase in non -dispensing general practitioners throughout England, as shown by the Rochdale report of May 3, has tended to enable the lower classes to recognize only a “ doctor’s shop,” by the presence of show bottles and nostrums displayed in the windows of our druggists, which were formerly the “sign posts” to the apothecary who dwelt within. Let the chemists seek to be legally permitted to prescribe behind the counter under the following re¬ strictions — the xvii. and xviii. clauses of the Apothecaries Act will certainly aid them in the attempt. After the Minor examination is over let the apprentice to the chemist devote two years of study, 1st to elementary anatomy and physiolog'y with dissections; 2nd, to attend¬ ance on the out-patient practice of a recognized hospital, infirmary or dispensary throughout the country. When such course is completed, let him present himself for the ‘‘assistant’s licence” at the Apothecaries’ Hall, where in addition to the present examination, his know¬ ledge in visceral anatomy and the elementary principles of medicine shall be tested. A sho.t Bill in 1874 amended the Apothecaries Act (37 and 38 Viet. c. 34) and removed the apothecaries’ appren¬ ticeship. Let the pharmacist seek for a brief Act to acquire this privilege at the hands of the Executive at Blackfriars and all would be finally and amicably arranged. The dental fee for special lectures and hospital practice required for L.D.S. is £31 10.«. The chemist’s outlay would not exceed £21. The present law restricting the dispenser to Wuik ouly in the premises would still remain untouched. With these brief suggestions for the consideration of the large body of pharmacists and chemists in England, I would conclude by adding a quotation from clause xviii. of the Act of 1815 : — “Five apothecaries in any county or counties respectively throughout England and Wales, except within the said City of London, the liberties or suburbs thereof, or within 30 miles of the same .... shall have full power and authority and are hereby authorized and empowered to examine all assistants to apothecaries throughout the county or counties, ia regard of which such apothecaries shall have been so appointed as aforesaid . The meetings shall take place monthly in some one of the county towns.” The whole wording of this clause xviii. sets forth the purpose of the Act to be one for the benefit of the publie and of the dispenser also. An Apothecary. Sir, — Tn my humble opinion the time is fast approaching w hen pharmacists as a body should endeavour all in their power to wrest the dispensing of medicine entirely from medical practitioners, but it must be accomplished so that no loss shall be sustained by either side. In cases where doctors receive large fees for their advice, they are satisfied and do not require also the profit accruing from the sale of the medicine. In districts where they could only get small fees they would prefer not to give a prescription at all, but to vend their medicine and advice for one charge, as they do at present. I would suggest the following arrangement as regards the latter class of prescribing, viz., that the medical man should write his prescription and place a certain mark on it which would signify that when it had been dispensed it was to be returned to the writer of it or else destroyed, that in no case, unless otherwise specified, should the prescription be given back to the patient. By this means I do not think anyone would be at a disadvan¬ tage. The chemist would necessarily have to dispense these prescriptions at a very moderate rate, but he would gain by reason of the quantity. C. H. F. Gas Supply. Sir, — 1 think we are all much indebted to Professor Red¬ wood for taking up the very difficult subject of gas supply, inasmuch as we have found our gas account to increase a good deal without sufficient cause to show, and on a recent occasion I took the liberty of questioning the right of this increase. The result was that we disconnected our meter and sent it down to Westminster to be examined, the cost of which was only one shilling, and the meter was condemned for registering too fast. I gather from this that it is quite within the province of any consumer to have his meter thus examined and tested, when, as in my case, the company would no doubt refund the difference and supply a new one. I think, howeyer, that there should he some more secure method, presenting less difficulty to the consumer, for cor¬ rectly estimating the quantity of gas burnt, and thus in a simple manner to check the reading of the company’s in¬ spector at each quarterly visit. A. W. Postans. R. Roberts. — 1 add 2 are correctly named. (3) Aspleidum tricliomanes. (4) Anthyllis Vulneraria. (5) Hypericum pulchrum. (6) Melicu nutans. T. C. — (1) Lithospermum arvense. (2) Echium vulgare, white-flowered variety. (3) Arctium ( majus ?), not ad¬ vanced enough to say what species. (4) Valeriana officinalis, white -flowered variety. W. Maunder. — We should think not, as long as no claim is made to the title of dentist. A. Mitchell. — Hottonia palustris and Melampyrum pratense. G. A. Thompson. — (1) Sanicula europcea. (2) Linum catharticum. (3) Vida hirsuta. “ Gulielmas.” — (1) Galium palustre. (2) Galium verinn. (3) Alcliemilla vulgaris. (4) Aira composita. (5) Lolium peren ie. (6) Hordeum pratense. (7) Plileiim pratense. W. Green. — (1) We know of no periodical in which the information required will be found to a greater extent than this Journal. (2) Blyth’s ‘Manual of Practical Chemistry., Communications, Letters, etc., have been received from Messrs. Hart, Pollard, Dallas, Story, Will, Price, 1 ulus. Nihil, Yolo semper juvare. August 2, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 81 MYRRH : ITS COMPOSITION AND IMPURITIES.* BY R. H. PARKER. The first market at which myrrh appears is Berbera — a small seaport town in Eastern Africa, nearly opposite Aden — where it is brought by the natives from the district about Hurrar and Somali¬ land. Here it is purchased by Aden agents (English and Indian goods being given in exchange) and shipped to Bombay. When sorted at the latter port, it is found to consist of all equalities of myrrh, together with opaque bdellium, foreign resins, such as juniper, and various other impurities (bark, stone, etc.).f The best selections are sent to Europe, the commoner to China, where it is probably used as incense.^ Bales of bdellium also appear at Berbera, consisting the opaque and perfumed kinds (bissa bol). Since myrrh is collected by uncontrolled natives, who probably know very little and care less about the quality of the gums taken to Berbera, it is not surprising that spurious gum resins and foreign sub¬ stances find their way into English markets. The sorting at Bombay is by no means carefully conducted and leaves a great deal to be picked out by London wholesale houses and dealers. Here it is of course most efficiently done and the best parcels of “Picked Turkey Myrrh ” contain but a very small proportion of impurity. Myrrh is first sifted in order to remove the small fragments and is then sorted by hand ; still, however, pieces ^ of spurious gums will occasionally find their way into the best parcels. I will, therefore, first describe myrrh and afterwards individually the various substances which occur in bales of the drug us imported, viz. : — 1 . Opaque bdellium. 2. African bdellium. 3. Bissa bol (perfumed bdellium). 4. Indian bdellium. 5. Perfumed amyriclaceous (I) gum resin. ■6. Odourless amyridaceous (?) gum resin. 7. Opaque tasteless gum. 8. Bitter gum. 9. Transparent gum. The relative preponderance of these varies con¬ siderably. Mr. E. M. Holmes found, in 1876, opaque bdellium in largest quantity, next, Indian bdellium, and third, bissa bol. At the present time in one bale of unpicked myrrh I found African bdellium chiefly, next, opaque bdellium. Of the “ spurious gums ” picked out from another bale, opaque bdel¬ lium constituted about one-third, the remainder being opaque tasteless gum, transparent gums and odourless amyridaceous (?) gum resin. Very little bissa bol or Indian bdellium occurred in any of the bales I examined. The substances thus rejected are commercially valueless. Myrrh and its impurities are readily distinguished by observing — (1) The characters of the fracture, . (2) The odour, and (3) The taste. African Myrrh “ Heera Bol,” the “ Turkey Myrrh” of commerce. * Read before the School of Pharmacy Students’ Asso¬ ciation, June 26, 1879. + Yaughan, Pharm. Journ. [1], vol. xii., p. 226. X Dyinock, Pharm. Journ. [3], vol. vi., p. 661. Third Series, No. 475. Botanical source, Balsamodendron Myrrha .* This may be divided into “ soft or oily myrrh ” and “ dry or gummy myrrh.” “ Soft myrrh ” occurs in irregularly roundish masses, varying in size from small grains to pieces as large as a hen’s egg and occasionally much larger ; it has a dull waxy fracture, is readily impressed by the nail, and gives at the same time an oily exudation. The fracture frequently exhibits whitish markings, which in the more globular pieces appear in narrow curved streaks arranged concentrically to the side which was attached to the tree. They are often broad but do not then exhibit the straight interstices or cracks filled with transparent resin characteristic of bissa bol. The fragrant odour of myrrh is too well known to need description and differs entirely from that of any of the impurities. The taste resembles the odour, it is aromatic and slightly bitter. The colour varies from deep reddish brown to light yellowish brown, some pieces are almost colourless. The paler kinds are to be preferred. Minute transparent resinous tears sometimes appear on the usually powdery surface, due to the exudation of oil which has resinified. Soft myrrh cannot be reduced to a fine powder ; indeed if beaten in a mortar for some time it gives a greasy paste. “Dry myrrh” occurs in masses having a very irre¬ gular surface, it is rarely rounded or globular. The fracture is conchoidal, shiny, resists the nail and gives no oily exudation. In odour and taste it agrees precisely with “soft myrrh,” but the white markings usually present in the latter are absent. It contains a large percentage of gum (75 per cent.). From the description in ‘ Pharmacograpliia,’ p. 129, this would appear to be identical with Arabian myrrh, but examination of the specimen in the Hanbury collection proves the latter to differ ; it is in small grains or tears, dark coloured, with an almost glassy surface, the larger pieces being formed by agglomeration of the smaller ones. It also is wanting in odour and the powdery exterior of African myrrh. The “meetiga” of the Bombay market, called Ara¬ bian myrrh by Dymock,f differs entirely from either “ dry myrrh ” or Hanbury’s “ Arabian myrrh.” % j > The “soft” and “dry” myrrhs, as above described, are very distinct and would almost suggest their being produced by different varieties of Balsamoden¬ dron myrrha-, but since (1) the chemical characters of both resins and gums agree (as shown subse¬ quently), (2) the odour and taste are identical, and (3) the relative percentage of gum is by no means constant, it seems more probable that they are pro¬ ducts of the same variety, but from plants either of different ages, or existing under dissimilar climatic conditions. It is possible that the same tree may, at different seasons of the year, give exudations as unlike as “ soft ” and “ dry ” myrrh. That “soft myrrh ” is not converted into “ dry myrrh ” by long exposure to air is proved as follows: — (1) The “ drying ” consists in oxidation of the oil, which would give increased weight § and therefore a relative increment of resinous percentage. Now, * Pharm. Journ. [3], vol. viii., p. 893. f Pharm. Journ. [3], vol. vi., p. 661. X See * Museum Catalogue,’ 139c and 139/. § 3 325 grams of soft myrrh in thin shavings exposed to the air for three weeks weighed 3'506 ; an increase equal to 5'4 per cent. 82 THE PHARMACEUTICAL JOURNAL AND ’PLANS ACTIONS. [August 2, IS791. “ dry myrrh ” has a very much higher gum per¬ centage ( vide subsequent table). The loss of water, if such take place, must be so small that the differ¬ ence would in no way be explained by it. (2). In a non-porous body like myrrh, oxidation would be confined to the surface. I have never found a piece of “dry m}7rrli” with a “soft” interior; on the other hand, a very small tear of “soft, myrrh,” not more than one-eiglith of an inch in thickness, which must have been exposed to the atmosphere ever since its exudation, proved on fracture to be very soft and oily close beneath the surface. “ Spurious Gums ” fou?id in Myrrh as imported. 1. Opaque Bdellium ( Balsamodendron Playfairiil) . — Identical with the bdellium opaque, of Guibourt* Dy mock’s specimen, however, of opaque bdellium, is a very brittle opaque gum, which agrees chemically with the “gum hotai” of Vaughan, but is rather darker coloured, Vaughan’s specimen being white. The latter is identified in the Hanbury collection as the gum resin of B. Playfairii. Opaque bdellium may be at once recognized by its opaque, yellow- ochre coloured, conch oictal fracture ; if resists the nail. It is very hard and difficult to fracture (difference from “gum hotai ”), almost odour¬ less, and its taste bitter without acidity. Occurs fre¬ quently in large elliptical tears with a coarsely granular surface. 2. African Bdellium (Balsamodendron Africanum ) is met with in large tears like opaque bdellium, but the granulation is less coarse and the surface is traversed by deep cracks. It is very hard ; the con- choidal fracture appears slightly opaque, of a dull bluish stony hue, with a characteristic resinous margin ; it is reddish and translucent in thin layers, almost odourless, and its taste feebly bitter. 3. Bissa bol (Balsamodendron Kafal ?), is identical with the perfumed bdellium or “habifk hadee” mentioned by Dymock; the “hebbakhade” of the Somalis, and the Myrrha Indica , of Martiny. Bales of “ bis -a bol ” are shipped from Berbera to Bombay; probably a large proportion of it goes to Cliina,t where it is used as incense and, according to Dymock, is mixed with the food of milch cows and buffaloes for the purpose of increasing the quantity and im¬ proving the quality of the milk. “ Bissa bol ” resembles myrrh much more closely than either of the bdelliums previously described. In external appearance it is very similar, the fracture is waxy, yields to the nail, giving an oily exudation like “ soft myrrh ;” yellowish white markings also appear, which, however, differ essentially from those of myrrh in being traversed by angular interstices filled with transparent reddish brown resin (or gum resin). It may be readily distinguished by its powerful aromatic odour, totally unlike myrrh, difficult to describe (perhaps because nothing re¬ sembles it), but easily recognized after one intro¬ duction to the olfactory nerve. It has been likened by Mr. Holmes to the taste of the spring mushroom (Agaricus gambosus), by Dymock to the odour of “lemon lollipop;” when diffused by evaporating the tincture on blotting paper, it is somewhat apple-like. The taste is aromatic and slightly bitter. 4. Indian Bdellium ( Balsamodendron Muhul and B. pubescens), or “ Googul,” collected in Deccan. * ‘ Histoire des Drogues/ tome iii., 515. f A specimen of bissa bol appears in Hanbury ’s collection of Chinese drugs. Occurs in large irregular masses of a dark reddish brown colour. The fracture resists the nail and is covered with characteristic minute shiny points of resin, which also appear on the outer surface. The odour is feeble and cedar like ; it appears to be de¬ veloped on keeping. The taste is slightly acrid and devoid of bitterness. 5. Perf umed Amyridaceous (?) Gum Resin. — Tins' substance does not appear to have been previously described,* but I have found a few pieces of it in parcels of myrrh obtained from different sources. In external characters it somewhat resembles olibanum or tacamahac, the colour varies fiorn light yellowish brown to light yellow, more translucent than myrrh, some pieces being transparent in mass. It has a waxy fracture, and from the presence of minute cavities filled with oleo-resin of treacly consistence, numerous silky strings join the fractured portions as they are pulled asunder. It is cheesy to the nail, softens in the hand and is very sticky. The odour is powerful, resembling some samples of elemi, but is more pleasantly aromatic. The taste is slightly aromatic without bitterness or acridity. When crushed in a mortar it gives a very adhesive paste. It is not entirely soluble in ether, alcohol, turpentine or chloroform. -6. Odourless Amyridaceous (?) Gum Resin. — This I have found in considerable quantity ; it has a bright yellow powdery exterior similar to the last mentioned gum resin, is very brittle, resinous and mostly trans¬ parent. It lacks, however, the cheesy character, the stringy fracture, and is odourless and almost tasteless. 7. Opaque Tasteless Gum occurs in irregular tears. It is very hard, fracture dull, somewhat opaque, nearly colourless, odourless and devoid oi taste. 8. Bitter Gum. — This is more transparent than the last; the colour varies from reddish brown to almost colourless ; its very bitter and acrid taste recalls ammoniacum. 9. Transparent Gum. — Very variable in appearance, but seems closely to resemble the inferior kinds of acacia gum in colour, taste and glassy fracture. Some pieces of white acacia gum frequently occur. Composition of Myrrh. The proximate constituents are — (1) . Resin (two according to Brandes). (2) . Two gums (one precipitable by both lead solu¬ tions, the other thrown out by subacetate only). (3) . Essential oil. The very variable relative proportion in which these occur is best seen by reference to different authors, f * The nearest approach to this substance is the Tacama- que jaune liuileuse, of Guibourt, (‘ Drogues Simples,’ 1870, tome iii., 483), the Luban Meyeti of the ‘Pharma- cographia,’ p. 135; but this author says it contains no gum. Now, 42 per cent, of perfumed amyridaceous gum resin is insoluble in cold or hot S.V.R., and dissolves to a large extent in water; the latter solution, however, is scarcely precipitated by acetate or subacetate of lead, f Planclion, ‘ Drogues Simples/ tome ii., 156. Brandes. Bracannot. Ruick- holdt. Huile essentielle .... 2*60 2*5 2*18 t, . . C molle 22*24 7 Resme . .jg|che j.ggJ 27*80 23* 44*76 n C soluble 54*38 7 G°mme | insoluble9'32 $ 63*70 {“}»* 40*81 Sels . 1*36 — 3*65 Impuretes . 1*60 — 3*86 Eau . — — 1*47 August *2, 1679.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. S3 Gum. — I have estimated the percentage of gum in different samples of myrrh, the results I have tabu¬ lated : — 5. Anoy- . 2. 3. 4. ridaceous *, “Soft “Diy Bissa psrfumed wyrm* Myrrh.” Myrrh.” bol. gum resin. Filter and gum . . G73 6 95 5 ’45 5'54 9'15 9 11 6 13 6 01 G'05 6-03 Filter . 2 '09 2 33 1*50 1*55 1‘65 1 60 1-80 1'72 1-83 1*77 4 64 4-62 3 95 3 99 7*50 7 ‘51 4'33 4’29 4*23 4'26 Gum, mean per cent 46-3 89 7 75*0 43* 1 42*4 Ten grams of the gum resin were powdered, ex¬ hausted with cold rectified spirit, the insoluble gum collected on a weighed filter and dried in a hot air chamber till the weight became constant. In each case the figures were checked by dupli¬ cated experiments. 1. Myrrli. — A representative sample of a large parcel of myrrh, powdered and well mixed. 2. “ Soft Myrrh.” — Very oily pieces selected, the outer portions rejected; was almost pasty when powdered. 3. “ Dry Myrrh.” — Characteristic specimen with bright glossy hard fracture, easily reduced to a light yellow powder. 4. “Bissa Bol” obtained from a parcel of myrrh, outer portion not removed, powder very yellow and oily. 5. Perfumed Amy ridaceous Gum Resin. — Specimen picked from parcel of myrrh, formed a very sticky paste when crushed. Equal weights of the dried gums from “ soft ” and “ dry ” myrrh were separately dissolved in equal volumes of water; the filtered solutions were pre¬ cipitated by neutral acetate of lead, again filtered and solution of snbacetate of lead added ; the amount of precipitates in the parallel experiments were approximately identical. Resin. — Brandes distinguishes two resins, (1) a soft resin, odorous, and (2) a hard resin (myrrhic acid), inodorous, both soluble in rectified spirit and in¬ soluble in ether. Unverdorben regards the soft odorous resin as a mixture of the hard resin with volatile oil. Volatile Oil , sp. gr. *988, b.p. 266° C. — Fluckiger and Hanbury in working on 25 lb. of myrrh obtained only | per cent. (‘ Pharmacographia,’ p. 1 28) ; Bley and Diesel produced 3*4 per cent. * If the liquid which exudes on pressing “ soft myrrh ” with the nail be volatile oil, a much larger proportion than 3 per cent, must be present. The following experiments were tried with the object of obtaining a greater percentage: — (1) . A sample of soft myrrh was made into a thin paste with water and distilled in a current of hy¬ drogen. The result was similar to that obtained by distillation with water in atmospheric air, viz., a very small quantity of nearly colourless oil, lighter than water, together with white flocks of a substance of butyraceous consistence, also lighter than water, but becoming heavier than it by prolonged contact. (2) . Some soft myrrh was macerated in a small quantity of chloroform and the filtered solution dis¬ tilled ; the chloroform came over rapidly and the residue soon acquired an empyreumatic odour. (3) . Soft myrrh was treated with a small quantity of benzole and the filtrate allowed to evaporate spon¬ taneously. The residue, however, soon became very viscid, proving that the solvent did not separate the oil from the resin. (4). About twelve ounces of “ soft myrrh ” were selected, reduced in a mortar to a pasty consistence, and subjected to powerful hydraulic pressure ; a reddish yellow liquid, of thin treacly consistence, heavier than water was expressed ; it is probably volatile oil holding resin in solution, if so, the quan¬ tity obtained (about an ounce and three-quarters by weight) would indicate at least 10 per cent, of oil in the sample. I obtained a similar liquid some twelve months since in making an emulsion of myrrh: — One ounce of myrrh was powdered (the odour indi¬ cated contamination with bissa b61) and rubbed with 3ij of water, the gum at once assumed a doughy consistence, from which 3iij of liquid was readily expressed by the pestle. This mixture (of oil and resin) was reddish brown, heavier than water and very slowly distillable therewith ; the distilled oil was lighter than water, but on prolonged contact became a heavier solid. Removed from the water and allowed to dry it formed a transparent brittle resin. I have several times endeavoured to repeat this experiment with myrrh free from bissa bol, but could in no case get any exudation. The expressed liquid is possibly that mentioned by Plaff* as being “ heavier than water and not distillable therewith.” Brandes describes a volatile oil also heavier than water and distillable therewith, but not with alcohol. The specimen of oil of myrrh in the Society’s museum, prepared at Plough Court (1873), is a light yellow mobile liquid. Formic acid is said to be produced during dis¬ tillation. From the above it appears probable that a large quantity of volatile oil exists in myrrh, only a small proportion of which has, as yet, been isolated, on account of its high boiling point (266° C.) and the readiness with which it is decomposed or resinified by contact with air and moisture at a high tem¬ perature. Probably distillation in vacuo per se, or distillation under reduced pressure in an atmosphere from which oxygen would be excluded might prove the correct¬ ness of this assumption. The colouring matter of myrrh is probably due to the presence of a small proportion of a deep reddish brown resin, which is almost absent from the paler specimens. The action of nitric acid at once distinguishes true myrrh from any of the “ spurious gums ” that have been mentioned. It is best observed by satu¬ rating white filter paper with the freshly prepared tincture (1 of gum resin and 6 of sp. rectif.), and when the alcohol is almost entirely dissipated, draw¬ ing across the paper a glass rod previously dipped in nitric acid (sp. gr. 1*42). True myrrh gives an imme¬ diate deep yellowish-brown colour, rapidly becoming almost black. The margin soon acquires a red tint, passing through bright crimson to dull purple, which is permanent. The presence of alcohol of course modifies the action of the acid ; the latter should be applied when the alcohol has evaporated, and yet avoiding undue exposure of the dried resin to air, i.e., when the paper begins to recover its stiffness. The resins from bissa b61 and African bdellium * ‘ Grnelin/ xiv., 413. 84 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 2, 187?. are much less powerfully acted upon; those from the remaining impurities give scarcely any colour at all. A few drops of the tincture evaporated on glass also give distinctive features. The residues from perfumed amyridaceous gum resin, opaque and African bdelliums, are opaque; those from myrrh and bissa bol are transparent. I cannot conclude without expressing my obli¬ gation to Mr. E. M. Holmes for much of the in¬ formation given in this paper and a great deal of valuable assistance with reference to the history of authentic specimens of the gum resins in the So¬ ciety’s museum. PHARMACEUTICAL EXTRACTS.* CRITICAL CONSIDERATIONS UPON THEIR PRE¬ PARATION, CLASSIFICATION, GENERAL CHA¬ RACTERS, USES, ETC. BY E. SCHMITT, Professor of Medicine and Pharmacy at Lille, The extracts are very important preparations, never¬ theless but little is generally known concerning their raison d'etre, their different modifications, the very diverse modes of their preparation, and their general or specific characters. I shall attempt in this paper to make a study of them under all these aspects, and in order to do so logically I shall proceed as follows : first, define an extract, then describe the origin and advantages of extracts, give the general rules of preparation, indicate the classification of the extracts and finish by giving theh general characters. I. An extract is the product of the evaporation of a natural or artificial juice to the consistence known as “ the consistence of an extract,” i.e., a paste that is soft, but nevertheless sufficiently firm not to run like a liquid or adhere to the well dried fingers. This primitive defi¬ nition can in the present day no longer be applied ; the consistence of the extract is more variable ; thus, the Codex indicates three different types, when it says, “ The extract is the product of the evaporation to a soft, firm or dry consistence, of a solution obtained by treating a vegetable substance with a vaporizable menstruum, such as water, alcohol or ether.” Some operators define the extract in a manner more simple still : to them it is the product of the evaporation of aqueous, alcoholic, ethereal or acetic liquids to a pasty consistence. Whatever may be the definition adopted, the extract may be characterized by two essential con¬ ditions : the concentration of a medicinal liquid (a natural or artificial juice) and a special consistence to which I shall refer further on. All the juices, and the juices of indigenous plants especially, contain within themselves germs of fermenta¬ tion and destruction ; they are besides exposed to a second alteration, due to external agents of decomposition. In concentrating the juices, their volume is diminished, the causes of internal decomposition are modified or destroyed and less access is permitted to external agents of fer¬ mentation ; the causes of disorganization of the juice are thus diminished. Preservation is the primary object of the preparation of an extract ; but it is not the only one, for the syrups, wines and tinctures answer to the same want. In concentrating the juice the pharmacist also, by successive operations, effects the removal from the liquid of useless and inactive matters, the albumenoid, pectic and amylaceous principles, for example. Lastly, the extract offers to the medical man a preparation that is active in a small volume, capable of reproducing im¬ mediately in a mixture or a syrup, the original juice with all its active elements and also lending itself with a * Repertoire de Pharmacie, vol, vii., p. 249, marvellous facility to other pharmaceutical preparations, such as pills, pastes, pomades, etc. To recapitulate, the extracts supply in a small volume the medicinal principles of plants and animals, and they include all the soluble elements of the plant or animal to the exclusion of inert principles. The active principles are moreover modified in such a manner that they can be better borne, and in higher doses, as has been demonstrated with the squill and digitalis. Further the extract is a good active preparation accommodating itself to all phar¬ maceutical forms. One single shadow there is to this picture: the preparation of an extract is a delicate operation and its preservation for any length of time is difficult. II. We are thus led to study in a general way the pre¬ paration of extracts. Some among them, — the commer¬ cial extracts, aloes, catechu, kino, etc., — are supplied by the druggists, all the others ought to be prepared in the laboratory of the pharmacist. When operating with a natural juice it may be concen¬ trated immediately or after clarification : we have thus two kinds of juice extracts, the extract from defecated juices and the feculent or non-defecated extracts, called also Storck’s extracts. Sometimes there is incorporated with the fresh juice as much powder of the plant as there is real dry extract in the juice and evaporation is carried on to dryness at from 40° to 50° C., extracts being thus ob¬ tained under the form of grumous dark green powders. In this way are prepared the narcotic extracts of the Belgian Pharmacopoeia (aconite, belladonna, conium, lactuca, etc.). These extracts are very active, but are difficult to preserve, so that the pharmacist ought to renew them every year. The name of “rob” is given to the product of the evapora¬ tion of the juice of fruits ; for instance the robs of buck¬ thorn, juniper and elder. The natural juices are rather rare: the questions of locality, collection and time interfering with their pre paration. In order to obviate this inconvenience the pharmacist prepares artificial juices by treating the dry products with menstrua capable of dissolving their active principles. When the menstruum is vapourizable the artificial juice can be concentrated, and we have then a new series of extracts, the aqueous, alcoholic and ethereal. To these may be added the acetic extracts, of which at present there are but two representatives, — the acetic extract of colchicum and Lalouette’s acetic extract of opium, — notwithstanding the efforts of Ferrari to extol the extracts prepared with vinegar. Finally there are the mixed extracts, in the preparation of which ether and alcohol and water and alcohol have been employed as menstrua successsively, as is done with the cubebine of Lab^lonye and the ergotine of Bon jean. In all the extracts it is necessary to commence with the study of the juice, then its concentration. Let us com¬ mence with the aqueous extracts, which ought always to be supplied when the medical man does not specially in¬ dicate the alcoholic or ethereal extract. Whatever may be the menstruum the substance ought always to be well divided, either by cutting or by coarse pulverization ; it is necessary to eliminate carefully the fine powder which would interfere further on with the decantations and filtrations. Thus prepared, the primary substance is exhausted by maceration or digestion, infusion or displacement with distilled water, when that is ordered, or at any rate with water very poor in carbonate of lime. Maceration is effected between 10° and 20° C., for opium and gentian, for example 5 digestion between 35° and 40° C., for cinchona. Infusion is made with water at 70° C., for digitalis, the extiacto-aromatic plants, and valerian root ; but these extracts ought to be replaced by alcoholic extracts, wrhich are very superior to them. Dis¬ placement is recommended for extract of liquorice, and with me it has succeeded very well for extracts of guaia- cum and couch-grass. Decoction I reject, because it determines the coagulation of albumenoid matters in the substance itself, and prevents the solution of some prin- August 2, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 85 ciples which, like astringent principles, form with vegetable albumen and starch insoluble compounds. The product of these operations is thrown upon a cloth or hair sieve, and the liquid thus separated is reduced to one-third by evaporation ; the evaporation can be con¬ ducted over the bare fire, ebullition being avoided and the liquid stirred continually. When reduced to one-tliird the liquid is removed to another vessel and placed in a cellar or some other cool place where it is left to stand two or three days, after which it is decanted or filtered if neces¬ sary. The juice is then ready for further concentration. The alcoholic and ethereal extracts are prepared by maceration or displacement with 60° to 90° alcohol, ether, or ether containing alcohol. The clear tincture is intro¬ duced into a distillatory apparatus to collect the greater part of the alcohol or ether, and concentration is effected generally as with the aqueous extracts. The evaporation of all these liquids is carried on in a water-bath; the temperature ought not to exceed 80° C. for alcoholic extracts and 50° C. for ethereal extracts. It is advisable to operate in flat vessels having a large surface but of small capacity; to add the liquid in portions and in pro¬ portion as evaporation goes on, and to agitate constantly to favour the disengagement of vapour and to prevent the adherence of the extract to the bottom of the vessel. The action of heat is continued until the attainment of the proper consistence, which it is proposed to define more closely than in the Codex. Formerly, only the “consistence of an extract” was known : the Codex only specified that the paste should be soft, firm, or dry. The following scale of consistence for extracts is now proposed : — (1) “ Soft or semi-fluid extract,” the mellcigo of the Ger¬ mans, of the consistence of fresh honey. Examples : The ethereal extracts of male fern, mezereon, semen contra and cantharides ; the alcoholic extract of thapsia and the “ robs.” (2) “Firm extract,” extmctum spissum, of the true con¬ sistence of an extract, not capable of running, like the preceding, when cooled, but allowing threads to be drawn from it by the spatula. Examples : the extracts of cin¬ chona, valerian and gentian. (3) “ Pilular extract,” extractum spissius, much firmer than the preceding, no longer yielding threads and capable of being used in the manufacture of pills without the incorporation of powder. (4) “ Dry extract,” extractum siccum, capable of being pulverized. Examples : the extracts of rhatany, monesia and cinchona (Lagaraye’s “sel essentiel”). To these may be added the resinous extracts or resins (jalap and scam- mony), which are in fact alcoholic or mixed extracts, and should not be placed in the saine category as Burgundy pitch, tar and the gum resins. To bring the extract to the dry consistence it is evapo¬ rated to the point when the mass becomes friable upon cooling ; it adheres no longer then to sized paper, and it may be spread while hot with the spatula upon sheets of paper having the edges turned up. The drying is finished in a stove at between 40° and 50° C. The product is then coarsely powdered and introduced into previously heated glass flasks, the mouths of which are closed with good corks. The soft, firm and pilular extracts are also placed in flasks, or tall porcelain pots having narrow openings. All extracts should be kept in a dry and cool place. These general rules having been laid down some modi¬ fications of the modus operandi will be described. Extract of opium is re-dissolved in water and again filtered. This fresh aqueous solution has for its object the elimination of fatty or aqueous matters, wax or sub¬ stances analogous to caoutchouc, which have been taken up in the first treatment, partly on account of their abundance and partly through the presence of other principles, such as sugar, gum and extractive matter, which favour their solution. The operator often desires to retain these resinous or resinified matters in the extract, but at the end of the operation they separate from the extractive (the total of the parts soluble in water) and the result is an extract of bad consistence and without homogeneity ; the defect is corrected by incorporating in the mass, at the last moment, a little alcohol, as recommended in the Codex for extract of guaiacum, and in the Belgian Pharma¬ copoeia for the dry extract of cinchona. Dry extracts less alterable and more easy to preserve may be obtained by incorporating in the mass, while still hot, vegetable powders or dextrin and finishing the drying in a stove at between 40° and 50° C. Extracts containing dextrin are prepared principally in Germany from the narcotic juices and the quantity of excipient added equals in weight the amount of real extract. It is only necessary then in making up prescriptions to use of these extracts double the quantity prescribed by the physician. A few words more upon mixed extracts requiring the employment successively of several menstrua. The cubebine of Labdlonye and the ergotine of Wiggers are prepared by treating with alcohol the ethereal extracts of cubebs and ergot ; the extracts are thus freed from waxy and fatty matters which are inert or even dangerous. Bonjean’s ergotine is obtained by treating the aqueous solution of ergot with 90° alcohol, which precipitates gummy and albuminous matters and the salts insoluble in alcohol ; the preparation is twice as active as the ordinary aqueous extract. Dausse has proposed the successive treatment with ether, alcohol and water for the exhaustion of the extracto-aromatic plants. Mohr also recommends this mixed treatment for the preparation of the narcotic extracts. According to this learned operator the purified juice ought to be evaporated to the consistence of a syrup, then treated with anhydrous alcohol, which precipitates the gums and insoluble salts ; the alcoholic liquid should then be evaporated to the consistence of an extract. Mohr’s extracts are very active and are easily preserved. The resins of jalap and scammony may also be included in the category of mixed extracts. In the laboratory of the pharmacist the concentration of the juices is effected by the action of heat : to accelerate the preparation of the extract and prevent prolonged contact with the air it has been suggested to operate in a vacuum. The preparation of extracts, in consequence of the apparatus this would require, would then necessarily become industrial, which ought not to be encouraged. Extracts should be prepared by the pharmacist; they are very active medicinal agents upon which the medical man ought to be able to depend, and notwithstanding the authority of such names as Grandval, Berjot, Dausse and others, I always prefer the extract prepared in a phar¬ macy, for the following reasons : — The dry extracts prepared in a vacuum are very hygrometric ; after a very short time and by simple contact with the atmosphere they form a mass more or less elastic and difficult to manipulate. Also, it is very easy for an isolated phar¬ macist to collect the two or three kilograms of the sub¬ stance which he requires for the preparation of his extract, but would it be possible to find the hundreds and thousands of kilograms required for an industrial manufacture in good condition and of certain origin ? The analysis of extracts is very little understood; the adulteration of commercial products is therefore too easy to execute and impossible to detect. Lastly, it has not been proved, so far as I know, that the extracts prepared in a vacuum ha,re a therapeutic value superior to that of the extracts prepared by the ordinary method. The following process appears to me to be preferable : — Quite recently an attempt has been made to substitute the action of cold for that of heat in the concentration of juices, and extracts have been prepared by congelation. This congelation may be effected by the cold of winter or by means of well-known apparatus, such as Carre’s. It is advisable not to purify the juices of plants or fruits before proceeding to congelation, for the coagulation of the vegetable albumen takes up much of the active 86 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 2, 18T*. principle, which is then wanting in the extract. The juice is submitted to two or three successive congelations, the frozen juice is broken up, put into a linen or hair bag, and then strongly pressed. The concentration is such that the evaporation of the juice may be finished by putting it on plates in a stove heated to 30° C. The alteration of the juice is much less than by the ordinary processes, and extracts of rhatany, catechu and aloes are obtained which are perfectly soluble. This process, employed by myself in the preparation of medicinal diastase, has given excellent results in respect of the yield as well as the quality of the product. Some milk after three congelations had lost 57 per cent, of its original volume ; its density had increased from 1032 to 1108, and by exposure on a plate to the sun this milk gave a very fine dry extract. The question of yield ought also to occupy the attention of the pharmacist; this is treated of in the Codex, p. 433, in a table very well drawn up. I would only wish to add to this table a column in which the figures 1, 2, 3, 4, should indicate to the operator the degrees of consistence, from the semi-fluid to the dry extract. The consistence is moreover strictly correlative to the yield, without which it has no practical value. I should like to see the preparation and employment of dry extracts more extended. Whether prepared by immediate desiccation, or by incorporation of vegetable powders or of dextrine, these extracts are better for preservation and they are more certain from a posological point of view. The German Pharmacopoeia orders several extracts to be dry which in French pharmacies are kept soft. For example, take the extract of opium : in Ger¬ many it is the powder of opium which should contain 10 per cent, of morphia, and the dry extract 20 per cent. These requirements are certainly very reasonable ; in the Codex it is absolutely indispensable to indicate the amount of water which opium and its extract may con¬ tain. The same remark applies to all the extracts of soft or firm consistence. In Germany, besides opium, the dry extracts are those of aloes, colocynth (simple and compound), campechy, calumba, myrrh, nux vomica (aqueous and alcoholic), rhatany, compound rhubarb and senega. The narcotic extracts dry and containing dextrine are often demanded ; they are besides necessary for the preparation of the compound powders. I have intentionally omitted to speak of the fluid extracts, the use of which has spread so rapidly in England and America. I think, and I hope to prove subsequently, that the fluid extracts ought to be excluded from medici¬ nal use. It now remains to treat of the general constitution of the extracts, their classification, and their general characters. {To be continued.) RECENT CONTRIBUTIONS TO THE HISTORY OF DETONATING AGENTS.* BY PROFESSOR ABEL, C.B., F.R.S. ( C1 99 99 99 99 99 5* 300 grams 99 99 99 99 9? 600 grams 99 99 99 99 N. BaCO-i. BaC-.O. at 100° 2*1 3*6 3*4 at 120 2*3 4*7 4*3 at 150 3*1 10*5 5*0 at 180 4*0 10*8 8*0 at 200 3*95 11*0 8*6 at 180 3*79 11*2 18*2 at 250 4*41 12*5 24*2 Acetic Acid. — The proportion of this acid is always relatively small, it varies with the temperature and the proportion of the baryta, as in the previous instances, the smallest quantity obtained being 2*7 per cent., and the greatest 5*4 per cent. Fixed Residue. — The total weight of this residue, obtained as before mentioned (including 6*53 per cent, of organic matter carried down by the barium carbonate), amounted in one experiment to 95*83 per cent., and in another to 96*5 per cent, of the albumin used ; it is evident therefore that the decomposition under the influence of baryta is accompanied by a fixation of the elements of water, inasmuch as the separate weights < f the com¬ ponents being added together, there is always an excess varying from 10 to 1 4 percent. The ultimate analysis 104 THE PHARMACEUTICAL JOURNAL AND TRANSACTION'S. [August 9, 1879, of the fixed residue gave very constant numbers, which did not vary greatly even under different formative conditions, the mean numbers being C = 4ST6 ; H = 8‘2 ; N = 11*03 ; O = 30-75 per cent. Volatile Oil. — There is formed, during the decomposition of albumin in the manner under discrission, a very small quantity of a volatile oil, about 1 or 2 per cent., which could hot be obtained in sufficient quantity for analysis under ordinary conditions. An operation on the large scale with 10 kilograms of albumin enabled about 50 or 60 grams of the oil to be collected and an examination to be made. It had no fixed boiling point ; on account of the small quantity at disposal it was not possible to separate its constituents by fractional distillation : it was therefore divided into four portions boiling from 113° to 120° ; 120° to 140° ; 140° to 180° ; and above 180°, and an analysis of each portion made. From the results of these analyses the author is of opinion that the oil is a mixture of two sub¬ stances, one, the more volatile, containing oxygen but not nitrogen ; the other, nitrogen but not oxygen. The presence of pyrrol in the oil was clearly established by means of its well-marked reactions. The formula, Ci6H23N03, calculates very nearly to the percentage obtained, from which if the formula of pyrrol be deducted (C4H5N) there remains 3 (C4H60), which may be con¬ sidered to represent approximately the composition of the remainder. A small quantity of a sulphuretted body is also contained in the oil. The quantity of this albuminol obtainable is so small that it is impossible to assign to it any important part in the constitution, or in the reactions representing the decomposition of albumin. The proximate analysis of the fixed residue was a work of very great difficulty, and every method that could be devised was tried with only partial success. It was eventually found that the best method was to treat the residue with neutral solvents, and to separate the con¬ stituents as far as possible by means of fractional crystal¬ lization. The identification of the various principles was afterwards effected by means of ultimate analysis, which, in the absence of any well characterized reactions, was found to be the only sure or practicable means of arriving at satisfactory results. More than 500 combustions were thus made. The two terms which were the easiest to isolate from the fixed residue, on account of their slight solubility, were tyrosine and leucine, the former, which is produced to an extent varying from 2‘3 to 3'5 per cent., was recognized by its crystalline form, and by its well-known colour reaction with mercurous nitrate ; the latter was also obtained in a well-crystallized condition, and gave results on analysis agreeing accurately with the formula CfiH13N02. . The successive crystalline deposits, obtained by pro¬ gressively concentrating the solutions from which the leucine, etc., had been partially separated, were composed of amido-valeric and amido-butyric acids, together with two new, definite, crystallizable products, tyroleucine C7HnN02(CnH2n-3N02) and a body corresponding with the formula C6H11N02(CnH2n-1N0o) : the quantity of tyroleucine obtained was about 60 or 70 grams from 10 kilograms of albumin. Tyroleucine presents itself as a white crystalline deposit of chalky aspect, possessing scarcely any taste, but soluble in about 20 parts of water at 15°. It melts and decomposes at 240°, breaking up into a white sublimate and a volatile oily base having an odour of radish ; it leaves behind an abundant yellow vitreous residue. The analysis of the chloroplatinate of the base gives it the formula of collidine, C8HnN, and of the vitreous residue the formula C14H]8N.,0„ ; the decomposition of tyroleucine may therefore be taken as proceeding thus — 2(C7HuN02) = C14H18N.,0o + 2Ho0 2(C7HuN02) = C02 + C8HnN + C5HnN02 Collidine. Amido-valeric acid. from which one is led to suppose tyroleucine to be a com¬ pound of amido-valeric acid with a body of the formula C9HnN02, the latter differing from tyrosine only by an atom of oxygen. This is rendered more probable by the fact that tyrosine, when heated under similar conditions, breaks up into C02 and a base, C8H14NO, which differs from collidine only by an atom of oxygen. Among the homologues of leucine, amido-valeric and amido-butyric acids were met with in quantity, but amido- propionic acid in very small proportion only ; its presence, however, was clearly and distinctly made out. To the compounds of the formula CnH2n + 2N02, the author gives the generic name leucines, and to those of the formula C^H^-iNO^ the names leucetnes {n~d). Both seem to be frequently produced by the splitting up on crystallization of bodies of the formula CmH2mN204. (wi — 10 or 12); however by repeated fractional crystal¬ lization the compound Cl2H24N204 gave always the same analytical numbers, from which it is fair to suppose that it has an independent existence. The supposition is more¬ over strengthened by the fact that similar results were obtained with the lower homologues containing 11, 10, 9, and even 7 atoms of carbon. For these latter bodies, the name glucoproteins has been adopted, on account of their sweet taste ; they crystallize less easily than the leucines, especially the lower terms * they are very soluble in water, but almost insoluble in cold absolute alcohol ; hot alcohol of 90 per cent, however dissolves them with ease. Another substance resulting from the decomposition of albumin, which is produced in important quantity, is a-, yellow viscous body obtained by precipitating certain mother-liquors from which leucines have been crystallized by ether. Dried at 120°, it is converted into a transparent amorphous mass, which on analysis gives numbers com¬ prised between the formulae C5H9N02 and C4H7N02, very often sensibly approximating to the formula C9H16N204 ; it appears in fact to be constituted in great part of butyric leucine with an admixture of some superior homologue. The longer the action of baryta on albumin is continued,, and the more concentrated the solution, the greater is the- proportion of leucines and of leuceines formed, whilst under the contrary conditions, the intermediate bodies, or glucoproteins, constitute the bulk of the fixed residue, representing the initial terms of the hydration of albumin ;; under all circumstances caproic leucine and tyrosine appear to be the ultimate terms of the decomposition. The mechanism of the reaction would therefore appear to admit of the following explanation. The albuminoid molecule losing ammonia and carbon as carbonic, oxalic,, and acetic acids, and assimilating water, is converted into a comparatively simple mixture of glucoproteins,, CnH2nN204, containing as its principle term C9H18N204: by the prolonged action of baryta and a high temperature^ these glucoproteins split up partly into leucines and leuceines, and partly into double compounds formed by the union of glucoproteins and leuceines with the leucines. The leuceines may perhaps be regarded as amido-acids- of the acrylic, or of an isomeric series. They reduce ammoniacal silver nitrate on warming, and are attacked by bromine in the cold with formation of HBr and an. acid of formula CnH2n~1N03. In the analysis of the fixed residue, the ratio of nitrogen to oxygen is never- rigorously 1 : 2, but there is always a slight excess of oxygen, so that the ratio is nearer 1 : 2T or 1 : 2’3 ; this difference indicating the presence of small quantities of non-nitrogenous compounds, or of bodies in which the atomic relation of nitrogen to oxygen is greater than 1 : 2.. A careful examination for such bodies among the crystal¬ line deposits resulted in the detection of a few grams of an acicl from 1 kilogram of albumin, offering a composi¬ tion very close to that of glutamic acicl, C5H9N04, and a. smaller quantity of a second, whose composition was that of glutamic acid minus water, C6H7N03, which has been called gluthnic acid. Judging from their amount, these- acids play but a secondary part in the constitution of the August 9, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 105 mixture resulting from the decomposition of albumin : the .acids, on the other hand, which are capable of being •extracted in reasonable quantity from the insoluble barium salts, do not exhibit a constant composition ; they appear to be residues of a progressive decomposition, and to be susceptible of being resolved by the continued action of baryta into a mixture of leucines and oxalic acid. Without following all the steps by which the author succeeded in tracing the presence of the various bodies which are met with in small proportions as constituents of the fixed residue, and modify slightly the ratio between the nitrogen and oxygen, we may sum them up as follows : — 1. Traces of succinic and lactic acids. 2. Tyrosine. 3. Amido-acids of the type of CnH2n-1N03 glutamic and aspartic acids. 4. Amido-acids of the type OnH2u— 3N03 glutimic acid. 5. Amido-acids of the types CmH2m-4N206 and CnH2n-1N03. 6. Intermediate compounds of the type CmH2mN205. The principle, which is the most constant among the ^products of the decomposition, and whose proportion is the most easy to determine on account of its sparing solubility, is tyrosine. The maximum quantity obtained of this body was 3*5 per cent. ; if, therefore, one molecule of albumin reacts in the formation of one molecule of tyrosine, it points to the approximate molecular weight 181 -5500 for the former, since ■— — - = 3*3. An expression of ODUU the form CO40H387N65075S3 corresponds with a molecular weight equal to 5473, which satisfies the conditions involved in the determination of the sulphur and tyrosine, as well .as the results ef elementary analysis, thus — Mol. C. H. N. 0. S. weight. Experiment 52*57 7*16 16*6 2T8 1*8 — Theory . . 52*62 7*07 16*62 21*94 1*75 5473 Again, taking as the basis of calculation the experiments made with 5 or 6 pai*ts of baryta at 180°, the centesimal proportions of the products were — N as NH3. BaC03. BaC204. H4C20.. 4*03 17*6 11*0 4*6 which corresponds very fairly for 5473 parts of albumin with — NU3. H2C204. C02. h4c2o2. 16 mols. 4 mols. 3 mols. 4 mols* Erom these numbers the following equation may be written, which moreover would give a fixed residue of 99*6 per cent. : — C240H387N65O75S3 + 60H2O = 16NH3 + 4C2H204 + 3C02 + 4C2H402 + C221H435N49O105 -f S3. Deducting a molecule of tyrosine from the formula of the fixed residue, we have C2l2H4o4N48O102, which approxi¬ mates very closely to an expression of the form CnH2nN02, differing from it only by a slight excess of oxygen. By taking in this manner the series of experiments made with different proportions of baryta and at different temperatures, a number of equations may be written, in all of which the theoretical composition of the fixed residue corresponds very closely with that obtained experimentally. There can be no doubt that, during the hydration of albumin, as many molecules of water are assimilated as there are molecules of ammonia liberated ; if then from the proposed formula for albumin we deduct the ammonia, carbonic, oxalic, and acetic acids in the proportion furnished by experiment, less a number of molecules of water equal to the number of molecules of ammonia (add¬ ing as many molecules of water as there are molecules of carbonic anhydride produced, since the latter probably results from the decomposition of urea) we shall have — [16NH3 + 4C2H204 + 3C02 + 4C2H402 — 16N20 + 3H.,0], which leaves C221H341N490581, an expression which corre¬ sponds with the type CnH2n-2NO quite as nearly as that of the fixed residue with the type CnH2nN02, the differ¬ ence on both sides being a slight excess of oxygen. The molecule of albumin therefore resembles that of a body whose formula is as(CmH2m-4N204), where m = 2 n, and undergoes hydration in two distinct steps. At 100°, with a limited proportion of baryta, the grouping fixes a number of molecules of water equal to one-half the number of atoms of nitrogen which it contains, and becomes £c(CmH2m-2N203). The latter, at a higher temperature, can in its turn fix a number of molecules of water equal to the number of atoms of nitrogen which it contains, changing itself to the formula r(CmH2mN204), the final result being the assimilation of as many molecules of water as the albumin contains atoms of nitrogen. Albumin is then probably an imido-derivative , which by hydration changes into a mixture of amido-derivatives. To return to the observed relation between the ammoniacal nitrogen evolved, and the carbonic and oxalic acids produced, it is noticeable that two molecules of ammonia are disengaged for each molecule of acid generated ; the simplest reaction which could account for such a phenomenon would be to suppose that the ammonia results from the hydration of urea or cyanamide and oxamide, a supposition which acquires a much greater degree of probability when it is shown that a very large majority of animal nitrogenous principles, when similarly decomposed, yield a quantity of ammonia which is pre¬ cisely the amount that should be furnished by the carbonic and oxalic acids produced at the same time, supposing the whole to result from the reaction above mentioned. The author has examined wool, hair, ossein, isinglass, gelatin, goat’s hair, silk, fibrin, and chondrin, in all of which the above relations held good. Summary. — It has been shown : 1. That the mixture of fixed principles derived from albumin by hydration contains only amido-derivatives. 2. That these derivatives can be divided into two unequal portions, one, the weight of which is about 16 to 18 per cent., containing the sub¬ stances in which the ratio of nitrogen is 1 : 3, or 1 : 4, or 2:5; the most important fraction of this portion con¬ sists of acids of the formula CnH2n-1N04, CnH2n-3, N03C2nH4n-4N20G, and CnH2n-1N03, the intermediate term being only a molecular combination of the terms CnH2n— 3N03 and CI1H2n-1N03. The second portion, which constitutes |ths of the residue, may be represented by the formula x(CnH2nN204) with a value for n a little less than 9. According as the limit of hydration is attained, the products formed belonging to the type CmH2mN204 (where m is a multiple of n) are progressively resolved into simple bodies belonging to the same apparent type ; these again are resolved into bodies of the type CnH2nN204, which in their turn are resolved into leucines, CuH2n + iN02, and leuce'ines, CnH2n-1N02. This inter¬ pretation is not affected by the presence of more highly oxygenated acids in the fixed residue, since they may be considered as derived from any of these bodies by substitution of O for H2. To the memoir is added an appendix, in which are given the results of some analyses made of fixed residues obtained from different sources. Albumin purified by Wurtz’s method was substituted for crude albumin ; the baryta was precipitated in one instance by carbonic anhy¬ dride, in another by carbonic anhydride and sulphuric acid, and in a third by carbonic anhydride, ammonia, and ammonium carbonate, but no important differences were observable in the products of decomposition. It was also found to be a matter of indifference whether the hydration of the albumin was begun by the action of other agents less energetic than baryta, such as dilute sulphuric acid ; on completing the action by the intervention of baryta as usual, the same result was obtained as in the previous instances. A fixed residue obtained by the action of baryta was subsequently boiled for twenty-four hours with a 20 per cent, sulphuric acid, but its composition was not found to be sensibly affected. In a final operation, conducted with the usual reagents, the action of baryta upon albumin was carried to its extreme limit. The fixed residue was carefully examined to see whether any substance was produced under such 106 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [Augu t 9, 1879. condition, which had not been found, or had been over¬ looked in previous experiments : nothing, however, was met with but the usual mixture of leucines and leuceines. The molecular weight of the various glucoproteins still remains to be determined. THE REMOVAL OF FIXED OIL FROM COLCHICUM SEED.* BY EMIL L. BCERNER. With the view of determining upon a suitable solvent for the fixed oil contained in colchicum seed, one which, while removing all of this for the preparation of the fluid extract objectionable constituent, would yet dissolve out none of the active principles of the drug, the following course was pursued, viz. : — Separate portions of the drug, in powder No. 60, were treated by percolation, the one with gasolin, a second with petroleum benzin, and a third with stronger ether, U. S. P. ; the several percolates resulting were carefully evaporated until entirely free from the odour of their respective solvents. The fixed oil thus obtained was of a density not unlike that of castor oil at a summer temperature, of a fatty odour, a pale olive colour, and very slightly bitterish taste in the case of the gasolin and petroleum benzin residues, while that exhausted with ether was of a some¬ what darker colour and more decidedly bitter. To ascertain whether the oil, as removed from the powdered seed by the process described, contained any colchicia, portions of each of the three residues were severally agitated with distilled water acidulated with hydrochloric acid, the liquids filtered and the filtrates treated for colchicia, as follows : — That from the ethereal preparation gave, with concen¬ trated nitric acid, concentrated sulphuric acid, hydro¬ chloric acid and carbonate of potassium, a lemon yellow coloration ; a slight white flocculent precipitate with tannic acid ; a denser, nearly white, flocculent precipitate with iodo-hydrargyrate of potassium ; a heavy, kermes coloured, flocculent precipitate with iodine and a tur¬ bidity with chlorine water — the solution becoming yellow upon the subsequent addition of water of ammonia — while the filtrates from the gasolin and petroleum benzin residues, when treated in exactly the same manner, gave no precipitates with any of the reagents mentioned, only a slight yellow coloration being produced by concentrated sulphuric acid. Upon subjecting a portion of fixed oil separated from a fluid extract prepared by the process of the U. S. P. of 1870 to the same treatment as was pursued in the fore¬ going experiments, a slight yellow coloration was pro¬ duced with each of muriatic, nitric and sulphuric acids. Ether, because of its solvent action upon colchicia, as well as on account of its greater cost, as compared with the other solvents used, was considered objectionable, and was accordingly abandoned for any further experiments. Gasolin and petroleum benzin having, apparently, about equal solvent powers, the former of these was preferred as being more readily expelled from the drug after perco¬ lation with it, and before subjecting to the usual treat¬ ment for the preparation of the fluid extract. Upon treating a larger quantity of the powdered seed with gasolin, in the manner above described, an oil answering to the description of that first mentioned was obtained to the amount of 9'05 per cent, and having a specific gravity of *922 at 60° F. A portion of this oil, tested for the presence of col¬ chicia, in the same manner as that obtained by a previous experiment, gave exactly the same results. A suitable solvent having thus been found for the fixed oil contained in colchicum seed, its removal from the drug, before treatment in the usual manner for the fluid extract, would seem practicable, as the product * From the ‘ Proceedings of the American Pharma, eutical Association,’ 1878. obtained, unlike that of the officinal process, which separates the oil upon standing and necessitates its removal, is a perfectly clear preparation. The advantages resulting from such a removal of the oil would seem to be quite evident, inasmuch as the fluid extract would not then be loaded with it, and would present a much more elegant appearance than does the officinal preparation. This extract being miscible with water, might perhaps even be used hypodermically by evaporating off the alcohol and diluting with water. The more evident may seem these advantages when it is remembered that nothing is sacrificed medicinally and only a slight expense incurred for gasolin, the quantity necessary for exhaustion being scarcely twice the weight of the powder to be treated with it. Aware of the difficulty of powdering colchicum seed, the writer sought to remove the oil by maceration before grinding, but was unsuccessful, as only a part can be extracted in this way. Though having no direct bearing upon the query here attempted to answer, the writer would state that, in availing himself of the suggestions offered in Mr. J. U. Lloyd’s papers, published on pages 408 and 409 of last year’s ‘ Proceedings,’ by omitting the use of glycerin and finishing the preparation with a mixture of three parts- alcohol and one part water, a more satisfactory pre¬ paration was obtained than when the Pharmacopoeia formula was strictly followed. ACETOUS PERFUMES.* 1. Concentrated Aromatic Vinegar. Concentrated Acetic or Glacial Acetic Acid . 8 ounces. Oil of Lavender (English) .... 2 drachms. Oil of Rosemary . 1 drachm. Oil of Cloves . b ,, Gum Camphor . 1 ounce. 2. Hygienic Vinegar. Strong Brown Vinegar .... 2 pints. Gum Benzoin . 1 ounce. Oil of Marjoram . \ drachm. Brandy . . 1 pint. Oil of Cloves . 1 drachm. Oil of Lavender (English) ... 1 ,, 3. Toilet Vinegar (d la Violet). White Wine Vinegar .... 2 pints. Extract of Cassie . h pint. Extract of Orris | „ Extract of Rose (triple) . . . . I „ 4. Toilet Vinegar (d la Hose). Extract of Rose (triple) . . . . A pint. Dx-ied Rose Leaves . 4 ounces. White Wine Vinegar . 2 pints. 5. Vinaigre de Cologne. Eau de Cologne . 1 pint. Glacial Acetic Acid . 1 ounce. 6. Cosmetic Vinegar (Pi esse and Lnbin's). Concentrated Vinegar .... 1 ounce. Gum Benzoin . 3 ounces. Alcohol, Pure . 1 quart. Balsam of Peru . 1 ounce. Oil of Neroli . 1 drachm. Oil of Nutmegs . i „ 7. Vinaigre a la Rose. Glacial Acetic Acid . 1 ounce. Oil of Rose . ^ drachm. 8. White Wine Vinegar . Filter best ordinary brown vinegar through animal charcoal till perfectly white. * From New Remedies , July, 1879. AugBt 9, 1879. J THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 107 §fmpaqttlital Jmtptl. - ♦ - SATURDAY, AUGUST 9, 1879. A MEDICAL TITUS OATES (?). When a ready writer is at a loss to find a subject on which to exercise his skill his pen is a weapon especi¬ ally liable to be engaged in the mischief which a nursery poet tells us is the inevitable consequence of idleness. At the present day, when the possession of a free press oilers such abundant scope for literary taleht, it is scarcely surprising that we should now and then meet with cases of this kind, referable partly to the inexorable necessity of filling a certain number of columns and partly to the exigencies of the young lions of the press. But besides the lack of subjects to write about there are other circumstances which tend to bring about the same mischievous exercise of literary skill, and chief among these is the love of sensation which prevails with so large a portion of the public. People demand highly spiced literary food for their daily entertainment, and if divorce cases or breaches of privilege do not afford the requisite 'pabulum the young lions must draw upon their inventive faculties, and manufacture something which will for the moment appease the desire for excitement. We have recently been made acquainted with a flagrant instance of this kind through the kindness of a friend who has forwarded to us some pages of the Philadelphia] Medical Times , of June 7. The managers of that journal appear to be impressed with the idea that correspondence between different parts of the civilized world is desirable in order to make the manners and customs of one country known in other countries for mutual benefit, and with that object, as we presume, they publish in the number we now refer to a “ London letter.’7 The writer of that letter is an English medical man resi¬ dent in London, and it might reasonably have been expected that he would have something to say in his letter that would be useful or instructive, and in that sense worth being read by his American colleagues. The first glance, however, at the London letter of the Philadelphia Medical Times serves to dispel such an idea, and it becomes evident that the London correspondent has either been in a state of literary destitution, without any suitable subject to write upon, or he has perversely devoted himself to the production of a sensational story no more fit to appear in the pages of a scientific journal than the ghost stories which school bo}^s delight to find in our illustrated papers at Christmas time. The article we refer to commences with the state¬ ment that amidst the varied "relations of the pro¬ fessions there is none more curious than that of consultants and chemists, and especially chemists’ assistants. Then it is remarked that any possi¬ bility of collusion between the two is not at first sight very apparent, and that of course it is natural for assistants in chemists and druggists’ shops to recommend any consultant who is either known to them by repute or in the habit of sending his patients to the shops in which they serve. It is also admitted that chemists and druggists’ assistants have some ojyportunity in common with other folk of seeing whose names most commonly occur in medical journals in connection with certain specialties, and it is lurther admitted that any reply upon such grounds to the inquiry, “ Who is the man to consult lor so and so?” would be quite unobjectionable. So far then chemists and druggists or their assistants may be grateful to the London correspondent of the Philadelphia Medical Times for the liberty he is pleased to accord them. But, as he says, “ the matter does not stop here he has penetrated deeper below the surface ; and then he proceeds to lay before his American readers a description of what he pretends to have discovered. No one yill deny that many persons who do not know anything about consult¬ ants, but yet wish to consult some one for an ailment or disease, think the readiest and surest plan is to drop into some well-known chemist’s shop and ask who is the best man to see f r such a complaint. What could be more natural than for the person whose daily avocations make him familiar with the repute of certain medical practitioners to be asked for such information ? But the unsuspecting and con¬ fiding inquirer who does so is thoroughly “ sold and liookwinked ” by the quiet and “ innocent looking youth who when thus interrogated immediately raps out some consultant’s name” — at least that is the statement made in the letter published in an Ameri¬ can medical journal for the information of medical men across the Atlantic. This instructive correspondent next proceeds to relate how this is done and the statements he makes in that part of his letter are of such a nature that we will not venture to give them in abstract. After referring to the importance attached by English people to a physician’s prescription and the anxiety to have it carefully dispensed, the writer says : — “ The youth to whom the prescription is handed looks at it sardonically, and remarks contemptuously, ‘ F or piles ? ’ Of course the patient is very much taken aback at this, and exclaims, ‘ Bless me ! no ! For bronchitis ! ’ The youth has achieved his end, and the surprised and startled patient’s confidence in the man he has just consulted is irrevocably shaken. That he should have got a prescription for piles when he went about his bronchitis, comes to him as a very unpleasant revelation. It is not only that he has spent his money in vain, but that he has been cheated into risking his health, and possibly ruining his constitution, by having the wrong medicine prescribed; the thought is very shocking that he should thus have been trifled with by ignorance or carelessness. In the midst of his pertur¬ bation he gasps out, ‘Who is the best man to consult about brochitis ? ’ The placid answer is, ‘ Oh, Dr. Vitreous Tendon, of course!’ The deed is done; an assassin-like stab has been given to the reputation of an unoffending man, and the young scoundrel chuckles at the skilful man¬ ner in which the blow has been delivered. The patient 108 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 9, 1S79. goes away wrathful and indignant that the doctor he had just consulted should have treated him so badly, and vows with genuine earnestness that he himself will never consult him again ; ‘No; nor, by Jove, shall anybody I know consult him either, if I can help it ! ’ Away he goes circulating the story among his acquaintances, getting this unlucky physician a bad name so far as he can. Now, this is certainly diabolical wickedness ; and the apparent artlessness with which it is done disarms all suspicion. That the chemist’s assistant had any motive other than of saving him from taking a medicine unsuitable if not possibly dangerous, any ulterior design in his apparently friendly action, never crosses the victim’s imagination. It is the apparent ii nocence of the scound- relism which is at once it strength and its protection. The utter guilelessness of the ingenious surprise of the young man behind the counter ‘ fetches ’ the victim, who never detects the trap that is so skilfully laid for him. That that young villain, that moral assassin, is ‘ squared,’ there can be no doubt ; and possibly enough he does not realize the injury he is doing to the unoffending physician to whose reputation he has delivered a nasty stab ; but he does it all the same, and as effectually as if his conduct had been inspired by the most deliberate malice. He wished to put a fee into the pocket of Dr. Vitreous Tendon, that was his main object ; we will hope, for the sake of humanity, that he does not realize the injury he is doing to another man. A less indecent but equally effective plan is for the chemist’s assistant to have three names on a card, and when asked about whom to consult, he declares his inability to decide, until the question is put home to him, ‘ Whom would he consult, if necessary ? ’ He then mentions the lowest name on the list. The ap¬ parent absolute bonafides of this crafty villain allays any possible suspicion of ‘ a plant ’ which might arise in the mind of the sold individual, and the inquirer goes away perfectly satisfied.” As regards the motive for such conduct as that described in the above paragraph very little more than insinuation is ventured upon by the writer of the letter who evidently perceives that some of the dirt he seeks to cast at chemists and druggists must stick to his brother physicians, for we are told there are two kinds of physicians, one like the writer who says “ Take your prescription to any good chemist,” without recommending anyone in particular. Then the phrase “secret understanding between pre¬ server and dispenser ” is slipped in and a story is told of a particular medical man being recommended by a chemist and druggist for syphilis, stricture, hemorrhoids, heart disease and every ill that man is heir to. In this way the suggestion of a dishonest influence is conveyed to the minds of the reader, and then we have the remark “ By what underground communi¬ cation the chemist’s assistant is rewarded for his “ share in the unholy compact has not yet transpired; “ but it is quite obvious some arrangement does “exist.” It is almost suggested that the chemist and druggist is the prime mover of the arrangement as well as the only culpable participator in it, for it is anticipated that “ doubtless the chemists’ journals will res. nt what is here written,” and “will cast doubts on the statements here made.” No such resentment is referred to, however, as being likely to come from the medical journals, for the charge is adroitly made only to affect chemists and druggists and “ black sheep ” in the medical profession. Perhaps a reason for this is to be found in the letter itself, since the writer says he has heard of a chemist and druggist’s assistant who stated that “There was no such medical man in London.” Such ignorance may be more reprehensible than we are disposed to consider it, but it certainly does not justify the designation of the assistant as a “youth¬ ful young sprig of rascality.” It is very difficult to come to any conclusion con¬ cerning such an effusion as the one we have above dealt with. Charity forbids us to entertain the latent suspicion that it is an ingenious mode of ob¬ taining the “ bold advertisement ” so much sought after by professional as well as trading men. But we cannot any the more regard it as wholesome criticism since it lacks the truthfulness and temper¬ ance that should always characterize a critic. More likely it is the result of an illusion provoked by the circumstance of being unknown to some chemist and druggist’s assistant, and that the writer brooding on this indignity has conjured up the form and semblance of a foeman worthy of his steel and madly possessed by this idea has made himself as ridiculous as Cer¬ vantes’ lanky and lugrubrious knight in attacking a harmless and inoffensive windmill. BRITISH PHARMACEUTICAL CONFERENCE. By the courtesy of the Secretaries we have been favoured with the following list of papers to be read at the meeting of the British Pharmaceutical Con¬ ference, at Sheffield, August 19 and 20 : — 1. Report on the Aconite Alkaloids. C. R. A. Weight D.Sc., F.C.S. 2. The Capacity of Different Organs to Absorb and Retain Arsenic in Cases of Chronic Poisoning. N. P. Hamberg, M.D., H.M.P.S. 3. The Growth and Development of Ergot. W. W. Stoddart, F.I.C., F.C.S. 4. The Application of Chloroform in the Testing of Drugs. Louis Siebold, F.I.C., F.C.S. 5. Note on the Specific Gravity of Liquids. Louis Siebold, F.I.C., F.C.S. 6. Proximate Analysis of the Rhizome of Zingiber officinalis. J. C. Thresh, F.C.S. 7. Soluble Essence of Ginger. J. C. Thresh, F.C.S. 8. The Polarimeter and its Use in Pharmacy. C. Symes, Ph.D. 9. The Assay of Commercial Disinfecting Powders containing Carbolic Acid. A. H. Allen, F.I.C., F.C.S. 10. Notes on Petroleum Spirit. A. H. Allen, F.C.S. 11. Cinnamon Bark. Mr. A. H. Jackson. 12. The Gelatinization of Tincture of Kino. Mr. T. H. Bamford. 1 3. Amylic Alcohol and Amylic Nitrite. Mr. Dott. 14. Extraction of Pilocarpine. Mr. A. W. Gerrard. 15. Anhydrous Air as a Therapeutic Agent. G. A. Keyworth, F.C.S. 16. Quillaia Bark, its Chemical Composition and Use in Pharmacy. Mr. H. Collier. 17. Note on Aricine. John Eliot Howard, F.R.S. 18. The Chemistry of Chaulmoogra. J. Moss, F.I.C. 19. The Determination of Water in Iodine. E. Davies, F.I.C., F.C.S. 20. The Presence of Tannin in Gentian Root. E. Davies, F.I.C., F.C.S. Augusts, 1879.] the pharmaceutical journal and transactions. 109 transit (jtions #J t| t ftaniutcmtiral MEETING OF THE COUNCIL. Wednesday, August 6, 1879. MR. GEORGE WEBB SANDFORD, PRESIDENT. MR. GEORGE FREDERICK SCHACHT, VICE-PRESIDENT. Present — Messrs. Atkins, Bottle, Gostling, Hampson, Hills, Mackay, Bimmington, Savage, Symes, Williams and Woolley. The minutes of the previous meeting were read. Previous to their being signed, Mr. Woolley said he wished to make an observation on two matters arising out of the minutes. The first referred to the conversation which took place respecting the Sale of Food and Drugs Act Amendment Bill. A friend of his had commiserated with him on the rap over the knuckles which it was thought he had received in the matter, but he did not want to say anything about that, except that he had never seen the Bill before. The im¬ portant point was that this Bill was ordered to be printed on April 29, but it did not seem to have ever been brought before the Law and Parliamentary Committee, and carefully considered. He was not one of those who complained of the Adulteration Act, which in many in¬ stances had been of great advantage, but that it needed amendment was evident from the new Act having been passed, and as this bore so directly on the trade, the Com¬ mittee ought at all events to have gone through it and seen .whether some improvements could not be suggested. For instance, it was a great hardship that an innocent man could never recover his costs. He should like to ask how it was that the Bill had not been brought before the Committee. . The President thought it had been many times men¬ tioned at that table or in the Committee. Mr. Woolley thought it ought to have been brought regularly before the specially appointed Committee for considering such questions, and gone through in a proper way. Mr. Bimmington said the Bill in the first place only referred to the strength at which spirit should be sold, and excited very little interest even in parliament. The President said that one gentleman who was examined before the Committee, the government analyst from Somerset House, called on him respecting a matter, which had been incidentally referred to and which would have affected chemists; that was mentioned at the Council table on more than one occasion. There never was any attempt on the part of the promoters of the Bill to intro¬ duce any clause which would specially affect chemists and druggists, and he had never heard a suggestion made by. the Committee or Council that alterations were re¬ quired. So far as Mr. Woolley had been in error, he thought all the members of Council were in the same boat, for none of them were aware of the last line in the Bill when the matter was discussed at the last meeting of Council. Mr. Woolley said the other matter he wished to refer to was the increase of salary voted to the Editor and Sub-Editor at the last meeting. He thought this was a matter of sufficient importance to appear in the report of the Council proceedings. The President said the members of the Society were apprised of any alterations in these matters by the balance sheet issued preparatory to the annual meeting. Mr. Williams said this matter arose out of the pro¬ ceedings of a Committee. If they were to publish all the reports of the Committees as well as the Council it would become a very serious matter. Unless it were made a practice to publish the reports of the Committees, such matters could not very well be published. Mr. Hampson thought Mr. Williams’s view was scarcely accurate, because the report very frequently contained a statement of what had been done by the Committee. For instance, in the General Purposes Committee, certain prosecutions were agreed to, and a notification of this effect was frequently made. Mr. Atkins was disposed to support the view taken by Mr. Woolley, though perhaps it would be discussed better at a later period in connection with a motion to which Mr. Symes had given notice. The minutes were then confirmed. The India Museum. The President said the Council was aware that it was the intention of the Government to break up the India Museum, and the Curator, Mr. Holmes, on going over it was informed that if the Society made applica¬ tion in all probability it would obtain certain things which were very interesting. He (the President) there¬ upon wrote to the Honourable E. Stanhope on the sub¬ ject, and had received a reply, promising to lay the matter before the Secretary of State for India in Council for his consideration, so that he hoped, if any distribu¬ tion of this collection were made, the Society would be thought of. The Vice-President wished it was within the province of the Council to express a disapproval of the course which the Government had thought fit to adopt. A more unfortunate resolution he could hardly conceive than that of scattering this fine collection of Indian products. Diplomas to Pharmaceutical Chemists The following, being duly registered as Pharmaceutical Chemists, were respectively granted a Diploma stamped with the seal of the Society Alcock, Frank Harris. Allan, James Henry. Betts, George. Bird, Henry. Dutton, Hugh Odard. Grimble, Albert. Horton, Thomas. Lapthorn, George. Lomax, Alban Edward. Mayger, William John. Nowell, Barnes. Pisani, Orestes Victoriano. Porter, Thomas. B.atcliffe, Henry Norman. Bemfry, Samuel Alfred. Bussell, James Lawson. Shirley, Stephen Shillito. Smithson, Thomas Henry. Yillar, Arthur. Elections. members Pharmaceutical Chemists. The following, having passed the Major examination and having tendered their subscriptions for the current year, were elected Members of the Society : — Alcock, Frank Harris . Stoke-on-Trent. Allan, James Henry . Stockton-on-Tees. Betts, George . Scottow. Horton, Thomas . Burton-Overy. Lapthorn, George . Southsea. Lomax, Alban Edward . Birkenhead. Mayger, William John . Northampton. Nowell, Barnes . London. Batcliffe, Henry Norman . Malmesbury. Smithson, Thomas Henry . Thirsk. Villar, Arthur . Taunton. The following, an Associate of the Society before 1842, having tendered his subscription for the current year, was elected a Member of the Society : — Ashmall , George . . . . W allingf ord. Chemists and Druggists, The following, who was in business on his own account before August 1, 1868, having tendered his subscription 110 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 9, 1*79. for the current year was elected a “ Member ” of the Society : — Moore, Francis Samuel . . Castle Cary. ASSOCIATES IN BUSINESS. The following, having passed the Minor examina¬ tion, being in business on their own account, and having tendered their subscriptions for the current year, were elected “ Associates in Business ” of the Society : — Davis, Henry John . Newbury. Hulland, Charles Richard . Framlingham. Pickles, Walter . Dewsbury. ASSOCIATES. The following, having passed the Minor examination and tendered or paid (as Apprentices or Students) their subscriptions for the current year, were elected “Asso¬ ciates ’ ’ of the Society : — Ballard, Frank English . Aylesbury. Bourne, Charles M. K . Wolverhampton. Bown, John Quinton . Nottingham. Bridge, George Edward . Maidstone. Carter, Francis . London. Clerke, William Burdett . Leamington. Crow, William . ..Berwick-on-Tweed. Crowther, Arthur . Tickhill. Davies, Thomas . Bridgend. De Peare, John Thomas . Spalding. Drew, Henry William . Southwark. Feaver, William . Truro. Green, William James . Yeovil. Harburn, Alfred . London. Hope, Arthur Peach . U ppingham. Humphreys, Griffith . Corwen. Kelly, Francis Charles . Great Yarmouth. Lindewald, Wilhelm Edvard ...London. Macaulay, William Henry . Rotherham. Manning, Alfred . Strood. Morgan, John Daniel . ..Swansea. Morris, David . Cardigan. Olden, Loathan . Romsey. Peck, Frederick William . Cambridge. Plattin, Henry Ramm . Fakenham. Powell, William . Swansea. Ratcliffe, George . London. Rossiter, Thomas Edward . Tiverton. Roughton, William . Loughborough. Selleck, William Robert . Bovey Tracey. Shrivell, Frederick WilliamE. .. .Hadlow. Smith, John Thomas . Spalding. Stableforth, John William . London. Stedman, Walter . West Mailing. Taylor, James Bennett . Bedford. Thompson, Arthur Stevens . Barking. Topliss, Walter George . Wainfleet. Wild, George Frederick . Hyde. Willis, Henry James . London. Willis, Joseph Darrington . Northampton. Wimshurst, Frederick . Southborough. Wood, Robert . Loughborough. Wyatt, Charles Frederick . Old Brompton. APPRENTICES OR STUDENTS. The following, having passed the Preliminary examina¬ tion and tendered their subscriptions for the current year, were elected “ Apprentices or Students ” of the Society : — Baron, Richard Edward . Alderney. Barnett, Henry Frederick . Uttoxeter. Bruce, Alexander Gibb . Brough ty Ferry. Butler, Ernest F. N. G . London. Callow, Ewan . Douglas. Clayton, Walter Flower . London. Cubey, Robert Hewison . South Shields. Edwards, Henry . Liverpool. Ellisson, Charles . Barnsley. Farthing, Thomas William . Devonport. Gibson, Matthew Henry . Gooch, Stephen Leeds . Green, Frederick . Grey, William . Grigs, Emerson Fenwick G. Grim wade, Edward H . Hopper, James Henry . Hutchinson, John . Inman, Thomas Leonard Joye, Joseph . Knox, John . Lawton, Ernest . McEwan, David . Melhado, Howard Emanuel Moore, Joseph Edward .... Morris, Harold Edward Morgan, Richard . Owen, William . Pawson, Frederick Thomas. Pumphrey, Arthur . Roberts, Griffith . Robinson, Thomas . Shepperd, William J ohn Taylor, George . Whaley, Thomas Cope . Young, John . .Matlock Bath. .Reepham. .London. .Blyth. .North Shields. .Croydon. .Ryde. .Kendal. . .Batley. ..Southport. ..March. ..Barnsley. ..Perth. ..Ramsgate. ..Bristol. ..London. ..London. ..Towyn. ..Banbury. ..York. ..London. ..Wigton. ..Newport, I. of W. ..Fairfield. ..Barnsley. ..Arbroath. Several persons were restored to their former status in the Society upon payment of the current year’s subscrip¬ tion and a fine. The names of the following persons who have severally made the required declarations and paid a fine of one guinea were restored to the Register of Chemists and Druggists : — William Halket, 74, Talbot Road, Bayswater, London, W., Richard Hammersley Forrester, 2, Merthyr Road, Abergavenny. Addition to the Register. The Secretary reported that — Thomas Farren Humble, Abergavenny, having made a statutory declaration that he was in busi¬ ness before the passing of the Pharmacy Act, 1868, and this declaration having been duly supported by medical practitioners, his name had been placed on the Register. Reports op Committees, finance. The report of this Committee was received and adopted, and various accounts ordered to be paid. BENEVOLENT FUND. The report of this Committee included recommenda¬ tions of the following grants : — £10 to the widow of a registered chemist and druggist. £15 to aid in the education of the younger son of the widow of a registered chemist and druggist. The appli¬ cant has had two previous grants. £10 to the widow of a pharmaceutical chemist. Appli¬ cant had a grant of £15 in September last. £17 for continuing the education of an orphan in an establishment in Belgium for another year. This case stood over last month for further consideration. £5 to a registered chemist and druggist who recently sustained an accident and had a grant of £10 in Feb¬ ruary last. A letter was read from Annie Isherwood, stating that she had a very happy and comfortable home. > The Committee had declined to entertain one applica¬ tion, as it appeared that the applicant was of intemperate habits. The report and recommendations of the Committee i were received and adopted. August £>, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. Ill LIBRARY, MUSEUM AND LABORATORY. The report of this Committee included the usual report from the Librarian, to the following effect : — Attendance during the day: highest, .26, lowest, 10, average, 20 ; evening, highest, 17, lowest, 7, average, 10. Circulation of books: town, 154; country, 49; carriage paid, £1 5s. 9 \d. He had also reported the following donations to the Library : — Cooley (A. J.), Cyclopteuia of Practical Receipts, 6 ed., 1879, pt. 18. Prom Messrs. Churchill. Dragendorff (G.), Bemerkungen in Bezug auf die Nachweisbarkeit des Strychnins in verwesenden Cadavern, 1879. Mandelin (K. F.), Chinincitrater, 1879. Scheibe (E.), Darstellung und Beschreibung der Borcitronensiiure and ihrer Salze, 1879. From Professor Dragendorff. Tilden (Dr. W. A.), Theory of Solution and Crystal¬ lization, being the substance of a Lecture given to the Bristol Naturalists’ Society, 1878. From the Author. Pifferi (G.), Breve cenno e preparazione di un nuovo composto di chinina, 1879. From the Author. The Committee recommended that the usual letters of thanks be forwarded. The Committee recommended the purchase of the fol¬ lowing books for the Library : — General Fund : — Allen (A. H.), Introduction to Commercial Organic Analysis; vol. i. Cyanogen Compounds, Alcohols, Phenols, Acids, etc., 1879. Hermann (L.), Elements of Human Physiology, translated by A. Gamgee, 2 ed., 1878. Neubauer (C.), and J. Vogel, Guide to Qualitative and Quantitative Analysis of Urine, translated by W. 0. Markham, 1863. Squire (P.), Pharmacopoeias of London Hospitals, 4ed., 1879. Unity of Medicine, its Corruptions and Divisions: by F.R.C.S., 1858. Yvon (P.), Traite de l’Art de Formuler, comprenant un abrege de pharmacie chimique, etc., 1879. llanbury Fund : — Baillon (H.), Natural History of Plants, vols. 1-5, 1871-8, and vol. 6 when published. Siebold and Zuccarini, Flora Japonica, 1825-70, 2 v., 150 coloured plates. Wallich (N.), Plantte Asiaticte rariores, 1829-32, 300 coloured plates. The Curator had reported the attendance in the Museum to have been as follows : — During the day, average, 17 ; evening, average, 6. He had also reported the following donations to the Museum : — Ninety-five specimens of drugs used in the United States and eleven specimens of active principles, com¬ prising three specimens of Podophyllin; two speci¬ mens of Hydrastine, one precipitated and the other crystallized; Cimicifugin ; Berberine; Sulphate, Hydrochlorate and Hypophosphite of Berberine; and Nitrate of Sanguinarina. From the Phila¬ delphia College of Pharmacy. Specimens of Paracoto Bark and the following sub¬ stances obtained from it: — Paracotoin, Hydroco¬ tom, Dinitro-coton, Leucotin, Oxyleucotin and Dibenzoy 1* hydrocoton. * Coto bark and Cotoin, Sulpho-carbolate of Quinine, Quinine, Chinamine, Aricine, Cusconine, Paricine; * With regard to these substances Dr. O. Hesse states that leucotin, oxyleucotin and dibenzoyl-hydrocoton are ethers of the hexatomic alcohol, hydrocoton; that dinitro-coton stands to hydrocoton in nearly the same relation as chinone to hydrochinone ; and that the formation of dinitro-coton is the origin of the peculiar coloration of leucotin and oxy¬ leucotin and dibenzoyl-hydrocoton when these are touched with strong nitric acid. and the following active principles of Opium, Laudanine, Cryptopine, Cryptopine Oxalate, Pseudo Morphine. Also the following liquids : — a. Paracotol, CigH240. 1). Paracotol, C18H40O2. c. Paracoto], C28H40O2. Paracoto-oil. The particulars concerning these bodies are promised in a future communication. From Dr. O. Hesse. Specimens of the undermentioned essential oils, in illustration of a paper read by Mr. W. E. Bush at the Students’ Association: — Almond, Aniseed, Bergamot, Camomile, Caraway, Cassia, Cinnamon, Cinnamon leaf, Citronelle, Cloves, Copaiba, Coriander, Cubebs, Dill, Geranium (Spanish), J uniper, Lavender (ExoticandMitcham), Lemons, pure, Mustard, Mustard (artificial), Neroli, Nutmeg, Orange peel, Origanum, Parsley, Pep¬ permint (Mitcham), Petit Grain, Pimento, Sassa¬ fras, Rose, Rosemary. From Messrs. W. J. Bush and Co. The Committee recommended that the usual letters of thanks be forwarded, with aspecial one for the Philadelphia College of Pharmacy. The Curator had reported that a shark’s skin had been sent by Mr. Fresson of Demerara, but as it was not suitable for the Society’s Museum, it was suggested that it should be offered to some society collecting natural history specimens. Professor Bentley had reported that his class was pro¬ gressing favourably, and had kept up better at the gardens than on any former occasion. Professor Redwood had stated that there was no special matter to report in reference to his class. It had been ordered that the Library and Museum be closed in the evenings during the months of August and September. A letter had been submitted from an assistant residing in the country, requesting that the regulation requiring the guarantee of a member for the safe keeping and due return of books might in his case be relaxed. The Com¬ mittee did not deem it advisable to make any exceptions to this rule. The Committee recommended that the Librarian should attend the annual meeting of the Library Association to be held in Manchester in September, and that ten guineas be allowed for his expenses. The Sub-Editor had reported that the manuscript of the Index to the Journal from 1868 to 78 was complete, and the Committee had directed that an estimate be obtained for printing the same. Professor Redwood had reported that he had made considerable progress with the continuation of Jacob Bell’s ‘Historical Sketch of Pharmacy,’ which he thought would make about 300 pages octavo, and he had sug¬ gested that the earlier part should be put into the hands of the printer in order that the manner in which he was continuing the work might be submitted to the Com¬ mittee for approval. The Committee recommended that estimates should be obtained for printing the book in the form suggested by the Professor. The Committee also recommended that the Editor and Sub-Editor should attend the meeting of the Pharma¬ ceutical Society of Germany at Hanover, and that £20 be allowed to meet expenses. The President said it would be noticed that the Han- bury Fund was exhausted, and he believed it had been as well laid out as possible. Mr. Rimmington asked if the index could be bound with the previous index. Mr. Williams said it would be a different size, owing to the change in the size of the Journal. Mr. Bottle said the same point had occurred to his mind, and he should like to know if it was a matter of 112 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 9, 1879 necessity that the index should be of the same size as the Journal. The Assistant-Secretary said the estimate had been obtained and all arrangements made on the footing of the index being the size of the Journal. Mr. Williams hoped that a sufficient number would be printed both of the index and of the “ Historical Sketch,” to allow of sending a copy to each member and associate of the Society. Mr. Hampson wished to know if the manuscript of the “ Historical Sketch” were complete. He thought it would be premature to make arrangements for printing before it was complete. Mr. Williams did not see how the Council or the Committee could sit in judgment on the work of two literary gentlemen to whom it had been entrusted. Mr. Rimmington said he should certainly object to giving these things away broadcast. The cheaper any¬ thing was made, the less it was appreciated. If people would not give Is. or 2s. for a copy of the “ Historical Sketch,” it was quite clear they did not want it, and to give them what they did not want was simply to waste. The same with regard to the index. It was certainly worth 2s. to anyone who had the J ournal, and if a person had not the set it would be entirely thrown away. Com¬ paratively few kept their Journals and bound them, perhaps not one in one hundred. The President thought the time had hardly arrived for settling these details. The present question Avas, who should print it. The Vice-President thought it was premature to discuss the printing of the “ Historical Sketch ” until the manuscript was in a more complete condition. The Council did not knoAV how much of it Avas ready. He thought it would be better to send the whole matter back to the Com¬ mittee. The President thought the Council should adopt the recommendation of the Committee that Avhen the “ His¬ torical Sketch ” was printed it should be in the form suggested, of Avhich specimens were submitted. But the Council might suggest to the Committee that the printing should not be commenced until the manuscript was com¬ plete or nearly so. Mr. Williams said the manuscript of the index was quite complete. The question to be decided was whether it should be printed for sale, in which case 1000 copies would be ample, or if copies should be given away, in which case 5000 Avould be required. Some details having been given as to the estimates which had been obtained, — Mr. Woolley thought it would be useless to giveaway the copies of the index. Mr. Mackay said he should not be in favour of giving away a single copy. The Vice-President thought it would be a mistake to distribute these things gratis. This might seem some¬ what different to the opinion he had expressed on a former occasion, but the subject matter was different. When the catalogue of the museum was published he was anxious that it should be given away, because he considered it had a certain educational value in itself ; but this index had no educational value, it was simply a matter of con¬ venience to those Avho Avanted to use the index. The “ Historical Sketch ” too, ought, he thought, to be paid for by those Avho desired to possess it. Mr. Atkins asked if a via media could not be adopted, to give the index to any person who applied for it. Mr Williams said this index was far superior] to the one appended to each volume. Mr. Atkins said it seemed to him rather strange to charge for an index to a book which was supplied to al. members in return for their subscriptions. He thought perhaps it would be wise to give it on application. The President said that was the regulation with regard to the catalogue. Mr. Savage said he was at first in favour o : adopting the same rule, but on further consideration he thought those Avho AA7anted the index should pay for it; that which was a small matter individually became a i.arge matter collectively. Mr. Williams could not agree with what seemed to be the opinion of the Council, and thought it was a pity it had undertaken the publication of the “Historical Sketch” if this was to be the result. It would be mere waste of money to bring out books the circulation of which it was mown would be very limited if they were sold. When the matter was initiated he trusted it would have done much good by arousing an interest in pharmacy and in the Journal, by members receiving the index for the last ten years. If members had been foolish enough to throw their numbers away they Avould probably regret it. He should not have taken so much interest in the matter unless he had thought the Council was going to carry it out in the liberal manner which it had lately talked so much about encouraging. Mr. Gostling sympathized very much with the remarks of Mr. Williams. It Avas quite possible more energy and enthusiasm might be put into the members if something Avere put before them. There was a work undertaken for the benefit of all, so that anything that had been published in the Journal for ten years might be referred to, and he thought it should be sent to every member even if it were in paper covers. The President said he was informed that the original proposition was that a copy should be sent to every member. The better plan would be to refer it back to the Committee to ascertain. Mr. Rimmington asked how many catalogues had been applied for. The Secretary said very few. The Vice-President asked what was the object of the Librarian attending the meeting of the Libra¬ rians’ Association ; and on what ground the Committee recommended the expenditure of ten guineas in this Avay. The President said when the Society of Librarians Avas established the Librarian attended the meeting at the request of the Committee. He was a member of the Association, of course as representing the Society, and he had quite satisfied the Committee that it would be an advantage that he should attend the conference. Mr. Williams said it was not a question of pharmacy but Jo f libraries. The Society’s was a large public library, and he thought it essential the Librarian should be in correspondence and communication with other librarians, and in fact be a part of the commonwealth of librarians. He was very glad to find that the Society’s Librarian took so much interest in the matter. Mr. Savage desired to endorse all that Mr. Williams had said. It Avas very important that the Council should be in possession of all the information accessible with regard to the arrangement and management of libraries in general. The President added that the same thing was done last year. Mr. Williams thought it Avas very desirable in the interest of the Journal that the Editor and Sub-Editor should attend the Conference in Hanover. The Editor came into personal contact with many gentlemen from Avhom he might afterwards receive communications which Avould be of interest. It was then resolved that the printing of the “Historical Sketch” be deferred until the completion of the work, and that further estimates be obtained for the printing of the index, and that the Committee report again to the Council. The remainder of the report of the Committee was adopted. Mr. Bottle having remarked that the shark’s skin referred to in the Committee’s report would be acceptable to the Dover Museum, it was unanimously resolved on the motion of Mr. Williams that it be presented to that ’ body. August 9, 1879. J THE PHARMACEUTiCAL JOURNAL AND TRANSACTIONS. 113 HOUSE. The Secretary had submitted to this Committee a table showing the quantity of gas consumed each year during the years 1873-79, by which it appeared that the late increase still continued. Professor Redwood had attended and stated the result of experiments he had made, showing that there was no leakage anywhere, but that there was a greater day pressure than formerly, and to this circumstance, together with the more abundant supply which the companies had recently provided, he ascribed the increased consumption. The Committee recommended that the gas used in the laboratories should pass through a separate meter. Mr. Atkins said he had mentioned on a former occasion that he had had his gas meter repaired ; but the result did not answer his expectations, for he found the consumption for the last quarter almost double that of the corresponding quarter in last year. He was satisfied, having taken great pains about it, that he burned less gas, and he therefore consulted the gas manager who told him that the com¬ plaint was very general, and his explanation was, that owing to complaints of insufficient pressure, the plant had been largely increased, and there was more than double the pressure and therefore more gas passed through the burners. The manager advised him to regulate the supply at the meter, and not allow more gas to pass than was requsite for a due supply to the burners ; and having done so he was satisfied there would be a reduction. Mr. Woolley said Mr. Atkins was quite right. He himself had Carnaby’s apparatus in use, which could be put up in any convenient place, and by it he could regu¬ late the supply at the meter down to a single burner if required. The report of the Committee was received and adopted. The Confekence. The Vice-President, as representing the British Pharmaceutical Conference, said last year delegates were appointed to that body from the Council and it would be considered an honour if the same course were followed now. It was moved by Mr. Mackay, seconded by Mr. Bottle, and carried unanimously — “ That the President and such members of the Council as are present at the meeting of the British Pharma¬ ceutical Conference be requested to represent the Society as delegates.” general purposes. This Committee had received the reports from the Professors as to the prize examinations, and opened the motto envelopes to ascertain the names of the successful candidates. Botany and Materia Medica. Professor Bentley had reported that six candidates had presented themselves for examination for the bronze medal and certificates of merit, all of whom passed a satisfactory examination and three were worthy of special distinction. With regard to the Terminal examination for the silver medal and certificates of honour and merit for the session 1878-9, fourteen candidates had presented themselves, being rather over the average for the last five years, and the answers of the majority were highly credit¬ able. The number of students attending his class during the last session had been notably in advance of last year, and the general attendance and uniform good conduct of the students, both at Bloomsbury Square and at the Botanic Gardens, proved that the school maintained its high character for order, progress and discipline. Herbarium Prize. Professor Bentley had reported that four collections had been sent in. The first in order of merit, that of Mr. Perkins was eminently worthy of the silver medal, it containing over 800 specimens. The second contained nearly GOO and reflected great credit on Mr. Walker, to whom he recommended that the bronze medal be awarded. The third also showed great merit and he recommended that a certificate of merit be awarded to Mr. Norman. Chemistry and Pharmacy. Professor Redwood had reported that in this class, the general conduct and industry of which had been very satisfactory, there were eleven competitors for the silver medal and certificates, the first six having furnished papers to which he had attached values entitling the authors to some marks of distinction. In the competition for the bronze medal and certificates there had been seven competitors, five of whom had acquitted themselves well, the first two remarkably so. Practical Chemistry. Professor Attfield had presented a report showing the number of marks obtained by the first eight out of seven¬ teen competitors. Council Examination Prizes. Mr. Moss on behalf of Mr. Southall and himself had presented a report of this examination, giving the mottoes and number of marks of the seven competitors. Legal and Parliamentary. The Solicitor had presented to the Committee his usual report. It stated that William B. Mason, 14, Arcade, Briggate, Leeds, had, prior to the hearing of the case against him, paid the amount of penalty and costs into Court, amounting to £5 8s. 3d. He had also reported that the Special Com¬ mittee on the Medical Act had concluded its sittings, and that no point had arisen in which the Society was specially interested. Various cases of alleged infringe¬ ment had been brought before the Committee, five of which were recommended to be placed in the Solicitor’s hands with a view to taking proceedings. The considera¬ tion of the question of the sale of patent medicines had been deferred. The Council considered in Committee, as usual, some of the cases of alleged infringement, and ultimately the report and recommendations of the Committee were re¬ ceived and adopted . Prize Awards. The following awards were made on the recommenda¬ tion of the General Purposes Committee : — Chemistry and Pharmacy. [Five months’ course.] Bronze Medal . Certificates of Merit . . Thomas Horton. I Henry William Drew. \ William Herbert Hyatt. j George Wale. ( William Inchle Gulliver. Silver Medal Certificates of Honour Certificates of Merit . Thomas Horton . Edward Jarrett Eaton. ( James Henry Allan. Frank Harris Alcock. Henry William Drew. [Ten months’ course.] James B. Lillie Mackay. Botany and Materia Medica. [Five months’ course.] Bronze Medal . . Certificates of Merit Thomas Horton. Henry William Drew. William Inchle Gulliver. [Ten months’ course.] Silver Medal . Certificates of Honour James B. Lillie Mackay. Thomas Horton. Frank Harris Alcock. Henry William Drew. Edward Jarrett Eatoa. 114 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 9, 1M9 Certificates of Merit f James Edward Williams. | William Inchle Gulliver, j Fred. Wm. Ed. Shrivell. ] James Henry Allan. | Percival C. Powrie. Isaac Leach. Practical Chemistry. Silver Medal . Frank Harris Alcock. Fredlc. Walm sley W ar rick Robert John Price. j Edwaid Jarrett Eaton. j James B. Lillie Mackay. Certificates of Merit . ; William Inchle Gulliver. j BeresfordF. H.Maudson. I Thomas Horton. Bronze Medals Botanical Prize. Silver Medal . Thos. Frampton Perkins. Bronze Medal . Charles Walker. Certificate of Merit . : . William Francis Norman Council Examination Prizes. Pereira Medal ( silver ) ; and Books value £5, presented by Mr. T. H. Hills. Frank Harris Alcock. Pharmaceutical Society's Medal ( silver ) ; and Books value £3, presented by Mr. T. H. Ilills. Marshall Leigh. Pharmaceutical Society's Medal ( bronze ) ; and Books value £2, presented by Mr. T. II. Ilills. Henry Allen. Jacob Bell Memokial Scholarships. The Committee appointed to award these scholarships, subject to the approval of the Council, reported that the examination was held on July 1, when eleven candidates competed, viz., in London, 8 ; Brighton, 1 ; Manchester, 1 ; Nottingham, 1. The mottoes adopted by the two candidates who had obtained the highest number of marks were “Alere flam- mam n and “ Minimus,” and the Committee recom¬ mended that the scholarships should be awarded to the competitors who had used those mottoes. The Committee had opened the envelopes bearing those mottoes, and the successful candidates were found to be — William Elborne and John Thomas. Superintendents of Examinations. The following list of Superintendents and Deputy- Superintendents of written examinations for the ensuing year was agreed to : — Aberdeen . . , Birmingham Brighton Bristol Cambridge Canterbury Cardiff . Carlisle . Carmarthen Carnarvon . . Cheltenham Darlington.. Douglas, Isle of Man Dundee . Edinburgh . Exeter . , Glasgow . , Guernsey Hull . Inverness J ersey Davidson, Charles. Southall, William. Gwatkin, James Thomas. Stroud, John. Deck, Arthur. Bing, Edwin. Ilollway, A. B. Thompson, Andrew. Davies, R. M. Lloyd, William. Smith, Nathaniel. . Robinson, James. Brearey, William A. Hardie, James. Mackay, John. Delves, George. Kinninmont, Alexander. Arnold, Adolphus. Bell, Charles B. Galloway, George R. Ereaut, John, jun. Lancaster . Leeds . Lincoln . Liverpool . London . Manchester . Newcastle-on-Tyne Northampton . Norwich . Nottingham . Oxford . Peterborough . Sheffield . Shrewsbury . Southampton . Truro . Worcester . York . Bagnall, William Henry. Reynolds, Richard. .Maltby, Joseph. Abraham, Thomas Fell. .Taylor, George Spratt. Wilkinson, William. Martin, Nathaniel H. Bingley, John. Sutton, Francis. F itzHugh, Richard. Prior, George T. Heanley, Marshall. .Ward, William. Cross, William Gowen. Dawson, Oliver R. Percy, Thomas B. Virgo, Charles. Davison, Ralph. Deputy-Superintendents of Examinations. Aberdeen . Kay, James Petrie. Birmingham . Churchill, Walter J. Brighton . Gwatkin, James Ross. Bristol . Tucker, Robert Lewis. Cambridge . Church, Henry James. Canterbury . Amos, Daniel. Cardiff . Sanders, W. J. Carlisle . Hallaway, John. Carmarthen . Davies, R. M., jun, Carnarvon . Hughes, Richard. Cheltenham . Barron, William. Darlington . Hutchinson, Rev. E. Douglas, Isle of Man . Brearey, Arthur W. Dundee . Kerr, Charles. Edinburgh . . Ainslie, W illiam. Exeter . Lake, J. H. Glasgow . Davison, Thomas. Guernsey . Collenette, Adolphus. Hull . Baynes, James. Inverness . . . . . Galloway, George. Jersey . Ereaut, John. Lancaster . Hall, William. Leeds . . Smeeton, William. Lincoln . Battle, John Scoley. Liverpool . Shaw, John. {Bremridge, Richard. Knapman, John W. Holmes, Edward M. Manchester . . . Wilkinson, George. Newcastle-on-Tyne . Stuart, Charles E. Northampton . ....Mayger, W. D. Norwich . Corder, Octavius. Nottingham . Rayner, John. Oxford . Thurland, Thomas Henry. Peterborough . Buckle, Frank George. Sheffield . Maleham, H. W. Shrewsbury . Cross, William G., jun. Southampton . Spearing, James. Truro . Fiddick, Thomas. Worcester . Lunn, Thomas. York . Sowray, Joseph. Reports of the Council Proceedings. Mr. Symes moved a resolution of which he had given notice, though he had slightly modified the wording of it to this effect : — “ That when any matter is considered in Committee during the Council proceedings, a record of the fact be stated in the Journal report of the Council pro¬ ceedings, except under some special circumstances where the Council by vote decide that it is un¬ desirable.” His idea was that everything taken into Committee should be reported in name, not necessarily in detail, but that the Council should still have the power by a special vote to decide that it was undesirable that some special matter should be reported. He scarcely knew August!*, 187 1 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 115 whether it was necessary to say much in support of the motion, but he had brought it forward under the full impression that there was a necessity for something of the kind. The first impression perhaps on reading it would be that it implied nothing which was not now provided for, and he did not wish to propose any innovation ; but it occurred to him that on several occa¬ sions the Council had gone in and out of Committee, and the members had hardly known where they were ; it had occurred that day and he was informed it had occurred frequently before, which rather showed that when the Council went into Committee it should do so more for¬ mally. The motion also suggested that at present the report was not as full as it might be, that it was not adequate to the importance or commensurate with the amount of work which the Council did. Its constituency had a right to be fully informed of the method of pro¬ cedure by which it was governed, and not only members of the Society, but chemists and druggists, for whom it legislated, had a right to be informed, not merely of the skeleton of its proceedings, but to have something more of the substance of them. It was complained sometimes that the members of the calling did not take as much interest in the proceedings of the Society as they might do, and the latter retaliated, when they had the opportunity, by saying that the Council did not con¬ sider their interests. It occurred to him that one means by which the Council might more fully do its part, would be by more deeply interesting these gen¬ tlemen in what it was doing. There was scarcely a subject considered there, of however little importance it might appear, the bearings of which had not some im¬ portance for persons who were concerned in the business in other matters. A report in the Journal would help to excite that interest which he was desirous of creating. They had been told that day that a matter which was not reported would appear in the balance sheet at the Annual Meeting, but if it were of sufficient interest to be stated there, it would be of more interest if it were found in the ordinary proceedings. The Annual Meeting lasted but a few hours, and when on the last occasion a gentleman got up and asked for figures, they all felt that he was straining a point too far in asking for such details. Probably he would not have asked for any figures at all if he had been able to read in the ordinary reports what had been done with the money of the Society. The Council met to conduct the business of the Society and to expend the money obtained from individual members. If those subscriptions came from wealthy men, it would not so much matter how they were expended, provided it was done wisely and not extrava¬ gantly, but many of these subscriptions came from men in a small way of business to whom it was really a tax, and they looked to get some equivalent for it. Their connection with the Society was the equivalent and they ought to have as mucli as possible for their money. By making the reports more full this would be done. The most interesting part of the work was generally done in Committee, and that the members of the Council should keep the most interesting part to themselves and hand over the least interesting part to their constituents, seemed a proceeding which it was not necessary to argue upon. Mr. Atkins seconded the motion. He did not pre¬ cisely know how it could be carried out, but he had had a strong conviction in his own mind for years that the constituency had a right to know what went on. He had known interesting questions occupy the Council for an hour or more, and yet in the country he had been asked why they had not been mentioned. He knew there might be a difficulty often as to what should be elimi¬ nated, but it had occurred to him that there was a middle course which r-!id not require a great amount of discrimi¬ nation to find, viz., to intimate that at a particular stage the Council resolved itself into Committee and discussed such and such a matter. Names need not be mentioned or any particulars which would frustrate legal action, if legal action were to be taken, but the fullest report consistent with prudence ought to be furnished. Certainly the unjust criticism which took place outside ought to be disarmed, that after spending four, five or six hours at the Council Board there was but a very sparse report of what had occupied the best intellects there for a number of hours. He hoped some means would be found of complying with the very reasonable suggestion contained in the motion. The President said he had no objection to the motion, the modification introduced having entirely taken the sting out of it. There was a very good example of un¬ authorized reporting in the Chemist and Druggist with regard to the proceedings last month, for as there put it was altogether a misrepresentation of the facts. Mr. Hampson said the Council had the cure in its own hands. If there had been an unofficial reporter present he would not have fallen into the error. He should be in favour of another reporter being admitted. The President said the inference expressed in the words he had quoted could not be drawn from the report which appeared in the Journal. Mr. (Jostling- said he had felt very strongly the injustice of the report which appeared in the Chemist and Druggist, and on reading it he thought he could not vote for Mr. Symes’s motion. What the Council did last month was perfectly consistent with the interests of the trade, viz., not to publish what was said with regard to the prosecution of co-operative stores generally. As the motion was now altered, he could vote for it with plea- ‘ sure. There was a good deal of point in some of the remarks made as to extending information amongst members as to what was done in Committee. The President, having read the Journal report, repeated that it contained nothing to justify what appeared in the Chemist and Druggist. Mr. Rimmington said he should like to know who communicated that to the Chemist and Druggist. The President said he was quite unable to answer that question. Mr. Williams said he had thought over this subject a good deal, and had long been of opinion that it would be well if the reports of Council meetings were fuller and more complete; but the present motion did not seem to him practical enough to be of real service, and he should like to see it modified so as to make it really practical instead of a mere expression of opinion. He thought he could see how the Council could get out of the difficulty. He could quite understand the difficulty which the reporter felt sometimes in knowing what to report and what to omit, and of course when the Council went into Committee he did not take down anything of the discussion, though frequently it turned out tha* there was no reason why the discussion should not be reported. He thought the best plan would be to have full notes taken of all transactions, whether in Council or Committee ; but that before being published they should be submitted to some one, either an individual or a Committee, who should take the responsibility of what was fit to be published, or rather of what it was necessary to omit. In his own opinion the President for the the time being would be the most suitable to undertake this office. If any check were required it could be afforded by the original notes with the alterations being placed before the next Council meeting. He thought it would be found in practice that very little alteration was required. Mr. Hampson asked if the doctoring would be done in the Editor’s room or there. Mr. Williams said certainly not in the Editor’s room. He should object to placing any paid servant of the Society in such a position. He only wished to prevent the publication of matter which would be decidedly objec¬ tionable, but to have as much unobjectionable matter as possible published. Mr. Mackay said he quite agreed with the principle 116 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 9, 1879. of the motion, for he had always argued that the pro¬ ceedings of the Council as reported were not satisfactory to the outside members. He had always felt that they were far too short, but he also felt that if the motion as originally drawn were carried, and everything that tran¬ spired were put into print the members of the Council would be running their heads against a post. As an ad¬ dition had been made to the original motion that difficulty was avoided, and therefore he could vote for it. He could see, however, that there would be some difficulty in carrying it out in detail. But Mr. Williams’s suggestion, he thought, was about the most unpractical he had ever heard ; he did not think the man was born who would take the office of President if he had to do what Mr. Williams suggested — to be reponsible, first for reporting what took place, and next to be called over the coals a month after¬ wards for having either published or omitted something he ought not. He had more than once advocated, and would again throw out the suggestion that the Editor should have a seat at the reporter’s table, and be repon¬ sible for giving a full account of the Council’s proceedings. Let him be furnished with full notes of what took place .and be responsible for what appeared. Mr. Bottle said, with every desire to follow up Mr. Symes’s wish to have a full account of all that occurred at the Council table, he could not help feeling that the mode in which the motion had now been put was peculiarly unfortunate, inasmuch as it would require that the Coun¬ cil should publish to its constituents that it had voted that a certain something should not be communicated to them. The members were to consider a certain thing n Committee and then in Council resolve that what they had done should be kept secret. He would rather put it the other way and let it be the vote of the Council that such and such a thing should be communicated. Mr. Symes said he was pleased to find that the opinion of the Council was so entirely with him, as he had indeed expected ; but he should like to reply to some of the remarks which had been made. If the report of the proceedings were a verbatim one there would be no difficulty in the mattei', because everything uttered would be reported ; but the Council now threw on the reporter a very serious responsibility. Mr. Mackay said the Pre¬ sident would not think of undertaking such a respon¬ sibility, and yet at every meeting the Council threw on the reporter the responsibility of sifting out what he thought desirable to report. Now the President, being a chemist and druggist, would have to some extent a long -education in what was required by chemists and druggists to be known; but the reporter was a professional re¬ porter, who could hardly be expected to be able to select such matter as would be interesting to chemists and druggists throughout the country, and it was most unfair to Iiim to cast this duty upon him. He had nothing to complain of as to the manner in which the reporter did his duty, but he was put in a false position. As to that report in the Chemist and Druggist, the first thing which occurred to him was that some one had been breaking faith in communicating it, but the second reflection was that no one had done so, but that it was a deduction from the official report, and it illustrated his position most forcibly. It showed that by giving these meagre reports and half sentences more danger was really introduced than a full report of the discussion would have done. There seemed a good deal of mystery .about the reporting. One gentleman at the last meeting, who had been a member of Council ten years, said he did mot know what became of the report when it left there, — whether the reports published were the same as the reporter furnished or not. He had no wish to suggest that the report was altered ; he hoped it was not ; but there seemed to be a vast amount of ignorance prevailing as to whether the reporter handed to the Editor certain matter which he was to publish, or whether the Editor had any right to alter it or cut it down. He quite agreed that it was desirable to make some suggestion of how the • reso¬ lution should be carried out. He had had some difficulty in maturing a plan; but it occurred to him that the vote could be taken in Committee in connection with the subject under discussion, so that if it were decided not to publish it, the vote would be part of the matter which would not be published, but if the majority of the Council thought it well to publish it, the fact might be stated. That would be a healthy thing too, as it would give the constitituency an opportunity of seeing how far the Council was disposed, and which of its members were, disposed, to give them a larger share of the information which they thought they ought to possess. The only thing he would suggest was that when the Council went into Committee — and it ought to go in and out of Com¬ mittee more formally than it often did — then it should ask the reporter to state what he proposed to report as the result of the discussion, or it might suggest to him what he should report. That seemed the only solution: that the Council should decide on the spot what should be reported, the form in which it should be reported, or how much and also what was not to be reported. The Vice-President wished to know in what respect the motion, if carried, would alter the existing state of things. Mr. Symes said it made a rule for what was now optional. The motion was then put and carried. The President stated that according to usual custom no business beyond what was absolutely necessary would be brought forward at the September meeting, so that only a quorum, which could be obtained in London, need attend. Report of Examinations. July , 1879. ENGLAND AND WALES. Candidates. Examined. Passed. Failed. Major, 9th . . .... 8 4 4 ,, 10th . . .... 8 2 6 ,, 16th . . .... 11 6 5 „ 17th . . .... 10 6 4 — 37 —18 —19 Minor, 9 th . . .... 18 10 8 „ 10th . . .... 21 9 12 „ 11th . . .... 27 8 19 „ 16th . . .... 18 10 8 ,, 17th . . .... 17 12 5 „ 18th . . 16 10 —127 — 65 —62 Modified, 9th . 4 • • • • * 3 1 — — — 168 86 82 Scotland . Candidates Examined. Passed. Failed. Major, 22nd . . .... 3 1 2 Minor, 22 nd . . .... 13 6 7 „ 23rd . . .... 13 5 8 „ 24th . . 7 5 — 38 —18 —20 Modified, 24th . .... 3 3 0 — — — 44 22 22 _ — Preliminary Examination. Candidates. Examined. Passed. Failed. 365 . . 184 181 August 9, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 117 6 Certi6cates in lieu of the Society's Examination had been received : — 2 from the College of Preceptors. 2 from the University of Cambridge. 2 from the University of Oxford. Erratum. — Page 93, column 1, line 31, for Macdonald Robert, Edinburgh, reac l Macgregor, Donald, Edinburgh. fvccjetUngs of Societies. SOCIETY OF ARTS. The History of Alizarin and Allied Colouring Matters, and their Production from Coal Tar.* BY W. H. PERKIN, F.R.S. (Continued from paye 98.) The anthracene, after the treatment with naphtha, should contain about 50 per cent of pure anthracene. It is not distilled in the same manner as for the preparation of dichloranthracene, but is heated in a retort, or more generally, in a semicircular iron pot. The lid of this is furnished with a safety valve, and also a steam pipe. The receiver consists of a tank, the top of which is sometimes made of canvas ; a perforated tube passes round this tank near the top, which is supplied with water and produces a gentle spray, which facilitates the condensation of the anthracene. When working this arrangement, a known weight of anthracene is introduced into the iron pot, which may be called a subliming pot, and is heated until it is quite fluid. Steam is then blown in ; this carries the anthracene vapour forward with it into the receiver, when both are condensed by the spray of cold water. The condensed anthraceneis found in a wet and extremely finely divided state, very suitable for oxidation. Its weight is known from the amount of washed anthracene used in the operation. Other methods of condensing the anthracene and steam are used, but the above, I believe, is the most common. Obtaining the anthracene in this finely divided state is a great improvement upon the old process of grinding it. The oxidation of this anthracene is performed much more slowly than it was at first, the solution of potassic bichromate and sulphuric acid being kept more diluted. In this way the amount of oxidizing agent required is smaller, less being expended on the useless impurities. In carrying out this operation in its present form, the potassic bichromate is first dissolved in water, and the wet anthracene well mixed with it. The requisite quan¬ tity of sulphuric acid, previously diluted with water, is then added by degrees, and the mixture kept gently boil¬ ing for ten or twelve hours. A Korting’s air injector should be used with the steam, to keep up the agitation of the mixture. The oxidized anthracene, which h^s the appearance of a yellow powder, is then collected in woollen bags, thoroughly washed, pressed and dried. The amount of potassic bichromate used is regulated principally by the proportion of pure anthracene con¬ tained in the product to be oxidized. Pure anthracene requires about 1‘66 times its weight of potassic bichro¬ mate to convert it into anthraquinone. The amount used by different manufacturers varies, some employing a little under two parts, others more ; but no fixed quantity can be given, as the amount required evidently must differ with the kind of impurities contained in different parcels of anthracene, some of these oxidizing more freely than others. It is remarkable that so little answers the purpose, and shows that the anthracene takes up the oxygen more greedily than the impurities. Too much oxidizing agent is injurious. The anthraquinone is still very crude, and needs puri¬ fication. The method that has been most generally adopted consists in treating it with concentrated sulphuric * From the Journal of the Society of Arts. acid. This dissolves tbe anthraquinone, but does not act upon it. The impurities, however, become soluble in water, being converted in sulpho acids, etc., so that after treating the crude anthraquinone in this manner, and then mixing the product with water, nearly pure anthraquinone is alone precipitated. This method of subliming anthra¬ cene, oxidizing it and purifying it with sulphuric acid, was first proposed, I believe, by H. Caro. The process is carried out as follows : — The crude anthraquinone is placed in large iron, semicircular, cast iron pots, capable of holding a ton or more of the product. These are fur¬ nished with a steam jacket, and a strong stirrer, also of cast iron, and worked by machinery, the blades being arranged so as to work the mixture constantly upwards. These pots are charged with crude anthraquinone and sul¬ phuric acid, in the proportion of one of the former to three or four of the latter ; the steam is turned on to the jacket,, and the mixture heated with continuous stirring for about twenty-four hours. The product is then run into shallow leaden trays, and exposed to the air, or the trays are arranged in a proper chamber, the atmosphere of which is kept moist by steam. In this way the acid becomes- very gradually diluted, causing the anthraquinone to cry¬ stallize out. In a proper chamber this occupies about two days. The crystalline product is boiled with water, and then washed by decantation, any anthraquinone found in the liquors being afterwards collected. The anthraquinone is then pressed and dried, and is usually so pure as to contain over 95 per cent, of anthraquinone. Instead of placing it on trays and allowing it to crys¬ tallize by the absorption of moisture by the sulphuric acid, some manufacturers pour it at once into water, boil the resulting mixture and wash it in filter presses. During the last year or two, a modification of our ori¬ ginal process has been coming into use ; I mean the process- of sublimation. The modification principally consists in assisting the process by passing superheated steam through the subliming retort, and this is important. Although anthraquinone is such a remarkably stable body, we often noticed that a good deal of loss occurred in our subliming operations, apparently from reduction, and especially if the charges were large, because the}' then required a high temperature continued for a long time, the residues being bad conductors of heat. This re¬ duction is probably caused by the steam and anthraqui¬ none coming in contact with the iron of the retort. To avoid this loss, it is evident that the temperature should not be higher than absolutely necessary, and the charge should also be spread out in thin layers, so as to be quickly volatilized. The anthraquinone vapour and steam may be condensed in a similar manner to anthracene. The- sublimed anthraquinone, which is pressed and dried, has to be still further pmified. It will be remembered that we used coal-tar naphtha for the purpose, but the sulphuric acid process above described, I believe, is now always employed. The large amount of chrome alum liquors produced in. the manufacture of anthraquinone has always been a source of trouble to manufacturers, their dark green colour and acid character making them objectionable in the drains, and chrome alum being of itself of very limited consumption. Processes, however, have been now devised for working this up again into a chromate. There is, however, another residue which, so far as I am aware, has not been turned to account, and that is the- acid liquors from the purification of anthraquinone, con. sisting of sulphuric acid, sulpho acids, etc., and it is difficult to see to what use they can be turned, especially as such enormous quantities are produced, probably over 3,000 tons of sulphuric acid being used in this process yearly. If the original process of crystallizing the sub¬ limed anthraquinone from naphtha were adopted, this difficulty would not exist. In converting the anthraquinone into the sulpho acids,, we at first used Nordhausen sulphuric acid, and heated, the mixture in glass retorts, such as are used in the con- 118 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 9, 1 87P. centration of sulphuric acid, but, owing to the fragility of these vesse's, we were induced to try cast iron pots. These we found to answer very well, though not quite so well as glass. On account of the expense and difficulty in getting Nordhausen sulphuric acid imported into this country — few vessels liking it as a cargo — we commenced ^working with ordinary sulphuric acid. We usually employed four or five parts of this to every one part of anthraquinone, and heated the mixture up to 270° — 280° C. The anthra¬ cene, as it sublimed from the operation, was put back into the acid. The sulpho acids produced in this way were treated with lime, etc., just as those obtained from di- chloranthracene, and alreadv described. I find we employed this process principally in our works until the middle of June, 1870. We then began to work on a larger scale than we had hitherto done with dichlor- anthracene, and carried both processes on for a time ; but finding the latter the most economical, partially on account of the ease with which it yielded the sulpho acids with ordinary sulphuric acid, we employed it almost exclusively after a time, although frequently making colouring matter by the other method. As already mentioned, in the early experiments made with anthraquinone, it was noticed that, by reducing the amount of sulphuric acid with which it was heated and keeping the temperature as low as practicable that the colouring matter produced with the resulting sulpho acids gave purples on mordanted cloth more closely resembling those produced with madder than when a large excess of s lphuric acid had been employed. The cause of this was not understood for some time, until it was eventually found out that a monosulpho acid was required to produce alizarin. I believe this was first discovered by Messrs. Meister, Lucius and Brtining, as they were the earliest to send practically pure alizarin into the market. The production of the monosulpho acid of anthra¬ quinone as the chief product, by means of ordinary sul¬ phuric acid, is difficult. I have generally thought it best to work with an excess of anthraquinone, to use a high temperature and only small operations, so that they may be quickly finished. When using ordinary sulphuric acid, every facility should be given for the escape of aqueous vapour which forms, so as to keep the acid as concentrated as possible. At temperatures over 260® C. sulphuric acid commences to oxidize anthraquinone, carbonic anhy¬ dride being slowly formed, so that high temperature should not be long continued. The large quantity of ordinary sulphuric acid which had to be employed to convert anthraquinone into the sulpho acids, and the high temperature which had to be used, causing a certain amount of destruction to take place, evidently showed that it was desirable to employ fuming sulphuric acid in this process. In this country we found it costly, but as it was more readily procurable in Germany, the manufacturers there used it. They were afterwards supplied with a very strong fuming acid from Bohemia, containing about 40 per cent, of sulphuric an¬ hydride. This was prepared, I believe, by distilling the sulphuric anhydride from one portion of ordinary Nord¬ hausen sulphuric acid into another. This very strong acid was found to be without action upon ordinary tinned iron and it is now actually stored in vessels made of that material. Within the last few years a very elegant process'* has been devised by Dr. Alessel and Mr. Squire for the pro¬ duction of sulphuric anhydride and fuming sulphuric acid. Sulphuric acid, when strongly heated, dissociates into steam, sulphurous anhydride and oxygen, thus : — S04H2 = 0H2+0 + S02. * Patented l$th September, 1875, and now manufactured largely in this country by Chapman, Messel and Co. Pro¬ fessor C. Winkler a short time afterwards also showed that fuming acid could be made in this manner. — Dingier , Polgt. Journ., ccxviii., 128 — 139. This decomposition is taken advantage of to give supply of sulphurous anhydride and oxygen in the proportions required, the water being condensed and thoroughly re¬ moved by passing the gases through sulphuric acid. The mixed gases are afterwards combined by passing them over heated platinized asbestos, and thus form sulphuric anhydride. so.,+o=so3. The sulphuric anhydride is then condensed, either alone or in ordinary sulphuric acid. It is remarkable that acid containing 60 to 70 per cent, of anhydride is liquid even below 0° C., acid containing 40 to 50 per cent, is solid, and acid containing 20 to 30 per cent., liquid. By this means fuming acid can be produced in any quantity, and of any strength ; that usually employed in the manu¬ facture of alizarin containing 40 or 50 per cent, of anhy- diide. We thus see that the demand for this acid in the production of artificial alizarin has created a new in¬ dustry" . On treating anthraquinone with fuming sulphuric acid, iron pots somewhat similar to those described for the conversion of dichloranthracene into sulpho acids are used, but, as but little acid vapours escape, very little pro¬ vision need be made for condensing them. In fact, if the anthraquinone be pure, there is no reason why they should not be entirely closed, though, of course, it would be desirable to have a safety valve, or some similar sort of arrangement. The sizes of the iron pots used for treating anthra¬ quinone with fuming sulphuric acid vary, but usually hold from 30 to 40 gallons. They should be fitted with stirrers, especially when required for the preparation of the monosulphanthraquinonic acid, and heated by means of an oil bath. The fuming acid, after being sufficiently heated to render it fluid, is emptied into these pots by means of a syphon, or by piercing the tins, after having placed them over the pots by passing an iron bar right through the top and then through the bottom ; the upper hole thus made serves as an inlet for the air, and allows the acid to flow freely through the hole in the bottom of the tin. When the monosulphanthraquinonic acid is required, a mixture of about one part of fuming acid, containing 40 to 50 per cent, of anhydride, is very thoroughly mixed with from one to one and a quarter parts of anthra¬ quinone. The mixture is then gradually heated up to about 170®, or even to 190°, and kept at this temperature for eight or ten hours, the stirrer being kept constantly in motion. The product thus formed consists chiefly of monosulphanthraquinonic acid, together with a little of the disulpho acid and unchanged anthraquinone. It is then removed from the pots whilst rather hot and diluted with water. The anthraquinone is then separated by passing this solution through a filter press or other con¬ venient arrangement. The monosulpho acid is easily separated from the disulpho acid by converting it into its soda salt, which is difficultly soluble in water, this solvent dissolving only about 5 per cent, at the ordinary temperature. The filtrate is, therefore, nearly neutralized with caustic soda. This causes it to become a thick crystalline mass, which is then thoroughly pressed from the mother liquors ; if required still purer, it can be re-crystailized, or purified by mixing it with about 15 or 20 per cent, of sulphuric acid, diluting with a little water and again pressing and washing with water. This salt forms beautiful small brilliant white pearly scales. When pure, sodic monosulphanthraquinonate gives, on heating with caustic soda and chlorate of potash, prac¬ tically pure alizarin. This operation I have already re¬ marked upon. To make the disulpho acid from anthraquinone, an excess of fuming sulphuric acid is used, about twice as much, or rather more, than in the preparation of the monosulpho acid ; the temperature is also raised (as com¬ bination of the products takes place) considerably higher; August 9, 1879.] THE pharmaceutical journal and transactions. 119 it may be allowed to rise, if a very red shade of colour is to be made, as high as 260°, but should not be taken much higher for any length of time. The product thus obtained is perfectly soluble in water, and, when sufficiently cool, should be removed from the pots and diluted. It may then be treated with lime, as when dichloranthracene has been used, or, as some prefer, neutralized at once with caustic soda. It will then, of course, be mixed with a considerable quantity of sodic sulphate, and, so far as my . experience goes, I have always found that the purer the soda salt the better it worked when treated with caustic soda to convert it into colouring matter. Dichloranthracene, if treated with about twice its weight of fuming acid, containing 25 per cent, of anhy¬ dride, instead of with five times its weight of ordinary acid, works very well, and undoubtedly could be used at once by neutralizing with caustic soda. It is remarkable that the artificial alizarin produced from disulpho acids, prepared from anthraquinone, does not yield such pure shades of colour on mordants as that made with the disulpho acids prepared from dichloran¬ thracene. The latter colouring matter gives the calico printer more delicate pink and red shades, and is, there¬ fore, also much liked by Turkey red dyers ; and, notwith¬ standing it is sent into the market in a weaker form than the corresponding anthraquinone colouring matter, still it demands a higher price. Taking both circumstances to¬ gether, the price it fetches is about 25 per cent. nDre than the colouring matter produced with anthraquiuone. Tne process with dichloranthracene has also the great advantage of always giving an artificial alizarin producing uniform shades of colour, according as ordinary or fuming sulphuric add is used, whereas with anthraquinone it is impossible to tell with certainty the exact tint the product you are making will give. Curiously, Continental manufacturers do not appear to have been as yet successful in manufacturing artificial alizarin from dichloranthracene in quantity, an I what little they have produced in this way does not seem to have been equal in quality to that produced in this country. The dichloranthracene and anthraquinone processes I have described are the only ones employed for the pro¬ duction of artificial alizarin. The method of converting anthracene into sulpho acids, and then oxidizing them so as to form sulpho acids of anthraquinone, although appa¬ rently very simple, does not work satisfactorily, the yield of colouring matter being small. The only process I have found to approach those in use is that patented by Meister, Lucius and Briining, in which mononitroanthx-a- quinone is use I. By this process the only colouring matter dyeing mordants produced is alizarin, and from experiments I made I found the yield of colouring matter to be, on the whole, satisfactory. It is, however, 'obtained in a brown and impure condition. When commencing to supply dyers and printers with artificial alizarin, we kn6w that we ha l to compete with m idder. And although the new product possessed certain advantages, yet we felt it was useless to ask prices rela¬ tively much higher than those of that product, and from the first we endeavoured to act upon this principle.* At first, nearly all the artificial alizarin we made was consumed by the Turkey red dyers of Glasgow and Man¬ chester. The colour at this time contained large quan¬ tities of anthrapurpurin, and therefore produced a more scarlet shade than madder or garancine, and for some time it was used along with garancine, as by this means shades of colour were produced which were far more brilliant than when garancine alone was employed ; but at the same time not too scarlet to be disliked by the Turkey red buyers. Of course, the use of garancine with artificial alizarin has now ceased, and much better results are * The prices given in the Moniteur Scientifique (April, 1879, p. 420), for the years 1870—1873, are very much higher than those ever obtained in this country. obtained by employing a mixture of the red shade and blue shade. Unfortunately, the market is now supplied, not only with the red or anthrapurpurin shade, and blue or pure alizarin shade, but mixtures of these in various propor¬ tions, so that there are more than a dozen shades in the market, and thus much of the manufacturer’s time is occupied with preparing these ; moreover, he is forced to keep a considerable stock of colour on hand. It would appear that on the Continent great difficulties were experienced in the use of artificial alizarin for Turkey red dyeing,* whereas in this country it was employed for this purpose from the very first, and no difficulties worth mentioning were experienced, the chief modification, being, I believe, the use of soap only in the clearing process, instead of soap and an alkaline carbonate. Several modifications, however, have since been made in oiling and mordanting the goods, which have rendered the process more simple ; and the colouring matter being a purer product than madder or garancine, the clearing ojoerations can be performed with greater facility. In dyeing ordinary printed goods the process can be conducted much more rapidly than when madder is used, as no loss of colouring matter is experienced by using a high temperature at once, as I showed you was the case with madder; however, I believe, when good pink and red shades are to be dyed, dyers do not usually allow their dye bath to rise much above 80° — 85° C. The use of a product called “ oleine,” prepared by treating castor and other oils with sulphuric acid, has been found of great service, as it increases the brilliancy of the shades, especially the red or scarlet ones. A good deal of artificial alizarin is used for topical printing. To fit it for this purpose it is mixed with a few per cent, of its weight of acetate of lime, and by dyeing patterns with light shades, say, with pure alizarin, and then printing on dark shades with anthrapurpurin, very beautiful results can be obtained. The use of artificial alizarin, in place of madder or garancine, has a very important influence in the pollution of our rivers, as when this is used the water from the dye baths is nearly pure, whereas when madder and garancine are employed it is full of ground woody matter and I think I shall be making a very low estimate if I say that over 10,000 tons of this was annually passed into our rivers before the introduction of artificial alizarin. Surely this is a great advantage in itself. Now that the production of artificial alizarin is equal to the demand, it is interesting to find that the supply of raw material anthracene, has been quite adequate, so that all the fears that were entertained on this subject have proved groundless; and it is also well to remember that up to the present time the anthracene contained in pitch has not been extracted to any large extent, so that much more anthracene could yet be produced if required. (To be continued.) Parliamentary and Sam proceedings. Sale of Food and Drugs Act Amendment Act, 1879. The following is the text of this Act, which has now received the Royal Assent : — Whereas conflicting decisions have been given in Eng¬ land and in Scotland in regard to the meaning and effect of section six of the Sale of Food and Drugs Act, 1875, in this Act referred to as the principal Act, and it is ex¬ pedient, in this respect and otherwise, to amend the said Act: Be it enacted by the Queen’s most Excellent Majesty, by and with the advice and consent of the Lords Spiritual and Temporal and Commons, in this present * Moniteur Scientifique , April, 1879, p. 417. 120 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 9, 1879„ Parliament assembled, and by tlie authority of the same, as follows : 1. This Act may be cited for all purposes as the Sale of Pood and Drugs Act Amendment Act, 1879. 2. In any prosecution under the provisions of the prin¬ cipal Act for selling to the prejudice of the purchaser any article of food or any drug which is not of the nature, substance, and quality of the article demanded by such purchaser, it shall be no defence to any such prosecution to allege that the purchaser, having bought only for analysis, was not prejudiced by such sale. Neither shall it be a gDod defence to prove that the article of food or drug in question, though defective in nature or in substance or in quality, was not defective in all three respects. 3. Any medical officer of health, inspector of nuisances, or inspector of weights and measures, or any inspector of a market, or any police constable under the direction and at the cost of the local authority appointing such officer, inspector, or constable, or charged with the execution of this Act, may procure at the place of delivery any sample of any milk in course of delivery to the purchaser or consignee in pursuance of any contract for the sale to such purchaser or consignee of such milk ; and such officer, in¬ spector, or constable, if he suspect the same to have been sold contrary to any of the provisions of the principal Act, shall submit the same to be analysed, and the same shall be analysed, and proceedings shall be taken, and penalties on conviction be enforced in like manner in all respects as if such officer, inspector, or constable had pur¬ chased the same from the seller or consignor under section thirteen of the principal Act. 4. The seller or consignor, or any person or persons entrusted by him for the time being with the charge of such milk, if he shall refuse to allow such officer, in¬ spector, or constable to take the quantity which such officer, inspector, or constable shall require for the purpose of analysis, shall be liable to a penalty not exceeding ten pounds. 5. Any street or open place of public resort shall be held to come within the meaning of section seventeen of the principal Act. 6. In determining whether an offence has been com¬ mitted under section six of the said Act by selling, to the prejudice of the purchaser, spirits not adulterated other¬ wise than by the admixture of water, it shall be a good defence to prove that such admixture has not reduced the spirit more than twenty-five degrees under proof for brandy, whisky, or rum, or thirty-five degrees under proof for gin. 7. Every liberty having a separate court of quarter sessions, except a liberty of a cinque port, shall be deemed to be a county within the meaning of the said Act. 8. The town council of any borough having a separate court of quarter sessions shall be exempt from contribut¬ ing towards the expenses incurred in the execution of the principal Act in respect of the county within which such borough is situate, and the treasurer of the county shall exclude the expenses so incurred from the account re¬ quired by section one hundred and seventeen of the Municipal Corporation Act, 1835, to be sent by him to such town council. 9. The town council of any borough having under any general or local Act of Parliament, or otherwise, a sepa¬ rate police establishment, and being liable to be assessed to the county rate of the county within which the borough is situate, shall be paid by the justices of such county the proportionate amount contributed towards the expenses incurred by the county in the execution of the principal Act by the several parishes and parts of parishes within such borough in respect of the rateable value of the property assessable therein, as ascertained by the valuation lists for the time being in force. 10. In all prosecutions under the principal Act, and notwithstanding the provisions of section twenty of the said Act, the summons to appear before the magistrates shall be served upon the person charged with violating, the provisions of the said Act within a reasonable time, and in the case of a perishable article not exceeding twenty-eight days from the time of the purchase from such person for test purposes of the food or drug, for the sale of which in contravention to the terms of the principal Act the seller is rendered liable to prosecution, and par¬ ticulars of the offence or offences against the said Act of which the seller is accused, and also the name of the pro¬ secutor, shall be stated on the summons, and the summons shall not be made returnable in a less time than seven days from the day it is served upon the person summoned. Poisoning by Carbolic Acid. An inquest has been held in the Coventry and War¬ wickshire Hospital, touching the circumstances attending the death of a girl named Edgington, from poisoning by carbolic acid. It appeared that some carbolic acid, which had been obtained for sanitary purposes had been placed on a shelf in a bottle similar to that in which some wine was usually kept, and for which it is probable that the deceased mistook it. A verdict was returned that deceased died from the effects of carbolic acid taken inadvertently, and the jury added a rider suggesting to the sanitary authorities of the town that in future a poison label should be attached to every bottle in which the acid was contained. %* No notice can be taken of anonymous communica¬ tions. Whatever is intended for insertion must be authenti¬ cated oy the name and address of the writer; not necessarily for 'publication, but as a guarantee of good faith. Tincture of Kino. Sir, — After the interesting paper by Mr. R. Pother, which appeared in the Journal of August 2, perhaps the following note may be of some value. Some fifteen or sixteen years ago, the idea occurred to my mind that the addition of a small quantity of glycerine to tincture of kino, might, by preventing the aggregation of the gum particles, do away with the annoying tendency to gelatinization. I found it answer the purpose admirably and have never been troubled with gelatinized tincture since. The proportion of glycerine I use is 5 per cent. August 5, 1879. John B. Merrikin. “ Gulielnius.” — (1). Send specimen with basal sheath. (2) . Carex remota. (3). Car ex divulsa. (4). J uncus bufonius. (5). Juncus effusus. (6). Juncus lampro - carpus. J. U. Dingle. — (1). Pteris aquilina. (2). TJsnea florida. (3) . Festuca gigantea, probably; send a more mature specimen. (4). Pinus sylvestns. T. J. S. Blaine. — Daphne Mezereum. B. Roberts. — (1). Vicia sylvatica. (2). Lathyrus syl- vestris. (3). Send a specimen with the lower leaves. (4). Correct. (5). Stachys palustris. . (6). Cichorius Intybus. J. M. — See a paper on Permanent Essence of Rennet in vol. ix., p. 307. “ Patent .” — A preparation is liable to stamp duty — (1) If it is a secret or occult preparation ; (2) If it is stated to be prepared only by the person whose name it bears; (3) If it is, or has been, recommended on the label, or on a handbill, or by any public advertisement, as a remedy for the cure or relief of any disorder. Messrs. Duncan, Flockhart and Co. — Your communica¬ tion has been forwarded to the publishers, Messrs. Churchill, New Burlington Street. Communications, Letters, etc., have been received from Messrs. Cowan, Eade, Strachan, Gulielmus, Congius, In¬ quirer, An Associate, Lavandula, M. R. I., J. A. August 16, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 121 NOTES ON INDIAN DRUGS. BY W. DYMOCK. {Continued from Vol. IX, page 1035.) Spilanthes oleracea, Linn., Composite ; Para cress of Brazil. Vernacular : Akurkura (Bomb)., is commonly cultivated in gardens in Bombay. It is a small annual plant with round smooth succulent branching stems ; the leaves are opposite, petioled, subcordifomi, subdentate. The flowerlieacls are solitary, at the ends of pedicels longer than the leaves, of a conical form and of the size of an acorn ; they are entirely composed of yellow or brownish yellow hermaphrodite tubular flowers. The achenes are compressed with ciliated margins and are surmounted by two naked awns. The whole plant is very acrid, but the flower heads are especially so, having a hot burning taste which causes profuse salivation. It is on this account that the plant has been named Akurkura by the gardeners. The name properly belongs to the pellitory root of the shops. The flower heads are sometimes chewed to relieve toothache. The S. acmella is a native of India and has similar properties. Artemisia Ixdica, Willd., Composite. The plant. Vernacular : Nagdoavn (Hind., Beng.); Dauna (Bomb.); Machipatri (Tam.). History , Uses, etc. — This plant, in Sankrit Nagada- mani, may be regarded as the wormwood of India. The Hindus consider it to be a valuable stomachic, deobstruent, and antispasmodic ; they prescribe it in infusion and electuary, in cases of obstructed menses and hysteria. Externally it is used in fomentations. In Hindu temples downa is placed upon the heads of the goddesses, but not on those of the gods. A. Indica is probably one of the kinds of afsanteen described in Mahometan works, but owing to the number of species which belong to the genus, and which all have very similar properties, it is difficult to decide this point. The authors of the Pharmacopoeia of India say the strong aromatic odour and bitter taste of this plant, scarcely distinct from A. vulgaris, indicate stomachic and tonic properties. Dr. Wight (Illust., ii., 92) states that the leaves and tops are administered in nervous and spasmodic affections connected with debility, and also that an infusion of them is used as a fomentation in phagedenic ulceration. Dr. L. Stewart describes an infusion of the tops and leaves as “ a good mild stomachic tonic.” Description. — Erect, suffruticose; leaves ashy and tomentose beneath, lower pinnatifld, upper trifid, uppermost undivided or with lanceolate lobes ; lobes of the lower leaves toothed or cut. Heads of the flowers racemose-panicled, ovate ; panicle leafy, spread¬ ing partial racemes pendulous before flowering, young involucre a little tomentose, at length glabrous ; exterior scales foliaceous, acute, interior membran¬ aceous, obtuse; corolla naked (Roxb. FI. Incl., iii.,419). Commerce. — The dry plant is sold by the herbalists and the fresh tops in the markets. Value Rs. 6 per Surat maund of 37£ lbs. Artemisia Sternutatoria. The plant. Vernacu¬ lar : Nakk-chikxee (Hind., Beng., and Bomb.). Description, Uses, etc. — According to Roxburgh this plant appears during the latter part of the cold season, on cultivated land. The whole plant does not cover a space more than about 0 — 8 inches in diameter. Third Series, No. 477. Root simple, the stems several, branchy, pressing on the earth ; all are somewhat woolly. Leaves numerous, sessile, wedge-shaped, deeply dentate, villous. Flowersaxillary, or in the divisions of the branches, solitary sessile, subglobular, hermaphrodite. Florets, from 10 — 12 in the centre, with their border 4- toothed, coloured and expanding ; the female ones very numerous in the circumference, most minute, with the border seemingly 3-toothed, and the tooth- lets incurved. Receptacle naked. It differs from A. minima in having sessile downy leaves and numerous flosculi in each flower. The minute seeds are used as a sternutatory by the Hindus, also the powdered herb. The plant does not grow in this part of India, but the dry herb, both entire and in powder, is always to be obtained in the druggists shops. Value about annas 6 per lb. Doronicum Scorpioides? Composite. The rhizome. Vernacular : Darunaj-i-akrabi (Pers., Bomb.). History, Uses, etc. — The author of the ‘Maklizan-ul- Adwiya tells us that Darunaj is a scorpioid knotted root, with a greyish exterior and white interior; that it is hard, faintly bitter and aromatic. He describes the plant as having fleshy yellowish leaves of the shape of those of the almond, which lie flat upon the ground. The flower stem he says is hollow ; it rises from the midst of the leaves to a height of two cubits, and bears from 5 — 7 scattered leaves, thinner and longer than the lower leaves. The flower is yellow and hollow. The plant grows in Andalusia and the mountainous parts of Syria, espe¬ cially about mount Yabroorat, where it goes by the name of Akrabi. There are two varieties of the drug, Persian and Turkish ; the latter is most esteemed. With regard to its medicinal properties, he says that it is a resolvent of phlegm, a remedy against bile and flatulencies, cardiacal and tonic, useful in nervous depression, melancholy and impaired diges¬ tion, also in pain of the womb and flatulent dyspepsia. Besides this it is prescribed for persons who have been bitten by scorpions and other venomous reptiles, and is hung up in houses to keep away the plague. Pregnant Avomen wear it round the waist suspended by a silken thread, which must be made by the Avearer. It is supposed to act as a charm, protecting the foetus and procuring a painless delivery. Hung up over the bed it pre Agents night terrors and ensures pleasant dreams. There Avould appear to be a demand for it in Bombay, as it is kept by all Mahometan druggists. Description. — Rhizomes scorpioid, occasionally branched, flat, jointed, of a dirty Avhite colour, 3 — 4 inches long, finch broad, and about inch thick. Upper surface scaly, under surface marked by the scars of numerous rootlets, a feAv of Avhich sometimes remain attached ; substance brittle and horny, yelloAArish white, central portion someAvhat spongy, odourless; taste at first insipid, but after a feAv minutes a sensa¬ tion of warmth and pricking is felt upon the tongue. Microscopic structure. — Sections sIioav that the bulk of the rhizome consists of a parenchyma, each cell of which is occupied by a mass having the appearence of inulin, inactive in polarized light, but which is coloured intensely black by iodine ; toAvards the circumference the cells become gradu¬ ally smaller, and upon the surface become scaly, forming a greyish epidermis. The vascular bundles are of a bright yellow colour, and consist of spiral vessels; they form one irregular ring round the 122 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 16, IS79-. rhizome, about midway between the circumterence and centre. No starch grains are to be seen in any part of the rhizome. Tricholepis procumbens, Wight , Ic, : Composite. Plant. Vernacular : Badaward (Pers. and Bomb.). This drug is described by Mahometan writers as the shaukat-ul-baida of the Arabs, the loofiniki of the Turks and the sanakhurd of the Syrians. Other Persian names given for it are kangar-i-sufed and asfar-i-baree. It is generally described as a thorny plant about two cubits high with downy triangular stems as thick as the thumb, or larger ; heads of seed like those of a thistle, thorny and full of down ; flowers purple ; seeds like these of carthamus, but rounder. M. Husain says, “Some have supposed this plant to be the same as the shukai ; this is not the case, but the two plants are nearly related. The true badaward has slender, white, round stems, little more than a span high, slightly downy ; flower heads white, surrounding them are three delicate soft spines like needles, so that altogether they have much the appearance of a brooch. Within is a quantity of white down, which when the seeds are ripe causes them to be carried about by the wind ; hence the name badaward. Medicinally the plant has tonic, aperient and deobstruent properties. It is said to drive away noxious reptiles when kept in the house ” (‘ Makhzan ’ article “ Badaward ”). The badaward of Bombay shops agrees with the de¬ scription of Meer Muhammad Husain. T. procumbens is found on sandy ground in Guzerat, and is thus described in the ‘Bombay Flora,’ “ Stem flexuose, short, ramous ; branches diffuse, procumbent, angularly striated, subglabrous ; leaves shortly pubescent or subglabrous, those of the stem lvrate, of the branches sinuatelv pinnatifid, the lobes spinously mucronate ; involucre ovate ; scales ovate, at the base araneose, terminating in a prickle-like appendage ; flowers purple, appear in the cold weather ; common in light soils in Guzerat.” Syn. : Carduus ramosus, Roxb. FI. Ind., iii., 407. The drug has a bitter taste. It is imported from Persia. NyCTANTHES ARBOR TRIST1S, Linn, : JASMINACE2E. Flowers, leaves and f ruit. Vernacular : Harsing- har (Hind.); Siuli (Beng.) ; Partak (Bomb.); Pagala mullai (Tam.). History, Uses, etc. — Royle in his ‘Himalayan Botany’ tells us that this tree is extremely common along the foot of the mountains which skirt the Deyra Dhoon, and may be seen for several hundred feet above Rajpore in the ascent to Mussooree. Hr. Wallich found it in a wild state near the banks of the Irrawaddy, on the hills near Prome. In Western India it is one of the commonest cultivated trees. Its flowers open at sunset, and fall before morning ; they have very strong perfume. The Sanskrit names for the tree are sephalika, parajatak, and rajanikasa. The author of the ‘ Makhzan’ gives a minute description of all parts of the tree and tells us that the Indians use the white portion of the flowers as a purple dye, which they call gul kamah, and the orange part as a yellow dye. The seeds and leaves are considered by them to have medicinal pro¬ perties. Six or seven of the young leaves are rubbed up with water and a little fresh ginger and administered in obstinate fevers of the intermittent type ; at the same time a purely vegetable diet is enforced. The powdered seeds are used to cure scurfy affections of the scalp. Directions for the preparation of gul kamah will be found in the ‘ Karabadeen-i-kabir.’' Chakradatta mentions the use of the leaves in fever and rheumatism. A decoction of the leaves prepared over a gentle fire is recommended by several writers as a specific for obstinate sciatica (Confer. Dutt’s ‘ Hindu Mat. Med.,’ p. 189). Description. — Tree, 15 — 20 feet ; young shoots four-sided : leaves opposite, short-petioled, cordate or oblong, pointed, entire or coarsely serrate,, scabrous ; panicles terminal, composed of smaller six-flowrered terminal umbellets ; calyx companulate, slightly five-notched, downy ; corolla tube cylindric, as long as the calyx, segments 5— 7 ; involucre of four inverse, cordate, opposite, sessile leaflets ; flowers numerous ; tube orange-coloured ; border white, fragrant (Drury). The fruit is a dry, flat, oblong, mucronate capsule, prominently veined, f inch loEg by | broad. It is of a brown colour when ripe and is divided into two cells each of which contains a flat foliaceous seed of a light brown colour ; the testa of the seed is thin, the kernel white, bitter and very astringent. The leaves have similar properties and stain the saliva yellow when chewed. Calotrobis gigantea, E.Br.; Calotropis procera, E.Br.: Asclepiade^e. The root, leaves and flowers. Vernacular : Ak, Mudar (Hind.) ; Akanda (Beng.); Akra, Rui (Bomb.); Erukku Erukkam (Tam.). History, Uses, etc. — The same Indian names are applied to both of these plants ; Sanskrit writers* however, notice two varieties, which are distinguished by the colour of their flowers, viz., alarka or white and arka or red. Dutt (‘Hindu Mat. Med.’), gives us the following summary of the uses of the plant, extracted from Sanskrit works, chiefly that of Chak¬ radatta. “The root bark is said to promote the secretions and to be useful in skin diseases, enlarge¬ ments of the abdominal viscera, intestinal worms, cough, ascites, anasarca, etc. The milky juice is- regarded as a drastic purgative, and caustic, and is- generally used as such in combination with the milky juice of Euphorbia neriifolia. The flowers are considered digestive, stomachic, tonic and useful in cough, asthma, catarrh and loss of appetite. The leaves mixed with rock salt are roasted within closed vessels, so that the fumes may not escape. The ashes thus produced are given with whey in ascites and enlargements of the abdominal viscera. The following inhalation is prescribed for cough : — Soak the powdered root bark of arka in its own milky juice and dry. Bougies are then prepared from the- powder, and their fumes inhaled. The root bark, reduced to a paste with sour congee, is applied to elephantiasis of the legs and scrotum. The milky juices of C. gigantea and Euphorbia neriifolia are made into tents with the powdered wood of Berberis Asiaticci, for introduction into sinuses and fistuloe in ano. The milky juice is applied to carious teeth for relief of pain.” An oily preparation (arkataila), made by boiling together 8 parts sesamum oil, 16 parts calotropis juice, and one part turmeric, is said to be useful in eczema and other eruptive skin diseases. August 10, 1879.1 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 123 In Western India and probably elsewhere there is a curious superstition that a leaf of the akra, fetched from the. tree with certain ceremonies, is of use in tedious labour. The friends of the woman take a packet of betel nut and leaf, and a piece of money, and proceed to the plant, which they address in the most respectful manner, placing the betel packet at its root and asking for the loan of one of its leaves which they promise to return shortly. They then ttake away a leaf and place it upon the head of the parturient woman, where it remains for a short time and is afterwards returned to the plant. This practice appears to be connected with the worship of Ma- irootee which is popular in this part of the country. He is the god of wind, and was born from a pinda under the shelter of an akra tree. The tree is con¬ sidered sacred to him, as it afforded him protection when all the other trees had been destroyed. Maho¬ metan writers describe it under the Arabic name of ushar. In Persian it is called khark. Meer Mu¬ hammad Husain gives a good description of the plant, mid notices the use of the silky cotton of the pods by the wandering Arabs and Tartars to make their makhad twist or yalisli (tinder). He says there are three varieties, 1st. A large kind with white flowers, large leaves, and much milky juice. It is found near towns and the habitations of man. 2nd. A smaller kind with smaller leaves, the flowers white externally but lilac within. 3rd. A still smaller plant, with pale yellowish green flowers. The second and third kinds grow in sandy deserts. The properties of all three are similar, but the first kind is to be preferred as it produces the largest quantity of milk. The juice is described as caustic, a purge for phlegm, depilatory, and the most acrid of all milky juices. Tanners use it to remove the hair from skins. Medi¬ cinally it is useful in ringworm of the scalp, and to •destroy piles ; mixed with honey it may be applied to aphthae of the mouth ; a piece of cotton dipped in it may be inserted into a hollow tooth to relieve the pain. Hakeem Meer Abdul Hameecl in his com¬ mentary upon the Tuhfat strongly recommends it in leprosy, hepatic and splenic enlargements, dropsy and worms. A peculiar method of administration is to steep different kinds of grain in the milk and then administer them. The milk itself is a favourite application to painful joints, swellings, etc.; the fresh leaves also, slightly roasted, are used for the same purpose. Oil in which the leaves have been boiled is applied to paralysed parts ; a powder of dried leaves is scattered upon wounds to destroy excessive granulation and promote healthy action. All parts of the plant are considered to have valuable alterative properties when taken in small doses. Lastly, some of our Mahometan writers give very exaggerated accounts of the poisonous properties of the plant. C. procera was observed in Egypt by Prosper Alpinus (1580 — 84), and upon his return to Italy was figured, and some account given of its medicinal properties (‘De plantis BKgypti,’ Yenet. 1592, cap. 25). 0. gigantea was figured by Rheede in 1679 (‘Hort. Malabar.’ ii. tab. 31). Ainslie in his ‘ Materia Medica of Hindustan’ (1813) mentions two kinds of calotropis, and in the ‘Materia Indica,’ he says, “ Both plants in their leaves and stalks contain much milky juice which when care¬ fully dried is considered as powerfully alterative and purgative, and has been long used as an efficacious remedy in the hoostura (lepra Arabum) of the Tamools ; the dose about the quarter of a pagoda weight in the day, and continued for some weeks. The root of the yercum has a bitter and somewhat acrid, or rather warm taste ; it is occasionally given in infusion as a stimulant in low fever. Of the other variety, the vullerkoo, the bark is warmish and when powdered and mixed with a certain portion of mar- gosa oil, is used as an external application in rheu¬ matic affections. In the higher provinces of Bengal the arka (6'. gigantea) is supposed to have antispas- modic qualities. Mr. Robinson has written a paper on elephantiasis, which may be seen in vol. x. of the Medico-Chirurgical Society, extolling the mudar root ( Yercum vagr ) as most efficacious in that disease, as also in venereal affections. In the elephantiasis he gave it in conjunction with calomel and antimonial powder, in a pill consisting of half a "rain of calomel, three of antimonial powder, and from six to ten of the bark of the root mudar, every eight hours. Mr. Playfair has also written a paper on the same root, which may be seen in vol. i. of the Edinburgh Medical Chirurgical Transactions , p. 414, wherein he speaks in praise of the alterative, stimulant, and deobstruent virtues of the bark, or rather rind below the outer crust of the root, reduced to fine powder, in cases of syphilis, leprohectic fever, etc.; dose from gr. 3 — 10 or 12, three times in the day, gradually increasing it. Messrs. Robertson, Playfair, and others seem chiefly to dwell on the virtues of the rind or bark of the root ; but I must observe that in lower India, where I was for many years, I found the simple dried milky juice considered as infinitely more efficacious, and later communications from the East confirm me in this opinion ( ‘ Materia Indica,’ vol. i., p. 487). The emetic properties of mudar were first brought to the notice of the profession by Dr. Duncan in 1829 ( Edinburgh Mediccd and Surgi¬ cal Journal, vol. xxxii., p. 65). They are noticed in the Bengal ‘ Dispensatory,’ where the drug is recom¬ mended as a substitute for ipecacuanha. Since the publication of that work abundant testimony in its favour has been collected, a summary of which will be found in the Pharmacopoeia of India. Duncan made a chemical examination of the root bark, the activity of which he referred to an extractive matter which he termed mudarine. Description. — The root barks of C. gigantea and C. procera are similar in appearance, as collected in Bombay, where they are removed by a few blows with a hammer or piece of hard wood. They occur in short quilled pieces £ to £th of an inch thick. The outer surface is yellowish-grey, soft and corky, fissured longitudinally, and can be easily separated from the middle cortical layer, which is white, friable, and traversed by narrow brown liber rays. The taste is mucilaginous, bitter and acrid, and the odour peculiar. Microscopic structure. — In both kinds of root bark the suber consists of large thin-walled cells, generally polyhedral. The parenchyma of the middle cortical Ayer is loaded with starch and contains some scler- enchymatous cells. The cells of the medullary rays also contain starch and crystals of oxalate of lime. In the middle layer are numerous lacticiferous vessels, the contents of which are of a brown colour. Chemical composition. — The authors of the ‘ Phar- macographia,’ following Duncan’s process, failed to obtain anything like his mudarine, they found, how¬ ever, that the plant contains an acrid, bitter resin, which is probably the active principle. {To be continued.) 124 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 16, 1879. PHARMACEUTICAL EXTRACTS.* CRITICAL CONSIDERATIONS UPON THEIR PRE¬ PARATION, CLASSIFICATION, GENERAL CHA¬ RACTERS, USES, ETC. BY E. SCHMITT, Professor of Medicine and Pharmacy at Lille. {Concluded from page 86.) III. The extract should contain all the soluble prin¬ ciples of the vegetable or animal substance to the exclusion of inert matters. The number of principles contained in a vegetable juice is very large ; but without entering into details apart from the subject it may be said that such juices contain immediate principles that are alka¬ line, neutral or acid, volatile oils, gums and mucilages, resins and gum resins, pectic and albuminoid matters, sugars, tannins, soluble and insoluble fecula, fatty and •waxy matters, organic and inorganic salts (especially those having lime and potash for a base), chlorophyll, debris of fibre and parenchyma (for the feculent extracts), and lastly, extractive matters, i.e., badly defined sub¬ stances, possibly belonging to one of the previous groups, or resulting from their transformation and slow destruc¬ tion. The extractive is characterized by its solubility in water. It may comprehend all the so-called colouring, bitter and depurative principles. It may exist in very small proportions in the fresh juice ; but with time, by the action of air, heat, ferments, etc., it may gradually augment in a preparation of extract, and frequently finish, in a badly prepared extract, by constituting the whole of the mass. It is very difficult to follow all these successive states of transformation, but some idea may be formed of them by recalling the modifications that crystallizable sugar undergoes under the influence of water and heat, starting with uncrystallizable barley sugar and finishing with caramel. The sugar is submitted to the phenomena of hydration and oxidation ; the oxygen of the air burns a part of the hydrogen and a little carbon ; vapour of water and carbonic acid are disengaged, and eventually there remains a compound richer in carbon and strongly coloured like caramel. The caramel is still soluble in water ; but in the preparation of extract there is always produced a more or less large proportion of a new sub¬ stance, coloured brown, green or black, and insoluble in water. This substance dissolves in alkaline liquors and acids re-precipitate it from this solution. It has much analogy with humic acid, and Berzelius named it “ oxy¬ genated extractive or apotheme.” Apotheme is very little known ; it is a very complex substance, and it re¬ mains as a residue when extracts are dissolved. Probably it ought not to exist in a typical or ideal extract, and it may be affirmed that the more care there is given to the preparation of extracts the less oxygenated extractive will be found in them. In generalizing the phenomena that take place in the preparation of extracts, — phenomena of hydration, oxi¬ dation, or others, — it may be said that the volatile principles disappear or are altered, that they are retained partially by the apotheme, either alone or united with fatty or resinous matters : the aqueous extract of vale¬ rian may be quoted for an example. These volatile principles at the moment of their elaboration are hydro¬ carbons, which become hydrated and oxidized and yield a series of alcohols, aldehydes and ethers that in the course of the operations are volatilized, decomposed or resinified. The sugar becomes glucose, and the fecula, bassorin and cerasin become soluble. The tannins alter more rapidly still, and it is probable that to the alteration of the astringent principles is due the greater part of the apotheme, which contains also the products of coagulation and destruction of pectic and albuminoid matters. * Repertoire de Pharmacie, vol. vii., p. 249. It may be concluded from this rapid glance at the phenomena that occur during the preparation of an ex¬ tract that the alteration would be most rapid in the extracts of juices and that this alteration would diminish in energy from the aqueous extract to the ethereal, which of them all is that which contains the least amount of alterable principles. It may be concluded also, that the preparation of extracts by congelation, when it shall have become more practical, will be the most rational, because all the principles that represent the juice of the plant will be certainly thus the least altered, cold being a condition of conservation and heat of destruction. IV. Should extracts be submitted to a pharmaceutical classification? Rouelle has divided the extracts into saponaceous extracts (containing only extractive matters), gummy extracts, gum-resinous extracts and resinous extracts. This classification is very primitive and in¬ complete ; it does not include nearly all the extracts employed at the present day. Without taking note of consistence, it appears tome more simple and more rational, from the pharmaceutical point of view, to classify the extracts according to the nature of the menstruum used in their preparation ; but it is necessary first to divide them into simple and compound extracts. The simple extract represents the active principles of a single species of a plant or animal ; the compound extract represents, on the contrary, a mixture of principles belonging to several plants, as the compound extract of rhubarb and the compound extract, of- colocynth. The compound extracts are little known, and not much employed in France. For the simple extracts I propose the following classi¬ fication : — 1. Aqueous Extracts. a. Commercial Extracts (aloes, catechu, etc). b. Extracts of juices (feculent or defecated, robs)- c. Aqueous Extracts, properly so-called. 2. Alcoholic Extracts. 3. Ethereal Extracts. 4. Acetic Extracts. 5. Mixed Extracts. It is necessary also to define clearly the part of the plant which has yielded the extract, so as not to confound the extract of aconite root or of henbane seeds with the extracts of the leaves of the same plants. The pharmacist has nothing to do with a therapeutic classification of these extracts, but it may be remarked that from this special point of view these preparations ought to be classified so as to take into account the phar¬ macodynamic object the medical man proposes to attain. The object being well defined, the physician and the pharmacist ought essentially to remember that the part of the plant, the menstruum and the consistence of the extracts are the elements which should occupy their attention, especially from a posological point of view. To cite only one example, it may be said there exist five extracts of aconite : the defecated and feculent extracts of the juice of the leaves, the aqueous and alcoholic ex¬ tracts of the leaves and the alcoholic extract of the root, and that this last, the most active of all, is given in doses of some milligrams. The pharmacist, on the simple pre¬ scription of “ extract of aconite,” will dispense in France, the soft defecated extract of the juice ; in Belgium, a dry extract, with aconite powder added, under the form of a greenish grumous powder; in Germany, the alcoholic extract of the roots. It may be mentioned also that the ergotine of Wiggers would be dangerous in the ordinary dose of that of Bon jean, which is itself more active than the aqueous extract of ergot. The necessity has thus incidentally been made manifest for a Universal Pharmacopoeia, especially for very active medicines ; this necessity has long been recognized by physicians having foreign patients and by travellers re¬ quiring the same prescription to be made up in different countries through which they pass. V. The next point is the general characters of the ex- August 16, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 125 tracts. Extracts ought to have, before al], the prescribed consistence ; they are always coloured brown or green, but should not be black, as happens with extracts prepared over the bare fire. They should have the odour and taste of the substance they represent, and especially should they be free from any empyreumatic odour. The surface should be smooth, not grumous ; further, it should not be covered with mould or puffed up with bubbles of gas, which would be a sign of fermentation. The aqueous extract ought to be nearly entirely soluble in water ; it dissolves better in water containing alcohol and in saccharine liquids than in pure water, so that in the preparation of a mixture it is often an advantage for the pharmacist to diffuse the extract in the syrup. The alcoholic and ethereal extracts ought to dissolve com¬ pletely in their original menstruum. Very fine crystallizations of organic or inorganic pro¬ ducts are often found at the bottom of pots containing soft extracts ; for instance, asparagin, oxalate of lime, chloride of sodium, nitrate and sulphate of potash. The extracts of bellodonna, henbane, borage and taraxacum are those which most frequently present these crystalliza¬ tions ; they are confined nearly always to the vegetable juices, and may also sometimes be the result of the action of atmospheric oxygen, as in the case of the nitrates. Besides these general characters, extracts present specific or even generic characters. Some are charac¬ terized by their colour (rhatany and campeachy), odour (valerian), or taste (aloes and rhubarb); others by their chemical characters, such as the alkaloids in opium, cin¬ chona and the narcotic plants, the astringent principles in catechu and rhatany, and the acids in opium, cin- • chona and the juices of fruits. Some extracts can be recognized rapidly by the action of certain reagents which produce a special odour or colour ; for instance, the odour produced by the action of caustic potash upon extract of conium, or the colour produced by the action of alkalies upon the colouring matter of rhubarb. These chemical characters have been given with care by MM. Patrouillard and Lepage in their ‘ Guide Pratique de l’Essai des Medicaments ; ’ but for the greater part of the extracts, and especially the “ saponaceous extracts ” of Rouelle, they are difficultly applicable. The study of the extractive is far from being complete, perhaps it never can be completed in consequence of the modifica¬ tions which continue to take place even in the finished preparation. If this problem, then, be one of the most arduous, if the spontaneous alteration of extracts be often inevitable, and if their adulteration be difficult to detect, it will be manifest that it is the duty, as well as the interest, of pharmacists to prepare their own extracts. This is not all ; the extract has issued from the shop of the pharmacist and become a food product. Originally a medicine and even a poison in the laboratory it has become an aliment in the manufactory. The scientific preparation of extracts upon the largest scale in the present day provides for food Liebig’s extract of meat, extract of milk or condensed milk, extract or essence of coffee, and the extracts of peas, hops, malt, etc. It would be easy to discuss the alimentary value of Liebig’s extract and to indicate the services rendered by concentrated milk, but to broach these questions in this paper would be to go completely outside the pharmaceutical domain. THE PREPARATION OF SALTS OF BERBERINA.* BY J. U. LLOYD. How can the salts of berberina be most easily prepared from the root of Hydrastis Canadensis ? What will be the practical yield and what are the solubilities of the different salts ? Of the many processes investigated, I suggest the * From the ‘ Proceedings of the American Pharmacev.- tical Association,’ 1878. following as applicable to small amounts. Owing to the slight yield of this yellow alka'oid, it is hardly advisable for experimenters to work lots cf less than ten pounds of hydrastis. Moisten sixteen troy ounces of Hydrastis canadensis in fine powder with eight fluid ounces of alcohol ; press firmly into a cylindrical percolator not exceeding three inches in diameter, previously prepared for percolation ; cover the surface of the powder with a piece of blotting- paper, held in position with a few fragments of glass ; add alcohol until the percolate appears at the exit, then close the orifice, cover the top of the percolator tightly by tying over it a sheet of soft rubber and place the percolator in a warm situation ; macerate twenty-four hours ; remove the rubber and replace with a cover of glass or tin. Cautiously open the exit and graduate the dropping so that the passage of each fluid ounce wrill occupy about thirty minutes. Suspend the operation when five fluid ounces have been obtained. Macerate until the next day under the former conditions and again procure five fluid ounces of percolate, observing the pre¬ ceding directions. A continuous supply of alcohol must be provided. The surface of the powder must not be¬ come exposed during the operation. Mix the percolates, surround the vessel with ice and reduce the temperature, then add sulphuric acid in excess and stir well. Keep the mixture cold for twelve or more hours, then pour it upon a muslin strainer or a filtering paper, and when the liquid ceases to pass return the precipitate to a vessel containing eight fluid ounces of cold alcohol ; mix well together and again separate the crystalline preci¬ pitate of impure sulphate of berberin. Dry by exposure to atmosphere. Sulphate of Berber in a. — Add one part of impure sul¬ phate of berberina, obtained as above, to sixteen parts of cold distilled water and cautiously drop in, with constant stirring, ammonia water until in slight excess, allow the mixture to stand in a cool place from twelve to twenty- four hours, then filter and surround the vessel containing the filtrate with ice and stir sulphuric acid into the solution until the ammonia and alkaloid are saturated. In a few hours the magma of minute crystals of sulphate of berberina can be separated with a muslin strainer or a filtering paper. Care must be taken to avoid an excess of sulphuric acid. If this occur the moist magma should be removed to a vessel containing cold alcohol, washed by decantation and drained on a muslin strainer. Lastly, dry the salt by exposure to atmosphere. Sulphate of berberina is of an orange colour, soluble in about 100 parts of wTater, temperature 60° to 80° E. It is readily decomposed by alkalies when in solution, yielding free berberina. I obtain from eighteen to twenty- one ounces from a hundred pounds of hydrastis. The specimen of salts exhibited represents the sulphate of berberina from a fifteen hundred pound batch of root. This batch yielded very nearly three hundred ounces. Although the ex¬ haustion was incomplete, with economy I could not carry the percolation farther. Sulphate of berberina is permanent; exposure to atmo¬ sphere does not affect it. If moisture be absorbed, either the salt is impure from hygroscopic extractive matter or free sulphuric acid. Berberina. — Rub eight parts sulphate of herberina in a Wedgewood mortar, cautiously adding ammonia water until in slight excess. Pour the dark liquid into thirty- two parts of boiling alcohol and allow the mixture to stand thirty minutes, then filter. Stir into the filtrate thirty-two parts cold sulphuric ether and cover tightly. Surround the vessel with ice and allow it to stand from twelve to twenty-four hours, then separate the magma of minute crystals of berberina with a muslin strainer or filtering paper and dry by exposure to atmosphere. Berberina is lemon-yellow when pure. It should not be dark or orange, which shade denotes impurity. It unites directly with acids and is a beautiful organic base. 126 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 16, 187P. It forms salts, some of which are very soluble, as, for example, the pyrophosphate ; others almost insoluble. I find it impossible to make one part of carbazotate of berberina dissolve in forty-five thousand parts of cold distilled water. Berberina and all its soluble salts are bitter. The carbazotate will not impart a trace of bitter¬ ness to distilled water, notwithstanding its constituents are both intensely bitter ; therefore, I believe it to be almost if not absolutely insoluble. Berberina is soluble in about four and a half parts of water, temperature 60° to 80° F. It dissolves moderately in officinal alcohol, is insoluble in ether and chloroform. It changes to orange colour when heated to 150° F., and slowly resumes its original shade when cooled. Phosphate of Berberina. — Dissolve berberina in its weight of boiling water and add two parts of dilute phosphoric acid, drain and dry the precipitate by expo¬ sure to atmosphere. Care must be taken that the acid be made from phosphorus and perfectly free from nitric acid. The orthophosphate is, according to Mr. Lord, soluble in 280 parts of water. Hypoph osph ite of Berberina. — This salt may be pre¬ pared by substituting in the above formula hypophos- phorous acid for phosphoric. Hypophosphite of berberina is soluble to the extent of from five to ten grains in the ounce of water. Muriate of Berberina. — Dissolve berberina in sixteen times its weight of distilled water and cautiously stir in lAdrochloric acid until in slight excess ; drain the preci- Prate and dry by exposure to atmosphere. Muriate of berberina was the first preparation of this alkaloid introduced to the medical profession from hy- drastis. It was discovered accidentally. It is soluble in about five hundred parts of water 60° to 80° F., scarcely soluble at all in cold alcohol, ether and chloroform. It is the most difficult of the berberina salts to decompose, holding its acid in presence of alkalies, and even long digestion with litharge fails to thoroughly remove it. Oxide of silver at once frees the berberina from a heated solution. When dry it is changed from the natural light lemon colour to orange by a heat of from 13S° to 150° F. LTpon cooling the lemon colour is resumed. It is rapMly falling into disuse, giving place to the more soluble salts. Nitrate of Berberina. — This salt can be obtained by substituting nitric acid for the muriatic acid of the preceding formula. It is of greenish yellow colour, soluble in about five hundred parts of water, temperature 60Q to 80° F., more soluble in hot water, scarcely soluble in alcohol, ether or chloroform. Its use is limited. Remarks. — Alcohol extracts from Hydrastis canadensis in addition to berberina a greenish fixed oil, an acrid resin, a white alkaloid, a vegetable acid, yellow colouring- matter and small amounts of other substances of little interest here. The materials named are intimately asso¬ ciated or combined while in the root ; such combinations being broken up by the addition of the acid, resulting perhaps simply in the formation of sulphate of the white alkaloid, hydrastia ; sulphate of the yellow alkaloid, berberina, and the liberation of the resinous substances, colouring matter and acid. The yellow sulphate of berberina quickly crystallizes, carrying down some of the other materials, the larger amount of the latter, however, remains in solution. This impure sulphate of berberina is difficult to dry even if well washed, the reason being the mechanical admixture of the oil alluded to ; consequently at this stage it has a greenish cast and imparts an unctuous feeling when rubbed 'between the fingers. Sulphate of berberina is decomposed by alkalies with the liberation of the alkaloid berberina. When we add ammonia water in slight excess to a mixture of the impure sulphate of berberina and water, sulphate of am¬ monium is formed, which dissolves, together with the liberated berberira, an alkaloid very soluble in water and alkaline solutions. The slight excess of ammonia pre¬ cipitates the hydrastia in an amorphous state, which, with the adhering resin and oil, are separated by filtra¬ tion ; afterwards sulphuric acid, added to the filtrate again, forms sulphate of berberina, which crystallizes. This is pure enough for all practical purposes. I«t con¬ tains a small amount of sulphate of ammonium and a little foreign matter. It can be purified further if de¬ sirable by repeating the last operation, dissolving in hot alcohol and crystallizing. For practical purposes this is unnecessary. When ammonia water is added to sulphate of berberina the salt is decomposed with formation of sulphate of ammonium and the liberation of berberina. Both sub¬ stances remain in solution, the berberina imparting a dark red colour. The addition of the hot alcohol pre¬ cipitates the larger portion of the sulphate of ammonium, and when the filtrate containing the berberina is poured into sulphuric ether, that alkaloid crystallizes in conse¬ quence of its slight solubility in ether and a mixture of alcohol and ether. The impurities may be traces of sulphate of ammonium. The other salts, simply combinations of berberina and the acids, do not require mention. Almost any salt may be produced in like manner by the substitution of various acids. I have met with little success in endeavouring to ob¬ tain berberina by evaporation of a solution of the alka¬ loid, unless by spontaneous evaporation, the heat of "expanded steam 150° to 180° F. seeming to decom¬ pose it. Fixed Oil of Hydrastis. — After separating the sulphate of berberina from the tincture, add to the liquid its bulk of water and evaporate the alcohol. Allow the residuum to remain in a cool place some days and carefully skim off the green oil which collects on the surface of the water associated with a little resin. It can be purified by dissolving in sulphuric ether. This oil has a disagreeable odour and taste, but is not bitter. It turns reddish-brown by age. Volatile Oil of Hydrastis. — In addition hydrastis con¬ tains a very small amount of volatile oil, which imparts the peculiar odour of the root. It may be procured in minute quantities by distilling water in contact with the root. Resinous Substances. — Decant the aqueous solution from which the oil was separated, and at the bottom of the vessel will be found a black tarry substance, thickly interspersed with yellow particles. Usually a yellow shining layer covers the top. This consists of resin, a little oil and mixtures of both the white and yellow alkaloids, with the resin and yellow colouring matter. Perhaps a combination exists between this substance and the alkaloids which settle with it. It is difficult to separate them by simply washing in hot water, which should scarcely be the case if they are disassociated, inasmuch as the sulphates of both alkaloids are quite soluble in this menstruum ; wash the precipitate well and dry. The black resinous substance is acrid to the taste, slightly soluble in hot water and dilute acids, , soluble in concentrated sulphuric acid, to which it im¬ parts a deep red colour and from which it is separated by the addition of water. It may be a mixture of several proximate principles. In some respects this substance reminds us of the amorphous material obtained from cinchona, known as chinoidine, and it may perhaps be largely composed of a principle from hydrastis, bearing a somewhat similar relation to hydrastia that chinoidine bears to the crystal- lizable alkaloids of the cinchonas. Hydrastia. — This white or yellowish-white alkaloid exists as sulphate in the liquid decanted from the last- named preparation. It is associated with small amounts of all the preceding substances and a soluble vegetable acid. To obtain it add an alkali, preferably ammonia water, in excess to the cold liquid and allow the brown August 16, 1879.] THE rHARKACETTTICU.il JOURNAL AND TRANSACTIONS. 127 or brownish-yellow precipitate to settle ; then decant the supernatant liquid and wash the precipitate with cold water. Add cold water enough to the drained precipitate to bring to the original volume and then slight excess of sulphuric acid. Allow it to stand in a cold place twenty- four hours and filter. To the filtrate add an alkali in excess and wash the precipitate as before. Dry the precipitate, dissolve in boiling alcohol, filter and crystal¬ lize. These crystals are of a deep daik yellow colour. They are not bitter, but impart a disagreeable acrid sensation to the throat and fauces. The yellow colour results from the intimate admixture of a yellow sub¬ stance, very soluble in acid solutions and imperfectly in neutral and alkaline. It is not berberina. Purify hydrastia by dissolving in a dilute acid, digest¬ ing with animal charcoal and filtering, repeating the operation several times. Or dissolve the crystals of impure hydrastia in boiling alcohol and crystallize, re¬ peating the operation several times. Specimens of small hydrastia crystals, apparently white, are found to be yellow when crystallized in large masses. It is very difficult to obtain an article free from yellowness if the crystals be large. I have none. Hydrastia is insoluble or nearly insoluble in water, freely soluble in cold chloroform and to an extent in cold alcohol, very soluble in boiling alcohol, from wffiich it crystallizes in beautiful crystals. It forms salt with acids, mostly very soluble in wrater, uncrystallizable or crystallizing with difficulty. These incidental products are of little general interest to manufacturers, as only berberina salts are in demand. I have already digressed from the direct line of my query. I wrill close by saying that there is a doubt in my mind as to ti e relations of these several principles while associated in the plant. I cannot believe they are as simple as we might expect and is generally believed. I doubt even if berberina and hydrastia are not mutually combined with other bodies. The splitting up of these organic compounds under the influence of chemical agents, drying the plants and the action of solvents, is with me very obscure. AEGAN OIL.* Except a brief notice of the exportation into Europe of Argan oil by the Danish Councillor of State, Georges Host, who travelled in the kingdoms of Marocco and Eez during the years 1766 — 1768, the only published account of the uses of the Argan is given in a very little known Danish work, published by P. K. A. Schousboe, entitled ‘ Iagttagelser over Voextriget i Marokko.’ Eorste Sty eke. Kiobnhavn, 1800, 4, 7 tab., of which a German edition appeared in 1801, in 8vo, by J. A. Markussen. It gives an account of seme Marocco plants ; and, after an intro- \ ductory sketch of the physical geography of Marocco, it contains descriptions of the plants of the country in Latin and German, with occasional observations in German. The account of the Argan under Betz’s name of Elceodendron Argan is long : first comes a technical description, follow'ed by a history of its syn¬ onymy, and then the following notes (kindly translated for us by Mr. Bentham) : — “ It is surprising that this tree should hitherto have been so little known ; as it is found in a country near Europe, and visited by many travellers, who speak in their diaries and descriptions of oil of Argan and of Argan trees, these last as constituting a considerable proportion of the forests of the countiy. It is, however, not to be met with in the northern provinces, but only towards the south. All those persons from whom I have sought more accurate information on the subject are unanimous in stating that it only grows between the rivers Tansif and Sus — that is, between the 29° and 32° N. lat. — and there constitutes forests of considerable extent. It flowers in the middle of June, and the fruit * Fiona the Gardiners’ Chronicle, August 2, 18/9. remains on the tree the greater part of the year. The young fruit sets in the end of July or beginning of August, and growls slowly till the rainy season com¬ mences towards the end of September. It now enlarges rapidly and attains its full size during that season, so as that by the middle or end of March it is ripe enough to be gathered for economical uses. Both the fruit and the wood are serviceable, but especially the former ; for from the kernel an oil is extracted which is much employed for domestic purposes by the Moors, and is an important production of the country, as it saves much olive oil, which can thus be thrown into commerce and made to bring money into the country. It is calculated that in the whole Ar-gan region 1000 cwt. of oil is annually con¬ sumed, thus setting free an equal quantity of olive oil for exportation to Europe. Our countryman, Host, in his ‘ Efterretninger cm Marokos,’ p. 285, says that the Argan oil is exported to Europe, where it is used in manufac¬ tures. Such may have been the case in former times w'hen it might be cheaper ; but now there would be no advantage in doing so, as it costs almost as much as olive oil. At present no Argan oil whatever is exported. “As the practice in preparing this oil is somewhat different from that of common olive oil, it may be useful to enter into some details on the subject. I have myself been present during the whole operation, and consequently speak from experience. “ In the end of March the countryman goes into the wood, where the fruits are shaken down from the trees and stripped of their husks on the spot. The green fleshy pericarp, which is good for nothing else, is greedily eaten by ruminating animals, such as camels, goats, sheep and cows, but especially by the first two. There¬ fore, wffien the Arab goes into the wrood to collect Argan nuts, he gladly takes with him his herds of the above animals, that they may eat their fill of the green husks whilst he and his family are collecting and shelling the nuts. The horse, the ass and the mule, on the contrary, do not like this food. When a sufficient quantity of nuts are collected they are brought home, the haid wooden shell is cracked between stones and the inner white kernels are carefully extracted. These are roasted or burnt like coffee on eaithen, stone or iron plates ; in order that they may not be too much done they are constantly stirred with a stick. When properly roasted they should be all over of a brown colour, but not charred on the outside. The smoke w'hich is disengaged during the process has a very agreeable odour. As soon as the kernels have cooltd, they are ground in a hanclmill into a thick meal, not unlike that of pounded almonds, only that it is of a brown colour, and the meal is put into a vessel in vvhich the oil is separated, which is done by sprinkling the mass now and then with hot water, and keeping it constantly stirred and kneaded with the hand. This process is carried on until the mass becomes so hard that it can no longer be kneaded : the harder and firmer are the residuary coarse parts, the more completely is the oil extracted. At the last, cold water is sprinkled upon it, in order, as they say, to expel the last particles of the oil. During the operation the oil runs out at the sides, and is from time to time poured into a clean vessel. The main point to be attended to in order to extract the greatest quantity and the best quality of oil, is that it should be well kneaded, and that the proper proportion of hot water for the extraction of the oil should be used; it is always safer to be sparing of it than to be too pro¬ fuse. The residuary mass, often as hard as a stone, is of a black-brown colour, and has a disagreeable bitter flavour. The oil itself, when it has settled, is clear, of a light brown colour and has a rancid smell and flavour. When it is used without other preparations in cooking, it has a stimulating and pungent taste w hich is long felt on the gums. The vapour which arises w’hen anything is fried in it affects the lungs and occasions coughing. The common people use it generally without preparation, but in better houses it is the custom, in order to take off 128 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 16, 1579. that pungency, to mix it previously with water, or to put a bit of bread into it and let it simmer before the fire. “ The wood, which is hard, tough, fine-grained and of a yellow colour, is used in house carpentry and for other purposes.” MORPHIOMETRIC PROCESSES FOR OPIUM.* * BY ALBERT B. PRESCOTT, M.D. The following pharmacopceial assay process for opium is submitted to the Committee of Revision : — Opium, when dried (in powder) at (about) 100° Centi¬ grade (212° Fahrenheit) until it ceases to lose weight, should yield (from 10 to 12?) per cent, of morphia.+ The proportion of morphia may be determined by the following'process : — Take of opium, in powder and dried as above required, 6J grams (100'3 grains) ; lime, freshly slaked with one-third its weight of water, 3 grams (46*3 grains) ; chloride of ammonium, in powder, 4J grams (6-9'4 grains) ; benzole (see List of Reagepts), 50 cubic centimetres (the volume of 772 grains of water); washed ether (List of Reagents), 6 cubic centimetres (the volume of 92 grains of water); distilled water, 70 cubic centi¬ metres (1080 grains), or a sufficient quantity. Place the opium in a paper filter of 4 inches (10 centimetres) diameter, in a small funnel; add benzole to fill and cover the powder, and when the filtrate begins to drop, close the neck of the funnel and leave to macerate one hour. Then percolate, by adding the remainder of the benzole, and dry the filter and its contents at a gentle heat until the odour of benzole has disappeared. Care¬ fully transfer the contents of the filter (which is to be preserved) to an exactly weighed flask, of the capacity of 100 to 120 cubic centimetres, add the lime, with 20 to 30 cubic centimetres of distilled water, agitate for several minutes, then stopper the flask and shake till a uniform mixture is obtained. Add distilled water enough to make the contents of the flask weigh 74J grams (11 49 ‘7 grains). Digest, by immersing the flask in nearly boiling water, with occasional agitation, for one hour. Cool, and add distilled water to restore the exact weight of 74*5 grams. Filter, through the paper filter previously used, into a test-tube or other cylindrical glass of the capacity of 80 to 90 cubic centimetres, and previously marked for the volume of 50 cubic centimetres (771*6 grains of water), until the filtered liquid reaches the mark. Should the filtrate lack a few drops of the re¬ quired volume, the filter-contents are gently pressed to bring the liquid to the mark, but in any case no more than this volume is received. To the filtered liquid (now representing 5 grams of the opium), add eight drops of the benzin, and 3 cubic centimetres of the washed ether (the volume of 46 grains of water), then stopper the tube and agitate. Add the chloride of ammonium, and when it has dissolved, agitate again, and set aside in a cool place for three to three and a-half hours. The crystalline deposit is now gathered by filtration, in a small filter previously weighed and moistened, collecting the deposit, and washing the filter with several portions of distilled water, using but a few drops in each portion. The filter- contents are now dried at about 50° Centigrade (122° Fahrenheit), washed with the remainder of the washed ether (3 cubic centimetres), dried again and weighed. t * From the ‘ Proceedings of the American Pharmaceu¬ tical Association,’ 1878. / t I would suggest, as others have done, that opium ought to be limited in maximum as well as in minimum strength. The Pharmacopoeia can hardly depend upon commercial interest alivays to carry over-rich opium to the morphia manufacturer. But I am not confident as to what limits should be fixed, and it seems to me that a requirement permitting a variation of only 2 per cent, is more strict than can be enforced. X Hager (after Jacobsen) directs to subtract from this weight its one -thirtieth for impurities (not removed by ether washing of the morphia previous). In his process, however, The weight represents the morphia in 5 grams (77*16 grains) of opium. The per cent, is found by multiplying the weight in grams by 2, or by dividing the weight in grains by 0*7716. The plan of Mohr : The use of lime solution in excess to dissolve morphia from opium or its infusion, and the use of ammonium chloride to neutralize the lime and precipitate the alkaloid — a plan corresponding to the successive use of potasea and ammonium chloride for aluminium separation- — has been well approved by the best authorities for the practical assay of opium. It has been adopted in the British Pharmacopoeia, with exhaus¬ tion of the opium with water before adding the lime, and with acidulation with hydrochloric acid and then evapo¬ ration, before adding ammonia to throw down the morphia. The addition of a little ether and benzole to hasten the crystallization of the morphia, and especially to prevent the crystals from adhering to the sides of the dish, was recommended by Hager ( Pkar . Centralhalle, Jg. 9, No. 1, u. 2), and the process so executed was designated Hager’s later process. Hager directed to deduct one- tenth the weight of the crystalline precipitate for im¬ purities. In view of the fact that some of the narcotina is dissolved by the lime solution, and crystallizes with the morphia, Jacobsen advised to wash the dried crystals with chloroform ; this suggestion, with preference of ether instead of chloroform, Hager accepted, directing the deduction of one-thirtieth for impurities. Hager Jacobsen’s process, with the lime solution of 5 grams of opium all washed through the filter (and consequent concentration of the filtrate) is chosen by Dragendorff, in his ‘Werthbestimmungen starkwirkender Droguen ’ (1874), p. 93, as the best process for practical uses, and only second to Schaeht’s prooess, with correction by amyl alcohol extraction and volumetric estimation, for a method of greatest exactness. Then Hager devised the improve¬ ment of taking 6^ grams of opium, and having 65 grams of water in the lime solution, taking the first 50 grams of filtrate, to represent 5 grams of the opium, thereby avoiding tlie washing of the filter and the concentration of the filtrate, saving the morphia from waste by wet heat, and shortening the operation. This form of Hager- Jacobsen’s process is given in Hager’s ‘ Untersuchungen,’ ii., 176; also in Hoffmann’s ‘Examination of Medicinal Chemicals,’ p. 268. I submit the process, very nearly as given in the two workg last named, but with addition of the preliminary treatment with benzole, for the con¬ sideration of the Committee of Revision.* With the desire to contribute some proof of the com¬ parative exactness of different processes of morphiometric assay, I have instituted a series of comparative trials, each process being applied in turn to each one of a set of samples of opium, holding the conditions as nearly parallel as possible. Then, as a test of each result, the purity of the morphia was estimated volumetrically by Mayer’s solution, and the morphia remaining uncrystallized in the mother liquor was sought to be extracted by -amyl alcohol and estimated volumetrically ; these means of correction, the one against overvalue and the other against under¬ value, being essentially those which were proposed and used by Dragendorff, in his ‘ Werthbestimmungen stark¬ wirkender Droguen.’ All the operations here reported were intrusted to the execution of Mr. Henry Stecher,f and I desire to acknowledge, still farther, the benefit of his counsel in conducting the work throughout the in¬ vestigation. there is no treatment of the opium with benzole. This treatment with benzole lessens the impurities of the morphia weighed, and probably wastes some morphia (not over 2uVo of the weight of the benzole used). The subtrac¬ tion of one -thirtieth is more fully discussed farther on. * A strong approval of Hager- Jacobsen’s process, by Dr. Schlosser, is given in the Am. Jour. Phar., 1871, p. 224. 4* Mr. Stecher has been Assistant in the Chemical Laboratory at Michigan University. August 16, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 129 The following named processes were tried : — A. The process here proposed for the U. S. P., Hager- Jacobsen’s, with a preliminary treatment of the opium with a limited quantity of cold benzole. B. The same, Hager- Jacobsen’s process, modified in treatment of the opium at the start with a sufficient quan¬ tity of hot benzole. C. Hager- Jacobsen’s process, as given by Hager, with-, out initiatory treatment of the opium with benzole. The results being taken before as well as after washing the morphia with ether. D. Procter’s Staples’s process (‘Am. Pharm. Asso. Proceed.,’ 1870, p. 130), the plan of the preparation of morphia by U. S. P., 1870, with initiatory treatment of the opium with benzole. E. Schachtrupp’s process for estimation of morphia and narcotina (‘ Zeitschrift fiir Analyt. Chemie,’ 1868, vii., 509). The plan of this method consists in exhaustion of the opium, made alkaline and dried, with hot benzole, the benzole solution being evaporated and its residue dissolved in acidulated water and titrated with Mayer’s solution, for narcotina, when the benzole-washed opium is exhausted with amyl alcohol, this solution evaporated, and its residue taken up in acidulated water, and ammonia added, for the crystallization of the morphia, so estimated, gravimetrically. The morphia gravimetric results of this process, as of the others, were subjected to volumetric trial. Four of the samples of opium used were obtained at different drug stores in Ann Arbor, and one was taken from the laboratory stock, all being “ powdered opium.” The samples were all dried at 100° C., till drying ceased to diminish the weight. Except for process C, only four samples were worked in the trial of each process. A. The process proposed by the writer, for the U. S. P., as described at the beginning of this paper, Hager- Jacobsen’s process, with initiatory treatment of the opium with a limited quantity of benzol not heated. The results represent 5 grams of opium (6‘5 grams being taken), as the directions stipulate. Corrections were undertaken, by volumetric estimation of the precipitates, and also of the amyl alcohol extract of the filtrates, with Mayer’s solution of potassium mercuric iodide, as described in detail below : — Process A. a. Crystalline precipitate of crude morphia* . b. Ether-washed mor¬ phia . c. By estimating b with Mayer’s solution . . d. From filtrate, by amyl alcohol and Mayer’s solution . . . . e. Total morphia by Mayer’s solution (c + d) . Percentages. No. 1. No. 'i. No. 3. .No. 4. Mean. 12-20 1310 12-32 12-05 12-42 10-74 11-94 11-84 11-68 11*55 7-40 8-80 8-48 8-80 8-37 2T2 1-92 2-76 3-21 2*50 9-52 10-72 11-24 12-01 10-87 /. Subtracting from b A (Jacobsen). . . . 10-38 11-54 11-44 11*29 11*16 fj. Subtracting from a fa (Hager)f .... 10*98 11-79 11-09 10-85 10-18 The quantities of benzole used upon the opium in this series of trials were larger than the directions specify, * The weight of these precipitates were, respectively for the four samples, 1st, 0 610; 2nd, 0’655; 3rd, 0"616 ; 4th, 0-6025 grams. t Hager’s directions to subtract A from the crude pre¬ cipitate and take the remainder for morphia, as well as Jacobsen’s direction, accepted by Hager, to subtract fa from the ether- washed precipitate and take the remainder as the morphia, were both given for processes without initiatory benzole washing of the opium. being, for No. 1, 100 c.c.; for No. 2, 80 c.c. ; for No. 3, 80 c.c.; for No. 4, 70 c.c. Even these quantities did not complete the removal of colour by the benzole, the last portions being still slightly coloured. The reason for restricting the quantity of benzole, and using it cold, is given under process B. For estimation with Mayer's solution, the volumetric potassium mercuric iodide, the precipitates were dissolved in sulphuric acidulated water, and so diluted that, at the final reaction in titrating, the solution should be about 200 parts to 1 part of morphia (as Dragendorff advises). Mayer’s solution* is made by dissolving 13 "55 grams mercuric chloride and 49"84 grams potassium iodide, both strictly dry, in water to make 1 litre. The solution is, therefore, twentieth normal (old decin(rrmal) of HgCl2 + 6KI. Mayer gave the value of 1 c.c. of the solution as 0*020 of alkaloid. Dragendorff reports trials giving (in solutions of 200 to 1) 0-0224 and 0’0221 of crystallized morphia, and of morphia, dried at 120° C., 0-0191 and 0-0205, respectively, for 1 c.c. Again, 0*020 of crystal¬ lized alkaloid. The precipitate is not insoluble in water ; therefore a uniform dilution of 200 to 1 is advised. If four molecules of morphia salt react with three molecules of the iodomercurate [(KI)2HgT2 + 2KI?], then 0-0202 should be the value of 1 c.c. of the solution, in crystallized morphia, c17h19no3 • H20 = 303, no allowance being made for the solubility of the precipitate in water. Dragendorff has stated that the precipitate was visible in a solution of morphia salt in 2500 parts of water. From all the evidence at command, and some trials with crystallized morphia, I believe that titration of morphia with Mayer’s solution, at 0*020 alkaloid to the c.c., gives results certainly not tco high, and possibly a little too low ; also that these results of titration are closer than can be obtained gravimetrically by methods of purification of the crystals. Nevertheless, more investigation is needed as to the conditions of accuracy in titrating with Mayer’s solution. The final reaction was found by patiently waiting for the precipitate to subside after each addition liable to be final, then taking a drop with a glass rod, upon a glass plate resting on black colour, and adding thereto a drop from the burette. If a precipitate appears, these drops are rinsed from the glass plate, into the solution, with a drop or two of water. In undertaking to exhaust the mother liquors (the fil¬ trates) of their remaining morphia, the following plan, after Dragendorff, was adopted : — The crude morphia was filtered out, at the time specified by the process, and the filtrate set aside some time longer for additional crystallization of morphia. The precipitate so obtained was filtered out, washed slightly with water, dried, and washed with ether, dissolved in sulphuric acidulated * F. F. Mayer, ‘Pro. Am. Pharm. Asso.,’ 1862, x., 238; Am. Jour. Plxarm., 1863, xxxv., 20 ; Cliem. News, 1863, 159. George Dragendorff : ‘ Werthbestimmungen stark - wirkender Droguen ’ (1874), 9; ‘ Gerichtlich-cliemische Ermittelung von Giften’ (1868), 227. f The solubility of morphia in pure water is about 1 milligram to 1 cubic centimetre, and Cleaver ( Phar . Jour, and Trans., vii., 243, 1876) advises to add to the weight of purified morphia crystals, one-thousandth of the weight of all the water of the mother liquors and washings, to compensate for the morphia so held in solution. It is of interest to note that this correction, with the 50 grams of mother liquor in the Hager- Jacobsen process, just makes one-tenth the morphia of U. S. P. standard opium, the correction formerly advised by Hager to be deducted for impurities (see result g of process A, above). But it has been clearly shown that opium mother waters, even when non-alcoholic, dissolve more morphia than pure water does. Cleaver states that “solutions of opium from which the morphia has been precipitated, if allowed to stand until the smell of ammonia has disappeared, will re-dissolve large quantities of morphia.” if, however, much excess of ammonia is left in the liquid, the amount of dissolved morphia is much greater (Phar. Jour., 1876, vii., 242). 130 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 16, wi water, and titrated with Mayer’s solution. The opium filtrate (from the morphia precipitate) was then shaken in a large test-tube with amyl alcohol, and the separated alcohol removed, three portions respectively of 15, 10 and 5 c.c. of amyl alcohol being so applied, each portion being heated in a mixture. The united amylic solutions were then evaporated to dryness, the residue dissolved in sulphuric acidulated water, and this solution titrated with Mayer’s solution. The following results were obtained : — In the work with Nos. 1 and 2, after treatment with ammonium chloride, the solutions were left twelve hours, and in Nos, 3 and 4, four hours, instead of the “three to three and a-half hours ” of the process, for the precipitate to form.* Supplementary to Process A. Percentages. a. Additionalprecipitates, estimated by May er’s No. I. No. 2 No. 3. No. 4. Mean. solution . b. From last filtration by amyl alcohol and 0-36 0-20 0 80 0-28 0-41 Mayer’s solution c. Total additional, as 1-76 1-72 1-96 2-93 2-09 given in A, d . . . 2T2 1-92 2-76 3-21 2’50 (To be continued.) ANTISEPTIC GAUZE AND COTTQN.f Although we have already given one or the other of the below-mentioned formulae for the preparation of anti¬ septic gauze, we take this occasion to republish a series of the most approved formulae, in order to answer the inquiries of several correspondents : — 1. Lister's Carbolized Gauze. Paraffin . . 7 parts. Resin . 5 parts. Carbolic Acid . 1 part. Melt the paraffin and resin and add the carbolic acid. The mixture contains 7'7 per cent, of carbolic acid. The original formula of Dr. Lister prescribed that the mixture should be applied by means of a syringe, provided with a sprinkling nozzle, upon the gauze, and that the latter should then be heated under pressure in an air-tight apparatus. For some time past, manufacturers of this gauze have found it more advantageous to dip the gauze into the mixture, and then pas3 it through rollers in order to remove the excess. All carbolized gauze must be kept in air-tight boxes, to prevent evaporation of the carbolic acid. 2. Bruns' Carbolized Gauze. Resin, in coarse ) , AA ,, . , _ . 400 §’ms* (14 av* oz- * 1 2 3 4 53 grs.) powder Castor Oil . Carbolic Acid Alcohol . . Dissolve the first 40 gms. ( 1 av. oz. 180 grs.) 100 gms. ( 3 av. oz. 230 grs.) 2 litres (67^ fl. £.) three ingredients in the alcohol. Saturate the gauze with it thoroughly, wring it out and * Dragendorff reports, from Mr. Fricker’s work (‘ Werth- bestimmung,’ 92) : — 1. Morphia by Hager’s process, 5'9 per cent.; by three days’ crystallization, 0 3 per cent. ; by amyl alcohol, T06 per cent. 2. Morphia by Hager’s process, 5 8 per cent. ; by three days’ crystallization, 0-85 per cent. ; by am>l alcohol, 0‘73 j>er cent. 3. Morphia by Hager’s process, 7'3 per cent. ; by three days’ crystallization, 127 per cent.; by amyl alcohol, 0‘56 per cent. 4. Morphia by Hager’s process, 6-24 per cent. ; by three days’ crystallization, 0‘80 per cent. ; by amyl alcohol, 0-46 per cent. 5. Morphia by Hager’s process, 0 38 per cent. ; by three days’ crystallization, 0’07 per cent.; by amyl alcohol, 062 per cent. t From New Remedies, August, 1879. dry it by hanging it up horizontally, or by shaking it, spread out in lengths of about seven yards ; if done in the latter way, two persons holding the two ends and shaking it up and down, it will be sufficiently dry in a few minutes. This gauze is much softer and pliable than Lister’s, and is free from the drawback of irritating the skin, which is sometimes caused by paraffin. The above solution contains 10 per cent, of carbolic acid. 3. Eilau's Carbolized Gauze. Linseed Oil, boiled . 4 ounces. Yellow Wax . 2 ounces. Resin . 4 ounces. Oil of Turpentine . 8 ounces. Carbolic Acid, Calvert’s No. 2 . 1 ounce. Melt the first three ingredients, then add the other two. Immerse the fabric in the liquid and pass it through a clothes wringer several times; then fold it, wrap it in oiled silk or carbolized paper, and keep it in a well closed tin box. The above solution contains a little over 5 per cent, of carbolic acid. 4. Pohl's Carbolized Gauze. Deprive the gauze of fat or grease by treatment with caustic soda, thorough washing and drying. Then make a mixture of 100 parts of pure carbolic acid and 5 parts of strong alcohol, of which about 4 grams (1 3) are sprinkled upon each square metre (a little over a yard) of the fabric. This is then introduced into a copper boiler which is provided with a safety valve, and is to be her¬ metically closed, where it is heated to a temperature of 120'*’ C. ( = 248° Ft). 5. Benzoated Gauze or Cotton (Bruns). This is either made with a 5 per cent, or with a 10 per cent, solution, namely : — a. 5 per cent, solution. Benzoic Acid . . 50 gms. (1 av. oz. 334 grs.) Castor Oil . . . 20 gms. (309 grs.) j or Castor Oil . 10 gms. (154 grs.) ) ( Resin. . . 10 gms. (154 grs.) ) Alcohol .... 2430 c.c. (82 fl. oz. 110 min.) b. 10 per cent, solution. Benzoic Acid . . 100 gms. (3 av. oz. 231 grs.) Castor Oil ... 20 gms. (309 grs.) ) or Castor Oil 10 gms. (154 grs.) ) ( Resin . . 10 gms. (154 grs.) ) Alcohol. . . . 2360 c.c. (79 fl. oz. 447 min.) The gauze or cotton (which latter should have pre¬ viously been deprived of oil), is dipped in the liquid, expressed, and dried at a gentle heat. 6. Salicylated Gauze or Cotton (Bruns). a. 5 per cent, solution, and b. 10 per cent, solution are prepared exactly like the preceding. 7. Benzoated or Salicylated Gauze or Cotton (Thiersch). These are prepared like those under Nos. 5 and 6; only in place of castor oil an equal quantity of glycerin is used. But this is found not to entirely prevent the loss of benzoic or salicylic acid in the shape of fine dust on handling. 8. Borated Gauze or Cotton. Boracic Acid . 10 oz. Glycerin . 4 fl. oz. Water . q. s. to make 100 fl. oz. Dissolve by the aid of a heat, which should not be raised higher than necessary, but should be kept up during the saturation of the cotton, so that the acid will not crystallize upon it. The cotton must have been pre¬ viously deprived completely of its fat by boiling with soda, and subsequent thorough washing and drying. 9. Borated Lint. Dr. Vulpius, of Heidelberg, directs to dissolve 1 part of boracic acid in 4 parts of boiling water, to saturate 1 part of lint with this solution, and to dry. August lfi, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 131 ©he $ftai;maqutual Jjarpral. - - SATURDAY, AUGUST 1C, 1879. Communications for the Editorial department of this Journal, hooks for review, etc., should he addressed to the Editor, 17, Bloomsbury Square. Instructions from Members and A ssociates respecting the transmission of the Journal should he sent to Mr. Elias Brkmridge, Secretary, 17, Bloomsbury Square, W.C. A dvertisements, and payments for Copies of the J ournal, Messrs. Churchill, New Burlington Street, London , IV. Envelopes indorsed “ Pharm. Journ .” THE CONFERENCE MEETING. By the time this Journal reaches the hands oi its readers many of them will, it is hoped, he turning their thoughts towards the steel metropolis and the gathering there of the British Pharmaceutical Con¬ ference during next week. It will, therefore, he of interest to them to know what are the arrangements made for that event hy the Local Committee. The meeting will he commenced on Tuesday morning, the 19th inst., at half past ten, in the Freemasons’ Hall, Surrey Street, under the presi¬ dency of Mr. George Frederick Schacht, of Clif¬ ton. After the usual preliminary business, the reception of the Report of the Executive and the Address of the President, the reading of papers— a partial list of which appeared in this Journal last week — ' will he commenced ; this will he continued until five o’clock, and resumed on the following day at half-past ten. On each day there will he an adjournment, extend¬ ing from one until half-past two o’clock, for luncheon, and on Tuesday the members will have the oppor¬ tunity during this interval of visiting the extensive cutlery works of Messrs. Rodgers and Son, under the guidance of some appointed members of the Local Committee. In the evening of the same day special cars will he provided to convey visitors to the Armour Plate Works of Messrs. J. Brown and Co., Limited. On Wednesday morning, at half-past nine, mem¬ bers of the Local Committee will he in attendance to accompany visitors to electro-plate and other works, previous to the resumption of the Conference. No arrangement has been made for Wednesday evening, in order that members may he at liberty to hear the Inaugural Address of Professor Allman, the President of the British Association. After two days of hard work the members of the Conference will he ready for a holiday, and should this most unseasonable of summers prove capable of yielding one more fine day on Thursday, the 21st, the Excursion to which the Local Committee invites the visitors, both ladies and gentlemen, should be a most enjoyable one. Starting at nine o’clock the company will be conveyed in carriages via Owler Bar, Frog- gatt Edge, Calver and Bake well to Haddon Hall, an old baronial mansion, situated on the banks of the Wye, and belonging to His Grace the Duke of Rut¬ land. This will be the most distant point of the excursion and here lunch will be provided. After ample opportunity has been given for exploring the old mansion, the company will leave for Chatsworth, where the celebrated mansion of the Duke of Devon¬ shire will be thrown open to the visitors. After a ramble through the park the road back to Sheffield will be struck where it crosses the Derwent at the village of Baslow. But before proceeding further “ high tea ” will be served at the Wlieatsheaf Arms. This it is expected will be brought to a close about half-past eight, and then the company will make their way northward to Sheffield. We do not presume to say which part of this pro¬ gramme is most enticing, the scientific conference or the scientific outing ; but we think that as a whole it is sufficient to decide the minds of any waverers in favour of being present at the Sixteenth Meeting of the Conference. We are glad to learn that, so far as can be judged from the number who have applied to Mr. Maleham, the Honorary Local Secretary, to secure them accommodation, there are already indi¬ cations of its being a most successful gathering. PHARMACOPOEIA REVISION. As mentioned on several occasions recently the question of Pharmacopoeia revision has been taken up by the pharmacists of the United States with considerable vigour. In that country the construc¬ tion of the Pharmacopoeia is not at present controlled by legislation, and among the consequences of this freedom are a multitude of suggestions and a large amount of volunteer work from pharmacists which under proper guidance will probably leave a benefi¬ cial impress upon future editions of the United States Pharmacopoeia and at the same time profit pharmacy generally. Such guidance may be expected from the American Pharmaceutical Association, which has shown considerable interest in the work, and a report of a committee of that body, presented at the last annual meeting at Atlanta, describes the general principles which it is recommended should be fol¬ lowed in the next revision. Language is the first subject dealt with, and with respect to this it is distinctly stated that whatever might be urged in favour of the use of the Latin lan¬ guage ill European pharmacopoeias, it would be im¬ practicable in the United States, for that if it were adopted the original text would be seldom consulted and most pharmacists would use a translation. In the arrangement it is proposed to abolish the divi¬ sion of the materia medica into primary and secondary lists, — a practice which has been recommended more than once for imitation in this country, — and to arrange all the articles in one alphabetical order, retaining however such headings as aquoe, infusa, decocta, etc., where it is thought desirable to give general direc- 132 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 13, 1879. tions referring to a whole class. It is also proposed to continue the plan of placing the name of a plant first, followed by the name of the particular part. The question as to the elimination of articles at present in the Pharmacopoeia and the introduction of others is next discussed and lists are given which are too long to quote entire. Among those it is proposed to discard are several indigenous remedies, some of which have more or less been recommended as substitutes for foreign ones, such as Americian elder flowers, Cannabis americana, Euphorbia Ipe¬ cacuanha , Gentiana Catesbcei. Chiretta and oil of rue are also included in this list. Among the crude drugs proposed to be added may be mentioned coca, guarana, tea, Eriodictyon Calif ornicum, Eucalyptus globulus , Ehamnus Frangula , Fucus vesiculosus . Grindelia robusta and G. squarrosa, Hamamelis Virginica and jaborandi. Seventy chemicals are proposed to be added, including clirysophanic, dilute hydrobromic, purified oleic and salicylic acids, cin¬ chonine and sulphate of cinchonidine, salicylates of iron, lithium and quinine, hypophospliites of cal¬ cium, iron, potassium, and sodium, and pilocarpine hydrochlorate. The list of pharmaceutical prepara¬ tions is still larger, and includes a number of extracts, oleates of the alkaloids and of mercury, tincture of gelsemium, hydrastin, viburnin, and leptandrin, and solutions of the silicates of potassium and sodium. The descriptions of crude drugs are to be sufficient to indicate the distinctive characteristics visible to the naked eye and when necessary such as are visible under an ordinarily good pocket lens. Common admixtures and falsifications are to be mentioned and the differences pointed out. The Committee further recommends that all chemicals of definite composition should have their formulae added, accord¬ ing to both the old and the new notation, together with their atomic weights; but that except when differences of process would give different results, chemicals should only be described and defined by concise but complete tests of identity and purity. Also, that temperatures should be stated both in degrees of Centigrade and Fahrenheit. In the expression of quantities the Committee thinks that all measures of capacity should be abandoned and quantities expressed only in parts by weight. It also recommends that the opportunity afforded by the reconstruction of the formulse for this purpose should be taken advantage of, in cases where a slight variation of dose is of no importance, to make the tinctures, wines, etc., of uniform strength, so far as relates to the proportion of the crude drug used to a definite quantity of product, and that in doing so the quantities of the ingredients entering into a compound should be expressed in the simplest possible terms and whenever possible in a decimal ratio ; but that in the case of very active prepara¬ tions the present strength should be as nearly as possible preserved. In cases where certain weights of ingredients are directed to be combined under conditions that may involve a partial loss of any of them— as for instance, when a variable quantity of water may be lost by heat— it is recommended that the weight of the end- product should be specified. Recognition of the progress the metric system is making in the United States is indicated in the proposition that wherever it is necessary to employ definite expressions of weight the quantity should be expressed both in apo¬ thecaries’ and decimal weights. The fluid extracts appear to be the most difficult problem the Committee has to deal with. It has decided to recommend that in regard to strength they shall all represent the drug, grain for grain ; but as to the practical process for their preparation the Committee hesitates between an improvement of Procter’s process and Squibb’s process of repercola¬ tion recently described in this Journal. Co-operative experiments are still being carried on under the superintendence of Professor Diehl to assist the Committee to come to a decision on this point. As an Appendix the Committee think the next edition of the United States Pharmacopoeia should be provided with a table of solubilities of the officinal chemicals in water and in alcohol, at 60° F., and the boiling points ■; a table of maximum safe doses of powerful remedies ; an alcoholometric table; an acidimetric table ; a table of reagents ; a list of synonyms ; a weight and volume table, to facilitate the introduction of the metric system in prescribing ; and a table comparing the strength of powerful galenical preparations of other pharmacopoeias 'with that of the corresponding preparations in the United States Pharmacopoeia. BRITISH MEDICAL ASSOCIATION. The Annual Meeting of this Association was held in Cork last week, commencing on Tuesday the 5th inst. The number of members present in the city on the first day is estimated at four hundred ; there were also many eminent foreign practitioners present. The new President is Dr. O’Connor. The Address in Medicine was delivered by Dr. A. Hudson, of Dublin, and that in Surgery, by Mr. Savory, the subject of the former being the labours of Laennec and their influence in medicine, and the latter being mainly a criticism of Lister’s antiseptic method. Amongst the business transacted was the award of the gold medal of the Association, for dis¬ tinguished merit, to Surgeon-Major Reynolds, in recognition of his services at Rorke’s Drift. SIR WILLIAM JENNER. We learn from the medical journals that Sir William J enner is suffering from an attack of whooping cough, and that he has ceased to practise for the present in order that he may not spread the disease. August 16, 1879.J THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 133 rocincial Sfransajfitms. LEICESTER CHEMISTS’ ASSISTANTS AND APPRENTICES’ ASSOCIATION. The half-yearly meeting of the above Association was held at the rooms, Halford Street, on Tuesday, August 5, 1879, the Vice-President, Mr. Brampton, in the chair. After transacting some preliminary business the following- report was read and adopted : — “ In submitting the report of the proceedings of the Association for the past session, your Committee con¬ gratulate the members upon the fact that the Association has now completed its twenty-first session. In looking at the results attained in the past through the medium of the Association, your Committee have every reason to be highly gratified; whilst at the same time they are assured that with the applianoes they now possess, mugh greater success may reasonably be looked for in the future. “ Your Committee regret to notice that the attendance of members has not been so good as could be desired, but are pleased that the rooms have been used by the members for private study on other than class nights to a considerable extent. “Your Committee are highly gratified at the success of Uhe botany class which has been conducted by Mr. W. J. Harrison, F.G.S.,in connection with the Science and Art Department of South Kensington. At the Government examination held in May, the following members were successful: — First Class, Mr. Burford; Second Class, Messrs. Brampton, Lewitt, Llewellyn, Shuttlewood and Raynor. “ Three lectures have been delivered during the past session, viz.: — By the Rev. E. Atkins, B.Sc., on ‘Elec¬ trolysis;’ Mr. W. B. Clark, on ‘Chemical Toxicology,’ and J. E. Weatherhead, Esq., on ‘Cetacea;’ to these gentlemen your Committee tender their sincere thanks for the very able and interesting lectures with which they have favoured the Association. “ Your Committee are pleased, to notice that a member of the Association, Mr. Raynor, has passed the Minor examination. “The library is in a flourishing condition, and the valuable books it contains have been in constant re¬ quisition. “ In conclusion, your Committee desire to thank those who have rendered help in the past, and to remind the members that the welfare of the Association depends, to a great extent, upon the efforts put forth by each individual member to further the interests of the Asso¬ ciation.” The Treasurer’s report, showing a balance in hand of 8s. 8|c?., having been received and adopted, Mr. Clark proposed that the Secretary be instructed to forward to the late President the following resolu¬ tion : — “ The members of this Association having heard with regret of the departure from Leicester of Mr. Raynor, beg him to accept their thanks for the many services he has rendered, and assure him that in whatever position he may be placed, he will have their best wishes for his future welfare.” Mr. Shuttlewood seconded the resolution. The Chairman having put it to the meeting, it was carried unanimously. The meeting then proceeded to the election of a Com¬ mittee for the ensuing session, with the following result : — President, Mr. J. J. Edwards; Vice-President, Mr. W. *3. H. Brampton; Honorary Seci-etary, Mr. S. F. Bur- ford ; Treasurer, Mr. W. B. Clark ; Messrs. Lewitt, Shuttlewood, Thirlby. Prmjrrdinjgs of ^cknlific Jsnrietifs. SOCIETY OF ARTS. The History of Alizarin and Allied Colouring Matters, and theie Peoduction from Coal Tar.* BY W. H. PERKIN, F.R.S. {Concluded from page 119.) The tars from different gasworks yield very different quantities of anthracene ; this is to a great extent due to the kind of coal employed and the temperatures to which the retorts are heated in the gasworks. To take two extreme cases. Newcastle coal yields a tar which is very suitable for the preparation of anthracene, whereas cannel coal gives a tar containing but little anthracene and a great deal of paraffin. Now, at some gasworks cannel coal is principally used, as in Scotland. At others, some is often mixed with Newcastle or other variety of coal to increase the illuminating power of the gas ; this is done frequently in cold weather. Thus tars of all sorts of qualities are formed, and consequently, the kind and quantity of impurities in the anthracene prepared from them differ. Further complications also arise in the tar works ac¬ cording to the way the distillation of the tar is conducted. If k is carried only so far as to leave a soft pitch in the still, it does not contain so many varieties of impurities as when the distillation is carried on until hard pitch is produced, or the pitch coked. Crude anthracene is, there¬ fore, found to be not altogether of value according to the percentage ©f anthracene it contains, but to a considerable extent upon the nature of the impurities associated with it. Thus, anthracene obtained from pitoh is scarcely a saleable article to those who purify their anthracene by washing it with naphtha, and then by sublimation. It would be very interesting to see if it would not be worth while distilling coal near the pit’s mouth, for the purpose of manufacturing benzol, anthracene, and other useful products, selecting the most suitable qualities of coal, and employing temperatures which experiment proved to be the most suitable. The gas and eoke, of course, could be utilized as fuel. Should the supply of coal tar from any circumstance become insufficient, as, for example, by gas being superseded by the electric or any other source of light, this undoubtedly would have to be done, and it would be a great advantage to get pro¬ ducts of a uniform quality. It will, perhaps, be of interest here to record the prices paid for anthracene during the first year or two of the manufacture of artificial alizarin. In 1870 — 1871, we gave from 9c?. to Is. 6d. per cent, per cwt., and in 1872 from Is. 6d. to 5s. , and a small quantity at 5s. 6d. This shows how the price advanced with the demand ;+ since then there have been great variations, and much higher prices are said to have been given by some buyers. The anthracene was at first valued by the bisulphide of carbon or petroleum and bisulphide of carbon tests, and also, by the alcohol process, the present anthraquinone method not being then proposed. For our own informa¬ tion, wTe employed from nearly the first an anthraquinone test, which consisted in oxidizing about ten grams of the anthracene, previously purified with petroleum and distillation with caustic potash, subliming off the anthra¬ quinone in a retort, crystallizing it from naphtha and then weighing. This, although not very accurate, we found to be practically of much value to us. As to the advantage of the use of naphtha or petroleum spirit for purifying anthracene, manufacturers differ in Opinion. It is evident, however, that petroleum spirit has the great advantage of dissolving less anthracene, and, at the same time, the other impurities are sufficiently soluble * From the Journal of the Society of Arts. f The prices of anthracene given in the Moniteur Scien - tifique, April 19, p. 420, are much too high. 134 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 16, 1H7P. in it to be removed if enough be employed, say two or three times as much as the crude anthracene to be puri¬ fied; it is also easily removed from the purified anthra¬ cene by steam, on account of its volatility. Coal-tar naphtha, however, dissolves out a good deal of anthracene; so that the impurities dissolved by it, and left after it has been distilled off, contain often seven or eight per cent, of anthracene, which is difficult to recover. Neither naph¬ tha nor petroleum remove much of the carbazol. The following is a table of solubilities of anthracene, etc., in benzene and petroleum : — Petrol* ;um. Benzene. B, .P. 70°- -100° C. B.P. S0°-10o° C. Anthracene . . ■115 per cent. . . ‘976 per cent. Phenanthrene . . 3-206 99 • . 21-94 „ Carbazol .... •016 99 . -51 Dichloranthracene T37 99 • '52 Anthraquinone •013 99 . -166 „ There is an impurity in anthracene which is sometimes very troublesome, and that is paraffin. This paraffin is of high fusing point, and of little solubility either in petroleum or in naphtha — very different in this respect from ordinary paraffin. It will dissolve in these solvents when they are hot, but on cooling is almost entirely deposited again. A small quantity of this left in the anthracene frequently greatly impedes the filtration in the succeeding operations, and being a stable compound, passes through most of the processes; it is, therefore, a very troublesome substance, and interferes with the value of a crude anthracene containing it. Crude anthracene is very much purified by being hot-pressed, so much so, that if it is thoroughly done, it is scarcely needful to treat it with naphtha or petroleum. The anthracene, which dis¬ solves in the fused impurities and is then pressed out, may be afterwards recovered. I will now make a few remarks upon the process of distilling anthracene with caustic potash. This process has been very much spoken against, as destroying a con¬ siderable quantity of the anthracene. I may remark that anthracene is not acted upon by heating with caustic potash ; and from all the experiments I have made on the subject, which are very numerous, I have not found that there is any more loss of anthracene by distilling it with caustic potash than by distilling it alone. The effect of caustic potash on crude anthracene is very remarkable, sometimes as much as forty and fifty per cent, of impurities being removed by distilling it with this alkali. The action appears to be twofold : first, it chars all the difficultly volatile and unstable products and bodies of a phenolic character ; and, secondly, it combines with the carbazol, forming with it a remark¬ able compound. Carbazol is present in considerable quantities ; crude anthracene, after being washed with naphtha, containing from ten to twelve per cent, of car¬ bazol ; washed anthracene, which has been distilled with caustic potash, consists chiefly of anthracene and phe- nanthrene. For the economical production of dichloranthracene, we found anthracene which had been purified by dis¬ tillation with potash essential. This, when properly chlorinated, gives a beautifully crystalline mass, con¬ taining a certain amount of oily bodies, which can easily be removed by pressure. Whereas anthracene, which has not been treated with potash, yields a confusedly crystalline mass mixed with sticky impurities, which cannot be pressed out until rendered fluid by the addition of coal-tar naphtha, which results in a considerable loss of product. One advantage of this process of treating anthracene is that it brings anthracenes of different origins to similar conditions — even pitch anthracene works perfectly well after being subjected to this process. It is also useful as indicating the origin of the anthracene. The further the distillation of the tar has been carried, it w ill be found the greater the loss of weight the crude anthracene obtained from it will suffer on distillation with potash,, on account of the impurities it contains being more easily charred. There is one curious fact in connection with the pro¬ cess. If anthracene which has been well washed with naphtha or petroleum be distilled with potash, it will be found that on treatment with these solvents again, a considerable amount of impurity will freely dissolve out,, apparently consisting chiefly of phenanthrene. I know of no method of procuring anthracene in a pure state easily and in quantity but by purifying it by dis¬ tillation with caustic potash. Anthracene thus treated, if washed with benzol or other suitable solvents, and then dissolved in boiling benzole, will crystallize out on cooling in a most beautiful manner- in nearly colourless plates with a blue fluorescence, one or two crystalliza¬ tions rendering it perfectly pure. And this brings me to the subject of the use of pure anthracene in the manu¬ facture of alizarin. Generally speaking, as a manufacture advances, so the- quality of the materials used are improved, and I quite think that the need of anthracene in a pure or purer condition than it is now employed in, will be found to be very desirable in the production of artificial alizarin. Just before I left off manufacturing this product, at the end of 1873, I was engaged upon experiments in this direction, for the purpose of improving the method of preparing dichloranthracene, so as to reduce the amount of chlorine oils formed, or to avoid their formation altogether. As chlorine forms, with pure anthracene,, the theoretical amount of dichloranthracene, it is evident, that if some convenient method were adopted to allow these bodies to freely react upon each other, pure- dichloranthracene could be produced very cheaply, as there would be no loss and no purification needed. I quite think this might be accomplished. The oxidation of pure anthracene for the preparation of anthraquinone does not succeed well by the process at- present adopted, so that this would likewise have to be modified ; but if it could be obtained pure, or nearly pure, at once, instead of having to be dissolved in oil of vitriol, or sublimed and then treated with this acid, it would be a great advantage. To obtain anthracene in a pure or nearly pure state on the large scale, I think that it would probably be found best to distil hot-pressed anthracene with potash ; then to grind it fine, wash it with petroleum or naphtha and lastly crystallize it from naphtha. I may here, perhaps, make a few remarks upon car¬ bazol, as it is quite probable that it may yet be found to be a valuable product. To obtain it, anthracene, pre¬ ferably hot-pressed or washed with naphtha, is distilled with caustic potash until no more anthracene passes over. The black residue is then freed from potash by being well washed with water, and on being distilled yields carbazol ; as I mentioned before, crude anthra¬ cene gives as much as 10 or 12 per cent, of this sub¬ stance. Another method consists in boiling the anthra¬ cene with fused caustic potash in a cylinder, until free from water, and then allowing the mixture to stand to cool. On opening the cylinder, the anthracene will be found as a layer on the top of the potash containing the carbazol, and can be scaled off. After this is removed,, the remaining product is treated as just indicated.* This remarkable compound of potash and carbazol, whtn heated to redness, gives off large quantities of hydrogen gas, the carbazol being decomposed. From experiments I have made, this compound appears to contain one atom of potassium to one of carbazol, its- formula probably being C12H8KN. It is now under investigation. * The process of distilling crude anthracene with caustic potash was communicated to H. Caro, of the Badische Aniline and Soda Fabrik, and it was by this means that the carbazol investigated by Graebe and Giaser was ob¬ tained. August 16, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS 135 Carbazol is a beautifully crystallized body, not unlike anthracene. When heated with mercuric chloride, or various other oxidizing agents, it produces a blue colour¬ ing matter. This, however, has not been found to be of practical value. It is probably the substance which was described several years ago as anthracene blue, the an¬ thracene used probably containing carbazol. In crude anthracene and oil, accompanying it, there is a peculiar organic base called acridine, having the formula C12H9N. It was first observed by Caro, and investigated by Graebe and Caro. It crystallizes in brownish yellow four-sided rectangular prisms, and is a most stable com¬ pound. The vapour causes sneezing and coughing, and it gives to the oils accompanying anthracene a very irritating action when rubbed on the skin. In hot weather the workmen employed in pressing or otherwise working with crude anthracene sometimes suffer very considerably from the pain it temporarily produces. Some improvement in the treatment of sulpho acids of antbraquinone with caustic soda in the production of colouring matter is very desirable. The amount of alkali used is often six or eight times more than indicated by theory, and, as no suitable means have been obtained for recovering this before precipitating the colouring matter, it is all converted into sodic sulphate, for which a large amount of sulphuric acid has also to be employed. The sulphate of soda, being in solution, does not pay for evaporation, otherwise it might be reconverted into caustic soda. Some experiments have been made to precipitate the colouring matter from the alkaline solution with lime, but this, unfortunately, especially with red shades of colours, acts very imperfectly, and is therefore of no value. It is also very desirable that the condition under which the a and jj disulphoanthraquinonic acids are formed as also of the disulpho acid giving the sulpho acid of alizarin should he studied, so that their separate formation may be effected at will. Having now given an account of the manufacture of artificial alizarin, it will be interesting to inquire into the commercial results of this industry, and, firstly, what has been its influence upon the sale of madder and its de¬ rivatives. I mentioned at the commencement of this piper that the annual value of the imports into the United Kingdom of madder and garancine, from 1859 to 1863, amounted to about £1,000,000 sterling, with prices averaging for madder 45s. and 50s. per cwt., and for garancine, 150s. In the subjoined table will be seen the remarkable changes that have taken place in the imports, and also the great reduction in price : — Average Annual Imports of Madder and Garancine into the United Kingdom. ! Year. . ■ -- , Madder. Garan¬ cine. French madder. Turkey roots. Garan¬ cine. 1859 ) 1868 \ cwts. cwts. s. s. S. 305,840 45,560 45 50 150 1875 ' 100,280 ( 25,860 15,396 ) — 1876 59,137 j or > — — _ 6,436 ) 1877 38,711 8,875 — — — 1878 32,990 2,790 18 17 65 Up to and during 1876 considerable quantities of artificial alizarin were imported from the Continent, and entered at the Customs as garancine or madder, which having been brought to the notice of the officials, the returns made subsequently are more reliable. The im¬ ports df garancine were returned by the Board of Trade in 1876 as 15,396 cwts. when first published, but in the following year, when the figures for 1876 were given for comparison with those of 1877 and 1878, the returns were stated as only 6436 cwts. The erroneous entries were most probably made to evade the penalties for the infringement of patent rights.* Dutch ground madder has been relatively much higher in price than the other qualities. This is owing to its extensive use in wool dyeing. For various reasons arti¬ ficial alizarin has made but little progress in its appli¬ cation to wool dyeing, and Dutch madder being mostly used for this purpose, its prices have been maintained at from 28s. for ordinary “ Ombro” to about 40s. to 45s. for crop madder. The wool dyers have, however, been working cautiously with artificial alizarin, and now some of them are using it somewhat largely, and, considering its cheapness as compared with Dutch madder, no doubt they will soon find how to use it successfully, and cease to employ madder. The decline in the sale of madder is still rapidly going on. During the first two months of last year the imports were — Madder . 6846 cwts. Garancine . 533 „ During the first two months of this year they were — Madder . 2185 cwts. Garancine . 175 „ Or about two -thirds less. And not only so, but the price is still declining. Turkey roots may now be bought at 11s. per cwt., whereas before artificial alizarin was intro¬ duced they were sold, on an average, at 50s. At the present prices of madder its cultivation is unremunerative, and will undoubtedly be soon a thing of the past. Such has been the success of artificial alizarin in competing with madder and garancine in this country, and it is equally true of other countries. The quantity of madder grown in all the madder-growing countries of the world prior to 1868 is estimated at about 70,000 tons per annum. The amount of artificial alizarin now produced is equal in dyeing power to considerably more than this ; in fact, the lowest estimate I have been able to get for 1878, and which is confirmed from other sources, is 9500 tons, which is equivalent to 950,000 tons of madder. This remarkable result has been arrived at in ten years °nly. To produce this quantity of artificial alizarin there are about nine manufacturers on the Continent and one in this country, Messrs. Burt, Bolton and Haywood, who have two large works for its production, viz., the original works at Greenford Green, and new ones at Silvertown. Graebe and Liebermann, in their paper in the Mpniteur Scientifique give some statistics of the production of artificial alizarin, which, however, require correcting. They also leave out the years 1869 and 1870. In 1869 we had advanced in the manufacture so far as to send colour into the market, the first invoice being dated October 4th, and that year we produced about one ton. In 1870 we produced 40 tons ; in 1871, 220 tons ; in 1872, 300 tons ; and in 1873, 435 tons. Up to the end of 1870 we were practically the only makers of this product. One of the largest chemical and coal-tar colour manufacturing firms of Germany, with whom we were in correspondence, stating that in November, 1870, they had only lately commenced producing 50 pounds of alizarin, 10 per cent, quality, per day, and that no one else in that country was supplying artificial alizarin ; and in 1871 we were practically the only producers of quantity, at any rate during the first part of the year, for in March, 1871, the firm already referred to, and who had great opportunities of knowing what was being done in their country, wrote that they had not received know- * A method so often resorted to as to render English chemical patents nearly useless as a protection against infringements by foreign manufacturers, the results of this being alike detrimental to the inventor and injurious to the national interests. f April, 1879, p. 416. 136 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 1 6, 1879. ledge of any establishment but their own manufacturing artificial alizarin. In November, 1871, however, Messrs. Gessert Freres announced to the Industrial Society of Mulhouse that they had produced 30,792 kilogrammes of alizarin in paste. This is equal to about 30 tons, an amount which was evidently considered by them a very large quantity.* Graebe and Liebermann’s statistics are as follows com¬ pared with our production : — Graebe and Lieber- Perkin and Son’s no arm. Production?. Tons. Tons. 1869 .... 1 1870 .... 40 1871 .... 125— 150 220 1872 .... 400— 500 300 1873 .... 900—1000 435 Without wishing to detract from Graebe and Lieber¬ mann’s original discovery, we may say that the birthplace of the manufacture of artificial alizarin was in England. It was in this country that the difficulties and doubts about the manufacture and supply of the raw material, anthracene, were solved, and the production of artificial alizarin by new processes successfully accomplished. After these results were obtained in this country, continental chemists were encouraged to manufactd^ on a compara¬ tively large scale, but up to the end of 1873 the English manufacturers had practically no competition in the home market. Having considered the amount of artificial alizarin now manufactured, it will be of interest to see what its money value is. Taking the lowest estimate, viz., 9500 tons, and calculat¬ ing its selling prices at £150 per ton, the annual value amounts to no less than £1,425,000, or nearly a million and a-half. =/ As a dye, it is now at most not more than one-third of the average price of madder in 1859-1868. Consequently, in the United Kingdom, when the annual value of madder imported was £1,000,000, the annual saving is very great. While collecting the statistics about alizarin, I thought it would be of interest to get, if possible, the statistics of the entire coal-tar colour industry, and to the kindness of H. Caro, of the Badische Aniline and Soda Fabrik, I am indebted for most of the following particulars : — Estimated Value of the Production of Coal-Tar Colours in 1878. Germany . . £2,000,000 of which four-fifths are exported. England . . 450,000 France . . . 350,000 Switzerland 350,000 Total. . £3,150,000 In referring to the works which have been set up for the purpose of making coal-tar colours, I thought it would be of interest to show a copy of a rough sketch of the first works erected for this purpose as they appeared in 186$, two years after the patent for the mauve was taken out. These works were not one year old when sketched, and the practicability of making the mauve commercially had only been proved a short time. In 1873 they had in¬ creased to such an extent as to cover about six acres. There are now in this country six coal-tar colour works ; in Germany, no less than seventeen ; in France, about five ; and in Switzerland, four. There are also three works in Germany and three in France which manufac¬ ture aniline in enormous quantities for the production of coal-tar colours. Such is the wonderful growth of this industry, which dates only from 1856. It is the fruit of scientific researches in organic chemistry, conducted mostly from a scientific point of view ; and, while this industry has made such a great progress, it has, in its turn, acted as a handmaid to chemical science, by placing at the disposal of chemists * Moniteur Scientifique, April 1879, 416. products which otherwise could not have been obtained, and thus an amount of research has beep conducted through it so extensive that it is difficult to realize, and this may before long produce practical fruit to an extent we have no conception of. One very important colouring matter related to coal-tar, and one of the original sources of aniline — a product of as great importance as alizarin — ha& yet to be produced on the large scale. I refer to indigo. Baeyer has shown that it can be produced artificially, but at present no practical means of accomplishing it have been discovered. No doubt, however, it will not be many years before this is achieved, and the cultivation of the indigo plant share the fate of madder. ROYAL INSTITUTION OF GREAT BRITAIN, A New Chemical Industry, Established by M. Camille Vincent.* BY PROFESSOR ROSCOE, LL.D., F.R.S. “After I had made the discovery of the marine acid air? which the vapour of spirit of salt may properly enough be called, it occurred to me that, by a process similar to* that by which this acid air is expelled from the spirit of salt, an alkaline air might be expelled from substances, containing the volatile alkali. Accordingly I procured some volatile spirit of sal-ammoniac, and having put it. into a thin phial and heated it with the flame of a candle, I presently found that a great quantity of vapour was discharged from it, and being received into a basin of quicksilver it continued in the form of a transparent and permanent air, not at all condensed by cold.” These: words, written by Joseph Priestley rather more than one hundred years ago, describe the experiment by which ammonia was first obtained in the gaseous state. Unacquainted with the composition of this alkaline air, Priestley showed that it increased in volume when electric sparks are passed through it, or when the alkaline air (ammonia) is heated the residue consists of inflammable air (hydrogen). Berthollet, in 1785, proved that this increase in bulk is due to the decomposition of ammonia into nitrogen and hydrogen, whilst Henry and Davy ascertained that two volumes of ammonia are resolved into one volume of nitrogen and three volumes of hydrogen. The early history of sal-ammoniac and of ammonia is very obscure. The salt appears to have been brought into Europe from Asia in the seventh century, probably from volcanic sources. An artificial mode of producing the ammoniacal salts from decomposing animal matter was soon discovered, and the early alchemists were well acquainted with the carbonate under the name of spiritus. salts urince. In later times sal-ammoniac was obtained from Egypt, where it was prepared by collecting the sub¬ limate obtained by burning camels’ dung. Although we are constantly surrounded by an atmo¬ sphere of nitrogen, chemists have not yet succeeded ir> inducing this inert substance to combine readily, so that we are still dependent for our supply of combined nitro¬ gen, whether as nitric acid or ammonia, upon the decom¬ position of the nitrogenous constituents of the bodies of plants and animals. This may be effected either by natural decay, giving rise to the ammonia which is always contained in the atmosphere, or by the dry distillation of the same bodies, that is, by heating them strongly out of contact with air; and it is from this source that the world derives the whole of its commercial ammonia and sal-ammoniac. Coal, the remains of an ancient vegetable world, con¬ tains about 2 per cent, of nitrogen, the greater part of which is obtained in the form of ammonia when the coal undergoes the process of dry distillation. In round numbers two million tons of coal are annually distilled for the manufacture of coal gas in this country, and the * Read at the Weekly Evening Meeting, Friday, February 21, 1879. August 16, 1879.3 THE pharmaceutical journal and transactions. 137 I I I ammoniacal water of the gas works contains the salts of ammonium in solution. According to the most reliable data 100 tons of coal were distilled so as to yield 10,000 cubic feet of gas of specific gravity Of), giving the following products, in tons : — Gas. Tar. Ammouia Water. Coke. 22*25 8*5 9*5 59*75 average. This ammonia water contains about 1*5 per cent, of ammonia, hence the total quantity of the volatile alkali obtainable from the gasworks in England amounts to some 9000 tons per annum. A singular difference is observed between the dry dis¬ tillation of altered woody fibre as we have it in coal, and woody fibre itself. In the products of the first operation we chiefly find in the tar the aromatic hydrocarbons, such as benzene, whilst in the second we find acetic acid and methyl alcohol are predominant. The year 1848 is a memorable one in the annals of revolutionary chemistry, for in that year Wurtz j roved that ammonia is in reality only one member of a very large family. By acting with caustic potash on the nitriles of the alcohol radicals he obtained the first series of the large class of compound ammonias, the primary monamines. Of these methylamine is the first on our list CHo CO N + 2 KOH = CH H2 n N + CO OK OK The years that followed, 1849-51, were prolific in ammoniacal discoveries. Hofmann pointed out that not only one atom of hydrogen in ammonia can be replaced by its equivalent of organic radical, but that two or all the three atoms of the hydrogen in ammonia can be likewise replaced, giving rise to the secondaiy and ter¬ tiary amines, by the following simple reactions : — H ) CH3 ) 1. ch3i + h[n=hi+ H'[N H ) H ) CH3 ) CU3 ) 2. CH3I + H f N = HI + CH., \ N H H3) ch3 ch3 ) 3. CH3I + CH3 > N = HI -f CH, N H ) CH3 ) To these bodies the names of methylamine, dimethyl- amine, and trimethylamine were given. They resemble ammonia in being volatile alkaline liquids or gases, which combine with acids to form crystalline and well-defined salts. Hitherto these compound ammonias have been chemi¬ cal curiosities ; they have, however, recently become, as has so often been the case in other instance'*, of great commercial importance, and are now manufactured on a large scale. We are all well aware that the French beet-root sugar industry is one of great magnitude, and that it has been largely extended in late years. In this industry, as in the manufacture of cane sugar, large quantities of molasses or treacle remain behind after the whole of the crystallizable sugar has been withdrawn. These molasses are invariably employed to yield alcohol by fermentation. The juice of the beet, as well as that of cane sugar, contains, in addition to the sugar, a large quantity of extractive and nitrogenous matters, together with consi¬ derable quantities of alkaline salts. In some sugar- producing districts the waste-liquors or spent- wash from the stills — called vinasses in French — are wastefully and ignorantly thrown aw*ay, instead of being returned to the land as a fertilizer, and thus the soil becomes impover¬ ished. In France it has long been the custom of the distiller to evaporate these liquors ( vinasses ) to dryness, and to calcine the mass in a reverberatory furnace, thus destroying the whole of the organic matter, but recover¬ ing the alkaline salts of the beet-root. In this way 2000' tons of carbonate of potash are annually produced in the- French distilleries. For more than thirty years the idea has been entertained of collecting the ammonia water, tar, and oils which are given off when this organic matter- is calcined, but the practical realization of the project has. only quite recently been accomplished, and a most unex¬ pected new field of chemical industry thus opened out thi'ough the persevering and sagacious labours of M- Camille Vincent, of Paris. The following is an outline of the process as carried, out at the large distillery of Messrs. Tilloy, Delaune and Co., at Courrieres. The spent-wash having been evapo¬ rated until it has attained a specific gravity of 1*31, is allowed to run into cast-iron retorts, in which it is submitted to dry distillation. This process lasts four hours ; the volatile products pass over, whilst a residue of porous charcoal and alkaline salts remains behind in the retort. The gaseous products given off during the dis¬ tillation are passed through coolers, in order to condense all the portions which are liquid or solid at the ordinary temperature, and the combustible gases pass on uncon- densed and serve as fuel for heating the retorts. The liquid portion of the distillate is a very complex, mixture oi chemical compounds, resembling in this respect the corresponding product in the manufacture of coal-gas. Like this latter, the liquid distillate from the spent-wash may be divided into — 1. The ammonia water. 2. The tar. The ammonia water of the vinasse resembles that of the coal-gas manufacture in so far as it contains carbon- ate, sulphydrate and hydrocyanide of ammonia ; but it differs from this (and approximates to the products of tho diy distillation of wood) by containing in addition methyl alcohol, methyl sulphide, methyl cyanide, many of the members of the fatty acid series and, most remarkable of all, large quantities of the salts of trimethylamine. The tar, on re-distillation, yields more ammonia water, a large number of oils, the alkaloids of the pyridener series, solid hydrocarbons, carbolic acid and, lastly, a pitch of fine quality. The crude alkaline aqueous distillate is first neutralized by sulphuric acid, and the saline solution evaporated, when crystals of sulphate of ammonia are deposited ; and these, after separating and draining off, leave a mother liquor, which contains the more soluble sulphate of tri¬ methylamine. During the process of concentration, vapours of methyl alcohol, methyl cyanide, and other nitrils are given off, these being condensed, and the cyanide used for the preparation of ammonia and acetioc acid by decomposing it with an alkali. Trimethylamine itself is at present of no commercial value, though perhaps the time is not far distant when an important use for this substance will be found. The question arises as to how this material can be made to- yield substances capable of ready employment in the arts. This problem has been solved by M. Vincent in a most ingenious wav. He finds that the hydrochlorate of trimethylamine, when heated to a temperature of 260°,. decomposes into (1) ammonia, (2) free trimethylamine,. and (3) chloride of methyl. 3 NMe3HCl = 2 NMe3 + NH3 + 3 MeCl. By bubbling the vapours through hydrochloric acid the alkaline gases are retained, and the gaseous chloride of. methyl passes on to be purified by washing w-ith dilute caustic soda and drying with strong sulphuric acid. This is then collected in a gas-holder, whence it is pumped into strong receivers and condensed. These receivers are wrought-iron cylinders, tested to resist a pressure of 20- kilos. per square centimetre, and containing 50, 110, 220 kilos, chloride of methyl. Both ammonia and chloride of methyl are, however, substances possessing a considerable commercial value- The latter compound has lip to this time, indeed, not 138 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 16, 1879. been obtained in large quantities, but it can be employed for two distinct purposes : (1) it serves as a means of producing artificial cold ; (2) it is most valuable for pre¬ paring methylated dyes, which are at present costly, inasmuch as they have hitherto been obtained by the use of methyl iodide, an expensive substance. Methyl chloride was discovered in 1804 by MM. Dumas and Pdligot, who obtained it by heating a mixture of common salt, methyl alcohol and sulphuric acid. It is a gas at the ordinary temperature, possesses an ethereal smell and a sweet taste and its specific gravity is 1 *738. It is somewhat soluble in "water (about 3 volumes), but much more in acetic acid (40 volumes) and in alcohol (35 volumes). It burns with a luminous flame, tinged at the edges with green, yielding carbonic and hydrochloric .acids. Under pressure, methyl chloride can be readily condensed to a colourless, very mobile liquid, boiling at — 23° C. under a pressure of 760 mm. As the tension of the vapour is not high, and as it does not increase very rapidly with the temperature, the liquefaction can be readily effected, and the collection and transport of the liquefied chloride can be carried on without danger. The following table shows the tension of chloride of methyl at varying temperatures : — At » 11 11 19 19 0° 15° 20° 25° 30° 35° the tension of CH3C1 is 2'48 atmospheres. 99 99 99 99 4-11 4-81 99 11 19 91 5-62 99 9 9 99 19 91 6"50 7-50 91 11 From these numbers we must of course subtract one to obtain the pressure which the vapour exerts on the -containing vessel. As a means of producing low temperatures chloride of methyl will prove of great service both in the laboratory and on a larger industrial scale. When the liquid is allowed to escape from the receiver into an open vessel, it begins to boil, and in a few moments the temperature of the liquid is lowered by the ebullition below -23®, the boiling point of the chloride. The liquid then remains for a length of time in a quiescent state, and may be used as a freezing agent. By increasing the rapidity of the evaporation by means of a current of air blown through the liquid, or better by placing the liquid in connection with a good air-pump, the temperature of the liquid can in a few moments be reduced to - 55°, and large masses of mercury easily solidified. A small freezing machine em¬ ployed by M. Camille Vincent consists of a double-cased copper vessel, between the two casings of which the methyl chloride is introduced. The central space is filled with some liquid, such as alcohol, incapable of solidification. The chloride of methyl is allowed to enter from the cylin¬ drical reservoir by a screw tap, and the screw left open to permit of the escape of the gas. As soon as the whole mass of liquid has been reduced to a temperature of - 23®, ebullition ceases, the screw may be replaced and, if a temperature lower than -23® be required, the tube placed in connection with a good air-pump. By this simple means a litre of alcohol can be kept for several hours temperatures either of -23° or- 55®, and thus a large number of experiments can be performed for which hitherto the expensive liquid nitrous oxide or solid car¬ bonic acid was required. M. Vincent has recently constructed a much larger and more perfect and continuous form of freezing machine, in which by means of an air-pump and a forcing pump the chloride of methyl is evaporated in the freezing machine and again condensed in the cylinders. This enlarged form of apparatus will probably compete favourably with the ether and sulphurous acid freezing machines now in use, as they can be simply constructed, and as the vapour and liquid do not attack metal and are non- poisonous, and as the frigorific effects which it is capable of produc¬ ing are most energetic. The second, and perhaps more important, application of methyl chloride is to the manufacture of methylated colours. It is well known that rosaniline or aniline-red, C20H]9N;!, yields compounds possessing a fine blue, violet, or green colour, when a portion of the hydrogen has been replaced by the radicals methyl or ethyl, and the larger the pro¬ portion of hydrogen replaced the deeper is the shade of violet which is produced. Thus we have triethyl rosani¬ line or Hofmann’s* violet, C20H16(C2H5)3N3. By replacing one or two atoms of the hydrogen of aniline by methyl and by oxidizing the methyl anilines thus obtained, Charles Lauth obtained fine violet colours, whilst about the same time Hofmann observed the pro¬ duction of a bright green colouring matter, now known as iodine green, formed during the manufacture of the violet, and produced from the latter colour by the action of methyl iodide. In order to prepare aniline green from the pure chloride of methyl, a solution of methyl-aniline violet in methyl alcohol is placed in an iron digester and the liquid rendered alkaline by caustic soda. Having closed the digester, a given quantity of liquid chloride of methyl is introduced by opening a tap, and the digester thus charged is placed in a water-bath and heated by a jet of steam until the temperature reaches 95° and the indi¬ cated pressure amounts to from four to five atmospheres. As soon as the reaction is complete, the hot water is replaced by cold and the internal pressure reduced by opening the screw tap of the digester. The product of this reaction, heated and filtered, yields the soluble and colourless base, whose salts are green. To the acidulated solution a zinc salt is added to form a double salt and the green compound is then precipitated by the addition of com¬ mon salt. By adding ammonia to a solution of the green salt a colourless liquid is obtained, in which cloth mor¬ danted with tannic acid and tartar emetic becomes dyed of a splendid green. If rosaniline be substituted for methyl aniline in the preceding reaction, Hofmann’s violet is obtained. The application of methyl chloride to the preparation of violets and greens is, however, it must be remembered, not due to M. Vincent ; it has been practised for some years by aniline-colour makers. M. Vincent’s merit is in establishing a cheap method by which perfectly pure chloride of methyl can be obtained, and thus rendering the processes of the manufacture of colours much more certain than they have been hitherto. The production of methyl violet from di-methyl aniline may be easily shown by heating this body with a small quantity of chloral hydrate and then introducing some copper turnings into the hot liquid. On pouring the mixture into alcohol the violet colour is well seen. In reviewing this new chemical industiy of the beet¬ root vinasses , one cannot help being struck by the know¬ ledge and ability which have been so successfully ex¬ pended by M. Camille Vincent on the working out of the processes. Here, again, we have another instance of the utiliza¬ tion of waste chemical products and of the preparation on a large scale of compounds hitherto known only as chemical rarities. All those interested in scientific research must con¬ gratulate M. Camille Vincent on this most successful issue of his labours. fartiamentarg amt Jtaa flroqicduujs;. Prosecution for the Sale of Adulterated Sweet Spirit of Nitre. At the Leeds Town Hall, cn Friday the 8th inst., William Greenwood, of Commercial Hoad, Kirk stall, + was summoned by the Corporation under the Sale of Food # Hofmann, ‘Proc. Roy. Soc.,’ xiii., 13 (1863). + Not on tho Register of Chemists and Druggists. — El. P. J. August 16, 1879. ] THE pharmaceutical journal and transactions. 139 and Drugs Act, 1875. The Town Clerk appeared on behalf of the Corporation, and stated that the proceedings were instituted under the 6th section of the above Act, which provided that “no person shall sell to the prejudice of the purchaser any article of food or any drug which is not of the nature, substance, and quality of the article demanded by such purchaser, under a penalty not ex¬ ceeding £20.” It appeared that Inspector Handford went on July 10th to the shop kept by the defendant and asked for six ounces of spirit of sweet nitre, for which he paid him Is. 6(7. He told the defendant he had purchased the nitre for the purpose of having it analysed by the public analyst. The Public Analyst stated that the medicinal value of the liquid depended chiefly on the quantity of nitrous ether contained therein, and that the sample submitted to him contained scarcely any of that element. The de¬ fendant stated that he had bought the spirit of nitre as it was from two chemists in the town. The defendant was fined 20s. and costs. — Leeds Mer¬ cury. JiU.iB !.i^ l r-ir t T*^' “ ©Mtnavjj. Notice has been received of the death of the follow¬ ing : — On the 6th of July, 1879, Mr. Thomas Britten, Che¬ mist and Druggist, Liverpool Road, Southport. Aged 56 years. On the 10th of July, 1879, Mr. William Griffiths, Che¬ mist and Druggist, Aberayron, Cardiganshire. Aged 51 years. On the 13th of July, 1879, Mr. Thomas Eyre, Che¬ mist and Druggist, Hayfield, Derbyshire. Aged 31 years. On the 24th of July, 1879, Mr. David Moir Mackay, Chemist and Druggist, Aberdeen. Aged 52 years. On the 3rd of August, 1879, Mr. Walter Ferguson Leadbitter, Chemist and Druggist, Sunderland. Aged 71 years. On the 8th of August, 1879, Mr. Edward Thurland, Pharmaceutical Chemist, Magdalen Street, Oxford. Aged 85 years. Mr. Thurland had been a Member of the Pharmaceutical Society since 1853. BOOKS, PAMPHLETS, ETC., RECEIVED. An Introduction to the Practice of Commercial Organic Analysis. By Alfred H. Allen, E.C.S. Vol. I. London: J. and A. Churchill, 1879. From the Publishers. International Medical-Pharmaceutical Dictionary, in Three Languages: French, English and German. Compiled by George Herman Moeller. Munich: J. Grubert. 1879. From the Publisher. Elements of Modern Chemistry. By Ad olphe Wurtz. Translated and Edited from the Fourth Edition, by Wm. H. Greene, M.D. Illustrated. London and Philadelphia: J. B. Lippincott and Co. 1879. From the Publishers. Jjtotyii and fipncrics. [621], SULLIVAN’S AMALGAM.— The reason of the non-amalgamation is, your precipitate was in too fine powder. Let the zinc remain twice as long in contact with the solution ; the result will be grains the size of ordinary filings. The fine powder should be thrown away with the washings. Dingwall, P. J. Dewar. [623]. EMP. COLCHICI. — I have several times had emp. colchici prescribed. It is an American preparation. Having failed to procure it from the wholesale house I shall feel greatly obliged if you will ask for the formula for making the same. M. R. J. THE INTRODUCTION OF CHLOROFORM AS AN ANAESTHETIC. — The following letter on this subject, from Mr. Henry Brown, of Northallerton, has appeared in the British Medical Journal : — The subject of anaesthesia is one ever of interest, and many have not taken the trouble to read the litera¬ ture of thirty or forty years ago bearing upon the question. I have for some time doubted the priority of Sir J. Y. Simpson’s discovery; but he must be credited with great patience and enormous working power ; and he never threw away a palpable suggestion, even if emanating from a babe in science, literature, or medicine. In regard to the composition of the chloric ether (or shall I say chloroform ? ) introduced into the practice of the Liverpool medical men, in 1838, by Mr. Waldie, I can find no reliable data. I am now referring to exact chemical composition. Whether the chloroform, as sug¬ gested by Mr. Waldie to Sir James Simpson, was the chloric ether of Thomson, Robiquet, and Colin, I am not able to say- I leave Liebig out of the discussion altogether: his analysis was defective and inaccurate, inasmuch as hydrogen is completely omitted in his calculation. In 1834, Dumas determined the true composition of chloroform, and gave it the name by which it is univer¬ sally known. Mr. Guthrie, of America, and Soubeiran, of France, in 1831, prepared chloroform; but does Guthrie’s description at all correspond to our modern article ? He writes, in 1832, that “he had used the product very freely during the previous six months to the point of intoxication ; that he had found it singularly grateful, producing promptly a lively flow of animal spirits and consequent loquacity, and leaving little of the depression consequent on the use of ardent spirits ; that it promises much as a remedy in cases requiring a safe, quick, energetic, and palatable stimulus ; and that, for drinking, it requires an equal weight of water.” Dr. Black, of Bolton, speakes of it, in 1833, as a new remedy, and considers it useful in asthma and adynamic conditions of the system. In 1847, the United States' Dispensatory, published in July, describes it thus : “It acts as a diffusible soothing stimulus in the same manner as sulphuric ether, but with this decided advantage, that, when sufficiently diluted, it possesses a bland sweet taste, which renders its admini s- tration easy even to children. The dose for an adult is a teaspoonful diluted with water. In affections character - ized by difficult respiration it may be used by inhala¬ tion.” We have thus Guthrie and the United States' Dispensa¬ tory speaking of a something called “chloroform,” but which is miscible with water. Now we know chloroform is only soluble in water to the extent of one in two hun¬ dred, and barely soluble in an equal weight of rectified spirit ; how, then, could pure chloroform be described by Guthrie and the United States Pharmacopoeia as possess¬ ing the properties above mentioned ? I believe it was a spirituous solution of chloroform that Waldie introduced into Liverpool, and it was called chloric ether ; but it was not the chloride of olefiant gas of Thomson and others. The question maj be asked, Was it chloroform as we now know it that was used by Sir James Simpson in his first experiments, or was it the spirituous solution? I have searched all available records, and confess that upon this point we are in ignorance. I know it is stated a liquid, by some means or other put aside, was used, and most unexpectedly answered the purpose — i.e., of anaesthesia. The party grew exhilarated, we are told, and some become insensible. I need not refer to the fact that, for more than ten years, ether and ether-anaesthesia were the rage, 140 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 16, 1.V9. and every medical and pharmaceutical journal literally u teemed with accounts of ether-inhalation and descriptions • of apparatus up to 1847. Mr. Jacob Bell, editor of the Pharmaceutical Journal, in a note on p. 357, No. viii., for February, 1847, thus writes: “Chloric ether has been tried in some cases with success ; it is more pleasant to . the taste, but appears to be rather less powerful in its effects than sulphuric ether.” Of the dead we must say nothing but in praise ; but I am bound to add, Sir James Simpson got his first hint in regard to the anaesthetic power of chloroform from Mr. Waldie; but the name cf Jacob Bell must not be over¬ looked. Bell’s note was written in February, 1847, and Waldie’s suggestion was offered in November of the same year. I thus leave the subject ; but with ample material behind to prove that, although Sir James Simpson was the first to put thoroughly to the test the anesthetic power of chloroform or chloric ether of 1847, he was in¬ debted to others for the suggestion, and Mr. Waldie followed in the wake of Mr. Jacob Bell. Mr. Bell does not inform us as to his authority ; but anesthesia with ether, and no doubt with chloric ether, was practised for reality’s sake, or for the purpose of scientific curiosity, years before the discovery of Sir James Simpson took the medical and civil world by storm. Ufcmmtantfa. In order to assist as much as possible our younger brethren, for whose salce partly this column was established, considerable latitude is allowed, according to promise, in ■the propounding of supposed difficulties. But the right will be exercised of excluding too trivial questions, or re¬ petitions of those that have been previously discussed in principle. And ive xoould suggest that those ivho meet tvith difficulties should before sending them search previous numbers of the Journal to see if they can obtain the re- ■quired information. [334]. In this prescription “An Apprentice ” does not give the quantity of calomel, and from the general character of the formula I should be disposed to regard it as one of those lay recipes which are dispensed from time to time rather than as the prescription of a qualified practitioner. In dispensing these the pharmacist has to draw largely as a rule on his judgment, and if the dose of calomel be not excessive I think “An Apprentice” would find mucilage of acacia go far to remove his difficulty. At the same time it is hard to see the object of the combination of calomel and bals. copaibae. Gulielmus. [335]. In answer to “Nihil ” the following formula for emp. iodinii is from Beasley’s ‘ Pocket Formulary,’ p. 126 : Lead Plaster . 3v.j Besin Plaster . 3^j Melt together and add iodine 7)j rubbed with olive oil ‘ 3s s- In the same work may also be found formulae for . emplastrum iodinii compositum and emp. iodinii c. bella¬ donna, and in Squire’s * Hospital Pharmacopoeias,’ a formula for emp. iodi co. as follows : — Iodine . 3ij Potass. Iodid . Emplast. Plumbi . ixvj Emp. Opii . ,3vj As the prescription ordered emp. iodinii merely, I should think the first of these formulae the proper plaster to have used. Gulielmus. An answer has also been received from “Lavandula.” [337]. In reply to query No. 337, I think “ G. W. W.” must have used hard water. Pure distilled water will make a perfectly clear solution with liq. ferri dialysati and syr. aurant., but if the mixture be only slightly alkaline, the iron will be immediately precipitated. (ji ^ rji ^ j (foiUtespiutynnt. The Benevolent Fund. Sir,— In reading over flie reports of the Benevolent Fund Committee, which are given in your Journal from time to time, there is food for much reflection, yet, strangely enough, there is too much reason to suppose that, by the vast majority in our community, they are not treated with the attention they deserve. Lying quite outside the pale of pharmaceutical politics, away from scientific controversy, and rigidly apart from all questions of trade and trade interests, there exists in our midst a neutral ground — a border- land, where charity and goodwill reign supreme, and where the cry of the sorrow- stricken is seldom heard in vain. When one sees, month after month, a system of relief, extended without ostentation to decayed fellow workers, to bereaved and desolate women, to orphans who have been dearer than life itself to those who have gone before, surely silence can be stretched beyond the point of en¬ durance and the iron-grip of apathy clog the efforts of good men who wTere working so wisely and so well. How it is possible for any individual amongst us to withhold his practical sympathy from a work which so per¬ sistently proves its nobility it is indeed difficult to say, and it would be a thought reflecting bitterly upon our boasted intelligence as a class if we could for one moment suppose that there existed the man who realized to the full the generous nature of the work done and who still could give some plausible reasons why he should not enlist side by side with those whose only object is to relieve the suffering and distress of fellow creatures— brothers in the close com¬ munion of a hard and earnest calling, and whose “ crown of sorrow ” may he the remembrance of brighter and better days. Surely, in such a course as this, argument must be unnecessary. I will simply ask my reader, if he should chance to be a non-subscriber to this fund, to turn through some of the back numbers of this Journal, to read over these recoids of charity — charity in the true sense of the word — to give them a few moments’ quiet thought, and then to ask himself “Can no more be done ? ” The issue I am con¬ tent to leave to himself and his conscience. Kilburn, N. IF. Charles B. Allen. Tincture of Kino. Sir, — Those who have been troubled with a gelatinized tinct. kino will, I am sure, be pleased to know that the remedy suggested by Mr. Merrikin is of the utmost value. But (having had at one time and another, considerable trouble with this preparation) I would suggest that the percentage of glycerine which he advises be doubled. As a revision of the B.P. is occasionally talked of, would it not be advisable to discard the present tincture and introduce a liquor kino in its place ? A preparation which I have used for some time, and which has given the utmost satisfaction, has been prepared as follows : — Kino in coarse powder . ^ij Sp. V. Kect . 5v Glycerine . 5V Aquae Dest. . . . • 3X Macerate for seven days. I have found the above to make a preparation which may be confidently relied upon, and I would therefore suggest to those who have been troubled in this matter to give it one trial. 1 am sure they will be pleased. Carey.’* on “ Permanent Essence of It is F. A. B.— Pereira’s ‘ Selecta e Prescripts, published by Churchill. “ Carbolic.” —See a paper Bennet,” in vol. ix., p. 307. J. Griffiths. — The Drugging of Animals Act, 1876. printed in the Society’s Calendar, p. 422. D. W. — The Act is for the protection of the title. G. J. Gostling.—We do not know, and must refer you to the gentlemen mentioned for the information. Communications, Letters, etc., have been received from Messrs. Mitchell, Harrison, Cairns, Watts, Cherry, Reynolds, Hesse, D. Howard, ltump, Maw, Minor, Dewar. Auguet 23, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 141 pmpaqntfeal Joupal - ♦ - SATURDAY, AUGUST 23, 1879. Communications for the Editorial department of this Journal , boohs for review, etc., should be addressed to the Editor, 17, Bloomsbury Square. Instructions from Members and Associates respecting the transmission of the Journal should be sent to Mr. Elias Bremridge, Secretary., 17, Bloomsbury Square , W.C. Advertisements, and payments for Copies of the Journal, Messrs. Churchill, New Burlington Street, London, W. Envelopes indorsed “ Pharm. JournJ THE CONFERENCE MEETING. After an interval of six years the British Phar¬ maceutical Conference has again visited the county of the ridings and for the second time experienced the hospitality of their Yorkshire confreres. In point of numbers the meeting has been a most successful one, one hundred and forty-five names having been signed in the visitors’ book. The company included many of the best known pharmacists in the three Kingdoms as well as delegates from several kindred associations, amongst them, notably, the Pharmaceu¬ tical Societies of Great Britain and Ireland, which were represented by their respective Presidents and several members of their Councils. N or do we think that the general verdict upon the papers read and the discussions, as compared with those of former years, will be an unfavourable one. Early in the meeting, however, one most unwelcome fact was revealed in the reading of the report, namely, that the Senior General Secretary, Professor Attfield, to whose energy and enthusiasm the present position of the Conference may be in a large measure attributed, had unexpectedly intimated his intention of resign¬ ing his present office, although at the request of the Committee he had consented to hold it during one more year. The appreciation of his services by the Executive Committee was evinced by the prompt formation of a provisional committee, to which many other members present added their names. The Honorary Secretary is Mr. M. Carteighe, and the business of the Committee will be to consider the best method of testifying to Professor Attfield the sense of the Conference as to its indebtedness to him. The Presidential Address was chiefly devoted to carrying out the contrast between the ideal and actual position of the pharmacist in Great Britain which Mr. Schacht had presented to the Conference last year. As the Address itself will be found in extenso at another portion of this Journal, we leave any more detailed reference to it until a future occasion. Once more Dr. Wright has provided a report on the aconite alkaloids, the present one being devoted to the alkaloids from Japanese aconite, atis root, and the leaves, flower 'and stalks of English grown Third Series, No. 478. aconite. From Japanese aconite Dr. Wright re¬ ports that he has obtained a crystallizable alkaloid, agreeing in composition with the formula C0(.H88N2On, which is itself in some respects more stable than aconitine and pseudaconitine, in not yielding “apo” derivatives, and he appears to think it may be a dehydrated derivative of a hypothetical parent base. As an incident of the research he also reports that “ treatment with alcohol alone, unacidulated by any acid at all, extracted practically all the alkaloids present in the roots examined.” These results confirm those obtained when Japanese aconite was first examined two years ago* in regard to the points of pharmaceutical interest, namely, that Japanese aconite contains more alkaloid — amountin '- to about 2-5 per cent, soluble Li ether — than any other kind of aconite, and that the crystallizable alkaloid obtainable from it is of a specific nature. In the course of the discussion Mr. Greenish suggested the desirability of ascertaining the botanical origin of the Japanese aconite roots worked upon, and expressed the opinion that as met with in commerce this drug is not always of the same character. This point is of special import¬ ance, as this kind of aconite, as pointed out by Mr. Umney, is now the kind almost exclusively met with in the market. The examination of atis roots ( Aconiticm heterophyllum ) has not led to any definite results sufficient either to confirm or controvert those recorded by Broughton, some years ago, in reference to the substance he termed “ atisine.” In the ex¬ amination of the flowers, leaves and stalk of aconite plants no definite result was obtained, and although the quantity of material worked upon amounted to nearly three hundredweight, it was only by inference from the comparative absence of inconvenience ex¬ perienced in working that the non-existence of poisonous alkaloids was conjectured. The next report presented to the Conference con¬ tained a statement of the results obtained by Mr. Thresh in carrying out the investigation of com¬ mercial ginger, for which a grant was placed at his disposal last year. These results show that ordinary Jamaica ginger contains, in the portion extracted by ether — (1) a crystalline fat, consisting of a dark red, tasteless and odourless portion, insoluble in strong alcohol, a white amorphous tasteless and odourless portion, soluble in alcohol, and a wax-like tasteless and odourless resin ; (2) a red fatty sub¬ stance, very pungent and soluble in alcohol ; (3) a limpid, volatile, straw-coloured oil of an aromatic, somewhat camplioraceous taste, having a sp. gr. of 0-853 at 15° C.; (4) a neutral resin, soluble in strong alcohol; and (5) acid resins of a dark brown colour. The pungent or active principle of ginger, to which Mr. Thresh gives the name of “gingerol,” is a viscid odourless liquid, about the consistency of treacle, readily soluble in alcohol even when dilute. * Pharm. Journ. [3], vol. viii., p. 172, and ‘ Year-Book’ (1877), P. 469. ]42 THE PHARMACE'JTICAL JOURNAL AND TRANSACTIONS. [August 23, i87». That portion of ginger which is insoluble in ether consists chiefly of mucilage, inorganic constituents, a substance precipitated by tannin, metarabin, cellulose, albumenoids, etc. The comparative ex¬ amination of different kinds of ginger showed that the variety most esteemed contains only half as much essential oil as the others, also less active principle than African or common Jamaica. The volatile oil of line Jamaica ginger has, however, the finest bouquet. The first paper read after the presentation of these reports was on the “ Soluble Essence of Ginger,” and it described a modification of the method originally proposed by Mr. Thresh for its preparation. The rationale of this process was to be gathered from a consideration of the constituents of ginger root ; in carrying it out, the alcoholic tincture which contains, together with the extractive soluble in water, neutral and other resins, gingerol, mall quantities of the red fat, wax, etc., is mixed with slacked lime, by which the greater part of the resin is precipitated. On adding dilute sulphuric acid to the clear liquid the dissolved lime is pre¬ cipitated, and by diluting the resulting clear liquid, and filtering through powdered pumice or silica, the wax, fat, extractive, and the rest of the resin is got rid of, together with any excess of volatile oil. The next paper gave an account of an investigation conducted by Mr. Stoddart, to ascertain the cause of a periodical fatality amongst sheep in the neigh¬ bourhood of Bristol. Though the inquiry was not originally of any apparent pharmaceutical interest, it incidentally furnished results of value in regard to the period at which ergot should be gathered for medicinal purposes. It was observed that the sheep fed on natural herbage alwavs had foot-rot, even in summer, and other circumstances led Mr. Stoddart to suspect that the mischievous effects might be due to ergotism. On examining the old mature plants of Lolium perenne he noticed well-formed purplish dark coloured ergots, but could not discover these upon the younger plants, which were greedily de¬ voured by the lambs, while they sought to avoid the old plants. In the following spring Mr. Stoddart ob¬ tained specimens of Lolium perenne the inflorescence of which was just commencing, and he traced the development of the ergot from this stage of its growth until the commencement of August, at which period he found the fungus had reached the limit of its vegetative or myceloid growth. It is at this stage that the peculiar medical effect of the Claviceps on the animal economy exists in greatest intensity, and it was at this period that the effect produced upon the sheep was greatest. After carrying out these observations for six or seven years he came to the conclusion that for all medicinal purposes ergot should be gathered in the months of August or Sep¬ tember, because at the end of the vegetative period its action k greatest. Dr. Symes then read a paper describing the construction and principles of the different forms of polarimeter and its application in pharmacy. Among other illustrations of this lie gave the results of the determination of the rotatory power of a number of essential oils. Another illustration of the utility of the polarimeter had reference to the examination of urine, a legitimate branch of the pharmacist’s calling, not subject to the influence of unfair competition on the part of uneducated outside traders. Next in order were three papers by Mr. Siebold. The first described the application of chloroform in the testing of drugs, and was based upon the prin¬ ciple indicated by Dr. Himley, that the presence of mineral adulterants in flour can be detected by their sinking in that liquid, while the normal constituents of the flour float at the surface. Mr. Siebold- described the results obtained in this way as being more satisfactory than those obtained by incineration. The second paper suggested that the difference in the coloration of chloroform by iodine according to> the presence or absence of alcohol afforded a means- of detecting the presence of alcohol in chloroform.. With a mixture of chloroform and alcohol the brown colour of the alcoholic solution of iodine predominates over the purple colour of the chloro¬ form solution sufficiently to give indications to- satisfy the requirements of the pharmacist, as in this way the presence of half per cent, of alcohol can be detected. The third paper was on the use of the hydrometer in determining the specific gravity of liquids, and described a number of experiments- undertaken with the object of deciding whether the indications of the hydrometer can be depended upon with liquids containing undissolved powders, oils, resins, etc., uniformly suspended. The results- tended to show that the presence of such substances does not affect the indications of carefully made hydrometers. The last paper read at Tuesday’s sitting of the Conference was by Mr. Gerrard, on the extrac¬ tion of pilocarpine by ammoniatecl alcohol, which he has found to be a much more convenient solvent than those hitherto used, it furnishing a larger amount of product and effecting the separation of the alkaloid from the dark colouring matter much more readily. It was pointed out by Mr. Williams* in the course of the discussion on this paper, that the use of ammoniated alcohol may possibly be adopted with advantage in the extraction of alka¬ loids from other materials. On the second dav’s sitting the business was com- menced by the reading, by Mr. Allen, of some “Notes on Petroleum Spirit,” describing some characteristic reactions of petroleum spirit as com¬ pared with those of benzene from coal tar, as well as a method of testing mixtures of petroleum spirit and benzole. The different behaviour of these substances when treated with nitric acid furnished the basis for this method of testing. August 23, 1679.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 143 Mr. F. W. Fletcher then read a paper on the moisture gave relief from the pain and inconvenience -“Valuation of Citrate of Iron and Quinine.” After caused by tension in various morbid conditions, adverting to the circumstance that the Pharmacopoeia such as cancerous growths, ulcers, etc. A jet of test furnished no indication whether the alkaloid dried air applied for an hour in the evening was obtained by its directions was or was not quinine, said to have been found to cause cessation of pain the author suggested the application of the plan of for several hours and secure a good night’s rest, fractional crystallization to the sulphate as a means Mr. PI. Collier read a paper on the use of of detecting the presence of cinchonidine. The tincture of quillaia bark as an emulsifying agent, necessity of employing this test was shown by the in which he described the efficacy of this preparation anention of the circumstance that certain foreign in producing emulsions with materials of a resinous makes of “sulphate of quinine” invariably contain or oily nature and suggested that on this account it a large proportion of cinchonidine sulphate. was deserving of consideration as a pharmaceutical Two papers by Mr. E. Davies were then read, agent. Some strong doubts were expressed in the The first, on the “Estimation of Water in Iodine,” discussion of this paper that the peculiar activity of by combining a known quantity of iodine with a quillaia bark would render it inappropriate for use weighed excess of mercury, and weighing the dried as the means of effecting emulsification, but the residue, elicited some useful information. The remarkable efficacy of the tincture in causing the -other paper, on the “ Presence of Tannin in Gentian rapid subdivision of mercury was considered to Root,” suggested the possibility that the tannin promise well for its application in the preparation of contained in the root is liable to decomposition when sheep ointment. the gentian is powdered, or that tannin is not a | Another paper by Mr. Collier dealt with the uniform constituent of gentian root. chemical condition in which saponin exists in the A paper on “ Amylic Alcohol and Amy lie Nitrite,” I quillaia bark, by Mr. Dott, consisted mainly of a reply to certain Next in order was a note on Aricine, by Mr. John criticisms* of the paper read by Mr. Dott upon this Eliot Howard. Referring to the recent paper on subject at the meeting of the Conference last year.f this subject by Dr. Hesse, and to the specimen of The author maintained the correctness of the state- aricine presented by that chemist to the museum of anents in his original paper and he was supported the Society, the author stated that he had compared in that position by speakers who stated their ex- this sample with the one deposited in the museum perience in the course of the discussion. by himself in 1852 and was satisfied as to their The “Gelatinization of Tincture of Kino” formed identity. He also found the bark from which Dr. the subject of a paper by Mr. Bamford. The author Hesse obtained his alkaloid to be exactly like his suggested frequent agitations of the tincture as an own, namely, the jaune cle Cuzco of Delondre and -efficient remedy of the inconvenience experienced Bouchardat, which was imported as Calisaya in by many dispensers from the behaviour of tincture of kino. In the course of the discussion that followed the reading of this paper it soon became -evident that gelatinization of tincture of kino is not by any means invariably experienced. Some of the speakers had never seen a case during many years ; others had observed it only on one or two occasions, 1829. This, Mr. Howard believes, is the only bark from wliieh aricine has been obtained, and he points out that the suggestion of the existence of aricine among the alkaloids of Cinchona succincbra is merely matter of conjecture. Mr. Howard disavows any claim to the discovery of aricine, though he has satisfied himself of the substantial accuracy of and it was suggested that the result was probably Pelletier’s observations, and has therefore main- due to some peculiarity in the kino used rather than tained the existence of the alkaloid described by a constant characteristic of this drug. Amongst him as aricine, although it has generally been denied, •other preventives of gelatinization the effect of the It is suggested that the further examination of bark addition of glycerine, as suggested by Mr. Ellinor, yielding aricine promises to be of interest as regards was in the main spoken of favourably, but it was also remarked that the glycerine might to some -extent counteract the astringent action of the kino. The judicious selection of the proper kind of kino for the preparation of tincture of kino will probably be the most effective remedy for this kind of diffi¬ culty and its attainment may therefore be intrusted to the relative intelligence of wholesale houses. The use of Anhydrous Air as a Therapeutic Agent was described in a paper by Mr. Keyworth, who had found that its application as an absorbent of - •» _ _ _ _ * American Journal of Pharmacy, for February, and Pharrn. Journ. vol. ix, p. 899. t Pharm. Journ. [3], vol. ix. p. 172. the classification of different species of the genus Cinchona, and that in connection with this inquiry it will also be desirable to study the physiological action of aricine, as well as that of paricine, which appears to occur among the alkaloids of Cinchona, succirubra. A paper on the “ Chemistry of Chaulmoogra Oil,” by Mr. Moss, showed that the existence of any alka- loidal substance in this oil was doubtful, at least so far as to account for any medicinal efficacy. Chemi¬ cally, the specific characteristic of chaulmoogra oil consists, according to the author’s results, in its con¬ taining a peculiar fatty acid, gynocardic acid, asso¬ ciated with palmitic acid, hypogoeic acid and cocini'e acid. 144 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. August 32, 187?, Dr. Hamberg’s paper on the “Capacity of Different Organs to absorb and retain Arsenic in Cases of Chronic Poisoning ’5 described the chemical results obtained in a physiological investigation carried ont for the purpose of elucidating this subject. The last paper read was on the “Estimation of Morphia in Turkey Opium/’ by Professor Fluckiger. The author recommended the exhaustion of the opium with cold water as being the most convenient for extracting the morphia. The clear liquid is then mixed with definite proportions of alcohol, ether and ammonia, and after shaking crystals of morphia are formed at the surface of the layer of ether. After a day Of two, the whole of it is deposited and can be collected and weighed. At the conclusion of the reading of papers, a ballot was taken for the election of officers of the Conference for the ensuing year, which resulted in the choice of Mr. William Southall, of Birming¬ ham, as President. The place of the next meeting, decided in accordance with the previous custom of accompanying the meeting of the British Association, is Swansea, and Mr. J. Hughes, of that town, has been elected Local Secretary ; the Vice-Presidents being Mr. Grose, of Swansea, Mr. Reynolds, of Leeds, Mr. Ward, of Sheffield, and Mr. Sandford, of London. The usual votes of thanks for the services rendered by the members of the Local Committee were then proposed, special mention being made of the names of Mr. Ward, President of the Sheffield Chemical and Pharmaceutical Association, Mr. Maleham, the Local Secretary of the Conference, and Mr. Learoyd, who has actively assisted him. These complimentary acknowledgments of the service rendered to the Conference were never more thoroughly well merited, and we think that all who were present at this meeting will share the opinion expressed by a Yorkshire man, that Yorkshire has reason to be ’ proud of the way that Sheffield has received the Conference and maintained the credit of the county. On the following day the prospects of fine weather at an early hour were very slender, but at the time fixed for meeting at the Freemasons’ Hall it had so far improved that there was a large muster of members, a few of whom were accompanied by ladies, and the excursion was carried out in accordance with the programme indicate! last week. With the ex¬ ception of one brisk shower, a kicking mare and some mountain dew there was nothing to mar the enjoyment of the entertainment that had been pro¬ vided by the zealous exertions of the Local Com¬ mittee. Before eleven o’clock at night the whole party had returned safely to Sheffield without any mishap and highly delighted with the excursion. Besides providing for the convenient lodging ac¬ commodation of visitors and for their amusement the efforts of the Local Committee were extended to obtaining for them access to some of the interesting manufactories existing in Sheffield. First amongst these must be mentioned the works where the manu¬ facture of steel according to the Bessemer method is carried on in the manner described in this Journal when the process was only in its infancy. It was- naturally at Sheffield that the inauguration of this- method took place, and those who had an opportu¬ nity of witnessing the enormous extent to which' it has developed during the last thirty years have- great reason to be grateful to the Local Committee* for having procured for them an opportunity o£ witnessing the operations of this interesting branch of manufacture. In addition to the treat thnw afforded, the members were also enabled to visit the electro-plating works of Messrs. Walker and Hall and the show-rooms of .Messrs. Rodgers, and so to* obtain an actual knowledge of the way in which two of the chief manufacturing trades in Sheffield are carried out. For these facilities the members are- under great obligation to the Local Committee, and they are no less indebted to the proprietors of the works visited, as well as to the various officials con¬ nected with them, for the extreme liberality with which everything was shown, and for the courtesy and attention displayed, no doubt at the cost of some- considerable personal inconvenience. In this superficial sketch of the Pharmaceutical Conference at Sheffield it has only been possible to indicate some of its most salient features, and there are many things we should have been glad to speak, of had time and space permitted. But we may,, from a general point of view, say that this has been,, in every respect, one of the most successful and satis- . factory meetings that have yet been held. THE BRITISH ASSOCIATION. The customary proceedings of the British Associa¬ tion commenced on Wednesday evening with the delivery of the Presidential Address, the attendance* at which was far from sufficient to fill the Albert Hall. A portion of this Address will be found at another part of the Journal. On Thursday the busi¬ ness of the sections commenced with the delivery of addresses, some of which we hope to print in subse¬ quent numbers. Up to the present time the number of visitors appears to be somewhat small. THE WEIGHTS AND MEASURES ACT. The following Order in Council, creating new denominations of standards of apothecaries’ weights, and measures under this Act, appeared in the London Gazette of the 15th inst. It will be ob¬ served that it differs from the draft Schedule for¬ warded by the Board of Trade to the Council of the Pharmaceutical Society* in including the half a scruple weight, and there is no doubt that this im¬ portant concession is due to the representation of the Council on the subject. Nothing is said as to the stamping of the small weights and subdivisions of * See Pharm. Journ. [3], vol. ix., p. 1003. August f3, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 145 glass measures, but probably, as suggested in tlie letter of the President to Mr. Trevor, of the 9th of May, the arrangements for carrying this out will be provided for in a less formal manner. At the Court at Osborne House, Isle of Wight, the 14th day of A ugust, 1879. Present — The Queen’s Most Excellent Majesty in Council. Whereas by “The Weights and Measures Act, 1878,” it is (among other things) provided that the Board of Trade shall from time to time cause such new denomi¬ nations of standards, being either equivalent to or multi¬ ples or aliquot parts of the imperial weights and measures ascertained by the said Act, as appear to them to be required in addition to those mentioned in the Second Schedule to the said Act, to be made and duly verified, and that those new denominations of standards, when approved by Her Majesty in Council, shall be Board of Trade Standards in like manner as if they were men¬ tioned in the said Schedule : And whereas it has been made to appear to the Board •of Trade that new denominations of standards of apothe¬ caries’ weight and measure, being multiples and aliquot parts of the imperial weights and measures ascertained by the said Act, are required, and they have caused the same to be made and duly verified and deposited in their custody : And whereas the Board of Trade have given to the said new standards of apothecaries’ weight and measure the several denominations set forth in the Schedule hereto: Now, therefore, Her Majesty, by virtue of the power vested in Her by the said Act, by and with the advice of Her Privy Council, is pleased to approve the several denominations of standards of apothecaries’ weight and measure set forth in the Schedule hereto as new denomi¬ nations of standards, and doth direct that the same shall be Board of Trade Standards in like manner as if they were mentioned in the Second Schedule to “The Weights and Measures Act, 1878.” C. L. Peel. SCHEDULE. Denominations op Standards of Apothecaries’ Weight and Measure. 1 . A pothecaries’j Weight. Denomination. Weight in grains in terms of the Imperial Standard Pound which contains 7000 such grains. Ounces. 10 ounces . . . 4800 grains 8 „ . . . 3840 „ 6 „ • . . 2880 „ 4 „ • • • 1920 „ 2 „ . . . 960 ,, 1 ounce . . . 480 „ Drachms. 4 drachms orhalf f 240 „ an ounce . . 2 drachms . . 120 „ 1 drachm . . . 60 „ Scruples. 2 scruples . . 40 „ 1^ „ or half a drachm . . } 80 „ 1 scruple . . . 20 „ half a scruple . 10 „ 6 grains . . . 6 „ 5 „ . . . ■5 „ 4 „ . . • 4 „ 3 „ . . . 3 „ 2 „ . . . 2 „ 1 grain . . . 1 grain half a grain . . 0-5 „ 2. Apothecaries'1 Measure. Denomination. Containing the following weight of Distilled Water. Temperature=62° Farenheit. Barometer=30 inches. Imperial Found=7000 grains. A fluid ounce and the ) multiples thereof from f one to 40 fluid ounces . t Half a fluid ounce . . . ) A fluid drachm and the ] multiples thereof from f one to 16 fluid drachms t Half a fluid drachm . . ) A minim and the multi- j pies thereof from one ;■ to 60 minims . . . . ) One fluid ounce contains 437'5 grains weight, or imperial gallon. One fluid drachm equals -i fluid ounce. One minim equals -Dg- fluid drachm. tuinmimiticat ^ociettr of J ret and. MEETING OF THE COUNCIL. Wednesday, August 6, 1879. Present — Charles R. C. Tichborne, LL.D., Ph.D., President ; Sir George Owens, M.D., Dr. Collins, Messrs. Allen, Brunker, Doran (Bray), Goodwin, Hayes, Hodgson, Holmes, Simpson. The minutes of the meeting held on July 2, were read and signed. Read a letter from Messrs. Ennis and Son, solicitors, with reference to proposed prosecutions, and also, in con¬ nection therewith, the Report of the Law Committee. Proposed by Mr. Simpson, seconded by Mr'. Allen, and resolved — “ That Messrs. Ennis be instructed to take legal pro¬ ceedings against the offenders in the two cases of illegal compounding in which proof has been obtained, as recommended by the Committee.” Read a letter from Mr. Harry N. Draper, Dublin, to¬ gether with a correspondence which he had had with the Clerk of the Peace, respecting his being summoned as a grand juror to the county court, at Kilmainham, and fined for non-attendance ; although as a pharmaceutical chemist he was exempt from service, under the provisions of the Juries Procedure (Ireland) Act, 1876. Proposed by Mr. Brunker, seconded by Mr. Hayes, and resolved — “ That Mr. Fennell be directed to send to the clerks of the North and South Dublin Unions a copy of a list of licentiate pharmaceutical chemists and request that they shall be returned as exempt in all future lists of persons liable to serve as jurors for the county or city of Dublin, and at the same time to state that this course has been rendered necessary by the fact that several of our body have been replaced on the jury lists after having been struck off in previous years.” Read a letter from Professor Schaer, of Zurich, thank¬ ing the Council for the books relating to the history of pharmacy in Ireland, which they had sent him. The reports of the examinations held in July were laid on the table. At the examination for Pharmaceu¬ tical Chemists, held on July 2, five candidates presented themselves. The following three passed — Thomas Batt, jun., 48, Fontenoy Street, Dublin. Robert James Hardy, Tandragee. John Patrick Henry, 160, York Street, Belfast. Eighteen candidates presented themselves at the Pre¬ liminary examinations held on July 7 and 8, of whom sixteen passed and two were rejected. 146 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 23, 1 8 79. William Whitla, M.D., 41, Victoria Place, Belfast, who was proposed and seconded at the July meeting, was now elected a member of the Society. On the motion of Mr. Hodgson, the Treasurer, seconded by Mr. Doran, it was resolved that £300 of the Society’s funds be invested in 3 per cent. Consols, in the names of the President, the Vice-President, and the Treasurer. Proposed by Mr. Holmes, seconded by Mr. Doran, and resolved — “ That the Pharmaceutical Society of Ireland be repre¬ sented at the forthcoming Meeting of the Pharma¬ ceutical Conference, to be held in Sheffield in August, and that the following be accredited as representatives: — the President; Mr. R. W. Pring, Belfast ; Mr. H. N. Draper ; Mr. W. Hayes ; Mr. E. M. Hodgson. jpro^fdinc;;; of gtoitniijty Jsocictks. BRITISH PHARMACEUTICAL CONFERENCE. The Sixteenth Annual Meeting of the British Phar¬ maceutical Conference was commenced on Tuesday, the 19th of August, in the Freemasons’ Hall, Surrey Street, Sheffield. The chair was taken at half -past ten o’clock by the President, G. F. Schacht, F.C.S. Prior to the commencement of the general business — Mr. W. Ward (Sheffield) welcomed the members of the Association on behalf of the Sheffield Committee, and after adverting to the pleasurable anticipation he and his confreres had enjoyed in the prospect of the visit of the Association to the town, said he trusted that the arrangements made were such that the members would carry away many vivid and lively impressions that would live in their memories for years to come. Reception of Delegates. The Senior General Secretary then read the following list of gentlemen representing other associations at the Conference : — From the Pharmaceutical Society of Great Britain. — Mr. G. W. Sandford, President, Mr. G. F. Schacht, Vice-President, T. Greenish, F.C.S., Treasurer, and Messrs. J. Robbins, W. D. Savage, J. Shaw, C. Symes and J. Williams. From the Pharmaceutical Society of Ireland.— Professor Tichborne, President, and Messrs. J. E. Brunker, H. N. Draper, W. Hayes, E. M. Hodgson and R. W. Pring. From the Bradford Chemists' Association. — Mr. Silson. From the Bristol Pharmaceutical Association. — Messrs . Pitman, W. W. Stoddart and G. F. Schacht. From the Brighton Association of Pharmacy. — Messrs. T. Billing and W. D. Savage. From the Glasgow Chemists' Association. — Mr. E. C. C. Stanford. From the Hull Chemists' Association.— Messrs. C. B. Bell and J. Oldham. From the Leeds Chemists’ Association . — Messrs. P. Jeffer¬ son, R. Reynolds and E. Yewdall. From the Leicester Chemists' Association. — Mr. J. W. Clark. From the Liverpool Chemist s\ Association . — Messrs. T. F. Abraham, A. H. Mason, R. Sumner and C. Symes. From the Manchester Chemists and Druggists' Asso¬ ciation. — Messrs. F. B. Benger, Robinson, L. Siebold and W. Wilkinson. From the Sheffield Chemical and Pharmaceutical Asso¬ ciation. — Messrs. G. Carr, J. T. Dobb, G. T. W. News- holme, J. Preston, J. Turner and J. Watts. Mr. F. Baden Benger, General Secretary, then read the following — Report of the Executive Committee. During the past year the various objects of the Association have been successfully promoted or accom¬ plished. It is again the pleasant duty of your Committee to- report a satisfactory condition of the British Pharmaceu¬ tical Conference. The annual Year-Book was issued in good time and fully maintained the reputation of its predecessors as a faithful resume of pharmaceutical pro¬ gress. The MSS. of the 1879 volume is now in the hands of the printer, and its issue to members will take place as soon as the report of the forthcoming meeting and the Editor’s introductory chapter can be added to it. At a meeting of your Committee, held in London on October 2nd of last year, applications for grants of money to aid authbrs to defray the cost of materials used in carrying out stated researches were received and con¬ sidered. It was resolved — “That £10 be placed at the disposal of Mr. Thresh for the purchase of materials for an analysis of the rhizome of Zingiber officinalis, and a Comparative Examination of the gingers of trade ; that £10 be at the disposal of Mr. Gerrard and Dr. Senier for the purchase of the drug termed Pituri, and for the materials for its pharmaceutical and chemical examina¬ tion ; and, that £40 be placed at the disposal of Dr, Wright towards the cost of the materials for an investiga¬ tion of the active principle or principles of Japanese aconite, and for an investigation of the active principles in the leaves and flowers of ordinary aconite.” Reports by these gentlemen will be presented. At a second Committee meeting, held on July 2nd, Pro¬ fessor Attfield, Senior General Secretary, reported in detail the work done since the last meeting of Committee, including matters relating to the editing, printing and publishing, and delivery to members of the Year-Book ; the grants in aid of research ; correspondence respecting improper use of the membership of the Conference ; correspondence respecting the Bell and Hills Fund books ; compilation and distribution of the list of subjects for research ; collection of subscriptions ; organization of the approaching meeting at Sheffield ; correspondence with members likely to work on the Executive Committee in 1879-80 ; and arrangements for inviting all registered chemists and druggists not already members to join the Conference. The very successful meeting held in Dublin last year will be still fresh in your memories. The pleasant relationships with our Irish brethren then formed or strengthened fully justified (if justification were needed) our acceptance of the invitation to visit Ireland, and proved with what satisfactory results two societies may form one conference. In returning once more to its native land, approaching indeed its very birthplace, the Conference is welcomed with a heartiness which must be highly gratifying to its members, but which is so invari¬ ably extended to it that there is danger of our accepting it more as a right than a privilege. On the present occasion we have perhaps a special reason for remarking on the thoughtfulness which has characterized the ar¬ rangements of the Local Committee. It has been repeatedly urged that the objects of the Conference are best promoted by the avoidance of formal entertainments, and whilst fully appreciating the generous impulse which has so often in the past disregarded this perhaps not sufficiently strongly expressed conviction, your Com¬ mittee venture to hope that the action of the Sheffield Local Committee in this particular may be allowed to form a precedent. The excursion, which usually takes place on the Thursday following the business meetings, affords an admirable opportunity for the renewal ot old friendships and the formation of new ones ; or to quote the words of the first article of our constitution, of pro¬ moting “the friendly reunion of those engaged in the practice or interested in the advancement of pharmacy.” The organization of reunions of this kind will, your Committee is assured, be always gratefully accepted by the Conference as an ample indication of the hospitable feelings of its entertainers. August 23, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS.' 147 Sufficient papers of pharmaceutical interest have been received to fully occupy the time which can be devoted to their reading and discussion at the present meeting. The names of many old and valued friends of the Con¬ ference appear in this list, as well as those of new contributors, to whom a cordial welcome will be given. The Committee have to announce with much regret that at a meeting held last evening they received a formal communication from their valued Senior Honorary Secretary, in which he tenders his resignation of the post he has so long filled with such distinguished success. The communication runs as follows — “ Ashlands, Watford, “ August 16, 1879. “ To the President of the British Pharmaceutical Con¬ ference : — “ Dear Schacht, ’ “ After sixteen years of pleasant labours as one of the Honorary Secretaries of our Association, I regretfully, and yet with a feeling of satisfaction at having done useful service, place my resignation in your hands. I thank my colleagues for the opportunities they have given me of joining them in promoting scientific development in pharmacy and good fellowship amongst pharmacists. From the birth of our organization we have all worked together with the utmost heartiness and harmony, and although I now return to the ranks, I trust I shall be allowed to con¬ tinue to support the objects of the Conference with undiminished enthusiasm and with all the experience and knowledge I have gained as a member of the staff. I hope and believe that the welfare of the Conference and its objects has not suffered either at my hands as a secretary or during my secretaryship, and I do not resign until I have assured myself that that welfare will be maintained, if not enhanced, by the change or changes that will, I know, necessarily be consequent on my resignation. “ I am, Dear Schacht, “ Yours faithfully, “John Attfield.” The Committee felt that the changes involved in Professor Attfield’s resignation were of so serious a nature that they shrank from the responsibility of accepting it until a very mature consideration had pro¬ vided the means for meeting them with a fair prospect of efficiency, and at their earnest request Professor Attfield consented to continue the duties for one year more, in order to afford them the necessary time. The Committee are sure every member of the Conference will concur in a feeling of real gratitude to Professor Attfield for this further manifestation of his self-denying devotion to the best interests of the Conference. Professor Attfield then read the financial statement, and the statement of the Hon. Treasurer in account with the Bell and Hills Library Fund, which is printed on p. 148. The President moved the adoption of the report and financial statement, and referred with great satisfaction to the fact that Professor Attfield had, waiving all personal feeling, decided to continue his services for one year longer, and said he had no doubt that he would act with the same energy, ability and skill as heretofore. Mr. G. Ellinor (Sheffield), an seconding the motion, adverted to the prosperous condition of the funds, which he was sure would be used well in promoting pharmacy in general in connection with the Conference. The motion was then put to the Conference, and car¬ ried unanimously. Professor Attfield read a communication which the President had received from Mr. H. B. Brady, one of the oldest friends of the Conference, apologizing for not being able to attend, and mentioning as evidence of the wide-spread influence of the Conference that he had observed in Japan that a native firm of booksellers offered the Year-Books for sale at four and a-half dollars per volume. The Gift of Books. Professor Attfield explained that the sum of ten guineas, placed at the disposal of the Committee from the Bell and Hills Library Fund, had been expended for the purchase of such books as the officers of the Local Asso¬ ciation thought would be the most useful in their library. In addition to those books there were two others — Han- bury’s ‘ Science Papers,’ and Fluckiger and Hanbury’s ‘ Pharmacographia,’ presented to the Local Association in memory of Daniel Hanbury by his brother Thomas Hanbury. There were, moreover, along with these books, engravings of Jacob Bell, William Alien and Jonathan Pereira offered to the Local Association by Mr. Thomas Hyde Hills. Mr. Ward and Mr. Learoyd returned thanks on be¬ half of the Sheffield Association. Mr. Schacht then proceeded to read the following : — President’s Address. Amidst the customs which rule this Conference in its relations with its President are two that in their co-existence may not always conduce to fortunate re¬ sults. The same individual is retained in his exalted position for two consecutive years, and he is expected to deliver an address on the occasion of each Annual Meeting. In defence of the latter, it may perhaps, with other considerations, be reasonably urged that he who is se¬ lected by the voice of this Association to a dignity so distinguished as the occupancy of this chair, may fairly be expected to have something to say to his fellow phar¬ macists, gathered from either his personal knowledge, his experience or his aspirations, worthy of being uttered. But when he finds himself called upon to repeat the duty after the short interval of one year, he may be excused for feeling, as I feel, that his chance of enlisting the im terest of those who listen is sadly diminished, and that he must, even more earnestly than on the occasion of his former effort, hope for indulgent sympathy. In days gone by, the course of events during the current year, so far as they affected scientific pharmacy, assisted much to indicate the plan and scheme of a Presidential Address ; and some of the ablest discourses recorded in our annals consist chiefly of judicious sum¬ maries of the progress of the sciences connected with our calling and of such movements within and outside our body as appeared to affect pharmaceutical culture. But the conditions which rendered such a course wise in the eai'iier Conference days are now much changed. The same interest, perhaps even greater interest, is felt in those matters, but the work of summarizing them appears to have passed to other hands. The press, which is ubiquitous, and whose chiefest apparent function is to absorb most other functions, has grown strong in our midst, and able editors obligingly offer to us all month by month, and journal by journal, a taste of the plums and a slice of the pie your Presi¬ dent might otherwise be fondly regarding as destined for his own gathering and maturing as a bonne louche for his expected guests ; and to complete his discomfort lurks the conviction that should even a stray blossom escape this scrutiny and he succeed in impressing it to his service, the Conference itself, in its own elaborate and well ordered Year-Book, will, a few weeks later, completely extinguish his puny entertainment and make the remem¬ brance of it stale and flat. The area for my choice appearing thus somewhat nar¬ rowed, I endeavoured last year to select a subject which for complete consideration would afford matter for two addresses, and which yet could be so arranged that the portion first delivered might stand fairly well by itself should any cross stream of events interfere with the original purpose, and I finally determined to make, as well as I could, two presentments of the same fact, viz., 148 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 23, 1870. FINANCIAL STATEMENT, 1878-79. THE GENERAL FUND. The Senior Hon. Secretary in Account with the British Pharmaceutical Conference. Dr. £ cl. Cr , £ s. cl. By Expenses connected with Year-Book : Butler and Tanner for printing, binding, and banding .... Editor’s Salary . Messrs. Churchill: — Com mission on Ad vertise- £410 150 5 9 0 0 ments 35 8 4 Advertising Year-Book . 2 1 0 Delivery to Members 53 16 9 Foreign Journals (Nutt) 3 1 6 654 18 4 General Printing : — Butler and Tanner 3 15 0 Stevens and Richardson . 3 15 3 Parkins and Gotto . 7 l 7 14 12 10 Printing and postage of 10,500 Invitations to Membership • • • 86 10 & Directing Circulars and En- vclopes . . 5 0 3 Assistant-Secretary’s Salary • • 40 0 O Postage (about 10,000 letters) ■ • 41 10 0* Sundries .... • * 13 1 6. Expenses of Meeting at Dublin • 12 6 4 Purchase of a few sets of Year-Books, 1870 — 1872 • • 24 3 4 Grants in Aid of Research • • 50 0 O Balance to Treasurer • 71 16 0 £1013 19 3 The Hon. Treasurer in Account with the British Pharmaceutical Conference. £ s. d. . 33 7 5 . 3 13 6 1878. Dr. To Balance in hand on July 1 July. To Dividend on £250 Consols 1879. Jan. To „ „ June 30. To Cash from Hon. Sec. 3 13 71 16 £112 10 5 1879. Cr. Jan. 29. By Power of Attorney By Balance .... Assets July 1, 1879 Cash in hand Consols (stock) £ 112 250 s. d. 4 5 0 0 THE BELL AND HILLS LIBRARY FUND. The Hon. Treasurer in Account with the British Pharmaceutical Conference for Year ending June 30, 1878. 1878. Dr. To Balance in hand on July 1 July. To Dividend on £350 Consols 1879. Jan. To £ s. d. 5 4 1 5 2 9 5 2 9 £15 9 7 1878. Cr. By Purchase of Books for Sheffield „ Balance . £ s. d. 10 10 0 4 19 7 £15 9 7 ( Cash in hand \ Consols (stock) Assets July 1, 1879 Examined and found correct, £ s. d. 4 19 7 350 0 0 W. HAYES, Dublin. G. A. CUBLEY, Sheffield .! Auditors. £ s. d. 0 6 0 112 4 5 £112. 10 5 August 23, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 149 the pharmacist as we see him ourselves, and the phar¬ macist as seen by others ; and further, should those two images be found to differ (and I scarcely expected them to coincide) to reflect upon some of the points that difference might suggest. Last year then I offered the first part of this scheme, & view of the pharmacist as seen by ourselves. It would doubtless be wrong to assume that the picture then offered was universally approved ; but I know it to have been the result of truth-seeking observation, and twelve months’ further experience assures me that it was fairly correct. I find that the more I know of my fellow labourers, the more good stuff I see in them, and the closer I become familiarized with the work they are doing the more I am able to respect it. Hence I feel no hesitation in repeating the opinion expressed last year, that the typical pharmacist “ stands the illustration of a high order of citizen.” But, lest there be danger that such an estimate resting long unchallenged provoke conceit, let me turn to what may prove an antidote of the severest kind, viz., the esti¬ mate of ourselves by others. Already I can fancy that the recollection of a well- worn couplet has passed through many minds, and has prepared their conceit, had it begun to develop, for a heavy fall — “ Oh wad some power the giftie gie us To see ourselves as others see us — for whatever was really prevailing in the poet’s mind when he penned those lines, the usual sense in which they are quoted is one that implies erroneous self-estimate, on the one hand, and wisdom, superior if not supreme, on the other ; and by this reading I and those who are in¬ clined to support my views ought to stand convicted by a jury of our own choice, not only of great conceit, but of great folly also. But to such -a position and to such a verdict I demur. A solicitude to ascertain what others think of us need not necessarily coincide with any such relation. “ Whom do men say that I am ?” was the in¬ quiry of one vfre should be little inclined to charge with folly or conceit; it was “ men,” not the speaker, that were likely to be the better for a correct appreciation of the speaker’s self; and at the risk of being charged with an unwise comparing of small things with great, I venture the opinion that what the public think of us pharmacists is of graver import to the public than to us. Every art must rest its claim for existence upon some great public want. The universality of disease created the art of medicine. The cure or relief of human suffer¬ ing is the great aim and purpose of that art, and hence in its pure and wholesome progress, every single creature of the public must ever have the profoundest interest. If public ignorance or public prejudice in any way warps that wholesome progress, it is the public that chiefly suf¬ fer ; they are the many, we are the few ; the penalties we may be called upon to pay are but sectional, theirs must be universal. We have but to accommodate our¬ selves to the conditions, they have to endure them. Con¬ versely, should the public wisdom tend, but in the least degree, to favour the full, fair, scientific progress of medicine, the benefit must be experienced in a thousand¬ fold degree where there is a thousand times the capa¬ city for its reception. Does that wisdom then display itself in a fashion most conducive to the best interests of the public ? Let us frankly and gratefully answer, that in many respects it is manifested with high intelligence, and with noble generosity. The hospitals that adorn our entire land, and many of the laws that grace our statute books stand .among the living monuments of both ; moreover few of the recognized professors of medicine pass through the labour of their lives without achieving fair reward in honour or in money, perhaps I might truthfully say in honour and in money. And if the same or similar sentiments pre¬ vailed towards pharmacy and its professors, the two pre¬ sentments I am supposed to be offering would probably coincide, and I should have to say but little more on this topic to-day. But with the majority of the public, certainly with the section that is called “society,” this is not the case, and but little of the honour, and as little as possible of the money, is given to us in exchange for our life-long work. The sole monuments of our professional existence are of our own raising, and “a House” can scarcely be got together to consider a bill, having for its object the regu¬ lation of so iminteresting a matter as pharmacy. It is true we are credited with being concenied in a “clean” sort of business, from which we are oddly enough accused of making very small incomes out of very large profits ; we are admitted to possess decent shops which it is not unseemly to enter, and which indeed it is quite correct to make use of for any purpose not demanding a fee ; we are supposed to be bound by some law of custom (certainly not by any sense of duty) to obey all behests, at all hours, on all days; we are credited, in short, with being “society’s ” most obliged and humble servants, slavishly ready to do whatever is told us, and to take for payment whatever cannot be conveniently bestowed upon the professional man on the one hand or the co-operative stores on the other. To find a man or woman “in society” content to be publicly seen in friendly talk with a pharmacist, or in¬ deed permitting the association of their children with ours at a public school, is to see a phenomenon of rare order. The doctor is the lady’s and sometimes the gentleman’s hero ; the pharmacist is the tradesman to both. Such, I fear is the view very generally taken of us by others, and I need scarcely say this presentiment does not coincide with the one I offered last year. Shall I endea¬ vour to account for the difference before passing to other reflections ? With my already declared estimate of ourselves, and of our art (so different from my lady’s), it is natural I should conceive that the phenomenon may be traced through a course that lies mainly outside us ; and remembering how many-headed is that great outside public, how prone to the instinct of speciation, and how prone is each species to become absorbed in matters of its own concern, taking impressions of other things mainly at second hand, seldom by original effort; I have thought that the first step should consist in the search for that section of the outside world which is likely to be chiefly responsible for the delivery of the initiatory bias. A very short consideration leads to the suggestion that the public would almost instinctively assume that the doctors would know more about pharmacy and pharma¬ cists than anyone else, and therefore that what they thought about us, and the attitude they assumed towards us, would be the proper thing to adopt and to imitate. And the public would have much to justify such an as¬ sumption. More or less the story is known to all (and the more it is remembered the better) that for a long period, until in fact quite recent times, pharmacy constituted both practi¬ cally as well as theoretically an integral portion of the medical art, and the pharmacist and the physician were one man. It is true this latter condition- no longer obtains; it has been found desirable to entrust the different depart¬ ments to distinct sets of hands in order that each may be worked to its fullest perfection, and under the completest personal responsibility. But the art remains the same, one portion being no more capable of repudiating another or declaring its independence of the rest than is the eye or the heart of the human body. And hence this assumption of a kind of perpetual alliance between the professors of all its departments would be both instinctive and reasonable, and the esti¬ mate of the one by the others would be deemed authori¬ tative. Whatever, then, the public estimate of us may be, I think it is mainly the echo and the reflection of that pre¬ viously adopted by our neighbours the doctors. I do not mean that they would pronounce as right the treatment which I have asserted so many of us receive at the hands 150 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 23, 1879*. of the public, but that their general tone and manner towards us have furnished the germ which has thus fructified. But does our experience with the profession justify this interpretation of their views towards us? I have heard of cases, and have experience of cases, in which individual members of the profession have mani¬ fested, by their thoughtful treatment of all pharmaceutical matters, an appreciation of their importance so high and just, and a respect for those engaged in them so fair, that, were the question to be answered from such examples, the reply would be to the effect that there is no justification for it whatever. I fear, however, that these cases are ex¬ ceptional. Of the large majority, some, the greater proportion, are as nearly as possible indifferent to ourselves and to our work. There exists, however, a third section of the profession, and I trust it is a diminishing one, that holds us at a very low estimate, that professes to believe us systemati¬ cally familiar with mean doings, and open to mean temptations. Prom the first of these divisions I pass with a cordial expression of respect, my chief hopes for the bettering of pharmacy in the future resting with its honoured mem¬ bers — from the last with a hope that they may be speedily delivered from their delusion; and our business for the present lies with the indifferentism that remains, and which is unfortunately only something less damaging than actual hostility. How is it to be accounted for ? I believe it to be mainly due to want of knowledge in two important directions. This large majority of medical men do not know enough of our subjects to appreciate them at their proper value, and they do not know the extent of our professional qualifications sufficiently well to give us due credit for them. Notwithstanding the fact to which I have already referred, the essential oneness of all the subjects that together make up the art of medicine, in no modern medical school do chemistry, botany and phar¬ macy rank in educational importance with, let us say, anatomy, surgery and medical practice ; the former are the off-subjects, and are very generally done any-how or no-how ; the latter are among the prime subjects and must be done well. The traditions of the school enlist all the student’s enthusiasm for what are called the medi¬ cal subjects proper, and as an inevitable consequence, a sentiment near akin to contempt pervades his view of the rest. Caring but little for them in the abstract, and taught to think but little of their practical value to his art, the student of medicine when he becomes the professor is but little likely to respect very highly even those he is com¬ pelled to admit as their recognized professors, and from the curious separation that has hitherto characterized the training of the pharmaceutical and the medical student, all that the latter knows of the former amounts to but hearsay, and he finds no particular reason in after life to mature or enlarge his information. For this state of things we must ourselves take some share of blame. There is no doubt that ignorance of mat¬ ters that should have ranged within our knowledge did, in past times, prevail, and, since miraculous changes in social phenomena do not frequently occur, that ignorance may not have entirely yielded yet ; but a great effort for improvement has been made, an effort be it remembered entirely from within our own body, and its practical results have been sufficiently remarkable to suffice in a large degree to absolve us from that portion of the blame. But the very circumstance that appears to stamp phar¬ maceutical progress as unique, and to give it a special dignity, I mean its self-originating and self-sustained character, has largely tended to limit all knowledge of it to those who have specially watched the phenomenon or taken part in it. The policy of those who initiated, as of those who con¬ tinued the effort was one that all can respect for its in¬ dependence, but which I cannot but fear time and experience will show to have been, in this one important respect, unwise. It has served to intensify isolation where unification should prevail. The withdrawal of ourselves and our educational processes from the general pro¬ fessional ken has tended to encourage the elimination of the sciences we specially cultivate from the complete medical curriculum, and to foster the notion I have already deplored that they are accessories of inferior value, and non-essential to medical culture. For this we must still bear our share of the blame. But wheresoever the blame should chiefly lie I think that the fact of the practical isolation of pharmacy and its professors, from the rest of medicine is due to the general defective acquaintance on the part of the professed medical man with both our subjects and our men. I must now pass to a consideration of the loss to the art of medicine that accrues from so extended an indiffer¬ ence to the pharmaceutical sciences. It would perhaps be in better taste to let others speak to this point rather than myself. I am content, therefore, simply to remind you of the frequent publicly expressed lament of many distinguished physicians that so much of their practice is still perforce empirical, and of their equally emphatic re¬ joicings when some ardent student of science has succeeded in wresting from its mysteries some secret that has offered a glimmer of firmer resting ground for their doctrines. The teaching of her highest authorities tells us that medi¬ cine cannot afford to fling away the help of her natural allies; that she is exposed to constant attack at almost every point ; that her growth is not in perfect comeliness and undisturbed proportions, but is liable to distortions and excrescences of formidable type ; and that her best hopes for future progress rest in the patient scientific work of her acutest and largest-brained sons — men who have the power to enlist within their sympathies every depart¬ ment of knowledge that can bring its modicum of truth, and focus all upon that one supreme point, the great problem, life. I think that among the first regions such men would wish to explore are the very subjects in which we are daily engaged ; and with such aspirations animating the great mind of medicine on the one hand, and such opportunities existing for practical co-operation on the other, is it not the simplest of all possible deductions that an effort- serving to bring all into better mutual estimation and closer mutual confidence, must be attended with a fair hope of distinct gain to the art itself ? So far I have attempted to show what the public estimate of us is ; who are chiefly responsible for it ; the probable causes that have led to it, and the mischief to medicine that attends it. One more consideration mnst be stated in order to- show that the error is, as I have said, of great practical interest to the public itself. We are not above the influence of that estimate. Who in this world, whether the question be asked of individuals or of communities, is so strong, either in good or evil as to be able to resist such influence ? Is “ the publican ” likely to become a patriot for being daily de¬ clared to be an outcast ? Branded as a social enemy, an enemy he will continue or become. Should we presume to expect brave deeds in the field if we systematically treated our soldiers as cowards ? Brave deeds alone being assumed as possible, brave deeds are done. In short the opinion of society reacts in a thousand ways upon society’s elements; and I fear the constant treatment to which some of us are subjected, — that says more forcibly than words can say, “You druggists are but hirelings, labour¬ ing like other hirelings for greed ; take your pay and be thankful” — exerts a power for degradation that cannot fail to promote the very condition it professes to re¬ probate. I say that for its own sake the public should make haste to see that we are of stuff much better than this. I am quite aware that at every step of these statements their accuracy may be challenged; I have attempted August 23, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 151 to do this myself in many ways, and during the process have had to admit, from our own side, how often my standard of pharmaceutical excellence is missed, and that ignorance, carelessness and looseness of principle are to be found amongst us ; and from the other side, that many just and considerate individuals can be found in English society, as also doctors whose scientific culture is as ample, and whose disposition to make the most of ours is as generous as heart could desire. Nevertheless, having taken these and kindred facts into full consideration, I allow the statements to stand as what I believe to be the truth. But to another challenge I have perhaps also laid myself fairly open, namely, to suggest some remedy for the condition of things I profess to have studied and to deplore. To this challenge I have but what may appear a feeble reply, I am prepared with no mature scheme, and can offer nothing that can claim to be regarded as a cure for all that is wrong, but being most anxious to see ground broken in the direction that appears to me most hopeful for the extinction of the isolation that besets us and thus give opportunity for a clearer view of ourselves and our doings to the rest of the profession, I am ready to suggest a first step. It is, that every student in medicine, whatever department of the art he may be aiming for as the sphere of his ultimate work, be brought at some period of his training through one single portal. So many practical objections have been found to exist against the mingling of medical and phar¬ maceutical students during their attendance at classes or during any portion of their actual studies, that I think the portal would have to consist of one of the sets of exami¬ nations ; but if that examination could be made a common one for all, whether ultimately destined for Medicine or Pharmacy, the step would be a useful one. It would serve to declare with authority that certain scientific studies were equally essential in all the departments of the medical art ; and it would demand of every student that he attain the required standard of proficiency in them. He would thus be prepared by actual personal knowledge (not through the traditions of his school) to estimate aright the proportionate value of those attain¬ ments towards his full professional equipment ; he would realize the serious amount of effort required to achieve that knowledge, and he would naturally conceive a feeling of respect for all who had laboured for its acquisition even as he himself had laboured. Whether such an experiment would be attended with results proportionate to the distinctness of the change, requires a better prophet than myself to declare. As far as we are concerned it would be the commencement of a reversal of much of our past policy. It would tend from isolation towards unification, from, estrangement towards co-operation, from suspicion towards trust ; but these very words seem to me to be full of hope. One possible comment upon the suggestion itself I should like to anticipate ; it may appear to some to involve the placing of our examinations in the hands of the medical profession. Were this the only course open for adoption, I should not shrink from its close consideration, nor fail to enter¬ tain it with great hope of ultimate benefit; but at present I do not think this by any means a necessary consequence. The story of our own progress, and my personal knowledge of the completeness of the organi¬ zation that lies within our midst, suggest rather the alternative, that for every man’s certificate of qualification in our subjects he might be required to come to our ex¬ aminations; I say “at present,” for in speaking of “our¬ selves” and “medical men” as distinct organizations I shall hope to be using but the language of to-day. My subject, however, now approaches somewhat too nearly the region of pharmaceutical politics to be con¬ tinued here; the arena for its discussion in detail lies else¬ where. But I sincerely hope and think that in urging it from this place to the point at -which I now leave it, I have acted in sympathy with the pervading spirit of the Conference. To this extent, at any rate, I know that I must carry with me the sympathy of all its members, namely, in a warm desire to exalt the dignity of Pharmacy and in an earnest hope that we pharmacists may ever be found, as truly in fact as in aspiration, Pharmacy’s worthy representatives. Mr. W. H. Maleham (Sheffield) said the members of the Conference were much indebted for the exhaustive address delivered by the President, Mr. Schacht, and he had great pleasure in moving a vote of thanks to the President for his valuable address. The time was rapidly coming when they must make a stand against the attacks launched against them, and it was by such' addresses that they could gain valuable information te aid them in repelling opposition. Mr. G-. W. Sandford seconded the motion, and ob¬ served how ardently the President loved the science he had adopted as his calling, and how anxious he was not only to elevate pharmacy but pharmacists. He could not refrain from saying, as a delegate of the Pharmaceutical Society of Great Britain, how heartily that Society ap¬ preciated the work of the Conference. It was his privilege to be connected with the Pharmaceutical Council, and he thought he was the President when this Conference was established. The objects of the Conference and the objects of the Society were identical, and he thought he might congratulate the Members of the Conference on having throughout the course of their work done much towards elevating pharmacy and pharmacists. Regretting that they would soon see the end of Mr. Schacht’s presi¬ dency, yet hoping the same good work would continue., he must say the Pharmaceutical Conference deserved great credit for the results it had already achieved. Mr. R. Reynolds, Vice-President, in putting the motion to the Conference, said it was an easy task when they were all agreed, and referred in terms of eulogy to Mr. Schacht’s philosophical conclideration of the position of pharmacy and his great interest in the welfare and elevation of pharmacists. The motion was carried unanimously. The President, in acknowledging the resolution, thanked the members of the Conference for the expres¬ sions of emotion that had graced the vote, and said he- was very grateful for their approval. He wished to say, however, that it must be understood that any expression of opinion on matters he had thought fit to introduce must be regarded simply as his opinion, for he should be very sorry to commit the Conference, outside those walls, to opinions which were only held by an individual. In expressing those opinions he wished rather to suggest the present position to maturer intellects, so that these ques¬ tions, might be pondered, not only for the benefit of pharmacists but of the community. THE BRITISH ASSOCIATION FOR THE ADVANCEMENT OF SCIENCE. The meeting of the above Association commenced on Monday, August 18, at Sheffield, under the Presidency of G. J. Allman, M.D., LL.D., F.R.SS.L. and E., M.R.I.A., Pres. L.S., who delivered the opening address : — The President’s Address. It is no easy thing to find material suited to an occasion like the present. For on the one hand there is risk that a presidential address may be too special for an audience necessarily large and general, while on the other hand it may treat too much of generalities to take hold of the sympathies and command the attention of the hearers. It may be supposed that my subject should have been suggested by the great manufacturing industries of the town which has brought us together ; but I felt convinced 152 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 23, 1879. that a worker in only the biological sciences coxild not do justice to the workers in so very different a field. I am not therefore going to discourse to you of any of those great industries which make civilized society what it is, — of those practical applications of scientific truth which within the last half century have become developed with such marvellous rapidity, and which have already become interwoven with our everyday life, as the warp of the weaver is interwoven with the woof. Such sub¬ jects must be left to other occupiers of this chair, from whom they may receive that justice which I could not pretend to give them ; and I believe I shall act most wisely by keeping to a field with which my own studies have been more directly connected. I know that there are many here present from whom I have no right to expect that previous knowledge which would justify me in dispensing with such an amount of elementary treatment as can alone bring my subject intelligibly before them, and my fellow members of the British Association who have the advantage of being no novices in that department of biology with which I pro¬ pose to occupy you, will pardon me if I address myself mainly to those for whom the field of research on which we are about to enter has now been opened for the first time. I have chosen, then, as the matter of my address to you to-night, a subject in whose study there has during the last few years prevailed an unwonted amount of activity, resulting in the discovery of many remarkable facts, and the justification of many significant generaliza¬ tions. I propose, in short, to give you in as untechnical a form as possible some account of the most generalized expression of living matter, and of the results of the more recent researches into its nature and phenomena. More than forty years have now passed away since the French naturalist Dujardin drew attention to the fact that the bodies of some of the lowest members of the animal kingdom consist of a structureless, semi-fluid, contractile substance, to which he gave the name of Sarcode. A similar substance occurring in the cells of plants was afterwards studied by Hugo von Mohl, and named by him Protoplasm. It remained for Max Schultze to demonstrate that the sarcode of animals and the protoplasm of plants were identical. The conclusions of Max Schultze have been in all re¬ spects confirmed by subsequent research, and it has further been rendered certain that this same protoplasm lies at the base of all the phenomena of life, whether in the animal or the vegetable kingdom. Thus has arisen the most important and significant generalization in the whole domain of biological science. Within the last few years protoplasm has again been made a subject of special study, unexpected and often startling facts have been brought to light and a volumi¬ nous literature has gathered round this new centre of research. I believe, therefore, that I cannot do better than call your attention to some of the more important results of these inquiries, and endeavour to give you some knowledge of the properties of protoplasm, and of the part it plays in the two great kingdoms of organic nature. As has just been said, protoplasm lies at the base of every vital phenomenon. It is, as Huxley has well ex¬ pressed it, “ the physical basis of life.” Wherever there is life, from its lowest to its highest manifestations, there is protoplasm ; wherever there is protoplasm, there too is life. Thus co-extensive with the whole of organic nature — every vital act being referable to some mode or property of protoplasm — it becomes to the biologist what the ether is to the physicist ; only that instead of being a hypothe¬ tical conception, accepted as a reality from its adequacy in the explanation of phenomena, it is a tangible and visible reality, which the chemist may analyse in his laboratory, the biologist scrutinize beneath his microscope and his dissecting needle. The chemical composition of protoplasm is very com¬ plex, ar.d has not been exactly determined. It may, however, be stated that protoplasm is essentially a com¬ bination of albuminoid bodies, and that its principal elements are, therefore, oxygen, carbon, hydrogen, and nitrogen. In its typical state it presents the condition of a semi-fluid substance — a tenacious, glairy liquid, with a consistence somewhat like that of the white of an unboiled egg. While we watch it beneath the microscope movements are set up in it ; waves traverse its surface, or it may be seen to flow away in streams, either broad and attaining but a slight distance from the main mass, or else stretching away far from their source, as narrow liquid threads, which may continue simple, or may divide into branches, each following its own independent course ; or the streams may flow one into the other, as streamlets would flow into rivulets and rivulets into rivers, and this not only where gravity would carry them, but in a direction diametrically opposed to gravitation ; now we see it spreading itself out on all sides into a thin liquid stratum, and again drawing itself together within the narrow limits which had at first confined it, and all this without any obvious impulse from without which would send the ripples over its surface or set the streams flowing from its margin. Though it is certain that all these phenomena are in response to some stimulus exerted on it by the outer world, they are such as we never meet with in a simply physical fluid — they are spontaneous movements resulting from its proper irrita¬ bility, from its essential constitution as living matter. Examine it closer, bring to bear on it the highest powers of your microscope — you will probably find dis¬ seminated through it countless multitudes of exceedingly minute granules ; but you may also find it absolutely homogeneous, and, whether containing granules or not, it is certain that you will find nothing to which the term organization can be applied. You have before you a glairy, tenacious fluid, which, if not absolutely homo¬ geneous, is yet totally destitute of structure. And yet no one who contemplates this spontaneously moving matter can deny that it is alive. Liquid as it is, it is a living liquid ; organless and structureless as it is, it manifests the essential phenomena of life. The picture which I have thus endeavoured to trace for you in a few leading outlines is that of protoplasm in its most generalized aspect. Such generalizations, how'- ever, are in themselves unable to satisfy the conditions demanded by an exact scientific inquiry, and I propose now, before passing to the further consideration of the place and purport of protoplasm in nature, to bring before you some definite examples of protoplasm, such as are actually met with in the organic world. A quantity of a peculiar slimy matter was dredged in the North Atlantic by the naturalists of the exploring ship “ Porcupine ” from a depth of from 5000 to 25,000 feet. It is described as exhibiting, when examined on the spot, spontaneous movements, and as being obviously endowed with life. Specimens of this, preserved in spirits, were examined by Professor Huxley, and declared by him to consist of protoplasm, vast masses of which must thus in a living state extend over wide areas of sea bottom. To this wonderful slime Huxley gave the name of Bathybius Haeclcelii. Bathybius has since been subjected to an exhaustive examination by Professor Haeckel, who believes that he is able to confirm in all points the conclusions of Huxley, and arrives at the conviction that the bottom of the open ocean, at depths below 5000 feet, is covered with an enormous mass of living protoplasm, which lingers there in the simplest and most primitive condition, having as yet acquired no definite form. He suggests that it may have originated by spontaneous generation, but leaves this question for future investigators to decide. The reality of Bathybius, however, has not been universally accepted. In the more recent investigations of the “ Challenger ” the explorers have failed in their attempts to bring further evidence of the existence of August 23, 1879.J THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 153 masses of amorphous protoplasm spreading over the bed of the ocean. They have met with no trace of Bathy- bius in any of the regions explored by them, and they believe that they are justified in the conclusion that the matter found in the dredgings of the “ Porcupine ” and preserved in spirits for further examination was only an inorganic precipitate due to the action of the alcohol. It is not easy to believe, however, that the very tlaborate investigations of Huxley and Haeckel can be thus disposed of. These, moreover, have received strong confirmation from the still more recent observations of the Arctic voyager, Bessels, who was one of the explorers of the ill-fated “ Polaris,” and who states that he dredged from the Greenland seas masses of living undifferentiated protoplasm. Bessels assigns to these the name of Proto- bathybius, but they are apparently indistinguishable from the Bathybius of the “ Porcupine.” Further arguments against the reality of Bathybius will therefore be needed before a doctrine founded on observations so carefully conducted shall be relegated to the region of confuted hypotheses. Assuming, then, that Bathybius, however much its supposed wide distribution may have been limited by more recent researches, has a real existence, it presents us with a condition of living matter the most rudimental it is possible to conceive. No law of morphology has as yet exerted itself in this formless slime. Even the simplest individualization is absent. We have a living mass, but we know not where to draw its boundary lines ; it is living matter, but we can scarcely call it a living being. We are not, however, confined to Bathybius for examples of protoplasm in a condition of extreme sim¬ plicity. Haeckel has found, inhabiting the fresh waters in the neighbourhood of Jena, minute lumps of proto¬ plasm, which when placed under the microscope were seen to have no constant shape, their outline being in a state of perpetual change, caused by the protrusion from various parts of their surface of broad lobes and thick finger-like projections, which, after remaining visible for a time, would be withdrawn, to make their appear¬ ance again on some other part of the surface. These changeable protrusions of its substance, without fixed position or definite form, are eminently characteristic of protoplasm in some of its simplest conditions. They have been termed “ Pseudopodia,” and will frequently come before you in what I have yet to say. To the little protoplasmic lumps thus constituted, Haeckel has given the nameofProtamoeba primitiva. They may be compared to minute detached pieces of Bathybius. He has seen them multiplying themselves by spontaneous division into two pieces, which, on becoming independent, increase in size and acquire all the characters of the parent. Several other beings as simple as Protaw ceba have been described by various observers, and especially by Haeckel, who brings the whole together into a group to which he gives the name of Monera, suggested by the extreme simplicity of the beings included in it. But we must now pass to a stage a little higher in the development of protoplasmic beings. Widely distributed in the fresh and salt waters of Britain, and probably of almost all parts of the world, are small particles of protoplasm closely resembling the Protamoeba just de¬ scribed. Like it, they have no definite shape, and are perpetually changing their form, throwing out and drawing in thick lobes and finger-like pseudopodia, in which their body seems to flow away over the field of the microscope. They are no longer, however, the homo¬ geneous particle of protoplasm which forms the body of Protamoeba. Towards the centre a small globular mass of firmer protoplasm has become differentiated off from the remainder, and forms what is known as a nucleus, while the protoplasm forming the extreme outer boundary differs slightly from the rest, being more transparent, destitute of granules, and apparently somewhat firmer than the interior. We may also notice that at one spot a clear spherical space has made its appearance, but that while we watch it has suddenly contracted and vanished, and after a few seconds has begun to dilate so as again to come into view, once more to disappear, then again to return, and all this in regular rhythmical sequence. This little rhythmically pulsating cavity is called the “ con¬ tractile vacuole.” It is of very frequent occurrence among those beings which lie low down in the scale of life. We have now before us a being which has arrested the attention of naturalists almost from the commencement of microscopical observation. It is the famous Amoeba , for which ponds and pools and gutters on the house-roof have for the last two hundred years been ransacked by the microscopist, who has many a time stood in amazement at the undefinable form and Protean changes of this particle of living matter. It is only the science of our own days, however, which has revealed its biological importance, and shown that in this little soft nucleated particle we have a body whose significance for the mor¬ phology and physiology of living beings cannot be over- • estimated, for in Amoeba we have the essential characters of a cell, the morphological unit of organization, the physiological source of specialized function. The term “ cell ” has been so long in use that it cannot now be displaced from our terminology; and yet it tends to convey an incorrect notion, suggesting, as it does, the idea of a hollow body or vesicle, this having been the form under which it was first studied. The cell, however, is essentially a definite mass of protoplasm having a nucleus imbedded in it. It may, or may not, assume the form of a vesicle ; it may, or may not, be protected by an enveloping membrane ; it may, or may not, contain a contractile vacuole ; and the nucleus may, or may not, contain within it one or more minute secondary nuclei or “nucleoli.” Haeckel has done good service to biology in insisting on the necessity of distinguishing such non-nucleated forms as are presented by Protamoeba and the other Monera from the nucleated forms as seen in Amoeba. To the latter he would restrict the word cell, while he would assign that of “ cytode ” to the former. Let us observe our Amoeba a little closer. Like all living beings it must be nourished. It cannot grow as a crystal would grow, by accumulating on its surface molecule after molecule of matter. It must feed. It must take into its substance the necessary nutriment ; it must assimilate this nutriment and convert it into the material of which it is itself composed. If we seek, however, for a mouth by which the nutri¬ ment can enter into its body, or a stomach by which this nutriment can be digested, we seek in vain. Yet watch it for a moment as it lies in a drop of water beneath our microscope. Some living denizen of the same drop is in its neighbourhood, and its presence exerts on the proto¬ plasm of the Amoeba a special stimulus which gives rise to the movements necessary for the prehension of nutriment. A stream of protoplasm instantly runs away from the body of the Amoeba towards the destined prey, envelops it in its current, and then flows back with it to the central protoplasm, where it sinks deeper and deeper into the soft yielding mass, and becomes dissolved, digested and assimilated in order that it may increase the size and restore the energy of its captor. But again, like all living things, Amoeba must multiply itself, and so after attaining a certain size its nucleus divides into two halves, and then the surrounding proto¬ plasm becomes similarly cleft, each half retaining one half of the original nucleus. The two new nucleated masses which thus arise now lead an independent life, assimilate nutriment, and attain the size and characters of the parent. We have just seen that in the body of an Amoeba we have the type of a cell. Now both the fresh waters and the sea contain many living beings beside Amoeba which never pass beyond the condition of a simple cell Many rl54 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. t August 23, 1>T9 •of these, instead of emitting the broad lobe-like pseudo¬ podia of Amoeba, have the faculty of sending out long thin threads of protoplasm, which they can again retract, :and by the aid of which they capture their prey or move from place to place. Simple strtxctureless protoplasm as they are, many of them fashion for themselves an outer membranous or calcareous case, often of symmetrical form and elaborate ornamentation, or construct a silicious skeleton of radiating spicula, or crystal clear concentric spheres of exquisite symmetry and beauty. Some move about by the aid of a flagellum, or long whip-like projection of their bodies, by which they lash the surrounding waters, and which, unlike the pseudo¬ podia of Amoeba, cannot, during active life, be withdrawn into the general protoplasm of the body; while among many others locomotion is effected by means of cilia — microscopic vibratible hairs, which are distributed in various ways over the surface, and which, like the pseu¬ dopodia and flagella, are simple prolongations of their protoplasm. In every one of these cases the entire body has the morphological Value of a cell, and in this simple cell •reside the whole of the properties which manifest them¬ selves in the vital phenomena of the organism. The part fulfilled by these simple unicellular beings in the economy of nature has at all times been very great, and many geological formations, largely built up of their calcareous or silicious skeletons, bear testimony to the multitudes in which they must have swarmed in the waters of the ancient earth. Those which have thus come down to us from ancient times owe their preservation to the presence of the hard persistent structures secreted by their protoplasm, and » must, after all, have formed but a very small proportion 'df the unicellular organisms which peopled the ancient world, and there fulfilled the duties allotted to them in natffre, but whose soft, perishable bodies have left no trace behind. In our own days similar unicellular organisms are at work, taking their part silently and unobtrusively in the great scheme of creation, and mostly destined, like their predecessors, to leave behind them no record of their ^ristence. The Red Snow Plant, to which is mainly due rfche foeautiful phenomenon by which tracts of Arctic and Alpine snow become tinged of a delicate crimson, is a microscopic organism whose whole body consists of a simple spherical cell. In the protoplasm of this little cell must reside all the essential attributes of life ; it must grow by the reception of nutriment ; it must repeat by multiplication that form which it has itself inherited from its parent; it must be able to respond to the - -stimulus of the physical conditions by which it is sur¬ rounded. And there it is, with its structure almost on • the bounds of extremest simplification, taking its allotted •part in the economy of nature, combining into living vmatter the lifeless elements which lie around it, redeeming from sterility tbe regions of never-thawing ice, and peopling with its countless millions the wastes of the snow land. But organization does not long rest on this low stage of unicellular simplicity, for as we pass from these lowest forms into higher, we find cell added to cell, until many millions of such units become associated in a single organism, where each cell, or each group of cells, has its •own special work, while all combine for the welfare and unity of the whole. In the most complex animals, however, even in man himself, the component cells, notwithstanding their fre¬ quent modification and the usual intimacy of their union, are far from losing their individuality. Examine under the microscope a drop of blood freshly taken from the human subject, or from any of the higher animals. It is seen to be composed of a multitude of red corpuscles, swimming in a nearly colourless liquid, and along with these, but in much smaller numbers, somewhat larger colourless corpuscles. The red corpuscles are modified cells, while the colourless corpuscles are cells still re¬ taining their typical form and properties. These last are little masses of protoplasm, each enveloping a central nucleus. Watch them. They will be seen to change their shape ; they will project and withdraw pseudopodia, and creep about like an Amoeba. But, more than this, like an Amoeba they will take in solid matter as nutri¬ ment. They may be fed with coloured food, which will then be seen to have accumulated in the interior of their soft transparent protoplasm ; and in some cases the colourless blood corpuscles have actually been seen to devour their more diminutive companions, the red ones. Again, there are certain cells filled with peculiar coloured matters, and called pigment cells, which are especially abundant, as constituents of the skin in fishes, frogs and other low vertebrate, as well as many invertebrate ani¬ mals. Under certain stimuli, such as that of light, or of emotion, these pigment cells change their form, protrude or retract pseudopodial prolongations of their protoplasm, and assume the form of stars or of irregularly lobed figures, or again draw themselves together into little globular masses. To this change of form in the pigment cell the rapid change of colour so frequently noticed in the animals provided with them is to be attributed. The animal egg, which in its young state forms an element in the structure of the parent organism, possesses in the relations now under consideration a peculiar in¬ terest. The egg is a true cell, consisting essentially of a lump of protoplasm enclosing a nucleus, and having a nucleolus included in the interior of the nucleus. While still very young it has no constant form, and is perpetu¬ ally changing its shape. Indeed, it is often impossible to distinguish it from an Amoeba; and it may, like an Amoeba, wander from place to place by the aid of its pseudopodial projections. I have shown elsewhere that the primitive egg of the remarkable hydroid Myriothela manifests amoeboid motions : while Haeckel has shown that in the sponges certain amoeba-like organisms, which are seen wandering about in the various canals and cavities of their bodies, and had been until lately regarded as parasites which had gained access from without, are really the eggs of the sponge ; and a similar amoeboid condition is presented by the very young eggs of even the highest animals. Again, Reichenbach has proved that during the de¬ velopment of the crayfish the cells of the embyro throw out pseudopodia by which, exactly as in an Amoeba, the yolk spheres which serve as nutriment for the embryo are surrounded and engulphed in the protoplasm of the cells. I had shown some years ago that in Myriothela pseudo¬ podial processes are being constantly projected from the walls of the alimentary canal into its cavity. They ap¬ pear as direct extensions of a layer of clear, soft homo¬ geneous protoplasm which lies over the surface of the naked cells lining the cavity, and which I now regard as the “Hautschicht,” or cortical layer of these cells. I then suggested that the function of these pseudopodia lay in seizing, in the manner of an amoeba, such alimentary matter as may be found in the contents of the canal, and applying it to the nutrition of the hydroid. What I had thus suggested with regard to Myriothela has been since proved in certain planarian worms by Metschnikoff, who has seen the cells which line the ali¬ mentary canal in these animals act like independent Amoebae, and egulph in their protoplasm such solid nutri¬ ment as may be contained in the canal. When the Planaria was fed with colouring matter these amoeboid cells became gorged with the coloured particles just as would have happened in an amoeba when similarly fed. But it is not alone in such loosely aggregated cells as those of the blood, or in the amoeboid cells of the alimen¬ tary canal, or in such scattered constituents of the tissues as the pigment cells or in cells destined for an ultimate state of freedom, as the egg, that there exists an indepen¬ dence. The whole complex organism is a society of cells, August 23, 1679.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 155 in which every individual cell possesses an independence, an autonomy, not at once so obvious as in the blood cells, but not the less real. With this autonomy of each element there is at the same time a subordination of each to the whole, thus establishing a unity in the entire organ¬ ism, and a concert and harmony between all the phenomena of its life. In this society of cells each has its own work to per¬ form, and the life of the organism is made up of the lives of its component cells. Here it is that we find most distinctly expressed the great law of the physiological division of labour. In the lowest organisms, where the whole being consists of a single cel), the performance of all the processes which constitute its life must devolve on the protoplasm of this one cell ; but as we pass to more highly organized beings, the work becomes distri¬ buted among a multitude of workers. These workers are the cells Avhich now make up the complex organism. The distribution of labour, however, is not a uniform one, and we are not to suppose that the work performed by each cell is but a repetition of that of every other, j For the life processes, which are accumulated in the single cell of the unicellular organism become in the more com¬ plex organism differentiated, some being intensified and otherwise modified and allocated to special cells, or to special groups of cells, which we call organs, and whose proper duty is now to take charge of the special processes which have been assigned to them. In all this we have a true division of labour, — a division of labour, however, by no means absolute ; for the processes which are essen¬ tial to the life of the cell must still continue common to all the cells of the organism. No cell, however great may be the differentiation of function in the organism, can dis¬ pense with its irritability, the one constant and essential property of every living cell. There thus devolves on each cell or group of cells some special work which con¬ tributes to the well-being of all, and their combined labours secure the necessary conditions of life for every cell in the community, and result in those complex and wonderful phenomena which constitute the life of the higher organisms. We have hitherto considered the cell only as a mass of active nucleated protoplasm, either absolutely naked or partially enclosed in a protective case, which still permits free contact of the protoplasm with the surrounding medium. In very many instances, however, the proto¬ plasm becomes confined within resisting walls, which entirely shut it in from all direct contact with the medium which surrounds it. With the plant this is almost always so after the earliest stages of its life. Here the protoplasm of the cells is endowed with the faculty of secreting over its surface a firm, resisting membrane, composed of cellulose, a substance destitute of nitrogen, thus totally different from the contained protoplasm, and incapable of manifesting any of the phenomena of life. Within the wTalls of cellulose the protoplasm is now closely imprisoned, but we are not on that account to suppose that it has lost its activity, or has abandoned its work as a living being. Though it is now no longer in direct contact with the surrounding medium, it is not the less dependent on it, and the reaction between the im¬ prisoned protoplasm and the outer world is still permitted by the permeability of the surrounding wall of cellulose. When the protoplasm thus becomes surrounded by a cellulose wall it seldom retains the uniform arrangement of its parts which is often found in the naked cells. Minute cavities or vacuoles make their appearance in it ; these increase in size and run one into the other, and may finally form one large cavity in the centre, which becomes filled with a watery fluid, known as the Cell Sap. This condition of the cell was the first observed, and it was it which suggested the often inapplicable term “ cell.” By the formation of this central sap cavity the surrounding protoplasm is pushed aside, and pressed against the cellulose wTall, over which it now extends as a continuous layer. The nucleus either continues near the centre, enveloped by a layer of protoplasm, which is connected by radiating bands of protoplasm with that of the walls, or it accompanies the displaced protoplasm, and lies embedded in this on the walls of the cell. We have abundant evidence to show that the impri¬ soned protoplasm loses none of its activity. The Charaae constitute an exceedingly interesting group of simple plants, common in the clear water of ponds and of slowly running streams. The cells of which they are built up are comparatively large, and, like almost all vegetable cells, are each enclosed in a wall of cellulose. The cellu¬ lose is perfectly transparent, and if the microscope, even with a low power, be brought to bear on one of these cells, a portion of its protoplasm may be seen in active rotation flowing up one side of the long tubular cell and down the other, and sweeping on with it such more solid particles as may become enveloped in its current. In another water plant, the Valisneria spiralis, a similar active rotation of the protoplasm maybe seen in the cells of the leaf, where the continuous stream of liquid proto¬ plasm sweeping along the green granules of chlorophyll, and even carrying the globular nucleus with it in its cur¬ rent, presents one of the most beautiful of the many beautiful phenomena which the microscope has revealed to us. In many other cells with large sap cavities, such as those which form the stinging hairs of nettles and other kinds of vegetable hairs, the protoplasmic lining of the wall may send off into the sap cavity projecting ridges and strings, forming an irregular network, along which, under a high power of the microscope, a slow streaming of granules may be witnessed. The form and position of this protoplasmic network undergo constant changes, and the analogy with the changes of form in an Amoeba becomes obvious. The external wall of cellulose renders it impossible for the confined protoplasm to emit, like a naked Amoeba, pseudopodia from its outer side; but on the inner side there is no obstacle to the extension of the protoplasm, and here the cavity of the cell becomes more or less completely traversed by protoplasmic projections from the wall. These often stretch themselves out in the form of thin filaments, which, meeting with a neighbour¬ ing one, become fused into it; they show currents of granules streaming along their length, and after a time become withdrawn and disappear. The vegetable cell, in short, wTith its surrounding wall of cellulose, is in all essential points a closely imprisoned Rhizopod. Further proof that the imprisoned protoplasm has lost by its imprisonment none of its essential irritability, is afforded by the fact that if the transparent cell of a Nitella, one of the simple water-plants just referred to, be touched under the microscope with the point of a blunt needle, its green protoplasm will be seen to recede, under the irritation of the needle, from the cellulose wall. If the cellulose wall of the comparatively large cell which forms the entire plant in a Yaucheria, a unicellular alga, very common in shallow ditches, be ruptured under the microscope, its protoplasm will escape, and may then be often seen to throw out pseudopodial projections and ex¬ hibit amoeboid movements. Even in the higher plants, without adducing such obvious and well-known instances as those of the Sensitive Plant and Venus’s Flytrap, the irritability of the proto¬ plasm may be easily rendered manifest. There are many herbaceous plants in which if the young succulent stem of a vigorously growing specimen receive a sharp blow, of such a nature, however, as not to bruise its tissues, or in any way wound it, the blow will sometimes be imme¬ diately followed by a drooping of the stem commencing at some distance above the point to which the stroke had been applied : its strength appears to have here suddenly left it, it is no longer able to bear its own weight, and seems to be dying. The protoplasm, however, of its cells, is in th;s instance not killed, it is only stunned by the violence cf the blow, and needs time for its restoration. i 156 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 23, 1879. After remaining-, it may be for some hours, in this droop¬ ing and flaccid state, the stem begins to raise itself, and soon regains its original vigour. This experiment will generally succeed well in plants with a rather large t er- minal spike or raceme when the stroke is applied some little distance below the inflorescence shortly before the expansion of the flower. In the several instances now adduced the protoplasm is in the mature state of the plant entirely included within n, wall of cellulose. Some recent beautiful observations, however, of Mr. Francis Darwin, have shown that even in the higher plants truly naked protoplasm may occur. From the cells of certain glandular hairs contained within the cup-like receptacles formed by the united bases of two opposite leaves in the Teazel { Dipsacus ) he has seen -emitted long pseudopodia-like projections of the proto¬ plasm. What may be the significance of this very •exceptional phenomenon is still undetermined. It is probably, as Mr. Darwin supposes, connected with the absorption of nitrogenous matter. That there is no essential difference between the proto¬ plasm of plants and that of animals is rendered further ■evident by other motor phenomena, which we are in the habit of regarding as the exclusive attribute of animals. Many of the more simply organized plants give origin to peculiar cells called “spores,” which separate from the parent, and, like the seeds of the higher plants, are destined to repeat its form. In many cases these spores are eminently locomotive. They are then termed “swarm- spores,” and their movements are brought about, some¬ times by changes of shape, when they move about in the manner of an Amoeba, but more frequently by minute vibratile cilia, or by more strongly developed flagella or whip-like projections of their protoplasm. These cilia and flagella are absolutely indistinguishable from similar structures widely distributed among animals, and by their vibratory or lashing strokes upon the surrounding water the swarm -spores are rapidly carried from place to place. In these motions they often present a curious semblance of volition, for if the swarm-spore meet with an obstacle in its course, it will, as if to avoid it, change the direction of its motion, and retreat by a reversion of the stroke of its cilia. They are usually attracted by light, .and congregate at the light side of the vessel which con¬ tains them, though in some cases light has the opposite •effect on them and they recede from it. Another fact may here be adduced to show the uniform character of protoplasm and how ver}T different are its pro¬ perties from those of lifeless matter, namely, the faculty which all living protoplasm possesses of resisting the en¬ trance of colouring matter into its substance. As many here present are aware, microscopists are in the habit of using in their investigations various colouring matters, such as solutions of carmine. These act differently on the dif¬ ferent tissues, staining some, for example, more deeply than •others, and thus enabling the histologist to detect certain elements of °tructure which would otherwise remain un¬ known. N ow if a solution of carmine be brought into con¬ tact with living protoplasm, this will remain, so long as it •continues alive, unaffected by the colouring matter. But if the protoplasm be killed the carmine will at once per¬ vade its whole substance, and stain it throughout with a colour more intense than even that of the colouring solution itself. But no more illustrative example can be offered of the properties of protoplasm as living matter, independently of any part it may take in organization, than that presented by the Myxomycetae. The Myxomycetae constitute a group of remarkable organisms, which from their comparatively large size and their consisting, during a great part of their lives, of naked protoplasm, have afforded a fine field for research, and Lave become one of the chief sources from which our knowledge of the nature and phenomena of protoplasm has been derived. They have generally been associated by botanists with the Fungi, but though their affinities with these are per¬ haps closer than with any other plants, they differ from them in so many points, especially in their development, as to render this association untenable. They are found in moist situations, growing on old tan or on moss, or decay¬ ing leaves or rotten wood, over which they spread in the form of a network of naked protoplasmic filaments, of a soft creamy consistence and usually of a yellowish colour. Under the microscope the filaments of the network exhibit active spontaneous movements, which in the larger branches are visible under an ordinary lens, or even by the naked eye. A succession of undulations may then be noticed passing along the course of the threads. Under higher magnifying powers, a constant movement of granules may be seen flowing along the threads, and streaming from branch to branch of this wonderful net¬ work. Here and there offshoots of the protoplasm are projected, and again withdrawn in the manner of the pseudopodia of an Amoeba, while the whole organism may be occasionally seen to abandon the support over which it had grown, and to creep over neighbouring surfaces, thus far resembling in all respects a colossal ramified Amoeba. It is also curiously sensitive to light, and may be sometimes found to have retreated during the day to the dark side of the leaves, or into the recesses of the tan over which it had been growing, and again to creep out on the approach of night. After a time there arise from the surface of this proto¬ plasmic net oval capsules or spore-cases, in which are contained the spores or reproductive bodies of the My- -xomycetae. When the spore-case has arrived at maturity, it bursts and allows the spores to escape. These are in the form of spherical cells, each included in a delicate membranous wall, and when they fall into water the wall becomes ruptured, and the little cell creeps out. This consists of a little mass of protoplasm with a round centre nucleus, enclosing a nucleolus and with a clear vacuole, which exhibits a rhythmically pulsating movement . The little naked spore thus set at liberty is soon seen to be drawn out at one point into a long vibratile whip-like flagellum, which by its lashing action carries the spore from place to place. After a time the flagellum disappears, and the spore may now be seen emitting and with¬ drawing finger-like pseudopodia, by means of which it creeps about like an Amoeba, and like an Amoeba devours solid particles by engulphing them in its soft protoplasm. So far these young amceba-like Myxomycetae have enjoyed each an independent existence. Now, however, a singular and significant phenomenon is presented. Two or more of these Myxamoebae, as they have been called, approach one another, come into contact, and finally become completely fused together into a single mass of protoplasm, in which the components are no longer to be distinguished. To the body thus formed by the fusion of the Myxamoebae the name of “ plasmodium ” has been given. The plasmodium continues, like the simple amoebiform bodies of which it is composed, to grow by the ingestion and assimilation of solid nutriment, which it envelops in its substance ; it throws out ramifying and inosculating processes, and finally becomes converted into a proto¬ plasmic network, which in its turn gives rise to spore- cases with their contained spores and thus completes the cycle of its development. Under certain external conditions the Myxomycetae have been observed to pass from an active mobile state into a resting state, and this may occur both in the amoebiform spores and in the plasmodium. When the plasmodium is about to pass into a resting state, it usually withdraws its finer branches and expels such solid ingesta as may be included in it. Its motions then gradually cease, it breaks up into a multitude of polyhedral cells, which, however, remain connected, and the whole body dries into a horny brittle mass, known by the name of ‘ sclerotium.’ In this condition, without giving the slightest sign of August 23, 1879.] THE pharmaceutical journal and transactions. 157 life, the sclerotium may remain for many months. Life, however, is not destroyed, its manifestations are only suspended, and if after an indefinite time the apparently dead sclerotium be placed in water, it immediately begins to swell up, the membranous covering of its component cells becomes dissolved and disappears, and the cells them¬ selves flow together into an active amoeboid plasmodium. We have already seen that every cell possesses an autonomy or independent individuality, and from this we should expect that, like all living beings, it had the faculty of multiplying itself, and of becoming the parent of other cells. This is truly the case, and the process of cell-multiplication has of late years been studied, with the result of adding largely to our knowledge of the phenomena of life. The labours of Strasburger, of Auerbach, of Oscar Hertwig, of Eduard van Beneden, Biitschli, Fol, and others, here come prominently before us, but neither the time at my disposal nor the purport of this address will allow me to do more than call your attention to some of the more striking results of their investigations. By far the most frequent mode of multiplication among cells shows itself in a spontaneous division of the protoplasm into two separate portions, which then become independent of one another, so that instead of the single parent cell two new ones have made their appearance. In this process the nucleus usually takes an important part. Strasburger has studied it with great care in certain plant cells, such as the so-called “corpuscula ” or “ secondary embryo-sacs ” of the Coniferse and the cells of Spirogyra ; and has further shown a close correspondence between cell division in animals and that in plants. It may be generally stated as the results of his obser¬ vations on the corpuscula of the Conifera?, that the nucleus of the cell about to divide assumes a spindle shape, and at the same time presents a peculiar striated differentiation, as if it were composed of parallel filaments reaching from end to end of the spindle. These filaments become thickened in the middle and there form by the approximation of the thickened portions a transverse plate of protoplasm (the “nucleus-plate”). This soon splits into two halves, which recede from one another towards the poles of the spindle, travelling in this course along the filaments, which remain continuous from end to end. When arrived near the poles they form there two new’ nuclei, still connected with one another by the intervening portion of the spindle. In the equator of this intervening portion there is now formed in a similar way a second plate of protoplasm (the “cell-plate ”), which, extending to the walls of the dividing- cell, cuts the whole protoplasm into two halves, each half -containing one of the newly formed nuclei. This partition plate is at first single, but it soon splits into two laminae, which become the apposed bounding surfaces of the two p»roti plasm masses into which the mother cell has been divided. A wall of celluose is then all' at once secreted between them, and the twro daughter cells are complete. It sometimes happens in the generation of cells that a young brood of cells arises from the parent cell by what is called “ free cell formation.” In this only a part of the protoplasm of the mother cell is used up in the production of the offspring. It is seen chiefly in the formation of the spore of the lower plants, in the first foundation of the embryo in the higher, and in the formation of the endosperm — a cellular mass wdiich serves as the first nutriment for the embryo — in the seeds of most Phanero¬ gams. The formation of the endosperm has been carefully studied by Strasbtirger in the embryo-sac of the kidney bean, and may serve as an example of the process of free cell formation. The embyro-sac is morphologically a large cell with its protoplasm, nucleus, and cellulose wall, while the endosperm which arises within it is com¬ posed of a multitude of minute cells united into a tissue. The formation of the endosperm is preceded by the dissolution and disappearance of the nucleus of the embryo-sac, and then in the midst of the protoplasm of the sac several new nuclei make their appearance. Around each of these as a centre the protoplasm of the mother cell is seen to have become differentiated in the form of a clear spherule, and we have thus corresponding to each of the new nuclei a young naked cell, wrhich soon secretes over its surface a membrane of celhdose. The new cells, w7hen once formed, multiply by division, press one on the other, and so combining into a cellular mass,, constitute the completed endosperm. Related to the formation of new cells, whether by- division or by free ce 1 formation, is another very inter¬ esting phenomenon of living protoplasm known as “rejuvenescence.” In this the whole protoplasm of a cell, by a new arrangement of its parts, assumes a new shape and acquires new properties. It then abandons its cellulose chamber, and enters on a new and independent- life in the surrounding medium. A good example of this is afforded by the formation of swarm-spores in Oedogonium, one of the fresh-water- Algse. Here the whole of the protoplasm of an adult cell contracts, and by the expulsion of its cell sap changes-, from a cylindrical to a globular shape. Then one spot, becomes clear, and a pencil of vibratile cilia here shows itself. The cellulose wall which had hitherto confined it now becomes ruptured, and the protoplasmic sphere,, endowed with new faculties of development and with powers of active locomotion, escapes as a swarm spore, which, after enjoying for a time the free life of an animal,, comes to rest, and develops itself into a new plant. The beautiful researches which have within the last few years been made by the observers already mentioned,, on the division of animal cel's, show how close is the- agreement between plants and animals in all the leading phenomena of cell division, and afford one more proof off the essential unity of the two great organic kingdoms. There is one form of cell which, in its relation to the- organic world possesses a significance beyond that of every other, namely, the egg. As already stated, the egg is, wherever it occurs, a typical cell, consisting essentially of a globule of protoplasm enveloping a nucleus (the “ germinal vesicle ”), and with one or more nucleoli (the “ germinal spots ”) in the interior of the nucleus. This cell, distinguishable by no tangible characters from thousands of other cells, is nevertheless destined to run through a definite series of developmental changes, which, have as their end the building up of an organism like that to which the egg owes its origin. It is obvious that such complex organisms as thus result — composed, it may be, of countless millions of cells — can be derived from the simple egg cell only by a process of cell multiplication. The birth of new cells derived from the primary cell or egg thus lies at the basis of embryonic development. It is here that the phenomena of cell multiplication in the animal kingdom can in gene¬ ral be most satisfactorily observed, and the greater number of recent researches into the nature of these phenomena have found their most fertile field in the early periods of the development of the egg. A discussion of the still earlier changes which the egg undergoes in order to bring it into the condition in which cell multiplication may be possible, would, however full of interest, be here out of place ; and I shall therefore confine myself to the first moments of actual develop¬ ment — to what is called “ the cleavage of the egg ” — • which is nothing more than a multiplication of the fegg cell by repeated division. I shall further confine myself to an account of this phenomenon as presented in typical cases leaving out of consideration certain modifications whish would only complicate and obscure our picture. The egg, notwithstanding the preliminary changes to which I have alluded, is still, at the commencement of development, a true cell. It has its protoplasm and its nucleus, and it is, as a rule, enveloped in a delicate mem¬ brane. The protoplasm forms what is known as the vitellus, or yolk, and the surrounding membrane is called 158 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 23, 1M the “ vitellary membrane.” The division which is now about to take place in it is introduced by a change of form in the nucleus. This becomes elongated, and as¬ sumes the shape of a spindle, similar to what we have already seen in the cell division of plants. On each pole of the spindle transparent protoplasm collects, forming here a clear spherical area. At this time a very striking and characteristic pheno¬ menon is witnessed in the egg. Each pole of the spindle has become the centre of a s}rstem of rays which stream out in all directions into the surrounding protoplasm. The protoplasm thus shows, enveloped in its mass, two sun-like figures, whose centres are connected to one another by the spindle-shaped nucleus. To this, with the sun-like rays streaming from its poles, Auei’bach gives the name of “ Karyolitic figure,” suggested by its con¬ nection with the breaking up of the original nucleus, to which our attention must next be directed. A phenomenon similar to one we have already seen in cell division among plants now shows itself. The nucleus becomes broken up into a number of filaments, which lie together in a bundle, each filament stretching from pole to pole of the spindle. Exactly in its central point every filament shows a knot-like enlargement, and from the close approximation of the knots there results a thick zone of protoplasm in the equator of the spindle. Each knot soon divides into two halves, and each half recedes from the equator and travels along the filament towards its extremity. When arrived at the poles of the spindle each set of half knots becomes fused together into a globular body, while the intervening portion of the spindle becoming torn up, and gradually drawn into the substance of the two globular masses, finally disappears. And now, instead of the single fusiform nucleus whose changes we have been tracing, we have two new globular nuclei, each occupying the place of one of its poles, and formed at its expense. The egg now begins to divide along a plane at right angles to a line connecting the two nuclei. The division takes place without the formation of a cell plate such as we saw in the division of the plant cell, and is introduced by a constriction of its protoplasm, which commences at the circumference just within the vitelline membrane, and, extending towards the centre, divides the whole mass of protoplasm into two halves, each including within it one of the new nuclei. Thus the simple cell which constituted the condition of the egg at the com¬ mencement of development becomes divided into two similar cells. This forms the first stage of cleavage. Each of these two young cells divides in its turn in a direction at right angles to the first division-plane, while by continued repetition of the same act the whole of the protoplasm or yolk becomes broken up into a vast multi¬ tude of cells, and the unicellular organism — the egg, with which we began our history — has become converted into an organism composed of many thousands of cells. This is one of the most widely distributed phenomena of the organic world. It is called “ the cleavage of the egg,” and consists essentially in the production, by division, of successive broods of cells from a single ancestral cell — the egg. It is no part of my purpose to carry on the phenomena of development further than this. Such of my hearers as may desire to become acquainted with the further history of the embryo, I would refer to the excellent address delivered two years ago at the Plymouth meeting of the Association by one of my predecessors in this chair — Professor Allen Thompson. That protoplasm, however, may present a phenomenon the reverse of that in which a simple cell becomes multi¬ plied into many, is shown by a phenomenon already re¬ ferred to — the production of plasmodia in the Myxomy- cetae by the fusion into one another of cells originally distinct. The genus Myriothela will afford another example in which the formation of plasmodia becomes introduced into the cycle of development. The primitive eggs are here, as elsewhere, true cell's with nucleolated nuclei, but without any boundary membrane. They are formed in considerable numbers, but remain only for a short time separate and distinct. After this they begin to exhibit amoeboid changes of shape, project pseudopodial prolong¬ ations which coalesce with those of others in their vicinity, and finally a multitude of these primitive ova become fused together into a common plasmodium, in which, as in the simple egg cell of other animals, the phenomena of development take place. In many of the lower plants a very similar coalescence is known to take place between the protoplasmic bodies of separate cells, and constitutes the phenomenon of con¬ jugation. Spirogyra is a genus of Algae, consisting of long green threads common in ponds. Every thread is composed of a series of cylindrical chambers of trans¬ parent cellulose placed end to end, each containing a sac of protoplasm with a large quantity of cell sap, and with a green band of chlorophyll wound spirally on its walls. When the threads have attained their full growth they approach one another in pairs, and lie in close proximity, parallel one to the other. A communication is then established by means of short connecting tubes between the chambers of adjacent filaments, and across the channel thus formed the whole of the protoplasm of one of the conjugating chambers passes into the cavity of the other, and then immediately fuses with the protoplasm it finds there. The single mass thus formed shapes itself into a solid oval body, known as a “ zygospore.’ This now frees itself from the filament, secretes over its naked surface a new wall of cellulose, and, when placed in the conditions necessary for its development, attaches itself by one end, and then, by repeated acts of cell division, grows into a many-celled filament like those in which it originated. The formation of plasmodia, regarded as a coalescence and absolute fusion into one another of separate naked masses of protoplasm, is a phenomenon of great signifi¬ cance. It is highly probable that, notwithstanding the complete loss of individuality in the combining elements, such differences as may have been present in these will always find itself expressed in the properties of the re¬ sulting plasmodia — a fact of great importance in its bearing on the phenomena of inheritance. Recent researches, indeed, render it almost certain that fertiliza¬ tion, whether in the animal or the vegetable kingdom, consists essentially in the coalescence and consequent loss of individuality of the protoplasmic contents of two cells. In by far the greater number of plants the protoplasm of most of the cells which are exposed to the sunlight undergoes a curious and important differentiation, part of it becoming separated from the remainder in the form usually of green granules, known as chlorophyll granules. The chlorophyll granules thus consist of true protoplasm, their colour being due to the presence of a green colour¬ ing matter, which may be extracted, leaving behind the colourless protoplasmic base. The colouring matter of chlorophyll presents under the spectroscope a very characteristic spectrum. For our knowledge of its optical properties, on which time will not now permit me to dwell, we are mainly indebted to the researches of your townsman, Dr. Sorby, who has made these the subject of a series of elaborate investiga¬ tions, which have contributed largely to the advancement of an important department of physical science. That the chlorophyll is a living substance, like the uncoloured protoplasm of the cell, is sufficiently obvious. When once formed, the chlorophyll granule may grow by intussusception of nutriment to many times its original size, and may multiply itself by division. To the presence of chlorophyll is due one of the most striking aspects of external nature — the green colour of the vegetation which clothes the surface of the earth; and with its formation is introduced a function of fundamental importance in the economy of plants, for it August 23, 1ST9.J THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 15& is on the cells which contain this substance that devolves the faculty of decomposing carbonic acid. On this depends the assimilation of plants, a process which be¬ comes manifest externally by the exhalation of oxygen. Now it is under the influence of light on the chlorophyll- containing cells that this evolution of oxygen is brought about. The recent observations of Draper and of Pfeffer have shown that in this action the solar spectrum is not equally effective in all its parts; that the yellow and least refrangible rays are these which act with most intensity; that the violet and other highly refrangible rays of the visible spectrum take but a very subordinate part in assimilation ; and that the invisible rays which lie beyond the violet are totally inoperative. In almost every grain of chlorophyll one or more starch granules may be seen. This starch is chemically isomeric with the cellulose cell wall, with woody fibre, and other hard parts of plants, and is one of the most important products of assimilation. When plants whose chlorophyll contains starch are left for a sufficient time in darkness, the starch is absorbed and completely dis¬ appears; but when they are restored to the light the starch reappears in the chlorophyll of. the cells. With this dependence of assimilation on the presence of chlorophyll a new physiological division of labour is introduced into the life of plants. In the higher plants, while the work of assimilation is allocated to the chloro¬ phyll-containing cells, that of cell division and growth devolves on another set of cells, which, lying deeper in the plant, are removed from the direct action of light, and in which chlorophyll is therefore never produced. In certain lower plants, in consequence of their simplicity of structure and the fact that all the cells are equally exposed to the influence of light, this physiological division of labour shows itself in a somewhat different fashion. Thus in some of the simple green algae, such as Spirogyra and H ydrodictyon, assimilation takes place as in other cases during the day, while their cell division and growth takes place chiefly, if not exclusively, at night. Strasburger, in his Remarkable observations on cell divisions in Spirogyra, was obliged to adopt an artificial device in order to compel the Spirogyra to post¬ pone the division of its cells to the morning. Here the functions of assimilation and growth devolve on one and the same cell, but while one of these functions is exei*cisei only during the day, the time for the other is the night. It seems impossible for the same cell at the same time to exercise both functions, and these are here accordingly divided between different periods of the twenty-four hours. The action of chlorophyll in bringing about the de¬ composition of carbonic acid is not, as was recently believed, absolutely confined to plants. In some of the lower animals, such as Stentor and other infusoria, the Green Hydra, and certain green planarioe and other worms, chlorophyll is differentiated in their protoplasm, and probably always acts here under the influence of light exactly as in plants. Indeed, it has been proved by some recent researches of Mr. Geddes, that the green planarize when placed in water and exposed to the sunlight give out bubbles of gas which contain from 41 to 55 per cent, of oxygen. Mr. Geddes has further shown that these animals contain granules of starch in their tissues, and in this fact we have another striking point of resemblance between them and plants. A similar approximation of the two organic kingdoms has been shown by the beautiful researches of Mr. Darwin — confirmed and extended by his son, Mr. Francis Darwin — on Drosera and other so-called carnivorous plants. These researches, as is now well known, have shown that in all carnivorous plants there is a mechanism fitted for the capture of living prey, and that the animal matter of the prey is absorbed by the plant after having been digested by a secretion which acts like the gastric juice of animals. Again, Nageli has recently shown that the cell of the yeast fungus contains about 2 per cent, of peptine, a substance hitherto known only as a product of the diges¬ tion of azotized matter by animals. Indeed, all recent research has been bringing out in a more and more decisive manner the fact that there is no dualism in life — that the life of the animal and the life of the plant are, like their protoplasm, in all essential points identical. But there is, perhaps, nothing which shows more strikingly the identity of the protoplasm in plants and animals, and the absence of any deep-pervading difference between the life of the animal and that of the plant, than the fact that plants may be placed, just like animals, under the influence of anaesthetics. When the vapour of chloroform or of ether is inhaled by the human subject, it passes into the lungs, where it is absorbed by the blood and thence carried by the circulation to all the tissues of the body. The first to- be affected by it is the delicate nervous element of the brain, and loss of consciousness is the result. If the action of the amesthetic be continued, all the other tissues are in their turn attacked by it and their irritability arrested. A set of phenomena entirely parallel to these may be presented by plants. We owe to Claude Bernard a series of interesting and most instructive experiments on the action of ether and chloroform on plants. He exposed to the vapour of ether a healthy and vigorous sensitive plant, by confining it under a bell-glass into which he introduced a sponge filled with ether. At the end of half an hour the plant was in a state of anaesthesia, all its leaflets remained fully extended, but they showed no tendency to shrink when touched. It was then withdrawn from the in¬ fluence of the ether, when it gradually recovered its irritability, and finally responded, as before, to the touch. It is obvious that the irritability of the protoplasm was here arrested by the anaesthetic, so that the plant became unable to give a response to the action of an ex¬ ternal stimulus. It is not, however, the irritability of the protoplasm of only the motor elements of plants that anaesthetics are capable of arresting. These may act also on the proto¬ plasm of those cells whose function lies in chemical synthesis, such as is manifested in the phenomena of the germination of the seed and in nutrition generally, and Claude Bernard has shown that germination is suspended by the action of ether or chloroform. Seeds of cress, a plant whose germination is very rapid, were placed in conditions favourable to a speedy ger¬ mination, and while thus placed were exposed to the vapour of ether. The germination, which would other¬ wise have shown itself by the next day, was arrested. For five or six days the seeds were kept under the in¬ fluence of the ether, and showed during this time no disposition to germinate. They were not killed, however, they only slept, for on the substitution of common air for the etherized air with which they had been sur¬ rounded, germination at once set in and proceeded with activity. Experiments were also made on that function of plants by which they absorb carbonic acid and exhale oxygen, and which, as we have already seen, is carried on through the agency of the green protoplasm or chlorophyll, under the influence of light — a function which is commonly, but erroneously, called the respiration of plants. Aquatic plants afford the most convenient subjects for such experiments. If one of these be placed in a jar of wa'er holding ether or chloroform in solution, and a bell-glass be placed over the submerged plant, we shall find that the plant no longer absorbs carbonic acid or emits oxygen. It remains, however, quite green and healthy. In order to awaken the plant, it is only necessary to place it in non-etherized water, when it will begin once more to absorb carbonic acid and exhale oxygen under the influence of sunlight. 160 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 23, 1*79. The same great physiologist has also investigated the action of anaesthetics on fermentation. It is well known that alcoholic fermentation is due to the presence of a minute fungus, the yeast fungus, the living protoplasm of •whose cells has the property of separating solutions of sugar into alcohol, which remains in the liquid, and car¬ bonic acid, which escapes into the air. Now, if the yeast plant be placed along with sugar in etheiized water it will no longer act as a ferment. It is unaesthesiated, and cannot respond to the stimulus which, under ordinary circumstances, it would find in the ^presence of the sugar. If, now, it be placed on a filter, and the ether washed completely away, it will, on re¬ storation to a saccharine liquid, soon resume its duty of separating the sugar into alcohol and carbonic acid. Claude Bernard has further called attention to a very significant fact which is observable in this experiment. 'While the proper alcoholic fermentation is entirely arrested by the etherization of the yeast plant, there still goes on in the saccharine solution a curious chemical ■change, the cane sugar of the solution being converted into grape sugar, a substance identical in its chemical •composition with the cane sugar, but different in its molecular constitution. Now it is well known from the researches of Bertholet that this conversion of cane sugar into grape sugar is due to a peculiar inversive ferment, which, while it accompanies the living yeast plant, is itself soluble and destitute of life. Indeed it has been shown that in its natural conditions the yeast fungus is amable of itself to assimilate cane sugar, and that in order that this may be brought into a state fitted for the nutrition of the fungus, it must be first digested and con¬ verted into grape sugar, exactly as happens in our own digestive organs. To quote Claude Bernard’s graphic account : — “ The fungns ferment has thus beside it in the same yeast a sort of servant given by nature to effect this di¬ gestion. The servant is the unorganized inversive ferment. This ferment is soluble, and as it is not a plant, but an unorganized body destitute of sensibility, it has not gone to sleep under the action of the ether, and thus •continues to fulfil its task.” In the experiment already recorded on the germination >of seeds the interest is by no means confined to that which attaches itself to the arrest of the organizing functions of the seed, those, namely, which manifest them¬ selves in the development of the radicle and plumule and other organs of the young plant. Another phenomenon •of great significance becomes at the same time apparent — the anaesthetic exerts no action on the concomitant chemical phenomena which in germinating seeds show themselves in the transformation of starch into sugar under the influence of diastase (a soluble and non-living ferment which also exists in the seed), and the absorption of oxygen with the exhalation of carbonic acid. These go on as usual, the ansesthesiated seed continuing to respire, as proved by the accumulation of carbonic acid in the surrounding air. The presence of the carbonic acid was rendered evident by placing in the same vessel with the seeds which were the object of the experiment a solution of barytes, when the carbonate became precipi¬ tated from the solution in quantity equal to that pro¬ duced in a similar experiment with seeds germinating in unetherized air. So, also, in the experiment which proves the faculty possessed by the chlorophyllian cells of absorbing car¬ bonic acid and exhaling oxygen under the influence of light may be arrested by anaesthetics, it could be seen that the plant, while in a state of anaesthesia, continued to respire in the manner of animals : that is, it continued to absorb oxygen and exhale carbonic acid. This is the true respiratory function which was previously masked by the predominant function of assimilation, which de¬ volves on the green cells of plants, and which manifests itself under the influence of light in the absorption of carbonic acid and the exhalation of oxygen. It must not, however, be supposed that the respiration of plants is entirely independent of life. The conditions which bring the oxygen of the air and the combustible matter of the respiring plant into such relations as may allow them to act on one another are still under its control, and we must conclude that in Claude Bernard’s experiment the anaesthesia had not been carried so far as to arrest such properties of the living tissues as are needed for this. The quite recent researches of Schiitzenberger, who has investigated the process of respiration as it takes place in the cell of the yeast fungus, have shown that vitality is a factor in this process. He has shown that fresh yeast, placed in water, breathes like an aquatic animal, disengaging carbonic acid, and causing the oxygen contained in the water to disappear. That this pheno¬ menon is a function of the living cell is proved by the fact that, if the yeast be first heated to 60° C. and then placed in the oxygenated water, the quantity of oxygen in the water remains unchanged; in other words, the yeast ceases to breathe. Schiitzenberger has further shown that light exerts no influence on the respiration of the yeast cell — that the absorption of oxygen by the cell takes place in the dark exactly as in sunlight. On the other hand, the influence of temperature is well marked. Respiration is almost entirely arrested at temperatures below 10° C., it reaches its maximum at about 40° C., while at 60° C., it again ceases. All this proves that the respiration of living beings is identical, whether manifested in the plant or in the animal. It is essentially a destructive phenomenon — as much so as the burning of a piece of charcoal in the open air, and, like it, is characterized by the disappearance of oxygen and the formation of carbonic acid. One of the most valuable results of the recent careful application of the experimental method of research to the life phenomena of plants is thus the complete demoli¬ tion of the supposed antagonism between respiration in plants and that in animals. • I have thus endeavoured to give you in a few broad outlines a sketch of the nature and properties of one special modification of matter, which will yield to none other in the interest which attaches to its study, and in the importance of the part allocated to it in the economy of nature. Did the occasion permit I might have entered into many details which I have left untouched ; but enough has been said to convince you that in protoplasm we find the only form of matter in which life can manifest itself ; and that, though the outer conditions of life — heat, air, water, food — may all be present, protoplasm would still be needed, in order that these conditions may be utilized, in order that the energy of lifeless nature may be converted into that of the countless multitudes of animal and vegetable forms which dwell upon the surface of the earth or people the great depths of its seas. We are thus led to the conception of an essential unity in the two great kingdoms of organic nature — a struc¬ tural unity, in the fact that every living being has protoplasm as the essential matter of every living element of its structure ; and a physiological unity, in the universal attribute of irritability which has its seat in this same protoplasm, and is the prime mover of every phenomenon of life. ( To be continued.) ^owfsjjotttlqtq. Messrs. Mclhuaine and Marshall. — We are not aware that any such code of rules has been published. E. Ware. — Artemisia vulgaris. _ Communications, Letters, etc., have been received from Messrs. Radclyffe, Wheeler, George, Reynolds, Mcllwaine and Marshall, Ware, Jarmay, Talbot, J. K. Nicol, Secre¬ tary of Leicester Association, Inquirer, Pendennis, Country Apprentice, H. S. N. August 30, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 161 “ THE MONTH.” When tho§e industrious little insects, the bees, cease working, or at all events collect but little honey, on account of the weather, it is hardly to be expected that flowers under such circumstances should prove more attractive to human beings, unless, like the Ligurian bees, they defy the weather. Studying plants under an umbrella is by no means an agreeable operation, and as sunny skies seem out of the question at present, our floral calendar this month may well be a short one. The terrific thunderstorm early in this month, which spent its fury chiefly in the neighbourhood of Kew and Richmond, committed such havoc, that the conservatories have had to be closed against the public for repairs, no less than 16,000 panes of glass having been destroyed. The house containing medi¬ cinal plants, however, appears to have been com¬ paratively uninjured, although great damage was done in its immediate neighbourhood. In the Economic House, at Kew, the cacao tree has the upper portion of its diminutive trunk and the lower branches studded with little white flowers, the size of which is absurdly small when compared with the large fruit, which is often a foot in length. The Indian variety of the arrowroot and the papaw tree (male plant) are also in flower, and the Guizotia oleifera, which yields the niger seed of commerce, is covered with handsome yellow flowers bearing some resemblance to those of the corn marigold ( Chrysan¬ themum segetum). Cinchona anglica is now in bud, and will shortly expand its flowers. Chlorantlius officinalis, used in Java as an aromatic stimulant in typhus fever, is also opening its minute green flowers. Adenantherci pavonina, which yields the bright scarlet seeds often used as necklaces, and which are used by jewellers in the east as weights, since they weigh almost uniformly 4 grains, is just showing its small yellowish flowers ; these are most disappoint¬ ing when compared with the brilliant colour and polish of the seeds. On the outside wall of the Economic House the jalap plant may be seen flowering freely. In the Herbaceous Ground several American medicinal plants may now be seen in blossom, including Eupa- torium purpureum, Liatris spicata, Leptandra vir- ginica and Monarcla didyma. Leptandra virginica is not unlike the ordinary Veronica genticinoides grown in gardens, but is a taller plant with rather smaller flowers. It has, however, a very pretty and neat appearance and seems to flourish well in the open air. Now that the root, or rather its active principle, leptandrin, is coming into use in this country, it might be worth cultivating. Monarda didyma is a very handsome plant ; its head of bril¬ liant crimson flowers and bracts forming a most striking object when surrounded by plenty of green foliage. The upper lip of the ringent corolla is remarkably long and narrow and conceals the two anthers. At Mr. Ware’s Nursery, at Tottenham, may now be seen in flower a mass of Nardostachys Jatamansi, the plant supposed to be the spikenard of Scripture. It is said to bear cultivation well. It is not, how¬ ever, a very handsome plant. The leaves are lanceolate and the flower stems are only 3 — 6 inches long, terminated by a cluster of small and not very attractive violet-coloured blossoms. The odour of the root somewhat resembles that of patchouli. Other medicinal plants in blossom now are Althcea Third Series, No. 479. officinalis, Cannabis sativa, Lactuca virosa, Artemisia Absinthium, Lobelia syphilitica and Origanum Dic- tcimnus. On chalky or calcareous banks the wild marjoram, Origanum vidgare, may now be seen giving quite a gay appearance to the waste places where it grows in any abundance ; indeed it is to this fact that it owes its name, derived from two Greek words or os and ganos, meaning mountain joy. This plant has a very ancient reputation, as it was used by the Greeks, both internally and for fomen¬ tations, and considered as a remedy for narcotic poisons, such as opium and hemlock. Gerarde speaks of it as being a diuretic, useful in dropsy, and externally of service in some skin diseases. The English or wild marjoram propagates itself extensively by slender stolons. Two forms are re¬ cognized in k English Botany,’ one with ovate few- flowered spikes, and the other with few prismatic many-flowered spikes. Specimens with pale pink and white flowers may occasionally be met with. The marjoram used as a sweet herb is not this plant, but 0. Majorana or 0. Onites. The former has small, roundish spikes and small, stalked, ellip¬ tical, smooth leaves, and the latter, oblong spikes and downy cordate leaves. Neither have the pretty appearance of the wild marjoram, which is largely due to the coloured bracts that subtend the flowers. There are few, probably, do not — “ Know a bank where the wild thyme blows.” But a few other facts connected with thyme do not appear to be so generally known as might be expected in these days of advanced education. In the adver¬ tisement columns of a contemporary may be noticed the statement that thymol is obtained from “ wild thyme ( Origanum vulgar e)T Wild thyme ( Thymus Serpyllum , L.) includes two forms, which by some authors are regarded as species. The form described in 1 Babington’s Manual ’ under the name of T. Ser¬ pyllum, L., forms dense cushions, consisting in great measure of barren shoots with comparatively few short, erect flowering stems rising one or two inches above the tuft. The other Thymus Chamve- drys grows in loose tufts with long slender flowering stems, five or six inches or more in height, and has altogether a different habit, by which, indeed, rather than by any good botanical characters, it is dis¬ tinguished. In the latter plant the upper corolla lip is more rounded and less notched than in T. Ser¬ pyllum. The common thyme of the gardens, Thy¬ mus vulgaris, L., is distinguished by its erect habit and revolute leaves, and is a native of the South of Europe. It is from this plant that the Oleum origani of the shops is obtained, and of which, when pure, thymol is said to form about one half. Thymol has, however, been obtained of late years from the essen¬ tial oil of the seeds of Ptychotis Ajowan, an umbel¬ liferous plant grown in India. The lemon thyme used as a culinary herb is Thymus citrriodorus, Schreb. A good idea of the variety of forms to which plants are subject may be obtained by studying the varieties of the common dandelion. The true natu¬ ralist will not be satisfied with knowing merely the typical form of any species, but will seek a know¬ ledge of the life-history of the commoner plants which come under his daily notice. With regard to the dandelion it would be an interesting inquiry as to which of the various forms yield the largest amount and best quality of extract, and how far the medi- 162 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 80, 1 879. eiual properties and forms of the plant are affected by the circumstances under which it grows. In Sowerhy’s ‘ English Botany,’ four varieties are described, a genuinum, with bright green decidedly luncinate leaves, and the outer bracts of the in¬ volucre recurved ; /3 erythrospermum, having dull green, deeply runcinate leaves, the segments reach¬ ing almost to the midrib, and the outer bracts of the involucre spreading horizontally ; y lacvigatum, with dull green leaves, deeply pinnatifid with triangular strap-shaped lobes, and the outer bracts loosely adpressed to the involucre ; and 5 palustre , with dull green leaves, having few broad spreading lobes, ©r almost entire. Yar. /3 prefers a dry sandy soil, and flowers in early summer. Yar. 5 grows in moist situations and flowers in the beginning of autumn. Those who are interested in knowing more of our sommon plants, will find useful monthly notes in ©ur excellent contemporary Science Gossip, under the heading of “Botanical Work for the Month.” In the Bulletin de la Societe de Pharmacie de Bor¬ deaux, M. Leon Perier gives an account of the hairs found on the leaves of digitalis. The structure ©f these hairs enables the microscopist to recognize the leaves of digitalis, even when powdered, from those of henbane, tobacco, aconite, stramonium, hemlock, etc., with the greatest ease, as anyone may find who will take the trouble to compare the hairs of these plants, first in their perfect state and then as found in powdered leaves. The present number of ‘Medicinal Plants’ contains figures of Balsamodendron Myrrha, Aloe spicata , Roccella tinctoria, Cetraria islandica, Claviceps pur¬ purea , Fucus vesiculosus, Chondrus crispms and Graci- laria lichenoides. Much light has been thrown upon the plants producing myrrh and the allied gum- resins mixed with it, by the excellent specimens collected by Mr. Wykebam Peiry, and presented to Kew Gardens, where the bissa-bol plant is still growing, although the myrrh plant is unfortunately dead. The authors think that B. Kafal will pro¬ bably turn out to be the plant yielding bissa-bol. Until the specimen at Kew flowers, however, this point cannot be satisfactorily determined. Those who choose to supplement the article on myrrh by the information contained on p. 81 of the current volume of this Journal will be in possession of the most recent contributions to our knowledge of this interesting subject. Aloe spicata, the drawing of which is a very characteristic one, has not previously been figured. The authors have followed Mudd in uniting Roccella phycopsis, Ach., and R. tinctoria, DC., and perhaps rightly so. So far as the writer has ob¬ served R. phycopsis, Ach., is the only form which occurs in this country, and may be readily distinguished when gathered by the yellowish colour of its point of attachment to the rock ; that of R. fnciformis and of R. tinctoria (at all events in dried specimens) being always white. No notice is taken of Roccella Mon- tagnei, Bel., as a plant yielding litmus or archil, although a large quantity arrives in this country for commercial purposes. This species is easily distin¬ guished from R. fuciformis by its soft texture. Variolaria, which the authors quote, is now not xecognized as a genus of lichens. The article on ergot is a remarkably clear and concise resume both ©f the botany and chemistry of the subject and is brought up to the most recent date. It may in¬ terest some readers to know that specimens of all the chemical principles obtained from ergot by Dragendorff, as well as crystallized ergotinine pre¬ pared by Tauret, may be seen in the Museum of the Pharmaceutical Society. The drawing of Fucus vesiculosus is a remarkably good one. The authors do not agree with Thuret in separating Fucus platycarpus, as a species. The two plants, besides differing in the shape of the organs of fructification, and in the latter plant being monoecious, may be seen growing together on the same shore and within a few yards of each other, preserving their distinctive characters. From the anniversary report of the Royal Botani¬ cal Society, Regent’s Park, it appears that 540 free students’ and artists’ tickets, for teims of one to six months each, have been issued during the year, and about 25,000 cut specimens given to the holders, besides which nearly 29,000 specimens of plants have been distributed to the several medical and art schools of the metropolis. The meteorological report of the same society shows that the mean temperature of the first six months of this year was 49*35 against 54*7 last year, and that the rain for the same period was in an excess of 3 inches over that of last year. From the Garden we learn that in Germany nearly every town has its botanical garden for fur¬ nishing means of instruction in botany. Berlin has two, the larger of which supplies 120 institutions of learning, including 100 common schools, requiring 3,000,000 specimens. The plants are arranged in bundles and. distributed in -waggons. The flower described by the teacher is illustrated by a living specimen placed in the hand of each pupil. In a letter to the same journal, a correspondent suggests that the nosegays of flow'ers sent to hospitals should contain svreet smelling green plants along with the flowTers, such as rosemary, lavender and gum cistus, an idea, which at first sight, when considered in connection with the ozone-producing power of some essential oils, would appear to be a very good one. It should not, liowTever, be forgotten that the per¬ fumes of some flowers are apt to cause headache and discomfort in peculiarly susceptible patients. Most botanists are familiar with the odour pos¬ sessed by the curious water plant Chara feetida. This odour has recently been attributed to a kind of camphor, which its discoverer, Dr. Phipson,* has called cliaracine. The name is perhaps ill- chosen, since he has obtained the substance also from Pal- mella cruenta, Oscillaria autumnalis, 0. tenuis and Nostoc. It is obtained from Palmella cruenta (a purplish-red substance, found at the base of damp walls, etc.) by drying it in the air at less than summer heat, then placing it in a covered glass vessel ; in thirty-six or more hours the characine torms a film on the water, and the clear decanted liquid is then shaken up with ether. On evaporation the ether leaves the characine as a white greasy substance having a strong marshy odour, lighter than water, and. disappearing either by volatilization or oxidation. To this substance the marshy odour of fresh-water algae in general is attributed by Dr. Phipson. From the Boston Journal of Chemistry we learn that an analysis of a Florida orange gave 23*33 per cent, for the weight of the rind, 2*84 per cent, for the seeds and 73*83 per cent, for the pulp, the free acid in the latter consisting of about equal parts of malic and citric acids. Reports from the Isle of Reunion state that most * Chemical News, August 22, 18/9, p. S6. AnguBt 30, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 163 ! i i I of the vanilla plantations there have been destroyed by a frightful cyclone of three days’ duration, and that those which have not been destroyed are greatly damaged, so that there will be hardly any harvest this year ; consequently, a high price for this article may be expected. In a recent report on the Government plantations at Adelaide, South Australia, Dr. Schomburgk states that a great demand has arisen in that colony for the Phytolacca decandra , which is freely used by homoeo¬ paths in the treatment of diphtheria. The parts of the plant official in the Homoeopathic Pharmacopoeia are the roots and berries. M. Colin, in the Revue Hebdomadaire des Sciences, states that santonin is a complete cure for the obsti¬ nate endemic diarrhoea of Cochin China, and that it acts by destroying the anguillulse by which the disease is occasioned. “ There is no new thing under the sun,” is a de¬ claration generally accepted with the reverence due to the wise preacher who uttered it, but it was hardly to have been expected that the noble savage could claim priority of Dr. Maclagan in the use of salicin in the treatment of rheumatism. Nevertheless the special correspondent of the Medical Times and ■Gazette in Zululand relates that having, in the year 1861, prescribed the usual remedies for a Dutch woman suffering severely from rheumatic swellings and pain, and meeting her two months afterwards looking well and hearty, he was about to congratu¬ late her when he was met by the exclamation, “ De doktor goot had nict gehelp the interpretation of which is, “The doctor’s medicine did not help a bit.” Upon inquiring what had helped lier, she said the old Hottentot shepherd had cured her with a decoc¬ tion of the tips of willow, which fringe the banks of the Orange river. And yet, had a list of South African drugs, including “ willow tips,” been pub¬ lished at that time, it would probably not have attracted the least attention. In a recent number of the British Medical Journal complaint is made by a correspondent of the varia¬ tion in character of commercial euonymin, one specimen which was received from a first class house consisting of brown particles mixed with the greenish particles of euonymin in considerable quantity. The euonymin used by Professor Rutherford and made by a New York firm, did not contain the brown particles. From the description given it would appear as if the euonymin alluded to were a mixture of a watery and spirituous extract in powder. The euonymin prepared by the same pro¬ cess as podophyllin is a very hygroscopic substance and cannot easily be kept in a powdered state. It is time that some of our practical pharmacists should experiment as to the best means of making euony¬ min in a convenient and active form. A correspondent of the British Medical Journal states that bromide of potassium given in doses of not more than 20 grains is a most valuable remedy for the sickness of pregnancy. Given in conjunction with other agents applicable to the local gastric irri¬ tation which may have ensued from the time sickness commenced, he has never found it to fail. Another writer to the Lancet finds that hydro- bromic acid in doses of 20 minims is very superior in its action to bromide of potassium in controlling the obstinate sickness arising from ulceration of the stomach. In the Louisville Medical News sulphate of eserine has recently been recommended by Dr. Cheatham as a means of delaying the use of spectacles, so that they are not required for several years, this alkaloid having the power of stimulating the ciliary muscle and thus assisting accommodation. The strength used is one grain of the sulphate of eserine to an ounce of water. One drop of this solution is put in the eye at night or when required. Professor Laden berg, of Kiel University, has been studying the artificial production of atropine, and has succeeded in recombining tropic acid and tropin e into atropine which is un distinguishable physically, chemically or physiologically from the original alka¬ loid. Among other interesting discoveries to which his inquiry has led is that of tropine being converted under special treatment with strorg hydrochloric acid into a new oily base called t.opidine, which bears a singular relation to conine and collidine. Thus, collidine has the formula C8HnN ; tropidine CsH13N ; and conine C8H15N. H. Weidel (Deut. Ch. Ges. Ber., xii., 410) has been repeating the experiment of Fleitmann, in the oxi¬ dation of berberine by means of nitric acid. Instead of obtaining oxalic acid, as reported by Fleitmann, he obtained a new tribasic nitrogenous acid, which he has named berberonic acid. It is prepared by heating berberine with eight or ten times its weight of nitric acid, concentrating the solution, and puri¬ fying the crystalline mass which separates on cooling by recrystallization from boiling water and conver¬ sion into a calcium salt. Upon decomposing this with an acid and crystallizing from hot water ber¬ beronic acid is obtained in groups of transparent prismatic crystals, sparingly soluble in alcohol and cold water, easily soluble in hot water, and insoluble in ether, benzene and chloroform. Freshly crystal¬ lized the composition is represented by the formula C8H6N0c + 2H20, but on exposure to air the crystals lose one molecule of water, and become opaque. A test to distinguish between tartaric acid and citric acid is published by Cailletet ( Chem . Centralbl., 1879, p. 14), based upon the difference in the be¬ haviour of these two acids towards a cold saturated solution of potassium bichromate, tartaric acid assuming a dark brown colour and giving off car¬ bonic anhydride, whilst citric acid is affected only slowly and gives a light brown colour. If 10 c.c. of * the potassium dichromate solution be added to a gram of pure oitrie acid the orange red colour is unaltered at the end of ten minutes ; if 5 per cent, of tartaric acid be present a dark brown colour is produced, and if 1 per cent, a coffee-browu tint. Vinegar made from wine, and containing tartrate, may be distinguished by this test from vinegar made from fruit and beer or wood vinigar. Another soluble albuminate of mercury for hypo¬ dermic use has been patented in Germany by a Mr. H. Drees. According to the specification it is pre¬ pared by mixing with an alkaline solution of albumen sufficient mercuric acetate to leave neither albumen nor mercury in excess, and removing excess of alkali together with the secondary salts produced in the reaction by dialysis or precipitation with carbonic acid gas and dilute alcohol. Or freshly precipitated mercuric oxide may be added to the alkaline solution of albumen, allowed to digest and the resulting albuminate separated as above. This albuminate is described as soluble in water rendered slightly alkaline by a trace of caustic alkalies, alka¬ line earths or ammonia. 164 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. August 3.0, 1879- Much confusion arises from the fact that henzol and benzin are often used as synonymous terms. In some works the name benzin is now applied to a light petroleum product. In the Archiv cler Phar- macie , it is pointed out that benzol is soluble in one- half to three-quarters its weight of alcohol, while benzin (used in the sense just named) requires six times its weight, so that the two may be thus dis¬ tinguished. In the Chemiker Zeitung, Maumene states that he considers the best characteristic test for oils is the amount of heat liberated when 10 c.c. of concentrated sulphuric acid are mixed with 50 grams of the oil. The acid is added with a pipette and the mixture stirred with a thermometer. Under these conditions olive oil gives a temperature of 42° C. and linseed 103° C. In the Technologiste it is stated that common rosin prevents the formation of acetic acid in fermented liquids without hindering alcoholic fermentation and the writer suggests that the peculiar effect of the hop may be due to its resinous matter rather than to its essential oil. The custom of using Burgundy pitch in lining beer-casks in Germany is thus evidently not without its value. The Lancet, commenting upon a statement that has appeared in various journals to the effect that arsenic is present in paper collars, etc., states that it has been ascertained by analysis that arsenic is not present, but that the substance used for glazing or facing them is sulphate of baryta. Mr. C. T. Gage, in New Remedies for this month, gives a paper on the structure and adulterations of powdered capsicum, with illustrations of the micro¬ scopical appearances of the drug. Out of seventeen samples analysed by him only three proved to be pure and free from adulteration, the chief adulterants being maize, wheat, oat and pea starches, with small quantities of black pepper, mustard and turmeric. A writer in the Deutsche Gartner- Zeitung recalls the fact that a decoction of the stems and leaves of the tomato plant forms a useful insecticide for the greenhouse. He has found that when the decoction is syringed over plants attacked by insects it at once destroys black or green fly, caterpillars, etc., and that it leaves behind a peculiar odour which prevents insects from visiting the plants for a long time. The Scientific American, which never misses an opportunity of extolling the progress of home in¬ dustries in the United States, says that the manu¬ facture of cream of tartar has so developed there that the imports of it from France have fallen in six years from 6,000,0C0 pounds yearly to none, whilst the price has been reduced from 32 to 24 cents per pound. In like manner the imports of citric acid from England have fallen from 250,000 pounds yearly to 27,000 pounds last year, the price having fallen to about one-half. In the case of borax the relations are even more completely reversed ; for in consequence of the development of the borax mines in Nevada, England now appears as a buyer of crude and refined borax in the United States market, where she used to be the principal seller. In the Moniteur Scientifique, M. Bardy points out that the actual amount of acid contained in glacial acetic aeid may be determined by the solubility of oil of turpentine in it. To a known volume of the aeid 8 to 10 times its volume of the oil is added and the mixture stirred two or three times. If the mixture remains clear the acid contains 97 to 98 per cent. In order to obtain comparable results the samples operated on should be of the same temperature, 15° C. being most suitable. The author found that the per¬ centage in the fifty-seven samples examined by him varied from 87 to 99 '5 j)er cent. In the same journal, M. Guyard describes the metal uralium, discovered by him in 1869 in commercial Russian platinum, as being, next to silver',, the whitest metal known, and as malleable as pla¬ tinum, but much more ductile and almost as soft as lead, while it is not volatile and its melting point is near that of platinum. Its sp. gr. is 2025, its mole¬ cular volume 6*25, and its atomic weight 187 ’25. The present year indeed promises to be an event¬ ful one in the history of the elements. On, the one hand scarcely a month passes without the reported discovery of some new substance to which this term is applied, and, on the other there is an accumula¬ tion of evidence that appears to give strength to the doubt whether more than a few, if any, known sub¬ stances are entitled to that name. Some most interesting speculations have been put forward by Professor Victor Meyer in a lecture delivered at Zurich last month, based upon results obtained whilst working out the determination of the vapour densities of various bodies by the process invented by himself and Herr Carl Meyer, and described in this Journal last May (vol. ix., p. 936). At a tem¬ perature of about 1567° C., results were obtained indicating that the molecular constitution of mer¬ cury, oxygen, nitrogen and sulphur is correctly indicated by the formulae usually adopted — Hg, 02, N2, and S2. But it has been found that at this tempera¬ ture the vapour density of chlorine is only two- thiids of what it is at 620° C., and that at 808° C. some kind of dissociation commences which becomes and remained constant at 1567°. Professor Meyer appears to think that the chlorine molecule as at present understood, having the molecular value of 70-4, must therefore contain at least six atoms of a hypothetic body, having the atomic weight of 11*4, and probably trivalent, and to this the name- chlorogene is given ; the hypothetic atom of iodine is similarly named iogene. Mr. Watson Smith, in reporting this lecture to the Chemical News (Aug. I), remarks that these results, considered in connection with the relationship between chlorine, bromine and iodine, and sulphur, selenium and tellurium, as to melting and boiling points, calculated from abso¬ lute zero, observed by Dr. Carnelly nd Mr. W. C. Williams ( Pharm . Journ. [3], ix., 1066), suggests the probability that all these “ so-called elements contain one and the same essence and will ulti¬ mately be decomposed so as to yield this essence common to all six.” But this is not all. Professor Meyer has pro¬ ceeded to a practical investigation as to the constitu¬ ents of chlorine, and following the hint of Berzelius, who looked upon chlorine as an oxygen compound, has tried to ascertain how far this opinion was based upon fact. After conducting his experiments with the utmost precaution, so as to eliminate causes of error as far as possible, he has arrived at the coiir elusion that “to all appearance” by heating chlorine oxygen is obtained. The theory put forward is that two atoms of oxygen exist combined with two atoms of a univalent body, to which the name “murium’* is applied, and that at a high temperature this com¬ bination is broken up, half the oxygen being set August 30, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 165 free. Dr. Armstrong, writing upon tliis subject in Nature (Aug. 14), says tliat some results obtained by Mr. Norman Lockyer in the spectroscopic inves¬ tigation of the non-metals are confirmatory of Professor Meyer’s discovery, and that Mr. Lockyer has shown him that “ with the spark at a particular tension the red line of oxygen is one of the most prominent lines in the spectrum of chlorine the freedom of which from admixed air is attested by the absence of the characteristic nitrogen and hydrogen lines.” In a letter to the Chemical News Mr. J. Gibbons suggests that the peculiar spectra sometimes observed in lightning may be due to metals with which the lightning comes into contact and that the instrumental observation of the spectroscopic character and direc¬ tion of the lightning, with the interval of flash and report, would be sufficient to determine the character and situation of exposed metalliferous deposits in unexplored districts. The veteran chemist, Chevreul, whose name is associated with researches on fats and fatty acids, although now in his ninety-third year, began his usual course of lectures on organic chemistry at the Museum of Natural History at Paris a short time since. Mr. Holloway appears to be bent upon the per¬ petuation of his name as a benefactor of his species in more than one direction. According to Nature he has purchased and vested in trustees ninety-five acres of land at Egham, upon which he intends to erect a building for a college, the object and scope of which is to be to afford the best education suitable for women of the upper and upper middle classes. The contract for the building of the college within four years has been signed, the price being upwards of £250,000, exclusive of fittings. It is the founder’s desire that power for the college to confer degrees should be sought at some future time, but that mean¬ while students should qualify themselves to pass the women’s examination of the London University. ■“ Denominational theology ” is not to be taught, and, instead of being regulated by the “ traditions and methods of former ages,” the system of education is. to be mainly based upon studies and sciences which the experience of modem times has shown to be most valuable and best adapted for the intellectual and social requirements of the students. Mr. Holloway has also agreed to provide an endowment fund of £100,000, in addition to such proceeds as may be derived from the sale of any portion of the land not required for the purposes of the College. It must be apparent from the continuous flow of inquiry that increased attention is being directed to these columns devoted to the difficulties which beset dispensers. The questions generally exhibit a very imperfect acquaintance even with prescriptions possessing no special characters, others refer to incom¬ patibilities which must have escaped the observation of the writer, and some have reference to obscure preparations, the formulae for which have never been published ; but there are those also which indicate that sufficient attention is not paid to the information supplied by correspondents, and recorded continu¬ ously in the Journal. This latter is to be regretted as repetition occupies valuable space, and should, unless in quite exceptional instances be unnecessary. The first question in the series refers to the result of a mixture of Donovan’s solution with liq. hyd. perclilor. in No. 331. Immediately on the addition being made there is a decomposition with a copious separation, and ultimately a deposit of red iodide of mercury, which settles at the bottom, the super¬ natant liquid being pinky- white ; the addition of a little iodide of potassium would render the mixture transparent, but, of course, this liberty cannot be taken with a prescription. The mixture is an in¬ elegant one, and most probably the writer was not aware of the result of mixing liq. hyd. perch, with liq. arsen. et hydrarg. hydriod. (Donovan ,s solution), an already delicately balanced compound. Gelatine is not suitable as a vehicle for tannin in pessaries or suppositories, as in No. 332. A decomposition occurs with the formation of tannate of gelatine, and the otherwise gelatinous vehicle breaks down in the preparation. In those instances where medical men require a gelatine vehicle it would be better that they left the most suitable relative proportions of the ingredients for that vehicle to the dispenser. It is usual to keep a gelatine medium ready prepared in proper propor¬ tions, and on liquefying this for the addition of the of the medicament, the pessaries are moulded in the usual manner. The usual vehicles for pessaries and suppositories are cacao butter or some such substance as a basis, on the one hand, and gelatine on the other, and it will be better for the prescriber to specify one or other of these, leaving the relative proportions to the dispenser, the writer of the prescription proportioning only the medicament. Very rarely do medical men give suitable propor¬ tions for the vehicle desired. The .same may be said of pill masses. A dispenser is often at his wit’s end in. too literally interpreting the excipient and its quantity ordered in a prescription. The in¬ gredients being written, those minor details, in fact, the mode of combining those ingredients so as to form a pill mass, may well be left to the practical ex¬ perience of the dispenser. The query No. 333 refers to ext. belte liq. Made according to the formula in the B.P. the result may be termed a dark brown syrupy liquid, which on standing deposits, the supernatant liquid being clear, and the portion containing the deposited matter opaque. It will be obvious from these remarks that the appearance of the ext. belce liq. will much depend on the time it has been allowed to stand subsequent to its preparation. The addition of spirit will also necessarily cause a separation of some of the constituents of the bael, which on standing deposits. The Pharmacopoeia does not direct it to be filtered. It is presumable, therefore, that the ext. belse liq. should be shaken each time that the prescription is dispensed, as the separated portion is not inert matter. If reference be made to the ext. ergot, liq. the distinction will be at once apparent. In that preparation the spirit is added to coagulate albumenoid matter, and then, after the addition of spirit, the liquid is directed to be filtered ; but the spirit in the ext. beke is more as a preservative than for the purposes of coagulation, though at the same time it probably promotes a subsidence of some of the proximate constituents of the bael, which forms an integral part of the finished preparation. The recipe No. 334 is very likely one of those sometimes met with by the dispenser. In its present condition it is not complete, and it would not be judicious or safe to put calomel into such a mixture to be taken three times a day. It is scarcely possible that such a formula could emanate from a 166 THE EH ARMACEU TIOAL JOURNAL AND TRANSACTIONS. (Augu>t 30. 1879.. duly qualified medical practitioner. The usual method of mixing copaiba is to emulsify that sub¬ stance by trituration with mucilage in a mortar, and gradually adding the other ingredients. In the presence of such a powerful agent as calomel, the dispenser, having no medical qualification, would not be justified in determining any proportion as a suitable addition to the other ingredients of the mixture. There is no formula for emp. iodin. in the B.P. ; but dispensers have facilities afforded them of re¬ ferring to other works for their guidance in similar difficulties. One that is frequently found useful is Squire’s ‘ Pharmacopoeias of London Hospitals,’ and again an extremely valuable little work, and one kept abreast of the time, is Beasley’s ‘Pocket Formulary.’ When a preparation met with in a prescription is absent in the B.P., and therefore unofficial, every dispenser is not bound to go t) the same source to supply the deficiency ; one may take a formula from Beasley, another from a foieign phar¬ macopoeia, and a third from a hospital pharmacopoeia. This may account for the emp. iodinii as sent out by different establishments not being of the same colour. It must clearly be annoying to a dispenser to be told that he does not know his business; but if his reading be so limited that he stands aghast in the presence of such a small difficulty, he must expect some such a remark, and should profit by the hint. The formula for emp. iodinii in Beasley is given by “ Gulielmus.” The formula for pomade, No. 336, corresponds with similar preparations which have been intended for promoting the growth of the hair. There being no official preparation of dialysed iron, difficulties are very likely to occur with liquors of different makers. The strength generally accepted as suitable is a liquor containing 5 per cent, of oxide of iron. Should it ever become official, probably a strength equivalent to that of the tr. ferri perchlor., containing about 6 per cent, oxide would for the sake of uniformity be better. The prescription No. 337 is readily made, and does not separate or deposit, but forms a clear transparent mixture, which keeps well without apparent change. If the medical pro¬ fession consider dialysed iron a remedial agent, having a therapeutic value, or some merit not possessed by other preparations of iron, which now occupy a place in the British Pharmacopoeia, the sooner a definite strength be determined on the better, that is that it should contain a definite quantity of oxide of iron, and probably a liquor of the same strength as the tinct. ferri perchlor. would be the best that could be adopted. Advertised medicinal preparations of unknown strength should be discountenanced, and their places supplied by preparations of definite strength. On this subject some remarks taken from a report on the progress of pharmacy, by Mr. C. L. Diehl, may be quoted here. He considers it under two heads : “ The progress that is secured by research and by the furtherance of educational facilities,” and, secondly, “ The progress that is made by the dis¬ couragement of empiricism* and the establishment ot a proper ethical and professional standard.” The first need not be considered here ; with regard to the second, he says: — “Pharmaceutic progress, as em¬ braced under the second head, however, is not so satisfactory. The relations of pharmacists to the public, to each other, and to physicians, leave much to be desired, and instead of being progressive, ap¬ pear rather to tend in the opposite direction. The- demand of the public for cheap goods, the variety demanded, competition, the profuse supply of ‘ready¬ made ’ pharmaceuticals, and the disposition of phy¬ sicians to prescribe medicines of a questionable composition or proprietary character, all have a tendency to reduce pharmacists to the condition of mere tradesmen, and to discourage those having higher aims.” CAVIAR* This substance, which is considered a great delicacy by gourmands, is the prepared roe of the sturgeon and has its origin in Russia. This roe differs materially from that of other fish, in being of a large size and very thin skinred, containing only an oily jelly which melts away in the mouth, leaving little or no residuum, and these are held together by a network of cellular tissue, fat and muscle in large masses, which generally exceed in size the head of the largest man. A net of very small mesh, spread over a frame, does duty as a kind of coarse sieve, and the roes being lightly pressed and kneaded over this, the eggs are detached and fall into wooden tubs placed below, each grain being of a very dark brown or black colour, and utterly distinct from the others. To make “ grained caviar ” the eggs are now sprinkled with salt ground very fine, of which from 3 to 5 pounds to thirty-six of eggs are used in the hotter months, while only If to 2^ pounds are sufficient in cold weather, the least possible quantity of salt being a great desideratum. A wooden fork with from eight to ten prongs is used to stir in the salt, and the eggs become first doughy, then swell, and finally give out a noise like the stirring of small scales of glass, a sure proof that the process is completed, after which the caviar is close packed in hard¬ wood kegs. In making “ grain caviar ” the eggs fall into tubs of brine stirred as before, and in lots of about one hundred¬ weight subjected to heavy pressure in coarse sacks, until the brine is expelled and the whole compressed into a cheesy mass. Nearly one-third of the contents of the eggs are pressed out with the brine, and the caviar thus made is packed in large casts lined with napkin linen, from whence it is called caviar d la serviette, or “napkin caviar.” Caviar a sac, as its name denotes, is choice pressed caviar, put up in linen sacks, and other choice preparations are shipped in hermetically sealed cans and boxes. The fattest caviar, made in midsummer, is merely soaked in brine and packed, without pressing, in casks holding from 180 to 360 lbs. each. Much roe which is tender to the touch and half spoiled is soaked in very strong brine, packed in large casks holding from 900 to 1000 pounds, and is worth only from six to eight cents per pound, while the fat summer caviar brings from twelve to eighteen cents. The choice kinds of fresh caviar packed in small kegs costs in Astrachan from sixty to seventy cents per pound, while the pressed brings but about forty-five to forty- eight cents ; that of the “ sterliad ” and some especially choice makes are never exported. Nearly 400,000 pounds are annually sent from Astrachan to Berlin, Dresden and Vienna, and England uses nearly 10,000 dollars worth yearly, but in the United States little is used except by foreigners, who have contracted a taste for it elsewhere. * From the Boston Journal of Commerce. Reprinted from N&iv JRemedies, August, 1879. August so, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS.' 1G7 ♦ SATURDAY, AUGUST 30, 1879. Communications for the Editorial department of this Journal, books for review, etc., should be addressed to the Editor, 17, Bloomsbury Square. Instructions from Members and Associates respecting the transmission of the Journal should be sent to Mr. Elias Bremridge, Secretary, 17, Bloomsbury Square, W.C. Advertisements, and payments for Copies of the Journal, Messrs. Churchill, Neio Burlington Street, London, JV. Envelopes indorsed “ Pharm. JournJ THE USE AND ABUSE OF EXAMINATIONS. The leading journal has within the last few days directed attention to some of the evils of the ex¬ amination system, and it has done good service by insisting upon the mischief likely to arise from the modern tendency to make examinations the sole test and crown of all processes of education. We quite agree with the opinion that this tendency entirely distorts every rational view of what educa¬ tion is and should be. But this is a result attribut¬ able more to the circumstance that too much faith has been placed in the virtue of examinations than to the absolute worthlessness of examinations as a test of merit, capacity and attainment ; it is a result of the misuse of examinations that has led students to look upon the passing of them as being of more importance than the acquisition of sound kliowledge, that has led teachers to devote their energies to the production of manuals by which superficial pro¬ ficiency can be readily acquired, and candidates enabled to pass the ordeal of examination without its being really that test of educational training that it was designed to be. From this point of view there is no doubt much reason to fear that however good examination may be when properly used, we are exposed to the possi¬ bility of having too much of a good thing, and as the Times remarks very many competent judges are already beginning to dread an educational surfeit in this respect. The exaggerated application of the examination system has not operated as a stimulus to sound and thorough education, but has rather called into existence and created a demand for facilities for passing examinations without under¬ going the preparatory educational labour necessary for acquiring a proficiency in the subjects. In this way the pupil has been made a mere racer and one who contends for heavy pecuniary stakes, while the teacher is made a trainer whose whole prosperity depends, not on his power of imparting sonnd know¬ ledge and drawing out the natural capacities of the mind, but on his skill in preparing his pupils for a particular examination . At the same time there is a tendency to make the examiner a judge not of mental capacity and general sound information, but of those qualities alone which are readily estimated in marks. These results are undoubted evils, and there are others not much less serious which justify the ques¬ tion put by the Times as to whether it is not possible that, as so often happens, we have confounded ends with means and made a successful examination the paramount purpose instead of merely the indispens¬ able test of educational training ? But while ad¬ mitting the existence of these we cannot share the opinion that the blame is entirely to be thrown upon examination. What in our opinion is needful as a remedy is not the abandonment of the examination system which some would recommend, but some means of reducing the exaggerated importance that has been attached to the passing of an examination. In many cases examinations are necessary as rough tests of required attainments, and where they are to be tested for some specific purpose it is indeed scarcely possible to dispense with examinations alto¬ gether, but even then they should not be placed higher than the category of necessary evils. Another remedy for^the mischievous influence of the examination system in limiting and restricting sound education is by some believed to be attainable by the establishment ol a compulsory curriculum, but we are far from sharing the opinion that such a plan would be effectual. At the best it would only furnish a guarantee that the student had enjoyed the opportunity of having the requisite education, but it would fail altogether to give assurance that he had made proper use of that opportunity. As regards this most important point we think that no real good would result from having recourse to the teacher’s testimony as to the assiduity of liis pupils in attending lectures, etc. It would be merely sub¬ stituting for the fallacious evidence of success in examination, the equally fallacious evidence of formal compliance with the requirements of a curri¬ culum. Neither is in itself sufficient to prove that the pupil has been properly educated. To take the case of pharmaceutical education, involving as it does the acquisition of a sound know¬ ledge of several branches of science and a practical training in their application to special objects, we are altogether averse to the establishment of a scholastic curriculum, because we do not believe it would ensure the education that is required. It is in the training of the apprentice in the shop that the proper curriculum of the pharmacist is to be sought for, and as the improvement in the practice of pharmacy in this country advances and becomes more general, it may be hoped that it will be found there more frequently than has been the case. In many cases the nature of a chemist and druggist’s business is not such as to afford apprentices much opportunity of studying science, but the de¬ ficiency in this respect might be largely compensated for by the local schools connected with provincial societies, and it is to be regretted that hitherto these provisions for the instruction of apprentices have not been more zealously taken advantage of. 168 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 30, 1S7&. VERIFICATION OF WEIGHTS IN NEW YORK. It is a little curious that whilst pharmacists in Great Britain have recently been under some anxiety as to the course that would he adopted by the State in respect to the verification of their weights and measures, their brethren in New York have had a similar experience. Some time ago, it was mentioned in this Journal that a Bill had been introduced into the Legislature of the State of New York, providing for the appointment of an Inspector of Apothecaries’ Weights, the amount of whose salary would have depended upon the number of penalties he succeeded in levying from persons whose weights he pronounced incorrect, although no provision was made that he himself should possess verified standard weights for use in the testing. The strong remonstrances of a committee of the New York College of Pharmacy procured the withdrawal of the Bill, upon a promise that the College would take the matter in hand and establish a bureau for the examination of apothe¬ caries’ weights, to be placed under the authority and control of the Board of Pharmacy for the city and county of New York. The arrangements for carrying this promise into effect having now been completed, and special balances and sets of troy and decimal weights, which have been verified by the United States Standards? having been provided, the New York College has sent out an appeal to all apothecaries, whether members or not, to help in carrying out its plan as aiming at a “wise and conscientious self-govern¬ ment.” It is proposed to deal with the weights first, leaving the measures untouched for the present. These the College offers to examine upon application of the owner, and to stamp as correct if found either absolutely identical with the standard or heavier up to a certain limit; if at all lighter or if heavier beyond the specified limit, they will be returned unstamped, and it is recommended that such weights should be at once destroyed. The limit of excess, as established for decimal weights ranges from not more than 0‘200 gram in the 1000 grams or 1 kilo weight to not over O- 00025 gram in the 0T gram and lesser weights. In the troy weights the limit of excess ranges from not exceeding 1 grain in the 12 ounce weight to not over 0'01 grain in the £ grain weight. The charge for examining weights, including the stamping of those found correct, is only five cents for each weight. The stamp of verification adopted consists of a monogram of the letters CP, and it will be noticed that it is proposed to apply it to weights so small as to be generally supposed to present almost insuperable difficulties in stamping them. Indeed the College offers to supply “ correct and stamped sets of weights ” of the decimal and troy systems reaching down to 1 milligram and of a grain respectively. If this offer is to be understood literally the method of carrying it out would prob¬ ably not be devoid of interest to the Board of Trade officials in this country just at the present moment. LEICESTER CHEMISTS AND DRUGGISTS’ AS¬ SISTANTS AND APPRENTICES’ ASSOCIATION. The first meeting of the twenty-second session of the Leicester Chemists’ Assistants and Apprentices’ Asso¬ ciation was held at the Rooms, Halford Street, on Tuesday evening, August 12. The proceedings of the evening were commenced by a tea, to which a good number of members sat down. After tea the newly elected President, Mr. J. J. Edwards, delivered an inaugural address, and in com¬ mencing referred to the necessity for individual effort and advised each member to attend regularly, to put his shoulder to the wheel, and to do all in his power to make the Association a success. Referring to past members of the Association who had passed their examinations, he stated that many of them had acknowledged the valuable aid they had received from the Association. Referring to the question what to read, the President said it was much more difficult to know how to read, so as not to follow the example of some, “who, like sponges, return ail they read in about the same condition, only a little dirtier ; ” nor of others, “ who, like strain bags, merely retain the dregs of what they read.” In concluding, the President reminded the members that not only was talent necessary to make a successful pharmacist, but it was imperative that there should be tact in conjunction with talent, for whilst “ talent knows how to do it, tact does it ; ” whilst “ knowledge is the treasury of the world, tact is the key to it ; ” and whilst “ talent beats about the bush, tact catches the bird.” The President announced that during the forthcoming session several lectures on subjects connected with phar¬ macy would be delivered by gentlemen of repute. Some remarks by Mf. W. B. Clark and Mr. Thirlby brought a very pleasant evening to a close. fjnnifMtinp of JlcmttiJiit foi’icties. BRITISH PHARMACEUTICAL CONFERENCE. ( Contin u ed from page 151.) The reading of papers was then proceeded with. The first paper was a — Report on the Aconite Alkaloids. BY C. R. ALDER WRIGHT, D.SC. (LOND.). Lecturer on Chemistry in St. Mary's Hospital Medical School. § 1. — Alkaloids of Japanese Aconite Roots. In the report presented last year there were briefly described some preliminary results obtained in the ex¬ amination of Japanese aconite roots. Since that date, several batches of roots have been examined with per¬ fectly uniform results ; as the numerical and other data on which these results are founded have been already published in the Journal of the Chemical Society (July, 1879, p. 387), it will be unnecessary to quote them here at full length. The first batch (about 14 \ kilos of ground roots obtained from Messrs. Wright, Layman and Umney) was worked up by the reporter and Mr. A. P. Luff, by percolating with alcohol acidulated with tartaric acid (1 part of acid per 100 of roots being used in all). The percolate was condensed to a small bulk by distillation, treated with water, filtered from precipitated resin, rendered alkaline with carbonate of soda and repeatedly shaken with ether, the ethereal solution being subsequently shaken with tartaric acid. The acid tartrate solution thus obtained free from resinous matters was then treated with soda August 30, 1879.] THE pharmaceutical journal and transactions. 169 and ether ; on spontaneous evaporation a copious crop of crystals was obtained, together with a quantity of varnish¬ like alkaloidal matters that wouH neither crystallize nor yield crystalline salts. The total yield of alkaloids from this batch was as follows : — crystallizable about 12 grams = 00S non-crystalline „ 25 „ = 0-17 37 0-25 | non-crystalline „ 20 „ = 0*14 )tal . 57 0-39 » The alkaloids insoluble in ether were separated by pre¬ cipitating as mercuriodide, and decomposing the pre cipi- tate by sulphuretted hydrogen; they appeared to be mainly identical with the non-crystalline alkaloid that was dissolved out by ether, being prevented from complete solution in ether by the solvent action of the soda liquors, just as is often the case with alkaline solutions of alka¬ loids, e.g., morphine and caustic potash, cotarnine and sodium carbonate. The non-crystalline alkaloids appeared, like the similar bodies obtained by analogous means from A. Napellus and A . ferox , to contain a higher percentage of carbon than the crystallizable base, and to possess a lower molecular weight ; on saponification with caustic potash, they yielded benzoic acid to nearly the same extent as the crystallizable base, whence it is probable that the two bodies are closely related. The second batch of roots examined was worked up by Messrs. Hopkin and Williams in precisely the same way as the first, about a hundredweight of roots being employed. From the rough alkaloids extracted by ether, etc., and sent to the reporter for examination, about 60 per cent, was isolated as crystallizable base, and 40 as non-crys¬ talline alkaloid. These two quantities of crystallizable base were purified by recrystallization, conversion into crystallized salts {the nitrate and hydrobromide being selected!, and re¬ generation by soda and ether. By fractional crystallization of the different portions, attempts were made to separate the crystals into two or more portions differing from one another. No success whatever attended these efforts ; in every case absolutely identical analytical numbers were yielded by the several fractions ; the melting point and general properties also were invariably the same, whence it results that only one alkaloid can be supposed to be present. The numbers obtained agreed closely with those re¬ quired for the formula, C66H88N2On, and with no other. On heating the base with strong tartaric acid solution to 100° for several hours no change whatever was brought about in its composition (aconitine and pseudaconitine become dehydrated to apo-derivatives by this treatment). From this circumstance it appears likely that the crys¬ tallized base was already as far dehydrated as possible, either by the effect of the tartaric acid in the alcohol used for extraction or by the heat alone. Accordingly, a third batch of roots was worked up, alcohol not acidulated at all being employed ; one hundredweight of roots was thus treated by Messrs. Hopkin and Williams, and the con¬ densed percolate sent to the reporter, who examined it (in conjunction with Mr. A. E. Menlce) as before, i.e., by treating with water, filtering, adding alkali and ether, etc. The crystallizable alkaloid obtained from this batch amounted to about 50 grams or OTO per cent., the non¬ crystalline bases dissolved by ether being about 55 grams =0T1 per cent. No difference whatever could be de¬ tected between the crystallized base thus obtained and the former samples, showing that if dehydration took place at all during extraction, it was brought about by the heat alone conjoined with the natural acids of the roots (the alcoholic extract was distinctly acid to test- paper). It is noticeable that the spent marc obtained in this process was percolated again by alcohol acidulated with sulphuric acid (about 30 grains of concentrated acid per gallon). This percolate, after condensation, was found to contain only between 2 and 3 grams of alka¬ loidal matter, of which half was non-crystalline, the other half crystallizable and identical with that above described; so that treatment with alcohol alone unacidulated by any acid at all, extracted practically all the alkaloids 'present in the roots examined. On examining the action of benzoic anhydride on the crystallized alkaloid thus obtained, it was found to be different from that occurring with aconitine and pseud¬ aconitine, inasmuch as three additional benzoyl radicals were thus introduced into the alkaloid per C33 present instead of one only. On treating the crystallized alka¬ loid with alcoholic potash, saponification ensued, benzoic acid being produced, and a new base very closely resem¬ bling aconine being formed. The following equations represent the actions of the benzoic anhydride and caustic potash : — CG6H88N2021 + 3 (C7HsO)0 = 2 c7hgo2 + (C26h89no7) (0.u7h50)4 ^66^88-^2^21 + 3HoO — 2C7H602 + 2C26H40InO10 These results may be conveniently represented, in har¬ mony with the formulae arrived at in the previous re¬ searches on aconitine and pseudaconitine, by supposing that the roots originally contain an alkaloid C33H47N012 differing from aconitine by containing H4 more ; and that this hypothetical parent base loses 14 molecules of water, producing the crystallized base above described, thus : — Hypothetical Parent Base. /o.c7h5o. - O.H. '7 8 -O.H. \O.H. Crystallized Base above described. o.c7h5o. ^C26H:isN07^ (c26H39N07)_q) (' o I C£6H39NO; \ — o. 7 -o.c7h5 0. Product of the Action of Caustic Potash. \ /O.H. c26h39no71=o. -8 7 \O.H. Product of Action of Benzoic Anhydride. )/o.c7h5o. — 0.C7H50. - O fl»H.O. o.c7h5o. \o.c7h5o. Aconitine. v /o.c7h5o. c20h35no7 ) :g;g; / \O.H. Apoaconitine. \/0.C7H50. C26H35N07 -O.H. \\o. Apoaconine. * / \/OH. Ic26h35no7)=o. V / \OH. Dibenzoyl apoaconine. , \ /0.07H50. 1 JCoCH35N07) = 0. V / \o.c7h5o. ( 170 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 30, 1*79. As above stated, attempts to isolate this hypothetical parent base in an unaltered state did not succeed; to avoid confusion it is proposed, for the present at any rate, to designate the crystallized base, C66H88N2021, above described, as jap aconitine, and the product of the action of potash upon it as japaconine. It is noticeable that the same tetrabenzoylated derivative is obtained when benzoic anhydride acts on japaconine as is formed with japaconitine itself. Japaconitine and japaconine respectively resemble aconitine and aconine so closely that, saving by actual combustion or studying the effects of benzoic anhydride upon them, it is practically impossible to distinguish the one from the other. Japaconitine melts at 184° to 186° when purified as far as possible, the purest aconitine tested side by side melting at 183°-184°. In physio¬ logical action the two are very closely allied, if not identical, so far as the involuntary observations made whilst working with them go. Dr. Eraser, of Edinburgh, is now investigating the two bases and their derivatives in these respects. Inasmuch as Japanese aconite roots appear to be con¬ siderably richer in crystallizable base than A. napellus roots, it is evident that this class of roots is likely to be in future a valuable source of active alkaloid ; further, it is evident from the above experiments that in working out the active constituents of roots of the kind, it is not necessary to acidulate the alcohol used, whereby chance of alteration during extraction is diminished. On contrasting the results above described with those obtained two years ago (‘ Year-Book of Pharmacy,’ 1877, 469) by Paul and Kingzett, it is open to some doubt as to whether the body obtained by those gentlemen was actually japaconitine ; their analytical numbers are quite compatible with their body being either japaconitine or pseudaconitine. On the one hand, they failed to obtain any crystallized salts from their alkaloid, whilst jap¬ aconitine yields a well crystallized nitrate, hydrobromide and hydrochloride with ease, pseudaconitine only yielding a crystallized nitrate by employing a particular mode of manipulation unknown at the time Paul and Kingzett’s experiments were made ; this would seem to indicate, as suggested at the time by the reporter, that the base ex¬ amined by them was simply pseudaconitine. On the other hand, Paul and Kingzett found that their base showed much greater tendency to crystallize than pseud¬ aconitine, and on boiling with dilute sulphuric acid it furnished a liquid capable of reducing Fehling’s solution. Whilst japaconine, like aconine, reduces Eehling’s solution pseudaconine does not do so ; whence these circumstances would tend to indicate that the base isolated by Paul and Kingzett was actually japaconitine ; a conclusion also in harmony with the fact that only japaconitine and no other crystallizable alkaloid of any kind was obtained from each of three different batches of roots examined by the re¬ porter. § 2. — Alkaloids of Atis Hoots [A. heterophyllum). Through the kindness of Mr. E. M. Holmes, the re¬ porter was enabled to examine the alkaloidal constituents of some 2 pounds of these roots. By percolating the coarsely powdered dry roots with alcohol containing a little tartaric acid, and evaporating the percolate, a con¬ densed liquid was obtained containing scarcely any resin; by adding water, filtering, and shaking with ether after rendering alkaline, a small quantity of an alkaloid was extracted. This agreed very well with the description given by Broughton of Atisine ; it was uncry stallizable but yielded a crystalline readily soluble hydrodichloride ; its taste was intensely bitter without the slightest tendency to produce the tingling characteristic of the active aconite alkaloids. The quantity obtained was not quite so much as a gram (less than 0"1 per cent.), where¬ fore its purification was impossible, and still more was it impracticable to find out if it was a mixture of alkaloids. The following numbers were obtained on analysis of the gold salt, which formed a yellow flocculent precipitate almost insoluble in cold water. The substance examined was dried by standing several days over sulphuric acid ; at 100° it fused, losing in weight and becoming apparently partially decomposed. 0-3710 gram gave 0*5175 C02 and 0T70 H20. 0"4565 gram burnt with soda lime gave 0-00882 nitrogen by titration, 0"070 Pt. by platinum salt. 0-3970 gram gave 0T140 Au. These numbers are close to those required for the' for¬ mula, C22H31N02, HC1, AuC13. Calculated. Found. Carbon . 38"82 38‘04 Hydrogen .... 4*71 5"09 Nitrogen .... 2"06 P93, 2T7 Gold . 28-82 28-72 Broughton deduced from his analysis of his platinum salt the formula, C46H74N205, which requires, carbon = 39"09, hydrogen = 5 "38, nitrogen = 1 ‘98, gold = 27"76, as¬ suming the gold salt to be C46H74N205, 2HC1, 2AuC13. It cannot, however, be concluded with certainty from the above experiments that his formula requires modification owing to the minute quantity examined. A priori the formula, C22H31N02, seems somewhat more probable than his di-nitrogenous one. The alkaline fluid from which ether had extracted this base still contained a small quantity of alkaloid permanently dissolved ; on slightly acidulating with acetic acid and addition of potassium mercuriodide, a dirty yellow precipitate was thrown down. After washing and drying over sulphuric acid — 0"432 gram gave 0*321, Ag I, iodine = 40T6. The formula, C22H31N02, HI, Hgl2, would require 41 ’19, whence it is very probable that the base dissolved by the soda was mainly the same as that dissolved out by the ether. § 3. — Alkaloids of the Flowers, Leaves and Stalk of Aconite. In order to examine the nature of the alkaloids present in the aconite herbs (distinct from the roots), it was found to be necessary to wait until the present spring for fresh material. Messrs. Wright, Layman and Umney obligingly undertook to prepare the raw material, and ultimately succeeded in obtaining 300 pounds of fresh aconite herb grown at Eoxton, Cambridgeshire. This was crushed under granite millstones, and the pulpy mass digested with 30 gallons altogether of methylated spirit of about 90 per cent, alcohol at the ordinary temperature for seven days, no acid of any kind being added ; as much of the tincture as could be removed by draining was so recovered, and the marc pressed in cocoa fibre bags ultimately with a pressure of 1 ton to the square inch. The total tincture was then filtered and distilled in four portions, so- as to expose to heat for as short a time as possible ; the residues were not completely freed from alcohol by heat for the same reason ; they were united and exposed to the air in shallow pans for a night to facilitate removal of some of the remaining alcohol, and then sent to the reporter as a brown aqueous fluid smelling somewhat agreeably, not unlike treacle, the total quantity being about 59 pounds. This material was thus worked up by adding soda and repeatedly shaking with ether, the ethereal solution bein^ shaken with tartaric acid, and then used over again. From the acid tartrates thus formed, there was obtained by shaking with soda and ether an ethereal solution which did not crystallize on quick evaporation in a watch glass. These operations having only been performed within the last few days, and the reporter being on the point of leaving town, it is impossible to report to the Conference, at this meeting, what is the nature of the alkaloids present. Judging from the comparative absence of inconvenience experienced in working out the crude alkaloid, the amount of active bases present is not large ; the ethereal solution finally obtained is being August so, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 171 abandoned to spontaneous evaporation in the hope that crystallizable bases will separate. _ The author of the paper was not present, and it was read by Professor Attfield. The President observed that Dr. Wright had given this subject very great attention, and had, in this last paper, arrived at much more definite conclusions. Mr. J. Williams (London) said the most important point in Dr. Wright’s investigation appeared to be the fact that he had now proved that it was no longer necessary to use acid in the preparation of aconitine, and it was proved pretty clearly that the use of acid was to be avoided. This was not known a year ago and therefore he thought the investigation was of great practical value. He had taken practical advantage already in a working sense of this discovery, and finding that it was really true that acid was not required, he might say that they as pharmacists had been benefited by an amount of know¬ ledge they had not previously possessed. With regard to the recent aconite plant he thought it was a very inter¬ esting portion of the research, and he was surprised that no more distinct result had been obtained. He thought it went to prove that the process of separating the alka¬ loid to be adopted would have to be rather different to get a satisfactory result. The process of merely shaking up with ether and carbonate of soda would fail in extracting the alkaloid out of such a large bulk. The quantity of recent plant used he should have thought must have contained a large amount of alkaloid, although not so much as in the root. The plant was of a highly poisonous character, for their knowledge of the poisonous nature of aconite was not derived from the root, but the plant itself. It would have been satisfactory if Dr. Wright had been able to isolate and show them the alkaloid of the plant, and he trusted further investigation would enable him to do so. Mr. Umney (London) said the great thing that had mili¬ tated against Dr. Wright in his observations on the aconite plant was time. Dr. Wright had only had the extract three weeks, and he hoped they might hear something further from him on the matter. He was glad to find the deductions he had obtained from his chemical experiments confirmed what they knew, that Japanese aconite was of excellent quality. In London large quantities had been put in the market and used almost exclusively in phar¬ macy, and there could be no question that it was a more powerful drug than that grown in Germany and England. Mr. Greenish (London) was anxious to know what kind of aconite Dr. Wright had used, for the broad term “ Japanese aconite” was not very definite. It was well known that in Japan there were at least three species of aconite. He had examined many samples of Japanese aconite, and had found at least two kinds continually mixed together, one root had a round, turnip shape, as described by Hanbury in ‘Science Papers,’ and the other root was more tapering. They were evidently to his mind distinct roots. It must leave Dr. Wright’s experi¬ ments in an uncertain condition until he made them from one species of aconite. These two roots mixed together in the Japanese aconite differed in character when sections were made from them. He had submitted one to Professor Fluckiger, who was of opinion that Japanese aconite was not from the same species as that which was imported from Germany, the produce of Aconitum Napellus. In course of time it might be ascer¬ tained from what aconites these roots were produced, and it was desirable that experiments should be made on the different roots, of which there were certainly two kinds, separately. Schroff had made experiments on aconite leaves, and had arrived at the conclusion that they con¬ tained but a very small portion of the alkaloid, even if they contained any. Prof ss or Attfield said the remarks made by Mr. Greenish were valuable, and members would like to know if he could suggest any method by which the experiments could be made on one species, and not on two or three different kinds. Unless some remedy were found he feared they must take Dr. Wright’s work as it was. Mr. Umney (London) said he could not state what was the particular aconite plant from which the Japanese aconite roots that had been used, had been derived, whether Aconitum Napellus, Aconitum ferox or Aconitum paniculatum, but he believed that Mr. Holmes was at the present time engaged in investigating the botanical source. Mr. Luff said that he had worked at the roots with Dr. Wright, and was able to state positively they only got one alkaloid from the Japanese roots, and the same alkaloid from the two batches. Mr. Greenish was of opinion that there would be little trouble in separating the aconites, and did not think they could arrive at a satisfactory conclusion, until they knew what species were used. If the species were separated, and the alkaloid were extracted from each species, he thought the investigators would arrive at something more definite. The President, in moving a vote of thanks to Dr. Wright for his paper and able report, said he was glad to hear that the grant was not entirely expended, and consequently they might expect further communications from him on the subject. The next paper read was the following : — Proximate Analysis of the Rhizome (Dried and Decorticated) of Zingiber Officinalis, and Com¬ parative Examination of Typical Specimens of Commercial Gingers. BY J. C. THRESH, F.C.S., Pharmaceutical Chemist. Part I. — Proximate Analysis of Rhizome of Z. Officinalis , The sample of ginger selected for analysis was a variety of what is known in commerce as Jamaica ginger. The decorticated irregular lobes were from 1 to 2 inches long, pale yellow brown externally, and yielded a decidedly brown powder ; fracture slightly resinous. Preliminary experiments lead me to the conclusion that it would be best to treat the powder with the following solvents, in the order given; — ether, water, rectified spirit, 1 percent, soda solution, 1 per cent, hydrochloric acid. As the constituents soluble in ether were known to be those most worthy of investigation, I got Mr. Umney to exhaust 28 pounds of the ginger with ether, to distil off the solvent, and forward me the extract and the marc. This extract was of a deep red-brown colour, semi-fluid consistency, and had the strong characteristic odour and pungent taste of ginger. It dissolved readily and com¬ pletely in ether, alcohol, chloroform and benzol, required a rather large proportion of 84 per cent, alcohol for complete solution, was imperfectly soluble in glacial acetic acid, and but slightly soluble in petroleum ether. A part of the ethereal extract was agitated first with water, then with successive portions of petroleum ether, until the solvent came off nearly colourless. After being treated a great number of times with this ether, the residue continues to impart to it both a slight colour and pungency, hence it was not deemed advisable to continue the treatment more than three or four times. The solution was of a deep red colour and very pungent. Upon allowing the petroleum ether to evaporate spontaneously, a quantity of deep red, apparently crystalline, fatty matter was de¬ posited. This was removed by filtration, washed with a little petroleum ether, and pressed between folds of bibulous paper. Let this be called^ “ crystalline fatty matter.” The fluid which had passed through the filter was ex¬ posed to a current of warm air until the last trace of the petroleum ether* was removed, then placed in a flask and * The petroleum ether employed boiled at 50° C. 172 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 80, 1879. a current of steam passed through it, and condensed so long as any volatile oil came over. The residue in retort consisted of a transparent red fat, about the consistence of lard. Call this “red fatty matter.” The residue of ethereal extract, insoluble in petroleum ether was of semi-fluid consistency, of a red-brown colour, with a scarcely perceptible odour, but intensely pungent taste. It dissolved readily in absolute and 84 per cent, alcohol, but when treated with 50 per cent, alcohol a residue was left which after washing with several successive quantities of alcohol of this strength, finally yielded nothing further to the solvent. This substance was of resinous consistency, nearly black in colour, and quite tasteless. “ Neutral resin.” The dilute spiritous solution when evaporated left a soft transparent red-brown residue, which although I soon found evidence of its compound nature, has proved most troublesome to resolve into its proximate constituents. It dissolved readily in benzol, bisulphide of carbon, glacial acetic acid, dilute alcohol and alkaline solutions. Its alcoholic solution precipitated most copiously with neutral and basic lead acetates, milk of lime and baryta water. In each case the precipitate first thrown down by the reagent differed in colour from the portions preci¬ pitated afterwards. In the former case the precipitate was a pale orange brown, in the latter orange yellow, and the supernatant fluid after addition of excess of the pre¬ cipitate was exceedingly pungent, and much paler in ■colour than the original solution. A quantity of the tincture was shaken with successive portions of slacked lime so long as anything was carried down, and the lime precipitate removed by filtration. After repeated wash¬ ings with spirit it still retained some pungency, and when treated with hot spirit, what was previously a soft sticky flocculent precipitate fused into a semi-transparent mass which adhered tenaciously to the sides of the flask. This was digested in alcohol and sufficient sulphuric acid added to completely decompose it, excess of acid removed with baryta, the solution filtered and evaporated to dryness. The residue was a dark brown-black, brittle solid, pos¬ sessed of a slightly pungent taste, but no odour. “ Acid resins.” The 50 per cent, alcohol solution from which the resins had been removed by lime when acidified with sulphuric acid gave an abundant precipitate of sulphate of lime, indicating the presence of a lime salt in the solution. This fluid was carefully freed from excess of sulphuric acid, filtered and evaporated to dryness. The residue was semi-fluid, transparent, pale red, and intensely pun¬ gent. “ Active principle.” There remains now to examine further — 1. Crystalline fatty matter. 2. Red fatty matter. 3. Volatile oil. 4. Neutral resin. 5. Resinous acids. 6. Active principle. 1. Crystalline Fatty Matter. — This had a slightly pun¬ gent taste, which, however, was easily removed by treatment with 84 per cent, alcohol, which when cold did not appear otherwise to affect the residue. Boiled with spirit, and filtered hot, the filtrate deposited voluminous flakes of t brownish colour. The portion insoluble in 84 per cent, alcohol was a soft red fat, which has resisted all efforts to resolve it into simple constituents, and hence may be regarded as a proximate constituent of the ginger rhi¬ zome. a. Soft Red Fat. — Properties, transparent, dark red, tasteless and odourless. Soluble in alcohol, petroleum ether, ether, benzol, carbon disulphide, and turpentine. Very slightly soluble in 84 per cent, alcohol, and forming with solution of potash an imperfect soapy solution. Not further examined. The brownish flocculent matter deposited by the spirit upon cooling, when collected and placed on a water-bath, shrivelled up to an exceedingly small residue, of a pale brown colour and waxy consistency. I at first regarded this as a kind of wax, but when pui'ified by being a great number of times dissolved in hot alcohol, and re-de¬ posited on cooling, a very small quantity of a snow white amorphous substance remained. b. White Amorphous Substance. — White, amorphous, pulverulent, odourless and tasteless. Heated on the mer¬ curial bath to 250° C., it did not fuse, but began to exhibit a slight brown coloration. At a higher tempera¬ ture it becomes darker in colour, melts and evolves in¬ flammable vapours which burn with a luminous smokeless flame, emitting no characteristic odour. It is insoluble in water, acid or alkaline solutions. Its behaviour with other solvents is somewhat peculiar. Cold ether dis¬ solves it very sparingly, but in boiling ether it is more soluble, depositing the excess as the fluid cools in a granular form. Benzol and carbon disulphide dissolve it rather more freely and the solutions when left to evaporate spontaneously, become covered with a trans¬ parent gelatinous film, which increases in thickness as the evaporation continues, until at length the residue is wholly of this consistence and the vessel may be upturned without losing any of the contents. If the evaporation be now continued on the water-bath, the bulky mass dwindles away, leaving a very slight residue. From boiling absolute alcohol it is deposited in granular waxy looking masses upon the side of the containing vessel. From boiling rectified spirit, if saturated, it is deposited in the gelatinous or bulky form, the whole becoming semi-solid, and resembling in appearance a strong solu¬ tion of an aluminium salt to which ammonia has been added. Boiling glacial acetic acid takes up a small portion, and deposits it upon cooling or dilution in the gelatinous condition. c. Resin 5. The wax-like appearance of the crude sub¬ stance “5” is due to the presence of a hard brittle fusible resin, which I have not isolated in the pure state. It appears to be but slightly soluble in alcohol, but soluble in petroleum ether, benzol, carbon disulphide and turpen¬ tine. It is tasteless and odourless. 2. Red fatty matter. This portion of the ethereal ex¬ tract was very pungent, but when treated with successive portions of 50 per cent, alcohol, the pungent principle passed into the alcohol, together with other substances which upon further examination proved to be identical with those contained in the alcoholic solution of the ethereal extract, which had been treated with petroleum ether. Besides these (gingerol, resins a and (3) there was the red fat already described, and traces of resin, and of the white amorphous substance. 3. Volatile Oil. — This is the only constituent of the ginger root hitherto examined, and the statements con¬ cerning it are somewhat conflicting. Gmelin says that its colour is yellowish, Neumann that it is red, and Morin affirms that it is greenish-blue. Paponselc ( Wien. akad. Ber. 9, 315), who submitted the oil to chemical examina¬ tion, obtaining the formula C10H16.H2O, states that it has a strong odour of ginger, and a burning aromatic taste, Bucholz on the contrary asserting that its taste is “rather mild at first but somewhat bitter and biting after.” Time has only allowed me to note the following physical and other properties of the oil obtained in the manner pre¬ viously described. It is a limpid, straw coloured fluid, with a peculiar aro¬ matic odour by no means recalling that of the rhizome from which it was prepared, and of an aromatic and some¬ what camphoraceous taste. Sp. gr. ’853 at 15° C. (Hanbury andFliickiger in ‘Pharmacographia,’ '878, Paponselc '893) It is neutral in reaction, forms no compound with sodium bisulphite, and is very soluble in absolute alcohol, benzol, petroleum ether, ether and bisulphide of carbon. One part of the oil dissolves in 25 of alcohol (sp. gr. *815), in 50 parts of alcohol (sp. gr. '834) but requires about 600 to 700 parts of alcohol of sp. gr. '920. These approximations were obtained by adding with agitation alcohol of the above strengths, to 1 c.c. of the volatile August 30 1379.J THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 173 oil contained in a flask, until a clear solution resulted. Dropped upon dry powdered iodine, instantaneous reaction takes place, accompanied by evolution of heat and effer¬ vescence. A few drops digested with a fragment of sodium produced a slight effervescence which continued for several days, the ultimate product being much darker in colour, and very viscid. The strange difference between the odour of the oil as it exists in the ginger and as obtained by distil¬ lation accounts for the statement made by Mr. Draper at the last Conference, that “an essence prepared from oil of ginger did not give the same results as that obtained from ginger itself.” A sample of this oil, obtained from a London firm who import it from Germany, is identical in colour, odour and taste with that prepared by myself, but its specific gravity is '907. A sample of oil obtained from an ethereal extract which had lost a great portion of its volatile oil from too long exposure to steam heat in the retort had a slightly darker colour and a specific gravity of *874. Hence it appears most probable that the oil of ginger really contains two or more volatile oils differing in specific gravity, boiling point, etc. 4. Neutral resin. — This is the most abundant constitu¬ ent of the ethereal extract, and, after treatment with 50 per cent, alcohol, remains as an odourless and tasteless brittle but somewhat soft resin, slowly taking the form of the vessel in which it is kept. Its colour by reflected light is nearly black, but by transmitted light, if viewed in thin layers, it appears transparent and of a dark red- brown colour. It dissolves readily in absolute alcohol, ether, benzol, carbon disulphide and turpentine. In rectified spirit it dissolves slowly but somewhat freely, but is almost totally unaffected by proof spirit and petro¬ leum ether. Glacial acetic acid dissolves it, but it is only slightly acted upon by solutions of potash, soda or ammo¬ nia. The alcoholic solution is neutral to test paper. 5. Acid resins. — This portion of the original extract evidently contained, as before stated, at least two resins, besides traces of the active principle, and possibly also of an oxidation product of the essential oil. When treated with benzol or carbon disulphide it separated into two portions, the one taken up by the solvent, the other unaf¬ fected by it. This residue after being treated repeatedly with benzol and carbon disulphide until nothing further | was dissolved I have called resin a. Resin a. — As above obtained is a dark brown rather soft solid, breaking with a short resinous fracture, readily soluble in dilute alcohol, ether and chloroform, but almost entirely insoluble in benzol, carbon disulphide and tur¬ pentine. Glacial acetic acid dissolves it freely, as also does solution of potash, the fluid becoming of a dark brown colour. The alcoholic tincture gives a pale brown precipitate with both acetate and subacetate of lead. Does not dissolve in liquor ammonise, and is precipitated from its solution in potass by addition of ammonium chlo¬ ride. The alcoholic solution is neutral to test paper. Boiled with absolute alcohol and so die carbonate the solution becomes of a dark brown colour, and sodium is readily detected in it. Hydrochloric acid does not affect the resin ; sulphuric acid forms with it a brown solution which is decolorized by addition of potassium bichrom¬ ate ; nitric acid gives a brown solution which evolves nitrous fumes and becomes orange red. The benzol solution of No. 5 was very pungent in taste, and when the benzol had been removed by evapo¬ ration and the semi-fluid residue dissolved in rectified spirit, addition of basic lead acetate gave a copious pre¬ cipitate; but when the precipitant was added very gradually it was noted that the colour of the precipitate varied from an orange-brown to an orange-yellow. By fractional precipitation, decomposition of the orange- yellow lead salt, resolution of the resulting resin in alcohol, and re -precipitation (partial) by subacetate of lead, a compound of lead and resin was obtained, from which the resin was finally extracted. Resin (3. — In external appearance, consistency, etc., it closely ressmbles resin a; like it also it is readily soluble in dilute alcohol, ether, chloroform, glacial acetic acid and solution of potash; but it differs from resin a in being soluble in benzol, bisulphide of carbon and turpen¬ tine, and in giving an orange precipitate with subacetate of lead and a deep orange solution with liquor potassm. It does not dissolve in ammonia, is tasteless and odourless, and in alcoholic solution has a barely perceptible acid reaction. Dissolved in absolute alcohol and boiled with sodium carbonate, the solution assumes an orange-red colour and contains sodium. By action of hydrochloric, nitric and sulphuric acids it can scarcely be distinguished from resin a. The alcoholic solution from which the resins a and /3 had been removed by lime yielded upon evaporation, etc. , as before stated, a reddish, thick, oily -looking substance, which was intensely pungent in taste. This was dissolved in as small a quantity as possible of 50 per cent, alcohol, and shaken with a little lime, whereby more of the resins a and (3 were removed. When neutralized with sulphuric acid, filtered and evaporated, the residue was found to be much paler than before, but when dissolved in liquor potassae it still gave a rich orange coloured solution. It undoubtedly contained traces of resin (3, to remove which is an exceedingly difficult matter. It can, however, be accomplished by boiling the impure substance (which I have called gingerol) in petroleum ether and rapidly de¬ canting. The ether as it cools deposits the gingerol in oily drops. By treating the crude substance several times with the same ether, collecting the still slightly impure principle, and subjecting it to a repetition of the above treatment, the pure or very approximately pure gingerol is obtained. Only the portions first taken up by the petroleum ether are employed (as by repetitions of the treatment the whole of the impure substance can be dissolved); hence the product of pure gingerol is small. Gingerol. — This, which is the pungent or active prin¬ ciple of ginger, is a viscid fluid of about the consistency of treacle, of a pale straw colour, entirely devoid of odour and of an extremely pungent and slightly bitter taste. It is very soluble in alcohol (even when diluted to 50 per cent.), benzol, volatile oils, carbon bisulphide, solutions of potash and ammonia and glacial acetic acid. It is very slightly soluble in petroleum ether. The alco¬ holic solution is neutral in reaction and gives no precipi¬ tate with the acetates of lead nor with lime. It does not yield glucose when treated with dilute sulphuric acid; strong sulphuric acid dissolves it with production of a brown colour ; hydrochloric acid does not affect it ; nitric acid converts it into a blood red resinous substance. The specific gravity of a slightly impure specimen was 1*09 at 15° C. Aqueous Solution of Ethereal Extract. — Upon evapora¬ tion this deposited a considerable amount of soft resinous matter; was acid in reaction and pungent in taste. It contained considerable traces of an alkaloid, malic acid and other substances, found in aqueous extract of the rhizome. A second lot of ethereal extract was treated in a some¬ what different manner. The whole was placed in a flask and the essential oil carried off by a current of steam. The residue was then treated first with petroleum ether and afterwards with proof spirit. What remained was completely soluble in benzol, but upon addition of a little petroleum ether the fluid separated into two distinct layers. The lower and darker coloured was removed and more benzol and petroleum ether added to it and the lower layer again removed. This residue was now found to consist almost entirely of resin a, and after treatment with successive portions of benzol to remove traces of gingerol and resin /3, pure resin a remained. The benzol and petroleum ether solution when shaken with slightly diluted alcohol (about 75 per cent.) yielded up nearly all the gingerol, together with a part of the resins. Upon repeating this treatment the active principle contained still less of the resins and was further purified by treat- 174 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August SO, 1U9 ment with petroleum ether as before described. The gingerol and resin a thus obtained are identical with those obtained by treatment with lime, decomposition of lime salt by acid, etc. Resin /3 can only be obtained by evaporating off the benzol and petroleum ether from solu¬ tion which has been treated with spirit, dissolving residue in dilute alcohol, fractional precipitation with lime, etc. Aqueous Extract of Ginger. — The ginger, or rather a portion of the ginger, which had been exhausted writh ether, was macerated for a couple of days in sufficient cold water to cover it, then transferred to a percolator, and water passed through until the marc was exhausted. The first portion of the percolate had an acid reaction, was limpid, and of a pale brown colour. It was carefully evaporated upon the water-bath to a small bulk, a pellicle constantly forming upon the surface, which readily dis¬ solved when the fluid was stirred. This solution gave with ammonia a copious crystalline precipitate, which when removed by filtration proved to be almost pure ammonio-magnesium phosphate. Both mineral and or¬ ganic acids gave a flocculent, very voluminous flesh- coloured precipitate which only re-dissolved in large excess of mineral acid. Both acetates of lead gave bulky precipitates, as also did admixture with alcohol. The concentrated solution was mixed with 3 volumes of 85 per cent, alcohol, and after standing some time the pre¬ cipitate was removed by filtration, and washed with a little alcohol. When now diffused in warm water, only part dissolved, a beautifully white crystalline powder re¬ maining behind. This was separated and washed, and proved to be almost pure phosphate of magnesia, but contained traces of manganese, potassium, ii'on, calcium and oxalic acid. The aqueous solution derived from the alcoholic precipitate, when mixed with a little acetic acid, gave a voluminous precipitate, and the filtrate when mixed with alcohol gave a further precipitate (mucilage or gum). From the filtrate the alcohol was removed at a gentle heat, and to the solution acetate of lead was added. This gave a brownish coloured precipitate, a part of which dissolved in boiling water, and was redeposited in an indefinitely crystalline form upon cooling. The fawn- coloured crystalline mass was diffused through water and decomposed by sulphuretted hydrogen. The resulting acid when neutralized gave no precipitate with calcium chloride until alcohol was added, and was apparently malic acid associated with a little impurity. The lead salt when ignited left a residue of lead oxide somewhat under the normal amount. The portion of lead precipitate not dissolved by boiling water yielded but little to acetic acid, and the residue was phosphate of lead together with a little oxalate and brown humus-like matter. The aqueous infusion which had been treated with neutral lead acetate was rendered slightly alkaline by ammonia and excess of basic lead acetate added ; the precipitate which fell was not further examined. The excess of lead was removed from the liquid by H2S, and the excess of H2S got rid of by warming the solution whilst exposed to a current of air. When rendered alkaline tannin pro¬ duced a most abundant precipitate, and phosphomolybdate of ammonia, Nessler’s reagent, and iodine gave indications of the presence of an alkaloid, but not in sufficient amount to warrant an attempt at its isolation. The tannin precipitate was collected, washed, dried, rubbed with lead oxide and rectified spirit, and digested at a gentle heat for several hours. The resulting solution when evaporated left a residue, which I will call “In¬ different substance precipitated by tannin.” The original infusion did not reduce Fehling’s solution. Acidified with acetic acid and filtered CaCl2 gave a precipitate which readily dissolved in hydrochloric acid. Evaporated to a small bulk, traces of Ca and Mg removed, then acidified with hydrochloric acid and perchloride of platinum added, abundant evidence of the presence of potassium was obtained. Tnese reactions together with the acid character of the infusion lead me to infer that the binoxalate of potash is a normal constituent of ginger rhizome. The substance precipitated by acids, mucilage, and indifferent principle precipitated by tannin were submitted to such further examination as my limited time allowed. Substance Precipitated by Acids. — This substance, when obtained, together with mucilage, by precipitating an infu¬ sion of ginger with alcohol, easily dissolves in pure water ; when obtained by addition of an acid it is not so readily soluble. Solutions of potash, soda, and ammonia dissolve it, and when an acid is added it is reprecipitated. When washed with a little water, and dried, the residue is transparent, reddish, very brittle, and readily reduced to a red-brown powder. It dissolves in strong hydrochloric, nitric, and sulphuric acids, the hydrochloric solution after some time acquiring a purplish yellow tint; the nitric solution is bright yellow ; the sulphuric solution is similar in colour to that in hydrochloric acid. In each case dilution with water causes precipitation of the original substance. When burnt upon a platinum dish it swells up considerably, leaving a voluminous char, which burns away with difficulty, leaving a little slightly coloured ash, which appeared to be chiefly Mg32P04. '4200 gram yielded '0105 ash or 2'5 per cent. A little of the dried substance when fused with sodium in a test-tube and the resulting mass treated successively with solution of oxidized ferrous sulphate and hydro¬ chloric acid, gave a copious precipitate of Prussian blue. '651 gram when burnt with soda lime yielded T35 gram of double chloride of platinum and ammonium, corre¬ sponding to 1'3 per cent, of nitrogen. (This substance is probably a mixture of albuminoid and arabinoid bodies.) Mucilage. — This is precipitated by alcohol, after the nitrogenous substance has been removed by addition of acetic acid and filtration. When dried it is an amorphous gum-like mass. As precipitated from a strong aqueous infusion of the ginger it contained 25 per cent, of mineral salts (chiefly Mg3P2Os and KH0204) ; as obtained from a more dilute solution it yielded 13 per cent, of ash. It is soluble in water, forming a slightly mucilaginous solution, which is not affected by solution of borax, precipitates slightly with neutral lead acetates, ferric chloride, and mercuric chloride (probably only oxalate and phosphates), and solidifies (in concentrated solution) upon addition of basic lead acetate. After boiling some time with dilute sulphuric acid the product reduces Fehling’s solution. No blue colour is exhibited when moistened with iodine and sulphuric acid. Indifferent Substance precipitated by Tannin. — The matter precipitated by tannin was left as a pale brown amorphous residue upon evaporation of the tincture obtained by digesting the tannic precipitate with carbonate of lead. It did not reduce Fehling’s solution after treat¬ ment with dilute acid. Its aqueous solution gave indica¬ tions of the presence of an alkaloid with the phosphomolybic, meta tungstic, iodine, and Nessler’s reagents, but it was evident that this existed in it only in minute proportion. From its aqueous solution tannin only precipitated it after addition of an alkali. Alcoholic Extract. — A portion of the powdered ginger which had been treated with ether and water was next percolated with 84 per cent, alcohol. The percolate was of a very pale red colour and when evaporated left an exceedingly small residue of a resinous character. It was insoluble in water or dilute acids, soluble in alkaline solutions, absolute and diluted alcohol. Did not affect Fehling’s solution after treatment with acid. Not further examined. The marc insoluble in ether, water and alcohol was digested in 1 per cent, soda solution for several days. The infusion was mucilaginous ; it filtered with very great difficulty, the filtrate being opalescent. Neutralized with acid, only a very slight turbidity was produced, but upon addition of 3 volumes of 95 per cent, alcohol, a very voluminous, white, flocculent precipitate fell, which rapidly cohered into lumps, leaving the supernatant fluid perfectly clear. August 30, 1679.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 175 Metardbin. — The substance, as above isolated, appeared to be an insoluble variety of gum, it was free from colour, and when dried left a brittle, slightly coloured residue. It contained a barely detectable trace of nitrogenous matter, and left upon ignition 5 per cent, of ash. It dissolved readily in alkalies, but very slightly, if at all, in strong hydrochloric acid. The alkaline solution (together with the marc) was diluted, boiled (to dissolve and remove the starch), and the insoluble residue washed by subsidence and decantation, boiled and digested with a 1 per cent, hydrochloric acid. The infusion when filtered and neutralized became slightly turbid, and upon admixture of alcohol a flocculent precipitate was formed. This, which appeared to be pararabin or a closely allied body, yielded upon incineration nearly 20 per cent of ash, chiefly calcium oxide (but possibly also a little phosphate), derived from the calcium oxalate contained in the rhizome. The quantitative analysis of the rhizome, the result of which will be found tabulated with those obtained upon examination of typical samples of commercial ginger, and given at end of part 2 of this paper, was made in a similar manner to that detailed in part 2, but not upon same quantities of ginger. The percentage of ethereal extract and of its constituents is calculated from amounts yielded by 28 pounds of powder, and the other con¬ stituents from 10 grams only. The total oxalates de¬ rived from analysis of a hydrochloric infusion, by pre- cipitation with calcium chloride after addition of excess of an alkaline acetate correspond to T52 per cent, of oxalic- acid. The phosphoric acid, as determined in solution from which the oxalate had been removed, equalled 'T per cent. Appended is a tabulated statement of the action of the various solvents, etc., upon the constituents of the ethereal extract : — Name. Alcohol. Petro¬ leum Ether. cs2. Benzol. Essential Oil. KHO solution. Glacial Acetic Acid. Physical Properties. Volatile Oil. . . Soluble Soluble Soluble Soluble Soluble Insoluble Soluble Straw coloured, limpid, not pungent in taste. Amorph. Substance Soluble* Soluble* Soluble* Soluble* Soluble* Insoluble Soluble* White, amor¬ phous. Red fat ... . Soluble* Soluble Soluble Soluble Soluble Forming a soapy solution Insoluble Deep red trans¬ parent fat. Resin 8 ... . Soluble Soluble — — — — — — Neutral Resin . . Solublef Insoluble Insoluble Soluble Soluble Insoluble Soluble Black, pitch like resin. a Resin .... Soluble Insoluble Insoluble Insoluble Insoluble Soluble (deep brown) Soluble Odourless and tasteless, soft but brittle resin. /3 Resin .... Soluble Soluble* Soluble Soluble Soluble Soluble (orange red) Soluble Odourless and tasteless, soft but brittle resin. Gingerol . . . . Soluble Soluble* Soluble Soluble Soluble Soluble Soluble Straw coloured, viscid, odour¬ less fluid ; taste extreme¬ ly pungent. * Slightly soluble. f Insoluble in proof spirit. {To be continued.) THE BRITISH ASSOCIATION FOR THE ADVANCEMENT OF SCIENCE. • The President’s Address. {Concluded from page 160.) We have seen how little mere form has to do with the essential properties of protoplasm. This may shape itself into cells, and the cells may combine into organs in ever-increasing complexity, and protoplasm force may be thus intensified, and, by the mechanism of organiza¬ tion, turned to the best possible account ; but we must still go back to protoplasm as a naked formless plasma if we would find — freed from all non-essential complica¬ tions — the agent to which has been assigned the duty of building up structure and of transforming the energy of lifeless matter into that of living. To suppose, however, that all protoplasm is identical where no difference cognizable by any means at our dis¬ posal can be detected would be an error. Of two particles of protoplasm, between which we may defy all the power of the microscope, all the resources of the laboratory, to detect a difference, one can develop only to a jelly-fish, the other only to a man, and one conclusion alone is here possible — that deep within them there must be a fundamental difference which thus determines their inevitable destiny, but of which we know nothing, and can assert nothing beyond the statement that it must depend on their hidden molecular constitution. In the molecular condition of protoplasm there is probably as much complexity as in the disposition of organs in the most highly differentiated organisms ; and between two masses of protoplasm indistinguishable from one another there may be as much molecular difference as there is between the form and arrangement of organs in the most widely separated animals or plants. Herein lies the many-sidedness of protoplasm ; herein lies its significance as the basis of all morphological expression, as the agent of all physiological work, while in all this there must be an adaptiveness to purpose as great as any claimed for the most complicated organism. From the facts which have been now brought to your notice there is but one legitimate conclusion — that life is a property of protoplasm. In this assertion there is nothing that need startle us. The essential phenomena 176 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August so, 1879. of living beings are not so widely separated from the phe¬ nomena of lifeless matter as to render it impossible to recognize an analogy between them : for even irritability, ■the one grand character of all living beings, is not more difficult to be conceived of as a property of matter than the physical phenomena of radial energy. It is quite true that between lifeless and living matter there is a vast difference, a difference greater far than any which can be found between the most diverse mani¬ festations of lifeless matter. Though the refined synthe¬ sis of modern chemistry may have succeeded in forming a few principles which until lately had been deemed the proper product of vitality, the fact still remains that no one has ever yet built up one particle of living matter out of lifeless elements — that every living creature, from the simplest dweller on the confines of organization up to the highest and most complex organism, has its origin in pre-existent living matter — that the protoplasm of to-day is but the continuation of the protoplasm of other ages, handed down to us through periods of indefinable and in¬ determinable time. Yet with all this, vast as the differences may be, there is nothing which precludes a comparison of the properties of living matter with those of lifeless. When, however, we say that life is a property of pro¬ toplasm, we assert as much as we are justified in doing. Here, we stand upon the boundary between life in its proper conception, as a group of phenomena having irrita¬ bility as their common bond, and that other and higher group of phenomena which we designate as consciousness or thought, and which, however intimately connected with those of life, are yet essentially distinct from them. When the heart of a recently killed frog is separated from its body and touched with the point of a needle, it begins to beat under the excitation of the stimulus, and we believe ourselves justified in referring the contraction of the cardiac fibres to the irritability of their protoplasm as its proper cause. We see in it a remarkable pheno¬ menon, but one nevertheless in which we can see un¬ mistakable analogies with phenomena purely physical. There is no greater difficulty in conceiving of contractility as a property of protoplasm than there is in conceiving of attraction as a property of the magnet. When a thought passes through the mind, it is associ¬ ated, as we have now abundant reason for believing, with some change in the protoplasm of the cerebral cells. Are we, therefore, justified in regarding thought as a property of the protoplasm of these cells in the sense in which we regard muscular contraction as a property of the proto¬ plasm of muscle? or is it really a property i*esiding in something far different, but which may yet need for its manifestation the activity of cerebral protoplasm ? If we could see any analogy between thought and any one of the admitted phenomena of matter, we should be bound to accept the first of these conclusions as the simplest, and as affording a hypothesis most in accordance with the comprehensiveness of natural laws ; but between thought and the physical phenomena of matter there is not only no analogy, but there is no conceivable analogy ; and the obvious and continuous path which we have hitherto followed up in our reasonings from the phenomena of lifeless matter through those of living matter here comes suddenly to an end. The chasm between unconscious life and thought is deep and impassable, and no transitional phenomena can be found by which as by a bridge we may span it over; for even from irritability, to which on a superficial view, consciousness may seem related, it is as absolutely distinct as it is from any of the ordinary phenomena of matter. It has been argued that because physiological activity must be a property of every living cell, psychical activity must be equally so, and the language of the metaphysician has been carried into biology, and the “cell soul” spoken of as a conception inseparable from that of life. That psychical phenomena, however, characterized as "they essentially are by consciousness, are not necessarily coextensive with those of life there cannot be a doubt. How far back in the scale of life consciousness may exist we have as yet no means of determining, nor is it necessary for our argument that we should. Certain it is that many things, to all appearance the result of volition, are capable of being explained as absolutely unconscious acts; and when the swimming swarm-spore of an alga avoids collision, and by a reversal of the stroke of its cilia backs from an obstacle lying in its course, there is almost certainly in all this nothing but a purely unconscious act. It is but a case in which we find expressed the great law of the adaptation of living beings to the conditions which surround them. The irritability of the protoplasm of the ciliated spore responding to an external stimulus sets in motion a mechanism derived by inheritance from its ancestors, and whose parts are correlated to a common end — the preservation of the individual. But even admitting that every living cell were a con¬ scious and thinking being, are we therefore justified in asserting that its consciousness, like its irritability, is a property of the matter of which it is composed? The sole argument on which this view is made to rest is that from analogy. It is argued that because the life phenomena, which are invariably found in the cell, must be regarded as a property of the cell, the phenomena of consciousness by which they are accompanied must be also so regarded. The weak point in the argument is the absence of all analogy between the things compared, and as the conclusion rests solely on the argument from analogy, the two must fall to the ground together. In a lecture to which I once had the pleasure of listen¬ ing — a lecture characterized no less by lucid exposition than by the fascinating form in which its facts were pre¬ sented to the hearers, Professor Huxley argues that no difference, however great, between the phenomena of living matter and those of the lifeless elements of which this matter is composed should militate against our attributing to protoplasm the phenomena of life as pro¬ perties essentially inherent in it ; since we know that the result of a chemical combination of physical elements may exhibit physical properties totally different from those of the elements combined ; the physical phenomena presented by water, for example, having no resemblance to those of its combining elements, oxygen and hydrogen. I believe that Professor Huxley intended to apply this argument only to the phenomena of life in the stricter sense of the word. As such it is conclusive. But if it be pushed further and extended to the phenomena of con¬ sciousness it loses all its force. The analogy, perfectly valid in the former case, here fails. The properties of the chemical compound are, like those of its components, still physical properties. They come within the wide category of the universally accepted properties of matter, while those of consciousness belong to a category absolutely distinct — one which presents not a trace of a connection with any of those which physicists have agreed in assign¬ ing to matter as its proper characteristics. The argument thus breaks down, for its force depends on analogy alone, and here all analogy vanishes. That consciousness is never manifested except in the presence of cerebral matter or of something like it, there cannot be a question ; but this is a very different thing from its being a property of such matter in the sense in which polarity is a property of the magnet, or irritability of protoplasm. The generation of the rays which lie invisible beyond the violet in the spectrum of the sun cannot be regarded as a property of the medium which by changing their refrangibility can alone render them apparent. I know that there is a special charm in those broad generalizations which would refer many very different phenomena to a common source. But in this very charm there is undoubtedly a danger, and we must be all the more careful lest it should exert an influence in arresting the progress of truth, just as at an earlier period tradi¬ tional beliefs exerted an authority from which the mind August 30, 1879.) THE pharmaceutical journal and transactions. 177 I I t r ; but slowly and with difficulty succeeded in emancipating itself. But have we, it may be asked, made in all this one step forward towards an explanation of the phenomena of con¬ sciousness or the discovery of its source ? Assuredly not. The power of conceiving of a substance different from that of matter is still beyond the limits of human intelli¬ gence, and the physical or objective conditions which are the concomitants of thought are the only ones of which it is possible to know anything, and the only ones whose study is of value. We are not, however, on that account forced to the con¬ clusion that there is nothing in the universe but matter and force. The simplest physical law absolutely incon¬ ceivable by the highest of the brutes, and no one would be justified in assuming that man had already attained the limit of his power. Whatever may be that mysterious bond which connects organization with psychical endow¬ ments, the one grand fact — a fact of inestimable import¬ ance — stands out clear and freed from all obscurity and doubt, that from the first dawn of intelligence there is with every advance in organization a corresponding advance in mind. Mind as well as body is thus travelling onwards through higher and still higher phases ; the great law of Evolution is shaping the destiny of our race ; and though now we may at most but indicate some weak point in the generalization which would refer consciousness as well as life to a common material source, who can say that in the far off future there may not yet be evolved other and higher faculties from which light may stream in upon the darkness, and reveal to man the great mystery of Thought ? - - Meetings of the Sections. The various Sections commenced their meetings on Thursday morning, the 22nd inst., when the proceedings were opened by addresses from their respective presidents as follows : — Section A. — Mathematical and Physical Science. — Pre¬ sident : G. Johnstone Stoney, M.A., F.R.S. Section B. — Chemical Science. — President: James Dewar, M.A., F.R.S. L. & E. Section C. — Geology.— President : P. Martin Duncan, M.B., F.R.S., F.G.S. Section D .—Biology. — President (Department of Zoo¬ logy and Botany) : St. George Mivart, F.R.S., F.L.S., F.Z.S. Vice-President (Department of Anthropology) : E. B. Tylor, D.O.L., F.R.S. Vice-President (Depart¬ ment of Anatomy and Physiology) : Dr. Pye Smith. This Department did not meet until Friday. Section E. — Geography. — President : Clements R. Mark¬ ham, C.B., F.R.S., F.L.S. Section F .—Economic Science and Statistics. — President (in the absence of Mr. G. Shaw Lefevre, owing to the death of his father) : Mr. Mundella, M.P. Section G. — Mechanical Science. — President : J. Robin¬ son, Pres. Inst. Mech. Eng. Soiries, Lectures, etc. On Thursday Evening a Soiree was given by the Mas¬ ter Cutler in the Cutlers’ Hall, and on Tuesday the 26th a Soiree was given by the Local Committee in this same building. On Friday Evening, the 22nd, Mr. William Crookes delivered a lecture on “ Radiant Matter,” ' to a large audience assembled in the Albert Hall. This lecture it is intended to print in an early number of this Journal. Another lecture was delivered in the Albert H,all on Monday evening, the 25th, the lecturer being Pi'ofessor E. Ray Lankester and his subject “Degeneration.” On Saturday, the 23rd, the lecture to the operative classes was delivered by Professor Ayrton, on “Electricity as a Motive Power.” Next Place of Meeting. At a meeting of the General Committee on Monday; for the election of Officers, Professor A. C. Ramsay, LL.D.j F. R.S., was chosen President of the Association for the meeting next year in Swansea. It was also finally decided to accept the invitation of the municipality of York to meet in that city in 1881. At the concluding meeting on Wednesday it was an¬ nounced that the total attendance had been 1404, against 2578 last year at Dublin, 1217 in 1878 at Plymouth, and 2652 in 1877 at Glasgow'. o The following is a list of the papers read in the Chemi¬ cal Section : — Report of Committee on the Chemistry of some of the lesser known Alkaloids. Read by W. Chandler Roberts, F.R.S. On some relations between the numbers expressing the Atomic Weights of the Elements. By Walter Weldon,, F.R.S.E. On the Synthesis of Diphenyl Propyl. By M. R. D. Silva. Recent Researches in Explosive Agents. By F. A* Abel, F.R.S. On Vapour Densities. By Professor Dewar, F.R.S. To Describe a large Crystal of Mercury Sulphate. By P. Braham. On the Manufacture of Crucible Steel. By Henry S. Bell, F.C.S. On the Separation of Iron and Phosphorus especially with reference to the Manufacture of Steel. By Thomas Blair. A new Process in Metallurgy. By John Hollway. A Lecture Experiment in Illustration of the Hollway Process of Smelting Sulphide Ores. By A. H. Allen, F.C.S On Lead Fume with a description of a New Process of Fume Condensing. By Andrew French. On the constitution of Aluminic Compounds. By Pro¬ fessor Odling, F.R.S. On the presence of Nitrogen in Steel. By A. H. Alien* Colour tests for Phosphorus and Sulphur in Iron and Steel. By A. Vernon Harcourt, F.R.S. To exhibit some experiments with Hughes’ Voltaic Induction Balance. By W. Chandler Roberts, F.R.S. Historical Sketch of the various Vapour Density Methods. By J. T. Brown. Note on certain Vapour Densities. By Professor Wanklyn. Note on Isocyan-propionic Acid. By Professor Wanklyn. Physical Constants of Liquid Acetylene and Hydro¬ chloric Acid. By G. Andsell. The Action of Ammoniacal Salts on Metallic Sulphides By M. De Clermont. On the Chemical Composition of a nodule of Ozokerite found at Kinghorn-ness. By W. Ivison Macadam. On some curious Concretion Balls derived from a Colliery Mineral Water. By Thomas Andrews. On some points in connection with Agricultural Che¬ mistry. By Dr. Gilbert, F.R.S. On the rare Metals of the Yttrium Group. By T. S. Humpidge, B.Sc. On the Synthesis of Hydrocyanic Acid. By Professor Dewar, F.R.S. On the amount of Nitrous Acid produced in Electric Illumination. By Professor Dewar, F.R.S. On the Kinoline Bases. By Professor Dewar, F.R.S. An account of some recent Experiments on Super¬ saturated Solutions. By John M. Thomson. Notes of some recent Spectral Observation. By J.. Norman Lockyer, F.R.S. Notes on Petroleum Spirit or Benzoline. By A. H. Allen* On the illuminative value of a mixture of Hydrogen. By A. Vernon Harcourt, F.R.S. On a new form of Condenser. By G. T. Hazelhurst. Notes on a sample of Fullers Earth found in an old Fullonica recently excavated at Pompeii. By W. Thom¬ son, F.R.S.E. On the detection of Milk Adulteration. By W. H* Watson. 178 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 30, 1879 Chemical researches on the Palmella cruenta. By Dr. Phipson. Description of a glass burette for collecting, mea¬ suring, and discharging gas over mercury. By Philip Braham. Ipartiamentarg and lam |roqtedtn()s. PROSECUTIONS UNDER THE PHARMACY ACT, IRELAND. In the Northern Division of the Dublin Police Courts, before Mr. J. W. O’Donnell, the chief magistrate, two summonses have been heard, brought under the Pharmacy Act, Ireland, by the Pharmaceutical Society of Ireland. The first case gone into was one against Messrs. George P. Beater and James North Hardy, trading under the name of Beater and Co., as druggists, of 17, Lower Sackville Street, the allegation being that they, “not being persons registered as a pharmaceutical chemist or chemist and druggist under the Pharmacy Act of 1875, did compound a certain prescription and sell same at Lower Sackville Street, in the Police District of Dub¬ lin Metropolis, on the 10th of July, 1879, between the hours of 10 and 11 o’clock, a,m., contrary to the form of the satute in such case made and provided.” Mr. Purcell, Q.C., instructed by Messrs. Ennis and Son, appeared on behalf of the Pharmaceutical Society of Ireland for the prosecution. Mr. Gerald Byrne ap¬ peared for the defendants. Mr. Purcell said the Society were proceeding under the 30th section of the 57th chapter of the Pharmacy Act of 1875. That statute enacted that the Society should be a body corporate, and the 30 th section was : “ So much of the Act of 1791 as prohibits the keeping of open shops within the meaning of the said Act by any person other than a licentiate of Apothecaries’ Hall shall be repealed ; provided always, that it shall be unlawful for any pei-son to sell or keep open shop for retailing, dispensing, or com¬ pounding poisons within the meaning of the Act of the session of the thirty-third and thirty-fourth years of the reign of Her present Majesty, chapter twenty-six, or medical prescriptions, unless such person is registered as a phar¬ maceutical chemist or a chemist and druggist under this Act, or to assume or use the title of pharmaceutical chemist, or pharmaceutist, or pharmacist, or dispensing chemist, or the title of chemist and druggist in any part of Ireland, unless such person shall be registered as a pharmaceutical chemist or as a chemist and druggist respectively under this Act ; and any person acting in contravention of this enactment, or compounding any medicines of the British Pharmacopoeia, except according to the formularies of the said pharmacopoeia, shall for every such offence be liable to pay a penalty of five pounds ; but no such penalty shall exempt any person from being liable to any other penalty, damage, or punishment to which he would have been subject if this Act had not passed.” On the 10th of July last, Messrs. Beater and Hardy, who carry on business as (chemists and) druggists in Lower Sackville Street, compounded a medical prescription and sold it to the party who pre¬ sented it, and he (counsel) held a receipt given by the defendants for compounding. He did not think that the facts were disputed, but if they were the Society had their witnesses ready who would prove the offence alleged. Mr. O’Donnell : What is the particular offence with which the defendants are here charged ? Mr. Ennis, solicitor: Selling and compounding medi¬ cines. Mr. O’Donnell : Then it is for the sale and compound¬ ing of medicines, and not of poisons ? Mr. Purcell : Yes. On the 10th of July a medical prescription, which we have here, was presented at the establishment of Messrs. Beater and Hardy, who are not registered pharmaceutical chemists under the Act of Parliament, and in the presence of our witnesses it was made up. But I believe they do not dispute the facts. Mr. Byrne, solicitor : I appear for Messrs. Beater and Hardy, and they admit that a breach of the law was committed in their establishment, but it was committed by one of the employes and not by themselves. Under the circumstances I hope the Society will not press the case. Mr. Purcell : If they express regret that it occurred and promise that there shall be no repetition of it in future we will not press for the full penalty. It is not the object of the Society to do so Under such circum- stances - Mr. O’Donnell : I am sure of that. Mr. Purcell : But we are bound to vindicate the law. Mr. O’Donnell : It is a very salutary Act. Mistakes occur every day in London in consequence of prescrip¬ tions being compounded by persons who are not properly qualified to do so, but, I am happy to say, there have been very few here. Mr. Byrne : My clients will take every measure to prevent a similar occurrence in future, and as far as Messrs. Beater and Hardy are personally concerned they knew nothing of it. Mr. Purcell : That is no justification. Mr. O’Donnell: They would be both personally and pecuniarily responsible for any neglect that might occur in their establishment. Mr. Purcell: On the undertaking of Messrs, Beater and Hardy that there will not be any repetition - Mr. O’Donnell : I will impose a nominal penalty of ten shillings. Mr. Purcell : I think that will do. And five guineas costs, your worship. Mr. O’Donnell : This is the first case of the kind that has been heard, and it settles the law on the subject. Should a similar case be again brought the penalty in¬ flicted will be very serious. Mr. Purcell: That is the object of the Society. Mr. O’Donnell: Of course, as a public body they act on public grounds and they will not prosecute in a mere squabble between different establishments. When they find anyone violating the law they should chasser him at once. The defendants are now fined 10s., but if any person, with that conviction in his face, commits a similar offence he will be severely dealt with. An order was made for the payment of 10s. and five guineas costs. The second summons, which was brought against Mr. Joseph Brownrigg, of Talbot Street, trading as Brown- rigg and Co., and was in respect of a similar offence alleged to have been committed by him on the 10th of July, was then heard. Mr. Brownrigg, when the case was called, denied that the prescription had been compounded in his establish¬ ment, and asserted that' he had sent it out to Messrs. Hamilton, Long and Co., where it was compounded. Mr. Purcell : We will prove the facts. Mr. Robert Cowan, 23, Geraldine Street, was examined by Mr. Purcell, and deposed : On the 10th of July I took this prescription (produced) into the establishment of the defendant. I was standing by all the time while it was being made up by Mr. Brownrigg himself. By himself ? — I saw him. Did you see the stamp put on it ? — I did. Was it done by him in your presence ? — It was. Who wrote the directions ? — He himself. Is that the box of pills that you got with the bottle ?— It is. And who wrote the directions ? — Mr. Brownrigg himself. I ask a conviction in this case for the full amount. Mr. Cowan, cross-examined by the defendant, who conducted his own case, stated : When I first went in you August 30, 1ST9.] THE pharmaceutical journal and transactions. 179 said it would require an hour to make up the prescrip¬ tion, and I went away for that time. On my return I stayed in the shop half an hour. Did you see me send out ? — No. I was looking at you all the time, and I saw' you making it up. To Mr. O’Donnell. — When I came back to the shop the defendant said he had not made up the prescription, and then he wrent and did it. He had not!.*- g done when I came back, and he made it up before my face. Mr. Brownrigg : I have a witness to prove that I sent to Hamilton, Long and Co.’s, and it was compounded there. I put on the labels myself. Mr. Cowan : I saw Mr. Brownrigg filling the bottle from the bottles on the shelves in the shop. Mr. Purcell: Not only is the label, as the witness swears, written in the handwriting of the defendant, but he actually has the audacity to have on it that he is a member of the Pharmaceutical Society — “Joseph Brown- rigg, M.P.S.’:' Mr. Cowan : I sawr him put his name to it. Mr. Purcell (to witness) : Did you go a second time to his shop ? — I did, on the 16th of July. Mr. O’Donnell : I will not take that as evidence. (To the witness.) Take the bottle in your hands. Did you see him write that on it ? — I did. Coidd any other person have written on the bottle ? — No. There was a young man sitting on a chair, but Mr. Brownrigg w'rote the label himself and put the wrapper on the bottle, and made up the prescription himself. Mr. Purcell : Look at the stamp on the prescription. Do you see Brownrigg and Company on it ? I do. The defendant W'rote on it in my presence. The letters “ M.P.S.” are after his name. That is “ Member of the Pharmaceutical Society ” of chemists and druggists and so forth, Talbot Street, Dublin, and he admits that he is not a member. Witness, in reply to Mr. Purcell : The receipt produced is the one that Mr. Brownrigg wrote. Cross-examined by Mr. Brownrigg : When I returned at the end of the hour you said the medicine was not ready, and that its preparation wrould take half an hour, but from the time you began to make it you were not twenty-five minutes. I saw you fill the bottle from bottles on your shelves. Mr. Brownngg (to Mr. O’Donnell) : I admit he got it from me, but it was made up elsewhere. Mr. Hugh James Pennell, Registrar of the Pharma¬ ceutical Society of Ireland, was sworn, but before he was examined, Mr. Brownrigg said : I admit I am not a member of the Pharmaceutical Society of Ireland. Mr. Purcell (to witness) : Do you see the letters “M.P.S.”?— I do. That is member of the Pharmaceutical Society ? — That is the usual meaning of the letters. Is it true or false ? — It is not true that Mr. Brownrigg is a member of the Pharmaceutical Society of Ireland. This closed the case for the prosecution. Mr. William Coulson, defendant’s assistant, was exa¬ mined for the defence. He stated, in reply to Mr. ! Brownrigg : I remember the prescription perfectly well . I took it to Hamilton and Long’s. Having some other things to get at the same time, I did not return at once with it. Mr. Cowan was kept near to an hour altogether. Was the bottle corked and labelled when you brought it in ? — It was. You then wrote a label yourself and put it on, taking off the other one. I saw the man (Mr. Cowan) when he came back. Prom where he was in the shop he could not possibly have seen you label the bottle, i He was sitting down. Cross-examined by Mr. Purcell: I am a chemist’s assistant. I do not know the name of the assistant at Hamilton and Long’s who made up the prescription. He would not put his number on it when it was for another chemist. I went out through the hall door of Mr. Brownrigg’s. What was your object? — Not to let the person in the shop know what we were doing. If we let every one see us go out for what we might be short of, people would say, “ It is no good going there for they have nothing.” Did you hear the evidence sworn here to-day ? — I did. And was it false or true ? — It is quite untrue that Mr. Brownrigg compounded the prescription himself. Mr. CVIJonnell : Suppose you brought the prescription to Hamilton and Long’s would they not make an entry of it? — Not when it was for another druggist. Mr. Purcell : Is it your evidence that they assist the druggists of Dublin in violating an Act of Parliament by making up prescriptions for them and letting them sell them? — It is no violation. Mr. Purcell: Well, I think it is. Mr. Coulson : That is the difference of opinion be¬ tween us. — It is made up by a qualified apothecary. Mr. O’Donnell: Are you in the habit of going to Hamilton and Long’s? — When we have prescriptions, but we have very few. Mr. Cowan : From the time I went in till when I came out, he (the witness) was not in the shop at all. Witness : The shop is a divided shop. Mr. O’Donnell (to Mr. Cowan) : You said there was a young man on a chair in the shop? — But this is not the one, nor did I sit down. He has told a falsehood. I stood and looked at Mr. Brownrigg mixing the things. Did any one bring in a bottle and hand it to him ? — No one. Mr. Purcell (to Mr. Coulson) : Have you a receipt from Messrs. Hamilton and Long? — No. Receipts are only given when they are asked for. If you came to my shop I would not give you a receipt unless you asked for one. Mr. Cowan asked for the one he was given. Mr. Purcell : Even if there were a shadow of founda¬ tion for this statement the Act covers it, for it is not only an offence against the 30th section to compound, but it is an offence to sell a medical prescription by a person who is not registered as a pharmaceutical chemist. The summons is not only for compounding, but selling. (To Mr. Coulson) : You brought the prescription to Messrs. Hamilton and Long’s? — Yes. Mr. O’Donnell : How long did that delay ? — From ten or fifteen minutes. Mr. Purcell: What did you pay at Messrs. Hamilton and Long’s? — One shilling. And got no receipt ? — And got no receipt. There is not a day I am not in the habit of going there. They know who I am and give me things at trade prices. Mr. Cowan, examined by Mr. Brownrigg, said: I did not see a glass counter dividing the shop. To Mr. O’Donnell : I was quite close to the defendant all the time he was making up the prescription. Mr. Brownrigg : Was not a little girl in the shop when I was called down first* — Yes, when I entered first. And you said very wrell you are at your breakfast ? — I said no such thing. Mr. Purcell : Then it appears there was only a little girl in the shop. Mr. Brownrigg : This was at nine o’clock in the morning. Cross-examination of Mr. Coulson resumed by Mr. Purcell : This pill box (produced) is not the one we got from Messrs. Hamilton and Long’s, as we could not wash the label off. Is that the bottle you got from Messrs. Hamilton and Long? — I don’t suppose they changed it. You don’t imagine we pay twopence for a bottle when we can get them so much cheaper by the dozen. Mr. O’Donnell (to Mr. Purcell) : You say the section embraces selling and compounding ? Mr. Purcell (reading) : “ Provided always that it shall be unlawful for any person to sell or keep open shop for retailing, dispensing, or compounding poisons .... or medical prescriptions.” To sell or compound medical prescriptions, for that it is so intended is shown by the 180 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [August 30, 1379. use of the disjunctive “ or.” — (To the witness) : Were the pills made up at Messrs. Hamilton and Long’s? — Yes. How much did you pay? — I paid a shilling in all. We charged Mr. Cowan one shilling and sixpence. Mr. O’Donnell (to the defendant) : At all events by the sale that day you made a profit of sixpence. I fine you £5 and £3 10s. costs. Mr. Brow-nrigg contended that the 31st section should be considered conjointly with the 30th, and in support of his argument quoted the following passage from the former, “ Nothing in this Act contained shall extend to or interfere with the making or dealing in patent medi¬ cines, or with the business of wholesale dealers in supply¬ ing poisons in the course of wholesale dealing or of chemists and druggists who are practising as such in Ireland upon their own account at the time of the passing of this Act, save and except the provisions against the compounding of poisons or medical prescriptions, and against the preparing of any medicines of the British Pharmacopoeia, except according to the formularies of the said Pharmacopoeia.” Mr. O’Donnell held that the provisions of the 31st section did not alter the meaning of those of the 30th, and refused to change his ruling. able to keep all the leeches alive for months, even during the hottest weather, when the mortality amongst them is usually very great. Edmund E. Cheery. COURT PLASTER. — Soak isinglass in a little warm water for seventy-four hours, then evaporate nearly all the whaler by gentle heat, dissolve the residue in a little proof spirits of wine, and strain the whole through, a piece of open linen. The strained mass should be a stiff jelly when cool. Now stretch a piece of silk or sarsenet on a wooden frame, and fix it tight with tacks or pack-thread. Melt the jelly and apply it to the silk thinly and evenly, with a badger hair brush. A second1 coating must be applied when the first has dried. When, both are dry, apply over the whole surface two or three coatings of balsam of Peru. Plaster thus made is very pliable and never breaks. INDELIBLE ANILINE INK. — Triturate If grams of aniline-black with 60 drops of strong hydrochloric- acid and 42 or 43 grams strongest alcohol; then add to- it a hot solution of 2 4 grams gum-arabic in 170 grams of water. This ink attacks steel-pens but little. It is not destroyed either by strong mineral acids or by strong lye. If fhe first alcoholic solution of aniline black be diluted giqiqismrj JJtmmpda. In order to assist as much as possible our younger brethren, for ivhose sake partly this column icas established, considerable latitude is allowed, according to promise, in the propounding of supposed difficulties. But the right will be exercised of excluding too trivial questions, or re¬ petitions of those that have been previously discussed in principle. And we xvould suggest that those who meet ivith difficulties should before sending them search previous number's of the Journal to see if they can obtain the re¬ quired information. [338]. Argent. Nitratis . ^ij. Aquae Destill . giij. Liq. Ammon. Port . q s. Ut ft. solutio secund. artem. How should the above be prepared ? Herbert Chambers. [339]. How should the following be dispensed ? — R. Ferri Ammon. Cit . ?jj. Quiniae Disulph . gr. xv. Aquae Fort . jjss. M. ft. Guttae. Five drops three times a day in sugar and water. Minor. and Queries. [624]. COLOUR OF CLOTH.— Will some corre¬ spondent kindly state what acid is generally used for testing the colour of cloth ? Minor. THE PRESERVATION OF- LEECHES.— Complaints are frequently heard of the inability of che¬ mists to keep their leeehes in health for any length of time. I have avoided the advertised leech aquariums and the like, and have for years kept leeches in perfect health by the following simple plan : — I got a 7 lb. ointment jar, made of glazed white earthen¬ ware, and put my leeches into it. Then instead of replacing the top I covered the jar with white muslin, and tied it round tightly. The w-ater was never allowed to go unchanged more than a week, and by these simple means I have been with a solution of grams of shellac (instead of gum- arabic) in 170 grams of water, an ink is produced which may be employed for writing on wood, brass or leather,, and which is remarkable for its deep black colour. (^oiir^sjond^nr^. *** No notice can be taken of anonymous communica¬ tions. Whatever is intended for insertion must be authenti¬ cated by the name and address of the writer; not necessarily for publication, but as a guarantee of good faith. J. C. Talbot. — See the Pharm. Journ. for February 22 last, p. 695, and May 21, p. 988. “ Tonic.” — We think the label would necessitate the use of a stamp, but recommend you to submit it to the revenue authorities who alone can decide the point. T. H. C. (Southsea). — Nostoc commune. By some it is considered an alga, by others a stage in the life-history of a lichen, Collena pulposum. J. H. Dingle. — Festuca gigantea is correct. The other plant is Pyrus torminalis. E. Parrett. — Veratrum nigrum. D. Dickinson. — 1 and 3. Send better specimens. (2) Veronica serpyllifolia. (4) Pmmella vulgaris. Diogeoxes. — Staphylea pinnata (bladder nut ? ). T. D. — Euphorbia Helioscopia. P. Roberts. — 1, 2 and 3 are correctly named. (4) Athy- rium Filix Mas. (5) Betonica officinalis , (6) Mentha arvensis. F. H. Fairweatlier. — (1) Beta maritima. (2) Sinapis nigra. (3) Sinapis arvensis. (4) Crepis virens. (5) Leycesteria formosa : not British. J. B. (who should have sent his name) is recommended to address his question to the editor of a veterinary journal. “Student.” — Potassium ferrocyanide is not a poison and is not included in Schedule A of the Pharmacy Act. “ Pendennis.” — The latest edition of the * Elements of Materia Medica ’ was published in 1872 by Messrs. Long¬ man and Co., and was edited by Professors Bentley and Redwood. This is an abridgment of the original work published by Dr. Pereira. R. Radclyffe. — See an article on Bisulphite of Lime and its use in Brewing, in the Pharm. Journal for March 3, 1877, p. 720. Communications, Letters, etc., have been received from Messrs. Howie, Prollius, Atkin, Moss. Attfield, Claypole, Fox. Pedler, Cocks, A. B., Sanders, Martindale, Benger. September 6, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 18 L NOTES ON CINCHONA BARE. BY DAVID HOWARD. Recent importations of East Indian cinchona bark have thrown light on several points worthy of the notice of those interested in the subject. The officinalis bark from the Government Planta¬ tion at Dodabetta gives us some valuable information as to the effect of age on the value of the bark. The date of the plantation from which each parcel was obtained was given, and we thus have a series of barks, classed as natural, mossed and renewed from trees planted each year from 1863 to 1867. As “ natural ” bark from the lower stems is only obtained from trees not yet treated for “ renewing,” it is evident that in the older plantations the natural bark will be chiefly from the upper stem or from saplings and inferior trees, and thus, as Dr. De Yrij has shown, will be of inferior quality. The result shows this to be the case, the best parcel of natural bark being from the plantation of 1867, that from the other plantations being of uneven quality showing no regular variation. The mossed bark on the other hand may fairly be taken to represent the oldest bark from the main stems in each plantation, and therefore is the best guide as to the influence of age on the quality of the bark. The result is highly satisfactory, showing that as yet the bark from the oldest plantations, so far from deteriorating, continues to improve. Both the quinine and the total crystallizable alkaloid steadily increase from the bark of the 1867 plantation to that of 1864, that of the 1863 plantation yielding the same quinine as that of 1864, and slightly more cinchonidine and quinidine. It is certainly more likely that so regular a pro¬ gression is the result of greater maturity than that the difference should be caused by any variety in the C. officinalis cultivated. This is a most important point, for recent importa¬ tions of the bark of G. succirubra confirm the opinion so often expressed by my uncle, J. E. Howard, F.R.S., and by Mr. Broughton, the late Quinologist to the Indian Government (‘ Quinology of the East Indian Plantations,’ p. 71), that in this species the bark deteriorates beyond a certain age. It is difficult to say exactly what that age may be, and it probably varies according to the growth of the tree, but some of the very finest of the red bark now coming from India, as far as appearance goes, certainly seems to have passed its maximum of rich¬ ness in quinine. As to the “ renewed ” officinalis bark, the time during which the different parcels have been forming is not given, nor is it stated whether it is from the first, second, or later crops, and therefore the com¬ parison may not be accurate ; but it is interesting to see that here also the older plantations show no deterioration, the best being from the 1863 planta¬ tion. From a private plantation I have received a sample of root bark of C. officinalis from trees which were coppiced three years ago. It gives quinine 2-2 per cent., cinchonidine, *2 per cent., quinidine, P5 per cent., and cinchonine, 3*3 per cent. The stem bark from this plantation, at the time when the trees were cut down, gave: quinine, 2-6 per cent., cinchonidine, *6 per cent., cinchonine, 1* per cent., and but a trace of quinidine. We find, therefore, that in this sample the Third Series, No. 480. ordinary tendency of root bark to produce the dextrogyrate alkaloids is developed to a most unusual degree, the percentage of quinidine is a most extra¬ ordinary one for bark from G. officinalis. I have also received from Darjeeling a very in¬ teresting sample of the bark of C. succirubra accidentally renewed. It is entirely the produce of accidental injuries to the trees (not deep enough to injure the cambium, and prevent the bark forming over the whole surface), no protection whatever having been given where the bark was removed. • The result is as successful as could have been expected from renewing under the most favourable conditions, the contained alkaloids being, quinine, 2’3 per cent., cinchonidine, 1*5 per cent , cinchonine, T2 per cent., quinidine, T per cent. Two parcels of the stem bark sent over at the same time from this plantation gave, first, quinine, •8 per cent., cinchonidine, T2 per cent., cinchonine, 1-2 per cent., and secondly, quinine, ’9 per cent., cinchonidine, 1*1 per cent., cinchonine, 2‘0 per cent. The improvement in value in renewed bark is therefore not owing to the covering, but is found equally in this accidentally renewed bark, and it would seem that the mossing is valuable chiefly as enabling the tree to produce the renewed bark with as little injury to its health as possible. It will probably be found that a less perfect shelter than moss may in some circumstances be sufficient to preserve the health of the tree under this process. It has been proposed by M. Moens to shave off the outer layers of bark without cutting quite through the bark. No doubt the cellular portion of the bark is richer in alkaloids than the inner fibrous layer (vide ‘ Quinology of the East Indian Plantations,’ by J. E. Howard, F.R.S., pp. 23, 24 and 38), although the corky excrescences thrown out by the variety of G. officinalis, the u knotty bark ot Jussieu,” contain but little alkaloid (Pharmaceutical Journal, third series, No. 454, p. 769; ‘ Quinology of the East Indian Plantations,’ p. 70). The inner and outer portions of a sample of the bark of G. succirubra gave the following results Quinine. Cinchonidine. Cinchonine. Inner . *6 per cent. T2 per cent. 1*4 per cent. Outer . 1*2 „ 1‘4 „ 1'7 „ It will be noted that not only is the total alkaloid more in the outer bark, but the quinine is in greater proportion, and therefore the outer bark would be of much greater value per pound to a manufacturer than the whole bark. The practical value of the process chiefly depends on the effect on the tree. If when thus treated the tree throws out fresh bark of a similar quality to that produced in the old method of renewing without greater injury to its health, the process may be successful, but of course it is essential not to cut so deeply as to injure the cambium, and thus destroy the recuperative power of the bark. AN IMPROVED METHOD OF MAK'NG PHOSPHORUS PILLS. BY E. F. CHERRY. Many have been the methods proposed for making phosphorus pills ; most of them however, have something in the process to which objection may be made. I believe the following process will be found iree 3 82 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 6, 1879. from all objection?, and it lias been in use now for years without a single instance of failure. For the sake of example let it be supposed that lot) pil. phospliori are to be made, each to contain one-fiftietk of a grain of phosphorus. For this quantity we shall, of course, require 3 grains of phosphorus. This is to be put into a 1 ounce wide- mouth bottle: on it pour ^ ounce of chloroform, close the bottle, and allow it to stand until the phosphorus is completely dissolved. Carbonic di¬ sulphide has been recommended as a good men¬ struum in which to dissolve the phosphorus, but it is open to two objections : 1st. It is unpleasant to use on account of its disgusting odour ; and 2ndly. It is not so volatile as chloroform, which is a disad¬ vantage in the after part of the process. When the process of solution is completed, pour the phospliorized chloroform into a mortar containing 150 grains of pulv. glycyrrhizse. By stirring continu¬ ously for a few minutes, a dry powder is obtained consisting of liquorice combined with the phosphorus in a minute state of subdivision. This forms a good pill-mass by the addition of equal parts of syrup and mucilage of acacia. These pills have been submitted to various eminent medical men, and have been found superior to those made by the B. P. process. In the latter it is often found that the presence of the wax pre¬ vents their solution in the stomach, and consequently their virtue is to a great extent lost. Another recommendation is that the pills made as above are much less trouble to make than the B. P. ones ; the latter process taking a long time to perform, while this new method only occupies a few minutes. A NEW METHOD OF MAKING TINCTURE OF IODINE. 13Y EDMUND F. CHERRY. The ordinary method of making tinct. iodi often entails the dirtying of several measures, and not unfrequently stains on the skin. By the following method this is avoided ; the tincture is made in a cleanly manner and can be allowed to proceed automatically, as it does not require any attention. Suppose 2 pints are going to be made. Into a measure pour about 30 ounces of spirit, then take a funnel and loosely but completely plug the narrow part with cotton wool. On this bed place the pot. iodid. and the iodine. Then introduce this into the measure, taking care that the level of the spirit outside is above that of the solid ingredients in the funnel. It will be found that by a simple process of displacement the spirit will rise in the funnel and gradually dissolve the iodine and iodide of potash. This solution, by reason of its superior specific gravity, will sink to the bottom and fresh spirit will rise to continue the operation. When the solids are completely dissolved, the remainder of the spirit may be added and the tincture is complete without any mess whatever. MQEPHIOMETRIC PROCESSES POE OPIUM.* BY ALBERT B. PRESCOTT, M.D. ( Concluded from page 130.) B. Process A, Modified by the Initiatory Treatment of the Opium with Hot Benzole. — Each portion of the opium was digested, with heat, for one hour, with 35 c.c. of * From the ' Proceedings of the American Pharmaceu¬ tical Association,5 1878. benzole, then washed on a filter with a little benzole, dried, and worked thereafter as directed in the process first given in this paper. The following results were obtained : — Process B. . Percentages. No. 1. No. 2. No. 3. No. 4. Mean. a. Crystallized precipitate of crude morphia* . 10*82 11 80 1P66 10*32 11-15 b. Ether-washed morphia. 10*26 11*18 11-08 9*84 10*59 c. By estimating b with Mayer’s solution . . 7*20 7*60 7*40 6"92 7*28 d. From filtrate, by amyl alcohol and Mayer’s solution . 3*08 2"72 3*60 3’72 3*28 e. Total morphia by Mayer’s solution . . 10-28 10-32 11-00 10*64 10*56 /. Subtracting from ^ At (Jacobsen) .... 9*92 10-81 1071 9*51 10*28 g. Subtracting from a ~ (Hager) ‘ . 974 10‘62 10*49 9*29 10-04 Comparison between Results of A and B. Percentages. Mean of A. Mean of B. a. Crude morphia . 12*42 11*15 b. Ether-washed morphia . 11*55 10*59 c*. By estimating b with Mayer’s solu¬ tion . 8*37 7‘28 d. From filtrate, by amyl alcohol and Mayer’s solution . 2*50 3*28 e. Total morphia by Mayer’s solution . 10*87 10*56 It appears, then, that the use of hot benzole, instead of cold benzole, upon the opium, causes lower gravimetric results and lower results of the sum of the volumetric estimation. Result b is lower with each sample, as well as in the mean, from the use of hot benzole. The ether- washed morphia is purer in process A than in process B ; the former giving of the mean 72 "47 per cent, and the later only 68"84 per cent, of absolute morphia, by Mayer’s volumetric estimation. Finally, the morphia precipita¬ tion is more nearly complete with process A than with process B; the former giving in the precipitate a mean of 77*00 per cent, and the latter a mean of 68*94 per cent, of the total morphia obtained by volumetric estima¬ tion. According to Cleaver ( Pharm . Jour. Trans., 1876, vii., 240), morphia is soluble in 2000 parts of benzole, at ordinary temperatures. The results of process B here seem to show that, when hot, benzole dissolves more morphia. The morphia volumetric yield is 0 0155 gram less after treatment with 35 c.c. hot benzole than after treatment with 50 to 100 c.c. cold benzole. I will not venture to surmise why hot treatment, with benzole should make the precipitate less pure and less complete, but it was found, not only in the mean, as above stated, but in each of the four samples, the hot benzole treatment gave precipitates less pure and less nearly complete. Therefore, it appears inadvisable to use the benzole hot. And, because morphia is not with¬ out waste by cold benzole, the quantity to be used is limited, in the process recommended. C. Hager- Jacobsen's Process, as given by Hager, without Initiatory Treatment of the Opium with Benzole. — (Hager’s ‘ Untersuchungen,’ii., 176.) The materials and directions are essentially the same given in the proposed U. S. Pharmacopoeia process, at the beginning of this paper, except that only eight drops of benzole are taken, and the initiatory treatment with benzole is omitted. The time of formation of the morphia precipitate was limited to three to three and a-half hours. As with processes A and B, the crude morphia was weighed, then ether- washed * The weights of these precipitates were, in grams, for No. 1, 0-541 ; No. 2, 0*590; No. 3, 0*583; No. 4, 0*516. eptember 6, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 183 and again weighed, and comparisons are given with crude morphia, minus tVj and then ether-washed morphia, minus gL. The precipitates were estimated volumetric- ally, and additional precipitates were obtained by twenty- four hours’ standing, and volumetrically estimated, but, I regret to say, the final filtrates were not exhausted with amyl alcohol. Process C. a. Crystallized precipitate of crude morphia . . b. Ether-washed morphia. c. By estimating b with Mayer’s solution . . cl. From additional pre¬ cipitate by Mayer’s solution . e. Total precipitates, by Mayer’s solution . . /. Subtracting from b ^ (Jacobsen) .... g. Subtracting from a -Jg (Hager) . No. 1. Percentages. No 2. No. 3. No. 4. Mean. 9*96 8*82 14*14 12*34 12*80 11*82 10*28 11*79 9*30 10*57 7*80 8*60 8*20 6*60 7*80 0*80 0*24 o*so 0*40 0*56 8*60 8*84 9*00 7*00 8*36 8*53 11*93 11*54 8*99 10*21 8*96 12*72 11*52 9*25 10*61 Here the gravimetric mean result of ether- washed mor¬ phia is lower than in process A, and nearly the same as in process B. The additional precipitates contain, in the mean, 0*56 per cent, against 0*41 per cent, in process A. Of the morphia in the last mother liquor (filtrate) no estimation was made. By the volumetric estimation of the ether- washed precipitate it was, in the mean, 73 ‘7 9 per cent, of morphia, a little purer than by process A (72*47 per cent.), and purer than B (68*84 per cent.). Judged by processes A and B (and D), the precipitation in C was deficient in No. 1, and notably impure in No. 2. Process C makes No. 2 to be 3*52 higher in per cent, than No. 1, A giving the difference 1*20, and B only 0*92 (for ether- washed morphia). The omission of the initiatory treatment with benzole leaves the opium-lime mixture loaded with the opium-wax and renders the filtrations more difficult and the entire operation less satisfactory. Indeed, one might say that the trouble of using the benzole was compensated for simply by the greater neat¬ ness of all the work afterwards. D. Procter's Staples's Process (‘Pro. Am. Pharm. Asso.,’ 1870, p. 130; Am. Jour. Pharm., 1871, p. 65; the first of the three methods tried by Procter). — The plan of the U. S. Pharmacopoeia preparation of morphia modified by the washing of the opium with benzole. The proportion of benzole used was 50 c.c. for the 100 grains of opium, the quantity taken by Procter. The benzole was applied by maceration in a filter and perco¬ lation, as directed for the proposed U. S. Pharmacopoeia process. Following the proportions and directions used by Procter, the following results were obtained : — Process I). Percentages. No. 1. No. 2. No. 3. No. 4. Mean. a. Crystallized precipitate of crude morphia* . 15*52 15*89 15*28 14*00 15*17 b. Ether-washed precipi¬ tate . 14*91 14*87 14*54 13*28 14.40 c. By estimating b with Mayer’s solution . . 11*20 11*11 11*60 10*40 11*08 d. From filtrates, by amyl alcohol and Mayer’s solution . Results not satisfactory. The results with Staples’s process were so evidently incorrect that I give them only as a confession of failure, * No. 1, from 2*5 grams opium, 0*388 crude morphia ; No. 2, 3*24 of opium, 0*517 crude morphia ; No. 3, 2*5 of opium, 0*382 crude morphia; No. 4, 2*5 of opium, 0*350 of crude morphia. the cause of which Mr. Stecher and myself had not time to investigate. In my own hands, and in the hands of those working under my instruction, Staples’s process has usually given results rather lower than Hager- Jacobsen’s. In this case the quantities of the samples were small, as given in the foot-note, but the balance was delicate and the work seemed satisfactory. The crude morphia was beautifully crystallized and of light colour, as is usual from Staples’s process. I can only surmise that the “ether-washed morphia” contained something besides morphia, which can react with Mayer’s solution. The results of working the filtrates were still less satisfactory. The filtrate from No. 1 was exhausted with amyl alcohol, this solution evaporated to dryness, the residue dissolved in sulphuric acidulated water, when it took 7*5 c.c. of Mayer’s solution, indicating 6*00 per oent. of morphia. Then, with Nos. 3 and 4, the amyl alcohol residue was dissolved, as before, in acidulated water, this solution made barely alkaline with ammonia, and a bulky, light-coloured precipitate obtained. Filtered out and dried, the precipitate turned dark, coherent and waxy. Dissolved in acidulated water, the No. 3 solution took 3*5 c.c. of Mayer’s solution (giving 2*80 per cent, morphia), and the No. 4 solution took 4*5 c.c. of Mayer’s solution (indicating 3*60 per cent, morphia). The am- moniacal filtrates from these precipitates, last above named, were washed with benzole, then acidulated and titrated, when that of No. 3 took 3 c.c. of Mayer’s solution (2*4 per cent, morphia), and that of No. 4 took 2*3 c.c. Mayer’s solution (1*84 per cent, morphia). These benzole washings evaporated, and their residue dissolved in acidulated water and titrated, used for No. 3, 1*8 c.c. Mayer’s solution (indicating of narcotina, 1*53 per cent.), and for No. 4, also 1*8 c.c. (same per cent, narcotina given by No. 3). I would advise, in extracting filtrates from Staples’s process with amyl alcohol, first to exhaust them with benzole, as was done for the estimations tabulated below. Narcotina, when free, is sufficiently insoluble in water, but narcotina, partially combined, may dissolve in the water solution of opium to a notable extent. If the crude morphia of process D, a, was loaded with narcotina, the ether washings have been insufficient to remove all nar¬ cotina, and the weights, b, may have represented this impurity. May there be something beside alkaloids which pre¬ cipitates Mayer’s solution, obtained in the amyl alcohol extract from Staples’s filtrates (though not so obtained from filtrates of Hager’s process) ? Dragendorff calls attention to the fact, that an aqueous extract of opium contains substances, aside from known alkaloids, which precipitate Mayer’s solution, whatever those substances may be. Some results of the titration of water solutions of opium, acidulated with sulphuric acid, were found to correspond to 50 and 60 per cent, of morphia (‘ Werth- bestimmung.,’ p. 88). Again, titrating ammoniacal filtrates from opium, Dragendorff reports that when additions showing 19 per cent, and 21 per cent, of morphia had been made, the precipitates were still in¬ complete. Certainly no results so widely out of the way are obtained by titrating the amyl alcohol extract (a method used by Dragendorff himself), but it is desirable to know more positively whether amyl alcohol (always aqueous) takes up anything at all to precipitate Mayer’s solution beside alkaloids. The work recorded in the next paragraph was entered upon before this question had defined itself in our investigation; but, although undertaken as a measure of the morphia left in Hager’s . filtrates and Staples’s filtrates, and not as a test of the accuracy of amyl alcohol extraction, nevertheless it may be said that the results have such reasonable proportions as to do credit to the amyl alcohol extraction by which they were obtained. Comparative Estimation of the Morphia remaining in a Set of the Final Filtrates of Hager's Process ancl of Staples's Process. — The estimation being done by Mayer’s 184 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 6, is:?. solution applied to amyl alcohol extracts, and the extrac¬ tion with amyl alcohol, being preceded with benzole washing in case of the Staples’s filtrates. These filtrates were obtained in a set of assays of tincture of opium, done by Mr. Henry Heim, in parallel operations by Hager’s and Staples’s process.* The work upon the filtrates, done by Mr. Stecher, was as follows : — The filtrates of Staples’s process were first exhausted with two successive portions of benzole ; those of Hager’s process were treated directly with the amyl alcohol, the total alkaloid so obtained being estimated as morphia. In every case the amyl alcohol was used in three portions, successively, of 15 c.c., 10 c.c.. and 5 c.c. — 30c.c. in all — each portion being shaken with the opium filtrate in a tube, the mixture left to separate, and the clear amyl alcohol layer drawn off. The united amyl solutions were evaporated to dryness on a steam-bath, the residue dis¬ solved in sulphuric acidulated water, and this solution titrated with Mayer’s solution. The results were as follows : — From Filtrates Left in Valuation of Opium Tinctures. With Hagf.u’s Process. No. Filtrate. Morphia. Morphia, per c.c. 1 45 c.c. 0*046 gram. 1*02 milligram. 2 50 „ 0*100 „ 2*00 3 33 „ 0*060 „ 1*82 4 40 „ 0*070 „ 1*75 5 38 „ 0 080 „ 2*10 6 40 „ 0 060 „ 1*50 7 40 „ 0*096 „ 2*40 8 35 „ 0*094 „ 2-70 9 35 „ 0*052 „ 1*51 10 40 „ 0*094 „ 2*35 11 — — 12 o 0*090 „ 2*25 With Staples’s Process. No. * Filtrate. Morphia. Morphia per c.c. 1 40 c.c 0*100 gram. 2*50 milligram. 2 40 „ _ 3 • 40 „ 0*110 „ 2-75 4 35 „ 0-062 „ 1*77 5 30 „ 0*090 „ 3*00 6 35 „ 0-096 „ 2-74 7 40 „ 0*108 „ 2-70 8 36 „ 0-072 „ 2*00 9 37 „ 0*080 „ 2*16 10 - 11 — _ _ 12 — — * Valuation of tincture of opium, twelve samples, in parallel assays by Hager’s process and Staples’s process, reported by the writer from works by Henry Heim See. The earlier process of Hager was used, differing from “ Hager- Jacobsen’ s ” in taking only 5 grams of opium (or the residue by evaporating an equivalent quantity of tinc¬ ture), washing the residue into the lime opium solution, and concentrating the latter to about 25 grams before adding the ammonium chloride (and benzole and ether), then leaving twenty-four hours for precipitating the crude morphia. (Dragendorff’s ‘ Werthbestimmung.,’ 91.) For Staples’s process, that given by Procter, ‘ Pro. Am. Phar. Mean morphia per c.c. for 8 Nos., omitting 2, 10, 11, 12; Hager’s, 1*85 milligrams; Staples’s 2*45 milligrams. For the total 436 c.c. of 11 Nos. with Hager’s process, the mean was 193 milligram morphia per c.c. of filtrate. The solubility of morphia in water, and to a greater extent in the mother liquor of morphiometric assays, even when no excess of ammonia is present, has been alluded to in a foot-note under process A. As the filtrate of Staples’s is alcoholic, it ought to dissolve more morphia than the filtrate of Hager’s process. Taking the solu¬ bility of morphia in pure water as 0*001 gram per c.c., it is indicated by this work that Hager’s filtrates dissolve, in the average, 1*9 times more than water does (the extreme being T02 times, and 2*4 times) ; while Staples’s filtrates dissolve, in the average, 2 ’45 times (in extremes, 1*77 times and 3 0 times) more than water dissolves. As having a bearing on the comparison of Hager’s process with Staples’s it may be quoted here that Mr. Heim’s gravimetric results, in valuation of tincture of opium give, as the average with the twelve samples, by Hager’s process, 3*103 grains ether- washed morphia per fluid ounce of tincture; by Staples’s process, 2*84 grains morphia per fluid ounce of tincture. E. Schachtrupp’ s Process for Estimation of Morphia and Narcotina. — ( Zeitschrift fiir Analyt. Chemie, 1868, vii., 509.) A weighed amount of opium (5 grams), is covered in an evaporating dish (porcelain), with a solution of sodium carbonate, heated on the water-bath, and when semi-fluid, evaporated to dryness. The dry mass is transferred to a perfectly dry beaker or flask, covered with benzole, agitated and heated moderately, then de¬ canted on a filter, and the residue treated two or three times with portions of benzole and filtered. [The quan¬ tities of benzole were not stated by Schachtrupp. The solubility of morphia in benzole has been discussed under “ Process B.” It is advised to use, in all, about 40 c.c. for 5 grams opium, but a good deal more was used in our operations.] (The benzole solution is reserved for estima¬ tion of the narcotina). The dried filter with its contents is now added to the residue in the flask or beaker, and the whole warmed to expel the last trace of benzole. Amyl alcohol is now added to the dry residue, in the flask, the mixture stirred and heated to near boiling, and while hot decanted upon a filter, adding successively two more portions of amyl alcohol. [Schachtrupp does not specify how much amyl alcohol to use.] Set the mixed filtrates aside for a few hours. Decant from crystals of crude morphia ; distil the solution to its one-third ; add dilute hydrochloric acid, in the retort, and shake. Re¬ move the amyl alcohol, the upper layer (from the water solution of morphia hydrochlorate, below); wash the decanted amyl alcohol with two or three additional portions of the dilute acid, and pour the united acid water solutions upon the crystals of crude morphia, pre¬ viously separated, to dissolve them. [Schachtrupp does not give strength or qualities of the dilute hydrochloric acid. Mr. Stecher used four portions, and found the last to take up a notable proportion of morphia. Dragen- dorff states that all the morphia can hardly be obtained in this way. It would be better to evaporate the amyl solution to dryness, and then dissolve in acidulated water, as done by Mr. Stecher in extracting mother liquors with amyl alcohol described under process A.] The acidulated water solution of morphia is now evapo¬ rated on the water-bath, to a weight double to that of the opium taken, filtered, the filtrate treated with am¬ monia in slight excess, covered loosely, and set aside for twenty-four hours. The precipitate (at first bulky and afterwards growing crystalline) is collected on a filter, washed several times with distilled water, and dried and weighed. [The gravimetric morphia of this process retains considerable colour.] The reserved benzole solu¬ tion is evaporated to dryness, the residue dissolved in Asso.,’ 1870, 131, was followed, evaporating tincture to one-half, and proceeding as directed, but leaving four days for the crude morphia to precipitate. September 6, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 185 sulphuric acidulated water, and the solution titrated for narcotina, with Mayer’s solution. Each c.c. of the latter precipitates 0 0218 gram narcotina. The following results were obtained by Schachtrupp’s process Process E. Percentages. No. 1. No. 2. No. 3. No. 4. No. 5. Mean. a. Coloured morphia, precipitate . . 7-53 8-82 1146 10-27 9-44 b. By estimating a with Mayer’s solution . . . 4-80 5-60 10-20 10-00 7-00 752 c. Benzole alkaloids, by Mayer’s solu¬ tion, estimated as narcotina . . . 14*91 1044 9 58 9"80 9'04 1045 Eliickiger and Hanbury mention percentages of nar¬ cotina, from l-30 to 10’30. Dragendorff gives results for narcotina, from 8 '8 to 14"7 per cent. (‘Werthbestimmung.,’ 83). As previously mentioned, Mr. Stecher used more benzole than should be used, and considerations of the benzole solubility of morphia make it certain that a notable proportion of morphia was obtained with the narcotina.* No work was done to separate morphia from the other alkaloids dissolved by the benzole, and it can only be declared that the results are untrustworthy, and the process of Schachtrupp an inexpedient one. The trial of process E gives additional evidence that the initiatory treatment of the opium with benzole cannot be used to remove all the narcotina, while leaving all the morphia behind. To dissolve all the narcotina, which is partly held in feeble combination alkali must be added, d as in Schachtrupp’s process, and then the use of another benzole to take out the wax, etc., seriously diminishes the morphia. The office of the benzole is to free the opium of caoutchouc-like matter, colour, etc., and the additional service of making it unnecessary to purify the crude morphia crystals seems to be more than benzole can accomplish. The advantages of preliminary benzole treatment appear from the results of process C, where¬ with they have been named. As to the results by the use of the benzole hot, see process B. It can hardly be said that the benzole treatment is very important ; but as it is otherwise required in the Hager- Jacobsen process, the preliminary use of the agent does increase the number of materials to be taken.J The purification of the crude morphia crystals is best done, I believe, by the ether, non-alcoholic or water- washed. I suggest to put water-washed ether in the list of reagents, unless otherwise included, with direction to wash shortly before use, because any pharmacist can, from any grade in stock, in a few minutes, make a uniform quality of ether, free from those common im¬ purities most objectionable for use as a solvent, alcohol and acetic acid, the latter derived in keeping. With the Hager- Jacobsen process as proposed for the Pharmacopoeia, I regret the unavoidable length of the directions, giving an appearance of complexity, perhaps forbidding to the pharmacist. In the execution of the process there is nothing difficult ; all the operations define themselves sharply and satisfactorily, and there is little more weighing and much less waiting than in other pro¬ cesses. Some features of leading processes may be com¬ pared as follows : — * Benzole dissolves narcotina, codeina, papaverina and narceina (slightly). f Obtaining, by Mayer’s solution, from the benzole extract of a sample of dried opium (not made alkaline), 2 3 per cent, of narcotina, I found from the similar extract of another portion which was made alkaline, 3‘3 per cent, of narcotina. X I hardly need mention that Mr. William Procter re¬ commended the adoption of. the benzole treatment, referring to its use by Fluckiger, and that the modification (of the Staples’ process) very properly bears the cognomen due to Mr. Procter’s important report on morphiometric methods. Process. Hager-Jacobsen’s . Quantity of Filtrate to 1 of Opium. 1 to 10 Time Required. 5 to 6 hours. >» with benzole pre¬ liminary treat¬ ment .... 1 to 10 6 to 8 hours. Staples-Procter’s . 1 to 6 or 7 (alcoholic) 48 „ British Pharma¬ copoeia .... 1 to 2^ 50 „ As to the purity of the morphia weighed, considered with the incompleteness of its extraction, and as to deduct¬ ing a fraction for impurities, I would only add to what is given under “Process A,” a remark of Dragendorff (‘Werthbestimmung.,’ 92), to the effect that, for ordinary purposes, the foreign substances left in the (chloroform- washed) crystals by Hager’s process may be left to balance the loss in mother liquor and washings. The reports made by careful analysts in different parts of the world render it evident that exact morphiometric methods for opium have not been attained, and the obstacles in the way towards exactness appear only the more apparent in the work I have undertaken. Indeed, absolute exactness is rarely if ever reached in human science. We must be patient with imperfection, always measuring our results by the truth beyond them, as nearly as we can, and we must work heartily for the uses of mankind with such approximate measures as we have. University of Michigan. CULTIVATION OF PERFUME PLANTS IN SOUTH AUSTRALIA.* A recent report on the progress and condition of the botanic garden and Government plantations at Adelaide, South Australia, by the Director, Dr. Schomburgk, con¬ tains some interesting remarks on the cultivation of perfume plants in that colony. A bianch of cultivation that promises to become of very great importance in South Australia is the syste¬ matic growth of perfume plants. Of the magnitude of the commercial aspect of the perfumery trade, we are reminded that British India and Europe consume about 150,000 gallons of handkerchief perfume yearly, and the English revenue from eau-de-cologne alone is about £8000 a year; that the total revenue from imported perfumes is estimated at about £40,000, and that one great perfume distillery at Cannes uses yearly about 100,000 lbs. of ■ acacia flowers ( Acacia farnesiana), 140,000 lbs. of rose petals, 32,000 lbs. of jasmine blossoms, 20,000 lbs. of tuberose, besides a great many other fra¬ grant plants. Dr. Schomburgk says: — “Most of the flowers which provide the material for perfumes grow most luxuriantly with us, viz. : mignonette, sweet verbena, jasmine, rose, lavender, Acacia farnesiana, heliotrope, rosemary, peppermint, violets, wallflower, laurel, orange, and the sweet scented geranium. I may say that these plants thrive probably in greater perfection here than in any other part of the world. No doubt South Australia should be a perfume-producing country. We see flourish¬ ing here some of the most valuable scent plants, and even some of our native plants will yield a valuable scent ; but two things are needed to encourage the enterprise. First if the scent is manufactured in South Australia, freedom of the still, so as to license distilling in vessels of less than twenty-five gallons capacity, and, secondly, the bond fide advertisement of a capitalist manufacturer that he will buy any quantify of specified flowers, leaves, roots, or plants, at a marketable price, then some farmers might be tempted to plant a few acres of lavender or mint ; another, geraniums or rosemary; another, jasmine ; whilst plantations in hedgerows, or - otherwise of roses, cassia, together with contributions of 'gardens, would lay the * From the Journal of the Society of Arts , August 22, 1879. 186 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 6, 1879 foundation of an export trade. Then it must also be noted that whatever the value which plants yield in flowers, fruit, leaves, and stems, it is increased threefold under manufacture, and this manufacture again consumes other local produce called into existence by it, such as olive and other oils, fats, alkalies, wheaten flour, colour¬ ing matter, pottery, and glass ware, which combine to make the farmer and the manufacturer contribute largely to the maintenance of the population and the wealth of perfume-producing countries.” Dr. Schomburgk further points out the profits likely to accrue from an extended cultivation of scent-bearing plants, as against the cost of land in England, acres of which in certain localities are under cultivation of peppermint, lavender, and other well- known plants of the same class. The failure of these crops, or more particularly those on the farms of Grasse, Cannes, and Nice, would be a serious disaster to this branch of commerce, the importance of which may be proved from the fact, that a member of a well-known perfumery house in Bond Street has thought it worth his while to visit Australia for the purpose of encouraging this branch of culture. Regarding the manufacture of the perfumes, an opinion is expressed which will no doubt be fully endorsed by practical men at home, that it is un- advisable to prepare them in the colony; this work would of course be much more effectually done in this country ; at the same time, the plants might go through some manipulation or partial preparation, so as to reduce their bulk and consequent cost of freight. The outcome of this endeavour to open a new branch of commerce with Australia will be looked to with much interest. The introduction and extended cultivation of the olive (Olea europea) in Australia is now un fait accompli ; it is nevertheless satisfactory to find that a choice variety — that which produces the famous Lucca oil — has been suc¬ cessfully raised. This new introduction seems due to the energy and liberality of a private gentleman, by whom it is hoped the plants will be freely distributed. VERATRUM VIRIDE— NOTES OF AN EXAMINATION.* BY CHARLES BULLOCK. When the root of Veratrum viride is digested in water acidulated with sulphuric acid at a temperature of 150° E., the mass becomes gelatinous and swells up to an in¬ creased bulk. When expressed and alcohol is added to the expressed liquor, a copious deposit of pectic acid is occasioned. The presence of pectose and the large amount of resin and fatty matter contained in the root makes the use of alcohol necessary for its exhaustion. Fifty-three pounds of Veratrum viride — rhizome with rootlets — from North Carolina, in powder, was exhausted with alcohol, the alcohol distilled off and the resulting extract exposed to a continued moderate heat until all of the alcohol was expelled. During this process the resin separated from the soft extract. It was removed and allowed to drain for several weeks during the warm weather of summer. Weight of the soft extract . 6 lbs. 10| ozs. Weight of the hard resin . 3 lbs. 4 ozs. Total weight of extract from 53 lbs. of root . 9 lbs. 14^ ozs. This extract furnished the material for examination. In separating the alkaloids, advantage was taken of the previously-ascertained fact that all of the alkaloids were imperfectly precipitated from acid solutions by caustic alkalies or alkaline carbonates at ordinary tem¬ peratures, but if the solution is heated to 150° F., the precipitation is almost complete. Trie Soft Extract . — 86 per cent, of this extract is soluble in water. Petroleum fcenzin removes 4 ’3 per * From the American Journal of Pharmacy, July, 1879. cent, of fatty matter. After removal of the alkaloids, the watery solution was treated in the usual manner with subacetate of lead, and after separating the excess of lead and neutralizing the free acid with carbonate of baryta, the filtered solution was evaporated to a syrup and thrown into alcohol. The filtered alcohol solution, evaporated and exposed to a temperature of 212° F. until it ceased to lose weight, gave a product representing 85 ‘5 per cent, of the extract. This product has a transparent red colour, a saccharine taste, with some bitterness, and acts energetically as a reducing agent with salts of copper and silver. In chemical character it appears to be almost entirely glu¬ cose. The amount of alkaloids contained in this extract was determined for the portion soluble in water and for the resin separately. 880 grains of the extract, representing the yield from one pound of root, was exhausted with water, the wash¬ ings were evaporated to reduce the volume and carbonate of soda added to alkaline reaction. After separating the precipitate, the solution was beated to 150° F. and a little caustic soda added. The precipitate occasioned was re¬ moved while the solution was warm. The weight of the first precipitate by carbonate of soda was . . 167 grains. The second, by caustic soda, was . 2‘6 „ Total . . 19-3 „ These alkaloids contained a large amount of colouring matter, from which they were purified by re-solution in acetic acid, filtering and precipitation from a warm solu¬ tion. The precipitate, when dry, weighed 107 grains. All of the mother- waters were made acid and evapora¬ ted, then made alkaline and treated with ether. The ether product was dissolved in acetic acid, filtered and precipitated as before. Weight of product, 17 grain; total weight of mixed alkaloids, 12’4 grains. The jervia was separated by precipitation, as a nitrate, from an acetic solution representing 3 grains in each ■ fluidounce, by addition of an equal volume of a saturated solution of nitrate of potassium. After standing six hours, the nitrate of jervia was collected on a filter and washed with a solution of nitrate of potassium, pressed between folds of bibulous paper and dried. Weight of nitrate of jervia, 7'9 grains. After the separation of the jervia the solution was evaporated, heated to 150° F. and precipitated by soda. Weight of other alkaloids, 3 '2 grains. Resin from the Soft Extract. — To prevent any change which might be caused in saponifying the resin with lime, the following process was adopted with this as also, subsequently, with the hard resin : — The fatty matter was removed by petroleum benzin. The resin, rubbed to a fine powder, was made into a smooth paste with water introduced into a bottle and a solution of carbonate of soda containing a little caustic soda added until the resin was dissolved. It was then agitated with ether and the ether removed. The washing with ether was then repeated. The product left on distillation of the ether was dissolved in acetic acid, filtered and precipitated by carbonate of soda, con¬ taining a little caustic soda. Weight of product, 9 '3 grains. The mother- water was made acid, evaporated, and after being made alkaline, treated with ether. The pro¬ duct, dissolved in acetic acid, filtered and precipitated, gave 07 grain more of alkaloids. Total weight of mixed alkaloids from the resin, 10 grains. The alkaloids separated by nitrate of potassium gave — Nitrate of Jervia . 8- 4 grains. Other Alkaloids . L6 ,, Hard Resin. — 429 grains, representing the yield from one pound of root, was powdered and digested in petro- September 6, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS.' 187 leum benzin. The loss of weight representing fatty- matter, was 847 grains. After removal of the benzin by evaporation, the resin was reduced to a fine powder and treated as in the previous experiment, by dissolving it in an alkaline solution and treating the solution with ether. The weight of mixed alkaloids obtained was 22’5 grains. The mother- water was made acid, evaporated, and, after addition of caustic soda, treated with ether. The pro¬ duct obtained weighed 0‘8 grain. The alkaloids, separa¬ ted in the manner preceding, gave — Nitrate of Jervia . . . . 14*1 grains. Other Alkaloids . 6 ’1 „ The resin from the soft extract and the hard resin were then precipitated from their alkaline solution by hydrochloric acid, and dried. The solution was made neutral with soda and evaporated to dryness. This pro¬ duct was added to the precipitated resin and the whole mixed with an equal weight of lime previously slaked, and the mixture boiled for a few minutes, then evapora¬ ted to dryness by steam heat. The dry mass was powdered and exhausted by hot alcohol. The product left on distillation of the alcohol was dissolved in diluted acetic acid, filtered and precipitated. Weight of mixed alkaloids obtained, 0'9 grain. The alkaloids, separated as before, gave — Nitrate of Jervia . 0’1 grain. Other Alkaloids ...... 0'8 „ The total amount of alkaloids obtained from the ex¬ tract representing one pound of root, was — From Soft Extract .... 12-4 grains. Resin from Soft Extract . . 10 „ Hard Resin . 24 '2 ,, Total yield of mixed Alkaloids, 46*6 When separated, the alkaloids represented- From soft Resin from extract. soft extract. Nitrate of Jervia. 7’9 grs. 8’4 grs. Other Alkaloids . 3'2 ,, 1’6 „ 6‘2 Total amount of Nitrate of Jervia . . 31 ’2 grains ,, other Alkaloids . . 11*0 ,, Hard resin. 14'9 grs. )> Loss 42-2 4-4 46’6 The loss of over 10 per cent, which occurred in separating the alkaloids is due both to separation of foreign matter and loss in manipulation. An examination under the microscope of the alkaloids, after separation of the jervia, was made by allowing a drop of their alcoholic solution to evaporate on a glass slide. Crystalline forms were found, differing in form from jervia, indicating the probable presence of another alkaloid which crystallizes from its alcoholic solution. When further purified by solution in ether, dissolving the ether product in acetic acid and precipitating by nitrate of potassium until a solution containing 1 part in 200 of acetic solution was no longer disturbed by addition of the nitrate, then precipitating the solution at 150° F., by caustic soda, a product representing 5 per cent, of the mixed alkaloids was obtained. Saponification of the Resin by Lime. — One pound avoirdupois of the hard resin was powdered and rubbed into a smooth paste with one pound of lime previously slaked. Sufficient water was added and the mixture boiled for a few minutes. After evaporation and drying on a steam-bath, the mass was powdered and exhausted with three gallons of hot alcohol. The product left on distillation of the alcohol was treated with warm diluted acetic acid,* filtered and precipitated while warm by caustic soda. The precipitate was purified by drying, re¬ solution and precipitation. The weight of mixed alka¬ loids obtained was 485 grains. A better result was obtained from a second pound of the resin, by first removing the fatty matter with benzin and using two pounds of lime. The yield of alkaloids by the process of saponifying with lime was 20 per cent, greater than by the ether process. Volatile Principles. — 300 grains of the hard resin, de¬ prived of fatty matter, was dissolved in water by addition of carbonate of soda mixed with a little caustic soda. The alkaline solution was submitted to distillation, collecting the product in a receiver containing water acidulated with acetic acid. The distillate was evapo¬ rated to reduce its volume, made alkaline and treated with ether. The result was negative. Note. — After concluding the examination recited in this paper, I have seen the abstract of a paper read by Dr. Wright before the Chemical Society, London, May 15th, “ On the Alkaloids of Veratrum Viride ,” in which the able and exhaustive examinations made by him con¬ tribute greatly to our knowledge of the constituents of this interesting drug. The name “ rubijervine ” has been given by him to the alkaloid which has claimed my attention, a name which is very appropriate to the reactions of the alkaloid. The alkaloid which I found to crystallize from solution in alcohol along with “rubi¬ jervine ” is probably his “ pseuclojervine.” The large amount of alkaloids which are associated with the resin, and removed from it only by saponifying with lime, render it probable that by his process of obtaining the alkaloids a considerable amount escaped his notice. The approximate yield of the bases which I obtained from 1 pound avoirdupois of the root by the ether process was 46'6 grains = 6 612 grams per kilo. The amount obtained by Dr. Wright was 0'80 gram per kilo. The amount obtained from the hard resin alone by saponifying with lime represented 297 grains for one pound of root = 4'21 grams per kilo. Philadelphia , June 6, 1879. SOAP BARK IN THE TREATMENT OF SKIN DISEASES.-! The Quillaia saponaria is indigenous to Chili. Its bark is imported in flat pieces, which are usually several inches wide, and from 2 to 3 feet in length. These are hard and tough and of light grey colour. In the shops it is generally found in raspings and small woody fibres mixed with an acrid dust which readily provokes sneezing. It contains, among other ingredients, saponin, sulphate of calcium and a small quantity of starch. A saturated alcoholic solution of saponin possesses the power of dissolving gums, resins and oils, and will form with them after being mixed with water, permanent emulsions. This same solution, when shaken with mer¬ cury, will keep it suspended. It will be seen that saponin in solution possesses all the chemical action of soap, and is often preferred to the latter. As a therapeutic agent this natural soap can be used in the form of infusion, tincture, or fluid extract. An infusion of the bark can be easily made by tying some of it in a piece of white flannel, and allowing it to remain in a bowl of water for one or two hours, until the saponin is dissolved. I resort to this method of extract¬ ing the active principle in order to avoid the irritating effect of the minute fibres of the bark. If this solution is applied to any part of the body it will be found to * Repeated treatment with hot water containing acetic acid until two gallons were used was necessary to exhaust the product. f From the Druggists’ Circular and Chemical Gazette, August, 1S79. 188 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 6. 1879. fulfil all the requirements of a mild soap, and act in addition as a moderate stimulant and astringent on the skin. I have used it with marked benefit in dandruff of the scalp. It causes the enlarged glands of the part to contract, and often removes all infiltration of the skin. It has often been of great service in removing the scales in simple pityriasis, and in producing at the same time its moderately stimulant and astringent action. Simi¬ larly, I have had some excellent results from its use in chronic ulcers and eczema of the extremeties. I usually saturate a roller bandage with the infusion and bandage up the part. The cases in which I tried this means had previously used both the simple dry and wet roller bandage, but no success was attained until the above method was adopted. The infusion is also a valuable remedy for aiding in arresting excessive secretion and fetid perspiration. The parts that are usually affected by these troubles are the face, armpits, hands and feet. In cases involving the face and armpits, I instruct the patient to dip a small piece of sponge in the infusion, and carefully mop over the surface once or twice daily. When the hands and feet are affected they should be bathed in the solution nightly, or on alternate nights, according to the condition. When a more active stimulant and astringent effect is required, the tincture of saponin can be employed with much advantage. The tincture is prepared by extracting the bark, as already mentioned, by means of strong boil¬ ing alcohol. The solution thus formed is clear and of a deep wine colour, and a pungent taste. It is chiefly em¬ ployed as an external remedy, and when applied to apart has a refrigerant effect. It is miscible with both water and oil, and has the power of dissolving, emulsifying, and removing fats and dirt from the skin. In many diseases, especially in Seborrhcea sicca, I have found it far prefer¬ able to the tincture of green soap. It has all the advan¬ tages that are claimed for the tincture of green soap, and at the same time is free from the high diffusive, pene¬ trating, and destructive action on the tissues that the latter possesses. I have used this tincture with great benefit, not only in the diseases to which the infusion is applicable, but also in general thinning and loss of hair in different parts of the body. It can be employed with great advantage as an addition to the internal treatment in that variety of the loss of hair in which the scalp is to all appearances healthy, but the surface is covered with short, fine, and downy hairs. In cases of this description it should be applied in full strength with a sponge, and should always be thoroughly rubbed into the scalp, and afterwards rinsed off with water. NOTE ON HYRACEUM* BY WM. H. GREENE, M.D., AND A. J. PARKER, M.D. Among the native remedies from the Cape of Good Hope, exhibited at the Centennial Exhibition, was a peculiar substance called hyraceum, which was supposed to be the inspissated urine of the Cape Hyrax ( Ilyrax capensis). The material was obtained from Dr. Leidy, who, in the ‘Proceedings of the Academy,’ December, 1876, p. 325, gave a short account of it. According to this account “ the hyrax is reputed to inhabit gregariously rocky places at the Cape of Good Hope, and the accumulated urine in the hollows of rocks, gradually evaporating, is supposed to give rise to the product in question. It is reported as having been employed in medicine with the same effect as castoreum.” * From the Proceedings of the Academy of Natural Sciences of Philadelphia, January 28, p. 12. Reprinted from the American Journal of Pharmacy, July, 1879. Professor Cope remarked that “a material resembling the concretion made by the urine of the hyrax was found in the fissures of the rocks of New Mexico. It is prob¬ ably the fecal and renal deposit of the wild rat, NeotomaP About two years ago we made an exhaustive examina¬ tion of this substance. It is a dark-brown, brittle and resinous material, having an aromatic odour and a bitter taste. About 56 per cent, of it is soluble in water, and nearly one-third of the residue from the aqueous extrac¬ tion is soluble in alcohol, ether and chloroform. The soluble material amounts in all to about 70 per cent., and the remainder is composed of 14 per cent, of woody fibre and insoluble organic material, and 16 per cent, of sand and other inorganic substances. On ignition, hyraceum yields about 34 per cent, of ash, which is composed of chlorides, sulphates, phosphates and carbonates of the alkaline metals, and of lime and mag¬ nesia. It also contains nitrates in small proportion. On precipitating the organic material contained in the aqueous extract with lead acetate, and afterwards decom¬ posing the suspended precipitate by means of sulphuric acid, a substanee was obtained which constitutes the greater portion of the organic material soluble in water. It was hard, horny and of a resinous character, trans¬ parent, and of a bright-brown tint. It probably consists of several substances, but we were unable to obtain a sufficient quantity for separation, and an ultimate organic analysis. It gives out a fecal odour, and seems to be derived from fecal matter. TThe analysis, the details of which are subjoined, shows that the substance is a mixture of various salts and organic matter, the latter constituting about one-half, and con¬ taining traces of urea, together with uric, hippuric and benzoic acids. We also obtained from the material a small quantity of a substance having a sweet taste, and which is probably glycocol ( ? ) derived from the breaking up of hippuric into benzoic acid and this substance. Hyraceum is undoubtedly derived from the urine of some animal, but the large amount of lime (6 per cent.) in proportion to the other salts, and the character of the organic matter contained, indicates that it also contains fecal matter. Analysis of Hyraceum. — Water, by desiccation, 7 per cent. A microscopical examination revealed nothing of im¬ portance. Woody fibres, particles of sand and a general granular appearance were found. Dried Material. Ash ^ . . . . . 34T5 Organic substances soluble in water . . 37'44 Organic substances soluble in water, alcohol, ether and chloroform . . . 14’54 Woody fibre and insoluble organic sub¬ stances; residue . 13‘87 100-00 A sh. Soluble in water . 1 9*20 Insoluble in water . 14 -95 Potassa . 2'95 Soda . 8*95 Lime . 6-00 Magnesia . 2’10 Iron . T2 Sand . 2'00 Sulphuric acid . *60 Carbonic acid . 3-64 Phosphoric acid . ‘97 Chlorine . 6-45 Traces of nitric acid, and loss .... '37 34'15 September 6, 1379.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 189 fjjhf phanntaqtttual Journal. - ♦ - SATURDAY, SEPTEMBER 6, 1879. PROTECTION OF THE PRACTICE OF PHARMACY IN IRELAND. The two cases of prosecution under the Pharmacy Act, Ireland, of which we published reports last week, serve to show that the Council of the Irish Pharmaceutical Society is resolved to maintain the character of the degree of pharmaceutical chemist, and we rejoice to be able to congratulate that body upon the manifestation of so laudable an intent. At the time the Irish Act was passed there were some misgivings in this country that the adoption of only one grade of pharmaceutical practitioners and the application of the title of pharmaceutical chemist to that grade might have a prejudicial influence on the value — acquired and anticipated — of the same designation in this country. The Irish Society was able to do -what could not be done here in legislating for the pharmaceutical practitioners that were to succeed the old apothe¬ caries. Here the practice of pharmacy was cast adrift to all comers, and in assuming new functions the English apothecaries abandoned the trust that was confided to them in the interest of the public. In Ireland, on the contrary, the right to compound physicians’ prescriptions has always been zealously guarded by the apothecaries as their exclusive privilege in virtue of special preparation for the duty, and though they, like the apothecaries of England, are gradually developing into medical practitioners simply, the protection of the public and of the qualified pharmacist has been secured by the provisions of the Irish Pharmacy Act in a manner that could not be done here when our Pharmacy Act was passed in 1868, though the eventual realization of this object is thereby pro¬ vided for. As an incident of the first of these cases we find that the magistrate gave utterance to one of those expressions of opinion which are sometimes exceed¬ ingly damaging in their influence upon particular classes, but at the same time are totally destitute of any just foundation, and should therefore be studiously avoided by magistrates or other judicial functionaries. We refer to the comments of the magistrate upon the propriety of the action taken by the Pharmaceutical Society of Ireland. It was natu¬ rally urged by the counsel for the plaintiffs that the prosecution was not intended to be oppressive, but that it was merely the action incumbent on the representatives of the Irish pharmaceutical body for the purpose of vindicating the law and protecting the public. This view was at once accepted by the magistrate, who also proceeded to observe — in illus¬ tration, we presume, of the salutary nature of the Act — that “ mistakes occur every day in London in “ consequence of prescriptions being compounded by “ persons who are not properly qualified to do so,” and he then went on to say that happily there had been very few such cases in Ireland. It is not our desire to open old wounds by following out the comparison thus instituted by the magistrate, though we think that if some members of the Council of the Irish Society had pointed out the total absence of any justification for the magis¬ trate’s remarks to the disadvantage of London he would not have done more than justice to his English colleagues nor would he have overdone that generous chivalry for which Irishmen are justly famous. But as this was not done it becomes our duty to give the most emphatic contradiction to the statement of the Dublin magistrate. Comparisons are always dan¬ gerous, no less than odious, and in this instance it would scarcely have been possible within so small a number of words to express a greater amount of inaccuracy. It is not the case that in London mis¬ takes occur every day in the compounding of pre¬ scriptions ; it is not the case that in London, or any other part of Great Britain, prescriptions are com¬ pounded by persons not properly qualified to do so. There is no contrast in these respects between Great Britain and Ireland which is to the disadvantage of the former. In the expression of a sense of what is necessary in the public interest as regards dispensing of medicines, Great Britain lies under the advantage of having led the way through the medium of the Pharmaceutical Society to establishing a regulation of the practice of pharmacy by which the competence and skill of pharmaceutists is ensured, and it is upon the model of the example thus afforded that phar¬ macists in Ireland have carried out the application of similar measures. In their labours to this end they have always had the cordial sympathy of their confreres in this country ; we trust their efforts may always be united in the same direction, and that these amicable relations may never be interfered with by unwise comments in the spirit of the Phari¬ see, whether they be accidental or intentional. THE FLOODS IN HUNGARY. We have received a communication from Mr. Gustav Jarmay, the President of the Hungarian Pharmaceutical Society, acknowledging the receipt of <£39 Is. in aid of the fund for the relief of the distressed pharmacists of Szegedin, and requesting us to express to those pharmacists of Great Britain whose contributions that sum represents the grateful thanks of himself and the other members of the Committee. We also will take this opportunity to express our hearty thanks to those who have sup¬ ported our endeavour to obtain on the part of British pharmacists a fitting expression of sympathy with the misfortunes of their brethren in Hungary. 190 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 6, is79. POISONOUS HONEY. In a report by Mr. Vice-Consul Biliotti on the trade of the port and district of Trebizond, he refers to the poisonous effects produced by some of the honey obtained near the coast of that province. Those who partake of it suffer from giddiness, vomit¬ ing and intoxication, exactly as did Xenophon’s soldiers in the same locality more than two thousand years ago. This poisonous quality has been on a former occasion attributed to the bees having col¬ lected the honey from the flowers of henbane and hemlock, which occur plentifully in the neighbour¬ hood, but Mr. Biliotti appears to be inclined to refer the mischief rather to the Datura Stramonium, which grows in abundance on the coast. Although therefore bees are reared on a somewhat extensive scale in the province of Trebizond, in the neighbour¬ hood of the coast, the hives are only remunerative in wax, but the honey produced in the high lands is innocuous, an 1 is said to be of superior quality. In the list of candidates who have passed the recent honours examinations of the London Univer¬ sity the first name in the first B.Sc. and Preliminary Scientific Examinations is that of Mr. A. P. Luff, formerly a Bell Scholar, whilst bracketed with another gentleman in the second place is Mr. W. A. Gostling, a son, we believe, of Mr. Gostling, of Diss, a member of the Council of the Pharmaceutical Society. Itasitittitmjs of tl]c fljarmaiptital JlDjittg. MEETING OF THE COUNCIL. Wednesday, September 3, 1879. Present — Mr. George Webb Sandford, President; Messrs. Atkins, Bottle, Churchill, Hills, Richardson, Robbins and Savage. The minutes of the previous meeting were read and confirmed. The Pharmaceutical Conference. The President said he might state that he and several ether members of the Council represented the Society at the Pharmaceutical Conference, and they were very warmly received. It was as good a meeting, he believed, as they had ever had, and the Sheffield chemists did everything to render their visit a pleasant one. Weights and Measures. The President read the following correspondence on the above matter : — “ Board of Trade, “ (Harbour Department), “ Whitehall Gardens, S.W., “August 21, 1879. “ Sir, — With reference to previous correspondence on the subject of providing proper standards of the weights and measures used in trade by apothecaries, I am directed by the Board of Trade to transmit to you, herewith, copy of the Order of Her Majesty in Council legalizing certain denominations of standards of apothecaries’ weight and measure. “ I am, sir, “ Your obedient servant, “ Henry G. Calcraft. “ The President of “ The Pharmaceutical Society of Great Britain, “17, Bloomsbury Square, W.C.” [The Order in Council here referred to was published in the Pharmaceutical Journal of August 23, p. 145.] “ Pharmaceutical Society of Great Britain, “17, Bloomsbury Square, W.C., “ August 27, 1879. “ Henry G. Calcraft, Esq., “ Harbour Department, “ Board of Trade, “ Whitehall Gardens, S.W. “ Sir, — In reference to your letter of the 21th inst., enclosing a copy of the Order in Council ‘ legalizing certain denominations of Standards of Apothecaries’ Weight and Measure,’ may I venture to refer you to a memorandum sent to F. H. Farrer, Esq., by the then President of this Society, on the 30th January last, especially on the subject of verifying small weights and certain sub-divisions on glass measures, which are in daily use by chemists, and stamping them ? “ If you will kindly favour me with the decision of the Board of Trade on these points or refer me for further information to the officer who has authority in the stamp¬ ing-department, I shall be greatly obliged. “ I am, sir, “ Your obedient servant, (Signed) “ G. W. Sandford, “ President .” The President said he had not received any answer to the last communication, and on inquiry at a scale- maker’s was informed that he had not at present received any instructions for stamping weights. It would be remembered that the question submitted was, whether the sub-divisions of glass measures would be verified. Mr. Richardson asked if it was intended that glass measures should be stamped. The President said no doubt they would be marked in some way — probably engraved. Elections. members. Pharmaceutical Chemist. Hugh Odard Dutton, Rock Ferry, having passed the Major examination and having tendered his subscription for the current year, was elected a Member of the Society. Chemists and Druggists. The following, who were in business on their own account before August 1, 1868, having tendered their subscriptions for the current year, were elected Members of the Society : — Carr, Walter Paterson . Berwick-on-Tweed. James, Joseph . Cheltenham. ASSOCIATES IN BUSINESS. The following, having passed the Minor examina¬ tion, being in business on their own account, and having tendered their subscriptions for the current year, were elected “ Associates in Business ” of the Society : — Jones, John . Liverpool. Scott, John . Newcastle-on- Tyne. Steele, John Cockburn . Glasgow. ASSOCIATE. John Carter, London, having passed the Modified ex¬ amination and tendered his subscription for the current year, was elected an Associate of the Society. Mr. Richardson asked when the Modified examina¬ tion would cease. I September 6, is79.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 191 Mr. Bottle said when they got a new Act of Parlia¬ ment. The President said all who were on a certain register were entitled to come up for the Modified examination. Mr. Robbins asked how many came up in the coarse of the year. The Secretary said about 20 or 25 per annum. There were, he believed, about 1200 men still eligible to pass the Modified examination. apprentices or students. The following, having passed the Preliminary examina¬ tion and tendered their subscriptions for the current year, were elected “ Apprentices or Students ” of the Society: — Allen, Ernest Edward . Winchester. Bradley, Frederick William ...Wisbeach. Clarke, William Seth . Coventry. Hall, Ernest Edward . Wednesbury. Hepple, Thomas . North Shields. Hill, Major . Sleaford. Ingham, William Linnell . London. Middleton, Burton . Ilkley. Mitchell, Charles Edward . Bolton-le-Moor. Newman, Alfred Pointon . Crewe. Staley, Henry . Burton-on-Trent. Skoulding, William George . Oakham. Talbot, William Widdowson ...Bulwell. Thomas, William Morgan . Glamorgan. Several persons were restored to their former status in "the Society upon payment of the current year’s subscrip¬ tion and a fine. The names of the following persons who have severally made the required declarations and paid a fine of one guinea were restored to the Register of Chemists and Druggists : — John Brierley, Barrow-in-Furness. Archibald James Millar, 2, Railway Terrace, York Road, Wandsworth, Surrey. Minutes op Committees. FINANCE. The report of this Committee was received and adopted, and sundry accounts were ordered to bo paid. BENEVOLENT FUND. The report of this Committee included a recommenda¬ tion of the following grants : — £15 to a pharmaceutical chemist, formerly in business, but now out of employment. Applicant has had five previous grants. £10 to the widow of a chemist and druggist, having three daughters dependent upon her. £10 to the widow of a late annuitant on the Benevolent Fund. £10 to a registered chemist and druggist, aged 67, suffering from partial paralysis. The report and recommendations were received and adopted. Mr. Savage said he was recently in the town where one of Isherwood’s children was placed, and he thought it right to make some inquiry about her. He had not an opportunity of seeing the child, but he heard from an independent source a very nice character, both of the child and the gentleman with whom she was placed. The Secretary said this information quite agreed with the letter received last month. Infringements of the Pharmacy Act. A letter was read from the Solicitor enclosing corre¬ spondence 'with regard to certain cases of alleged infringe¬ ment. The Council, according to the usual practice, went into Committee to consider the various matters referred to. rowcdugfi of Scientific ^kicidifs. BRITISH PHARMACEUTICAL CONFERENCE. (Continued from page 175). Proximate Analysis of the Rhizome (Dried and Decorticated) of Zingiber Officinalis, and Com¬ parative Examination of Typical Specimens of Commercial Gingers. BY J. C. THRESH, F.C.S., Pharmaceutical Chemist. Part II. — Comparative Examination of the Gingers • of Commerce. For the above purpose Mr. Umney kindly selected for me a typical specimen of each of the varieties found in commerce, viz., Jamaica, Cochin and African. No. 1. Jamaica ginger. A fine B.P. specimen. Ir¬ regular lobed decorticated pieces, three or four inches long, sub-compressed, yellowish-white, but not chalky on surface. Fracture short, mealy. Powder yellowish- white. No 2. Cochin ginger. Irregularly lobed pieces, decor¬ ticated, two or three inches long, a little smaller than the Jamaica, and pale brown externally. Fracture, fibrous, short. Powder yellowish- white. No. 3. African ginger. Short irregular coated lobes, of a brown colour. Fracture short, rather resinous. Powder brown. Moisture and Volatile Oil. — A quantity of each of the above was reduced to powdery and small weighed portions placed in tared dishes on the water-bath, until they ceased to lose weight and no longer retained an odour of ginger. No. 1. l-652 grams lost *234 or 14T7 per cent. „ 2. 1-311 „ „ -195 or 14-88 „ 3. 1-476 „ „ -235 or 16*13 Ash. — The above quantities were burnt at a dull red heat, cooled in dry air, and rapidly weighed. No. 1 yielded ash weighing "059 or 3*57 per cent. „ 2 „ ,, -063 or 4-80 „ „ 3 „ „ -063 or 4-27 „ Ethereal Extract. — Twenty grams of each were packed in small percolators, and ether passed through to exhaus¬ tion. For this purpose the African required twice as much of the solvent as the Jamaica and Cochin. The ether was driven off at a low temperature, and the residue kept on water-bath until the loss of weight between con¬ secutive weighings at short intervals was trifling. • No. 1 extract weighed "658 grams. 2 3 •993 1-613 Volatile Oil. — The above residues were kept for eight to ten hours upon a chloride of calcium bath, until they no longer lost weight. No. 1 extract lost -150= -75 per cent, volatile oil. „ 2 „ -270 = 1-35 „ „ 3 „ -323 = 1-61 A second determination of above was made by treating fresh portions of the powdered ginger with petroleum ether (boiling at £0° C.), removing ether by, first, a current of air, and, second, exposure for a few minutes to a temperature of 100° C. The extracts were then kept at about 115° C. until the weights were constant. No. 1 gave results corresponding to "830 per cent, volatile oil. No 2 gave results corresponding to 1*14 per cent, volatile oil. No. 3 gave results corresponding to 1"97 per cent, volatile oil. No. 4 gave results corresponding to 1*38 per cent, volatile oil No. 4 was the sample used in investigation of proxi¬ mate constituents of ginger. The amount of volatile oil 192 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. iSeptember 6, 1879. actually obtained from 28 lb. of this ginger was as before stated ozs. or 1*23 per cent., and as this was un¬ doubtedly not the whole of the oil contained in the ethereal extract, the above determinations may be taken as close approximations. Deducting the volatile oil, from the moisture + volatile oil, we have — Moisture in No. 1, 13 '42 per cent. „ ,, 2, 13*53 „ „ „ 3, 14-515 „ Soft Fat, Resin 8 and Wax (?). The ethereal extracts were next treated with small portions of petroleum ether to extract the fat, etc., the ether driven off, the residues washed with a little proof spirit, dried and weighed. No. 1 yielded *140 grams or *7 per cent. „ 2 „ -241 „ 1-2 „ „ 3 „ ‘245 . 1-22 „ Neutral Resin.— -The residues insoluble in petroleum ether were exhausted with proof spirit, and the washings of petroleum ether extracts added thereto. The portions insoluble in proof spirit consisted of the neutral resin, which was dried and weighed. No. 1 weighed -173= '865 per cent. 2 „ T90 = -950 33 -461=2-305 Gingerol. — The above proof spirit solutions were pre¬ cipitated with basic lead acetate, filtered, evaporated, and residue washed with dilute acetic acid, dried and weighed. This residue consisted of the active principle with traces of resins a and (j . The lead precipitate retained traces of active principle, so that these determinations, gingerol and resins a and /3 are mere approximations. No. 1 yielded *132 or *66 per cent. „ 2 „ ‘120 or -60 „ „ 3 „ ’290 or 1'45 „ Resins a and (3. — Calculated by difference we have from — No. 1. "063 gram or ’315 per cent. 2. -172 „ or -860 99 99 3. -294 or 1*470 99 Aqueous Extract — The portions of the original gingers insoluble in ether were dried and mixed with water until each measured 400 c.c.’s. The mixtures were stirred at frequent intervals for several days, the insoluble portions then allowed to subside, £0 c.c. ( = 1 gram ginger) of the clear supernatant fluid removed from each, evaporated to dryness and weighed, and the ash afterwards ascertained by ignition and re-weighing. No. 1 gave -143 extract less -023 ash = 12-0 per cent. 2 „ -146 „ '025 „ =12-1 99 99 *105 •030 99 7-5 99 Substance Precipitated by Acids. — Other portions of 100 c.c. each ( = 5 grams ginger) were acidified with acetic acid, allowed to stand for a few hours, then warmed, and filtered through tared filters, the precipitates washed with a little dilute acid, dried and weighed. No. 1 yielded -266 less ash -0035 = 5*25 per cent. 2 „ -262 -0045 = 5-35 33 •235 •005 =4-60 99 Mucilage. — The acid filtrate and washings from above were evaporated to 20 c.c., and mixed with 60 c.c. of 95 per cent, alcohol. (In each case during the evapora¬ tion a little flocculent matter was deposited, but the amount was too small to materially affect the estimations.) The mixtures were set aside for a day, the precipitates then thrown upon tared filters, washed with a little alcohol, dried and weighed, and the ash afterwards determined and deducted. No. 1 yielded *1725, ash -053 = 2-39 per cent. „ 2 „ -1155 „ -043 = 1.45 „ 3 „ -097 „ -038 = 1-19 Organic Acids, etc. — The combustible portion of aqueous extract unaccounted for consisted of malic (?) and oxalic acids, an indifferent substance precipitated by tannin and possibly other bodies. These amount in No. 1 to 4-36 per cent. „ 2 to 6"80 „ „ 3 to 1’70 „ Alcoholic Extract. — The marcs insoluble in ether and water were drained upon filters, re- packed in the per¬ colators, and 84 per cent, alcohol passed through so long as anything was dissolved. (200 c.c. in each case ) The Jamaica and Cochin tinctures had a pale amber tint, the African a pale brown. 40 c.c. of each were evaporated to dryness and the residue weighed. No. 1 gave "016 or *4 per cent. „ 2 „ ‘Oil or -28 „ „ 3 „ *025 or -625 „ The residues from treatment with ether, water and alcohol were next digested in sufficient 1 per cent, soda solution to measure 400 c.c. The Jamaica ginger yielded a mucilaginous solution, in which the insoluble matter settled very slowly; the Cochin ginger gave but a slightly mucilaginous solution, whereas the African variety yielded a perfectly limpid infusion. 50 c.c. ( = grams ginger) were neutralized with acetic acid mixed with 100 c.c. of 95 per cent, alcohol, and allowed to stand for a day. The precipitates were then collected on tared filters, washed, dried, weighed, then ignited and the ash estimated. No. 1 yielded "731, ash -029 = 28*08 per cent. „ 2 „ -210, „ -007= 8-12 „ 3 „ -049, „ -001 5 = 1-86 Starch. — The remainder of the alkaline infusions were in each case diluted to 1200 c.c., boiled for a few minutes, allowed to cool to 50° and digested at the latter temperature for forty-eight hours with a little diastase- 50 c.c. were then taken and boiled with 8 c.c. of dilute sulphuric acid (1 in 8) until the fluid ceased to react with iodine, or the volume was reduced to 50 c.c. After cooling the solutions were each run into 10 c.c. of Fehling’s solution ( = -044 gram starch), until the blue tint disappeared. No. 1. 14'9 c.c. = -044 starch or 18-12 per cent. „ 2. 17-1 „ =-044 „ 1579 „ 3. 20- „ =-044 „ 13-50 Pararabin and Calcium Oxalate. — The residues in¬ soluble in caustic soda and boiling water were slightly washed by subsidence and decantation, and mixed with sufficient 1 per cent, hydrochloric acid to measure each 400 c.c. After macerating twenty-four hours, they were boiled for a few minutes, and 50 c.c. ( = 2J grama ginger) of each, filtered, neutralized with ammonia, and diluted with three volumes of 95 per cent, alcohol. The addition of ammonia to the Jamaica infusion caused a slight turbidity ; the Cochin infusion was not affected,, but a rather bulky brown gelatinous precipitate was produced in the African solution. The ammonia and alcohol precipitates were collected on tared filters, dried and weighed, then incinerated and the ashes weighed. The ashes from the Cochin and Jamaica gingers con¬ sisted of CaO derived from the calcium oxalate in acid solution ; the African ash was of a brown colour, and contained manganese. No. 1. Pararabin and calcium oxalate -025 = 1*00 percent. No. 2. Pararabin and calcium oxalate -374 = 14"96 per cent. No. 3. Pararabin and calcium oxalate, etc., *273 = 10*92 per cent. The ash of No. 1 weighed "010 = *914 per cent, of cal¬ cium oxalate. The ash of No. 2 weighed *006 = "580 per cent, of cal¬ cium oxalate. The ash of No. 3 weighed *085, but of this only *022 was CaO, equivalent to 2 04 per cent. CaC204. Deducting the proportions of this salt from the result of last experi¬ ment, we have the yield of pararabin in No. 1. *086 per cent. „ 2. 14-40 „ „ 3. 6*36 „ (the ash not CaO also being deducted). ) September 6, 1879. J THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 193 Cellulose. — The marcs from treatment with dilute acid were digested for several days with constant agitation in nitric acid of sp. gr. 1*16, to which a little powdered potassium chlorate had been added. The insoluble por¬ tions, which were nearly colourless, were washed succes¬ sively with water, dilute ammonia and alcohol, then dried and weighed. No. 1 yielded 7 cellulose = 3*5 per cent. „ 2 „ *75 „ =37 „ „ 3 „ 1*25 „ =6-25 „ Albuminoids. — Portions of the original gingers in powder were burnt with soda lime as in Will and Varentrap’s method, and the ammonia estimated as double chloride of platinum and ammonium. As the precipitates were rather dark in colour, one of them was ignited, and the platinum weighed. The results were closely concordant. l-069 gram No. 1 yielded ‘245 pt. salt = l*38 per cent. N. 1-360 „ „ 2 „ -193 „ = *891 „ 1-130 „ „ 3 „ -094 „ = *522 In a second determination of the No. 1, "833 grams yielded *211 pt. salt = 1*44 per cent. N. Taking one part of nitrogen as representing 6*25 parts of albuminoids, and neglecting to take into consideration the small percentage of nitrogen in the substance precipi¬ tated by acids, we obtain the following proportions : — No. 1. 8-8 per cent, albuminoids. „ 2. 5-57 „ „ 3. 3*27 „ „ Vasculose, Pectose, Loss, etc. — These have simply been calculated by difference. Thus, in No. 1, 91*908; in No. 2, 85*237 ; and in No. 3, 67*695 per cent, has been ac¬ counted for, leaving in No. 1. 8*092 per cent. „ 2. 14*763 „ „ 3. 32*305 „ to represent the fibrous and pectic matters, loss, etc. Tabulated Results of Analyses. Original Sample. No. 1. No. 2. CO © Volatile Oil . . . 1*380 750 1*350 1*615 Fat, Wax (?) and Resin (P. ether solution) . *835 700 1*205 1*225 Neutral Resin . . . *915 *865 *950 2*305 a and 0 Resins . . 1*300 *315 •865 1*470 Gingerol .... 1*210 •660 •600 1*450 Substance precip. by acids • • • • • 4*600 5*250 5*350 4*650 Mucilage . . . . 1*600 2*390 1*450 1*190 Indifferent Substance precipitated by Tannin . . . . Organic Acids, etc. . 1*500 1*750 J 4*360 6*800 1*700 Extractive (soluble in S. V. R., not in Ether or Water *800 *400 •280 •625 Alkaloid . a trace. a trace. a trace. a trace. Metarabin . . . . 23*880 28*080 8*120 1*860 Starch . 18*750 18*120 15*790 13*500 Pararabin . . . . 2*490 •086 14*400 6*360 Oxalic Acid (as CaC204) . . . 1*240 •642 *427 1*440 Cellulose . . . 5.710 3*500 3*750 6*250 Albuminoids . . . 6*880 8*809 5*570 3*270 Vasculose, etc.. . . 9.080 8*092 14763 32*305 Moisture . . . . 11*020 13*420 13*530 14*515 Ash . 5*060 3*570 4*800 4*270 100* o o 100* 100* Original Sample. No. 1. No. 2. No. 3. Ethereal Extract . . 5*64 3*28 4*97 8*06 Aqueous „ . . 9*45 12*00 12*10 7*50 Alcoholic „ . . *80 *40 *28 *63 Alkaline „ . . 23*88 28*08 8*12 1*86 Starch . 1875 18*12 1579 13*50 Acid Extract . . . 4*32 1*00 14*96 10*92 Cellulose, etc. . . . 21*08 20*13 25*45 3874 Moisture . . . . 11*02 13*42 13*53 14*52 Ash . 5*06 3*57 4*80 4*27 100* 100* 100* 100* Comparison of these results reveals the singular fact that the variety of ginger most esteemed contains only about half the quantity of essential oil found in the other varieties, and less of the active principle than either the African or common Jamaica, and about as much as good Cochin. It would be interesting to have prepared samples of the essential oils from these various sources, in order to ascertain their physical and chemical properties. But as possibly in all cases the aroma would be affected by distillation, it would be necessary to devise some other method of obtaining them. Undoubtedly the volatile oil in the finest Jamaica gingers possesses a finer bouquet than the others. The very dark colour of tincture of ginger when made from the African rhizome is evidently due to the large percentage of the neutral, a and 0, resins contained therein, and as these are tasteless and apparently inert, their pre¬ sence only deteriorates the value of the ginger. The most striking difference in the constitution of the varieties examined is the relative proportions of metarabin and pararabin which they contain. It is easy to dis¬ tinguish between a sample of Jamaica and one of Cochin ginger, when in powder, by maceration for forty-eight hours in a 1 per cent, soda or potash solution. If, however, the fibrous portion of the rhizome has been removed by sifting, as is generally the case with the finer qualities of powder, the test does not give such decided indications, from which it may be inferred that the fibrous portion is the seat of this metarabinoid substance. The same author also read a paper on — Soluble Essence of Ginger. BY J. C. THRESH, F.C.S. Since the publication of my short paper on the above subject, which was read at the Conference last year, I have received a number of letters from chemists, and others interested, some containing suggestions, others queries. These chiefly referred to the essence becoming turbid after being kept some time, and to the evident loss of active principle, in the magnesia precipitate, this being exceedingly pungent. To remedy these defects the following modification of the process was devised, by which almost all the active principle is removed from the precipitate, and the product does not become turbid by keeping, as is evidenced by the sample upon the table, which was made before last Christmas. Take of strong tincture (1 to 1) of finest Jamaica ginger one pint, add in small portions at a time finely powdered slacked lime, shaking vigorously after each addition, until the tincture ceases to lose colour, throw the whole upon a filter, and pass through the residue proof spirit until the product measures two pints. Now add drop by drop dilute sulphuric acid until the rich yellow colour of the tincture suddenly disappears, let stand for twenty-four hours, filter, dilute with water 194 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 6, W*. to four pints, shake with a little powdered pumice or silica (by no means lime or magnesia), and filter at 0° C. if possible. Rationale of the Process. — As may be gathered from a consideration of the constituents of ginger root, the alcoholic tincture will contain besides the extractive soluble in water, which need not further be considered, essential oil, neutral resin, a and resins, gingerol, and small quantities of the red fat, wax (?) and peculiar extractive insoluble in ether. Upon agitating the tincture with lime the greater part of the a and /3 resins is re¬ moved, and by addition of the acid the lime which has entered into solution is precipitated. The addition of wnter precipitates the neutral resin, wax, fat, and peculiar extractive, and unless the ginger from which the original tincture was prepared was poor in oil, the excess of volatile oil also. As in probably all cases the soluble essence is saturated with essential oil, the final filtration must be effected at a lower temperature than any to which the essence is likely to be exposed. The product as thus obtained is very pale in colour, but if a darker essence is preferred it is only necessary to add one or two drops of solution of potash to give an alkaline reaction, when the rich orange tint due to the action of the alkali upon the @ resin will be immediately produced. The President congratulated Mr. Thresh upon his able report, and congratulated the Conference on being the means of inducing him to pursue his inquiries on this truly pharmaceutical subject. Mr. Umney (London) said scientific chemists and pharmacists were greatly indebted to Mr. Thresh for having brought this subject forward. It had been a stand¬ ing disgrace that a drug they daily handled in a variety of forms, such as African, Cochin and Jamaica ginger, was not thoroughly understood by them. Mr. Thresh had placed the subject before them very exhaustively, and from his paper they would be able to follow with certainty the phar¬ maceutical aspect of ginger. The soluble essence of ginger wTas a most elegant preparation, and useful for the manu¬ facture of aerated water. The difference noticed in specific gravity of portions of the volatile oil was probably due in the main to the different processes by which the oils had been obtained. Those who had distilled essential oils knew that according to the heat used in their pro¬ duction they differed slightly in specific gravity. ' No doubt, according to whether this oil were made with petroleum spirit, or by distillation, the specific gravity would vary somewhat. Mr. Greenish remarked that he had examined micro¬ scopically sections of Jamaica and African ginger root, and found that a very large amount of starchy matter was developed in the Jamaica root as compared with the African ginger; but African ginger, if subjected for a series of years to the same amount of cultivation as Jamaica ginger, might possibly lose some of its pungent character, and develop starchy matter to an equivalent extent. Mr. W. L. Howie (London) adverting to Mr. Thresh’ s statement that the oil of ginger odour did not recall that of ginger, said he was inclined to think that possibly the smell was masked by that of the petroleum spirit used in its extraction. The difference in the specific gravity of the oils was due to some extent to the method followed, but it might also be due to a change which he believed took place in the oil when it had been kept some time. A small quantity of oil of ginger, which he had had in his possession some years, and wLich had, he believed, been made by distillation, he found to be but sparingly soluble in rectified spirit — not more perhaps than one in ten, and even with one in fifty there wnre still left some small whitish globules, which, when separated and exposed to heat, dried into a clear glassy resin, with scarcely any odour or taste. After exposing a little of the oil, for some days, in a watch-glass to a temperature of 100° F., there remained a resinous residue like the other in appearance. He made these remarks in order that Mr. Thresh’s attention might be directed to the further examination of the oil so as to discover whether or not it was a com¬ pound, and what was the character and extent of the change which occurred in it when kept for a long period. Mr. Martindale (London) observed that from a medical point of view and having before them the prospect of a new Pharmacopoeia, it was doubtful whether it would be advisable to introduce soluble essence of ginger into it or not ; although as a commercial article it might be very useful. The syrup of ginger was, in the present Pharma¬ copoeia, prepared from the essence and did not make a very elegant preparation. It might be improved if it were not opaque, but prepared from a soluble essence. The old London syrup was made from an infusion, which contained the metarabin Mr. Thresh had mentioned and made it a mucilaginous, and not very satisfactory pre¬ paration. Mr. P. B. Benger (Manchester) remarked that the paper, which was by a pharmaceutical chemist actively engaged in their business, was of great practical value and might be taken as the type of the sort of papers it was desirable to bring before tbe Conference. Mr. Thresh, in replying, said that he thought the essential oil exhibited did not smell of petroleum spirit. He had distilled a sample of the oil directly from an ethereal extract, and found that it had exactly the same odour as that distilled from petroleum extract; it was therefore quite impossible for it to have the odour of petroleum. He had observed (as also had Mr. Umney) that in distilling an ethereal or alcoholic essence of ginger a considerable quantity of oil came over at that low temperature, and he felt confident that this more volatile portion, which was lost, had the finest aroma. Again, he did not think it desirable to put the soluble essence of ginger into the Pharmacopoeia for its own sake ; but, as suggested by Mr. Martindale, it might be advisable to employ it for making the syrup of ginger, as the syrup thus prepared was really a much more elegant one than that made by the officinal process. The active principle was certainly very soluble in dilute spirit, but as the soluble essence must contain some essential oil also, it was impossible to make it of equal strength with the B.P. strong tincture ; nevertheless by removing the inert resins they were enabled to make a stronger solution than would otherwise be possible. The President asked if Mr. Thresh had made any special examination into the nature of the oil itself, as to its boiling point. Mr. Thresh said he had not. His time was limited and the isolation of the active principle took so much time that he had not been able to pursue the subject further. Professor Attfield hoped Mr. Thresh wTould continue the inA'-estigation further, and examine the oil as well as the other principles, applying to the committee for a grant to cover any outlay. The President was exceedingly glad so many able men had spoken of the value of the paper, and he hoped they would join him in passing a very hearty vrote of thanks to Mr. Thresh for his able report. The motion was carried unanimously. The Conference then adjourned for luncheon. After returning from luncheon the first paper read AA'as on — The Growth and Development of Clayiceps Purpurea (Tulasne). BY W. \V. STODDART, F.C.S., F.G.S., ETC., Lecturer on Forensic Medicine at TJniv. Coll., Bristol. At the end of the year 1877, a farmer residing in the neighbourhood of Bristol requested me to investigate the death of some sheep which had taken place every autumn without any assignable cause, so much so that a heavy September 6, 1879. j THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 195 loss was annually incurred. Many visits were conse¬ quently paid to the farm for the purpose of finding out the cause of disease. I noticed that the sheep were fed only on the natural herbage grown on the spot. It con- •isted of two kinds of clover, the ordinary Dutch ( Tri¬ folium repens , L.), and the common purple (A pratense. L.). With these were the ray grass [Lolium perenne, L.), or as it is commonly but erroneously spelled “rye” grass. A strict inquiry being made as to the symptoms, the farmer informed me that they were always the same and generally supervened in the month of August, when this very peculiar illness on the farm became prevalent. It took the form of dysentery, inflammation of the bowels, diarrhoea, the evacuations resembling coffee grounds, afterwards succeeded by exhaustion, collapse and death. Analyses of water and the soil were made for the purpose of detecting any deleterious metal or other irritant poison. No satisfactory result followed and the cause of the illness seemed to be mysterious and inex¬ plicable. At length 1 heard that the ewes sometimes slipped their young, which gave a remote suspicion that the cause, of all might be due to ergotism. An inquiry was then made as to the presence of gangrene, when the unexpected but significant remark was made, that although the farm was on a dry, porous, sandy slope, yet the sheep always had the “foot rot,” even in the summer, which defied all the remedies that usually proved effectual . With this idea in my mind and while watching the lambs feeding I noticed that they avoided the old mature plants, while they greedily devoured the young green ones. On examining more minutely the former, I noticed several well formed, purplish, dark coloured ergots were projecting from the palese, but could not discover a single specimen on the younger fresh plants. Several of these ergots were then taken home for chemical and microscopic examination. I made a considerable number of sections which exactly coincided with the beautiful and truthful engravings in the paper by Tulasne, in the ‘ Annales Sc. Nat.’ for 1853, Sur l’Ergot des G-lumacdes. While here, I must stop to express my admiration both at the accuracy of these microscopic delineations and the description of the metamorphoses of this curious fungus. I thought that this would be a good opportunity of studying the growth of this vegetable, and that the result of my observations during the following year may prove to be of some service in the cause of pharmacy. During the next few months I had only the olcl and nearly dead stems of the Lolium on which I could work, but on the 12th of April I obtained some specimens of the Lolium 'perenne in which the commencement of the inflorescence was just to be observed. Soon afterwards I made several sections of caryopsides, on which were many thousands of conidia, which seemed rapidly to multiply and to completely fill some of the grains till they protruded far beyond the glumes. In two or three days the sclerotium stage of the mycelium began to change colour and assumed a purplish brown tinge. The sclerotium seemed now to have arrived at what was formerly termed the “ sphacelia ” condition, and was soft, while the upper portion was wrinkled. The exterior was white from the growth of the liyphae, which seemed to grow with marvellous rapidity till at length only a small portion of the pistil remained free. Although the conidia were so numerous, I never noticed any on the androecium, even when examined with a one-sixth of-an- inch object glass, while close to them four or five of the caryopsides were completely filled with the little conidia, which are blunt and ellipsoid bodies about mm- to mm. in length, and from iTtVtf mm- to iTXothy mm. in breadth. They are curved and divided into two parts, each part containing a nucleus. On touching them with a drop of diluted sulphuric acid, a cilium or minute flagellum was extruded, and when placed in water had a vibratile motion. On examining suspected flour, bread or pastry, the microscope would always show these conidia, especially with the addition of a little chromic acid. In the third week of May several small drops of a syrupy substance made their appearance on the stem near the spikelet. If dissolved in a little distilled water and placed under the microscope, the solution would be seen to contain the conidia, and hence I suppose gave rise to the supposition that the honey-dew was intimately con¬ nected with the formation of ergot by aiding the growth of the mycelium. But it most probably only attracts and adheres to insects, who by this means convey the conidia to other spikelets and thus spread the infection to other grains. This saccharine mixture instantly re¬ duces the copper solution of Trommer’s test, thus showing the presence of sugar. When boiled, a slight milkiness is produced and not removed by nitric acid in excess, pointing out the presence of albumen. At this period the ergot attains its full development and gives no blue with iodine, because by the well-known metastatic power of fungi all starch is removed and an oil substituted. Of this oil, ergot sometimes contains about a third part of its weight. At this period of its growth each sclerotium gives off the odour of trimethylamine when treated with potass, and produces a red colour. With spontaneous evapora¬ tion, after mixing the honey- dew with alcohol and a little ether, minute octahedra of mycose are formed and may be seen with the lens. On July 18th I first gathered fully formed and mature ergots, which I now produce. They have a dark exterior with a white interior and give the ordinary red infusion. On August 1st one of the lambs was taken ill with the usual inflammatory symptoms. The feet also in a few days had a gangrenous appearance, which did not seem to be alleviated by any of the usual applications of silver nitrate, carbolic or cresylic acids. The affection of the feet strongly reminded me of “ clavellization,” so destructive among the flocks of Italy, France and Moravia, and has frequently been supposed to have been a variety of variola. The fungus has now reached the limit of its vegetative or myceloid growth, which plainly ends at the sclerotium stage as our medicinal agent called ergot, by means of which the embryo and most of the caryopsides have been destroyed. The hyphae are now ready to spread in every direction and thus extend the vegetative growth, from which only we derive the peculiar medical properties of the Claviceps in their greatest intensity and power on the animal economy, and it is now that the greatest effects are pro¬ duced which are included under the name of “ ergotism.” A poU mortem examination of the sheep showed the presence of the conidia among the “ coffee ground ” looking fasces. The fungus having now ari-ived at this stage awaits for appropriate weather and other suitable conditions for the fructifying metamorphosis. At the end of August one or two of the ergots that had fallen with the stems of the grass on the damp ground I placed, for more convenient observation, on the moist soil of a flower pot. In a few days I noticed on the dark cuticle of the sclerotium several minute excres¬ cences from which gradually emanated some stalks about 11 to 18 millimetres in length, each supporting a minute round head about 4 millimetres in diameter, in fact furnishing good characteristic specimens of Claviceps purpurea. It is' not to be wondered at that these fungi should have received the names of sphoeria or torrubia, because they so much resemble the growth so often desci’ibed as being found on the heads of caterpillars or larvae, and used as a medicine in China and Japan. A very remarkable change now took place in the oil that was so noticeable as long as the condition of sclero¬ tium continued, but directly the mature Claviceps appeared the oil oxidized, dried up and was found no longer. The round heads of the fungus now became I 196 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. ISeptomber 6, 1879. covered with a large number of brown dots, which even¬ tually became the openings of pear-shaped sacs or asci of the perithecium. If a section was made with a sharp scalpel each ascus was seen to be filled with a glutinous substance containing seven or eight spores. These last adhered to the ergot, looking like a powdery coating and causing the production of many thousands of conidia on each ergot and ready for the evolution of fresh mycelium. This seems to me the true mode of development of Claviceps. It commences and proceeds with the vegeta¬ tive growth till it reaches the sclerotium stage and at that period possesses in the greatest vigour the medicinal characteristics of ergot. I have, I think, conclusively found that ergot has the greatest medicinal power in the month of August, and that the experience of six or seven years shows that the same changes take place in the plant at the same period of every year. It has been known to medical men that the so-called essences of ergot are so uncertain in their efficacy that many, in order to ensure success, have determined to use the powder itself. Dr. Kluge, of Berlin, observed some years since, that for some reason or other the properties of ergot varied according to whether it was gathered before or after the harvest. In the former case it had an energetic action, while in the latter it was frequently powerless. The sheep were distinctly seen to choose the young green grasses and to particularly avoid the older and ripe ones, probably directed by the odour of trimethylamine, for I found that I could not produce this odour till the sclerotium was fully developed and the starch completely gone. I therefore think the following conclusions may be safely drawn — 1. That for all medicinal purposes, or pharmaceutical preparations, ergot ought to be gathered in the months 0? August or September. 2. That ergot always attains its greatest intensity at the end of the vegetative period. 3. That the medicinal powers of ergot diminish or dis¬ appear as soon as the fructifying period commences. I have chemically and microscopically examined the ergots produced from the Lolium perenne while the plants have been living. The infusion was first treated by the ether process of Stas. On the evaporation of the ether an oily residuum was obtained containing a minute quantity of a resinous substance. The extract was then dissolved in alcohol, afterwards mixed with water and filtered. Chloriodide of mercury caused a precipitate reminding one of a vegetable alkaloid. I did not detect any crystals of cholesterine that are said to exist in Sccale cornutum, but phosphoric acid was clearly shown by using molybdate of ammonia and nitric acid. In toxicological investigations the microscope is the most to be depended upon. The conidia are very abundant and may always be detected in bread, pastry or flour, especially if acetic or chromic acids be used to make their presence more evident. The one-sixth or one-eighth of an inch is a sufficiently high power. I always find that this mode of detection is preferable to the use of potass and distillation alone. The little conidia may be generally observed in the intestinal canal of a poisoned person or animal. The President, in inviting discussion, remarked that the Conference had been favoured by Mr. Stoddart with an extremely suggestive and interesting paper. Mr. Luff said he should like to ask two questions of Mr. Stoddart. Some months ago a toxicological case was entrusted to him for investigation. It was that of a young woman’s stomach in which ergot was found. He would ask Mr. Stoddart whether he noticed in the stomachs of thesheep during post mortem examinations very rapid decomposition. He was present at the post mortem examination of the young woman and very rapid decompo¬ sition set in during the course of twenty-four hours. At the inquest the medical witnesses wished to show that that proved the presence indirectly of ergot. He also wished to ask Mr. Stoddart whether he noticed the pre¬ sence of the poison in the second or in the fourth stomach of the sheep. Mr. Thresh said he should like to know definitely whether it was the same fimgus that produced ergot in the rye grass as produced it in the rye. Mr. Greenish thought this an extremely interesting subject to pharmacists, because ergot was the only fungus in the Pharmacopoeia. To investigate the subject properly it really required a knowledge of botany, of the microscope and of fungology. It was important to observe that the ergot just referred to was not ergot of rye, but an ergot from one of the grasses, and it appeared to have been ex¬ ceedingly active and very poisonous. There had been lately presented to the Museum of the Pharmaceutical Society some of the ergot of Diss, also a grass ergot from Algeria which was longer and more slender than the ordinary ergot of rye. It was said to be a much more active ergot. There had not been sufficient opportunity yet to enable this point to be decided, but it would be possible to get any quantity from Algeria. There was one point he could not very well understand. Mr. Stoddart had said that the ergot on the young grass was very poisonous to sheep; and he (Mr. Greenish) assumed that on the young grass it would not be the fully developed ergot. At the same time Mr. Stoddart had stated that the ergot for pharmaceutical purposes would be best ob¬ tained fully developed, and the fully developed ergot could not be got until about the month of August. He asked how it was that the ergot was more active before it was fully developed on the young grass, and yet that it should not be obtained for pharmaceutical purposes until it was fully developed. Mr. Umney said, with regard to the closing statement of Mr. Stoddart’ s remarks on the pharmacy of ergot, viz., “that the preparation of ergot must either be an ethereal or an ammoniacal one,” he would say that he must take exception. The ether directed in the Pharmacopoeia process was used to extract the fixed oil, and for the preparation of the extract the ether was driven off and the oily residue thrown away, the prepara¬ tion therefore was an aqueous one. Professor Attfield said that probably many cases of poisoning which had hitherto puzzled analysts were ex¬ plicable now with the facts which Mr. Stoddart had brought forward. A few weeks ago he had had one of these puzzling cases brought under his own notice ; and he mentioned it because he thought a great deal of light had been thrown upon it by what he had heard from Mr. Stoddart, and because it to some extent supported Mr. Stoddart’s conclusions. Some heifers which were turned into a particular pasture died. He examined the contents of the stomachs of these animals, but could find no trace whatever of any of the ordinary poisons or even of unusual poisons. He suggested that the farmer should instruct a botanist to examine the pasturage for poisonous plants or plants which would be likely to produce irritation enough to cause death; but he examined the contents of the stomach microscopically as well as chemically and found present crowds of minute bodies which he now thought must be the conidia to which Mr. Stoddart had referred. They were minute things seen very easily with a quarter inch power. They were somewhat sausage shaped, only thicker at one end than the other ; and they afforded evidence of structure. He believed they were identical with those alluded to by Mr. Stoddart. Mr. Stoddart, in summing up the discussion, alluded first to the question put by Mr. Luff as to putrefaction taking place in the stomach. He generally found that blood was the first thing to putrefy; and he believed that what he had alluded to as being comparable to coffee grounds was simply coagulated blood. Whenever he got a s ptember 6, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 197 stomach — and they were very frequently brought to him — and he saw there was much congestion — in other words, much blood— he assumed that probably strychnine had been used. So accustomed had he been to see the effects of strychnine that he was often able to say whether animals or men had been poisoned by that means, as decomposition would set in sooner than by the use of any other poison. He had usually found that to be the case. In answer to Mr. Greenish he repeated what he had pre¬ viously stated, that the best time to gather ergot was in its maturity in the sclerotium condition. With regard to Mr. Umney’s observation it only proved what he had said, that doctors differed considerably. The President said the Conference was much obliged to Mr. Stoddart for his extremely interesting paper, and gave him a cordial vote of thanks for his labours in this direction. (To be continued.) BRITISH ASSOCIATION. The Process of Investigation in the Exact Sciences.* BY G. JOHNSTONE STONEY, M.A., F.R.S. The process of investigation in the exact sciences is fundamentally one in all cases. It has been well described by Mill in the third book of his ‘ Logic.’ Nevertheless it is notorious that minds which are well fitted for some branches of physical inquiry find difficulty — sometimes insuperable difficulty — in pursuing others. It is not every eminent mathematican who would have made an equally good chemist, or vice versa. This is because there exists a practical distinction separating the investigation of exact science into two well-marked classes when they are viewed, not as they are in them¬ selves, but in their relation to the powers of us human beings. I refer to the distinction between the experi¬ mental method or the method of observation, on the one hand ; and the deductive method, or the method of reasoning, on the other. All valid investigations in exact science appeal to what can be directly perceived, and all lead to a conclusion which can be reasoned out from it ; but there are some of these investigations in which the main difficulty consists in making the appeal to the senses, and there are others in which the main difficulty lies in the process of reasoning. To contend with these difficulties successfully requires very different qualities of mind and body. In experi¬ mental science the powers principally called into re¬ quisition are readiness and closeness of observation, dexterity in manipulation, skill in devising expedients, accuracy in making adjustments, and great patience. It also requires that the investigator should have an accurate memory of what else he has witnessed resembling the phenomenon under observation, that he should be quick to detect every point of agreement and difference that can be perceived, and be skilful to select those which are significant, and to employ them as materials for provision to guide his further proceedings. But the strain on the reasoning powers is generally less, often of trifling amount. The question is put to Nature, and it is Nature usually that gives the bulk of the answer. The most striking monument of splendid achievements by the experimental method of investigation unaided by the deductive method is to be found in the science of chemistry. An equally typical instance of the power of the deductive method is the science of mechanics. This science, which has sunk deeper into the secrets of Nature than any other science, and which is the science towards whom all other physical sciences are at present more or less gravitating, is essentially deductive. There is little or no difficulty about its fundamental data. They are facts of Nature so patent to all men, and so indelibly implanted in human conception, that some persons have * Extract from a Presidential Address to the Mathematical and Physical Science Section, August 21, 1879. supposed that we have an intuitive perception of them. But, while the materials from which the mind is to work are thus easily obtained, it lias taxed to the utmost the reasoning powers of understandings like Newton’s to evolve the few consequences of them which are already known, and the investigator has to call to his assistance every aid to prolonged consecutive thought which mathe¬ maticians can devise. In grappling with the problems of Nature we are seldom allowed the choice of the method of investigation we shall employ. This is commonly settled for us and not by us. Where we cannot advance without further information, we must make further observations, i.e., we must employ the experimental method, the appeal ad experientiam : where we cannot advance without under¬ standing better what the information we possess really amounts to, we must employ the deductive method. No reach of intellect applied to the materials in existence before 1860 could have elicited the fact that iron exists upon the sun. This great discovery was made by Professor Kirchhoff, a scientific man who was equally versed in both methods of investigation. On the present occasion it was the experimental method he employed. He applied to the scrutiny of the sun’s spectrum four prisms of the most homogeneous glass that could be procured, figured with the greatest accuracy that the eminent artist Steinheil could attain. He expended far more pains on their adjustment for each successive part of the spectrum than any of his predecessors had done, and he was rewarded by a more perfect vision of the sun’s glorious spectrum than had met the human eye before. In a collateral inquiry, suggested by an observation made by Foucault, he and Bunsen placed a metallic vapour emit¬ ting bright rays in front of a still brighter incandescent body, so that the light from the brighter background had to pass through this vapour, and they found that this vapour now caused dark lines in the spectrum occupying the positions which its own bright lines had before filled. Professor Kirchhoff thereupon added an appliance to his spectroscope which enabled him to bring a metallic spec¬ trum and the solar spectrum together into the field of view, alongside of one another. On accomplishing this he saw sixty of the brightest of the iron rays as continu¬ ations of sixty of the strongest of the dark lines in the sun’s spectrum ; and by an elaborate scrutiny, he satisfied himself that the observations had been pushed to a suffi¬ cient degree of exactness to make ' sure that a deviation would have been detected in any one of these sixty cases if it had amounted to as much as one-fourth of the average interval between consecutive lines of the solar spectrum. From this it was obvious that the sixty coin¬ cidences are not due to chance, but indicate that there is really iron vapour in the path of the rays. It will be observed that Kirchhoff’s great merit and the real diffi¬ culty of his work lay in the scientific foresight and the in¬ dustry which were required to frame hypotheses that were worth testing, to guide the investigation by these hypotheses, to contrive, construct, and adjust adequate apparatus, and to make with it the elaborate observations and the exact observations and maps which were neces¬ sary. But when by these means the new facts had been brought to light, the inference from them that there i3 iron in the atmosphere of the sun was an easy one. This example will better convey than a definition what are the characteristic features of an experimental inquiry. On the other hand, no series of observations or experiments, however skilfully arranged, could have enabled anyone to understand the cause of that familiar but truly surprising phenomenon that a top stands upon its peg while it is spinning. But a full explanation of it is within the reach of any student who will train his mind to reason consecutively, and avail himself of the aids to prolonged consecutive thought which mathema¬ ticians have contrived. He will then see that the most obvious and familiar mechanical facts involve as necessary consequences all the phenomena which he finds in the i 198 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 6, 1879. schoolboy’s top, in the physicist’s gyroscope, and in the precision and nutation of the heavens. This then is a problem of Nature which falls within the province of the deductive method. Wherever data are known exactly, these inferences from these data, however remote, may be depended upon as corresponding with what actually occurs in Nature. And if in such cases the mind of man has proved equal to the task of drawing inferences which can effectually grapple with the problems he finds around him in the Universe — which is, alas! as yet but too seldom — then will the deductive method, our plummet, explore depths in the great ocean of existence which our anchors of experiment could not have reached. The distinction which is here made between deductive and experimental investigations would have no place in a logical system. But it has dii'ect reference to human convenience, and derives its importance from this circum¬ stance. It is obvious, too, that an investigation may partake of both characters — that it may require all the powers of the scientific observer to get at the facts, or even to appreciate them, and all the resources of the mathematician to elicit the consequences of them. For instance, on beginning his electrical studies, the student of Nature must master a mixed experimental and deduc¬ tive inquiry to get at the elementary fact that free electricity resides either at or outside the surfaces of conductors ; and he must engage in a further inquiry, and one only within the reach of a trained mind, to deduce from this the law of the inverse square. And, again, no full appreciation or even intelligent use of the common electrostatic and electrodynamic measures which he meets at the threshold of his electrical studies is within the reach of the mere experimentalist or the mere theorist. And if this treacherous ground lies before the immature student at his entrance, what shall we say of the bogs he struggles into as he advances ? We are per¬ petually meeting with inquiries of this mixed character in electricity and some of the other physical sciences, but they are comparatively rare in either medicine or che¬ mistry, and none that is difficult lies in the path of the beginner. How many students are there who are made to slur over the above and a multitude of similar difficul¬ ties, and who are told that they are learning science, when in fact what they are really learning is the perni¬ cious habit of being content to see Nature through a fog or through other men’s mental eyes ? In mechanics valuable progress can be made by the mere mathematician, the student of deductive science ; and in chemistry similar progress can be made by the mere ex¬ perimentalist. Of all the physical sciences these are the most purely deductive, and the most purely experimental. What I desire particularly to invite attention to is that the two great methods of investigation may best be acquired in these two sciences, and that for a really sound grasp of the remaining physical sciences, and especially with a view to further advance in physical science, a com¬ mand of both methods of investigation is essential. We must bear in mind, too, that either method of in¬ vestigation may be misapplied, and that this is a risk carefully to be guarded against. The deductive method when misapplied lands us in speculation, the experimental method becomes empiricism ; and it so happens that the sciences of mechanics and chemistry are not only monu¬ ments of the power of the two great methods of investi- gation,but instructive examples of their weakness also. For in chemistry, scarce any attempt at prolonged reasoning, carrying us by any lengthened flight to a distance from the experiments, can be relied on. The result has seldom risen to any thingbetter than speculation. And on the other hand, in mechanics, conclusions which depend on experiments only are empirical ; that is, they are deficient in accuracy, and their relation to the other phenomena of the science is left in darkness. Here, then, we find in these two sciences not only how strong these two methods of investigation are, but how weak they may become if misapplied. fjarliamentarg aiut Ifoui ^ro^dtngs. An Act to Continue and Amend the Petroleum Act, 1871. Be it enacted by the Queen’s most Excellent Majesty, by and with the advice and consent of the Lords Spiritual and Temporal, and Commons, in this present Parliament assembled, and by the authority of the same, as follows : — 1. This Act may be cited as the Petroleum Act, 1879. This Act shall be construed as one with the Petroleum Act, 1871, and together with that Act may be cited as the Petroleum Acts, 1871 and 1879. 2. Whereas by the Petroleum Act, 1871, it is enacted that the term “ petroleum to which this Act applies ” means such of the petroleum defined by that Act as, when tested in manner set forth in Schedule 1 to that Act, gives off an inflammable vapour at a temperature of less than 100° of Fahrenheit’s thermometer, and it is expedient to alter the said test : Be it therefore enacted that — In the Petroleum Act, 1871, the term “petroleum to which this Act applies” shall mean such of the petroleum defined by section 3 of that Act as, when tested in manner set forth in Schedule 1 to this Act, gives off an inflammable vapour at a temperature of less than 73° of Fahrenheit’s thermometer. Every reference in the Petroleum Act, 1871, to Schedule 1 to that Act shall be construed to refer to Schedule 1 to this Act. 3. A model of the apparatus for testing petroleum, as described in Schedule 1 to this Act, shall be deposited with the Board of Trade, and the Board of Trade shall, on payment of such fee, not exceeding five shillings, as they from time to time prescribe, cause to be compared with such model and verified every apparatus constructed in accordance with Schedule 1 to this Act which is sub¬ mitted to them for the purpose, and if the same is found correct shall stamp the same with a mark approved of by the Board and notified in the London Gazette. An apparatus for testing petroleum purporting to be stamped with the said mark shall, until the contrary is proved, be deemed to have been verified by the Board of Trade. All fees under this section shall be paid into the Ex¬ chequer. 4. The Petroleum Act, 1871, shall continue in force until otherwise directed by Parliament. 5. This Act shall come into operation on the thirty- first day of December one thousand eight hundred and seventy nine, which day is in this Act referred to as the commencement of this Act. 6. The Petroleum Act, 1871, shall be repealed after the commencement of this Act to the extent in the third column of the Second Schedule to this Act men¬ tioned. Provided that any sample of petroleum taken before the commencement of this Act shall be tested in manner set forth in Schedule 1 to the Petroleum Act, 1871, and any offence committed before the commencement of this Act shall be prosecuted, and any investigation, legal pro¬ ceeding, or remedy in relation to such offence, or to any act done before the commencement of this Act, shall be instituted, carried on, and have effect as if the provisions of this Act, other than those continuing the Petroleum Act, 1871, had not been passed. FIRST SCHEDULE. Mode of testing Petroleum so as to ascertain the Tempera¬ ture at which it will give off Inflammable Vapour. Specification of the Test Apparatus. The following is a description of the details of the ap¬ paratus : — The oil cup consists of a cylindrical vessel 2" diameter, i 2t‘2q " height (internal), with outward projecting rim TV' September 6, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 199 wide, §'•' from the top, and 1-|» from the bottom of the cup. It is made of gun metal or brass (17 B.W.G.) tinned inside. A bracket, consisting of a short stout piece of wire bent upwards and terminating in a point, is fixed to the inside of the cup to serve as a gauge. The distance of the point from the bottom of the cup is 1J". The cup is provided with a close-fitting overlapping cover made of brass (22 B.W.G. ), which carries the thermo¬ meter and test lamp. The latter is suspended from two supports from the side by means of trunnions upon which it may be made to oscillate, it is provided with a spout, the mouth of which is one- sixteenth of an inch in dia¬ meter. The socket which is to hold the thermometer is fixed at such an angle and its length is so adjusted that the bulb of the thermometer when inserted to its full depth shall be 1^" below the centre of the lid. The cover is provided with three square holes, one in the centre, TV' by TV'> and two smaller ones, To" by jVb close to the sides and opposite each other. These three holes may be closed and uncovered by means of a slide moving in grooves, and having perforations corresponding to those on the lid. In moving the slide so as to uncover the holes, the oscillating lamp is caught by a pin fixed in the slide, and tilted in such a way as to bring the end of the spout just below the surface of the lid. Upon the slide being pushed back so as to cover the holes, the lamp returns to its original position. Upon the cover, in front of and in line with the mouth of the lamp, is fixed a white bead, the dimensions of which represent the size of the test flame to be used. The bath or heated vessel consists of two flat-bottomed copper cylinders (24 B.W.G.), an inner one of 3” dia¬ meter and 2^» height, and an outer one of 5|" diameter and 5f '' height ; they are soldered to a circular copper plate (20 B.W.G.) perforated in the centre, which forms the top of the bath, in such a manner as to enclose the space between the two cylinders, but leaving access to the inner cylinder. The top of the bath projects both outwards and inwards about ■§" ; that is, its diameter is about greater than that of the body of the bath, while the diameter of the circular opening in the centre is about the same amount less than that of the inner copper cylinder. To the inner projection of the top is fastened, by . six small screws, a flat ring of ebonite, the screws being sunk below the surface of the ebonite, to avoid metallic contact between the bath and the oil cup. The exact distance between the sides and bottom of the bath and of the oil lamp is one-half of an inch. A split socket similar to that on the cover of the oil cup, but set at a right angle, allows a thermometer to be inserted into the space between the two cylinders. The bath is further provided with a funnel, an overflow pipe, and two loop handles. The bath rests upon a cast-iron tripod stand, to the ring of which is attached a copper cylinder or jacket (24 B.W.G.) flanged at the top, and of such dimensions that the bath, while firmly resting on the iron ring, just touches with its projecting top the inward-turned flange. The diameter of this outer jacket is 6%". One of the three legs of the stand serves as support for the spirit lamp attached to it by means of a small swing bracket. The distance of the wick holder from the bottom of the bath is 1 “ . Two thermometers are provided with the apparatus, the one for ascertaining the temperature of the bath, the other for determining the flashing point. The thermo¬ meter for ascertaining the temperature of the water has a long bulb and a space at the top. Its range is from about 90° to 190° Fahrenheit. The scale (in degrees of Fahrenheit) is marked on an ivory back fastened to the tirbe in the usual way. It is fitted with a metal collar, fitting the socket, and the part of the tube below the scale should have a length of about 3^" measured from the lower end of the scale to the end of the bulb. The thermometer for ascertaining the temperature of the oil is fitted with collar and ivory scale in a similar manner to the one described. It has a round bulb, a space at the top, and ranges from about 55° F. to 150° F. ; it measures from end of ivory back to bulb 2^". Note. — A model apparatus is deposited at the Weights and Measures Department of the Board of Trade. Directions for applying the Flashing Test. 1. The test apparatus is to be placed for use in a position where it is not exposed to currents of air or draughts. 2. The heating vessel or water-bath is filled by pouring water into the funnel until it begins to flow out at the spout of the vessel. The temperature of the water at the commencement of the test is to be 130° Fahrenheit, and this is attained in the first instance either by mixing hot and cold water in the bath, or in a vessel from which the bath is filled, until the thermometer which is provided for testing the temperature of the water gives the proper in¬ dication, or by heating the water with the spirit lamp (which is attached to the stand of the apparatus) until the required temperature is indicated. If the water has been heated too highly, it is easily re¬ duced to 130 9 by pouring in cold water little by little (to replace a portion of the warm water) until the thermo¬ meter gives the proper reading. When a test has been completed, this water-batli is again raised to 1309 by placing the lamp underneath, and the result is readily obtained while the petroleum cup is being emptied, cooled, and refilled with a fresh sample to be tested. The lamp is then turned on its swivel from under the apparatus, and the next testis pro¬ ceeded with. 3. The test lamp is prepared for use by fitting it with a piece of flat plaited candle wick and filling it with colza or rape oil up to the lower edge of the opening of the spout or wick tube. The lamp is trimmed so that when lighted it gives a flame of about 0T5 of an inch diameter, and this size of flame which is represented by the pro¬ jecting white bead on the cover of the oil cup is readily maintained by simple manipulation from time to time with a small wire trimmer. When gas is available it may be conveniently used in place of the little oil lamp, and for this purpose a test- flame arrangement for use with gas may be substituted for the lamp. 4. The bath having been raised to the proper tempera¬ ture, the oil to be tested is introduced into the petroleum cup, being poured in slowly until the level of the liquid just reaches the point of the gauge which is fixed in the cup. In warm weather the temperature of the room in which the samples to be tested have been kept should be observed in the first instance, and if it exceeds 65° the samples to be tested should be cooled down (to about 60°) by immersing the bottles containing them in cold water, or by any other convenient method. The lid of the cup, with the slide closed, is then put on, and the cup is placed into the bath or heating vessel . The thermometer in the lid of the cup has been adjusted so as to have its bulb just immersed in the liquid, and its position is not under any circumstances to be altered. When the cup has been placed in the proper position, the scale of the ther¬ mometer faces the operator. 5. The test lamp is then placed in position upon the lid of the cup, the lead line or pendulum, which has been been fixed in a convenient position in front of the operator, is set in motion, and the rise of the thermometer in the petroleum cup is watched. When the temperature has reached about 66° the operation of testing is to be commenced, the test-flame being applied once for every rise of one degree, in the following manner : — The slide is slowly drawn open while the pendulum performs three oscillations, and is closed during the fourth oscillation. Note. — If it is desired to employ the test apparatus to 200 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 6, 1379. determine the flashing points of oils of very low volatility, the mode of proceeding is to be modified as follows : — The air-chamber which surrounds the cup is filled with cold water, to a depth of 1^ inches, and the heating vessel or water-bath is filled as usual, but also with cold water. The lamp is then placed under the apparatus and kept there during the entire operation. If a very heavy oil is being dealt with, the operation may be commenced with water previously heated to 120°, instead of with cold water. SECOND SCHEDULE. Act repealed. Year and Chapter. Title. Extent of Repeal. 34 and 35 Yict. c. 105. The Petroleum Act, 1871. Section three, from “ and the term petroleum to which this Act applies ” inclu¬ sive to the end of the section. Section eighteen. i gispensiitjg Ukwopitdit. In order to assist as much as possible our younger brethren, for whose sake partly this column was established, considerable latitude is allowed, according to promise, in the propounding of supposed difficulties. But the right will be exercised of excluding too trivial questions, or re¬ petitions of those that have been previously discussed in principle. And we roould suggest that those who meet ivith difficulties should before sending them search previous number's of the Journal to see if they can obtain the re¬ quired information. [340]. Will any readers of the Journal kindly inform me if it would be right in making “ung. sulph. iodidi” to rub the iodide of sulphur with a little glycerine before mixing the lard, glycerine being a solvent for iodide of sulphur ? Inquirer. [341] , The following prescription was presented to me to-day. Will some of your readers kindly inform me what the first ingredient is ? — R Ung. Calcis Hydr. Alb . 3ij. 01, Amygd. Dulc, Aq. Calcis . aa § j. M. ft. ung. (Cream for the face). H. S. N. [342] . Would some reader kindly inform me the cause of my failure in making ung. plumbi subacetatis com- positum ? I strictly followed the directions given in the B.P., but in the course of a week or so, the ointment began to change to a pale orange colour. The jar in which it is kept is free from lead, but it being standing next to the iodine ointment jar I thought that might be the cause. Having thrown the first lot out I began again, this time isolating the jar, but with no better results? An Apprentice. The Introduction op Chloroform. Sir, —Referring to Mr. Brown’s note on the introduction of chloroform, 1 subjoin the following extract from my laboratory book : — 154 lbs. chloride of lime, 631 pints of wood naphtha. The above mixed with a sufficient quantity of water was distilled in a large still heated with steam and the product distilled with strong sulphuric acid and again distilled with carbonate of baryta and dried chloride of calcium. The purified product weighed 13 lbs. 2 oz. and was supplied to Dr. Simpson, of Edinburgh, early in November, 1847, having been prepared by myself at the end of October and during the first few days of November in that year, and was, I believe, the first chloroform ever prepared as a commercial article in this country. Subsequently I prepared large quantities from pure spirit of wine which was found to yield a larger and purer product. At the time in question I was an apprentice to Mr. George Simpson, of Kennington, the head of the subsequently well-known firm of Simpson, Maule and Nicholson, manufacturers of aniline dyes. 13, Curzon Street, W. E. N. Butt. Weights and Measures Act. Sir, — In the schedule of apothecaries’ weights abstracted from the London Gazette of the 15th ult. and published in the Journal (Aug. 23), p. 145, 1 observe the largest single measure of weight is 10 ounces, equal to 4800 grains. I am at a loss to understand why this is the case when the troy pound contains 12 ounces and the sets of cup-weights in general use have always had this— the troy pound — as their largest weight. And will the 12 ounce weight now become illegal, or will it still be a lawful weight as being the silversmith’s troy pound? I have not the late Act at hand, but I think the latter was legalized. When the subject was before the Council, in your report I noticed the above peculiarity, but thought it was a mis¬ print in the numerals 10 to 12, to which 1 had intended to draw attention. It had escaped my memory till now, when I again see the 10 ounce weight in print, with its equivalent in grains, which I think was not the case before. This new weight will be a decimal blunder and a reproach on the originators of the Act for having discarded the metric decimal system. Winchelsea. Wm. Martindale. The Health of the Drug Trade. Sir, — From frequent perusal of the Obituary in the Pharmaceutical Journal, and from other sources, my atten¬ tion has been drawn to the peculiar fact that nearly 80 per cent, of chemists and druggists die at an age when men are generally supposed to be in their prime, both intellectually and physically, and a considerable number even under that age, while very few reach the allotted span of three score and ten years. The subject seems to me to be of sufficient importance to warrant a short discussion on the matter in the Journal. The question naturally arises, what are the causes of this lamentable fact? can that odour which is so characteristic of a chemist’s shop be injurious to health ? The atmosphere of our shops must frequently be vitiated by the escape of gases from many drugs and chemicals, whose injurious qualities, overloading the normal impure atmosphere which is generally found in large towns, cannot improve the condition of the respiratory organs. In the absence of correct statistics as to the actual causes of death in each individual case, a just decision is imprac¬ ticable, but I have been led to believe that consumption and cardiac affections are the two principal agents at work in our ranks. Do these insidious enemies find a footing amongst us through any fault of our own ? Do the anxiety, the long hours, the constant deep attention which every druggist requires to devote to all the little minutije which go to make up his daily duties, and the want of that active exercise to the muscular system which is to be found in almost every other trade, induce towards an enervated nerve power ? This letter, I hope, will be the means of inclining some who are abler than I to give an explanation of the causes, so that those of our suffering brethren whose pale faces and degenerated nervous system may apply the remedy. Edinburgh. _ J. K. Nicol. “Inquirer.” — Under the circumstances you mention there may be a kind of acid fermentation set up, resembling lactic fermentation, but we are not aware that there would be any formation of valerianic acid. “ Country Apprentice.” — You are learning the business of a chemist and druggist as it is not unfrequently carried on in country districts. You are recommended to prepare for future eventualities by studying chemistry, botany and materia medica. September 13, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 201 NOTES ON SOME JAPANESE DRUGS. BY E. M. HOLMES, F.L.S., Cw'ator of the Museum of the Pharmaceutical Society. (' Continued from page 103.) HERBS AND LEAVES. Hakka (57) : — Mentha austriaca, Jacq.1? Fr. et Sav. yoI. i. p. 366. Syn. Mentha arvensis , L., var. Jcivanica, Bl.; Phar- macographia, p. 434, note 1 ; Mentha arvensis , var. vulgaris, Benth. Megusa, So mokou Zoussetz, vol. xi. tig. 27 ; Phonzou Zoufou, vol. xii. fol. 10. This drug consists of the dried herb. - The leaves are lanceolate and nearly glabrous, with a tapering base and with few short but sharp serrations. The taste is powerfully pungent and strongly resembles that of Mentha 'piperita. The oil, ho-wever, of the two plants is not identical, as ■shown by Fluckiger, since it does not give a fluores¬ cence when treated with nitric acid. *■ The leaves are probably used as tea by the Japanese. Mr. T. Christy informs me that he ex¬ perienced great relief when in China, in an attack •of sunstroke, by the application of the oil, which a Chinese doctor rubbed over his head. It produced a most profuse perspiration and tranquil sleep. . The Japanese peppermint plant has been attributed •to Mentha javanica, Bl., by Fluckiger and Hanbury ; but all the specimens of that plant which I have seen have the taste of Mentha viridis , L., not of Mentha piperita , L. In the So Mokou Zoussetz the figure of the Japanese peppermint plant exactly •corresponds to the drug ; but is by mistake referred to M. arvensis, var. vulgaris, Benth., which is quite a different plant, with leaves widest below, like those of M. arvensis, and a similar taste. All the speci¬ mens of M. Austriaca, Jacq., including a type speci¬ men, to which I have had access, have not the taste of peppermint. The plant yielding the Japanese peppermint oil must therefore be regarded as a yet unnamed form. In shape of the leaf and character •of the calyx it seems to approach most nearly to M. u Canadensis , but the leaves of that species, according to a living specimen of the hairy variety, kindly supplied by Professor Asa Gray, have a taste more approaching to pennyroyal. Kei-ning-soh (10) : — Digenea simplex, Ag. (Alg?e). This seaweed is of a dull green colour, having lost its original purplish red tint by exposure to air and heat probably. It is well known that all sea¬ weeds contain chlorophyll, the green colour of which in the case of red algce is hidden by a red colouring matter, phycerythrine, and in the black or olive algse by phycoplueine and pliy coxanthine. f By the action of fresh water and heat the colouring matter which conceals the chlorophyll is destroyed, and the presence of the latter becomes evident. From the quantity of sand and foreign matter pre¬ sent, the decoloration in this case would appear to be due to the action of the heat of the sun on a sandy shore, rather than to the effects of fresh water. King-ki-yo (15) : — Malm sylvestris, Lin. Syn. Zeni-aoi, So mokou Zoussetz, vol. xii. fig. 54. This drug consists chiefly of the leaves of this well-known plant mixed occasionally with fragments * Pharm. Journ. [3], vol. i., p. 682. t Millardet, Comptes Rendus, Feb. 22, 1869. Third Series, No. 481. of those of Althaea rosea, L. (Tachi-avi) and appa¬ rently also of Malva pulchella, Bernh. (Fuyu-avi). See So mokou Zouss., vol. xii. figs. 53, 55. Shisso (21): — Perilla arguta, Benth. ; Fr. et Sav., vol. i. p. 365 ; So mokou Zouss. , vol. xi. fig. 24 ; Phonzou Zoufou, vol. xii. p. 113 (calyx bad). Syn. Sissoo, Jakosju, Miq. Prol., p. 36. Shisso consists of the stems and leaves of the plant. The leaves are ovate, lanceolate, acuminate, the largest about two inches long by one inch broad, sharply serrate, and of a purplish tint underneath. Shisso blossoms in September. To-yak (17) : — Pleurogyne rotata, Griseb. (Gentian- aceoe) ; Swertia rotata, Thunb. FI. Jap., p. 115. Syn. Senburi, Toyaku ; So mokou Zoussetz, vol. iv. f. 54. This is a small plant, having a slight resemblance to centaury, but with pinkish-white flowers striped with purple, somewhat similar in size and shape to those of Ghlora perfoliata ; the leaves are linear- lanceolate, about one inch long and two or three lines broad in the middle. The taste is extremely bitter, like that of chiretta, and the odour hardly anyl To-yak flowers in October. This plant is interesting botanically on account of the stigma being prolonged downwards over the edges of the valves of the ovary. The corolla has also at its base little glands terminating in hairs. FLOWERS. Chacj-to-ko (13) Uncar ia Gcimbir, Roxb. (Cin- chonacese). Syn. Tiax-t'ang, Porter Smith, Chinese Mat. Med. p. 224. This drug consists of short portions of the slender stems half an inch to one inch in length and one to two lines broad, with one or two strongly recurved hooks. The whole is of a brown colour and has an as¬ tringent taste. These curious hooks do not consist, as described by Dr. Porter Smith, of the stipules, but of the stalk which bears the flower-heads. The flower stalks, as described in Bentley and Trimen’s ‘Medicinal Plants/ are furnished near the m iddle with a few bracts, beyond which the peduncle is more slender. After the fall of the fruit the portion of stem below the bracts elongates, hardens and forms a strong recurved hook by means of which the plant climbs. On some of the hooks the traces of the fall of the peduncle and bract may still be seen, on others, which have probably arisen from abortive inflorescences, there is no sign of them. It is probable that these hooks are also obtained from U.acida, Roxb., a plant which is used in the Malay Islands in the same manner. The hooks possess astringent properties, and a wine is made from them used for infantile diseases, according to Dr. Porter Smith. Neither of these species are mentioned in Franchet and Savatier’s work, and this drug may therefore be a J apanese importation from China. Biak-tau kah (52): — Amygdalus persical Syn. Too, Thunb. Flor. Jap., p. 199; T‘au, Porter Smith, Chinese Mat. Med. p. 168. These flowers evidently belong to some species of Amygdalits , and are called by Mr. Takemura “peach flowers.” They are apparently derived from some cultivated species, since the majority of the blossoms 202 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 13, i879v are partially double. Kali means flowers, and Tan or Too is a sort of generic name both in Japanese and Chinese for fruits of the peach kind, and Biak means white, according to Mr. Takemura, so that some variety of Amygdalus Persica with white flowers may be the source of Biak-tau-kah. The dried flowers however have a slight pinkish tinge. Thunberg mentions a variety of peach with simple white flowers called “Sato Momu.” Hoh-oh (32) : — Typha japonica , Miq. Syn. P’u hwaug, Porter Smith, Chinese Mat. Med., p. 224. This yellow powder consists of the pollen. It is inflammable, like lycopodium, but shows a tendency to agglomerate into lumps. Dr. Porter Smith states that in China it is obtained from Typlia Bungeana, and is used as a desiccant, astringent, styptic and sedative remedy, and also that it is made into a confection for external and internal use. It has neither taste nor odour. The Chinese character, translated P’u liwang, is exactly the same as the Japanese character, Hoh-oh. P’u or Hoh being the name of the plant, and Hwang or Oh meaning yellow. The spikes are said by Miquel to be used as a styptic. The only species mentioned by Fr. and Savatier as a native of Japan is T. japonica, although the Phonzou Zoufou, vol. 33, figures two which are supposed to be (fig. 19 Kobo) T. japonica, Miq., and (fig. 29, Rindziakou) T. angustifolia, L. In t’ying (31): — Artemisia capillaris, Tliunb. Syn. Intsjin; Fki Iamogi and Kawara Iamogi; Ksempf. Amoen., p. 897 ; Iamma Intsjin ; Thunb. FI. Jap., p. 30.9; Kawara Yomogi, So mokou Zouss. vol. xvi. fig. 27 ; Phonzou Zoufou, vol. xiv. fol. 2. This consists of the flower heads, and bears some resemblance to Levant santonica, than which the flower heads are smaller. The paleae are oval, obtuse and membranous, about six in number, and closely imbricated. The scales separate more readily than in santonica, and are mixed with the flower heads, as well as portions of the capillary leaflets. The taste is slightly pungent and aromatic, but not bitter. The plant flowers in August, and is not an inland, but a littoral species. Set-kotz-mo kah (22) : — Sambucus nigra, L. Syn. Niwa Toka, Tonga, Kiempf. Amcen. fasc. v. p. 787 ; Thunb. FI. Jap. p. 126. This drug consists of the flowers freed from the stalks, and dried just before expansion. They are of a clark brown colour, and not to be compared in quality with those dried in this country. The species of Sambucus is given on Mr. Takemura’s authority. Thunberg states (p. 126) that neither this species nor S. canadensis, L., matures fruit in Japan, and are therefore evidently not natives. Probably for this reason S. nigra is omitted by Fr. and Savatier, in their Enum. PI, Jap., p. 198. Sbin-ee (4) : — Magnolia Yulan, Desf. Syn. SiN-if Porter Smith, Chinese Mat. Med., , P* 142. Shin-ee consists of the very young flower buds of a this tree. The two outer scales are smooth, and the- two inner are covered with a dense coat of silky hair ; when these are removed the flower in a very rudimentary state may be traced. The taste is bitter- and aromatic ; of odour there is almost none. According to Dr. Porter Smith, a kind of snuff made of the powdered drug was formerly used in China. It is probably imported from that country. . FRUITS AND SEEDS. Gobo see (25): — Arc'.ium Lappa, L. (Composite). Syn. Lappa Major, Gaertn, Fr. et Sav. vol. i.. p. 262; Gobo, LTmma Busuki ; Koempf. Amcen.. p. 828 ; Thunb. FI. Jap. p. 304 ; Kouma tori bokoudsi, Phonzou Zoufou, vol. xv. fol. 23 Gobo, So mokou Zoussetz, vol. xv. fig. 33. The small fruits of this plant are about a quarter of an inch long, linear, somewhat flattened, about one line wide at the apex, and tapering thence to the base. The taste is bitter and slightly pungent. They are of a greyish brown colour, speckled with minute black dots. In Japan the burdock is cultivated as a vegetable under the name of gobo, and the root is used to put in soups. For this purpose it is taken up before the flowering stem appears (Koempfer). It is probably identical with the Arctium edule of Siebold. I have- no information concerning the uses of this seed in Japan. Rather more than one hundred years ago- they were used in this country in doses of one- drachm as a diuretic and aperient, and the root is still used by herbalists in this country as an alterative in skin diseases and syphilis. The Japanese character for “ see ” is exactly the same as the Chinese for “ tsze,” and stands for “ seed ” in both cases. Gome see (6) :— Schizcmdra nigra, Max. Syn. Madzi-ssa, Maximowicz, Diag. PI. Nov. Jap., et Mandsh. Dec. x. p. 370. This drug consists of reddish or black wrinkled fruits about the size of a pea, each containing two* flattened kidney-shaped seeds. The seeds have a minutely tuberculatecl testa, and contain an oily albuminous nucleus. The berry is sweetish and mucilaginous, and the kernel of the seed has a slightly bitter oily taste, but no odour. Gomichi is given by Franchet and Savatier as the Japanese name for Schizandra Chinensis , Baill. That plant, however, has smooth seeds. Maximowicz, in the work above quoted, states that S. nigra is at once distinguished from all the other species of this genus by the black berries with a glaucous bloom and the tuberculated seeds. S. nigra is a climbing plant, clothing the pine and fir trees with its foliage in alpine woods, especially those of the Kundslio san chain of mountains in central Kiusiu. The fruit is ripe in October, and is considered edible. The Chinese character Wu-wei-tsze, which, ac¬ cording to Dr. Porter Smith, is the Chinese name for the fruits of Kadsura Cliinensis ( Schizandra Chinensis, Baill.), is identical with the Japanese character above translated, gome-see, and means in both languages five-tasted seeds. The berries abound in a viscid mucus.* Go-siu-ju (50) : — Evodia rutcecarpa, Benth. Syn. Boymia rutcecarpa, Sieb. et Zucc, vol. i. p. 50 ; Go-sju-ju ; Kawa hasikami, habite kobtjra, * Porter Smith’s 7 Chinese Materia MedicaJ p. 126. September 13, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 203 Fr. et Sav. vol. i. pp. 71, 72 ; Phonzou Zoufou, vol. lxx. fol. 11. Tins drag consists of the pedicels and very young fruits of the plant. The stalks are cylindrical, about one line in diameter, covered with down consisting of minute spreading hairs. The fruits are reddish brown, deeply pitted with oil glands, varying in size from a swan shot to a small pea, and divided half way down into five segments. The taste is decidedly rutaceous and pungent, although not exactly that of rue. The odour is very similar, but less powerful. Possibly the young fruits of E. glauca, Miq., are -also used, since “koshiou you” is given as the Japanese name for this species in ‘ Phonzou Zoufou, vol. lxx., fol. 10. Boymia rutcecarpa is a handsome shrub, six to ten feet high, and frequently cultivated in the south of -Japan for its beauty. The flowers, which are dioe¬ cious, are produced in May and June. By the Japanese doctors of the Chinese school this drug is considered to be a most valuable remedy, and is used as a purgative, emmenagogue, sudorific and stimulant, and, in fact, seems to possess properties very similar to those accredited to the common rue. Kee-kock (45) : — Citrus fusca, Lour. 8yn. Chi-koh, Porter Smith, Chin. Mat. Med. p. 66; Cay Baong, Chi xac, Chi rest, Lour. FI. Oochinchinensis, p. 467. This drug consists of what appears to be fruits gathered when unripe, and then cut in half and dried. The rind is thick and externally of a dark or brownish black colour, internally whitish ; the dried pulp is blackish. The taste is bitter and the odour very faintly that of orange. The drug is identical with that presented to the Museum of the Pharmaceutical ■Society by Dr. Porter Smith under the name of Citrus fusca. The Japanese character is not, however, abso¬ lutely identical with the Chinese one given by Dr. Porter Smith. The Japanese character translated “ kee,” and the Chinese “ chi,” is identical, but the one translated u kock ” is not identical in appearance, although Mr. Takemura assures me it is identical in meaning with the Chinese character for “ koh.” Loureiro, however, gives as a synonym “ chi xac,” which more nearly approaches the Japanese name in sound. Thunberg (FI. Jap., p. 294) gives the very similar name “ kikokf” as a synonym of Citrus trifoliata, L. Citrus fusca is supposed by the Chinese to possess cooling, deobstruent and stomachic properties. Ketz-may see (49): — Cassia Tora, L. (Leguminosm). Pharm. Journ. [3], vol. vii. p. 350. Syn. Kiueh-ming-tsze, Porter Smith, Chinese Mat. Med. p. 54 ; Keue-ming tsze, Hanbury Science Papers, p. 231 ; Tagaray-elley, Ainslie Mat. Med. vol. ii. p. 405 ; Ketsumei, Miq. Prol. p. 243 ; Yebisugusa, So mokou Zoussetz, vol. viii. fig. 1; Phonzou Zoufou, vol. xviii. fol. 12. The seeds, which are to be seen in most collections ■of drugs from India or China, are of a dark brown colour and polished, about two lines long, quad¬ rangular, oblique at both ends, but blunt at one end and pointed at the other, and having two very faint stripes on opposite sides. Dr. Porter Smith states that in China they are used both externally and internally for sore eyes -and for herpetic or furunculoid sores. In India, according to Udoy Chand Dutt (‘Hindu Mat. Med.,’ p. 156), the seeds are dipped into the juice of Euphorbia neriifolia and made into a paste with cow’s urine for keloid tumours ; or equal parts of them mixed with the seeds of Pongamia glabra and a fourth part of the root of Tinospora cor difolia are made into a paste for ringworm. Fr. et Savat. ‘FI. Jap.,’ vol. i., express the opinion that neither this plant, nor C. occidentalism nor C. Foplioragrow spontaneously in Japan. The seeds of C. Tora are therefore probably imported into Japan. The J apanese and Chinese characters for Cassia Tora seed are identical, although in Chinese the word is pronounced, according to Dr. Porter Smith, Kiueh- ming-tsze. Kieu-ess (44) : — Allium senescens, Thunb. , FI. Jap. p. 132. Syn. Yama-rakkyo, Phonzou Zoufou, vol. xlv. fol. 13; So mokou Zouss. vol. vi. fig. 37; Allium japonicum, Regel., Fr. et Sav. vol. ii. pt. 1, p. 77. These seeds have the appearance of ordinary onion seeds. They are black and angular, without odour, and have only a very slight alliaceous taste. In China they are used for various fluxes and for haemorrhages. In ‘ Loureiro FI. Cochin Chinensis ’ the term kieu is applied to three species, A. triquetrum , L., A. odorum, L., and A. angulosum, L. (To be continued.) LIQUID PREPARATIONS OE L ACTU CARIUM. * BY JOSEPH L. LEMBERGER. In accepting the query to give a formula for a con¬ centrated liquid preparation of lactucarium, from which can be made the syrup, tincture, or other preparations, the writer is fully aware of the difficulty usually met with in making the lactucarium preparations occasioned by the caoutchouc principle always present in this as well as most, if not all, the products from the lactescent plants ; in order to overcome this difficulty petroleum ben- zin has been found the most practical, being efficient and cheaper than most of the solvents for caoutchouc. It was found that by beating the lactucarium in an iron mortar until it is well crushed it separates into layers, or plates, or very coarse granulation (according to its degree of dryness), as the nearest possible approach to comminu¬ tion, it being impossible to powder it without the addition of sand or other foreign substance. Thus treated and macerated with benzin the caoutchouc principle is readily dissolved and the lactucarium is fitted for treatment with other menstruum. After numerous experiments the fol¬ lowing is offered as a practical working formula for the — Fluid Extract of Lactucarium. Take of — Lactucarium . 16 troy ounces. Petroleum benzin deodorized . 32 fluid ounces. Diluted alcohol a sufficient quantity. Beat the lactucarium thoroughly in an iron mortar, then introduce it into a wide-mouth bottle of about three pints capacity, adding the benzin, corking tight, and allowing it to macerate, with frequent agitation, for twenty-four hour3 ; then let it rest about twenty-four hours, or until the lactucarium subsides and the benzin solution becomes clear or nearly so ; then, haying de¬ canted the benzin solution, transfer the lactucarium to a stone or glass slab or other similar vessel, spreading it as thin as possible, allowing it to remain in this situation until completely dry (at least twenty-four hours); then * Prom the ‘ Proceedings of the American Pharma¬ ceutical Association,’ 1878. 204 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 18, 197»- rub it up in an iron mortar with an equal bulk of clean sand; next introduce it into a cylindrical percolator, first prepared with a disc of flannel and a thin layer of sand, pack lightly and add sufficient diluted alcohol to cover several inches, and after closing the outlet with a cork or otherwise allow it to macerate twenty-four hours; then percolate to exhaustion, reserving the first four fluid ounces. By means of a still reclaim the alcohol and evaporate the residue in a water-bath to ten (10) fluid ounces, mixing this with the reserved percolate and filter, adding sufficient diluted alcohol to wash the filter and remaining residue until the product weighs sixteen troy ounces. With this fluid extract you can readily make — - Tincture of Lactucarium, as follows : — - Take of — Fluid extract lactucarium . . 1 troy ounce (^j). Diluted alcohol . q. s. for f 5viij. A fluid drachm representing 7h grains. For — Syrup of Lactucarium , Take of — Fluid extract of lactucarium . 1 troy ounce (3j). Simple syrup . q. s. for f§xvi. A fluid drachm representing 3§ grains. SMILAX GLAUCA * BY JOHN BLANKENHOKN, PH.G. With the view of ascertaining the constituents of the long cylindrical light-coloured rhizome, a sample furnished by Professor Maisch was submitted to the following treatment : — Two pounds of the ground rhizome were exhausted by a mixture of two parts alcohol and seven parts water, and the percolate concentrated at a low tem¬ perature. After cooling, the whole was treated with acetate of lead until no further precipitate occurred, then filtered. The filtrate, thus deprived of nearly all colour¬ ing matter, was subjected to the action of sulphuretted hydrogen, in order to free it from lead, and again filtered The sulphide of lead after thorough washing with water, was treated with boiling alcohol, filtered, the filtrate con¬ centrated and spread on glass to scale ; attempts were made at crystallization, but without success. The precipitate with acetate of lead was thoroughly washed, suspended in water and decomposed by sulphu¬ retted hydrogen, then filtered. The liquid was now evaporated ; at first the colour was dark-red, and the colour of blue litmus was changed to red. Both charac¬ ters became greatly augmented as the process of evapora¬ tion went on. A small quantity diluted with water gave the following reactions : — With alkalies, the colour was deepened ; with ferric chloride, a greenish-black colour ; with Mayer’s test, a yellowish colour ; with subacetate of lead, gelatinous precipitate; with solution of gelatin, gelatinous precipitate. These reactions showed the presence of tannin. After concentration to a small bulk, and setting aside for a few days, crystals of what appeared to be a magnesium compound were deposited. The filtrate from these crystals was now treated with twice its bulk of alcohol, filtered, and then found to be free from tartaric, citric and malic acids. After having been treated with ammonia and solution of alum, no pre¬ cipitate was abtained with salts of iron, calcium, mercury and copper, but lead acetate occasioned a white precipitate. The sulphide of lead remaining after the decomposition of the lead precipitate by IBS was thoroughly washed and treated with boiling alcohol, filtered and allowed to evaporate spontaneously, then spread on glass to scale. The product was of a beautiful red colour, perfectly trans¬ parent, taste slightly bitter, wholly soluble in alcohol and partially so in water, but insoluble in ether and chloro¬ form. Ammonia dissolved it, deepening the colour, and on the addition of an acid the colour was discharged. A small quantity dissolved in water with the aid of alcohol, * From the American Journal of Pharmacy, June, 1879. and agitated, produced copious foaming, and was precipi¬ tated by acetate of lead. On digesting with water, a portion was dissolved, and on being evaporated was left behind as a red transparent mass ; the portion insoluble in water dissolved in alcohol, and after evaporation left a brown transparent mass, both portions foaming on being agitated with water. The filtrate, after precipitation by acetate of lead, left,, on evaporation, an amorphous dark red-brown mass, with a tint of green, and perfectly transparent ; the taste is very bitter and slightly acrid. It is freely soluble in alcohol and water, insoluble in ether and chloroform. With strong sulphuric acid it produces an orange-red coloration chang¬ ing to brown. The presence of starch, sugar, albumen, resin and pectic compounds was also incidentally noticed. CHEMICAL NATURE OF PEPTONE.* BY R. HERTH. Peptone was prepared by digesting the finely powdered white of egg from 50 to 60 boiled eggs for 24 to 30 horns with a 1 per cent, solution of phosphoric acid, then treat¬ ing with hot water, and digesting with 4 litres of a 0'65 per cent, solution of phosphoric acid and 40 c.c. of a clear pepsin solution which had been purified by dialysis, and was free from calcium and chlorine. When the liquid had become clear (after 5 or 6 hours) it was heated on a sand-bath, and freshly precipitated lead carbonate was added to neutral reaction. The small quantity of lead present in the filtrate was removed by means of sulphur¬ etted hydrogen; the liquid was again filtered, concentrated on the water- bath, precipitated, and digested with con¬ centrated alcohol, again dissolved, and the liquid repre¬ cipitated. This process was repeated three times. The precipitated lead phosphate was quite white, showing the absence of sulphide. A concentrated solution of the pep¬ tone thus prepared gave a slight turbidity with potassium ferrocyanide and acetic acid. Various methods of purifica¬ tion were employed, but the reaction with ferrocyanide was invariably obtained. Whether this reaction is due to a trace of unchanged albumin in the peptone, is regarded by the author as a yet unsettled point. In the original paper a number of analyses of the pep¬ tone are given, both of the substance prepared as described above and of the various precipitates obtained by fraction¬ ally precipitating with alcohol and with lead acetate and ammonia. These analyses show that peptone is not a mixture, but a distinct chemical compound. The percent¬ age composition of peptone appears to be identical with that of albumin obtained from egg white. The author regards albumin as a polymeride of peptone, and the change brought about by the action of pepsin solution in albumin as analogous to the action of heat in effecting the change of paraldehyde into vapour of aldehyde. A solution of peptone is not precipitated by many o£ the salts of heavy metals, by acids, or by boiling. Alcohol, mercuric chloride, and lead acetate, followed by ammonia,, cause precipitates in solutions of peptone. The statement of Adamkiewicz (Die Natur unci Ncihrwerth des Peptons, Berlin, 1877) that those reagents which precipitate egg albumin also precipitate peptone is regarded by the author as incorrect. Peptone forms compounds with metals, analogous to those formed by albumin, but the compounds of peptone are generally soluble, while those of albumin are insoluble. The author claims for his process of preparing peptone that it ensures a complete or almost complete conversion of the albumin into peptone, that it entirely removes syntonin, and that the absence of salts of the alkaline earths is also ensured. These salts are very difficult ta remove from solutions of peptone. The amount of ash in the peptone prepared by the author’s process is not more than 1 per cent. * From the Journal of the Chemical Society, August* 1879 (Wien. Akad. Ber. [ii], 76, 986-890). September 13, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 205 Ske papaqutual Jonptl - ♦ - SATURDAY, SEPTEMBER 13, 1879. PROCEEDINGS UNDER THE PHARMACY ACT. Although the present month is to a great extent devoted to holiday making by pharmacists, as well as others who have opportunity to do so, it has, as yet, not been altogether wanting in incidents of im¬ portance and interest to those engaged in this business. As will be seen from our report of legal proceedings this week, a step has been taken towards repressing the unlawful trade in scheduled poisons without the labels required by the Pharmacy Act, stating the name and address of the seller, and bearing the word “poison.” The prosecution was instituted by direction of the Council of the Phar¬ maceutical Society in reference to the illegal sale of laudanum, a practice that has frequently been cause of complaint among chemists and druggists, besides being one that is extremely prejudicial to the well¬ being of the public. In some parts of the eastern counties, as many of our readers are aware, the habitual consumption of opium, in the crude state and in the form of laudanum, is carried on to a degree that is almost incredible, and the demand for the drug or preparations of it is so considerable that they are to be obtained at many of the small grocers’ or other village shops throughout the district. Of course the trade thus carried on by persons who are not registered in conformity with the provisions of the Pharmacy Act involves a breach of the 15th section of that Act, and renders the persons selling opium or any of its preparations, such as laudanum, liable to the penalty therein prescribed. It is there¬ fore competent for the authorities of the Pharmaceu¬ tical Society, as charged with the execution of the law regulating the practice of pharmacy, to institute proceedings against offenders under this 15th section of the Act ; but in the great majority of cases the persons so offending by the sale of laudanum or opium belong to the class of very small shopkeepers in villages, and owing to the difficulty as well as the expense of obtaining information and proceeding against offenders in distant parts of the country it has been found undesirable to have recourse to this mode of procedure as a general plan. The illegal sale of opium and laudanum in the manner we now refer to is no doubt to some extent an interference with the privileges which are by law accorded to the legally qualified chemist and druggist in virtue of his conforming to those require¬ ments as to education and examination which are held to be necessary for the interests of the public. The sale of these drugs by unqualified persons de¬ prives those who have a right to deal in them of some business they might otherwise have, and of the profits arising from that trade. It may also be the case that the sale of these drugs will eventually lead to the usurpation of other parts of the business properly belonging to the chemist and druggist. In such cases, when clearly made out, it would un¬ doubtedly be proper to enforce the provisions of the 15th section of the Pharmacy Act as a means of protecting the interests of the pharmaceutical body, and with that object to make use of the funds and resources of the Pharmaceutical Society. But this protective application of the Act being only in¬ cidentally a result of the provisions for securing the main object of protecting the public interests, and the petty sale of laudanum, etc., being more directly pernicious to the public health than to the trade interests of chemists and druggists, it is more fitting that its prosecution should be conducted under the 17th section of the Pharmacy Act. It is in that section declared to be unlawful to sell poison with¬ out a distinct label having the word “ poison ” and the name and address of the seller. This is a pro¬ vision made for the safety of the public, to warn people against the dangerous character of certain drugs or preparations, and designed, in case of their criminal misuse or of accident, to furnish a clue to the dis¬ covery of the person by whom they have been misapplied. It is entirely a provision for the pro¬ tection of the public ; it is fully sufficient for that purpose, and as the capability of enforcing it is not confined to any particular body or set of individuals any person can be the prosecutor in a case of the kind now referred to. One of the devices by which it has been sought to make this illegal sale of poison evade the provision of the Pharmacy Act has been to affix a label bearing the name of some registered person, but the present case at Horncastle serves to illustrate the insuffi¬ ciency of this proceeding to protect the seller against conviction, and it is to be hoped the decision of the magistrates will be a timely warning to others en¬ gaged in similar ways. It is also evident that the plea of selling with a patent medicine stamp will not avoid conviction, and that if some trouble be taken to obtain definite evidence of this mode of selling laudanum or other preparations, as suggested by Mr. Hampron, it may soon be demonstrated that unregistered persons adopting this plan are liable nevertheless as con¬ travening the law. THE WEIGHTS AND MEASURES ACT. Among other matters that have attracted attention within the past few weeks is the new Act in reference to weights and measures. Some uneasiness is ex¬ perienced in regard to the carrying out of the provisions of this Act, but we believe there is really no reason to fear vexatious interference. We understand that no arrangements have yet been made for affixing a Government mark of verification to the glass measures used by chemists. An idea seems to prevail that all weights and measures must have the stamp of the particular dis- 206 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 13, i87». trict in which they are used. This is clearly an error and should he corrected. The Act does not thus needlessly interfere with traders, hut it specially provides that a -weight or measure stamped hy a duly appointed authority shall he deemed legally authorized for the whole kingdom irrespective of districts. FORMATION OF A PHARMACEUTICAL SOCIETY IN CONSTANTINOPLE. Although the regeneration of Turkey is not a very hopeful subject, the pharmaceutical portion of the Turkish community appear to be making an effort to raise themselves more nearly to the position occupied hy followers of the same calling in other lands. Nor have they taken action a minute too soon, for never was pharmacy at a lower level in Turkey than now. It is true that the cumbrous alembic and pan of former times have disappeared, but they are not replaced by the glass retort or the porcelain capsule ; neither is it to the delicate modern balance or graduated burette that the old weighing machine and rude measuring vessels have given way. The laboratory as a rule is absolutely wanting and the shelves are now filled with foreign specialties, drugs which were originally derived from the country now coming back to it in the shape of preparations from Paris, Vienna and other places. This appears to be attributed to a great extent to the law regulating the practice of pharmacy, -which sets no limit on the number of pharmacies, and whilst pharmacists are placed by it under severe restrictions as to the sale of poisons and active medicines it is alleged that the sale of such articles by lower classes of traders is winked at. On the 9th of June last a number of pharmacists met in the room of the Imperial Society of Medicine in Pera and agreed to form a “ Societe de Pharmacie de Constantinople,” which should have for its ob¬ jects to raise the level of pharmacy in Constantinople and other cities of the Ottoman empire, to assist the authorities in all scientific questions within its com¬ petence, and the defence of professional interests. After the election of officers, — C. Bonkowski Effendi being chosen the first President and J. Zanni the General Secretary, — the statutes of the Society were agreed to, and a copy ordered to be sent to Munif Effendi, Minister of Public Instruc¬ tion, with a request for his approbation and pro¬ tection of the Society as a work of public utility. The President was also requested to put himself in communication with other societies abroad asking for their advice and assistance. The second meeting was attended by the Minister of Public Instruction, who assured the Society of the sympathy of the Imperial Government, and, what was quite as important, the Secretary was able to state that one hundred and forty pharmacists had expressed their desire to become foundation members. Several papers were read, and it was decided to make arrangements for the publication of the pro¬ ceedings ; the outcome has been the appearance of the first number of a journal, which is to be supplied free to the members. Steps have also been taken for the foundation of a library and museum, and in order to bring the literature of other countries within the reach of the members generally, committees of gentlemen acquainted with the respective languages have been appointed to prepare reports on the salient features of the journals and other books received, to be read at the weekly meetings. It is a somewhat “far cry” from London to Con¬ stantinople, but we feel justified in assuring the members of the new Society that they have the hearty sympathy of British pharmacists in their efforts to improve the status of their common calling in the East. THE METRIC SYSTEM. Those of our readers who are interested in the progress of the metric system will be glad to learn that the subject came under the consideration of the British Medical Association during its recent meet¬ ing in Cork, and that, on the motion of Mr. Ernest Hart, a committee was appointed to consider and report whether it would be desirable to adopt the metric system in medicine in Great Britain and Ireland, and whether the British Medical Association should by any means, and if so by what, facilitate its introduction. The Committee consists of Dr. Clifford Allbutt, Dr. Lauder Brunton, Dr. A. Carpenter, Dr. Farquharson, Dr. T. Frazer, Dr. Harvey, Dr. Quain, Dr. Sieveking and Mr. Ernest Hart. In introducing the subject Mr. Hart said the metric system had made great progress, and now the profession in Great Britain was to some extent isolated, since foreigners were cut off from following the results of work carried out by their English colleagues through not being able to follow the British system of notation, while the British medical man could not follow the system now adopted in foreign countries. Dr. Seguin, in supporting the motion, gave an account of the “ brilliant metric campaign” in America, which has resulted in the adoption of the metric system in many public de¬ partments and by several medical societies, including the American Medical Association. In the new edition of the ‘ National Dispensatory,’ by Stills and Maisch, the metric weights are given second ; but Professor Maisch states that had he not been hindered he would have given all the weights and measures of this book either preeminently or ex¬ clusively in the metric language. EXEMPTION OF PHARMACEUTICAL CHEMISTS FROM JURY SERVICE. As the lists of persons liable to serve on juries are now being exhibited at the doors of all places of public worship, we take the opportunity of suggest¬ ing to pharmaceutical chemists the advisability of examining them. If their names have been impro¬ perly included it is necessary, in order to secure exemption from service, to give proper notice to the parish authorities within the specified time. September is, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 207 jprooimjiat iCransautions. LEICESTER CHEMISTS’ ASSISTANTS AND APPRENTICES’ ASSOCIATION. A lecture was delivered by Mr. S. F. Burford, on Thurs day evening1, August 14, before the above Association on ■“The History of Chemistry,” being the opening lecture of a course on chemistry. The lecturer said he thought it advisable in commenc¬ ing a series of classes on chemistry to give the members a general view of the history of chemistry from the earliest times. Quoting from the works of Frankland and Fownes for a good definition of the term chemistry and what was embraced therein, and the various laws which governed it, he went on to say that as far as could be learnt the origin of chemistry was lost in antiquity. Tubal Cain has been considered its founder, as he was conversant with the art of working in metals, but it was more likely that it took its rise among the early Egyptians. Thoth or JEthotis is the first Egyptian of whom men¬ tion is made as having been a chemist. Siphoas, sur- named Hermes by the Greeks, 1900 B.C., wrote forty-two books on philosophy, and from him chemistry was en¬ titled the Hermetic philosophy. The priests of Egypt, though they studied chemistry with considerable success, veiled their discoveries in mystery and hieroglyphics, so that their studies were lost to others. Nevertheless they seemed to have been well acquainted with the arts of making imitations of precious stones, working metals, etc. They were also conversant with the uses of nitrate of silver, which they employed to write on linen, evidence of which is to be found on the linen bandages around mummies. From the Egyptians the Israelites gained some knowledge of chemistry, and Moses must have been acquainted with it to enable him to dissolve the Golden Calf, which Stahl states was rendered soluble in water by means of liver of sulphur. During several centuries the study seemed to have been neglected till it appeared among the Arabians. In the ninth century Gebber, of Thus, in Persia, wrote three excellent books on chemistry; and so this study passed through the various stages of superstition and alchemy when men spent best part of their lives in the vain effort to trans¬ form the baser metals into gold and to discover the elixir of life. Even as late as 1825 the study of alchemy was pursued in England. The lecturer then reviewed in detail the various studies •of Lavoisier, Boyle, Locke, Brandt, Glauber, Roger Bacon, Leibnitz and Newton with their discoveries, goingminutely into the studies of Priestley, Faraday, Davy, to our own time, passing to the statements of Lockyer and the an¬ nouncement that Meyer had decomposed the element chlorine. The lecturer concluded by remarking that it was im¬ possible to glance around without seeing the benefits which every day accrue from the study of chemistry in the arts, manufactures, and in medicine, contributing to the health and happiness of the human race. The human mind cannot depict in its entirety the mag¬ nificent future of chemistry, but overwhelmed with the vastness which everywhere surrounds them, the noblest, purest minds return from contact with this awful infinity, and like the Angel in Jean Paul Richter’s •dream can only find relief in tears. At the conclusion of the lecture, which was listened to with marked interest, a vote of thanks to the lecturer was proposed by Mr. J. J. Edwards, seconded by Mr. Brampton and carried. MEETING OF CHEMISTS AND DRUGGISTS AT LIVERPOOL. A general meeting of the chemists and druggists of Liverpool was held on September 1, at the Royal Institu¬ tion, to resist the tendency to reduction of prices of pro¬ prietary articles. The chair was taken by Mr. A. Red- ford, President of the Registered Chemists’ Association. The good attendance showed the interest generally taken in the subject of the meeting. Communications were received from Messrs. C. Jones, Birkenhead; Greenall, Flint; Stanton, Rock Ferry; Barton and Williams, approv¬ ing the object of the meeting. The Chairman, Messrs. Shaw, Symes, Edisbury, Marson, M. Hughes, Turner, T. F. Abraham, Peet, Woodcock, Warhurst, Wright, Hocken, Paddock, Wharrie, Mackin- lay, Fletcher, Lloyd of Garston, and Messrs. Ball, Fore and Cooke, of Birkenhead, spoke with only one exception strongly against departing from makers’ advertised prices. It would inevitably lead to reduction in other departments of the business, and the opinion was strongly expressed that its effects would be disastrous, and that no sufficient reason at present existed to justify its adoption. The meeting adopted resolutions affirming the determination of the trade generally to maintain the uniformity attain¬ able by adhering to the makers’ advertised retail prices. rorwMttgs of Jsrirntijk poddies. BRITISH PHARMACEUTICAL CONFERENCE. [Continued from 'page 197). The next paper read was on — The Polarimeter and its Use in Pharmacy. BY CHARLES S1AIES, PH.D. For the development and perfecting of the science and practice of pharmacy, various instruments and forms of apparatus have from time to time been introduced ; it is not, however, to a new instrument that I am desirous of directing your attention, but to one which, although it came into existence some sixty years ago, has not in this country and in recent times received the amount of attention which it appears to me to merit, nor has it been applied to many purposes for which it seems calcu¬ lated to be of use. In its variously modified forms it is known as the polariscope, saccharimeter, polaristrobometer and polari¬ meter, men of science and manufacturers having pro¬ gressively introduced such alterations as appeared desirable for the better accomplishment of the object aimed at, viz., polarizing a ray of light and accurately measuring the amount of rotation produced in that ray when it is passed through an optically active liquid or liquid possessing rotatory power. My chief aim in bring¬ ing this subject before the members of the Conference is to offer for their consideration some of my experience and to render familiar, as far as I am capable of so doing, this instrument which has hitherto been dealt with chiefly in works of a purely scientific character, and which has been regarded by the working pharmacist as outside his province and useful only in the prosecution of abstract science. That too little is known of its general applica¬ tion has long been my opinion, but this was brought more forcibly to my mind in June of last year, when (in com¬ pany with Mr. Greenish) I paid a short visit to M. Petit, of Paris, and found him using the instrument of Laurent practically in his business for determining the purity of certain alkaloids, etc., and was assured by him that the results obtained were as trustworthy as those of the most accurate chemical analysis. To accomplish the object already mentioned and render the subject thoroughly clear to those who have not previously given any atten¬ tion to it, I may be allowed to say a few words on polarized light. A ray of common light, as you will be aware, is assumed to consist of vibrations in the ethereal medium or luminiferous ether occurring in two directions at right angles to each other, and by interference the primary planes are constantly shifting. If, however, these two 208 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 1 3 879. vibrations are split up by the absorption, reflection or dispersion of one, or by refraction of both, the remain¬ ing portion, or one of the portions separated, constitutes a ray of polarized light and as the phenomenon of inter¬ ference ceases it vibrates in one plane only. If now this is made to traverse certain media, the plane no longer remains in this direction, but is deviated either to the right or left, and is caused to rotate or assume a spiral form, and it is as already stated for the measurement of the amount of rotation caused by different fluids when so traversed that the polarimeter has been constructed. The property possessed by quartz of circularly polariz¬ ing a ray of light was known to Sebeck and Arago, but it is to Biot in 1818, that we owe the discovery of the property possessed by many fluids of rotating a ray of plane polarized light. He states that this occurred to him accidentally whilst examining crystallized laminae, placed in highly refractive media, such as oil of tur¬ pentine. He thoroughly investigated the phenomenon, and laid the foundation of a very important study, his early results being obtained by means of an instrument devised by himself, not unlike the polariscope attached to the microscope, except that the polarization was ob¬ tained by reflection from a blackened mirror and that the analyser was placed in the centre of a graduated disc. When the analysing prism was so placed as to obscure the polarized ray, on interposing a tube containing an active fluid the light was again found to pass until the analyser had been rotated through a certain number of degrees; that number being taken as the rotatory power of the fluid ; but it was found difficult to determine the exact point of maximum darkness, and somewhat wide and inaccurate results were obtained. M. Soleil, an in¬ strument maker of Paris, next constructed with con¬ siderable ingenuity and skill an improved form, by the use of which much greater accuracy could be obtained. In it the light first passes through a doubly refracting prism as analyser, then through a plate of quartz 375 mm. thick (subsequently replaced by a double plate) ; then through the fluid under examination, another plate of quartz, the compensator consisting of two wedges of quartz, and finally through the analyser. To this there was added what Soleil called a produce of sensible tints , consisting of a prism, Galileo telescope and quartz plate. On one occasion I spent a profitable hour or two in tho¬ roughly examining this instrument, taking it to pieces and tracing the tortuous course of a ray of light through it ; the study was interesting as showing what optical skill can accomplish and what complicated means had here been employed to surmount difficulties, which have since been overcome in a more simple manner. The special features in this instrument are first, that the ray of polarized light emerging in a vertical plane from the prism meets the double plate of quartz, one half of which rotates to the right, the other half to the left, the rotation being sufficiently great (90°) to decompose the ray and to produce a rose- violet tint uniformly over the whole field. This is known as the sensitive or transition tint, also the tint of passage. Secondly, the analyser is fixed with its axis corresponding to that of the polarizer, the amount of rotation produced being measured by compensation, effected by a plate of quartz, divided into two wedges and fitted with rack and pinion motion, by which they are moved over each other so as to increase or diminish the thickness ; they are also attached to a vernier and scale. When the compensator is at zero, the whole of the disc is rose-violet, but the introduction of an active fluid causes one half to become red ; the compensator is then moved through a sufficient number of degrees to restore uniformity and the amount of rotation is thus ascertained. Actual degrees are not marked in the scale, but the rotation produced by a plate of quartz 1 mm. thick, equal to that given by 200 mm. of solution of sucrose (1679 grams in 100 c.c. of water), being marked on the scale and divided into 100 equal parts. The instrument was specially constructed with a view to its use for sugar solutions and is best known as Soleil’ s saccharimeter, of which there are several modifications, such as the Soleil- Yentzke, Soleil-Scheibler, etc. Accurate as were the results obtained by this means, there were some difficulties, such as the interference of coloured solutions with the sensitive tint, the shortness of the scale, etc., which have caused it to be superseded by more simple forms in which, as in Biot’s instrument, the analyser is made to rotate, and these forms have been adopted by the two opticians Duboscq and Laurent, who may be regarded as the successors of Soleil. In 1860, Professor Jellett, of Dublin, described to the. British Association at Oxford, a new analysing prism, which he had invented, by which greater accuracy could be obtained than by any previous arrangement. The report is as follows: — “Professor Jellett described to the section a new analysing prism, by which the plane of polarization of polarized light may be deter¬ mined with great precision. This instrument consists of a large prism of calc-spar, which is reduced to the form of a right prism by grinding off its ends, and sliced lengthwise by a plane, nearly, but not quite perpendicular to its principal plane. The parts into which the prism is thus divided are joined in reversed positions and a diaphragm with a circular opening is placed at each end. The light which passes through both diaphragms pro¬ duces a circular field, divided by a diametrical slit into two parts, in which the planes of polarization are slightly inclined to each other. If then light, which has been previously polarized, be transmitted, it will be extin¬ guished in the two parts of the field of view in positions which lie close together, and the light will become uni¬ form in a position midway between these. This position determines the plane in which the incident light was polarized with a precision much greater than has been otherwise attained. Professor Jellett stated that the different observations did not differ from one another by an angle greater than a minute, and that the instrument was equally applicable to the case of homogeneous light.” The first practical application of this invention was in the construction of a polarimeter for the Professor by Bryson in that year, and the manufacture is continued by the same optician at the present time ; it is the most simple form with which I am acquainted, efficient and inexpensive ; it is the instrument now before you, the one ’with which my observations have been made, and which I have com¬ pared with those of Wild, Laurent and Duboscq, with very satisfactory results. The instrument of the last named maker still retains the double quartz plate of Soleil, but dispenses with the compensator, having been fitted with a Jellett’ s prism as analyser on a suggestion made by him in 1869. That of Laurent has as its special feature the polarized ray passed through a diaphragm with circular opening, one half of which is covered by a plate of quartz, the division of the field by this means giving great precision, to the readings ; the analyser is an ordinary Nicol’s prism. By this means the optical work is simplified as- compared with the old form and the perfection of work¬ ing is enhanced. Wild’s polaristrobometer, manufactured by Hermann and Pfister, of Berne, is a special form of the instrument. It is somewhat elaborate in construction ; the readings are taken at the disappearance from the centre of the field of certain lines or bands which cross it and which are produced by two plates of calx spar crossed at right angles to their principal faces. Those who work with this instrument speak of it as giving very satisfactory results. In 1872, Professor Jellett, in a paper read before the Royal Irish Academy, de¬ scribed a “ new optical saccharometer,” an ingenious arrangement by which the polarized ray is made to- traverse a fluid, the rotatory power of which is previously determined and which is opposite in character to that of the fluid to be examined. In general terms it might be , described as an instrument by means of which the relative September 13, 1379. ] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 209 rotatory power of any transparent fluid to that of a stan* dard fluid may be accurately determined. Although delicate in its results it is somewhat troublesome in work¬ ing and does not appear to have come into general use. Originally, ordinary daylight, or that from an Argand lamp was used; but on discarding the more complicated instrument of Soieil, with its compensator, whereby the decomposition of the light due to the unequal refrangi- bility of the different rays was overcome, monochromatic light was adopted. Different operators, however, used different coloured rays with, as a matter of course, dif¬ ferent results; hence it became necessary when stating the rotatory power of a body to indicate by what ray the reading was taken, andldiis still obtains to a large extent; thus, in the Agenda du Chemiste last year there are four tables giving the rotatory power of 76 bodies — 12 by the “ teinte du passage," 7 by the red ray, 10 by the yellow, and 20 without any indication as to the ray, and the remainder indicated by letters corresponding to certain Fraunhofer lines, as used by the authorities from whom the results are quoted. It is true we have a factor, *7 67, by which to multiply the values obtained by the yellow ray to convert them into those which could be obtained by the red, but it has been shown that this is not constant for all bodies. Further, one object of a table is to show at a glance without calculation the relative rotatory power of different bodies; now this clearly cannot be the case with such tables as those referred to. This chaotic state of things is to some extent in process of rectification, and modern instruments are all constructed with a special view to them use with the yellow flame, corresponding to the line d of the spectrum, or in other words, with a Bunsen flame containing a salt of sodium. This gives a grey field quite as sensitive as the transition tint, and where observations are continued for any length of time it is far less fatiguing to the eye of the observer. Certain natural crystals possess high rotatory power. Thus a plate of quartz 3’75 mm. in thickness gives a rotation of 90°, whilst a column of English oil of turpentine, 100mm. in length, gives only 14°’30. Some few salts, such as bromate and chlorate of sodium, acetourate of sodium, and hypo¬ sulphite of lead possess double rotatory power; but most inorganic salts, and some liquids, such as water, alcohol, ether and chloroform, are inactive. The activity in crys¬ tals and liquids depends on different causes, the former belongs to the domain of physics, the latter to that of chemistry, and it is this, viz., the molecular rotatory power, which we are more especially considering. The rotation produced by any given liquid (all else being equal) depends on the length of the column ; it will be evident therefore that to have uniformly correct results the greatest accuracy must be observed in this respect, and that either the same length of tube must always be used or the readings must be brought to the same standard by calculation. The usual working length is 200 mm., but most operators supply themselves with tubes of 100, 50, and even 25 mm., as some of the fluids to be operated on possess so much colour that light will not pass through a larger column satisfactorily. It is desirable to use the larger tube whenever available, inasmuch as the error will be thereby diminished; but whatever be the dimen¬ sions of the tube used the results should be stated in terms corresponding to a column of fluid 100 mm. in length, this now being generally accepted, and [a] is used to indicate the molecularly rotatory power of such a column. Hesse, however ( Chem . Centr., 1875,369; Journ. Chem. Soc., 1S76, 667), in referring to the results obtained by De Montgolfier, Weiss and Biot, points out the dif¬ ference obtained by the ray D, the red and transition tints, and concludes that this symbol is equivocal, and suggests that it is better to use a0 for the rotatory power obtained by the yellow ray, as has indeed been the practice for some time in Germany. When the transition tint was almost exclusively adopted the sign [a] was used to indicate the rotatory power read by it, otherwise it would have been more simple to have adopted this sign where the sodium ray was used, and to have used the qualifying letter only when other rays were employed, which is now rarely done. Temperature influences the rotatory power to some extent, 15'5° C. (60° F.) being that at which readings are usually taken, and it has been found that the rotation decreases as the temperature increases, and vice versd ; but Landolt has shown that the diminution is not always uniform at all temperatures for the same body, or equal for all bodies. He gives as examples — Oil of Turpentine [a]0 360,61 : diminished rotatory power for an increase of 1° C. =’004437. Oil of Orange [«]0 115°*31: diminished rotatory power for an increase of 18 C.r=T2371. This diminution being represented graphically, not by a straight but by a slightly curved line. This, I think, would depend entirely on the expansion and rate of expansion of the liquid, inasmuch as an increase of temperature would necessarily increase the volume and reduce the number of molecules in a column of a given length; the slight expansion of the tube would tend in some degree to compensate for this, and in most fluids the difference for two or three degrees of temperature is so slight that it might be disregarded as being less than the probable error of observation. Magnetism also influences rotation; indeed some bodies which are void of this property under ordinary circum¬ stances will under its influence exercise it in a marked degree. The discovery of this phenomenon we owe to Faraday (Phil. Trans., 1846, p. 1), and it has been further investigated by De La Rive ( Archives des Sciences, etc., vol. xxxii., p. 193 : Annales de Chimie, 4th series, vol. xv., p. 57 ; Phil. Mag., 4th series, vol. xl., p. 393) ; this is, however, a study in itself, and those who wish to prosecute it will find abundant matter of interest in the papers quoted ; suffice it to say that under the influence of mag¬ netism the same law holds good as regards decreased rotation for increased temperature. The advantage of having certain commonly occurring liquids, such as those mentioned, void of activity, is ob¬ vious, as it enables us to make concentrated solutions of most solid substances, such as sugar, camphor, the alka¬ loids, etc., and to select a menstruum in which the body is most soluble, since concentrated solutions are most desirable, inasmuch as the calculation is made for the solid substance, and any error in observation will be in¬ creased in proportion to the dilution. Not only so, but it has been shown by Landolt (Deut. Chem. Ges. Ber. [9], 901 — 904) that to obtain accurate results, saturated solu¬ tions are absolutely necessary, for as in the case of tem¬ perature so in dilution, the effect cannot be represented graphically by a straight line. In concentrated solutions the divergence is only a few tenths of a degree, and the rotatory power of the body remains the same whatever be the (inactive) solyent employed, but observations taken with dilute solutions are utterly worthless. He further finds (Liebig’s ‘Analen,’ clxxxix., 241 — 337) that some substances have an increased proportional rotation by dilution, whilst others are diminished; turpentine and ethyl tartrate always show increase, nicotine and camphor both show diminution, and these results are constant wirh all solvents. Organic liquids and solutions are sometimes so much coloured that light will not pass through even 25 mm. sufficiently for our purpose. In such cases filtration through charcoal is usually resorted to ; this under ordi¬ nary circumstances removes enough of the colour to admit of the observation being made, or indeed some¬ times entirely decolorizes. But this procedure intro¬ duces a possible source of error, inasmuch as it has been shown by Dr. Stammer ( American Chemist, from the Sugar Cam, Pliarm. Journ. [3], vol. i., p. 926), that in the case of saccharine solutions the char absorbs sugar from the first portion of the liquid, which passes through and so reduces the strength and rotatory power. This would doubtless occur equally with solutions containing 210 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 13, i87». alkaloidal bodies and possibly some others ; but as the char becomes saturated before it loses its decolorizing property, if a sufficient quantity be passed through, and the latter portion be taken for examination, the chance of error on this point is obviated. The great commercial industry in which the polari- meter has been most useful is the sugar trade, and as the expenditure of large sums of money is not unfre- quently dependent on the results so obtained, it is not surprising that the greatest perfection in construction and working has been sought for its special requirements.* There is, however, good reason to believe that of the other spheres of usefulness as yet unknown (in addition to those which are known) some are closely allied, whilst others belong to the domain of pharmacy. By its means (as already stated) the purity of the alkaloids can be readily determined ; castor oil, croton oil, and doubtless some others of this class possess their specific rotatory powers, whilst the majority of essential oils do so in a high degree. Landolt, who has worked largely with bodies of a definite and constant chemical constitution, does not appear to have as much faith in its application to essential oils on account of some amount of variation dependent on soil, climate, etc., and in his recently pub¬ lished memoir he devotes but little space and consideration to them. Oil of turpentine and other volatile oils were, however, amongst the first liquids examined in this way, and connected with which an interesting incident occurred. Biot, in announcing his discovery in 1818, called special attention to the fact that whilst in quartz or rock crystal there existed two opposite direc¬ tions of rotation, in oil of turpentine the rotation was in one direction only, viz., from the right to the left of the observer, and this was the same in direction, although slightly different in degree for all samples examined. This statement remained unchallenged until 1843, when Dr. Leeson read a paper before the Chemical Society of London, entitled “ Observations on the Circular Polariza¬ tion of Light by transmission through Fluids.” In this paper he stated that every sample of oil of turpentine which he had examined possessed a right handed rotation coinciding in direction with that produced by essence of lemon. These conclusions were so thoroughly opposed to those of Biot, that Dr. Pereira undertook to further investigate the subject, and by procuring reliable samples of French oil of turpentine from M. Guibourt, of Paris, he was enabled to demonstrate the fact that both ob¬ servers were correct ; that the French oil rotated to the left, the English or American to the right, and that a mixture of the two in proper proportions possessed no rota¬ tory power whatever. ( Pharm . Journ. [1], vol. v., p. 67.) My first experience in the use of the polarimeter was in a direction not altogether pharmaceutical, but one which nevertheless merits attention from pharmacists, viz., in the examination of urine ; it is a legitimate branch of our calling and one which medical men are usually willing to delegate to us ; it possesses considerable interest and the remuneration is not influenced by unfair competition on the part of uneducated outside traders. It was diabetic urine containing in round numbers only 2 grains sugar per ounce ; subsequently other experiments were made with samples containing larger quantities, but my ex¬ perience led me to the conclusion that this method of determination is more troublesome and not more accurate than the copper test of Fehling or the recent one of Pavy, although its use has been recommended by Mdhu and others. Passing on to essential oils, the work became in¬ teresting, although occasionally disappointing ; for example, essential oil of bitter almonds distilled in this country, that from abroad which is often obtained from a mixture * Those who are interested in the various kinds of sugar will do well to peruse an excellent paper by Dr. O. Hesse, ‘ The Behaviour of Solutions of some Substances to Polar¬ ized Light’ {Pharm. Journ., 3rd series, vol. vii., pp. 191, 410 and 473). of peach kernels and almonds, and the artificial, or oil of mirbane, are all optically inactive, hence the polarimeter does not furnish us with a means of distinguishing between them. Other results were very satisfactory. Thus, finest imported otto of rose is levogyrate, giving a rotation of - 3-52°. A common quality was found to be dextrogy¬ rate giving + 1'50°. Now the lower qualities of otto are known to contain varying proportions of oil of geranium; but on examining the only sample of this oil which was then at my disposal and which had been received from the south of France, it was found to give — 6*73°. This, then, could not have been the article used in adulterating the sample in question ; but subsequently on examining the Turkey oil of geranium a solution of the problem was furnished, since it gave a rotation of +1*72° and indicated that it constituted the bulk of the so called common otto of rose. It was found too that otto of rose distilled in this country possessed an opposite rotatory power to that of the finest imported, as indicated in the table appended to this paper. On examining many samples of oil of lavender it was found that some of the commoner were adulterated with turpentine, and there was no diffi¬ culty in determining whether this had been done in France or England, on account of the different rotatory powers of the turpentines in the two countries. Whilst prosecuting this study my attention was directed to an excellent paper by Dr. J. H. Gladstone on essential oils {Jour. Chem. Soc ., new series, vol. ii., p. 1), in which he gives the specific gravity, rotatory power and refractive indices of a number of essential oils ; also to a less important paper by Dr. J ulius Maier, of New York, “Detection of the Adulteration of Essential Oils with Oil of Turpentine” {Chemical News , vol. xi., p. 301, from the Amzr. Joum. Science, xxxix. ; p. 273). Since the publication of these, some oils have come into use which were then less known than at the present time and some others are now supplied from different localities ; it was therefore thought desirable to go over the ground anew and to compile a table giving the rota¬ tory power and specific gravity of a somewhat larger number. Such a table is appended to this paper, the samples of oil operated on being the most reliable I could obtain, except where a second quality is mentioned for comparison, and all that were sufficiently colourless to be viewed through a column of 200 mm. were so examined. Some oils, such as those of hops, cassia, chamomiles, myrtle, etc., could only be read through 100 mm. ; whilst some, such as patchouli and cajuput, admitted only sufficient light through 50 mm. All have been calculated to 100 mm. and at a temperature of 15*5° C. Many results were obtained which being unimportant are not here recorded, but all tended to experience, and as deductions from which might be mentioned that turbidity even though very slight, materially interferes with the accuracy and sharpness of the readings; it is therefore necessary to filter any oils or solutions which are not perfectly bright. Age does not influence to any extent the optical activity of essential oils. Oil of cloves, new and colourless, and samples of a light sherry and dark sherry colour all registered very nearly the same, and samples of English oil of lavender less than a year, four years and five years old differed from each other less than one degree. The modus opcrandi is exceedingly simple. A correct zero must be first obtained thus — one of the tubes being filled with distilled water, the glass disc is slid on so as to exclude air bubbles, and screwed firmly down. It is then placed in position and the instrument brought opposite to a sodium flame ; the operation must be conducted in a dark room, or a black covering cloth be used. The analyser is then set so that the arrowhead on the vernier points to 0 on the scale when the whole of the disc is at a maximum of obscurity, i.e., both halves equally obscure ; it is necessary to take several readings of this and note down the results, taking the mean of the observations, and if, as sometimes happens, there is any difficulty in getting an exact zero it is convenient to make a note of the error and add or subtract this from the subsequent readings. September 13, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 211 If now the tube be replaced by one containing an optically active liquid, it will be found that the field is entirely illuminated, or that one half is so whilst the other is obscure; The analyser is then rotated until equal obscurity is regained and the number of degrees, minutes or decimal parts of a degree, through which it has been moved, as well as the direction, is noted. For each of the following results ten readings were taken ; two of these (the highest and the lowest) were struck out, and the sum of the others divided by 8 gave the mean reading, or where the 200 mm. tube was used, division by 16 gave at once the correct mean for 100 mm. It is, of oourse, necessary from time to time to check the accuracy of the zero, just as a careful dispenser does the correctness of his scales. With solid substances, a saturated solution being made in water or other suitable inactive liquid the specific rotatory power [a] is found by dividing the amount of observed rotation a, by the length of the column in deci¬ metres l , by the weight of the active body in each unit of liquid w, and by the density of the solution d thus, — [>]=—”■-- = L J txwxd For the loan of authentic specimens of some of the following oils I have to thank Mr. E. M. Holmes, Curator of the Pharmaceutical Society’s Museum. Specific Gravity and Rotatory Power of Essential Oils. Oil of — Anise Do. Ajowan . Angelica Almond, Eng. . . Do. Foreign . . Do. Artificial . Amber . Bay . Bergamotte . . . Birch . Canada Balsam . . Clove Bark . . . Cardamoms . . . Ccdrat . Cedar, Commercial . Do. Red . . . . Caraway . . . . Cassia, Pure . . . Do. Commercial . Cascarilla . . . . Chio Turpentine . . Cinnamon . . . . Do. Leaf . . Citron . Cherry Laurel . . Citronelle . . . . Cloves, Eng. . . . Do. Foreign . . Chamomile, Eng. Do. Foreign Coriander . . . . Cummin . . . . Cajuput . . . . Cubebs . Copaiba, New . . Do. Old . . . Camphor . . . . [a]=100 mm. 15 56° C. Sp gr. . Pimpinella Anisum . 0"936 + . Illicium Anisatum . 0'980 - . Ptychotis Ajowan . 0-919 . Archangelica offici¬ nalis .... . Amygdalus communis 1 '0 49 Rot. 1°' 0°' 0 P- 00 82 Do Mirbane . Succinum . . . . Laurus Nobilis . . Citrus Limetta . . Betula alba. . . . Abies Balsamea . . Dicypellium Caryo- phyllatum . . . Elettaria Cardamo- mum . Citrus medica. . . 0-897+ 1 °*78 0 0 0 ? 1-063 1-152 0-859+ 0° 0-904-18° 0-872 + 31° 0-872+ 2° 0-914-30° ■85 ■88 25 18 07 1-052- 2°-25 . 0-976 + 14° .0-969- 3° 0-968-16°' Juniperus Virginiana 0*960 —28 Carum Carui Cinnamomum maticum . . 0-940-20 aro- , . .1-053- 1° 1-021+ 2° Croton Eluteria . .0”88S+ 8 Pistacia Terebinthus 0'889 + 22° Cinnamomum Zeyla- nicum . 1*025 0 Do. 1-060 0 Citrus medica . . .0-901+38° 0 0° 0° 0° 0° 6° Dm Lauro- Cerasus. . . 1-046 Andropogon Nardus. 0"881 Caryophyllus aroma- ticus . 1*064 + Do. 1-064 + Anthemis Nobilis . 0-906 - Do. 0-910 + Coriandrum sativum 0*876 + 10° Cuminum Cyminum 0*933 + 4° Melalueca minor . .0‘924- 1° Piper Cubeba . . .0*924-29° C opaif era multi j uga 0-920-13°" Do. 0-920 - 12° Dryobalanops aroma- tica . 0*956+ 7° Anethum graveolens 0*860 — 6° 59 00 00 75 68 00 02 65 55 31 ■81 50 32 95 16 65 29 52 07 50 52 87 24 Oil of-^ [a]=103nrm. 15-56° C. Sp. gr. Rot. p. Elemi . Canarium commune . 0-867 - 3°-65 Eucalyptus . . . Eucalyptus Globulus 0’881 - 36° -30 Do. . .* . E. Amygdala, odorata 0*912 — 42°-33 Erigeron .... Erigeron Canadense . 0*885 + 72°-41 Fennel . Foeniculum dulce. . 0‘998 + 25°*7l Geranium, French . Pelargonium species. 0*906 — 6°‘73 Do. Turkey . AndropogonSchoenan.0-880 + 10,72 Do. Indian . Andropogon . . . 0’896 0 Do. Spanish. 0-911— 4°*45 Ginger, Jamaica . . (Eng. dist.) . . . . 0‘853- 27°’15 Do . Do. 0-870 -52°*25 Do . (Distilled Abroad) . 0-907 — 65°-00 Ginger Grass . . . Andr. Schoenanthus . 0-951 + 39°-65 Hyssop . Hyssopus officinalis . 1*005— 23°*63 Hops . Humulus Lupulus . 0*890 + 1 *42 Horsemint, Amer. . Monarda punctata. .0-934— 0 *76 Juniper, English . . Juniperus communis 0 -882— 5 *00 Do. Foreign. . Do. 0-855-18 *71 Jaborandi. . . . Pilocarpus pennati - folius . 0-879- 4 -10 Lavender, Eng., New Lavandula vera . 0-887- 8 -29 Do. Do. Old . Do. 0-903- 8 -48 Do. Foreign petal 0-876- 5 -93 Do. Do. spike Lavandula Spica . . 0-880 + 13 -75 Lemons, best Com- mercial .... Citrus Limonum . . 0-856 + 52 -05 Do. extracted by Spirit . Do. 0-852 + 57 -23 Do. Distilled. . Do. 0-848 + 22 -10 Do. obtained by Sponge Process (Hanbury) . . . Do. 0-957 + 24 -26 Limes . Citrus Limetta . . 0-887-43 -80 Lign Aloe .... Elaphrium species 0-925- 2 -45 Mustard . . . . Sinapis nigra . . 1-000 0 Do. Artificial . Sulphocyanide of Al- lyi . 1-010 0 Myrrh . Balsamodendron Myrrha . . . . 0-989 — 59o,06 Myrtle . Myrtus communis . 0-89S + 18°-79 Myrcia . Myrcia acris . . . 0-939+ 6°-59 Neroli . Citrus vulgaris Flowers . . . . 0-873 + 10 -62 Nutmeg . Myristica officinalis . 0-988 + 24 -22 Olibanum .... Boswellia Frereana . 0-872- 4 -61 Origanum Y ulgare, true . — 0-891- 30 -27 Do. Commer- cial, white . . . - > 0-877-16 -20 Do. Commer- cial, yellow . . . — 0-877-23 -74 Do. Commer- cial, red .... — 0-876-15 -15 Oreodaphne Opifera (from British Guiana) .... — 0-917 + 27 -56 Orange, Sweet . . Essence de Portugal. 0-848-16 -40 Orange Bitter, Bi- garade .... — 0-856- 2°-30 Do. Bi- garade, distilled . — 0-850- 3°-10 Patchouli, French . — 0-988- 57°-10 Do. Penang . — 0-970 — 48°-26 Parsley . Petroselinum sativum 1 -000 - 8o,90 Do. Seed . . . Do. 0-945- 14°-75 Pennyroyal, English Mentha Pulegium . 0-945+ 7°‘10 Do. Foreign — 1-019- 8°-30 Do. American Hedesma Pulegioides 0-938 + 29Q,82 Pimento .... Eugenia Pimenta 1-038+ 2°*35 Peppermint, English Mentha piperita . . 0-912 - 21°-23 Do. Foreign Do. 0-924- 7°*49 Do. Japanese Mentha Canad ? . . 0*880 - 21°*81 Petit Grain . . . Citrus vulgaris, leaves and shoots . . .0:900- 4°-14 Rhodium .... Genista Canariensis . 0*931 — 10°*28 212 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 13. l»79. Oil of— Rose Otto (distilled in England) . . Rose Otto, Finest Imported . . . Do. Common Rosemary, English . Do. Foreign . Rue . . Sassafras (English distilled) . . . Do. Commercial Sandal Wood (Eng. distilled) . . . Do. Foreign Spearmint, E nglish . S olidago 0 dora, s we et scentedGoldenRod Savin, English . . Do. Foreign . . Sweet-flag .... Do. Commercial Sage . Silver-fir .... Scotch-fir .... Tansey . Thyme . . . . . Turpentine, Ameri- cftn • • • • • Do. French V erbena .... Valerian . . . . Wintergreen . . . Wormwood . . . Wormseed .... Ylangylang . . . [a]=100 mm. 15-56° C. Sp. gr. Rot. p. — 0-854 + 2°-50 — 0-877- 3°T5 — 0-867+ l°-50 Rosmarinus officinalis 0"881 — 16^-47 — 0-952+ 4°'47 .0-886- 3°-61 Ruta graveolens Sassafras offic. Do. Santal. Alb. Mentha viridis Juniperus Sabina Calamus aromat. Salvia officinalis . Abies pectinata . Pinus sylvestris . Tanacetum vulgare Thymus vulgare . Andropogon Citra tus . Valeriana officinalis Gaultheria procum lens .... Artemisia Absin thium .... Chenopodium an thelminticum . 1-072 + 1-084 + 2°-64 2°-64 .0-958+ 2°-36 0-986+ 8°-29 .0-950-30°-28 0-912 0-927 0-884 0.926 0-957 ,0-925 , 0-864 , 0-886 0-923 0-891 + 10°*53 — 32°*78 + 2°-25 + 14°-31 + 19°-60 + 12° -23 — 14Q- — 9°" + 29°- '18 •78 •48 •10°-60 0-870 + 14°-30 0-938 -25°-35 0-890- 2°-61 0-971-31 -50 1-162+ 0 -81 0-971 + 17°-43 0-941- 8°-53 0-056— 20°-10 Mr. Stoddart referred to the extensive use of the polarimeter in the examination of sugar, but said that the value was affected by the difficulty of determining the zero, as in Soleil’s polarimeter, different people arriv¬ ing at different conclusions respecting shades of colour. Mr. Umney, adverting to the results Dr. Symes had obtained from the various oils, said he should expect to get a different result from the grass oil of India (Andro¬ pogon), than from the geranium oil obtained in the south of France. Professor Attfield observed that the substances Dr. Symes had examined were nearly all mixtures of distinct things. The polariscope was extremely useful in examin¬ ing a solution of a single substance, such as sugar, but it was not so useful in other cases unless the nature of the constituents of the mixture was known. Nevertheless, such observations as Dr. Symes’s must be useful if they were multiplied, especially as a substance such as an essential oil, when properly obtained and pure, might give a fair average amount of rotation to a polarized ray of light. But he would suggest that many observations would be necessary on the same essential oil before they could well trust to the figures given to them. He hoped D*. Symes would continue the subject. Perhaps, also, Dr. Symes with his intimate knowledge of the modes of construction of polariscopes would eventually be able to put pharmacists in the way of obtaining a cheap variety of the instrument. The President said Dr. Symes had spoken of the use of the polarimeter in detecting sugar in urine, and it was a nice point for the physician to discover when the last trace of sugar disappeared from a patient's urine. Before the sugar was lost altogether it became a • very difficult matter to estimate the exact percentage by the ordinary process, and he found when sugar existed in less than 1 per cent, in urine it was difficult to determine the exam, percentage by the ordinary process. If this instrument, therefore, would detect more minutely the exact propor¬ tion when it arrived at such a degree of dilution it would be very useful. Although they might arrive at the exact figure as to the rotatory power of different essential oils, would not the figures have to be varied according to the age of each particular sample ? Dr. Symes, replying, said that most persons had no difficulty in getting the coloured zero with the Soliel instrument, but the maker finding that it did not suit the eyes of all observers introduced what he called a producer of sensible tints, whereby the flax flower tint could be changed for some other ; it consisted of a Galileo tele¬ scope and quartz plate. He could scarcely understand any difference existing between the estimation of sugar by chemical means and by the polarimeter. Reading sugar solutions was almost a profession in itself, and the French who are sellers of sugar usually read higher than the English who are buyers. He regarded both Fehling’s and Pavy’s tests for diabetic urine as equally accurate with the results obtainable by the polarimeter; they were less troublesome, and the work could be with more con¬ fidence delegated to another person. He hoped to go on with the study and that others would take it up, so that ultimately the subject migh tassume a more definite and important position pharmaceutically. He then spoke of the desirability of obtaining cheaper instruments, and agreed with Professor Attfield that they ought to get them at half their present price. A vote of thanks was then passed to Dr. Symes for his paper. The next paper read was on — The Application of Chloroform in the Testing- of Drugs. BY L. SIEBOLD. In the ‘Year-Book of Pharmacy’ for 1877 there occurs an abstract of an article by Dr. C. Himly on the Detection of Mineral Adulterants in Flour by means of Chloroform. Having frequently tried this test and finding it extremely useful both as a qualitative and as a quantitative process, it appeared to me desirable to ascertain to what extent it might be advantageously employed in the testing of powdered vegetable drugs. As many of the latter are lighter than chloroform, and the usual mineral adulterants sink in that liquid, it was but reasonable to infer that this mode of separation might prove of value to the phar¬ macist. I will not trouble the meeting with the details of ray experiments, but confine myself to a brief summary of the results. In each experiment a small quantity of the dry powder was well shaken with about half a test-tubeful of chloroform, and the mixture allowed to stand at rest for twelve hours. The following drugs were found to rise so completely to the surface of the chloroform, that the obser¬ vation and estimation of any mineral adulterant became a very simple and easy task : — Acacia, tragacanth, starches, myrrh, Barbadoes aloes, jalap, saffron, cinchonas, nux vomica, mustard, white pepper, capsicum and guarana. Known quantities of selenite and of chalk were added to these drugs, and subsequently determined by running the lower stratum of the chloroform with the sediment into a small dish, carefully pouring off the chloroform, drying the sediment at a gentle heat and weighing it. The result in each case was very satisfactory. No such accuracy could be attained by incineration, as in the presence of chalk there was always a loss of carbonic acid, and in that of selenite a loss of water and of oxygen, the sulphate being partly reduced to sulphide. An estimation of these adulterants by the usual analytical processess would, of course, give exact results, but prove much more tedious. Both for qualitative and for quantitative purposes, the chloroform test therefore answers extremely well with the drugs named. In the case of the following substances no September 13. 1879. j THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 213 complete rise to the surface of the chloroform took place, but a portion was found to float and another portion to sink, though the absence of mineral adulterants was proved by analysis : — Gamboge, scammony, opium, socco- trine aloes, liquorice root, ginger, colocynth, cousso, ipe¬ cacuanha, cinnamon and cardamoms. Of the last two by far the greater portion was found to sink in chloroform. But even in these cases the test is not altogether without value, for a careful inspection of the sediment will show whether or not it is a mixture of various substances, differing in appearance, weight, etc. The mineral adul¬ terant will generally, in such a case, form the lowest stratum of the sediment. A comparison with a genuine sample helps to arrive at a correct conclusion. More¬ over, the chemical examination of the sediment gives results which cannot always be obtained by testing the ash. Take the case of cinnamon, for instance, which contains organic calcium salts. These upon incineration leave calcium carbonate, and a qualitative analysis of the ash would therefore fail to show whether this calcium oarbonate was solely the result of ignition, or whether a part of it pre-existed in the cinnamon powder as an adulterant; while the addition of hydrochloric acid to the lowest stratum of the chloroform sediment would settle this point at once. It is, however, in the case of the drug first named that I wish specially to recommend this mode of testing to pharmacists. The next paper was by the same author on — Note on the Behaviour of Iodine to Chloroform, and a New Test for the Detection of Alcohol in Chloroform. Every chemist knows the beautiful purple colour of a solution of iodine in chloroform. It does not seem to be so generally known, however, that this colour varies with the degree of purity of the chloroform employed, and that this variation of colour is due to the presence or absence of alcohol. A solution of iodine in pure chloroform is deep purple- violet, or if very weak it is purplish-pink, while a solu¬ tion of the same substance in alcohol is brown, red or yellow, according to its strength. In solutions of iodine in mixtures of chloroform and alcohol, the colour of the alcohol solution so predominates over that of the chloro¬ form solution, that the presence of even a small per¬ centage of alcohol may be readily recognized in a sample of chloroform by comparing the colour of its iodine solution with that of a solution of iodine in perfectly pure chloroform. This mode of testing, however, would necessitate the use of exactly equal proportions of iodine, and of iodine of the same quality and purity, as otherwise the difference in the depth of coloration would materially interfere with the result. I therefore propose the fol¬ lowing modus operandi, which on the strength of numerous trials I can recommend as a very simple, expeditious and reliable one : — Introduce a small quantity of iodine into about 10 to 15 c.c. of the chloroform to be tested, shake until the solution has acquired a deep purple or purplish-red colour, not so deep, however, as to render it opaque, and decant the solution from the undissolved iodine. Divide the solution into two equal parts, which place in two separate test tubes of equal diameter, shake one with about four times its volume of water, and keep the other as it is, for comparison. The water will absorb the alcohol, and what settles down is a solution of iodine in pure chloro¬ form, the colour of which will be exactly the same as that of the other portion if the chloroform was pure, but will distinctly differ from it if the sample contained alcohol. With 2 per cent, of alcohol or more, the difference of colour is very striking indeed ; with 1 per cent, it is very distinct, and in the presence of only half a per cent, it is still clearly discernible. As little as half a per cent, of alcohol can therefore be readily detected in this manner. By resorting to distillation, a quarter of a per cent, and even less of this impurity may be detected by using the first portion of the distillate for the test. It is a curious fact that, though chloroform boils at 62° C., and alcohol not under 78° C., the first portion of the distillate is richer in alcohol than the original sample, and that the distillation, if continued, finally leaves pure chloroform quite free from alcohol in the retort. The cause of this must be sought in the different densities of the vapours of alcohol and chloroform, that of the former being 23, while that of chloroform is nearly 60. I think, however, that the test as above described, without the trouble of a distillation, is sufficiently delicate for all practical purposes, and that it will commend itself in that form especially to pharmacists, on account of its sim¬ plicity and ease of application. A third paper, by the same author, was a — Note on the Specific Gravity of Liquids. While the great usefulness of the hydrometer for the rapid determination of the specific, gravity of all kinds of clear liquids is universally recognized, there appears to be anything but unanimity of opinion as to the value of this instrument as an indicator of the specific gravity of mixtures owing part of their weight to the presence of undissolved or suspended matter. I have therefore made a number of experiments with the object of deciding whether or not the indications of the hydrometer may be depended upon in the case of mixtures containing insoluble powders, oils, resins, etc., uniformly suspended. The results were as follows : — Mixtures of Precipitated Chalk, Mucilage of Acacia, Syrup and Water — Specific gravity by liydiometer. No. 1. 1106 „ 2. 1-070 Specific gravity by balance. 1T066 1-0710 Mixtures of Magnesia, Mucilage and Water — Specific gravity Specific gravity by hydrometer. by balance. No. 1. 1-059 1-0598 ,, 2. 1-036 1-0359 Mixture of Precipitated Chalk and Water only — Specific gravity Specific gravity by hydrometer. by balance. 1-037 1-0396 The difference in this case arose from the fact that it wasi mpossible to read off the specific gravity quickly enough, for in the absence of mucilage or any otker binding substance, the chalk began to subside immediately after shaking, thus causing a continual decrease in the specific gravity. Mixtures containing subnitrate of bismuth, heavy spar and other mineral powders, each suspended by mucilage, were tested in the same manner and likewise gave con¬ cordant results. Emulsions of Water — Oil of Almonds, Gum Acacia Specific gravity by hydrometer. Specific gravity by balance. No. 1. 1-010 1-0110 „ 2. 1-007 1-0070 Emulsion of Copaiba, Mucilage and Water — Specific gravity by hydrometer. Specific gravity by balance. 1-014 1-0144 Various Samples of Milk — Specific gravity by hydrometer. Specific gravity by balance. No. 1. 1*030 1-0305 „ 2. 1-028 1-0278 „ 3. 1-032 1-0316 ,, 4. 1-029 1-0300 and 2 1.4 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. iSeptemoer 13, W9 Officinal Mucilage of Acacia — Specific gravity Specific gravity by hydrometer. by balance. 1T65 1-1670 The last determination was made in order to see whether the great viscosity of the liquid would have any notable effect on the indications of the hydrometer. All the determinations were made at 62 Q F. The set of hydrometers used consisted of instruments specially made for very short ranges of specific gravities, the correctness of which I had frequently -checked in previous determinations. The foregoing experiments prove that carefully made hydrometers afford reliable indications of the specific gravities of liquids, no matter whether their gravity is due to dissolved or suspended substances. The President having invited discussion on these three papers — Mr. Martindale asked a question as to the detection of chloroform in dichloride of ethidene. Mr. C. Umney much admired as a chemist the simple test for detecting the presence of minute quantities of alcohol in chloroform. But the Pharmacopoeia recognized the presence of 1 per cent, of alcohol in chloroform of trade, and they as pharmacists must not encourage the idea that chloroform was not medicinally pure because the specific gravity was l-490. The accuracy of this statement could be checked by calculating the specific gravity of a mixture of 100 parts of chloroform at l-500 and 1 part of alcohol at ‘795. Mr. E. C. C. Stanford said in using chloroform he did not know whether the presence of alcohol did not very often give a disagreeable colour to the iodine solution. He had now discarded it for some years, and used no¬ thing but bisulphide of carbon. That was an exceedingly good method of testing certain substances, such as kelp, where the actual amount of iodine was not more than 0*5 per cent. Professor Attfield asked Mr. Siebold whether there really was any adulteration in powdered drugs ; his own experience was that there was little or none. Mr. Reynolds referred to the use of chloroform for testing drugs, and mentioned that he had by this means easily ascertained that the active constituent of . an an¬ thelmintic lozenge was santonin. Mr. Siebold said he had observed adulterations of powdered drugs during his experiments, but not many, and in order to see to what extent the test might prove available, he had himself adulterated most of the drugs experimented with. With regard to the solubility of alkaloids and some other constituents of drugs, alluded to by one of the speakers, he said that in every case in which chloroform dissolved anything from the substance under examination, it was necessary of course to wash the sediment with chloroform before drying and weighing it. He thought this mode of separating mineral from light organic substances might also prove valuable in cer¬ tain toxicological analyses. Respecting the purity of commercial chloroform, he stated that among the samples he had examined those manufactured in this country were, on the whole, very pure. A vote of thanks to Mr. Siebold for his papers was passed. The last paper read at this sitting was on — The Extraction of Pilocarpine. BY A. W. GERRARD, F.C.S., Demonstrator of Materia Medica at University College. Having during the past year worked some large quanti¬ ties of the leaves of jaborandi ( Pelocarpus pennatifolius) for the alkaloid pilocarpine, I on three occasions varied my process with the view of obtaining the most economi¬ cal results. Exhaustion of the leaves with water instead of alcohol was tried and abandoned, as the volume of water required for a thorough exhaustion was so large as to necessitate the employment of much time and unnecessary heat in its evaporation ; and moreover the large yield of extractive, most of which was albumenoid, required considerable and prolonged washing with alcohol to free it entirely from commingled alkaloids. A process similar to that adopted by Wright for ex¬ hausting aconite root, viz., treating the root with alcohol acidified with tartaric acid, was tried with the jaborandi leaves; the presence of the acid did not in any way influence the process or result, neither to its advantage nor dis advantage, simple alcohol being equally efficient as a solvent. In my first process for the preparation, of pilocarpine {vide Pharmaceutical Journal), I found on treating the con¬ centrated washings of the alcoholic extract with ammonia instead of potash, that much brownish black colouring matter subsided, freeing the mother liquor from a very objectionable accompaniment; this observation several times repeated led me to believe that ammoniated alcohol might be with advantage substituted for ordinary alcohol as the solvent of the pilocarpine. Another reason why I considered the use of ammonia might prove advantageous was that most salts of pilocarpine are only sparingly soluble in cold alcohol, but the hydrate is freely soluble, and in the percolation of the ammoniated spirit through the drug, the ammonia would liberate the alkaloid, which would be freely taken up by the alcohol. Tested on a small scale this process was successful, and the experiment was repeated upon 100 lbs. of jaborandi leaves as follows: 84 per cent, alcohol was treated with 1 per cent, of strong solution of ammonia, and the leaves percolated to exhaus¬ tion with this solvent, the alkaline alcoholic percolate was made neutral with tartaric acid, the alcohol distilled, and the residue treated with excess of ammonia and alcohol, again distilled and the pilocarpine dissolved out from the residue with chloroform converted into nitrate and crys¬ tallized to purity from boiling absolute alcohol. The yield of alkaloid by the above process was greater than I had previously attained by other methods of work¬ ing upon the same sample of leaf ; the yield being *7 per cent., and the ammonia (as I inferred it would) effectually liberated the pilocarpine, so that a comparatively small volume of alcohol was required for its solution, also leav¬ ing behind the brownish black colouring matter. The contact of free ammonia with the alkaloid during percola¬ tion might be objected to as likely to produce decomposi¬ tion. This does not appear to be the case judging by the yield. To purify the nitrate of pilocarpine, which is by far the best and most convenient salt for medicinal use, it is usual to boil the crude brown coloured salt of the first crystal¬ lization with absolute alcohol and set aside for a few hours, when the separated crystals may be thrown on a filter and washed with cold alcohol until colourless ; the mixed washings will by further treatment yield a further supply of crystals, and the process may be carried on until at last will be obtained a viscous dark brown mass still contain¬ ing alkaloid but no longer crystallizing. This residue is best worked up by treating with a large volume of water, and allowing to stand for twenty-four hours, when the larger part of the colour separates in flocks, falling to the bottom of the vessel; the solution now evaporated will again crystallize, and the crystals can be treated as before- mentioned. The percentage of pilocarpine in different samples of jaborandi is very variable, one specimen yielding me only *03 per cent, whilst from others I have obtained ‘3, '5, ’7 per cent., the leaf giving the lowest percentage possessed the true characters of Pilocarpus pennatifolius, except that it was much thinner. I was unable to trace its source, but the differences I have alluded to lead one to think that it may be a second variety or grown in a different locality than that from whence we obtain our regular supplies of September 13, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS 215 jaborandi. At any rate it is important to know that there are inferior qualities of the drug which if used in making tinctures, extracts, etc., would possess but little therapeutic value and this is an additional argument for the use of definite principles in medicine such as is found in the alkaloid pilocarpine, which is one of the most powerful and certain diaphoretics known in materia medica. Mr. Martindale said that having worked at pilo¬ carpine he thought he might have a prior claim to Mr. Gerrard for having first purified the crude crystals of nitrate of pilocarpine. Mr. Gerrard read a paper and showed specimens of nitrate of pilocarpine at the Bristol meeting. The crystals exhibited were contaminated with uncrystallizable matter. Towards the end of 1875, he (Mr. Martindale) worked some bark and stem of jaborandi, from which he got two drams of crude pilocarpine, and on January 18, 1876, experimenting with this, he dissolved it in one ounce of absolute alcohol, and added fifteen minims of nitric acid previously diluted with fifteen minims of distilled water. The small crystals separated readily and were purified by pouring off the spirit, by dissolving in boiling absolute alcohol, from which they separated free from colour. A quarter of a grain admin¬ istered by the mouth produced the usual perspiration and salivation in forty minutes. The action was over in three hours. A physiologist who had worked a great deal at the subject had informed him lately that pilocarpine did not produce all the actions of jaborandi. It possessed the sialogogue and diaphoretic properties, but did not produce the same action on the heart as the extract of jaborandi. This was probably the effect of a second alkaloid. He should have liked to have asked Mr. Gerrard if he had sought for this in the uncrystallized residues in making this nitrate of pilocarpine. Mr. Williams said Mr. Gerrard had suggested a new and very important process and they ought to thank him very much for his discovery by which they could get a better yield at a smaller expense of spirit. Not only was credit due to him for this discovery, but for the liberality with which he had made it known. A vote of thanks was passed to Mr. Gerrard for his paper, and the first day’s sitting of the Conference terminated. The proceedings on Wednesday morning were com¬ menced by the reading of a paper entitled — Notes on Petroleum Spirit or “ Benzoline.” BY ALFRED H. ALLEN. Although it is well known to professional chemists that petroleum spirit is composed of hydrocarbons quite dis¬ tinct from those constituting coal-tar naphtha, among the general public, and to a certain extent among people possessed of some knowledge of chemistry, great con¬ fusion has arisen as to the nature of the liquids known in commerce as “ benzine,” “ benzene,” “ benzol,” and “ benzoline.” Of these, the hydrocarbon benzol or benzene, C6Hn, is the chief and characteristic constituent of coal- tar naphtha, while it is present in very insignificant amount in petroleum spirit or mineral naphtha. The terms benzine and benzoline have no scientific application, and are merely commercial names for petroleum spirit. It is owing, in a great measure, to the similarity of these names to those of the chief constituent of coal-tar naphtha that confusion has occurred, but it has been made far worse by the accidental or intentional substitution of one liquid for the other, until it is difficult to obtain the coal- tar product retail, even when it is asked for by its proper name. This would be of but little consequence if the two liquids were of exactly similar nature, but in certain cases they present decided differences of behaviour, although in general characters there are very close re¬ semblances. The following tabular statement of the characteristic differences between petroleum spirit and coal-tar naphtha has been compiled from various sources and includes a few original tests. All the characters given have been carefully verified by actual experiment on representa¬ tive samples of commercial petroleum spirit and coal-tar benzol. Petroleum Spirit, “benzo¬ line,” or “benzine.” 1. Consists of heptane, C7Hlfi, and its homologues. 2. Heptane contains 84 0 per cent, of carbon. 3. Burns with a some¬ what smoky flame. 4. Commences to boil at 54° to 60° C. 5. Specific gravity about •69 to -72. 6. Smells of petroleum. 7. Dissolves iodine, form¬ ing a solution of a rasp¬ berry red colour. 8. Does not sensibly dis¬ solve pitch, and is scarcely coloured by it, even on pro¬ longed contact. 9. When shaken in the cold with one-third of its volume of fused crystals of absolute carbolic acid, the latter remains undissolved. 10. Requires two vo¬ lumes of absolute alcohol, or four or five volumes of methylated spirit of *828 specific gravity for com¬ plete solution at the or¬ dinary temperature. Coal-Tar Naphtha, or “ benzol.” 1. Consists of benzene, C6H6, and its homologues. 2. Benzene contains 92 ’3 per cent, of carbon. 3. Burns with a very smoky flame. 4. Commences to boil at about 80° C. 5. Specific gravity about *88. 6. Smells of coal-tar. 7. Dissolves iodine, form¬ ing a liquid having the colour of a solution of po¬ tassium permanganate. 8. Readily dissolves pitch, forming a deep-brown solution. 9. Miscible with absolute carbolic acid in all propor¬ tions. 10. Miscible with abso¬ lute alcohol in all propor¬ tions. Forms a homo¬ geneous liquid with an equal measure of methylated spirit of ’828 specific gravity. Although the foregoing tests are abundantly sufficient for the distinction of petroleum spirit and benzol, when applied to mixtures of the two products they are of but little value even as qualitative indications, and in that case the density is the only one of the above characters which is capable of giving even an approximation to the quantities in which the constituent liquids are mixed. The action of nitric acid on coal-tar naphtha is well known to result in the formation of nitrobenzene and its homologues, and has been employed by Scborlemmer for detecting traces of benzene, etc., in petroleum. On the other hand, the action of nitric acid on the hydro¬ carbons of the paraffin series, which constitute practically the whole of petroleum spirit, is almost nil in the cold, even if fuming acid be used, and is very limited in extent if hot acid be employed, provided that the very strongest be avoided. I found by experiment that the action of nitric acid on petroleum spirit was, under certain conditions, even more limited that I had supposed, and eventually I found that by employing the acid in a particular manner it was not only possible but easy to effect a tolerably perfect quantitative separation of coal- tar naphtha and petroleum spirit. The following was the mode of treatment eventually employed, and, by adhering to it, it is possible to detect and approximately estimate the proportion of petroleum spirit existing in a mixture of it with benzol, in ten or fifteen minutes : — A known measure of the sample (from 4 to 6 c.c.) was treated with four times its measure of yellow nitric acid of 1‘45 specific gravity. The mixture was made in a flask, to which a condensing arrangement was attached. Slight heat was applied externally by means of a flame if the spontaneous action was not sufficiently vigorous. After about five minutes the contents of the flask were cooled, and then poured into a narrow graduated tube. Any oily layer was measured and removed with a pipette, 216 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 13, 1879. and the remaining liquid poured into a large excess of water. When ordinary petroleum spirit is thus treated the nitric acid becomes coloured more or less brown. Very little heat is evolved, but on applying moderate heat externally the production of red fumes proves the occur¬ rence of a certain amount of action. The effect, however, is not so violent as I had anticipated from a perusal of Schorlemmer’s description of the reaction, and, if the experiment be carefully made, the petroleum spirit em¬ ployed forms a layer on the nitric acid, and on transferring the liquid to a graduated tube is found to occupy the original volume of the sample used. This is true whether petroleum spirit alone be operated on or whether it be previously mixed with various proportions of coal-tar naphtha. If the proportion of the latter be large, the quantity of nitrobenzene formed is larger than can be retained in permanent solution in the nitric acid. This fact causes no inconvenience, for the nitrobenzene forms a separate layer below the petroleum spirit, and in pre¬ sence of nitric acid is not miscible with it. Nitrobenzene and petroleum spirit are perfectly miscible alone, but on shaking the mixture with strong nitric acid the nitro¬ benzene is dissolved out. It will be seen therefore that the reaction with nitric acid may be conveniently em¬ ployed for the determination of petroleum spirit in admixture with benzene. Very fair approximate results are obtainable. If the layer of petroleum spirit be removed with a pipette and shaken with water to remove dissolved nitrous fumes, it is obtained in a suitable condi¬ tion for further examination. If, after removing the layer of unacted-on petroleum spirit, the nitric acid solution be poured into water, a very sensible turbidity is usually produced, even with petroleum spirit free from coal-tar products, and on filtering off the precipitate, or allowing it to settle, and decanting the liquid, distinct evidence of the formation of nitrobenzene is obtainable by the aniline test. When the more volatile portion of petroleum spirit is thus treated, the nitric acid is scarcely coloured at all, and hardly a trace of milkiness is produced when the acid is poured into water. The brown colour and turbidity on dilution increase with the boiling point of the sample of naphtha, and are strongest with kerosine oil ; but in all cases in which petroleum products are treated with nitric acid, the quantity of precipitate on dilution is very insignificant. Although nitrobenzene is recognizable among the products of the action of nitric acid on petroleum spirit, as was shown long since by Schorlemmer, I do not think the turbidity produced on dilution is due solely to its formation. It is probably rather due to the production of various nitro-substitution products, as it is well known thet the higher numbers of the paraffin series are far more readily acted on by nitric acid than their lower homologues. I have attempted to determine the proportion of benzene in a mixture with petroleum spirit, by measuring the nitrobenzene produced, but the results have not been satisfactory, partly in consequence of the solubility of nitrobenzene in water and acid liquids. By employing 250 c.c. of water for dilution, allowing the nitrobenzene to settle completely, decanting the greater part of the water, and pouring the “bottoms” into a graduated tube, the nitrobenzene may be readily measured. If an allow¬ ance of 1*5 c.c. be made for solubility in the one-quarter litre of acid liquid, the measure of benzene present in the sample taken may be roughly ascertained by multiplying the number of c.c. of nitrobenzene obtained by the factor 0-S5. Thus if V be the volume in c.c. of nitro¬ benzene, then the benzene in the amount of sample taken was (V + 1’5) x ‘85. The method is not capable of giving accurate residts, but may be useful in some cases as a check on the determination of petroleum spirit by measurement of the layer insoluble in nitric acid. With a view of learning something respecting the proportion of heptane present in ordinary petroleum spirit, I made a mixture in equal measures of four samples of commercial “ benzoline,” such as is used for sponge lamps. This mixed specimen had a density of *7001 at 15‘5° C., and commenced to boil at about 54° C. It was distilled in the manner first described by Warren, in a flask furnished with an inverted condenser, filled with water, maintained at a temperature of 70° C., a second condenser being kept well cooled by a current of cold water. The distillation ceased when the temperature in the flask was 84° C., that is, 14° C. above that of the first condenser. The water in the first condenser was then raised to the boiling point, and the distillation continued till scarcely anything more came over, by which time the contents of the flask were at 114° C. The result of the distillation was as follows — for 100 measures of petroleum spirit taken Condensed below 70° C. Percentage by measure . . 16 Density at 15‘5° C., com¬ pared with water at same temperature . *667 Condensed Condensed between above 70° and 100° C. 100° C. (residue). 56 26 •707 *742 The loss was about 2 per cent, of the original measure. Another specimen of petroleum spirit gave 22^ measures of distillate with the receiver at 70° C., 42 per cent, between 70° and 100° C., and 32 per cent, of residue; the loss being 3J per cent. The densities of the three products were almost identical with those previously obtained. The observed specific gravities of the first and second distillates correspond approximately with the recorded densities of hexane and heptane, and from this and the known boiling points of these liquids it is evident that the portion of petroleum spirit not condensed at 70° C. will consist chiefly of hexane and lower homologues, while the part condensed at 70° C., but distilling at 100° C., will be chiefly heptane and isoheptane. As, in the experiments described, this fraction measured from 42 to 56 per cent, of the entire spirit, it is evident that the proportion of heptane present equals if it does not exceed that of all the other constituents.* The President said Mr. Allen’s paper was an exceed¬ ingly useful and able one, and invited discussion of it by those who had knowledge of this particular class of chemicals. Professor Tichborne (Dublin) said the paper they had just heard represented a class of papers exceedingly valuable to the analytical chemist, papers dealing with questions bearing on the reactions and detection of admixtures in articles met with in commerce. He should be glad if Mr. Allen would answer two questions. Mr. Allen mentioned that the solvent action of benzole and American light oils were different as regarded pitch. He presumed Mr. Allen meant coal-tar pitch. There were many pitches. One used in road making in Ireland was a pitch procured as a residue in distilling these American oils, and it was probable that that pitch would behave in the same way as regarded the heptane as the coal-tar pitch would behave as regarded benzole, that was, it would be soluble. He wished to know whether Mr. Allen had tried any experiments as regarded the action of these two solvent bodies upon creosote, and whether there was any difference. They knew already * The physical properties of the benzoline examined by me are very different from those attributed to the liquid by Wiederhold, who on fractionally distilling benzoline of *715 sp. gr., which commenced to boil at 60°, obtained — 48 6 per cent, of ‘70 sp. gr., boiling at 100°* 45‘7 „ ‘73 „ „ 200°. 5‘7 „ ‘80 „ ,, above 200°. September 13, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 217 that creosote was frequently adulterated with carbolic acid, and he desired to know if they had any means of distinguishing the adultei’ation by means of these solvents of creosote and carbolic acid. Dr. Symes said with regard to the odour of the two bodies in question, although they appeared to be some¬ what similar, they smelt quite differently. If they were at all compared the odour was a very satisfactory test of the difference between the two, and if the admixture was agitated with water there always seemed to be quite sufficient evidence, not of the quantity, but of the pre¬ sence of petroleum spirit. The difference in the solvent properties was very great. In separating chrysarobine from araroba the solvent powers of benzole were con¬ siderably greater than those of petroleum spirit, and a much larger yield was obtained. In exercising this great solvent property in this particular instance it perhaps produced a less pure product; but he had tried the solvent powers comparatively on some other bodies, and he thought it was exceedingly desirable to know thoroughly what they were using when they were supposed to use either petroleum spirit or benzole. A quantitative test which would readily determine the proportions in which the two had been mixed would doubtless prove valuable. Professor Attfield said some varieties of petroleums were so highly cleaned, that he questioned if they would be detected in benzole by their odour. Mr. J. T. Dobb said Mr. Allen in his statement had referred to pitch. He should like to know if the kind of pitch that was used to ascertain the solubility was Swedish, Stockholm or mineral pitch. The gentleman who had pi’eviously addressed them spoke of pitch as a product of petroleum spirit from America, and used for roads only in Ireland. He found that in the distillation of tar the residue was pitch, commonly and commercially called mineral pitch. He had found himself that it was only partially soluble in petroleum spirit ; but was perfectly soluble in coal-tar naphtha. He wished to ask Mr. Allen what kind of pitch he used to ascertain the solubility of petroleum spirit and the solubility of coal-tar naphtha. Mr. Allen, in reply, said he was very glad gentlemen had called his attention to the kind of pitch he used. He certainly ought to have explained that he used coal-tar pitch. It seemed probable, as Professor Tichborne had suggested, that pitch from petroleum would dissolve in petroleum spirit better than the other. He might add that anthracene, one of the most characteristic constitu¬ ents of coal-tar pitch, was much more soluble in benzol than in petroleum spirit. He had not made any experi¬ ments on wood pitch or petroleum pitch. He had never seen any petroleum pitch, and he would like to obtain a sample. In a paper, written by himself, that appeared in the ‘ Year-Book,’ he had said, “ Absolute carbolic acid dissolves half its volume of petroleum spirit, forming a clear liquid. On addition of a larger portion of petroleum spirit precipitation occurs. With one volume of carbolic acid and three of petroleum spirit, the layers have about the same measures as the original liquid. Each layer, however, contains both liquids, as may be proved by cooling the tube with a freezing mixture (or by wrapping filter paper round it, and dropping ether on the outside) when carbolic acid crystallizes out. Absolute carbolic acid is permanently soluble in about ten measures of petroleum spirit at 15'5° C. ( = 00° F.).” When carbolic acid was shaken with petroleum spirit it must not be supposed that the layers which separated consisted of the original liquors. Each was a solution of the one in the other. With ten measures of petroleum spirit to one of carbolic acid complete solution took place at ordinary temperatures. The solubility was enormously increased by rise of temperature, so that carbolic acid and hot petroleum spirit were miscible in all proportions. Mr. Allen was thanked for his paper. {To be continued.) Parliamentary and Ham §nn[Mliiujs. Prosecution under the Pharmacy Act. At the Horncastle Petty Sessions, held on Saturday,, the 7th inst., before the Rev. Thomas Livesey (Chair¬ man) and the Revs. Samuel Lodge and Arthur White, magistrates, a summons issued by Messrs. Clitherow ancl Elsey, of Horncastle, as agents for Messrs. Flux and Co.„ of London, solicitors of the Pharmaceutical Society of Great Britain, in respect of a sale of laudanum, by Robert Croft at his shop at Horsington on the 19th of July last,, contained in a bottle not distinctly labelled with the name and address of the seller of the poison, was heard. In the absence of the accused, a police constable proved due service of the summons. Mr. Flux, addressing the Court, said that he appeared to support the case on the instructions of the Council of the Pharmaceutical Society of Great Britain, and as he understood that no prior case under the Pharmacy Act. had been under the consideration of their Worships, he; would shortly read the 17th section as being the one most especially applicable to the offence of the accused, and with the Court’s permission would refer to earlier clauses as showing that in some respects the Pharma¬ ceutical Society were specially charged with sundry duties concerning sales of poisons, and thus that the Council was justified in bringing this case before; the Court in order to direct the attention of offenders- and the public in the county to the law regulating; the sale of poisons. He might mention that the consumption of laudanum in the county of Lincoln was excessive, that his clients had special means of information in regard to it, and had knowledge that the consumption of the dangerous and pernicious drug in. and about the fen country had engaged the serious atten¬ tion of the medical officers of the Privy Council. Lau¬ danum was undoubtedly a poison, and Parliament had by the statute expressly enacted that opium and all prepara¬ tions of opium should be deemed poisons, and that sales- of them should be conducted by duly qualified persons* known as chemists and druggists, and with certain for¬ malities, which included labelling with the name and address of the seller. In respect of sales by unqualified persons, penalties were enacted, and in the instance under consideration, the sale had been made by a person not duly qualified, but with that class of penalties the Court had not to deal. The offence of the accused was that of having sold a poison without a label bearing the name and address of the seller so that on any improper use of the article there would not have existed, for the public protection, those traces concerning, the sale which the law contempl ited. He submitted that in thus bringing one case to the Court’s attention and under public notice, his clients fulfilled their mission, and that it was now for the public and those generally charged with the administration of the law within the district to enforce the provisions of the statute. In regard to irregular sales any person might be the prosecutor in a case of the- kind, whether the offender was or was not a duly quali¬ fied seller. Mr. Flux then read from the statute 31 and. 32 Yict. c. exxi, section 17, “It shall be unlawful to sell any poison, either by wholesale or retail, unless the box,, bottle, vessel, wrapper, or cover in which such poison is- contained be distinctly labelled with the name of the; article and the word poison and with the name and address of the seller of the poison, and any person selling, poison otherwise than is herein provided, shall upon a- summary conviction before two Justices of the Peace, be liable to a penalty not exceeding five pounds for the first offence, and to a penalty not exceeding ten pounds for the second or any subsequent offence, and for the pur¬ poses of this section the person on whose behalf any sale; is made by any apprentice or servant, shall be deemed to- be the seller.” 218 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 13, 1879. Police Constable Samuel Kempston, examined by Mr. Flux, proved knowing Robert Croft, who keeps a grocer’s .shop at Horsington. The name of Robert Croft appears over the door. On the 19th July last witness went to the shop, and asked of a person in charge of it if they sold laudanum, and was supplied with the article in a bottle, for which he paid 8%d. The bottle bore a label which did not mention the name or the address of Robert Uroft. He kept the bottle in the condition in which he had received it until Wednesday, the 3rd instant, when he handed it to Dr. George May-Lowe. By the Court : — The label bore the words “ Laudanum — poison,” and also the name of J. H. Elmitt, chemist, Horncastle. Dr. George May-Lowe, of Lincoln, lately public .analyst for the county, examined by Mr. Flux, proved having received the bottle from the constable, and having analysed the contents, and that the contents consisted of a preparation of opium called laudanum. As the magistrates were engaged in consultation, the accused arrived and made a statement not disputing the facts proved, but adding that the bottle was stamped with a patent medicine stamp. The Bench fined the accused £2 10s., and ordered him t) piy costs, £2 12s. 6c?. The accused expressed his inability to raise the amount. The Court (on the suggestion of Mr. Flux) informed the accused of the clause in the Act of Parliament which would expose him to a penalty of £10 on a second or any subsequent offence. Arbitration in a Plaster Dispute. In the High Court of Justice, Queen’s Bench Division, there has recently been decided a case which should be of interest to those engaged in pharmacy. The parties to the suit were Leslie and Co., Limited, -of Walbrook, plaster spreaders, plaintiffs, and Gale and Company, wholesale druggists, of Bouverie Street, defen¬ dants. The warehouses of both firms being within the city of London, the case was heard at the Guildhall, before Mr. Justice Field and a jury. Scientific evidence was given in support of plaintiffs’ case by Mr. Oxton, F.C.S., and for the defence by Pro¬ fessors Redwood and Attfield. The plaintiffs’ claim was one of damages arising, it was alleged, out of defects in the manufacture of resin and white soap plasters, which the defendants, as whole¬ sale druggists, had supplied to them in the ordinary •course of their business. The plaintiffs’ practice was, it would seem, to purchase the crude plaister, and spread upon tapes and other material for which their firm had obtained a reputation. In addition, it was also alleged That on account of the rancidity of the plaster, after it had been spread but a short time only, they had sustained ■a considerable loss. After the case had been fairly opened, the learned -counsel contended that it was one of those disputes that should have been referred to an arbitrator, and that even at this stage it would be much better for a referee to be appointed under the authority of the Court. As both parties, seemed desirous that the case should be decided at the present hearing a mass of evidence extending into the second dav was taken, when the foreman of the jury expressed his conviction that the •case ought to be decided by reference to an expert, in which opinion Mr. Justice Field quite concurred, and directed that both parties should agree upon some one conversant with the subject. Mr. C. Umney, (Wright, Layman and Umney), of Southwark, was accordingly elected as referee, and his appointment was confirmed by Mr. Justice Field, who gave him full liberty to examine the respective parties and their witnesses upon oath. Evidence was taken upon three days at the Cannon Street Hotel, in the City of London, supported on both sides by the same scientific evidence as at the first hearing at Guildhall, Mr. Courtenay appearing for the plaintiffs and Mr. St. John Wontner for the defendants. Mr. Umney ’s award was as under : — 1. That the plaintiffs in this action were a firm of plaster spreaders, who had, during a period of several years supplied the medical profession and the public with adhesive and other plasters in a novel and most con¬ venient form, but that the plaintiffs did not in any way manufacture the crude plasters of which their spread plasters were composed, neither did they, either through their managing director, Mr. J. S. C. Renwick, or their foreman, Mr. Wallace Burnett, profess to have knowledge of such manufacture. 2. That one of the shareholders in the company of which the plaintiffs’ firm was composed, viz., Frederick Henry Smith, doctor of medicine of St. Andrew’s Univer¬ sity, and Fellow of the Royal College of Surgeons of England, who lays some claim to a knowledge of manu¬ facture of crude, as well as spread plasters was, and is, entirely ignorant of the former, and the composition of plaster as detailed in the specification of letters patent of himself for the manufacture of tape plasters or bandages, dated January 16, 18.74, was not only im¬ practicable, but that he himself did never prepare any plaster either of such composition, or from such recipe that was suitable for producing spread plasters. 3. That the plaintiffs not being possessed of that special knowledge of manufacture which is necessary in order that the business of a plaster spreader may be successfully conducted resorted for the purchase of such crude plasters as they manipulated, viz., resin and white soap plaster, to wholesale druggists and others, part of whose business it is to prepare crude plasters (either from formulae tabulated in the British Pharmacopoeia, or from recipes which they find are generally approved by medical practitioners and pharmacists to whom they generally supply them), and that such crude plasters are made of different proportions of ingredients (notably in litharge and oil), as compared with those designedly made for spreading purposes, a fact well known to those conversant with each branch of this industry. 4. That the defendants were in the habit of preparing various plasters, including those used by the plaintiffs, and that they did from time to time supply such from their private recipes in preference to those compounded from official formulae. 5. That the complaint made by the plaintiffs against the defendants’ plasters was in the main non-adhesiveness and rancidity. 6. That the formula given in evidence by the de¬ fendants through one of their firm, Mr. J. S. Walton, who regulated the manufactures of their laboratory, was although non-official, a recipe from which good plaster could be made, and that, when carefully prepared, such plaster, from the fact that it contained to 100 parts of oleaginous or fatty basis upwards of fifty (54) parts of litharge, would not either be rancid or likely to become so during such time in which plasters are generally ex¬ pected to remain in a sound condition, neither could it have been non-adhesive made from the proportion of ingredients combined with the amount of resin prescribed in the formula. 7. That the plasters sold by the defendants were divided into two portions, the one comprised in the total supply from May to September 12, 1877, and the other that manufactured and supplied subsequently. 8. That the plaster supplied previous to September 12, 1877, was prepared from commercially pure ingre¬ dients and was of good average quality, and although jt occasionally contained specks caused by slight defects in certain brands of litharge, these were not uncommon, and might in all probability have been removed by judicious melting, straining and subsidence (by no means an uncommon process in the manipulation of plasters) September 13, lsTf.] TIIE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 219 had plaintiffs or their workmen been conversant with such treatment. 9. That the defendants’ plasters were good and fairly uniform, but even if this were not so, as applied to that supplied subsequent to September 12, 1877, no claim should be made for any defect therein, inasmuch, as re- melting had been resorted to, and this was opposed to a stipulation made by the defendants in a letter written on or about that date which contained conditions upon which the defendants would continue to do business with the plaintiffs and their accountability for their plaster being only so long as it remained in the state supplied, and not after its condition had been altered by melting, spreading or any other process ; the defendants having had at this time a clear notion that the complaint of previous plaster was in the main due to and caused by, the unskilled treatment to which the same was subjected in plaintiffs’ factory prior to spreading, and they, there¬ fore, clearly thought it expedient thus to protect them¬ selves. 10. That plaintiffs’ factory men were in the habit of melting the plaister in pipkins and other vessels over gas burners (Bunsen’s) constructed to give a maximum of heat, and that they did not exercise proper precautions in so doing, stirring of the plaster during the melting process being only sometimes resorted to, as stated by W. Metzner, when diligent stirring to prevent decom¬ position was necessary. 11. That a plaster prepared since hearing evidence, in accordance with defendants’ recipe gave, when chemi¬ cally examined, results corresponding to those obtained from plaister put in evidence and fully corroborated the statements of Professors Redwood, and Attfield. 12. Finally, that for the reasons previously stated the plaintiffs have not proved their case, and judgment, therefore, should be entered for the defendants. The above award being taken up by defendants was handed to Mr. Justice Field, the plaintiffs raising ob- , jections to the same upon finding that it was adverse to them. Mr. Justice Field, however, confirmed Mr. Umney s award, and gave judgment for the defendants with costs. Sis^nsing $fU'moramt;t. In order to assist as much as possible our younger brethren, for whose sake partly this column was established, considerable latitude is allowed, according to promise, in the propounding of supposed difficulties. But the right rvill be exercised of excluding too trivial questions, or re¬ petitions of those th^at have been previously discussed in principle. And ive would suggest that those who meet with difficulties should before sending them search previous numbers of the Journal to see if they can obtain the re¬ quired information. [338]. Add the Liq. Ammon. Fort, drop by drop to the Arg. Nit. solution until the precipitate first formed is re¬ dissolved. It is the formula for a dark brown hair dye, which I inserted in this J ournal two or three years ago. HuU. F. Stayeley. [338]. In this prescription it is evidently intended that the Liq. Ammon. Fort, is to be added to the nitrate of silver dissolved in the water, until the precipitate which is at first produced is redissolved. This is a common receipt for hair dye, and is used after an application of a solution of pyrogallic acid. W. Fowler. [340]. Iodide of sulphur should be triturated with a few drops of S. V. R. in making the B.P. ointment. It is less objectionable than glycerine, and it ensures the production of a faultless ointment. In the next edition of the B.P. the form might, with advantage be altered to — Take of Iodide of Sulphur . 30 grains. Rectified Spirit . 15 minims. Prepared Lard . 1 ounce. Triturate the iodide of sulphur with the spirit in porcelain mortar, and gi'adually add the lard, rubbin them together until the ointment is perfectly smooth. R. H. Parker. International Medical Pharmaceutical Dictionary,, in three languages, French, English and German, com¬ piled for the use of physicians and chemists in inter¬ course with foreigners, by George Herman Moeller, chemist, professor, etc. Munich : 1879. Jul. Grubert, publisher. Perhaps a good dictionary may be considered one of the most valuable books in a library, and a library, how¬ ever well chosen, must, without a dictionary, be considered incomplete; but there are dictionaries and dictionaries, and whilst there exists so great a variety and “ still they come,” it is necessary to use some discrimination as regards their choice. The general principle in the arrangement of a dic¬ tionary should be that it contain the words or subjects of which it treats arranged in alphabetical order ; but in modern times, to meet the extension in several branches of science, and the daily increasing desire for knowledge, works of very varied kinds have been prepared on the principle of alphabetical arrangement, and are termed dictionaries. The title of the one before us is attractive; it professes to give the equivalent terms in three different languages necessary for mutual understanding of the medical man and the pharmacist in their intercourse with foreigners. The book is divided into four parts ; the first embraces materia medica, the second, man and his maladies, or the human body and its physiology, the third, phai-maceutics, the fourth, chemistry and physics, and these again are sub-divided ; for instance, materia medica is subdivided into the therapeutic classification of medicaments, the pharmaceutic classification of the same, patent medicines with their prices, and finally the art of prescribing. The materia medica proper embraces probably all the organic and inorganic materials that ever have formed a part of the materia medica of any European country, from “ Ping-war-har-jamby” to “spirit of treacle.” The second division, man and his maladies, is subdivided into physiology, including every part of the human body and diseases with all the “ills that flesh is heir to.” The third, pharmaceutics, has in its subdivision every article required in pharmacy, from a bung to a thermometer, and every appliance found in the laboratory from a screw press to a gridiron. The fourth, chemistry, is so sub¬ divided as to include the elements, simple combinations, and chemical analysis, from a simple element to a “compound atom,” together with botany and zoology. Every object in the several sciences named, with every term required to be used in their pursuit, are here given in three languages, followed by a complementary vocabu¬ lary, and a copious index in the German language, from which it may be inferred that the work is primarily in¬ tended for the German aerzte and apotheker. If it were leasonable to ask a person to employ his leisure time in learning a dictionary, doubtless much information would be acquired from this one, but life is too short to admit, of such a luxury. The work may sometimes prove useful, but it is too diffuse to be readily available. Where there is a dictionary it can scarcely be said to supply a want, or where there is not one to compensate for the deficiency; and the labour bestowed upon it by the author will, we fear, be ill requited if its sale be dependent as a? THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 13, 1379. ^20 •on its being used by physicians and chemists in Great Britain as ai assistance in their intercourse with foreigners. df o ititcsg o n d r No notice can be taken of anonymous communica¬ tions. Whatever is intended for insertion must be authenti¬ cated by the name and address of the writer; not necessarily for 'publication, but as a guarantee of good faith, A Request. Sir, — With your permission, I wish to ask those who are in a position to give it, for tangible proof that the patent medicine stamp is used to cover the sale of scheduled poisons. As the sale of poisons under the guise of so-called patent medicines is likely to engage the attention of the Pharmaceutical Council, I am anxious to demonstrate by ample proof that the Act of Parliament is thus infringed. May I ask therefore that members of the trade will kindly obtain for me, as soon as convenient, samples of pokons sold under cover of the medicine stamp, and that they may be sent to my address as annexed ? 205, St. John Street Road, E.O. Eobt. Hampson. How can a Chemists’ Assistant register Himself as a Dentist in bona fide Practice? Sir, — The above question has been asked me during the last few months by numerous friends in both the dental and medical piofessions; in consequence I have been at considerable trouble to ascertain if any chemists’ assistants really had registered as such, and I find that they have. I have also had chemists pointed out to me who have never done any dental operation beyond extracting a tooth, and have probably never seen inside a dental laboratory, and know absolutely nothing of “ dentistry,” who have registered as being in bond fide practice as dentists. Now the Act never contemplated registration by any persons other than those known as being engaged in the practice of dentistry, either separately or iu conjunction with pharmacy or surgery. It does not follow that because a chemist placed an en¬ graved plate with the word dentist on it, upon his door, at the passing of the Act, that the law will recognize him as a dentist. A dentist in the eye of the law must have been a person engaged in every branch of the dental art, i.e., able to undertake any operation and do any mechanical woik that may be required for the mouth by the public. The various dental associations, formed for the express purpose of sifting out fraudulent registrations, have an agent in every town now busily engaged in compiling a list of such registrations. Section xxxv. of the Dental Act, 1873, provides for such by fine and imprisonment. Many think that because they have filled up the declara¬ tion paper sent by the Registrar, and received from him the “Dental Registration Certificate,” that they are now safe ; such, however, will not be the case without legal evidence of qualification and fitness, which will be de¬ manded by the “ British Dental Association.” No chemist regularly engaged in “ bond fide practice as a dentist” need fear any annoyance or subsequent trouble from the requirements of the Dental Act ; such, however, as cannot bear the strictest investigation as being bond fide in practice at the passing of the Act had better at once, and previous to the publication of the register, apply to Mr. Miller, and have their names erased to prevent “ Section xxxv. ” being carried into effect. 1, St. Domingo Vale, Liverpool. J. J. Musgeave. SP. iETHER. NlTROSI. Sir, — In your issue of August 2, there appeared a letter on this subject by Mr. W. Pollard in reference to the paper by me in the Journal of July 19. The usual derangement of business consequent upon holiday time must be my apology for the delay in replying. Two questions appear to have suggested themselves to Mr. Pollard, and upon which he asks information. 1st. How is it that 2 per cent, of aether. is separated by the solution of calcic chloride, and only 1*72 is obtained by analysis? In answer to this query, I must refer Mr. Pollard to the discussion that followed the reading of a paper at Blooms¬ bury Square, reported in the Journal, on page 377, vol. viii., 1877, and he will find it stated by some of the speakers that the ethereal fluid that rises in the tube is not all nitrite of ethyl, and the analysis I have given shows this to be true. 2nd. What becomes of two-thirds of the nitric acid used in the process P Some of the nitric acid is decomposed by the alcohol, aldehyde and -water being formed, a further portion remain¬ ing in the retort unused. Bradford, Sept. 10, 1879. F. M. Rimmington, Weights and Measures. Sir, — Mr. Martindale in his note says that “the troy cup weights in general use have always had this, the troy pound of 12oz., as their largest weight.” This is certainly not “ always ” the case, all the troy cup weights I have ever seen run thus— 5ij, 5ij, 5iv, 5j, 3u» §iv, gviij, going on to 16 and 32oz., the larger cup being always of the same weight as those fitting into it. I would give a hint to people having the larger cups of 16 and 32oz., that if the inspectors see them it may not be altogether pleasant, as these weights are not mentioned in the schedule and there is no standard for them ; but in this as in some other matters connected with the Act, we can only hope the authorities will not ask too many questions. Manchester. W. Wilkinson. Liq. Kino (‘Year-Book,’ 1873). Sir, — I take the opportunity now the subject is again before the members of the Conference and readers of your Journal to make a necessary correction. In the ‘ Year-Book ’ for 1873, in the paper on page 554, line 12, “four” should be “one and a half,” which dilution would then bring the solution to the same strength as the tincture, i.e., 2oz. Kino to Oj. I would ask those possessing the ‘ Year-Book’ to make the necessary alteration. I did not observe the mistake till after the ‘Year-Book ’ was published, and had not that paper been mentioned at the Sheffield Conference by Mr. Benger, I should not have thought it necessary to call attention to the error which was an oversight of mine at the time of writing the paper. Sheffield. G. Ellinor. Gilvach, M. — See a letter on the subject in the previous column. F. Watts. — (1) Ballota nigra. (2) Stachys Betonica. (3) Origanum vulgare. “ Querist .” — The latest edition of Fownes’s ‘ Chemistry ’ is the 12th, published in two volumes iu 1877. J. Thompson. — Salvia verbenaca. G. R. P. — Ohenopodium album. J. H. Dingle. — (1) Peplis Portula. (2) TJsnea plicata. (3) Molinea ccerulea. 4 and 5 belong to the genus Ampelopsis, but the materials are not sufficient to deter¬ mine the species. “Fred.” — The Army Medical Department. “ Spes.” — We are unable to give the inforinatioh asked for. “ Apprentice .” — If possible, send the original prescrip¬ tion ; probably you have misread it. A. N. — See the discussion in the “Dispensing Memo¬ randa” in vol. viii., pp. 19, 38 and 67. “ Associate .” — There is no such preparation in the United States Pharmacopoeia. B. T. Gregory. — You should apply to a respectable book¬ seller for the information. T. P. Blunt.' — The substance in question is not included in the schedule, it not being a cyanide. D. Dickinson. — Registration in America does not protect a title in England. W. J. Sanders. — Probably Galangal root (Alpinia offici - narum, Hance). Communications, Letters, etc., have been received from Messrs. Parsons, Hamilton, Long and Co., Dickson, Hop- kinson, Fletcher, Howard, Benger, Robinson, Pope, Rim¬ mington, Tait, Mason, Atkins, Naylor, Collier, Elton, Gosling, Draper, Landerer, Corder, Musgrave, Bostock, Barnaby, Stoner, Abraham, Laing, Norman, Chadwick, Tupholme, Junior, Tyro, Inquirer, Epsilon, Greek Fire, Ignoramus, Junius, Minor, Sandford, R. W., M. P. S., J. T., W. L., T. S. W. September 20, 1879.) THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. ! 221 NOTE ON GENTIAN ROOT. BY 0. CORDER. Whilst walking through the Engadine, Switzer¬ land, this summer, I found in some valleys, as in the Beveos Thai, great quantities of Gentiana punctata, and in one chalet saw several tons dug up for medicinal use ; in others as in the Fex Thai, only G. lutea was noticed, and upon inquiry from a local botanist, M. Cavretzel of Pontresina, he informed me that I was correct in supposing that hotli are indis¬ criminately collected for pharmaceutical purposes. The two plants differ but little in the growing state, but when in flower would never be mistaken, G. lutea, having a yellow corolla and G. punctata a yellowish green one profusely spotted over with black dots. THE PHARMACEUTICAL EXHIBITION IN HANOVER. One of the most interesting features of the meetings of the Deutsche Apotheker-Verein consists in the exhibition of objects more or less closely associated with pharmacy, and the display in con¬ nection with the recent meeting in Hanover, although including many exhibits which have lost the charm of novelty, well recompensed the trouble of a careful examination. The larger portion of this exhibition was shown in the basement and gallery of a good sized hall in the “Odeon,” adjoining the hall in which the meetings of the Association were held, but the machinery and larger pharmaceutical ap¬ paratus overflowed into the concert grounds, where they were placed under a long shed. The number of exhibitors was considerable, the Catalogue containing 161 names. It was rather noticeable, however, that the manufacture of che¬ micals, as distinct from pharmaceutical preparations, was almost entirely unrepresented. On the other hand, several of the exhibits might be looked upon as being rather excrescences of pharmacy than pharmaceutical. Paper and labels, bottles and boxes, infants’ foods and extracts of meat, condensed milk and soluble cocoa, aniline dyes and phosphorus paste, all had their exhibitors, and most of the cases were praiseworthy, but they presented in this direc¬ tion little beyond what pharmacists are accustomed to see in this country. 1 Amongst the knickknackeries of elegant phar¬ macy one could hardly help being struck by the development in the preparation of gelatine capsules and perles. Some very fine and elastic specimens of these were exhibited by H. Kalile, of Konigsberg, and G. Pohl, of Schonbaum. In fact the gelatine capsule has developed in more ways than one, speci¬ mens being shown as containing 15 grams of oil. A remark as to the large size of these led to a practical demonstration with one by an obliging bystander, and the capsule was bolted without any indication of present difficulty or —what was quite as noticeable, perhaps — fear of subsequent inconvenience. Pas¬ tilles were also shown in considerable number, and of tempting appearance, one of sal ammoniac being frequently met with. Much nattiness was also evident in the getting up of plaster in small quan¬ tities, long strips of different widths being rolled up and enclosed in tin boxes for sale for a few pfennigs. Allied with these were also to be seen small rolls of linen, charged with plaster of paris, put up in air¬ tight cases, requiring only to be wetted to be ready Third Series, No. 482. for use as plaster bandages. It may be remarked here, that some of the plasters appeared to be of admirable quality; especially may be mentioned an adhesive plaster on silk, exhibited by R. H. Paulcke, of Leipzig. This exhibitor also showed a fine speci¬ men of glass wool, prepared from crystal glass and warranted to be free from lead, which metal has been alleged to be a source of impurity when glass wool is used as a filtering material. Some very good specimens of drugs in powder, both coarse and fine, were shown by different ex¬ hibitors, notably by Dr. Brunnengraber, of Rostock, in whose case was also a fine cake of expressed oil of nutmeg. Many specimens of barks and roots cut small, but to a uniform size, for the convenience of pharmaceutical operations, were also to be seen, though perhaps the best show of these was made by W. Kathe, of Halle. Especially noticeable in this display were the fine specimens of rhizoma iridis, rhizoma galangae, radix liquiritise, and radix rhei cut into small cubes. Some remarkably fine ergot was also shown by Mr. Kathe. It was stated to be the choice pickings of large parcels of ergot of rye collected in different parts of Germany, especially in Prussian Silesia, but the size was so enormous as to suggest the idea that it might have been parasitic on some other plant than rye. A very fine case of pharmaceutical preparations was displayed by Dr. F.. Witte, of Rostock. It con¬ tained a very large and handsome crystallization of caffein, but of not less interest was a series of pre¬ parations of pepsin and peptones. Amongst these was an “Eisen-pepton,” prepared from a fibrin pep¬ tone. It is claimed that iron administered in combi¬ nation with peptone is presented to the stomach in a form in which it does not cause irritation to the mucous membrane and is very easily assimilable. This preparation is in the form of powder, is said to be easily and perfectly soluble in water at a temperature of 28° C., and to contain 5 per cent, of iron oxide. A “ tinctura episcopalis ” gave rise to some specu¬ lations as to its possible origin, which were by no means allayed by the subsequent visit to the old cathedral at Hildesheim, where the remains of several bishops are supposed to lie at rest. Attention has recently been directed to the subject of crystallization, and especially to the behaviour in this respect of solutions of isomorphous salts to each other. ■ A case of crystals exhibited by F. Meyer, of Geestemiinde, contained some very fine crystals, which well illustrated some principles laid down in two papers that have appeared in this Journal during the present year.* One very fine and perfect octahedron of chrome alum crystallized over ordi¬ nary alum weighed 1550 grams. From mixtures of solutions of the two alums the crystallization of chrome alum appears to take place most rapidly at starting, as indicated by the centre of the crystal being much darker than the outer portion. J udging from similar evidence, when a crystallization of magnesia sulphate is grown over nickelous sulphate the greater part of the deposit takes place at the ends of the prism as compared with the sides. In the exhibit of Schmidt and Haensch, of Berlin, was an instrument that promises to respond to what was mentioned at the recent Conference meeting at Sheffield as a desideratum. This was a small pola- rimeter, which is described as a “ half-shade Mit- scherlich.” From a cursory examination it appeared * 1'twi m. Jour.L. p>], voJ. ix., pi . 6.r8 and 7a>. 9,9,9, THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 20, 1879; to "be a fairly good and delicate instrument,— tlie vernier being graduated to degrees representing each 1 per cent, of sugar, — and the price was five guineas. It is probable that an opportunity of examining this instrument, as well as a low-priced, but apparently very good, students’ microscope, will be afforded at an evening meeting in the coming session. Some of the microscopes of this firm were fitted with an ingenious arrangement by which, after the traveller has carried the object glass from end to end hori¬ zontally across the field of vision, upon reversing the movement the object glass is, by a ratchet action, shifted vertically just sufficiently to expose a fresh field, and thus a systematic examination of an object can be attained. In the machinery and apparatus shed were some very handsome and comprehensive pharmaceutical apparatus, aiming at the same objects as those described and illustrated in this Journal in the papers by Mr. Corder and Mr. Schacht* A small vacuum apparatus, valued at £35, was also exhibited by F. H. Meyer, of Hanover. There were also several pharmaceutical presses. One consisted essentially of two vertical plates, with cavities to contain hot water, and was worked by a double screw (one to each plate). In another the pressure was effected by drawing four rvedges placed above the pressure plate from an inclined into a perpendicular position. Mills, appa¬ ratus for filling, corking and washing bottles, etc. , were also shown, but these call for no particular remark. There was also a small stove, adapted for the use of petroleum as a source of heat. Different people have different tastes, and to some probably the small side room, devoted to the “His- torisch-pliarmaceutische Austellung,” was the most acceptable part of the whole. This was the first time in connection with this Association that an attempt had been made to gather together literary and other antiquities more or less belonging to pharmacy, and the committee at Hanover maybe fairly congratulated upon the success that followed their effort. This is not the place for a catalogue, but it may be men¬ tioned that the collection included some very curious old specimens of pharmaceutical utensils, including a brass mortar, which has just completed its five hundredth year, as would appear from the inscrip¬ tion, “ ghegote van ian verpiet. 1379.” Some bezoar stones, mounted in gold filagree and formerly worn as charms, recalled a materia medica that has passed away. But this was done more vividly by a case of ancient remedies from the Altstaclen Apotheke . It contained a large number of specimens in small bottles, and among those of which the labels could be deciphered -were the following : — viperarum spinoe, viperarum exuvite, dentes lupi, dentes lio- minis, pili cervi, pili leporis, pili liirci, calculus ex vess. fel. bovini, calc, ex vess. humance, priapus cervi, testiculi equi, testiculi cervi, testiculi cervis, testae fiuviatilis, succinum rubrum, succinum artifici- ale, stercus pavonis, stercus murium, stercus hiru- dinum, stercus equorum, stercus columbarum, and stercus anseris. There was a considerable collection of old documents, consisting of “ privilegiums,” indentures, certificates, and the like, most of them bearing a date in the latter half of the eighteenth century, but some much earlier. Many of these documents were elaborately emblazoned and other¬ wise ornamented, and most of them were written in the German language and characters. Amongst the # Phcwm. Journ. [3], vol. vii., p. 349, and vol. viii., p. 225. — . ' ' ' - : - ^ books were several very old herbaria and herbals, a number of old pharmacopoeias, mostly of German states, but some British, and several ancient works on alchemy and chemistry. Perhaps, as Victor Meyer has recently shown that it is not always safe to overlook as exploded the theories of these old masters, there may be a tendency just now to hunt up the literature of the past for hints. It will not therefore be out of place to conclude this notice with mention of the ‘ Zymotechnia Fundamentalis, or. the General Principles of the Art of Fermentation,’ published at Frankfort in 1734, a book which ap¬ pears promising forage ground at a time when the- nature of the “ elements ” is so much discussed, since it claims on the title-page to describe how a true sulphur may be artificially produced (“ wie ein wahrer Schwefel durch Kunst zum Vorschem zu bringen ”) . CITRATES OF QTJINIAA BY A. F. MANDELIN. The author has made investigations in the pharma¬ ceutical laboratory of the University of Dorpat, under - Professor G. Dragendorff, on the composition of various citrates of quinia which may be obtained of a definite - composition. He first gives an historical review of the labours of his predecessors. Dr. Guleani, of Venice, was the first who proposed (in 1832) a method for preparing a citrate of quinia by double decomposition of sulphate of quinia and sodium citrate. The former salt may be either neutral or acid according to its nature the proportions of the two salts required to react upon each other will somewhat vary, but they will yield in each case the same product, namely,, a neutral salt.f a.) 3(2Qu.H2S04) + 2Na3H3(C6H507)2t = neutral quinia sulphate + “acid ” sodium citrate = 3Na2S04 + 2(3Qu.2Ci). sodium sulphate + neutral quinia citrate. h.) 3(Qu.H2S04) -!- 2Na3C6H507. acid quinia sulphate + neutral sodium citrate. = 3Na2S04 + . 3 Qu.2 Ci. sodium sulphate + neutral quinia citrate. Wittstein analysed the crystallized salt and found it to- correspond to a formula which in the new notation would- be 2Qu.Ci.5JH20. Dr. Hager, in 1859, directed to prepare it from Id- parts of citric acid and 29 parts of pure quinia. Its composition was given as 3Qu.2Ci.l0H2O. In 1875, the same author changed his directions to 1 part of citric acid to 3-5 parts of pure quinia. He called the resulting salt neutral citrate of quinia, and gave its composition as 2Qu.Ci.7H20. In 1876, however, he reduced the proportion of quinia to 3 parts, and returned to the original formula, namely, 3Qu.2Ci. 10H2O. The Austrian Pharmacopoeia directs to saturate citric acid with freshly precipitated quinia hydrate. Dcebereiner (1861) gives for this the following formula: 2Qu.Ci. Geiger, in 1845, directed the same method of pre¬ paration. The Netherland Pharmacopoeia (1871) directs 1 part of citric acid and 3 parts of quinia hydrate, which yield, according to Stceder (1878), a salt of the composition 3Qu.Ci.lOH20. * Prom New Remedies, September, 1879. Abstract of a paper by K. P. Mandelin. Chinincitrater : TJndersok - ningar i farmaceutisha laboratoriet i Dorpat. Af K, F. Mandelin, fr. Jcensuu i Finland. 8vo. Dorpat, 1879. + Throughout the above text we have abbreviated the formula for quinia (C2oHo4N202) by “ Qu.,” and the for¬ mula for citric acid (CgHgO-) "by “ Ci.” X This stands really for 2 Na;jCtiH507+2H3C;iHa07. September 20, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 223 Wurtz gives the composition 2Qu.Ci.5H20. The author now proceeds to give an account of his •own investigations. He brought together citric acid and quinia in four different proportions, and analysed •the resulting crystallized salts with the following re- •suits : — a. Three molecules of quinia and two molecules of citric acid. He obtained a salt containing 0'3963 per cent, of water, 72 ‘99 per cent, of anhydrous quinia, and (28*14 per cent, corrected) 26 '62 per cent, of citric acid, and corresponding to the formula 3Qu.2Ci. b. One molecule of quinia and one molecule of citric acid. The resulting salt was anhydrous, and contained i64*55 per cent, of anhydrous quinia and (32 '43 per cent., •corrected) 35*45 per cent, citric acid. Composition : 'Qu.Ci. c. One molecule of quinia and two molecules of citric •acid gave a salt containing, when dried in the air, 0'60 per cent, of water, 63*79 per cent, of anhydrous quinia .and 35*59 per cent, of citric acid (calculated by dif¬ ference). The composition is, therefore, probably the same as that of the preceding salt. Hesse has already stated that by treating one molecule of quinia with a little more than one molecule of citric acid, a salt of the composition Qu.Ci. is obtained. d. Two molecules of quinia and one molecule of citric .acid. This salt contained 1*14 per cent, of water, 78*28 per cent, of anhydrous quinia, and 20 '32 per cent, of citric .acid. Composition: 2Qu.Ci.£H20. The solubilities of the three obtained citrates are the following in 100 parts of water : — Cold. BjiliDg part8 parts Basic Quinia Citrate (2 Qu.Ci.) 0'1093 2*25. Neutral „ „ (3Qu.2Ci.) 0 'll 33 2*39. Acid „ „ (Qu.Ci) 01566 2'60 PETROLEUM FROM THE CASPIAN.* A correspondent of the Daily News, writing from Baku, on the Caspian, gives an account of the petroleum springs •existing there. All around Baku the ground is sodden with natural issues of naphtha. In some places the earth is converted into a natural asphalte, hard during cold weather, but into which the foot sinks a couple of inches at midday. Add to this that, owing to the scarcity of water, the streets are moistened with coarse black residual naphtha. It effectually lays the dust during fifteen days. After this period a thick ih-own dust lies four or five •inches deep in the roadway, over which the numerous “ phaetons ” or street carriages glide so softly and noise¬ lessly that the foot passenger is frequently in danger of being run over. When a north or west wind arises, the air is thick with impalpable marly earth, combined with •bitumen. The least glow of sunshine fixes this indelibly in one’s clothes. No amount of brushing or washing can remove it. The shores of Baku bay north of the town trend towards the east, and some five or six miles distant are the petro- . leum, or, as they are termed, the naphtha springs. The surrounding district is almost entirely destitute of vegeta¬ tion ; and in its midst are some black-looking brick buildings, interspersed with curious wooden structures, twenty feet high, resembling Continental windmills. ‘These latter are the pump or well-houses covering the borings for oil, and in which the crude liquid is brought ■ to the surface. All around smells of petroleum, and the ground is black with waste liquid and natural infiltrations. Boring for naphtha is conducted much in the same manner as that for coal. An iron bit, gouge-shaped, is fitted to a boring bar, eight or ten feet in length, which is successively fitted to other lengths as the depth of the piercing increases. This depth varies from fifty to one * From the Journal of the Society of Arts , August 29, hundred and fifty yards, this difference existing even at very short horizontal distances, sometimes not over forty yards. Layers of sand and rock have to be pierced. It is in the sand that often the greatest difficulties have been met with. A loose boulder will meet the boring tool, and displacing itself leave the passage free. But when the l’ods are withdrawn to allow the introduction of the tubes which form the lining of the well, the boulder falls back to its place, and baffles all attempts to continue the orifice. This boulder difficulty is the great terror of those commencing to bore. Sometimes, after a lengthened discharge of heavy carburetted hydrogen, the naphtha rises to the surface, and even flows over abundantly, as in the case of the artesian well. Under ordinary circum¬ stances, it has to be fished up from a considerable depth. The boring is generally ten, or at most eighteen inches in diameter. A long bucket, or rather a tube stopped at bottom and fifteen feet in length is lowered into the well, and drawn up full of crude petroleum, fifty gallons at a time. This, which is a blue-pink transparent liquid, is poured into a rudely constructed, plank-lined trough at the door of the well-house, whence it flows by an equally rude channel to the distillery. The distillation is con¬ ducted at a temperature commencing with 140 degrees Centigrade, much lower, I am told, than the first boiling point for that from Pennsylvania. When no more oil comes over at this heat, the result is withdrawn and the temperature increased by ten degrees. This second result is also laid aside, and the heat being again increased a third distillation is carried on until no further easily evapo¬ rated liquid remains. This last is the best quality of petroleum for lamps. That which preceded it is the second quality; and the first, or highly volatile, liquid is either thrown away or mixed with the best and second best % j an adulteration. The thick dark brown treacly fluid remaining after distillation is termed astalki, and is that used for the irrigation of the streets. The distilled petro¬ leum, if used in lamps, would quickly clog the wick with a carbonaceous deposit. Previous to being offered for sale, it is placed in a large reservoir, within which revolves a large paddle-wheel. Sulphuric acid is first added, and after being allowed to settle, the clear top liquor is drawn off, and similarly treated with caustic potash. After this it is ready for sale. Up to the present, the residues, after the acid and potash treatments, have not been utilized. I have no doubt but that, later on, valuable products can be derived from them. With the astalki, or remnant after the first distillation, it is different. For years past it has been the only fuel used on board the war ships and the mercantile steamers of the Caspian. At Baku its price is only nominal, vast quantities being poured into the sea for lack of stowing space or demand. In cooking apparatus it is used, and for the production of gas for lighting purposes. In the latter case it is allowed to trickle slowly into retorts raised to a dull red heat, pure gas with little graphite being the result. Weight for weight this waste product gives four times as great a volume of gas as ordinary coal. By distillation at a high temperature and treatment with an alkaline substance, a product is obtained which is used as a substitute for oil in greasing machinery. Apart from the local use of petroleum for lighting purposes, and its exportation for a similar use, comes its application to steam navigation. With the old-fashioned boilers in use, having a central opening running longitu¬ dinally, no modification is necessary for the application of the new fuel. A reservoir, containing some hundred pounds weight of the refuse (astalki), is furnished with a small tube, bearing another at its extremity, a few inches long, and at right angles with the conduit. From this latter it trickles slowly. Close by is the mouth of another tube, connected with the boiler. A pan containing tow or wood saturated with astalki is first introduced to heat the water, and once the slightest steam pressure is pro¬ duced, a jet of vapour is thrown upon the dropping bitu¬ minous fluid, which is thus converted into spray. A ligh 224 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 20, 1879. is applied, and then a roaring deluge of fire inundates the central opening of the boiler. It is a kind of self-acting blow-pipe. This volume of fire can be controlled by one man by means of the two stop-cocks as easily as the flame in an ordinary gas jet. This I have repeatedly witnessed on board the Caspian steamers. As regards the expense, I give the following data on the authority of a merchant captain who has used naphtha fuel for years. His steamer is of four hundred and fifty tons, and of one hundred and twenty-horse power. He burns thirty poods per hour of astalki to obtain a speed of thirteen nautical miles in the same time. One pood is about thirty-three English pounds (16 kilogrammes), and costs on an average from five to six pence. Thus a twenty hours’ voyage at full speed for such a vessel costs about twelve pounds sterling. The fuel is as safe and occupies much less space than the amount of coal necessary to produce a similar effect, not to speak of the enormous difference in price, and the saving of manual labour. Two engineers and two stokers suffice for a steamer of a thousand tons burden. With the immense supply of natural petroleum, as yet only very slightly developed, and its application to the already guaranteed railway from Tiflis to Baku, and to the in¬ evitable future ones beyond the Caspian over the plains of the far East, I think this subject is worthy of every attention. Yet there are proprietors of large tracts of petroleum-bearing ground Avhose capital rests unproduc¬ tive because of a want of demand. The island of Tchili- can, not far from Krasnavodsk, teems with the precious liquid. The sea-ward cliffs are black with its streams flowing idly into the sea ; and a natural paraffin, or ‘•'mineral wax,” is found abundantly in the island and in the low hills a hundred versts west of Krasnavodsk. All round Baku the ground is full of naphtha. I11 hundreds of places it exhales from the ground and burns freely when a light is applied. Only a couple of months ago the volatile products produced a remarkable effect a couple of miles south of Baku. A large earth cliff front¬ ing the sea was tumbled over as by an earthquake shock and, as I saw myself, hugh boulders and weighty ship’s boilers were thrown a hundred yards. In some places I have seen fifty or sixty furnaces for burning lime, the flame used being solely that of the carburetted hydrogen issuing naturally from fissures in the earth. OIL OF GATJLTHERIA.* BY JOSEPH BRAKELEY, PH.G. The manufacturers of this oil are generally men of limited means and knowledge, and the apparatus used is very crude and simple in its arrangement, being easily taken down and removed to other parts when the supply of leaves is exhausted. This generally occurs in two or three years. The first point in locating, after finding where the plant grows plentifully, is to secure a stream of water with enough fall to allow it to be carried to the top of the refrigerating tub. Under a rough shed the apparatus is erected, consisting generally of an ordinary copper whisky still with a capacity of from two to four hundred gallons, enclosed in brick work, and with the head only projecting. The still is connected with a copper worm, and a cask or tub to receive the distillate completes the arrangement. The process followed is the one generally used in dis¬ tilling volatile oils. The leaves are placed in the still, covered with water, and heated by an open fire beneath. The steam carrying the volatile oil passes through the worm, is condensed, and the product is collected in the receiving vessel. The oil settling to the bottom, most of the water is dipped out and used again with the next lot of leaves, while the oil is collected by means of a tin _^*^From the American Journal of Pharmacy , September, separating funnel. The advantage of using the same water in each succeeding operation seems to be under¬ stood and is in general practice. The above method is the one nearly always followed, and the amount of volatile oil obtained varies from ‘66 per cent, to ‘80 per cent. This is the percentage as given to me by a number of manufacturers. From their statements I believe the average yield to be abont seven- tenths of one per cent. From certain facts given to me by one manufacturer I believe that were a close wooden cask or vessel substituted for the metallic still, and live steam introduced and passed through the leaves, a larger product would be obtained. This process was the only excejffion to that usually followed. He made his still of heavy tin plate in place of copper ; this would be of the usual size and shape, and one would last five or six months. He always noticed that when the still was new and first used the amount of oil produced was very large, and gradually and steadily grew less as the still became older. Finally he would hardly get -o per cent of oil, and would be obliged to throw the still aside. On ex¬ amining it then he would find it very much corroded and eaten away inside where the steam and oil came most in contact with the metal. He also noticed that a brown spongy mass would collect in the bottom of the receiving vessel, and that the amount of this deposit seemed to be inversely in proportion to the yield of oil. That is, when the still was new it would be almost wanting, and would gradually increase with the age of the still. This decrease in yield could hardly be ascribed to the plant giving a greater quantity of oil at one season of the year than at another, as the stills were renewed at different times in the year, and always with the same result. The most probable couclusion is that the oil acts on the metal at the temperature used in distilling, and forms the deposit referred to as collecting in the oil. I could not ascertain if other manufacturers using copper stills had noticed the same corroding effect, but as the average yield with all seemed to be about the same, I should think it very probable. This same party used also a false bottom in his still, srqrporting the leaves over a small quantity of water, merely the steam passing through the leaves. He found this arrangement to give better results. There was an arrangement by which the overflowing water from the receiving tub was returned directly and continuously to the still, thus retaining the water there at a constant level. The oil as thu3 obtained has the specific gravity 1T7 and is of a pale red to a deep brown colour, and by most manufacturers is thus sent into the market, packed in tin cans of various shapes and sizes. One party uses animal charcoal, obtaining a product entirely colourless. He tried redistilling the oil with water and a small quantity of fixed oil, but did not get a satisfactory result; then he tried filtering through animal charcoal and was still unsatisfied. Then he adopted the plan of maceratiug the charcoal with the oil for several o’ays and then filtering off the oil, which is thus well decolorized. The filter and charcoal are returned to the still with the next lot of leaves, thus losing no oil. The leaves are gathered principally by woman and children. The price paid varies with the locality and abundance of the plants, seldom going below 1 ‘00 dollars or over 1*75 dollars per one hundred pounds. To gather fifty pounds of leaves is considered a good day’s work. The average is less, being nearer twenty-five or thirty pounds. The wages earned are small, but the entire family will turn out in the morning, so that by evening they will have collected a good quantity. The people, though, are apt to be indolent, and the manufacturer often finds himself without the material to operate on, and so earns rather a precarious living. None, so far as I know, have ever grown rich at the business, and the decline in the price of the oil in the market of late years has still further reduced their profit. September 20, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 225 §harnt;i apical Journal - ♦ - SATURDAY, SEPTEMBER 20, 1879. Communications for the Editorial department of this Journal, books for review, etc., should be addressed to the Editor, 17, Bloomsbury Square. Instructions from Members and Associates respecting the transmission of the Journal should be sent to Mr. Elias Bremridge, Secretary, 17, Bloomsbui'y Square, W.C. Advertisements, and payments for Copies of the Journal, Messrs. Churchill, New Burlington Street, London , W. Envelopes indorsed “ Pharm. JournJ THE STATE OF PHARMACY IN GERMANY. Pharmaceutical affairs in Germany are at tlie present time in a state of agitation in reference to several important questions, the discussion of 'which will not be without some interest on this side of the Channel as throwing a light upon subjects which have here engaged the attention of pharmacists during the last few years. As our readers are prob¬ ably aware, the practice of pharmacy in Germany has been for ages carried on under conditions especi¬ ally favourable for the interests of those engaged in the business. The old established usage by which the possibility of competition was almost done away with is a condition so foreign to our experience at home that some will be inclined to envy the position of a German pharmacist under that regime , and almost to wish that something of the same kind could be established here. Unquestionably the system of limitation of phar¬ macies in Germany has been productive of good, inasmuch as it has tended to make the business one eminently attractive for men of capital and scientific ability, and it has had the further effect of making the position of the pharmacist in Germany one very superior to that which must be taken as obtaining in regard to the general body in this country. But as in process of time it happens with most old insti¬ tutions, their merits fall into disregard, so with the established system of limitation of pharmacies in Germany ; there has grown up a feeling of dissatis¬ faction with it and a desire to replace it by a more free exercise of individual inclination. Even among the proprietors of old-established German pharmacies the opinion is held that the restrictions which have been in force to prevent the opening of pharmaceutical establishments are out of date and not suited to the present require¬ ments of society. Consequently there is an eager controversy going on as to the relative advantages of the protective system and that which is proposed as its substitute on the basis of absolute free trade principles. Since Germany became one, the two pharmaceu¬ tical associations of North and South Germany have been united, but the official amalgamation has not obliterated either in the north or in the south the desire to hold a prominent, if not a preponderating, position in the regulation of pharmaceutical affairs. The union of Germany has in this respect, as in others, given additional force to the desire of Prussia to take the lead, and of Berlin to imitate the role of Paris in being Germany as Paris has been France. Those who know the character of the Germans who are not Prussians will be able to understand that this endeavour meets with strenuous opposition among those whom we may term provincial Germans, and hence it is possible to recognize in many of the proceedings of the German Pharmaceutical Associa¬ tion an expression of this contest between centraliza¬ tion and provincialism which gives marked animation to the discussions of various subjects. The constitution of the German Association is especially representative, and the maintenance of active centres for the transaction of business relating to pharmaceutical affairs, is one of the best features of this body. It is one which, if properly used, scarcely admits of the complaint that the provinces are not adequately represented or that the ruling body can be insensible to the representations of its provincial members. Among the subjects which commanded most atten¬ tion at the late meeting in Hanover, the re- construc¬ tion of the statutes of the Association is perhaps the most important to those immediately concerned, but as it would be unreasonable to expect that it would have the same interest here, it will suffice to say that most of the principal pharmacists in Germany are actively engaged in the consideration of this matter. Next in order and in import for the well being of the pharmaceutical body, comes the question as to the system of education to be adopted. On this point there is great diversity of opinion, some adhering to the old system of education in the pharmacy, while others lean to or advocate the adoption of a system of university education. For both views cogent arguments are adduced and equally cogent objections are brought forward on either side. A special com¬ mittee has been appointed by the Association to consider and report upon this matter, and we shall take the opportunity, when this report appears, to place before our readers the substance of the views put forward on the subject. The preparation of a new Pharmacopoeia is another subject which engaged the members of the Associa¬ tion at the late meeting. At the meeting in Coblentz last year a committee vTas appointed to deal with this subject and some steps were taken to that end, but a number of difficulties have arisen to prevent the presentation of a report, and at the meeting in Hanover various questions connected with the subject vrere discussed. As the chief among these we may mention the following : — Whether the Pharmacopoeia should be published in Latin or in German ? Whether chemical formulae should be used ? Whether in naming metallic com¬ pounds the name of the metal should be placed first? Whether the use of synonyms should be limited l 226 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. >r eptember 20, 1879. The discussion of these and other questions occupied a considerable time, and from the interest manifested by the speakers it was evident that the pharmacists of Germany are determined to have some consider¬ able voice in the construction of their new book of law. In speaking of the Coblentz meeting last year we pointed out that one of the most striking impressions produced upon us as strangers was the amount of attention devoted to matters connected with “ trade interests.” The same tendency was this year equally manifest, and though running in a direction some¬ what remote from the mere endeavour to monopolize the trade in patent medicines it served to show that if the material well-being of the pharmaceutical body is to be maintained, or if possible augmented, it is only by the active co-operation of those engaged in the business that this can be done. While looking over the records of the work done by the provincial branches of the German Pharmaceutical Associa¬ tion it was impossible to avoid drawing a com¬ parison, or rather a contrast, between the general activity there displayed and the small extent to which this is the case throughout this country. The number of our provincial associations is also dispro¬ portionately small, and though some of them are well kept up there is too frequently an absence of any sustained effort to advance the interest of the busi¬ ness or even total quiescence except when some burning question is being agitated. In this respect there is much to be learnt with profit from the example of our German colleagues and we trust the opportunity may not be missed. THE LOCAL GOVERNMENT BOARD ON THE WORK. ING OF THE SALE OF FOOD AND DRUGS ACT. It is satisfactory to learn from the returns in the Report of the Local Government Board just issued that the proportion of the samples analysed under the provisions of the Sale of F ood and Drugs Act in the year 1878 reported to have been adulterated is lower by 2 per cent, than in the preceding year. The total number of samples reported upon was 16,191, and of these 2,782, or 19’2 per cent., were returned as adulterated. Too much importance, however, must not be attached to these figures, for irrespective of the fact judiciously emphasized in the Report, that these percentages are based on the results of analyses as given in the quarterly reports of public analysts, and not upon the number of cases that have been tested in a law court, it needs only a glance at the abstract of returns to see that the figures may be affected seriously by local condi¬ tions and the number of samples examined, as well as the idiosyncrasy of the analyst. Thus in the column showing the percentage proportion of samples reported to be adulterated in the different counties we find Bucks returned as 0; Rutland, 0; Anglesey, 7-4 ; Bedford, 7*7 ; and Gloucester, 7*8 ; whilst Essex stands at 71 '4 and Cumberland at 62*5 per cent. It can hardly be contended that these figures represent correctly the relative proportions in which trading in adulterated articles exists in these counties. Moreover, the whole returns would be affected to the extent of 2 per cent, if spirits were excluded from the calculation, and the diversity of opinion as to what constituted an adulteration of spirit, until the passing of the Act of last session, is notorious. The number of samples of “ drugs” reported to have been examined is 491, of which 125, or 25’4 per cent, have been returned as adulterated. Here again there is great diversity, Lancaster returning 22 adulterated out of 45, or nearly 50 per cent., whilst Lincoln reports none adulterated out of 25. The Board expresses regret that more samples of drugs are not submitted to analysis, “ for it is obvious that prescriptions may have very different effects, accord¬ ing as they are made up with genuine or with adulterated medicines,” and it then goes on to quote the report of the analyst for the West Riding of Yorkshire as to the evil results attending the dilu¬ tion of sweet spirit of nitre with water. The aptness of the apposition is not, however, quite evident, in the face of the fact that in few, if any, recorded cases of a conviction for the sale of adulterated sweet spirit of nitre has the vendor been a registered chemist and druggist. Moreover, “ sweet spirit of nitre ” is not a preparation that would be used in dispensing. On the 31st of December, 1878, the number of authorities who had appointed analysts was 196, — 49 counties, 108 boroughs, and 39 district boards and vestries in the metropolis, — and 5 other boroughs had made arrangements with the county analyst or the analyst of a neighbouring borough. THE LOCAL SECRETARY OF THE CONFERENCE AT SHEFFIELD. Those who had the opportunity of taking part in the very successful gathering of the British Pharma¬ ceutical Conference at Sheffield will be able to understand that very much of their enjoyment in various ways was due to the exertions of the Local Committee. Organizations of this kind sometimes fail to do what they should do, and then they are very difficult to get at for punishment by those who suffer for their shortcomings ; but though in general they may be destitute of some of the usual attributes of humanity it is certain that when they do their work well they must possess a head to direct and a working hand to execute. In neither of these was the Sheffield Local Committee wanting, and it is with great pleasure we learn that the services of Mr. Maleham, the Local Secretary upon whom devolved the arduous labours of preparing for the meeting, have met with recog¬ nition from his colleagues, and that they have expressed their appreciation of his zealous exertions by presenting him with a handsome piece of silver plate as a token of their respect and admiration. We are sure that few who were present at the Sheffield meeting will fail to be gratified at hearing this. September £0, 1879. THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS.' 227 off J^crnttific Storieliqs. BRITISH PHARMACEUTICAL CONFERENCE, {Continued from page 217.) The next paper read was on — The Valuation of Citrate of Iron and Quinine. BY FREDERICK W. FLETCHER, F.C.S. Notwithstanding the large number of papers which have been published during the last few years on the estimation of quinine in the Citrate of Iron and Quinine of the British Pharmacopoeia, there still appears to be a lack of trustworthy information upon one point in the process which ought by no means to be overlooked. Re¬ corded observations have hitherto been confined, with scarcely an exception, to the determination of the total alkaloid present in the citrate, without regard to its purity as quinine. That such should have been the case is not, however, surprising, when it is remembered that, until recently, the separation of quinine from some other cinchona alkaloids closely resembling it in their behaviour to certain solvents was a matter of extreme difficulty. But the process described by Dr. Paul, in the valuable paper which he communicated to the Pharmaceutical Society at an Evening Meeting in February, 1877,* may be said to have revolutionized the subject of quinine analysis. In that paper, it will be recollected, the author stated that a sample of sulphate of quinine, containing an admixture of no less than thirty per cent, of sulphate of cinchonidine might, if examined by the Pharmacopoeia test, be passed as pure quinine. That this astonishing statement was well grounded, any¬ one who has since interested himself in quinine analysis can testify. Nor indeed was the possibility of such an extensive adulteration a matter of fancy. Not long since I met with a parcel of German quinine containing over twenty-five per cent, of sulphate of cinchonidine, and the opinions of those most competent to judge, con¬ firm my own experience that from ten to fifteen per cent, of cinchonidine is invariably present in certain brands of foreign quinine. The question now arises, whether if such sulphate is used in the manufacture of citrate of iron and quinine the Pharmacopoeia test will detect the cinchonidine. The reply, as might have been expected, is in the negative. The alkaloid obtained from the citrate in ‘'the manner directed in the Pharmacopoeia will dissolve in pure ether, even though 25 per cent, of its weight is cinchonidine. But this is not all. The process of extraction of the alkaloid by ether, which has now superseded the charac¬ teristically indefinite official test, will not eliminate cin¬ chonidine for the same reason that it fails to do so when applied to sulphate of quinine. It is therefore necessary to have recourse to some other method. The process which I have devised for the purpose, and which I have found to succeed remarkably well, is simply an adaptation of Dr. Paul’s plan of fractional crystalliza¬ tion. It is exceedingly easy of application, and although a considerable quantity of the citrate has to be operated upon, there is little or no loss of quinine, most of the alkaloid being recovered as sulphate. It has, moreover, the advantage of combining three operations in one, as the results indicate: — (1) The exact amount of anhy¬ drous alkaloid ; (2) The proportion of the latter which can be converted into crystallizable sulphate of quinine ; and (3) The percentage of alkaloids other than quinine. The operations involved are briefly as follows: — Place 20 grms. of the citrate in a 100 c.c. flask, dissolve in 50 c.c. of distilled water, and add gradually an excess of ammonia (*960), shaking well after each addition. This is important, in order that the quinine may separate in a state of fine division, as otherwise it is apt to be thrown out in tough lumps, difficult of subsequent solution. * Pkarm. Journ., [3] vol. vii. (1877), p. 653. Pour in 25 c.c. of washed ether, and agitate with a rotatory motion till the alkaloid has completely dissolved. Transfer the mixture to a small glass separatory funnel, and having rim the lower stratum of liquid back into the flask, pour the ethereal solution into a 100 c.c. platinum capsule. Treat the liquid in the flask with 20 c.c. more ether, and proceed as before. Repeat this operation a third time. The capsule containing the mixed ethereal solutions is then placed in a saucer of water, and the ether blown off by a current of air from a Fletcher’s bellows. This immersion of the capsule in water obviates the tendency of the ether to creep up the sides. The platinum dish, which will now contain a pasty residue, is next placed in the air-bath, previously heated to 120°, and in fifteen minutes desiccation is complete. After cooling in an exsiccator, the capsule is covered and re¬ moved to the balance. The weight, minus that of the capsule and cover, multiplied by 5, is the percentage of total alkaloid. I may mention that having made many hundreds of analyses by this process, I can testify to the accuracy of the results obtained. In cases where a de¬ termination has been repeated, I have never found the results to vary more than 0T per cent. When an esti¬ mation of total alkaloid only is required, 2 grms. of citrate is a sufficient quantity to operate upon. The anhydrous alkaloid is now to be converted into basic sulphate. Since a molecule of the latter salt contains 648 parts ofquinia to 98 parts of sulphuric acid, and as decinormal sulphuric acid contains 4*9 grms. of H2S04 per litre, it follows that one grm of anhydrous quinia will require 30*86 c.c. of decinormal sulphuric acid to effect its conversion into basic sulphate. The weight of anhydrous alkaloid in grms. is, therefore, multiplied by 30*86, and the number of c.c. of decinormal sulphuric acid thus indicated are run into the platinum capsule from a burette, and the former being placed on wire gauze over the flame of a rose burner, the • contents are briskly stirred until the alkaloid is all taken up and a clear solution obtained. This is then transferred to a flask and allowed to cool spontaneously. The crystalline mass which will then have formed is thrown on to a small calico filter, about three inches square, stretched over a beaker, and, when drained, tightly squeezed to remove the last few drops of liquid. The latter is then filtered into a stoppered graduated tube of about 150 c.c. capacity, and its volume noted. 20 c.c. of washed ether and an excess of ammonia are then introduced, and the whole, after being well agitated, is set aside for six hours. In the meantime the squeezed residue is detached from the calico filter, dried in the air-bath at a temperature of 100 degrees C. and weighed as anhydrous sulphate of quinine j (C20H24N2O2)2. H2S04 = 746 j ’ To express the result in terms of ordinary crystallized sulphate | (C20H24N2O2)2 H2S04j72H20 = 881 | the weight found is multiplied by = j 1*18. To this is added the amount of the latter contained in the mother liquor which has been separated (and which may be estimated to contain 1 part in 750), and the total will then represent the proportion of anhydrous alkaloid which can be con¬ verted into sulphate. At the expiration of the time mentioned, the tube which has been set aside is examined, when the cinchoni¬ dine and quinidine present will be found to have crystal¬ lized out at the junction of the two liquids. The stratum of ether is removed by a small Nessler pipette ; the crystals washed with two successive portions of 10 c.c. of ether, the last few drops of which can be absorbed by a little roll of filter paper. The crystals are then thrown upon a double-tared filter, made of two papers weighed one against the other, dried at 120°, and placed on the balance, the outside paper acting as a counterpoise. In practice I find that the weight of this first crop of crys¬ tals represents on an average two-thirds of the total cin- 228 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. (September 20, 1879 clionidine or quinidine present. If, therefore, the amount does not exceed '1 grin, the percentage of these alkaloids may be estimated to be below 5 per cent. Should the first weighing exceed this limit, the sulphate obtained from the first crystallization must be dissolved in 100 c.c. boiling water, and treated as before, the weight of alkaloid separated by ether being of course added to the amount first obtained. As thus described the process may seem tedious, but in reality it is not so. Not counting the time which must be allowed for crystallizing, the entire estimation may be completed in something under two hours. The method, of course, does not distinguish between quinidine and cinchonidine, the usual tests for which must be applied to the solution of the mixed sulphates. This, however, is a point of minor importance, as the question of chief interest for the pharmacist is the determination of the exact amount of pure quinine present in the citrate. Two examples will be sufficient to illustrate the working of the process. A. 20 grins, citrate taken. Yield of anhydrous alkaloid — extracted as above, by ether and dried at 120° C., = 2‘67 grms., or 13 '3 5 per cent. The number of c.c. of deci- normal sulphuric acid required to convert it into sulphate was therefore (2-673 x 0‘86 — ) 82’5 c.c. This volume was run in from a burette and the alkaloid dissolved in the manner described. When cool, the filtered mother liquor, which measured 85 c.c., was treated with ether and ammonia. The first crop of crystals of cinchonidine weighed when dry T13 grm., the second ‘06 grm., there- (•113 + *06) x 100 „ , ,. _ A xl fore - — - = 6*4, which represents the per- Z'O ( centage of cinchonidine in the total alkaloid. The sulphate obtained in the first crystallization weighed, when dried at 100°, 2*67 grm., or (2*67x1*18 = ) 3’1 grms. of ordinary crystallized sulphate. On adding to this the amount present in the 85 c.c. mother liquor, which will equal = T1 grms., we get (3T + T1 = ) 3*21 grms. of sul¬ phate of quinine. The weight of anhydrous alkaloid found by experiment being 2*67 grms. would be equi¬ valent to 3 '6 grms. of sulphate ; the cinchonidine found represents To grms., so that the crystallizable salt would stand as 3'4 grm. found against 3’6 grm. calculated, proving the absence of any appreciable amount of amor¬ phous alkaloid. B. 20 grms. of citrate taken. Yield of anhydrous alkaloid 3’06 grms., or 15*3 per cent. Weight of cin¬ chonidine found, first crystallization, *120; second, •065 (T20 + -065.)x 3-06 6‘04 per cent, of the total alka¬ loid. The hot aqueous solution of the sulphate was sherry-coloured, and the sulphate which separated on cooling was very far from being white. It weighed when dry 2'46 grms., equal to (2*46x1*18 = ) 2*9 grms. crys¬ tallized sulphate. This amount, 'plus *113 grms., the quantity estimated to be present in 85 c.c. mother liquor, and *15 grms. allowed for first crop of cinchonidine, gives a total of 3T6 of crystallizable salt. But the weight of anhydrous alkaloid found was 3-06 grms., equivalent to (3*06 x|f| = ) 4*16 of crystallized sulphate; the difference of 1 grm. must therefore be considered to be amorphous alkaloid — which would thus constitute over 30 per cent, of. the whole. Whether the presence of 5, 10 or 20 per cent, of cin¬ chonidine would bring a sample of citrate of iron and quinine, which nevertheless answered the B.P. test, within the reach of the Adulteration Act, is a point upon which I offer no opinion. An eminent analyst, with whom I was lately discussing the subject, took the nega¬ tive view. If such is really the case, a revision of the Pharmacopoeia will come none too soon. The plausible excuse which is sometimes set up, that manufacturers cannot perfectly separate the cinchonidine from the quinine except at a greatly enhanced cost, is utterly without foundation. The white sulphate manufactured both by Messrs. Howard and Mr. Whiffen I have never found to give the slightest reaction with Paul’s test, and what is a still more striking fact, the so-called unbleached quinine of the latter maker is frequently quite free from cinchonidine. Certain of the foreign makes are also, as a rule, unimpeachable in this respect, whilst on the other hand, some others are systematically adulterated. It may be worth noting, as a matter of practical interest, that the substitution of 1 per cent, of cinchon¬ idine for quinine, in the manufacture of citrate of iron and quinine, reduces the value \d. per ounce for each such addition ; and when it is remembered that the Pharmacopoeia test will easily pass 20 per cent, of cin¬ chonidine, and that the consumption of the citrate is considerably over 100,000 ounces per annum, the valuation of this preparation resolves itself from a chemical into a question of commercial interest. The President said this was one of those useful prac¬ tical papers the importance of which appealed to them, and as there were practical manufacturers of the article present it would tbe interesting to hear what they had to say on the subject. Mr. Umney said that the subject of citrate of iron and quinine had for some years been of interest to him. In a paper by himself in the Pharmaceutical Journal, August 30, 1873, he endeavoured to show that the Phar¬ macopoeia directions and its test for this salt were written in somewhat of a haze. Those who remembered citrate of iron and quinine in its infancy would bear him out that it was customary for the labels to bear the words “this preparation contains an equivalent of 25 per cent, of sulphate of quinine.” Even latterly the same labels have been affixed, but to some the statement “ that this preparation contains 16 per cent, of quinia ” has been added. The compilers of the Pharmacopoeia presumed that from one part of quinine sulphate they would obtain by the formula indicated four parts only of citrate of iron and quinine. Now as a manufacturer he knew that from 100 ounces of sulphate of quinine he could produce 445 to 450 ounces of citrate of iron and quinine. The starting point, therefore, was wrong, and it was absolutely im¬ possible to get a preparation working by that formula that would contain the equivalent of 25 per cent, of sulphate of quinine. This had been pointed out in the Pharmaceutical Journal, and he had no doubt some alteration would in the next Pharmacopoeia be made in this respect. The Pharmacopoeia in directing the pre¬ cipitation of the alkaloid limited them to the quantity of water. It prescribed that 50 grains should be dissolved in one ounce of water, and that the precipitate when dried should weigh eight grains. They were therefore to infer that it contained 16 per cent, of anhydrous quinia. Now the experiments of Mr. Fletcher would show that citrate of quinine and iron would not give 16 per cent, of anhydrous quinia. To obtain the alkaloid anhydrous they must resort to a temperature of about 225° F., and such heat must be continued for four or five hours, for at 212° F. the precipitate would for hours continue to lose weight. He maintained that the tests in the British Pharmacopoeia wanted revising, or one day pharmacists might find themselves landed in great difficulty with gentlemen known as public analysts. It had been given on the authority of a public analyst, in the case Mr. Fletcher had mentioned, that a prosecution would be with a negative result. Another point required modification. Mr. Fletcher had referred to the dissolving of cinchonidine by ether. Had the Pharmacopoeia limited the quantity of ether used they might have prescribed the ether test with advantage. The question of the purity of the quinia precipitate was a very important one, for cinchonidine was now largely used, and was unques¬ tionably a valuable remedy. He thought the paper was a most important one, and that the observations on the revision of the Pharmacopoeia were not the least important part of it. September 20, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS 229 Mr. A. H. Mason (Liverpool) said that whilst it was universally admitted that the Pharmacopoeia test was faulty, it was quite possible to guard against trouble from public analysts by adding such a quantity of quinine to the formula as shall yield the desired per¬ centage to the Pharmacopoeia test, and this plan was now adopted by some manufacturers. Professor Attfield said it was only fair to the editor of the British Pharmacopoeia to say that at the meeting of the Conference in Glasgow that gentleman admitted that the quantitative test for quinine in citrate of iron and quinine was not all that could be desired, and thought that it was important to go a step further so that they might arrive at more accurate results. Mr. Symes said it had been shown in Mr. Fletcher's paper and the discussion — indeed, it had become a re¬ cognized fact — that the Pharmacopoeia process strictly followed did not yield the product it described, and the tests given would not detect a considerable amount of impurity if present. Professor Attfield had stated that in justice to the editor of the work he should say that he was now aware of this. He (Mr. Symes) wished to remark that this being the state of things with regard to so important a preparation, it furnished further evidence of the necessity for a new edition of the Phar¬ macopoeia, and he thought in justice to pharmacists this work ought to be proceeded with in a much more active manner than it appeared to be doing. The President said he might be pardoned for the reflection that the discussion seemed to indicate how desirable it was that in the re-arrangement of the next Pharmacopoeia pharmacists proper should be well repre¬ sented. He hoped they would join him in a vote of thanks to Mr. Fletcher. Mr. Fletcher said he quite agreed with Mr. Umney that the B.P. test was most unsatisfactory, and as a manufacturer he could also endorse Mr. Umney’s state¬ ment that citrate prepared strictly in accordance with the directions of the Pharmacopoeia would not be found to contain 16 per cent, of quinine. With regard to what Mr. Mason had said respecting the 16 per cent, of alka¬ loid, it should be borne in mind that the Pharmacopoeia method of weighing the alkaloid precipitated by ammonia was not intended to give anhydrous quinia. The preci¬ pitate was generally regarded as a tri-hydrate, 16 parts of which were equivalent to 13 *7 parts of anhydrous quinia. He had verified this experimentally by adopting a slight modification of the process described in the Pharmaceutical Journal a few months since by Mr. W. Stevenson. Instead of dissolving the citrate in water he dissolved it in a saturated aqueous solution of quinine, containing a very small quantity of ammonia. The quinine, precipitated in the usual way, was then thrown upon a double tared filter, washed free from iron by a further quantity of the ammoniacal solution of quinine, and the precipitate dried without heat. Proceeding in this way, a sample of citrate which yielded to ether 13 7 per cent, of anhydrous quinia would afford very nearly 16 per cent, of air- dried alkaloid. Mr. E. Davies, F.I.C., sent a paper on “ The Esti¬ mation of Water in Iodine,” which was read by Mr. Benger. The Estimation of Water in Iodine. BY EDWARD DAVIES, F.C.S., F.I.C. In endeavouring to discover a method for quantitatively determining the moisture in iodine several difficulties had to be overcome, owing to the conditions laid down in the blue list, namely, that the process should be “ handy and direct.” By the first requirement I understand that it should be performed with such ordinary apparatus as may usually be found in a chemist’s shop, that the manipulation should be easy and simple, and that the time should not be very long. The second requirement, strictly construed, is that the water should be weighed, and, so far, I cannot claim to have complied with it. All attempts to retain the iodine whilst the water passed on into an absorption tube were failures. The best was to volatilize the iodine in a current of carbon dioxide over clean iron filings gently heated. The apparatus was troublesome to put together, and practically it was impossible to heat the iron suffi¬ ciently to make it absorb the iodine without decomposing some of the water. I was therefore driven to adopt an indirect method and I think that the following process will answer the purpose satisfactorily : — It consists in combining the iodine with mercury and weighing the resulting iodide. A small thin porcelain dish, about 2J inches in diameter and weighing about 250 grains, is fitted with a small glass pestle, made from a piece of solid glass rod, 3 inches long and about Jg thick, by heating one end in the blowpipe flame until soft, and then pressing it on the bottom of the dish so that it may have the same curvature. About 60 grains of dry mercury are put in the dish with the pestle, and the whole accu¬ rately weighed. Twenty grains of the iodine are then added and a few drops of absolute alcohol to moisten it. The iodine and mercury are rubbed together until com¬ plete combination takes place, which is shown by adding a few more drops of alcohol, and allowing them to flow upon the side of the dish. If there is no free iodine the alcohol remains colourless. The rubbing requires about five or six minutes if much water is present, but only about one minute with dry iodine. The dish and its contents are now dried in a desiccator over sulphuric acid for twelve hours and weighed. The loss of weight of the dish, mercury and iodine, represents the amount of water contained in the iodine. The residue must be dried at ordinary temperature of the air, as mercury is far too volatile for a temperature of 212° F. to be used. The iodine used in these experiments was resublimed and dried over sulphuric acid in vacuo. The mercury used was the commercial article not quite pure. The following are some of the results obtained, from 60 to 80 grains of mercury being used in each case : — 1. 2. 3. 4. 5. Mercury, pestle and dish . . 494 "23 509 "35 493 21 532 "Ho 52*2*03 Resublimed Iodine . 20'00 20*00 20*00 30*00 30 00 Water added . 5*87 6*86 6*59 7*77 6*29 Total . 520*10 536*21 519 80 670*1*2 558*32 Residue after drying . 514*10 529*20 513*10 662*20 551*90 Water found . 6 00 7*01 6*70 7*92 6*42 Excess . *13 *15 *11 *15 *13 As these results showed a constant excess of about *13 grain, the iodine was examined with a view to ascertain if it contained water which was retained on drying in vacuo over sulphuric acid. Two results gave : — Mercury, pestle and dish 513*4*2 509-92 Iodine . 20*00 20-00 Total . 533*42 529-92 Residue after drying . . . 533-42 529*92 The iodine being thus found to be free from moisture and the mercury also by the same experiment, the only expla¬ nation of the excess of loss which I can suggest is, that as five or six times as long is required to bring about the combination when water equal to about 20 per cent, is present, some of the iodine escapes with the alcohol vapour. The drying was continued for twenty-four hours and in some cases for forty-eight hours, but no perceptible loss was experienced after the first twelve hours. The trifling excess which would amount at the outside to ^ per cent, in an excessively wet sample, and is abso¬ lutely nothing in dry iodine, cannot be considered a great objection to the process. A sample of resublimed iodine 230 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 20, 1879 purchased in Liverpool contained 0’60 per cent, of moisture. A sample of commercial iodine contained 0'70 per cent. Professor Attfield remarked that he had made some experiments on the best means of estimating water in iodine, but he had not come to a very satisfactory con¬ clusion. He believed the method adopted by those who used iodine tolerably largely was to expose a given weight of the iodine over sulphuric acid under a small bell-jar at as low a temperature as possible. No great amount of iodine escaped, and the loss suffered by the substance represented the amount of water present. That was a crude method, and he hoped they would arrive at a more exact one on the lines followed by Mr. Davies, namely, to endeavour to find some metal which would at, if necessary, a high temperature, and in large excess, absorb all the iodine, allowing the moisture to pass off in some way or other, and be collected and weighed. Hitherto he had found, that however large the excess of the metal might be, and whatever the amount of affinity of that metal for iodine, a little iodine did escape along with the moisture and gave an inaccurate result. With regard to Mr. Davies’s suggested defect in the process followed, namely, that a little of the iodme itself escaped, and caused the percentage of water to appear too high, he thought many samples of iodine would give a loss due to another cause, namely, the presence of sulphuric acid in iodine. This would probably decompose iodide of mercury and form sulphate of mercury, an equivalent amount of iodine previously combined with the mercury passing off. Mr. E. C. C. Stanford was surprised to hear this spoken of as a new process. It was one he had adopted for several years ; it was first suggested by Bolley, and would be found in Slater’s ‘ Commercial Analysis.’ His method was to use eight times the quantity of mercury and to use it dry ; they used five times the quantity, and found the process correct to 0T per cent. It was also rapid and convenient. Mr. R. R. Talloch, of Glasgow, used zinc, and had kindly sent him the details of the process employed : — Place a weighed quantity of the iodine in a weighed platinum capsule or small basin, in which has been placed a weighed quantity (say twice that of the iodine) of zinc sheet clippings in size about one-eighth of an inch square, add a little water and move the capsule and contents gently about. Immediately the iodine acts upon the zinc, the first small portion of iodide of zinc produced dissolving the free iodine, which is thus presented to the zinc in a dissolved state. The fluid by- and-by becomes colourless, after which the contents are carefully evaporated to dryness, and the dry residue heated till it ceases to lose weight, taking care that no iodide of zinc is volatilized, which, however, is not easy. With the clippings the temperature does not rise beyond control. The dry residue which remains in the capsule is that of the zinc originally added, plus that of the dry iodine which has combined with a portion of it. Professor Tichborne had used the process for many years, and he preferred that of drying over sulphuric acid. If a small bell jar was used practically the process became correct, or nearly so; the error in the loss of the iodine would depend in a great measure on the size of the vessel in which the iodine was dried. As regarded the old process in connection with mercury he might suggest that perhaps the best means of performing that would be to use a large excess of mercury, and to do it with a stopper bottle, shaking it up with the addition of alcohol. In that case there would be no loss from the volatilization of the iodine. In such a process as that detailed in the experiment they must make every allowance, and de¬ termine separately the presence of bromine, cyanogen, etc. Mr. Foster observed that he had had some little experience in the estimation of iodine, and he had adopted the usual method, that was to expose a weighed quantity of iodine over sulphuric acid to which some iodine had been previously added, observing the precau¬ tion of having a very limited atmosphere in the way Professor Tichborne had pointed out. With these pre¬ cautions he thought the ordinary process met the requirements of manufacturers, buyers and sellers. The other processes, ingenious as they were, scarcely met the requirements of the case. Mr. Draper asked what was the objection to the use of hyposulphite of soda. Professor Attfield explained that the use of hypo¬ sulphite of soda was a very good process when there were no other substances to be estimated. A vote of thanks was passed to Mr. Davies for his paper. The next paper read was on — The Presence of Tannin in Gentian Root. BY EDWARD DAVIES, F.C.S., F.I.C. The paper on this subject by Professor J. M. Maisch, in the American Journal of Pharmacy, 1876, p. 117, would seem to have settled the question of the presence of tannin in gentian root in the negative. The researches of M. Yille, reported in the ‘Year-Book of Pharmacy,’1877, p. 217, on the other hand, are directly contradictory in their result. The subject thus presents some interest, both with regard to the fact itself, and to the reason of the discordant results obtained in such an apparently simple matter. My first experiments were made on a sample of ground gentian root. A hot infusion was first made, but as it was impos¬ sible to get this perfectly clear, an infusion was made with cold water. This solution gave negative results ; gelatine gave a very faint precipitate after long standing, tartar emetic with chloride of ammonium gave no precipitate, and ferric chloride only produced a slight darkening of the colour. This appeared decisive, but I thought it better to test some of the unground root. A piece, which probably had been kept some time, was thinly sliced and digested with cold water for two or three days. The solution had a bright yellow colour, and although considerably less material had been used than in the previous one, it gave a decided precipitate with gelatine. I then obtained a quantity of roots as fresh as possible, for which I am indebted to Messrs. Evans, Sons and Co., and made a cold infusion of the sliced root. In the liquid obtained gela¬ tine gave a decided precipitate, acetate of chinchonine a strong precipitate, tartar emetic small precipitate, ferric chloride distinct darkening of colour. This result was so decided that I made an attempt to obtain an approximate determination of the amount of tannin. Making use of an improvement in volumetric analysis made by Mr. A. Haddock {Chemical News, 1879, April 10), consisting in the use of a mirror instead of the usual black glass plate, by means of which the faintest turbidity is shown whilst the effect of colour is eliminated, a drop of the clear solution of the gentian root, 300 grains in 3000 of water, was put on a mirror, a drop of perfectly clear gelatine solution added, and a strong turbidity was produced. By the side of this a drop of a dilute solution of tannin was placed, and gelatine added to it. The tannin solution was diluted until the turbidity in the two drops was apparently identical. In this way the amount of tannin was estimated at 0‘08 per cent, two tests agree¬ ing very closely. It is possible that this trace of tannin is liable to decomposition when the root is powdered and so exposed to oxidation ; or that it is not a constant constituent of gentian root. Either of these suggestions, if correct, will explain the discrepancy in the results obtained by com¬ petent observers. The small quantity contained in the root renders its isolation a matter of great difficulty, and until it can be so separated the proof that the tannin in the root is September 20, 1H79.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 231 gallotannic acid is only partial. So far as the tests ehow, they indicate gallotannic acid. A vote of thanks was accorded to the author. The next paper was a note on — Amylic Alcohol and Amylic Nitrite. BY D. B. DOTT. It was not my intention to write anything further on the subject of amylic nitrite, but a paper which has appeared in the American Journal of Pharmacy, by Dr. W. H. Greene, containing an adverse criticism of my contribution to the work of last year’s Conference, almost necessitates some notice on my part. I think I ought to say at the outset that Dr. Greene seems somewhat to have mistaken the nature and scope of my paper. It was intended more as a contribution to pharmacy than as a research in pure chemistry. Be that as it may, however, I have carefully gone over the same ground as last year, with the general result of substantiating what was then said. Dr. Greene’s vague allegation of inaccuracy resolves itself on examination into three points, that is to say, I stated erroneously : — 1st. That amylic alcohol may be obtained boiling at 128°— 129°. 2nd. That nitrite of amyl does not distil at a constant temperature. 3rd. That nitrite of amyl decomposes when distilled. As regards the first of these assertions I have now proved its accuracy by more rigorous experiment than was formerly applied. Fusel oil from a large Scotch distillery was rectified at first roughly in a capacious flask, the portion passing over at 125° — 135° being -retained. This was then distilled from chloride of calcium and repeatedly rectified. No distillate was obtained at so high a temperature as 132°. If any small quantity of that boiling point existed it must have been left behind in the syrupy solution of calcic chloride. It was soon found that the greater part of the above-men¬ tioned fraction distilled at 128° — 129°. The portion obtained at these temperatures was rectified at 129°, but even after many distillations it still yielded 2 or 3 per cent., passing over at 128°. This liquid was mixed with caustic baryta and agitated therewith from time to time. After forty-eight hours the alcohol was distilled from fresh portions of baryta, but without any alteration in the boiling point, the calcic chloride having doubtless completely removed the water originally present. The liquid obtained in this way had the characteristic odour of amylic alcohol and possessed the specific gravity of *814 at 60° F. A quantity of it was oxidized by means of potassic dichromate and sulphuric acid, the alcohol being mixed with the acid and the mixture dropped into the strong aqueous solution of the dichromate. The flask containing the solution was attached to a reversed con¬ denser and the solution gently boiled for two hours, after which the acid was distilled off. The distillate was neutralized with sodic carbonate and evaporated to dry¬ ness ; the residue mixed with sulphuric acid and distilled. The valeric acid obtained was equal to about 20 per cent, of the alcohol used. The acid was converted into sodium salt, and the solution of the latter mixed with solution of argentic nitrate. The resulting valerate of silver was washed with cold water and dried in exsiccator. By ignition — 6 *1 70 grs. gave 3*195 Ag. = 51*78 per cent. 9-035 „ „ 4*685 „ =51*85 C8H.AgOt= 51*67 „ Ag. When we consider this result along with the circumstance that the alcohol in question yielded a product by the action of nitrous acid having the well-known properties of amylic nitrite, I think there can be no doubt that the liquid obtained from fusel oil at 129° was amylic alcohol. This is said with all the more confidence that my results agree exactly with those of Alexander Pedler, mentioned in his memoir on the valerianic acids ( Chem . Soc. Journ. [2], vi., 74). It may be here mentioned that the apparatus used, both in distilling the alcohol and nitrite, was essen¬ tially the same as that of Le Bel and Henninger, described and figured in the Comptes Rendus (vol. lxxiv., p. 480). It consisted of an ordinary three-bulb condensing tube, with a contraction under each bulb, so that the ascending vapours had to pass through portions of liquid before reaching the condenser. We come now to the second statement previously referred to, viz. : “ That nitrite of amyl does not distil at a constant temperature.'’ I never affirmed that it is impossible to prepare a nitrite of constant boiling point, but simply that I had found it impracticable to purify the medicinal nitrite to such an extent, and that therefore the Pharmacopoeia test of a liquid boiling at 96° was one which the commercial nitrite could not reasonably be expected to answer. However, I think I am now in a position to state that even pure amylic nitrite does not distil at a constant temperature, in case it has been pre¬ pared from the 128° — 129° alcohol. A quantity of the nitrite was prepared by passing the vapours obtained by the action of nitric acid on starch through amylic alcohol (B.P. 128° — 129°). After saturation with the gas the liquid was of a bright green colour. It was agitated with water and after being separated therefrom was shaken up with anhydrous sodic carbonate. The product was now quite neutral to test paper and had a specific gravity of *881. On being distilled it evolved dense red fumes and yielded 78 per cent, between 95° and 100°. This fraction was retained and shaken up thrice with solution of sodic carbonate in successive portions and then with dry carbonate before being rectified. At the commence¬ ment of the distillation red vapours were given off and the first portions of distillate were strongly acid. The fraction 95° — 98° was retained and re-distilled, the por¬ tion coming over at 96° — 97° being collected apart. Very little was obtained at 96°, the greater part distilling between 96° and 97°. Can it be that the nitrites corre¬ sponding to the 128° and 129° alcohols boil at 96° and at 97° ? After twelve rectifications the nitrite had diminished to 20 per cent, of the original product and even then did not distil entirely at 96° — 97°, the last three rectifications showing no increase in the percentage of the correct fraction. When this result is considered along with the fact that the amylic alcohol had been rectified sixteen times, it will surely be admitted that it is not easy to obtain an amylic nitrite of nearly constant boiling point, and that such a process is out of the question for a pharmaceutical preparation. Regarding the third statement, “ That nitrite of amyl decomposes when distilled,” I certainly think that a very fair inference from the phenomena observed. If a liquid which has been washed with an alkaline solution until quite neutral to litmus be distilled, and the distillate is strongly acid, it is manifest that decomposition has occurred ; and this is just what takes place with amylic nitrite, at least with as pure a preparation as I have examined. In the twelfth rectification red fumes were evolved as at first. Of course it is open to anyone to say that some impurity may persistently adhere to the nitrite, which former, by its decomposition under the influence of heat, may evolve nitrous vapours. That may be quite within the bounds of possibility, though I do not think it is probable; but even supposing it to be the case, it only confirms my original assertion, which obviously referred to medicinal nitrite of amyl obtained at 90° — 100°, and not to a compound which (as then stated) I had never seen. The President said the paper was a refutation of the charges brought against the author, and it struck him that Mr. Dott had succeeded in perfectly establishing his case. Mr. Williams said he could to a great extent confirm the statements in the paper. In making nitrite of amy 232 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 20, 1-79. he had had considerable experience in one or two of the points, and the fact of its decomposition by constant dis¬ tillation he could quite confirm. With respect, however, to the statement concerning amyl alcohol, he thought there could be no question that it had a constant boiling point. A paper read a year ago contained another point which he should like to refer to, and that was that nitrite of amyl might have a higher boiling point than that given in the Pharmacopoeia and still be a justifiable and good pharmaceutical product for use ; but he did not agree with that, and thought that as the higher boiling point might be due to the presence of other bodies like nitrite of caproyl, the nitrite of amyl used in medicine ought not to have a higher boiling point than that indicated in the Pharmacopoeia. Professor Tichborne also bore testimony to decom¬ position of nitrite of amyl in distillation. Mr. Abraham said in these experiments one or two degrees of boiling point were matter of considerable importance. Did the experimentalists take cognizance of the variation in barometric pressure, for half an inch would make about one degree variation in the boiling point? Mr. Mackenzie asked if nitrite of amyl became de¬ composed with keeping. Mr. Williams thought perhaps it would ke^p any length of time if properly preserved ; still it was ques¬ tionable whether it was as good at the end of twelve months as at the end of one. Mr. Naylor maintained that it could not be kept for any great length of time, and that he had known it, turn acid when kept at a low temperature. In reply to Mr. Williams, it was admitted by Mr. Naylor that the specimen spoken of had not been re¬ distilled. A vote of thanks was passed to Mr. Dott for his paper. The following paper was then read on : — The Gelatinization of Tincture of Kino with a Possible Remedy for its Prevention. BY THOS. H. BAMFORD. One of the very first subjects discussed at the evening meetings of the Pharmaceutical Society on its institution, was the gelatinization of tincture of kino, introduced by Dr. Redwood, and the general opinion expressed was, that this tincture kept best in small corked bottles in preference to large stoppered and partially filled bottles. However this may be, it has always been a source of trouble to the dispenser, which would be greatly aggra¬ vated if the tincture were a more popular one with pre- scribers. In the majority of establishments, along with other seldom used preparations, it lies on a shelf in some out of the way place, and on the second or third occasion of its being required, it is usually found to have become con¬ solidated into a stiffish, translucent, pinkish jelly, very elegant in appearance, bearing as it does a tolerable re¬ semblance to red currant jelly, but altogether useless as a medicine. Then, if the dispenser be inexperienced and unaccustomed to this phenomenon, he begins a series of experiments in the hope of inducing the fickle tincture to resume its normal condition ; the agency of heat and the addition of more spirit will sometimes induce it to leave the bottle, but hardly in a state of solution, and in this condition it should never be used by the conscientious pharmacist, since it would altogether fail in its action on the patient, as in passing into the gelatinous condition it likewise loses its astringency. Pereira, in the article on kino in his ‘ Materia Medica,’ dismisses the fact in a brief sentence, and accounts for it as follows : — “ It is said that by keeping this tincture has, in some instances, become gelatinous and lost its astringency. Where this occurred, probably the Botany Bay kino (the inspissated juice of the Eucalyptus resinfera) had been employed,” It is doubtful whether the use of inferior specimens of kino will account for the deterioration of the tincture, as- I have seen samples of all kinds, made expressly and kept under what were supposed to be the most auspicious cir¬ cumstances, fail entirely as regards their keeping qualities, and the experience of any practical dispenser will bear out the statement that nine out of ten tinctures of this- gum will pass into the gelatinous condition with more or less rapidity. In the Pharmaceutical Journal for 1842, is the above named paper, entitled, “The Gelatinization of Tincture of Kino,” and in thisDr. Redwood states as his opinion that the change is dependent on the conversion of the tannin into a partially insoluble substance, ulmic acid, and in the discussion which took place after the reading tif the paper, a general opinion was expressed that this change was- expedited by the contact of atmospheric air in partially filled bottles. Messrs. Bell, Morson, Ince, and other well- known pharmacists took part in the discussion, and the general opinion seemed to be that to its storage rather than preparation were we to look for the means of com¬ bating its unfortunate peculiarity. A somewhat pro¬ tracted acquaintance with a sample kept in an unusual manner convinced me that I had at last seen a perfect panacea for this failing. The sample in question has- now been kept in its present position (this is written from notes made in 1876), about twelve or fourteen years, and is to all appearances as good as on the day it was received into stock. It was placed in an ordinary quart stoppered round, in such a position that it was necessarily taken up and dusted every morning, and consequently was well shaken every twenty-four hours ; the bottle was likewise- covered with blue paper so as to perfectly exclude the light. The bottle was never full (possibly now there are 8 ounces in a 40 ounce bottle), so that it has always been in contact with air. When it is stated that it was pro¬ cured from a London drug house, some time between 1862 and 1864, and has been in its present position since that time, all that is known of its history has been told.. My advice to any druggist who has been troubled with this tincture is to remove his stock of it into a position where it must necessarily get a daily shaking (that is amongst the bottles which are dusted daily), and also coat the bottle with blue paper. As during fifteen years’ experience this is the only tincture of kino I have seen keep for twelve months, I am convinced that I have brought a remedy to the notice of the British pharmacist. P.S. (1879). — The experience above recorded has re¬ ceived strong confirmation from the fact that a fresh supply was obtained three years ago from a local (Liver- ' pool) house and turned into the same bottle, and remains- to this present day in as good a condition as on the day of its reception into stock. Mr. Umney thought before this question could be- finally settled, experimenters must operate upon authentic specimens of kino. They had three distinct varieties that occasionally appeared in commerce. The official kino,, the product of Pterocarpus marsupium, of the East Indies, the kino from Pterocarpus erinaceus, and the Australian or eucalyptus kino, from the Eucalyptus resinifera. (See- Hanbury’s ‘ Pharmacographia.’) Anyone in the habit of visiting the drug warehouses of London where these imports were shown previous to sale was able, after a little practice, to distinguish one kino from another by tasting and observing the effect upon the palate and saliva. Mr. Mackenzie said he had had great experience in the use of kino, and he had no faith whatever in shak¬ ing it. Mr. Martindale was of opinion that much depended upon the age of the kino as to whether it was astringent or not. Mr. Cottrell paid the London houses a high compli¬ ment for great intelligence and probity, but expressed the ! September 2 \ 1879. J THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 233 opinion that some of the samples of kino sent out were not perfectly pure. Mr. Benger referred to a paper read by Mr. George Ellinor at the Bradford meeting of the Conference in 1873, in which a liquor was recommended as a substitute for tincture of kino. If he remembered rightly Mr. Groves on that occasion expressed the opinion that old kino yielded a tincture liable to pectization, whilst that which was fresh did not. Mr. Long thought the subject of tincture of kino a very interesting one. From the immense range of remedies they had to contend with, there were difficulties in keeping all their preparations in a proper state unless they had a very large practice, and he thought as new remedies were introduced that old and useless remedies should be knocked out. Mr. Hasselby said he had been familiar with kino for twenty-five years and only recently had he seen a specimen of it gelatinized. Mr. Greenish said in a paper on this subject introduced nearly forty years ago by Professor Redwood the same diffi¬ culties presented themselves as now had to be contended with. He hoped it would occupy a place upon the blue paper of the Conference, and that some phar¬ macist capable of undertaking the subject would ascer¬ tain whether gelatinization depended upon a particular kino or upon the age of the kino. * Mr. Chipperfield said he had never known any tincture of kino that had not gelatinized sooner or later, from the fact he supposed that it had been kept a some¬ what unusually long time. Mr. T. F. Abraham stated that he had known tincture of kino for fifteen years, and he had never seen it gelatinize. The only difficulty he had had with it was that it wedged the stoppers of the bottles. To provide for this in their •establishment there were two bottles, one a standard bottle which was placed on the ordinary shelves and with the other bottles, dusted and consequently shaken once a week, and another a bottle which was kept in the back part of the shop and which was shaken perhaps not once in two months. The contents of both bottles were made at the same time from the same variety of kino and both kept equally well. The gentleman whose paper they had listened to, before he sugested remedies should have been C[uite sure that what he used was really B.P. tincture of kino. j Mr. Preston stated that their tincture of kino had gelatinized once in seventeen years, and he believed that was caused by the stopper of the bottle having become a little loose. Mr. Robbins had known tincture of kino for some time and only once, had he known it gelatinize. Mr. Savage gave his experience with the tincture, which was to the effect that at one establishment it had gelatinized, and at the other it had not, but had kept exceedingly well. The little that had gelatinized had been put carefully away in a cupboard ; the one that had kept well had been exposed to the light and dusted every day. Mr. Elltnor said he had ordered kino from different houses and the tincture made from some of them would gelatinize, and that made from others would not. That which tinged saliva was the best kind and it never gelatinized as far as his experience went. He had, in a paper read at Bradford, recommeaded the substitution of a liquor containing glycerine in the place of the tincture, the object of which was, a3 far a3 possible, to avoid the use of spirit, but he had somewhat modified his opinion in consequence of Mr. Brady having then pointed out the extraordinary extent to which glycerine sometimes affected the characteristic property of astringents. He had ob¬ served in the Journal two recommendations for the use of glycerine in preparing the tincture, one preferring Aouble the quantity of glycerine to be added to the other, but he thought they should be careful before altering a Pharmacopoeia formula. If necessary at all to add gly¬ cerine the smallest possible quantity to effect the object should be ascertained. Dr. S YME3 remarked that he had only met with tincture of kino that had gelatinized once, and he did not believe its gelatinization was so common as was generally supposed. Mr. Bamford had suggested a remedy in the keeping rather than in the preparation, but his own opinion was that the real remedy was in the pre¬ paration itself. The addition of a small quantity of glycerine appeared to be effectual, but it remained to be proved whether it affected prejudicially the astringency of the tincture. Mr. Lee said he had known tincture of kino to keep for years in a fluid transparent condition when exposed to a strong light and frequently removed. The President, in presenting the thanks of the Con¬ ference to Mr. Bamford for his paper, said it was his opinion that the remedy lay not so much in the manage¬ ment of the preparation as in the selection of the material of which it was composed. The Conference then adjourned for luncheon and upon resuming the first paper read was — Anhydrous Air as a Therapeutic Agent. BY G. A. KEYWORTH, F.C.S. Some time since my attention was drawn to the great pain and inconvenience caused by tension in various morbid conditions. It occurred to me that air artificially dried and heated and so made an energetic absorbent of moisture would give relief by causing shrinking of the parts. This I found to be the case. Frequent oppor¬ tunities were presented of observing this effect upon a cancerous growth affecting the hand, with moist fetid surface. The jet was applied for an hour in the evening and caused cessation of pain for some eight hours, en¬ suring a good night’s rest. After the application the surface presented a dried, shrivelled appearance. The loss of pain and stiffness was well marked and repeatedly verified. Anhydrous air as a mechanical anodyne may therefore prove a useful addition to the therapeutic armoury. The medical practitioner may see fit to apply it to gouty and edematous swellings, to inflamed surfaces, to indolent ulcers and intractable wounds with a view to promote healing by desiccation, and to various tumours and cancerous growths to relieve the pain and if possible check their increase. The apparatus I employed consisted of an eprouvette of glass, containing fragments of calcic chloride, through which large volumes of air were driven by means of a foot bellows of the Fletcher type. The exit end of the eprouvette was connected by india-rubber tubing with an iron tube 3 feet in length, with a diameter of J an inch, having a spirit lamp burning beneath the centre, and a piece of india-rubber tubing attached to the extremity for the purpose of applying the current. In this manner a stream of dried air heated to 100° F. could be maintained. A plug of cotton wool inserted within the entrance tube to the eprouvette acts as a filter when the jet is applied to unsound skin. The air might (if desirable) be impregnated with carbolic acid or other volatile substance by introducing a portion with the wool. Large volumes of air must be used and for a considerable time (sometimes several hours) in order to produce sen¬ sible effects. If the process should be found useful in medical practice dispensing chemists will probably be called upon to supply the apparatus on hire. An econo¬ mical form of it will be supplied by the usual dealers in pharmaceutical apparatus. If used in hospitals on a large scale, a small gas engine or hydraulic motor could be adjusted in order to drive large bellows or a fan wheel, the eprouvette being of increased dimensions and the spirit lamp replaced by a Bunsen flame. The addition of india-rubber gas bags and pressure boards or other methods of compression can be made if increased force to the jet is required. It may be remembered that warm dry air ha3 long been observed to promote, and cold air 234 THE r H ARMACEUT1C AI j JOURNAL AND TRANSACTIONS. ISeptemoer 20, i*T» o retard the healing- of wounds. Anhydrous air, though not a caustic in the usual sense, shares with such sub¬ stances a certain power of disintegration by its affinity for moisture. The Michel process, introduced in Paris for removing tumours, consisted in the application of a paste of asbestos and sulphuric acid, the latter effecting destruc¬ tion by absorbing moisture. Caustic potash, soda and lime act in the same manner. The effect of nitric acid is due partly to this and to its power of oxidation. Anhydrous air is, however, free from the dangers and objections which attach to the use of these energetic chemical agents. Mr. Keyworth’s paper was read by Mr. Benger. There was no discussion on this paper, and a vote of thanks was awarded to the writer. The next paper was on — Saponine from the Bark of Quillaia Saponaria. BY H. COLLIER, Teacher of Pharmacy at Gay's Hospital. One of the subjects on the list of the Pharmaceutical Conference for investigation is Quillaia bark, its chemical composition, properties and uses. This bark had been under my notice for some time before the issue of this list, but as my chief aim has been to determine more precisely the nature of the saponaceous principle which it contains, I have adopted the above title for my paper. I have been assisted in my endeavours by my friend, Mr. Scard, F.C.S., chemical assistant to Dr. Pavy, F.R.S., Guy’s Hospital, to whose practical chemical knowledge I am indebted for the various analyses of saponine which I am able to lay before you. I have by no means ex¬ hausted the subject ; in fact, what I have to say must not be regarded as a complete investigation of saponine. I have obtained some results which may be looked upon as so many steps of progress towards the goal, but never¬ theless there remain many points which are still obscure. A principle which'tmakes a froth with water, similar to that formed by ordinary soap, is very widely diffused throughout the vegetable kingdom. Although generally known as saponine, from its original source, Saponaria officinalis , it has other names according to the plant from which it is obtained. All these saponaceous principles may be one and the same substance modified perhaps by the impurities belonging to its extraction. Saponine has been the object of numerous investigations, but most dis¬ cordant results have been published respecting it by different experimenters. Thus Bussy, Henry, Plisson and Overbeck state it to be a white non-crystalline friable powder. Rochleder and Schwartz that it is colourless, and Quevenne that it is yellowish white. Again, according to Henry and Plisson it is inodorous, whilst Quevenne asserts that it has a peculiar aromatic odour, and Shar¬ ing that the aqueous solution has a repulsive odour. There is also a great difference in the formulas assigned to saponine. According to Rochleder and Schwartz it is C24H40OJ4, Overbeck C42H76O30, and Bolley C36H56024. Before proceeding any further with the consideration of saponine, I think it will be well to say a few words re¬ specting the source, character and microscopic appearance of quillaia bark. The following description is from the ‘Treasury of Botany,’ part ii., 952 : — “Quillaia saponaria, quillaia or cullay of the Chilians, is a tree from 50 to 60 feet high, with smooth, shining, short stalked, oval leaves and usually terminal white flowers. Its bark, called quillaia or soap bark, is rough or dark coloured externally, but consisting of numerous regular whitish or yellowish layers, and contains a large quantity of carbonate of lime and other mineral matters. It is rich in saponine, a vegetable soap principle, and on this account it is commonly used as a substitute for washing clothes, two ounces of the bark being sufficient to wash a dress. It is also said to remove all spots or stains, and to impart a remarkable lustre to wool, and it is used to wash the hair, for which purpose it is powdered between stones, then rubbed with the hands in water, making a foam like soap.” The cortex quillaiae which I have examined consisted of heavy flat or slightly curved pieces varying in size from 1 to 4 feet in length, 4 to 8 inches in breadth, and from a \ to | an inch in thickness. The outer bark had been removed ; there were, however, a few scattered pieces still remaining. Le Boeuf, who described the colour of the tincture he obtained as “d’une couleur orang^e foncee,” no doubt employed the bark without removing the remaining outside portions. Now this is an important matter, as this outer bark contains a colouring principle which contaminates the saponine. In all my experiments I have operated upon a bark from which every portion of outside layer had been removed by planing and the use of the chisel. The tincture from this is of a pale yellow colour. It is not difficult to reduce the bark to coarse powder, if it is thoroughly dry, but if exposed te the air it absorbs moisture, and although it may easily be separated into layers, it is not friable. It is rather an unpleasant substance to powder, the fine dust which arises causing a great amount of coughing and sneezing. Examined by the microscope an opaque longitudinal section of the bark with one inch object glass and oblique light gives a general view of the woody tissue, upon and among which lie large crystals of what are undoubtedly oxalate of calcium, as they are unaffected by acetic acid, but are dissolved without any effervescence by hydro¬ chloric. A longitudinal transparent section, part of which is stained with aniline, shows principally the woody fibre with crystals lying about. In the coloured section some cellular tissue may be observed, and a few resinoid looking bodies of a brown colour. I have one section here which is made in a part where the resinoid bodies are chiefly deposited. These are somewhat of an oval form, and I have every reason to believe they consist of saponine with impurities, giving them a brown colour. The bark ignites very readily, and during combustion gives off an aromatic odour somewhat resembling cedar wood. It yields 11*8 per cent, of ash which consists chiefly of calcium carbonate ; there is also a trace of iron. Henry and Boutron-Charland were, I believe, the first who investigated quillaia bark and separated its sapon¬ aceous matter, which they described as an acrid principle. The method they adopted was to boil the aqueous extract with water, filter at the boiling heat, and the saponine which fell down on cooling and concentration was purified by solution in alcohol with aid of animal charcoal. I have prepared saponine by this method, but I was unable to obtain it pure; it would persistently remain brown after all treatment. The best process is that of Le Boeuf, which consists in boiling the bark with 84 per cent, alco¬ hol, filtering at the boiling point, and upon cooling the saponine deposits. It is purified by washing with alcohol and ether. The principle of the above process is that saponine is more soluble in boiling rectified spirit than in cold, so that the excess deposits upon cooling, leaving above a saturated solution of saponine with colouring and other matters. This tincture upon evaporation yields 2-24 per cent, of solid residue. The first saponine I ob¬ tained by this process, after thorough washing with alcohol and ether and drying over a water-bath, was a white friable amorphous mass. There were some portions how¬ ever which were not white but of a decided brown colour, and there appeared an oily stain upon the filter paper round the edge of the saponine. I found it to be very soluble in water, but ether, chloroform, benzol, carbon bisulphide appeared to have no effect in dissolving it. A portion heated on platinum foil burnt very easily, and a white ash remained. This was insoluble in water, but dissolved at once with considerable effervescence in hydro¬ chloric acid. A platinum wire dipped into this solution and held in the flame of a Bunsen burner produced a very well marked red colour. The acid solution neutralized with liq. ammoniae gave on the addition of ammonium oxalate a white precipitate insoluble in acetic but dissolved September 20, 1879 ] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 235 by hydrochloric acid. An examination for other bodies ■gave negative results so, that the ash of saponine is com¬ posed entirely of calcium carbonate. Now Bolley’s sapo- mine contained 1 per cent, of ash, and one sample examined by Rochleder and Schwartz contained 4*3 per cent. These investigators are I believe the only persons who mention anything about an ash. This discovery of the fact that my saponine contained an ash was the result of a pre¬ liminary examination before submitting it to analysis ; it was therefore necessary to obtain the amount before pro¬ ceeding. The plan adopted was to ignite the saponine in a platinum dish; when the carbonaceous residue had become quite white it was cooled and moistened with solution of ammonium carbonate, evaporated to dryness and again heated gently to expel excess of ammonia. The ash was thus weighed as carbonate: '49 of saponine yielded *0195 of ash carbonated as described, which gave 3'979 per cent. I could not regard this saponine as a pure substance. It had been most carefully prepared accord¬ ing to the process given by Le Bceuf, but the oily stain on "the filter paper upon which the saponine had been dried, and the brownish tinge of some of it were so many in¬ dications of impurities. It was necessary for me, there¬ fore, to endeavour to ascertain what was the nature of the impurities associated with saponine, and if possible to •obtain a pure specimen in order to determine the formula ■of it. I have worked upon three different lots of bark obtained at various periods, and the saponine prepared from all of fhem upon ignition left an ash consisting of calcium car¬ bonate : — Saponine from 1st bark 3'979 per cent, of ash. „ 2nd „ 3'904 „ „ ,, 3rd ,, 3*843 „ ,, The saponine prepared by boiling watery extract of bark with rectified spirit and deposition on cooling contained 4 ’37 per cent, of ash. It is a question in what state the calcium exists in ■saponine ; from its mode of extraction and after treatment it is hardly possible to suppose that the calcium oxalate existing in the bark had been dissolved out with the ■saponine, and then appeared in the ash as carbonate. The fact that the saponine from different specimens of bark should yield such nearly equal amounts of ash is very strong evidence that saponine from quillaia bark is a calcium salt. I have endeavoured to obtain saponine free from calcium, but up to the present time I haVe failed to •do so. It is stated by Rochleder and V. Payr that baryta water added to a strong watery solution of saponine pre¬ cipitates saponine-baryta, and that the white precipitate washed with baryta water, dissolved in water and then C02 passed through the solution gives carbonate of baryta which separates out, and after its removal the saponine may be precipitated by ether-alcohol. My saponine threw down a brown gelatinous precipitate with the baryta; which did not appear to dissolve in water, and C02 pro¬ duced no effect in the filtrate from the digestion of the barium precipitate. I next tried precipitating a watery solution of saponine with neutral acetate of lead ; the precipitate, which was a very gelatinous one, after washing was dissolved in water and a current of sulphuretted hy¬ drogen passed through the solution for several hours. No precipitate was produced but simply a black coloured liquid which upon dilation with water formed a clear dark brown solution. Afterwards to a similar solution of saponine in water I added oxalic acid until the liquid was distinctly acid. It was then laid aside for several days by which time the bottom of the beaker was covered with a white precipitate of calcium oxalate. The clear super¬ natant liquid was decanted and then neutralized with barium carbonate. It was impossible to filter quite bright and so it was allowed to remain for a week. At the end of that time the clear upper liquid, which I hoped was nothing but saponine in solution, was drawn off and carefully evaporated to dryness ; the result was a brown amorphous mass, which upon ignition left some amount of ash in which barium was present. I next turned my attention to an examination of the tincture from which the saponine had been deposited upon cooling. I considered, that as this tincture was only a solution of impure saponine, a knowledge of its composition might suggest the purification of the saponine. The tincture evaporated over a water-bath left a soft reddish-brown sticky extract. This was digested with washed ether for some days ; by this treatment it lost much of its colour but still retained its tenacious character. The ethereal solution was of a yellow colour, and when mixed with water became opaque, and after a short time a fatty matter appeared adhering to the sides of the tube. If hydrochloric acid instead of water were employed, the fatty substance at once separated in the form of distinct lumps floating on the surface of the liquid. These were not dissolved on the addition of alcohol, and no change of colour was produced by the application of heat to the alcoholic mixture. Upon evaporating the ethereal solution a soft oily substance remained, which imparted a perma¬ nent greasy stain to white paper ; it was insoluble in water and alcohol, but readily dissolved by benzol. It was unaffected by alkalies or diluted acids. A similar oily matter may be obtained by adding tincture quillaia to water acidulated with hydrochloric acid. After standing for some time a yellowish precipitate separates which collected upon a filter and well washed with water dissolves entirely in ether and this solution upon evaporation gives this oily residue. If washed ether be added to the tincture this oily principle is also precipitated together with saponine. In this case the precipitate after being well washed with rectified spirit and then dried over a water-bath is resolved J into an oily fluid which soaks through the filter. The extract after being treated with ether as above was then digested with absolute alcohol for a week; at the end of this time the alcohol had acquired a reddish-brown tint and the extract had become a grey amorphous powder entirely devoid of stickiness. The alcoholic solution acidified with hydrochloric acid and then heated became of a cherry-red colour, which was changed to a dark olive green by alkalies and restored again upon the addition of acid. The residual extract treated with water dissolved entirely and appeared to be only impure saponine. I had thus acquired two facts, that the impurities present in precipitated saponine were an oily matter soluble in ether, and a colouring principle soluble in alcohol. It would be necessaiy therefore only to treat with alcohol and ether in order to obtain pure saponine. But this had been the method of purification always adopted and I have never obtained saponine without a marked oily stain upon the filter paper and more or less brown colour. I tried digestion with alcohol and ether for several days, but the product was still impure. At last after numerous experiments I found that by boiling the saponine in rectified spirit, filtering at a boiling heat, allowing the precipitate to settle by cooling, and digesting this in absolute alcohol and ether, that a very much whiter product was the result : it still, however, gave a red colour when heated with rectified spirit and hydrochloric acid. The saponine of which the analysis is given was purified as above, but the solution, deposition, and digestion were repeated a second time. It was a white amorphous substance, and the filter upon which it had been dried presented no appearance of any oily stain, and dissolved in rectified spirit, and acidified with hydrochloric acid, upon heating no red colour was produced. I thus believed it to be a perfectly pure specimen of quillaia bark saponine. It contained 4T3 per cent, of ash, which is higher than that yielded by the other saponines prepared in a similar manner, but not subjected to so thorough a process of purification. Now the saponine obtained from the watery extract gave 4'37 per cent, of ash which corresponds more closely to the amount obtained from purified saponine. I can say in explanation of this that the last sample being free from oily matter would yield a higher percentage of ash, and that the product from the 236 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. : September 20, 18?» watery extract probably contained no oil, as this is not soluble in water, so that its ash approaches more closely that of pure saponine. The absence of this oily impurity made a perceptible difference in the amount of carbon contained in the last sample of saponine compared with the first in which it was present. Now this has an important bearing, for the amount of carbon contained in the first saponine I prepared and submitted to analysis was 49-31 per cent, and this corresponds closely to the amount given in the published analyses : thus — Rochleder and Schwartz. . . 52 T 7 per cent. Overbeck . 47*54 „ Bolley . 49‘54 „ Rochleder and V. Payr . . . 5 2 ‘97 „ Bussy . 50'00 „ It is therefore very probable that these saponines containing such a high amount of carbon were not pure and that the different results are owing to various degrees of purity of the sample examined. The following is the result of the analysis of purified saponine. Calculated from formula (OgH^CkhoCaO. c 43-63 H 8-88 O 45-23 CaO 2-26 Found. 43-51 8-88 45-30 2-31 100-00 100 00 Deducting the CaO the percentage composition runs as follows : — C 44-53 H 9-09 O 46-38 100-00 Corresponding to the formula C9H2207 which requires — C 44-62 H 909 O 46-29 100-00 Considering the large number of atoms in combination with one of lime it may be inferred that the lime is simply united with the saponine and that it does not displace any hydrogen or compound radical, therefore, we should be justified in calculating the formula for saponine in deducting the lime found, and recalculating the percentage proportion. In fact, it may be assumed that saponine has a similar structure to that of arabine, which is said to be a calcium salt. Another paper read by the same author was — Tincture of Quillaia as an Emulsifying Agent. EY HENRY COLLIER, Teacher of Pharmacy at Guy’s Hospital. I now pass on to a consideration of the use of a tincture of the bark of Quillaia sapor aria for the preparation of emulsions. The tincture which has been employed in the preparation of the various mixtures upon the table has been made according to the following formula, which is taken from Guy’s Hospital Pharmacopoeia : — Quillaia Bark, in coarse powder . 4 oz. Rectified Spirit of Wine .... 1 pint. Digest for three days and then strain. The bark before powdering is carefully freed from all remains of outside layer, and the tincture produced is of a pale yellow- colour. Into this bottle I have put some mercury and shaken it up with tincture of quillaia, the result is that the mer¬ cury has been reduced to a very fine state of division. It has very much the appearance of hyd. c. creta, and examined with a lens it is seen to be composed of distinct globules of mercury. So long as there is some tincture present this division of the metal remains; if it be dried, it at once runs together and appears in its ordinary liquid state. This is a remarkable power which tinct. quillaiae- possesses of destroying the cohesion between the globules of mercury, breaking them up and preventing them from uniting together, and it is this property which renders it so valuable an emulsifying agent. A true emulsion consists, as is well known, of a number of oily or resinous particles floating about in a watery liquid by means of some agent which prevents them from cohering. To be perfect the emulsion should have a milky appearance, and the suspended particles should not subside or rise too rapidly. In the British Pharmacopoeia there is a preparation containing mercury in a very fine state of division, and which is in fact an emulsion con¬ taining mercury finely divided. The preparation I mean is the Linimentum Hydrargyri , which Squire says “ should be a lead- coloured cream, but is curds and whey.” By using tinct. quillaiae a lead-coloured cream may be formed which does not turn to curds and whey. The preparation here contains the same proportion of active ingredients as is ordered in the Pharmacopoeia ; if left undisturbed for some time the ung. hydrargyri settles to the bottom, but a vigorous shaking blends it again perfectly. The follow¬ ing is the formula : — Lin. Camph . %j. Tinct. Quillaiae . fpj], (Liq. Amm. Fort. 3ijj 1Tl 40 Aq. ad). 3V- Ung. Hydrarg . 1 oz. M. Chloroform is made into an excellent emulsion by means of this tincture. Chloroform . trix. Tinct. Quillaiae . 3j* Aq. Destil . ad §j. Misce. Although chloroform is such a heavy liquid, yet it remains suspended for some minutes after shaking. It finally settles as a creamy layer at the bottom of the bottle. A solution of saponine in water shaken with chloroform converts it into a thick creamy fluid ; the water separates, but the chloroform permanently retains its creamy character. Here is a mixture of castor oil made according to the following formula : — 01. Ricini . gss. Tinct. Quillaiae . ' 3ss. Aq. ad The tincture is first put into the bottle, afterwards the oil, and shaken together, then the water is added and again shaken. The emulsion thus formed resembles its prototype milk in appearance and like it separates after the lapse of some time into a cream at the top, w-hich mixes again upon agitation. Emulsions prepared in a similar manner of oleum morrhuse and oleum olivse are of as perfect a character. Ext. Filicis Liquid . 3j- Tinct. Quillaiae . 3SS* Aq. Destil . ad ^j. Misce. This forms an excellent emulsion, and with the addition of syrup zingiberis 3SS constitutes the Mistura Filicis. Maris of Guy’s Hospital. Copaiba* . 3SS- Tinct. Quillaiae . 3SS* Aq. Destil . ad Misce. The copaiba in this mixture is perfectly emulsified. S pteraber 20, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 237 Here is an example of an essential oil. 01. Terebinth. ........ itlxx. Tinct. Quillaue . Rlxx. Aq. Destil. . . . * . . . .ad 3j . Misce. This formula, with the addition of tinct. limonis, is the mistura terebinthinae (Guy’s). I have found that resinous tinctures require more than their bulk of tinct. quillaise to prevent any separation of resin. Tinct. Tolut . in. 40. Tinct. Quillaise . 3j- Aq. Destil . ad §j. Misce. The resin deposits after some time, but upon shaking it is easily diffused. This mixture contains the soluble matter of 12 grains of guaiacum resin in every fluid ounce, so that it is about the same strength as mist, guaiaci, B.P. The following is the formula : — Resin Guaiaci . gr. xij. Tinct. Quillaise . 5j* Aq. Destil . ad §j. Dissolve the guaiacum in the tincture, filter, and then mix with the Avater. Resin of copaiba is largely used at Guy’s Hospital where it is considered a valuable diuretic. It does not appear to me to make so perfect a mixture with tinct. quillaise as the hospital formula with pulv. tragacanth co. The liquid is not thick enough to prevent the resin separating too rapidly. Here are mixtures of copaiba resin made after the folloAving formulas : — Mist. Resince Copaibce {Guy's). Resin of Copaiba . 15 grains Rectified Spt. of Wine ... 20 minims Compound Powder of Traganth. 15 grains. Syrup of Ginger . 1 fl. dr. Distilled Water to . 1 fi. oz. Misce. The resin and spirit are put into an evaporating dish and blended together by heating over a water-bath ; then poured into a mortar containing the pulv. tragacanth co. previously made into a thick mucilage with a little of the water and well rubbed together, the syrup and the re¬ mainder of the water being gradually added. Resinse Copaibas . gr. xv. Tinct. Quillaise . 3j. Aq. Destilat . ad §j. The resin is dissolved in the tincture and the water gradually added with agitation. Bals. Peru . ill xv. Tinct. Quillaise . 3j* Aq. Distil . ad §j. This mixture is open to the same objection — the bal¬ sam subsides too rapidly. The above quantity of balsam with gr.xv. of pulv. tragacanth co. gives an excellent result. I have now placed before you examples of emulsions of the various substances which are administered in that form, and I have no doubt but that you will agree with me that tincture of quill aia is worthy of a place in phar¬ macy for the preparation of this class of medicines. Mr. Benger asked Mr. Collier if the taste of the tinc¬ ture of quillaia was not sometimes objectionable. Mr. Reynolds said he should like to extend the ques¬ tion put by Mr. Benger. The use of quillaia bark for these necessary purposes of pharmacy would divide itself into two sections : — Its use for external and its use for internal purposes. The question of physiological action and ques¬ tionable taste might be taken as parts of the same subject. He would like to inquire if there were any other instances than the use of the male fern oil emulsion for which Guy’s Hospital would reccommend the use of quillaia in an in¬ ternal application, and if they were to understand that the half drachm close containing 6 grains of bark was the maximum. Dr. Soulle had recommended an emulsion so as to bring carbolic acid into the form of a lotion and had written very highly of its effects in the treatment of wounds after certain operations. Mr. Greenish observed that tincture of quillaia had been highly recommended by the Paris Pharmaceutical Society as an emulsifying agent. He had tried it in many instances, and had found it exceedingly useful. Dr. Vogl, of Vienna, had written most exhaustively on this bark ; not only on its chemical composition, but its microscopical structure. There was also a valuable paper on its microscopical structure by Schlesinger in Wiesner’s ‘ Untersuchungen.’ He believed that tinct. quillaia would occupy a place in pharmacy. Mr. A. H. Mason (Liverpool) remarked that the author spoke of quillaia bark in the natural state ; his experience was that only the inner bark was offered for sale in this country ; this was frequently stained, and he would like to ask if this was caused by exposure or if any decomposition took place likely to deteriorate the bark. He would like to know, moreover, if the frothing power of quillaia bark was due to the presence of saponine, and if so whether saponine obtained from other sources had the same properties. He would also ask whether the watery or the alcoholic extract yielded the greater per¬ centage of frothing power and what the yield of extracts was. Mr. Lee asked what strength of spirit Avas required to extract saponine from quillaia bark, and what tempera¬ ture should be used. Mr. Umney said he knew this bark Avas occasionally used medicinally, also that it was a most poAverful drug applied externally. It entered into the composition of one well -known patent medicine, which had been before the public for years, and it was well known as a stimu¬ lant in certain skin diseases. Before it Avas recommended broadcast as an emulsifying body for .all kinds of mixtures they ought really to ascertain if it Avas harmless in its nature when administered internally. Dr. Symes referred to the use of quillaia bark in tooth powders and mouth Avashes as objectionable on account of its nauseous acrid taste, and asked if saponine in the purest form in which Mr. Collier had been able to obtain ^it still possessed this objectionable character. Mr. Fletcher asked if the saponifying property was peculiar to the lime compound. Mr. Hasselby asked how the author broke up the mercury, and said the process seemed so simple and effective that it might be u-ed Avith advantage in sheep ointment. Mr. Collier said as regarded the physiological action of quillaia bark he could only refer to Husem aim’s ‘ Fflanzenstoffe,’ in which saponin AAras mentioned as being poisonous to the lower animals ; but the fact of its being adopted by the Paris Society of Pharmacy induced him to think there could not be any harm in the substance. He had made a considerable quantity of emulsions Avith it, but more particularly of cod liver oil. The tincture of quillaia added to cod liver oil, and flavoured with cin¬ namon, made really a very palatable mixture, and he knew one person, Avho having an objection to oil, even liked it in this Avay. He explained the process of break¬ ing up mercury, and showed that it would do well to make sheep ointment. The thanks of the Conference were given to Mr. Collier for his paper. {To be continued.) ©bituarg. Notice has been received of the death of the follow¬ ing : — On the 10th of August, 1879, Mr. William Rowland, Chemist and Druggist, East Street, Chichester. On the 15th of August, 1879, at Chelsea, Mr. William 238 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 20, 1«!9. Bartlett. Aged 75 years. Mr. Bartlett was one of the Founders of the Pharmaceutical Society, and served as a Member of the Council in the years 1845-46 and 1846-47. On the 16th of August, lb79, Mr. Joseph Barnett, Chemist and Druggist, New Street, Burton-on-Trent. Aged 35 years. On the 22nd of August, 1879, Mr. Thomas Rush worth, Chemist and Druggist, Wellington Street, Leeds. Aged 63 years. On the 22nd of August, 1879, Mr. Joseph Pearce, Chemist and Druggist, Sheep Market Street, Crewkerne. Aged 67 years. Mr. Pearce had been a Member of the Pharmaceutical Society since 1869. On the 22nd of August, 1879, Mr. Clement Dallas, Chemist and Druggist, Lavender Hill, Clapham, S.W. Aged 42 years. On the 31st of August, 1879, Mr. Thomas Pass, Chemist and Druggist, Melbourne. Aged 72 years. On the 1st of September, 1879, Mr. James Holiday, Chemist and Druggist, St. Dunstan’s Street, Canterbury. Aged 76 years. On the 6th of September, 1879, Mr. John Joseph Nicholson, Pharmaceutical Chemist, High Street West, Sunderland. Aged 42 years. Mr. Nicholson had been a Member of the Pharmaceutical Society since 1861. On the 13th of September, 1879, Mr. Richard Flower Ellis Wilton, Chemist and Druggist, Bridgwater. Aged 33 years. d|oiit[«8]jon inches in circumference. A similar patch of the plant was recently noticed by the writer, near Dartford, quite an effort being re¬ quired to reach the fruits with an outstretched arm, the plants, which were not measured, being probably close upon 9 feet high and much branched. Fungi also, which might have been expected from the damp state of the ground and the recent warmth of atmosphere, at all events in the day, to have been •abundant, are in fact unusually late and scarce. A recent search for Amanita muscaria, in a well known locality for it, near London, proved quite a failure. So great is the scarcity of fungi that it is feared that the fungus foray of the Woolhope Club at Hereford this year will prove less successful than usual, which would be rather an unfortunate occur¬ rence, since several fungological celebrities from France are coming over to attend the meeting. The unusual abundance of insects this year is ■another curious circumstance, and it would be in¬ teresting to ascertain how far it has affected the crops of medicinal plants. The writer recently observed a patch of peppermint completely stripped of leaves by one of the common garden caterpillars, Mamestra persicaricz. Most insects appear to dislike strong odours, but whether the moist weather has diminished the quantity Of oil usually present in the leaves, or whether it is possible for insects to become habitu¬ ated to unusual food, it is not possible to say. At all events, neither the elder nor the peppermint appears to be generally attacked by insects. In damp meadows, in localities where it occurs, the colchicum may now be seen in full beauty, and almost reminds one of the early spring time when the crocus displays the same delicate hue. Many spring plants often blossom again in the autumn if the weather be damp and mild. This year there may be seen at the Botanical Gardens the bistort, Actcea spicata, crosswort, comfrey, and several others. The same thing often happens when flowers which naturally blossom in spring, are transplanted at that season. Thus primroses transplanted in spring will sometimes flower in autumn for two or three years in succession. Among the rarer wild plants to be seen in flower this month are, Linosyris vulgaris, Artemisia campes- tris, JJrtica pilulifera, Spiranthes autumnalis, Lactuca Scariola, L. saligna, and Bupleurum tenuissivium. The first three may now be seen in blossom in the Herbaceous Ground at Kew, where several families are still well represented by plants in flower. Those which more especially afford abundant material for study are, Chenopodiacece, Polygonaceai, Composite, Scrophulariacece, Labiate, Convolvulacea3,Dipsacace9e and Boraginaceie. The Chenopodiacece are, even to advanced botanists, a very troublesome group, but a veritable bete noir to the tyro in botany, to whom it may be useful to know that although it is neces¬ sary to gather specimens in flower, as well as speci¬ mens having the lower leaves, it is best not to attempt to name the species until specimens with ripe fruit can be obtained. Third Series, No. 483. Among medicinal plants at Kew a number which were recorded for last month still remain in blossom, such as lavender, peppermint, borage, camomile, hyssop, tansy, tobacco, melilot, wormwood, alkanet, and Monarda didyma. Another species of Monarda, M. fistulosa, with pale pink flowers, presents a much less brilliant appearance than M. didyma, but its leaves give off a highly fragrant odour, like bergamot, when bruised. It is a curious coincidence that the odour both of lemon and bergamot should occur in more than one plant of the Labiate, while that of the orange does not seem to occur in that natural order. A solitary flower of the cochineal cactus, Opuntia vulgaris, may be seen in the Herbaceous Ground, a sight of apparently rare occurrence in this country. Among the plants in the same ground worth a pass¬ ing attention, at least, are several species of Eryngium, with their curious thistle-like habit. In the Com¬ posite may be noticed several plants of the genus Echinops , of which we have no indigenous repre¬ sentative, and which derive their name of globe thistle from their spherical capitulum, differing from ordinary composite flowers in each floret having an involucre of its own, while a general involucre is absent, or perhaps it would be more correct to say that what is apparently a flower-head consists of an aggregation of eapitula, each of which contains only a single flower. In the Onagracese bed may be observed a flower, Lopezia coronata, worthy of notice on account of its unusual structure. The parts of the flower in this family are usually four in number, or the stamens are sometimes reduced to two, but in this case theie are apparently five petals, which gives an irregular appearance to the flower. This is due to one of the two stamens having no anther at its apex, but the filament developed instead in the form of a petal. In hedgesides and damp waste places near old towns and villages, the soapwort, Saponaria officin¬ alis, may be seen in blossom, its pretty pink flower frequently showing a tendency to become double. This plant has lately been spoken of as likely to be useful in carcinoma. Gerarde in his ‘ Herball ’ speaks of it as being used “ for greene wounds, to hinder inflammation and speedily to heale them,” and quotes from Ludovicus Septalius a remark which would have been doubtless much resented, had it been written in these democratic days. “ I have some¬ times used it with happy success in the most con¬ tumacious (venereal) disease, but it is of a somewhat ungrateful taste and therefore must be reserved for the poorer sort” It derives its name from the lather which may be made with water and the bruised leaves, and which is due to saponine, first obtained from this plant. By the .sides of streams may be seen the gipsy wort (Ly copus europoeus), remarkable for having only two stamens, the upper two being imperfect. This plant has the reputation of being one used by the gipsies to dye their skin. The curious little plant Samolus Valerandi, may now be looked for in wet marshy or dripping places. Although the flowers are small and have an un¬ attractive appearance, they are interesting on account of possessing, in the modified form of small scales, the second row of stamens, which is absent in most Primulacecz, and by reason of which absence the stamens in this order are opposite to the petals, 242 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 27, i879„. instead of alternate with them, as should, if the flowers were normal, he the case. On damp sandy turfy heaths the Calathian violet, Gentiana Pneumonanthe, may now be found in flower. It is one of the prettiest of our native species, but is somewhat local and rare. The flowers differ from those of the commoner species, G. Amarella, in the stamens coming to maturity "before the stigma, so that the pollen is carried by bees (which can only creep half way down the corolla) from the flowers in which the pollen is ripe to the older in which the anthers are withered and the stigma is viscid. As the stigma is higher up the tube than the stamens, self-fertilization is not possible. In Gentiana Amarella, which is common on chalky hills at this time of year, although the anthers and stigma are mature at the same time, the stigma is above the stamens by reason of the style being longer than the stamens, so that cross-fertilization must also take place in this case. The G. Amarella is still sometimes gathered by herbalists under the name of English Gentian. Most of those who have attended botanical lectures at Regent’s Park Gardens are acquainted with the curious leaves of Bryopliijllum calycinum, which when placed on damp earth in a warm place give rise to young plants from each notch at the margin of the leaves. Dr. W. Berge, of Zurich, has recently been examining the origin of these buds and their development into plants, and has found them to be of exogenous production and entirely developed from a meristem tissue in the base of the notches of the leaves. Some interesting experiments on the action of anaesthetics on the sensitive plant have been made by M. Arloing. He found that chloral had not the same action on the plant as upon animals, while the contrary was the case with chloroform and ether. The anaesthetics were administered in the form of watery mixture to the roots, and the vessels contain¬ ing the plants were then covered over so as to arrest evaporation, so that the anaesthetics must of necessity penetrate the plants either by the roots or leaves. The experiments showed that the rate of ascent of liquids in the plant increased from the base of the stem upwards, being one and a half to twice as great in the petioles as in the stem. In the Gardeners’ Chronicle , this month, Mr. W. G. Smith points out that a fungus very common at this time of the year possesses poisonous properties. A gentleman observing that it wras eaten by slugs or snails most erroneously supposed it was therefore suitable for human beings and suffered severely for his theory. The fungus in question, known tofungo- logists as Paxillus involutus, is remarkable for the rim of the pileus or cap being distinctly curled under. The pileus is pale brownish and the gills run down the rather stout stem. The flesh when broken is dirty white, becoming brown, and the spores are reddish. At the drug sales in London there has been noticed this month some spurious matico, with an aromatic odour between that of aniseed and sassafras, and another kind with leaves extremely similar to those of matico, but quite inodorous. A bag of the fruits of the doum palm, Hyplicene thebctica was also observed, but with what object they were imported it wras not possible to as¬ certain. The fruit is said to be eaten by the lower classes in Egypt and to taste like gingerbread, — . - whence it is sometimes called the gingerbread tree; its dry fibrous fruit, however, look so little like “gingerbread nuts” that there is not much temptation to try them. The seeds which are hard and horny are sometimes made into beads for rosaries. Goa powder of good quality was noticed and Calabar beans appeared to be more plentiful than of late. Several inquiries concerning Alstonia bark have recently been made, and as some confusion appears to exist between Alstonia scholaris and Alstonia con - stricta, some readers may be glad to know that an account of the former may be found in Bentley and Trimen’s ‘Medicinal Plants,’ No. 173. This bark is also called Echites scholaris • and Dita bark. Attention was called to it so long ago as 1853, by Dr. Gibson. In his paper in the Pharmaceutical Journal, series 1, vol. xii., p. 422, a formula for the tincture (3 oz. of the coarsely bruised bark to a pint of proof spirit) is given, and some idea as to the dose and uses. Alstonia constricta is an Australian bark used in Queensland as a substitute for quinine and is now coming into use in the United States. It is also known under the name of Queensland Fever Bark. It is quite different in appearance from Dita bark,, which is used for dysentery rather than for fever. At the meeting of the International Congress of Medical Science, at Amsterdam, among the papers read was one by Mr. Van Gorkom, on the culture of the different species of cinchona barks in Java. His experience, as superintendent of the quinine plantations in Java, naturally gives great value to his opinions. He considers that regular culture has done much to increase the value of the cinchonas for medical purposes, but that neither by outward nor by anatomical structure is it possible to determine the richness in active principles of any given sample of the bark and that chemical analysis alone can determine this point. He also finds that the properties of each species remain the same, although growing in foreign lands. Their tendency to hybri¬ dization, however, renders careful supervision of the plantations necessary, so as to secure seed of the best varieties only, or in other words, such, as yield the largest amount of quinine. He believes that the growth of cinchonas in the East Indies is more in¬ fluenced by the local condition of the climate and the soil than by a difference in the elevation of the land and that it is best not to attempt to grow them above 4500 or 5000 feet. In the Gardeners' Chronicle an interesting extract from the Colonies and India is given concerning the collection of kauri gum. It is there stated that the districts in which the gum is found are generally covered with small mounds which indicate its presence. The gum hunter carries a steel-tipped spear with which he probes the mass, a little ex¬ perience enabling him to ascertain the existence of the gum without further search. It is found in blocks from a few ounces to 50 or 60 pounds. The gum which is dug up is said to be used in this country for dressing calicoes, while the recent resin,, or that from the existing tree, is employed princi¬ pally in varnish making. In the Lancet for September 6th attention i3 called to the fact that the use of sulphate of duboi¬ sine is liable to produce giddiness or even in some cases delirium. The writer says : — “ When the supply of pure alkaloid becomes large enough to ensure uni¬ formity of strength in the solution made by different ••September 27, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 243 chemists, it may he unsafe to prescribe a four grain solution of sulphate of duboisine, and the use of the drug for rapidly dilating the pupil or paralysing the accommodation in the out-patient or the con¬ sulting room may not be free from disadvantage.” On this subject Dr. J. Tweedy remarks in a sub¬ sequent paper, in the same journal, that “ Duboisine, like many other remedies, has been and still is ex¬ travagantly abused. It is of immense power and value and necessary only in special cases, for which it should be reserved. Bulk for bulk, it is much stronger than atropine and should be employed with corresponding caution.” From these remarks it is evident that duboisine is an unsafe drug to be used by patients themselves, and it behoves chemists, •should they meet with prescriptions containing it, to tell the patient to be extremely careful not to exceed the quantity directed to be used. Apropos of the above remarks it is not quite evident in what way uniformity in streligth of the solution made by different chemists depends upon the supply of the pure alkaloid. Does the writer mean to imply that chemists do not make solutions of the strength ordered, because duboisine is an expensive article ? Solutions of alkaloids, etc., are usually made at the request of medical men, and such solutions naturally differ in strength according to the requirements of the prescriber; therefore it must rest with the prescriber alone to regulate the strength in the absence of a published formula. This experience of duboisine does not appear to be universal with experimentalists, for in Dr. H. Macnaughten Jones’s able summary, in the British Medical Journal , no mention is made of giddiness or delirium being induced by its_ application ; on the contrary, he observes, “ of the two (atropine and -duboisine), so far as my experience teaches me, save for its expense, I prefer the sulphate of duboisine to the sulphate of atropine.” The production of these symptoms may therefore be due to a peculiar intoler¬ ance of the drug similar to that which is well known to occur in some persons as regards atropine, and which is alluded to by Dr. Jones in the above paper. Benzoate of sodium is said to be much us:d in Germany at present. It is stated that it reduces fever less rapidly than quiniie and salicylate of sodium, but that the effect lasts longer. The dose given is 5 to 6 grams for children and 10 to 20 grams for adults. In the Medial and Surgical Reporter, Dr. Mary J. Matlack calls attention to the value of asparagin as a diuretic. She considers it to be one of the best remedies in dropsy dependent on disease of the heart, and to be especially valuable in chronic gout. The dose given is 1 grain, three times a day, in conjunction with 12 grains of bromide of potassium. Many of our readers have probably heard of the singular case of Alexis St. Martin, who had an open¬ ing into his stomach from a bullet wound which never closed, and who w'as the subject of experiments on gastric digestion, by Dr. Beaumont. The Detroit Lancet , for August, states that he is still alive and lives at Joliette county, Quebec province, Canada, and although seventy-nine years old, is strong and healthy. The hole in his stomach is an inch in dia¬ meter, yet his digestion has never failed. It should be added that he has been a hard worker all his life. A new use for thymol has been discovered by Dr. Emil Stern, of Breslau, who states in the Breslaue drztliche Zeitschrift (No. 8, 1879), that so far as he has been able to observe a mixture of a one per 1000 aqueous solution of thymol preserves vaccine lymph from decomposition, while it does not destroy its specific action and the mixture is not more irritating than ordinary vaccine matter. It does not appear, however, that tliymolized lymph is infallible in its action, it seeming to vary in activity according to its age. The discovery, however, that thymol does not, like carbolic acid, destroy the power of the vaccine lymph is a remarkable one. From the Ammi Visnaga , an umbelliferous plant common in Lower Egypt, and the rigid pedicels of whose umbels are used by the Arabs as toothpicks, Mr. Ibrahim Mustaplia has extracted a glucoside to which he has given the name of kelline, from kell, the Arabic name of the plant. It is obtained by treating a mixture in equal parts of the powdered seeds of the plant and slacked lime with alcohol, evaporating to dryness in a water-bath, exhausting with ether, filtering and treating with boiling water the yellowish residue and filtering while warm. On cooling crystals are obtained which are purified by recrystallization first from hot acetic and then from boiling water. Kelline is described as a white very bitter substance, very slightly soluble in water, methylic, ethylic and amylic alcohols and chloro¬ form when cold, but much more soluble in them when hot. Pelletierine, the alkaloid isolated by Tanret from pomegranate root bark, and considered by him to be the active tsenicide principle, appears to be making its way into favour on the Continent. The free alkaloid is a volatile oleaginous liquid, and the salts described by Tanret in his original paper ( Pharm . Journ. [3], ix., 1023), — the sulphate, hyclrochlorate and nitrate, — although obtainable in the crystalline form, are very hygroscopic and liable to undergo alteration through atmospheric influences, and are consequently qot suitable for dispensing. For this purpose Messrs. Gehe recommend as most con¬ venient the tannate, which forms a dirty white powder, stable when exposed to the air. In bringing the subject before the Paris Society at its August meeting M. Petit said that judging from the com¬ position of the tannate of pelletierine the dose would vary from 1*50 to 2-0 grams, but as he admitted that the results of a polarimetric examination were abso¬ lutely different from those reported by M. Tanret it is not quite certain that the substances obtained by these two chenists were identical. Aspidospermine, the alkaloid of the bark of Aspi- dosperma Quebracho, which has been recently recom¬ mended in the treatment of dyspnoea accompanying diseases of the lungs and other organs, has been the subject of a further examination by its discoverer, Herr Fraude ( Ber . cl. deutscli. chem. Gesells, xii. , 1561). The author represents it by the formula C^F^NgC^, and states that at 14° C. one part of it is soluble in 48 parts of 99 per cent, alcohol, in 106 parts of ether free from alcohol and water, and in 6000 parts of water, the aqueous solution having a distinctly bitter taste. In many of its reactions it closely resembles strychnia, but its reaction with hypochlorous acid is characteristic. If a very small quantity be boiled for a few minutes in a tew c.c. of aqueous solution of hypochlorous acid, sp. gr. 1T3 to 1T4, the liquid acquires an intense red colour, resembling that of a solution of fuchsin, which is persistent during a week’s exposure to air and light. Brucine under similar conditions gives a dark Madeira colour, and strychnine a reddish yellow colour. The cinchona and opium alkaloids, veratrine, caffeine, 244 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 27, 1879.. atropine, nicotine and coniine give no colour reaction with the solution of hypochlorous acid. Bromide of zinc having come recently into use in medicine M. Yvon recommends its preparation by double decomposition between zinc sulphate and potassium bromide. Upon triturating equivalent quantities of these in a mortar liquefaction quickly takes place, the water * being afforded by the zinc sulphate. This product is left in contact about twenty minutes, then suspended in double its weight of perfectly rectified 95 per cent, alcohol and filtered. The solution of zinc bromide, which should pass through colourless, is evaporated to dryness first in a water-bath and then in a sand-bath. The product should be volatile, without residue and entirely soluble in water, alcohol and ether. In the French Academy of Medicine, M. Vulpian has called attention to the fact that pepsines de¬ livered from different pharmacies vary much in their digestive power, some of them modifying albumen so slowly as to make it doubtful what good effect they can have when administered to dyspeptics. He also confirmed a conclusion arrived at some time ago by Dr. Symes ( Pharm . Journ. [3], iv., 1), that the action of pepsine is retarded by the presence of alcohol. Wines and elixirs of pepsine are very much used in France, and as M. Vulpian went on to say that some of the most renowned elixirs contained an extremely small quantity of pepsine, the rest in¬ tended to have been present having probably been precipitated by the alcohol during the manufacture of the preparations, the statement has caused some little sensation amongst the makers. M. Vulpian also described some experiments made by a pupil, M. Mourrut, which appeared to indicate that sufficient hydrochloric acid to correspond to the acidity of the gastric juice, added to a liquid containing dias¬ tase or pancreatine, retards the action of the diastase and stops that of the pancreatine, the former recover¬ ing its activity upon the neutralization of the liquid, but the latter remaining inert. Some interesting experiments on the propagation of sponges, made by Dr. Schmidt, of the University of Gratz (Stvria), have just been reported to the Paris Acclimatization Society ( Bulletin , xxvi., 374). Dr. Schmidt has found that if a sponge be taken early in the spring, cut into small pieces, and immersed in water by attaching the pieces to wooden stakes, growth soon commences and eventually in about three years each piece may become a perfect sponge worth ten centimes. An estimate based upon what appears to be rather slender experience sets the probable profits from the investment of capital in this direction at about 60 per cent. The disastrous consequences that might result from a person affected with colour blindness being placed m charge of a vessel induced the Board of Trade at the beginning of 1877 to issue instructions that persons presenting themselves for examination for masters’ or mates’ certificates should undergo a preliminary test as to their ability to distinguish the following colours, which enter largely into the combinations of signals used at sea - black, white, red, green, yellow and blue. As a result, out of 5967 candidates 26 — or rather less than half per cent. — were finally rejected as colour blind, and 13 others were only allowed to proceed to examination after a second trial. Green seems to have been the greatest stumbling block, it having been described wrongly by each of these 39 men, and in 25 cases referred to red. On the other hand, 12 referred red to green. It may be remarked that some time since it was stated in La France Medicate that this infirmity could be overcome by looking through a layer of fuchsine in solution. A M. Javal has made a practical application of this observation by interpos¬ ing between two glasses a thin layer of gelatine tinted with fuchsine, and it is claimed that by the use of such spectacles the errors caused by colour blindness are corrected. According to the Medical and Surgical Reporter , some experiments made in Philadelphia have confirmed this statement. Still more additions to the “elements,” and again the spectroscope has been the principal instrument used in the detection. M. Cleve reports to the Academy of Sciences {Compt. Rend., September 1) that he has dis¬ tinguished in erbia two new elements, making four that have been separated from this substance, which was until recently looked upon as itself being the oxide of a single element, erbium. A writer in the Chemical News asks some pertinent questions as to the manner in which these strangers are to be treated in the text-books. Since June, 1877, the following new elements have been named — davyum, neptunium, lavoesium, mosandrum, philiipium, ytterbium, deci- pium, scandium, norwegium, uralium; and to these are now added, thullium and holmium. Whilst some workers are thus increasing the list of elements, others- are steadily seeking to reduce it. In a short note read by Mr. Lockyer before the British Association he makes the following statement, leaving to others apparently to draw their own inferences: — “When carefully distilled metallic sodium was condensed in a capillary tube, placed in a retort, and heated in a Sprengel vacuum, it gave off twenty volumes of hydrogen. Phosphorus, carefully dried, and sub¬ mitted to the same treatment, gave off seventy volumes of a gas which appeared to consist chiefly of hydrogen.” Magnesium is said to have given off two volumes of hydrogen, and from sulphur sulphur¬ ous anhydride was always obtained. Iridium always gave off hydrogen in vacuo without heating, whilst lithium gave off as much as one hundred volumes. Corresponding with the advance of science there must necessarily occur in national pharmacopoeias successive changes in the names of many of the chemicals employed as therapeutic agents ; with the lapse of time some of the earlier names have become quite obsolete. When, therefore, a prescription con¬ taining a well-known chemical, but with its more ancient name, is placed before a pharmacist whose acquaintance with drugs and chemicals dates no further back than the advent of the British Phar¬ macopoeia, he is ignorant of the preparation when ordered by a name not found in that volume. The library of everyone engaged in a business composed of the usual mixture of the retail of drugs and the dispensing of prescriptions may 'with ad¬ vantage have on its shelves, in addition to the British Pharmacopoeia, subsidiary works of reference* in which category may be named as specially useful Beasley’s ‘ Pocket Formulary,’ also Gray’s ‘ Supple¬ ment,’ a valuable work and one that well merits, another edition, together with Jourdain’s ‘Pharma¬ copoeia Universalis, or a complete encyclopaedia of the. materia medica contained in the pharmacopoeias of London, Edinburgh and Dublin, as well as of all those: of Europe and America, and of dispensaries formu¬ laries, etc.,’ and, as hospital formulae very frequently September 27, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 245 I I : find their way into private practice, to the above may with advantage be added that valuable little work, Squire’s ‘Pharmacopoeias of -the London Hos¬ pitals.’ It must be obvious that the number can be greatly increased, but the few above named may be considered almost essential as works of reference in a well regulated pharmacy, and these should be so placed as to be readily accessible to the dispenser. Some of the questions asked and repeated in these pages may be taken to indicate that in many establish¬ ments no such facilities exist of easy reference when a difficulty occurs in the case of synonyms or formulae which the British Pharmacopoeia does not supply- Correspondents would materially assist their less favoured brethren by naming works of reference which they have found valuable and could recom¬ mend to others similarly situated. The first formula, No. 338, is evidently intended for a hair dye and the inquiry has been answered by several correspondents the answer of Mr. Staveley is definite. As regards the addition of liq. ammon. fort, to the solution of argent, nit., the ammonia should be added drop by drop with constant stirring and discontinued just before the disappearance of the last trace of precipitate. The addition of ammonia to a solution of argent, nit. precipitates the silver in the state of oxide, which is redissolved in excess of the precipitant, and care should be taken towards the end of the process that no more ammonia be added than is barely sufficient to dissolve the oxide precipitated. The prescription No. 339 may be dispensed by rubbing the quinine to a fine powder, and then mixing it with one half the water ordered, and the ferri am. cit. being dissolved in the other half, they should be mixed. The result will be a turbid mixture, which will require being shaken before the administration of each dose. Probably the question refers merely as to whether the quinine should be dissolved by the addition of an acid, previously to its mixture with the ferri am. cit. The writer has not added an acid, its addition by the dispenser would consequently not be justifiable. The presence of an acid produces a more elegant result, and may with propriety be suggested to the prescriber, but should not be employed without his sanction, as he may have sufficiently satisfactory reasons of his own for the omission. No. 340 contains the question whether it would be right in making ung. sulph. iodid. to rub the iodide with a little glycerine before adding the lard, “ glycerine being a solvent of iodide of sulphur.” In making the ointment it is very desirable that it should be smooth and without grit, and although any addition to a prescription must be adopted with great care, to either a few drops of glycerine or spirit in this case there can be no objection, and more especially as one correspondent says the addi¬ tion of one of them “ ensures the production of a faultless ointment.” Mr. R. H. Parker, in his reply to the question regarding the production of this ointment, states that in the next edition of the British Pharmacopoeia the formula may with advantage have the addition of the rectified spirit. This remark points to another direction in which the discussions taking place in these columns may be of value, namely, in improving the formulae for the next Pharmacopoeia. It is well known that the accumulation of small but valuable facts with regard to the make of these and similar preparations, and their general application in practice, constitute that essential difference which is now and then observed in the same prescription dispensed at different establishments. The prescription No. 341 contains an ingredient well known under its present name, hydrarg. ammon., but it is not so generally known by pharmacists of the present day under its former one, calx hydrargyri alba. It is one that in name has seen many changes, and probably the present one will not be final. A formula for the ointment occurred in the £ Pharma¬ copoeia Londiniensis ’ of 1788, and is quoted by a correspondent in another column. An ointment of this preparation is frequently used as an external application in eruptions of the skin on the head or face. No. 342 refers to a change of colour which takes place in ung. plumbi subacet. co. after being kept some time. This subject has been discussed on previous occasions, and it can only be necessary to refer “ An Apprentice ” to the remarks on this change in prescriptions Nos. 130 and 243, and some observations on the same in “ The Month,” Feb. 22, 1879, p. 698, and July 7, 1878, p. 65. MELIA AZEDARACH, LIN.* BY J. JACOBS, PH.G. This beautiful tree is highly appreciated in the Southern United States for the beauty of its flowers, the elegance of its foliage and the medicinal uses to which it is applied ; as a shade tree its popularity is equal to that of the maple in the North. It appears to be indigenous to Asia, but is planted as an ornamental tree in southern Europe, whence it was introduced into and naturalized in the United States at an early period, after the settlement of Carolina and Georgia. It is not found farther north than Virginia, as \h e severity of the climate of the more northern districts destroys it. The common names, pride of China and pride of India, undoubtedly originated from its rare beauty ; Indian lilac from the resemblance of its flowers to those of the common syringa, and bead tree from the use of the nuts in rosaries, to which also, the German name Paternosterbaum (paternostertree) alludes. In the southern States it is known as China-berry , and to the young as popgun tree, in allusion to the use of its green fruit. The tree attains a height of 30 to 40 feet, aud from 15 to 20 inches in diameter ; it grows rapidly, reaching the height of 12 or 15 feet in four years. The green fruit is very astringent, but when ripe it is a fleshy -yellow drupe, of a sweet taste, rather larger than a cherry, and contain¬ ing a five-celled bony nut. The green fruit is used in Texas for making blacking. The ripe berries were largely used in Georgia during the late war for the purpose of obtaining alcohol, by the usual process of fermentation and distillation ; the whisky thus obtained was preferred by many to that produced from corn or rye. By expressing the fleshy part of the fruit, like the olive, a fixed oil is furnished from which a “ Poor Man’s Soap ” is made. Remarkable qualities are said to reside in the fruit, such as will intoxicate robins, which are particularly fond of and feed upon them during their annual migration southward { the seeds are widely dispersed by these birds, and hence trees are found in secluded places. Instances are known of the fruit being destructive to hogs, by what means it is not yet ascertained. A decoction of the berries sprinkled on plants prevents the depredations of * From the American Journal of Pharmacy , September, 1879- 246 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. September 27, 1 879. the grub-worm. The leaves and berries will preserve dried fruit from insects, and when packed with clothing will prevent the attack of moths. The dried berries in whisky have been employed against ascarides, tape- worm and verminous maladies. The pulp of the berries stewed in lard has been used with success as an oir.tment in scald head. The decoction of the leaves has been employed in hysteria, and is astrin¬ gent and stomachic. A decoction of the green bark, 4 ounces to the pint, is administered as an anthelmintic in doses of 1 or 2 fluid ounces, followed by a cathartic. When prepared in March or April, while the sap is ascending, unpleasant effects have been observed, such as stupor, dilation of the pupil, etc., which symptoms, however, pass off -without perceptible injury to the system. For the following experiments the bark of the root was employed, and as the liber is very easily separated, and this portion is the most effective in the Nim Bark ( Melia Azadirachta , Lin.), this alone was used. The liber is of an extremely bitter taste, devoid of astringency, and its decoction gave no evidence of tannin ; the outer portion, on the other hand, is very astringent, and its decoction gave abundant evidence of tannin by gelatin and ferric chloride. I may also mention that the inner bark is the portion used in making the decoction for administering. After several preliminary experiments made with the view of determining the best course to pursue, one pound of the powdered bark was percolated with diluted alcohol until thoroughly exhausted. Upon distilling off the alcohol the aqueous residue held in suspension a con¬ siderable amount of insoluble matter. This residue was divided into two parts, one being filtered ( A ), the other evaporated (B). The aqueous filtrate, A, was treated with solution of acetate of lead as long as a precipitate was produced ; the precipitate was brought on a filter and washed well with water. The filtrate was treated with subacetate of lead, and this precipitate likewise collected and washed. The filtrate was freed from lead by sulphuretted hydrogen, separated from the sulphide of lead, and the sulphuretted hydrogen expelled by heating. The sulphide of lead yielded nothing to hot water, but when treated with hot alcohol, a small amount of resinous or extractive matter was obtained. The filtrate from the sulphide of lead was concentrated to a syrupy consistence ; alcohol produced a slight precipitate, and on the addition of ether a slight semi-fluid mass se¬ parated. Both precipitates occasioned by alcohol and ether redissolved in water and alcohol, respectively, and, evaporated spontaneously, left a dark amorphous residue, which was also obtained from the filtrate after ether and alcohol had been expelled ; the ether precipitate proved to be sugar. The examination of the lead precipitate did not lead to any decided results. The evaporated portion, B, had a peculiar odour and bitter taste ; it was treated with hot water, acidulated with hydrochloric acid and filtered from the residue, C. The filtrate w-as treated with magnesia and tested for an alkaloid, but none was found. The residue, C, was well washed with water, had a brownish-yellow colour and a strongly bitter taste, was not affected by hot or cold water, was slightly soluble in carbon bisulphide, insoluble in petroleum benzin and oil of turpentine, and soluble in alcohol, ether and chloroform, which solutions, on evaporation, refused to crystallize. The alcoholic solution was acid to test paper, but apparently did not combine with alkalies. On dissolving the substance repeatedly in alcohol, and precipitating it by water most of the colour was removed, the resinous principle remaining as a yellowish-white mass. It was given as an anthelmintic to a child aged four years, in the quantity of 3 grains, followed by a mercurial purgative, and proved to be at least as effectual as other vermifuges which had been previously given. The results of his observations and experiments lead the author to the following conclusions : — 1. The activity of the bark resides in the liber, and this alone should be employed. 2. The active principle is a yellowish -white resin. 3. The drug is one of the best anthelmintics, and a fluid extract, prepared with diluted alcohol, or a tincture, would be a valuable preparation that would seem to' deserve a place in the Pharmacopoeia. CHEMICAL NATURE OF THE ESSENCE OF LAURO- CERASUS AND OF BITTER ALMONDS.* BY M. FILETI. The great difficulty of separating the whole of the hydrogen cyanide from essence of bitter almonds, and of the laurocerasus, renders it probably that it is present in some form of combination with the benzaldehyde ; this compound would be the nitril, C6H5.CH(OH).CN, corre¬ sponding with mandelic acid. In order to test the truth, of this supposition, the crude essences were treated with zinc and hydrochloric acid, in presence of alcohol and a platinum plate ; twenty-four hours afterwards, the mix¬ ture was precipitated with water, and evaporated at lOO01 to remove alcohol. After filtration from the hydroben- zo'in, the liquid was supersaturated with potash, and agitated with ether, the ethereal solution being sub¬ sequently washed with water, and agitated with dilutes hydrochloric acid. On evaporating the acid solution, the hydrochloride of a base was obtained, which was converted into the platinochloride and analysed, as was also the. hydrochloride. The results correspond with the formula. C6H5.CH2.CH2NH2 for the base. From this it would appear that the nitril C6H5.CH(OH).CN is present in the crude essences, and that by the action of nascent hydro¬ gen it is not converted into the amide C6H5.CH(OH).CH2.NH2, as might have been expected, but that an atom of oxygen, is eliminated in the process, so that the final product is- the base C6H5CH2.CH2.NH2. A mixture of pure benzal¬ dehyde and hydrogen cyanide, when treated with zinc, and hydrochloric acid in a similar manner, yields a base having the composition and properties of methylamine. In a similar manner, both chlorine and fuming sul¬ phuric acid act differently on the essences to what they do on a mixture of pure benzaldehyde with hydrogen cyanide. W ith the crude essence, a solid crystalline sub¬ stance is formed, which Zinin has shown to be benzylidene- formobenzamide, Ph.CH(OH).CO.N : CHPh; whilst the author finds that no solid substance is produced by the action of fuming sulphuric acid on the mixture, and with chlorine it fields ammonium chloride and mbnochloro- benzoic chloride. The base above described is obtained in much larger quantity by the action of zinc and hydrochloric acid on amygdalin in aqueous solution. The hydrochloride of the base is more soluble in water than in alcohol, crystallizing from the latter in large plates, melting at 217°, and subliming near its fusing point. It would appear to be identical with that obtained by Colombo and Spica, by the action of nascent hydrogen on the compound of benzyl cyanide with hydrogen sulphide ( Gaz ., 5, 124). On decomposing the solution of the hydrochloride with potash, agitating with ether, and leaving the ethereal solution to evaporate, the free base is obtained as a syrupy liquid, which after a time crystallizes in large plates (m. p. 101—104°). The author proposes to continue his examination of the more obscure reactions of the essences of bitter almonds and laurocerasus. * From the Gazzetta chimica italiana, 8, 446 — 452. Reprinted from the Journal of the Chemical Society, Sei - tember, 1879. September 27, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 247 SUhf $hat;maqutuat Jmtptl. - ♦ - SATURDAY , SEPTEMBER 27, 1879. QUESTIONABLE PROSECUTION UNDER THE SALE OF FOOD AND DRUGS ACT. We have not unfrequently had occasion to com¬ ment upon the oppressive and vexatious mode in which the provisions of the Food and Drugs Act are brought to bear upon chemists and druggists without in any way serving the purposes for which that Act was passed, though at the same time tending to inflict serious personal inconvenience and injury. We regret especially that it has been necessary to make this complaint against the application of an Act which in its spirit harmonizes so thoroughly with the endeavours of the Pharmaceutical Society to expose and put a stop to the falsification of drugs. Without going back to past instances we may refer to the case that has just been 'decided at the Cliertsey Petty Sessions as affording a fair illustra¬ tion of what is meant. According to the report of this case, which will be found at page 257, it will be seen that Police-constable Waters, acting upon the instructions of his superintendent, went to the shop of Mr. Boyce, an old-established pharmaceutical chemist at Chertsey, and purchased sundry articles, namely, quinine wine, citrate of iron and quinine, citric acid and cream of tartar. After having ob¬ tained and paid for these articles, he informed Mr. Boyce’s assistant that they would be handed over to the county analyst for examination, and he offered to leave a portion of each article under seal. In due course these articles were passed through the hands of Superintendent Bungard to the county analyst, who examined them and reported the results he had obtained. So far there is absolutely nothing to complain of in the manner of carrying out the provisions of the Act. The subsequent reports of the county analyst represented three out of the four articles in question to be genuine, as they might reasonably be expected to be when obtained from such a source. As regards the cream of tartar, however, the report of the analyst represented that it contained tartrate of lime to the extent of 11 *7 per cent., and sulphate of baryta to the extent of 0 6 per cent. Both of these substances were spoken of in the analyst’s report as being “ foreign ingredients,” and hence, we presume, the local authorities inferred that the analyst’s report showed the cream of tartar not to be of the nature, substance and quality of the article demanded by the purchaser. It is true the analyst’s report also stated that the “ foreign ingredients ” were insoluble, and not injurious to health, so that on this score, ac¬ cording to him, there was no ground for concluding that their presence would be to the prejudice of the purchaser, or the consumer, and it might have been expected that the vendor’s freedom from liability to penalty under the provisions of the Act would have beefi apparent. But it cannot be expected that the local authorities of a town like Chertsey are always qualified to judge of such matters and they may well be excused for having, as it seems, put such an interpretation upon the analyst’s report as to induce them to institute a prosecution under the sixth section of the Act against Mr. Boyce, for selling cream of tartar that was not of the nature, substance and quality, etc., demanded by the purchaser. It is in this way that Mr. Boyce has found himself arraigned on a charge of having transgressed the law by selling an adulterated article and called upon to defend himself from the most damaging imputations that could be made against him in his business capacity. And now let us consider what are the data upon which this grave charge has been brought against him. Of the two so-called u foreign ingre¬ dients ” reported to be present in the cream of tartar, the one that was in the largest proportion, and that, according to the analyst’s report, would consequently have been chiefly to the prejudice of the purchaser, is the tartrate of lime, the other foreign ingredient, the sulphate of baryta, is of itself too small in amount to justify the inference that it was added as an adul¬ teration. What then is the origin of the tartrate of lime 1 Is there any reason to suspect that it was added fraudulently to increase the weight of the cream of tartar, for that is the imputation conveyed by the charge preferred ? Upon referring to the British Pharmacopoeia for information on this point, we find under the head of Potassse tartras acida, a description of the sub¬ stance commonly known as “ cream of tartar.” It is there stated to be an acid salt obtained from the crude tartar which is deposited during the fermenta¬ tion of grape juice. Proceeding on this basis for further information from other sources, we find that crude tartar, the raw material from which the Pharmacopoeia article ,“ cream of tartar,” is prepared, generally if not invariably contains tartrate of lime; moreover, that grape j uice itself contains tartrate of lime as well as tartrate of potash, and that in conse¬ quence of this association of these two tartrates in the primary source of crude tartar as well as of “ cream of tartar,” they continue to be associated in its products, so that tartrate of lime is not, as the analyst for the county of Surrey represents, “ foreign” to cream of tartar, but a natural ingredient of it. And if we return now to the British Pharmacopoeia we find this fact recognized by that authority. The solution of the charred substance in hydrochloric acid is described as becoming slightly turbid when neutralized with ammonia and mixed with oxalic acid and the presence of lime is thus indicated. But this indication that acid tartrate of potash, in the sense referred to in the British Pharmacopoeia, contains some proportion of tartrate of lime is totally ignored by the analyst for the county of Surrey. He 248 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 27, 1879. like the peculiar people is above considerations which regulate the proceedings of more ordinary folk, and acting upon the esoteric conception that the term acid tartrate of potash is to be interpreted from an absolute chemical point of view, expects a policeman’s request for “ cream of tartar ” to be responded to by a pro¬ vincial druggist by the supply of perfectly pure bitartrate of potash. This and this alone is the basis upon which tartrate of lime has been treated as a “ foreign ingredient ” of cream of tartar, and it is only by allowing such superfine and unauthorized views to regulate his proceedings that the analyst has brought about the prosecution of Mr. Boyce. Nor is this the only point in vThich exception is to be taken to the report now in question. From an analyst it might be expected that in such a docu¬ ment, fraught with possible prejudice to another man’s reputation, care would be taken not to state anything contrary to well-established chemical know¬ ledge. Unless, indeed, it be unreasonable to expect a public analyst to respect chemical fact, we protest against the representation that tartrate of lime, as an ingredient of cream of tartar, is “ insoluble.” The assumption that it is an insoluble substance may in¬ duce the belief that it is also a “ foreign ingredient,” but certainly this belief has no better foundation. It is scarcely to be wondered at that a very simple statement of facts relating to the presence of tar¬ trate of lime in cream of tartar should have led the magistrates unanimously to dismiss this case. Pro¬ vision had been made to support the defence of the case in this particular by reference to authorities, and by direction of the Council of the Pharmaceu¬ tical Society, Mr. Flux attended to watch the case and assist the defence in case of need. At the same time, Mr. W. Hodgkinson, appeared on behalf of the firm from which Mr. Boyce obtained the cream of tartar to testify that they had always been in the habit of supplying him with the very best drugs. While thus loyally supporting his customer he was also able, with the aid of Mr. Allem, to prove that the conditions under which cream of tartar passed into his hands and was supplied to retailers pre¬ cluded the possibility of its being adulterated or in any way tampered with. In these results there is a reason for satisfaction, but it certainly seems to be a somewhat superfluous thing that with the object of protecting the public against adulteration individuals should thus be put to the severest social torture that can be devised. The mere fact of having to appear before a bench of magistrates charged with an offence of the kind that Mr. Boyce has been charged with is sufficient to furnish evil-disposed persons with opportunity for damaging a man in his reputation and in his busi¬ ness. In the present instance it has been satis¬ factorily proved that the charge was unfounded; it has also we think been made evident that the prose¬ cution should never have been undertaken and Mr. Boyce should never have been exposed to the pos¬ sibility of being asked as he was on coming out of court how his “ little job ” had been settled 1 This experience is one that may fall to the lot of any member of the trade who happens to become “ corpore vili ” upon which the public analyst chances to operate. Surely some arrangement could be de¬ vised by which this kind of human vivisection might be avoided without counteracting anv beneficent influ- ence that the Food and Drugs Act is calculated to< exercise. While public analysts produce such certi¬ ficates as that upon which the case in question was based, would it not be well to submit these docu¬ ments to some competent central authority for deci¬ sion* whether prosecution is requisite or justifiable ? At any rate, such proceedings as that above described are calculated to bring the Act into contempt, and to make the public analyst, for some sections of the community, a public nuisance. THE NEW SESSION. Two or three more days will bring the summer vacation of 1879 to an end, and during the coming 'OO week the medical and pharmaceutical schools of the metropolis will be alive with audiences who have- assembled to hear the Introductories. On Wednes¬ day the new session in Bloomsbury Square will as usual be inaugurated by an Evening Meeting of the Pharmaceutical Society, the special business of which will be the reception of the reports of the Professors of the School of Pharmacy, the Distribution of the Prizes awarded to the successful competitors of last session, and an Introductory Address to the Students of the present. The occasion promises to be of special interest, as the Address is to be delivered by a former Bell Scholar, Prizeman and Teacher in the School Dr. W. A. Tilden, of Clifton. It will not be out of place to point out that the invitation given to the Students and Friends extends to the ladies, and we hope that on this, as on former similar occasions, the meeting may be graced by the presence of many of the fair sex. COUNTER PRACTICE IN NEW SOUTH WALES. The counter practice controversy appears to have spread to the antipodes, a Dr. Bowker having intro¬ duced into the New South Wales Legislative Assembly a Medical Bill which the chemists and druggists of the colony condemn as ignoring the rights, customs, immunities and privileges secured to them by the Imperial legislation in the Apothe¬ caries Act of 1815. At a recent Annual Meeting of the New South Wales Pharmaceutical Society, held in Sydney, a petition was adopted asking for the erasure of the obnoxious clause and the insertion of one repeating the saving clause of the Apothe¬ caries Act ; the construction of which has furnished so much food for argument in this country. It was also decided at the same meeting to take steps to draft a new Pharmacy Bill to be submitted to the Legislature. «Ptember27, ls79.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 249 $rcrindal ®ran8a#ti and that “ around this are gathered other species of cinchona, which, viewed in this light, constitute a very exceptional and anomalous group of plants ;+ which most certainly belong to the genus cinchona, but in which the typical cinchonaceous elements are superseded by those corresponding to, and perhaps identical with, the pro¬ ducts of other families of plants. I have shown under the heads C. lutea ( quod vide) and C. decurrentifiolia, in my illustrations of the ‘Nueva Quinologia,’ how botanical and microscopical researches illustrate and confirm each other; and how microscopical examination comes in to^ aid the diagnosis of the barks ; all tending to show the Ladenberyia-like character which pervades them ; and under the C. lutea it appears that Pavon’s careful obser¬ vation of the living plant brings out indirectly the same fact. He says that “a milky juice flows out when the tree is cut down or amputated that is to say, the milk cells are abundant and full of their peculiar product, in which respect the tree symbolizes specially with' the kindred genus. I refer to the “Report” itself for further observations on these yellow barks, and to my remarks^ under C. lutea for the yellow colour. In conclusion I would briefly add that, the red barks are equally a group of plants of which the C. succiruba may be looked upon as the centre. (See my account of specimens of C. succirubra in my ‘Nueva Quinologia, pp. 4, 5.) The red bark is only beginning to be fully investigated as to its alkaloids, and even less so as to its other constituents, as I have partly remarked in. the work alluded to ; but this much may be said with certainty, that the physiological effects must be consider¬ ably different from those of other barks. The Spanish physicians had an opinion about it, to which I cannot at the moment refer. I understand that a fluid extract of C. succirubra has recently obtained some celebrity, but have not yet had an opportunity of examining it. It is probable that its medicinal effects may vary from those of a tincture of pale bark, and still more widely from a tincture of yellow (cordifolia) or of Calisaya bark. A vote of thanks to Mr. Howard was passed. * Report, p. 208. f The group comprehends C. Pelletierana, C. cordifolia, C. lutea, C. decurrentifolia, C. villosa, C. ovata, C. obovata, C. microphylla. X Vide ‘ Nueva Quin.,’ sub C. lutea. September 27, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS 251 The author of the next paper not being present, an abstract of it was given by Mr. W. H. Naylor. The full text is as follows : — The Chemistry of Chaulmoogra Oil. BY JOHN MOSS, F.I.C., F.C.S. BOND. ET BER. A body possessing well marked physical characters, and capable of producing effects interesting alike to the physiologist and the therapeutist is sure to excite that spirit of inquisitiveness which is the moving force in all scientific inquiry. The physiologist and the therapeutist both want to know what is the proximate cause of the phenomena noted by them, and the chemist busies him¬ self to find it out ; separating by his art the inert and diluting material. The members of this Conference sympathize most with the latter, and if each could be persuaded to tell the conclusion to which a scientific use of the imagination has led him in speculating as to the nature of the said proximate cause, nine times out of ten he would suggest an alkaloid. There is about an alkaloid something so definite, so’tangible and real; it is so compact an expression of ideas and properties, is so representative and genuine, that to discover it is a desirable thing, and its presence is easily assumed where strongly marked properties exist. The thought is begot by a powerful desire, and is itself strong — so strong that all others relating to the same body are for the time subservient to it. That Chaulmoogra is a most powerful drug need not be insisted on here, seeing that the widely known favour¬ able testimony of highly qualified observers in Europe and Hindoostan is concurrent with the position it occupies in the ‘Pharmacopoeia of India,’ and the almost veneration with which it is regarded by the native Hindoos. That an alkaloid should be the first thing looked for when an examination of the oil was resolved upon, was a matter of course ; had one been discovered further investigation had probably been stayed. As a guide and a warning to others who may be encouraged by this failure, the method adopted in searching for the possible alkaloid is here i Siven- § 1 . Exami nation for A Ikalo id. a. Volatile. — One pound of chaulmoogra was placed in a retort with twice its weight of water and boiled. The collected distillate, (4 ozs.), was perfectly clear, possessed the odour of the oil in a marked degree, and was neutral to test paper. With acetate of lead a precipitate was thrown down, as also with chloride of barium when made perfectly neutral with potash. W ith the usual alkaloidal reagents no change was produced in the liquid, which was accordingly precipitated with lead acetate, the precipitate collected, de¬ composed with hydrochloric acid and agitated with ether. Evaporation of the ethereal solution gave a fatty body, which was not further examined. The contents of the retort were now made alkaline with solution of soda and the distillation was continued ; this time the distillate gave no indication with any of the reagents used in the first instance and was returned to the retort along with sufficient sulphuric acid to be in excess. Twelve ounces of distillate were collected and on the surface of it were floating aggregations of white, silky needles. The liquid was negative to reagents. The white needles were collected and found to weigh 2 grains. They possessed all the characters of cocinic acid, treated of afterwards. b. Non-Volatile. — A pound of the oil was agitated with successive portions of warm water, acidulated with hydrochloric acid in a Winchester quart bottle. After each agitation the bottle was inverted and allowed to stand till cool, when the oil formed a solid cake, from which the liquid could be easily run away below. The ► united liquids were reduced in bulk over a water- bath and tested with the usual alkaloidal reagents, namely, phos- phomolybdic acid, iodo-hydrargyrate of potassium, iodine in iodide of potassium, iodide of bismuth and potassium, and iodide of cadmium, each one of which produced a precipitate. The whole was now rendered alkaline by soda, filtered, and half the filtrate agitated with chloroform. The chloroform on evaporation to dryness gave a residue which was treated with very dilute sulphuric acid, and the acid solution was shaken with chloroform after addition of sufficient ammonia to make it alkaline. The chlor©- form solution was separated and divided, one portion being shaken with water containing sulphuric acid, and the other with hydrochloric acid. Very slightly coloured residues were obtained on allowing each of these solutions to evaporate spontaneously. The residues when micro¬ scopically examined exhibited after a time well defined isolated needles and prisms, few in number and widely scattered ; the quantity of these crystals was so very minute that any attempt at a chemical examination was entirely precluded, even if its minuteness as compared with the original bulk of oil had not robbed them of all significance. The residues when dissolved in weak acid — they would not dissolve in water — gave a precipitate with ammonia which was found to agree in character with the ammonia salt of a fatty acid. A like result attended the treatment of the second half of the filtrate with ether in place of chloroform. A further search for an alkaloid was made on the liquor pro¬ duced when one pound of oil was saponified. The treat¬ ment was precisely as the foregoing after addition of soda. The precipitate formed by soda in the first instance, and already existing in the second, and which consisted of the hydrate and phosphate of calcium, vegetable tissue, etc., was digested in chloroform and further examined for alka¬ loid. Each attempt was rewarded with non-success. Satisfied either that chaulmoogra contained no alkaloid at all, or that if it did the quantity was so very small that no share in the properties of the drug could be reasonably claimed for it, a fuller and more systematic examination than was at first contemplated seemed to be desirable. Such examination was accordingly instituted, and it grew in interest as fact after fact was slowly and laboriously laid bare. And here I would say that I know of no re¬ search drawing more frequently and more largely upon the patience and the resources both of mind and fingers of the chemist than the unravelling of the constitution of a com¬ plex fatty body, and my thanks a, re due and are cheerfully given to my friend and assistant, Mr. W. A. H. Naylor, for his unwearied and painstaking attention to my wishes and for his suggestive interest in the work, which was rendered more difficult by the exigencies of a busy labora¬ tory where numerous and varied operations were proceed¬ ing at the same time. § 2. General Examination. To make this account more complete it is necessary that I should refer to a previous paper published in the Chemist and Druggist for December, 1878. To a general description there given of chaulmoogra were joined certain remarks having industrial and pharma¬ ceutical interest ; and besides these, the paper furnished results obtained in a preliminary examination undertaken as stated “ with a view to obtain indications of the direc¬ tion in which more particular investigation would lead to the most interesting and valuable results.” A summary of these results will not be out of place here, inasmuch as it will assist in avoiding subsequent explanations. a. Summary of results previously obtained. — Chaulmoogra oil has a decided acid reaction. The melting point is 42° C. and at that temperature the specific gravity is '930. It froths freely when agitated with warm water and after standing separates over the surface of a milky emulsion. At the ordinary temperature alcohol (’807) dissolves a con¬ siderable proportion, including those constituents of higher melting point and aodd reaction possessing the character¬ istic odour and acrid taste of the oil and giving Dymock’s reaction (a rich olive-green colour with oil of vitriol) very readily. The portion not dissolved by cold alcohol exhibits a pale green colour with oil of vitriol and is completely dissolved by repeated treatment with warm alcohol of the same strength. Ether (’720), chloroform, carbon disulphide 252 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 27, i™ and benzine ('872) completely dissolve the oil, except (and the exception equally applies to alcohol) a minute propor¬ tion of flocculent dust consisting of oxalate and phosphate of calcium, sodium and potassium salts, vegetable tissue and albumenoid bodies. The albumenoid bodies are present in sufficient quantity to form a milky emulsion with a small proportion of whatever quantity of oil is agitated with water. By saponification with potash and decomposition of the resulting soap by hydrochloric acid 81 T1 per cent, of fatty acids are obtained, which after exposure assume a white bloom similiar to that observed on the surface of Japan wax. The fatty acids give a fine green colour on the application of Dymock’s test. b. The results which follow have been obtained since the publication of the paper above referred to, and though they still leave the chemical history of chaulmoogra oil in a somewhat incomplete state they form an interesting addition to our knowledge of this important drug. The melting point of the fatty acids just as obtained from the oil in a mixed condition is 44°C. Numerous pre¬ liminary trials were made of processes for separating and identifying them which promised well on paper and were serviceable as illustrating the behaviour of the acids and their compounds under certain treatment, and which in addition to this, did indeed suggest the probable presence of acids afterwards found, but however interesting and instructive to the experimenter, the details would prove but tedious to others, and accordingly I shall confine myself to describing the processes finally adopted, by which the proximate principles to be described were actually separated. , c. Free fatty adds in the oil. — The strong acidity of the oil and its solutions indicates the presence of one or more free acids ; to separate and identify these was the first part of the problem to be attacked. Half a fluid ounce of the oil was shaken with three fluid ounces of a saturated aqueous solution of hydrate of barium at 100° F. The watery liquid was removed and the oil washed with successive quantities of water at the same temperature as the solution originally used, until the washings came away neutral. The united liquids were filtered, acidified with hydro¬ chloric acid, and boiled. There was no separation. The oil therefore does not contain any compound of a fatty acid, and does not form with hydrate of barium any such compound, which is soluble in water or baryta water. d. Oil treated as above will contain the fatty bodies originally present in it, and barium compounds of the free acids originally present. From this oil cold alcohol ("807) and ether (*735), used successively, dissolve away the former, leaving all the barium compounds ; boiling alcohol dissolves a very few grains of the residue. The residue consisting of barium compounds was then fused by admixture with boiling water, hydrochloric acid added, and the fatty acids collected on a filter and washed with hot water till the washings were neutral and free from barium chloride. After this the fatty acids were kept melted on a water bath till dry, when they were treated w>th alcohol and the solution set aside. In a little while crystals appeared which when first tried melted at 55° C. By repeated crystallization from warm alcohol these were finally obtained of a pure white colour and having a constant melting point of 62° C. With the aid of a microscope and selenite plate this crystalline body was recognized as palmitic acid. The crystalline form and the arrangement of the crystals corresponded exactly with a beautifully executed photograph of palmitic acid forming one of a number in a pamphlet* published by Price’s Patent Candle Company, and besides it corresponded in all characters to a specimen of chemically pure palmitic acid, for which as well as the pamphlet I am indebted to the kindness of the company. On the first treatment with alcohol of the fatty acids * 1 Examen der A-cides G-ras par la lumiere olarisee.’ separated as above a portion remained undissolved, which was subsequently found to go into solution when more alcohol was used, especially when warmed. This portion consisted of palmitic acid solely. e. The alcoholic solution first obtained, from which crystals of impure palmitic acid separated as the alcohol slowly passed away into the air, yielded on evaporation to dryness a fatty acid, which when purified by repeated treatment with small quantities of cold alcohol had a fixed melting point of 29° C. This body is more fully described later on ( h ). /. Turning now to the fatty acids obtained by decom¬ posing the soap of chaulmoogra,, 317 grams of the mixed acids were dissolved in just sufficient alcohol for the purpose and the solution was saturated by adding solution of ammonia (-959). This converted all the acids present into ammonia salts. Acid palmitate of ammonia is not freely soluble in spirit and separated'out at once ; the acid from this precipitate was prepared in the free’state and identified. It was not pure but contained another acid not recognized at the time, which will be found freely described in h ; this acid is also mentioned in e. The spirituous solution of the ammonium salts was now treated with chloride of ammonium and acetate of mag¬ nesium. These failed to produce any visible chang'e in the solution, thus indicating the absence of more than traces of palmitic acid. On the further addition of an aqueous solution of chloride of barium a precipitate fell of a viscous character. JThis was collected and digested with cold alcohol, which dissolved a small portion, leaving a precipitate which was decomposed, washed', dried, dissolved in alcohol, and exposed to cold. The solution separated from the crystalline deposit of palmitic acid was now treated with lead acetate in presence of ammonia and warmed, and the precipitate resulting from this treatment was likewise set aside. The filtrate was kept warm until all the alcohol was expelled, and 'the liquid containing the lead salt thrown out of solution by the expulsion of the alcohol was treated with ether, by which it was completely cleared. Hydrochloric acid was now added, the chloride of lead produced removed by a filter, and the ethereal solution of fatty acid allowed to evaporate spontaneously. A crystalline substance separated in rosettes, which when subsequently crystallized from alcohol was quite colourless, but turned yellow in a few hours. It melted at 33° C. This is the melting point of hypogseic acid, which moreover possesses the characteristic of turning yellow a few hours after it is prepared. -^-yP°S3ea^e lead is readily dissolved by ether; it also dissolves in warm alcohol, but the greater proportion separates out upon cooling. It is not precipitated by magnesium acetate in presence of alcohol. The barium compound also dissolves in hot alcohol but falls out of solution on cooling. The compounds of the acid under consideration possessed all these characters, and its identity with hypogseic acid was established by a combustion. 0781 gramme was burned with chromate of lead and yielded -1369 gramme of carbon and -0217 gramme of hydrogen ; side by side I give the numbers obtained, calculated into percentages, with those required by the formula for hypogaeic acid, C16H30O2. Numbers Obtained. Theoretical Numbers Carbon . . 75'63. 75-59. Hydrogen . 11-99. 11-81. O' The precipitate produced by acetate of lead and not dissolved by warm alcohol was freed from adhering liquor by pressure between folds of bibulous paper and then digested in ether ; hypogaeate of lead was dissolved away. The insoluble portion was decomposed by hydro¬ chloric acid and the free fatty acid crystallized from ether. It melted at 38"5° C. and crystallized in a form very closely resembling that assumed by palmitic acid, but when crystallized under the same conditions it is not so . delicate as the latter. A further small quantity of this acid, as also of hypogaeic acid, was obtained from the September 27, 187?. J THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. £53 cold alcohol washings of the viscous barium precipitate. To examine it more particularly 660 grains of the mixed fatty acids were used for preparing some by a method slightly modified from the above. The acids were dis¬ solved in alcohol and the solution was treated with ammonia and magnesium acetate. The precipitate, which will be considered later, was collected on a filter. Lead acetate was added to the filtrate and after two days standing the mixture was filtered. The precipitated lead I salt was washed with cold alcohol, dried and digested in ether. The insoluble portion was again dried, fused on the surface of warm water, and decomposed by hydro¬ chloric acid. The liberated fatty acid being removed by agitation with ether, was freed from the solvent and then dried over oil of vitriol. It weighed 18 grains, and by observation of the melting point was found to be still impure owing to the presence of palmitic acid. This was removed by fractionation from alcohol and th finael pure product, a white crystalline mass, weighed when perfectly dry 10 grains. The melting point was constant at 385° C. 0T71 gramme burned with chromate of lead gave T84 gramme of water and '446 gramme of carbonic acid, corresponding to '0204 gramme of hydrogen and T216 gramme of carbon, or in 100 parts. i Numbers Obtained. Calculated from C11H22O2. Carbon . . 71T1. 70'97. Hydrogen . 11*92. 11*82. By the side of these numbers I have placed others with which they closely agree, calculated from the formula CuH.>202, an acid not usually mentioned in the text-books, but which I find very fully described under the name of cocinic acid in a paper by M. Saint Evre — “ Recherches sur les Acides Gras du Beurre de Coco.”* He says “II cristallise par le refroidissement de sa dissolution al- coolique en aiguilles incolores groupies en etoiles autour d’un centre commun. II fond a la temperature de 3 4 '70 et se dissout aisdment dans lather et 1’alcool a 36 degrds. II est depourvu de toute espbce d’odeur, et lors qu’il a ete maintenu en fusion pendant longtemps, puis sounds a Faction du vide, il se prdsente sous la forme d’un masse incolore, dure et cassante. II se volatilise, mais seulement dans un courant de gaz.” This desciiption applies per¬ fectly to the acid separated from chaulmoogra with the single exception of the melting point. According to Dumas’ theory a body having carbon atoms in the series CnH2n0.2 should melt at 36*5° C. Saint Evre’s observation was as much below this point as that here recorded is above, and looking to the source whence his acid was obtained it was quite as likely to contain a minute trace of oleic acid as the cocinic acid from chaulmoogra is likely to have still held a trace of palmitic. Referring more particularly to the volatility of cocinic acid in a current of gas it will be seen in the section which describes the examination for alkaloid, that silky needles possessing all the properties of this acid were found in the distillate from chaulmoogra and water with sulphuric acid. The position of cocinic acid is between rutic or capric acid and lauric acid in the series CnH2n02. h. The magnesium acetate precipitate obtained in the last process was decomposed by hot dilute hydrochloric acid and the liberated fatty acids were washed till free from chlorides. Palmitic acid was separated from the mixture at first by dissolving in warm alcohol and cooling, but this method was altogether inadequate to its complete removal and a method of fractional precipitation was adopted; first, by the cautious addition of a concentrated aqueous solution of magnesium acetate to the simple alcoholic solution of the acid, and afterwards by similarly treating the solution when it had been made neutral by ammonia. After the separation of the fractions the alcoholic * Annales de Chimie et de Physique, troisieine serie, 1847, xx., 91. strength and solvent power of the solution was reduced by the addition of water, and on standing a small quan¬ tity of magnesium salt separated out. That the last traces of palmitic acid were thus removed was shown by the follow¬ ing treatment of the filtrate. This was decomposed by hydrochloric acid, the fatty acid removed, washed and dissolved in alcohol. To the solution water was added till feebly opalescent and then the mixture was exposed to a temperature of 6° C. for some time without any further separation. The weak alcoholic solution was gently eva¬ porated and allowed to crystallize. After repeated crys¬ tallizations a body was obtained of a feeble yellow tinge, which under the microscope shot out as it cooled into crystalline plates with a more or less deep thalloid fringe, polarizing at the margins only. The melting point was 29*5° C. Fractionated from alcohol the fractions were homogeneous, exhibiting precisely the same crystalline form and melting at exactly the same point. 0*348 of the acid burned with chromate of lead gave 0*3465 gramme of water, and 0*955 gramme of carbonic acid gas equivalent to 0*0385 gramme of hydrogen, and 0*2604 of carbon; or 11*06 per cent, of the former and 74*84 of the latter element. In a second combustion 0*381 gramme gave 0*382 gramme of water and 1*048 of carbonic acid gas ; equiva¬ lent to 11*13 per cent, of hydrogen and 75*01 of carbon. In a third combustion 1 1 *2 per cent, ©f hydrogen was obtained. The results placed side by side show as follows : — No. 1. No. 2. No. 3. Carbon . . . -74*84 75*01 Hydrogen .. 11*06 11*13 11*2 The numbers correspond to a member of the little known series CnH2n_402, and the probable formula is C14H240.2, which by calculation gives — Carbon, 75; Hydrogen, 10*7. Though additional data will be required to determine the formula I think it is certain that this body has not been previously examined and described, and accordingly, having reference to its source, I propose to name it Gynocardic acid, and trust shortly to be able to announce the correct formula. This is the acid referred to in e and /, and as already stated has a pale yellow colour and a well marked crystal¬ line form. Gynocardate of ammonium is soluble in water. The magnesium salt is insoluble in water, but dissolves in alcohol (*807) and falls out of solution on diluting. The lead and barium salts are insoluble in water, ether and cold alcohol. § 3. Dymock' s Test. Reference has been made in this paper to Dymock’s test for chaulmoogra oil. Fuller reference will be found in the paper from which I have already quoted (vide p. 251), where the opinion was expressed that the reac¬ tion on which it is based was characteristic of the oil, and taken in connection with physical characters might be used as an indicator of genuineness. In the course of investigation I have been compelled to modify this opinion, and take the present opportunity of qualifying it. As progress was made in the work of separating the proximate parts of chaulmoogra, each was subjected to the test, with the result, at first, that the colour was invariably obtained. One of the first separated quantities of palmitic acid, gave the colour in so marked a degree that certain natural substances known to contain palmitic acid as well as the pure acid itself were submitted to the test. It was thus ascertained that pure palmitic acid does not present the reaction, nor do any of the bodies experimented with, including Japan wax and butter, except palm oil. This gives a splendid green colour with sulphuric acid when applied as Dymock directs, a colour of the same character as that afforded by chaulmoogra. The green coloration is therefore not peculiar to the oil, as was supposed by Dymock, but is a property which equally belongs to palm oil. As the working processes 254 THE rHARMACETTTICAL JOURNAL AND TRANSACTIONS. [September 27, iw. improved with additional knowledge of the material, the constituents of chaulmoogra which gave the green colour, were reduced and narrowed by purification till only the last, gynocardic acid, remained. It still remains. It has not been found possible by any means to deprive gyno¬ cardic acid of this colour-giving power. A quantity of it has been dissolved in alcohol and crystallized from it in successive small portions — each fraction has given the colour with equal intensity. It has been digested with animal charcoal, and after such treatment the colour has been verdant as before ; it is inherent and a characteristic. Gynocardic acid also produces the acrid burning taste which is noticed when chaulmoogra is swallowed, and altogether appears to be a constituent of such importance as to deserve further attention, not only from a chemical point of view, but also in regard to its medicinal activity. § 4. Constituents Separated and Recognized. Chaulmoogra oil then, so far as it is at present known, contains : — Gynocardic Acid . 11*7 Palmitic Acid . 63 ’0 Hypogseic Acid . 4* Cocinic Acid . 2*3 in combination with glyceryl as fats, and the two former in the free state as well. No attempt was made to determine accurately the proportion of each acid present, as the loss in purifying was necessarily considerable, but the figures against each represent fairly well the quantity of acid in 100 parts of oil. The President said this paper was a very exhaustive and admirable one, and the members of the Conference owed their thanks not only to the writer, but to Mr. Naylor, whose clear and comprehensive condensation of its contents had placed the subject so lucidly before the Conference. Mr. A. H. Mason said as some of the members present might be unacquainted with this oil, it would be well if information were given as to its origin and supposed properties. Mr. Naylor said the oil was obtained from a plant known as the Gynocardia odorata, and had been used very successfully in cutaneous diseases. It was an oil much used in India, and had been sold in the bazaars there for a great number of years. It had also been used with considerable success in this country in cases of phthisis, but had not been previously studied chemically, except by Dr. Dymock. Mr. Willmott quoted a case in which it was found that the medical properties of chaulmoogra oil were not so great as those of gurjun oil. Mr. Baxter spoke of chaulmoogra oil as a cure for itch and mange in dogs. Mr. Greenish said that the green coloration produced by a drop of sulphuric acid brought into contact with the chaulmoogra oil, being considered by Dymock a test of the genuine oil, he would like to know from Mr. Naylor if he had tried it on oil extracted, for instance, by benzine, to ascertain if the coloration proceeded from the oil or from some organic matter which may have been pressed out into the oil. Mr. Naylor, in reply, said chaulmoogra oil had been used for a variety of purposes, but it was never intended to be a panacea, and in some cases it had not been so successful as others. He had known it to be largely used in mange in dogs, and he had not heard of a case in which it had failed. With reference to the green colour pro¬ duced with sulphuric acid, whatever solvent might be used, providing gynocardic acid was present, the fat from the solution would give a green colour. That test had been applied to the oil which had been extracted with benzol and oil obtained by pressure. The next paper, which was read by Professor Attfield, the author not being present, was entitled — The Capacity op Different Organs to Absorb and Retain Arsenic in Cases of Chronic Poisoning. BY N. P. HAMBERG, M.D., H.M.P.S. This paper called forth some adverse criticism, on the ground that the subject was foreign to pharmacy ; and, as it did not contain anything which had not previously been established, its publication does not appear desirable. The last paper read was — Note on the Estimation of Morphine in Turkey Opium. BY PROFESSOR FLUCKIGER. The estimation of morphine is the subject of many valuable papers which have been published in the various pharmaceutical periodicals. Numerous and elaborate as they are, these investigations have not, as far as I can see, arrived at a thoroughly satisfactory result. Without further discussing in this place the merits of these methods, I beg to submit to the Conference another process, of the utmost simplicity, yet of sufficient accu¬ racy. How far this accuracy is attained by the method I now recommend remains for the profession at large to decide. It must be remembered that it is exclusively intended for the assay of official, i.e ., Turkey, opium. Valuable as may be the drug produced in other countries with regard to the industrial extraction of alkaloids, no modern pharmacopoeia has ever admitted any other kind of opium than that of Asia Minor. My method will possibly prove less satisfactory if applied to Indian or Persian opium, although in my opinion, for a fair standard opium, it is a good and elegant process. It is as follows : — Take of powdered opium 8 grammes ( = 123*5 grains), cold water 80 grammes ; shake the mixture frequently ; filter after twelve hours. The filter should have a dia¬ meter of five inches. The operation will afford on an average 65 to 70 grammes of clear liquid. No washing is to take place. 42 *5 grammes of the liquid are col¬ lected in a little phial, the weight of which should have been marked on it. Then add to the solution 12 grammes of alcohol (sp. gr. 0*812-0*815), 10 grammes of ether and 1*5 gramme ammonia water of 0*960 sp. gr. The mixture after shaking will remain clear and allow a colourless layer of ether to make its ap¬ pearance. The phial is corked and allowed to stay without further shaking it. After an hour or two, crystals of morphine begin to be formed, mostly at the border of the two layers. By and by they sink down to the bottom, and after a day or two the whole amount of whitish or white crystals of the alka¬ loid will be deposited. They are then to be collected by using two folded filters having a diameter of four inches. The phial is rinsed out with a mixture of 6 grammes of alcohol and 5 grammes of ether, and lastly with 10 grammes of ether, (these liquids being gradually poured on to the crystals in order to wash them. The funnel in the meantime is carefully covered. The crystals are subsequently cautiously pressed between the folds of the two filters, which will almost completely absorb the mother liquor which the crystals of morphine may still retain. It will now be easy to remove the alkaloid very neatly from the filter ; it must be weighed in the very phial in which some crystals may have remained obstinately attached to the walls. The phial lastly dried at 100° C. then contains the whole amount of morphine precipitated, that is to say its hydrate, viz., Cl7H19N03 + 0H2. As to the mother liquor, it is to be observed for a day more in another corked phial ; it does not usually afford a further crop of crystals. Yet in an open vessel amor¬ phous matters are soon deposited. A good Turkey opium being under examination will thus afford about 0*40 to 0*48 gramme of morphine, which September 27, 1679 ] THE PHARMACEUTICAL JOURNAL ANL TRANSACTIONS. 255 are to be considered as deriving from half the weight of the sample, i.e., from 4 grammes opium ; the percentage would then be 10 to 12. The alkaloid must next be identified by resorting to the usual tests for morphine. Among them there is the official nitrate of bismuth, which I have pointed out some time ago* * as one of the most characteristic tests for that alkaloid. If morphine is rubbed with con¬ centrated sulphuric acid the liquid turns dark brown or black as soon as a little nitrate of bismuth is strewn on it. An excess of nitric acid present in the official nitrate of bismuth would at first produce rather a red hue. Lastly, there is also to be ascertained the purity of the crystals. To this effect take 1 decigramme of the mor¬ phine and dissolve it in 10 grammes of lime-water. If the lime-water is duly saturated, in the cold, the quantity mentioned will be a little more than sufficient. The morphine will then prove to leave a very trifling amount of colouring matter, quite insufficient to influence appre¬ ciably the percentage of the alkaloid. Should narcotine be present it would remain undissolved, and might be weighed if the whole quantity of morphine be treated with lime-water. But it would, in such a case, be much more advisable to get rid of the narcotine by repeating the experiment with another sample of opium. I would recommend then, as I have already urged in the ‘ Pharma- cographia,’ page 59, to dry the opium previously and to deprive it of narcotine by exhausting it with boiling ether. It must be borne in mind that we have to do now with perfectly dry opium, whereas in the beginning we started with air dry opium, the latter containing, possibly, as much as 7 or 8 per cent, of water. If to the solution of morphine in lime-water a little chlorine water is added, a remarkable reaction is dis¬ played : the mixture assumes a permanent bright red hue, which is highly characteristic ; this is, in fact, an excellent new test for morphine. The assay as just described somewhat minutely is of the utmost practical simplicity; it must be granted that it claims no special rapidity, but it is by no means longer than any other process hitherto devised for the same purpose. A few explanatory remarks must be still added. As a solvent for opium, cold water is by far the best, for the simple reason that it affords immediately a liquid ready for the precipitation of the alkaloid. It is true that the drug yields a less coloured solution by using alcohol, but this would require a distillation. If opium is to be exhausted by means of water it is extremely difficult to point out how far the extraction must be carried on. Cold water on an average dissolves about 60 per cent, of standard Turkey opium if it is absolutely exhausted. By treating 8 grammes of opium with 80 grammes of water we should consequently obtain very nearly 85 grammes of solution. As it is practically almost impossible to get really as much as this, it will be safer to use just half the amount of the calculated liquid, namely, 42*5 grammes. The analyst who does not feel satisfied with this average number may ascertain exactly the amount of soluble constituents which his sample of the drug is able to yield ; he may then act accordingly. I believe the morphine to be present in the opium as a sulphate, at least for the most part. This is evidenced by the fact that the alcoholic solution of opium is found to contain both the alkaloid and sulphuric acid. In the aqueous solution inorganic sulphates are also present chiefly sulphate of calcium, but in alcohol of all the sul¬ phates only that of morphine (or other alkaloids) can be in solution. The sulphuric acid met with in the alcoholic solution of opium must therefore be due to sulphates of alkaloids. The solutions of opium display a slightly, yet undoubtedly acid reaction as the vegetable juices — - - - - - - * See my ‘Pharmaceutical Chemistry/ Berlin, 1879, page 373. generally do. The acidity of opium becomes more distinctly manifest if its solutions are cautiously con¬ centrated ; it is no doubt due to meconic acid. It is important to precipitate the morphine from a solution containing alcohol and ether. By adding am¬ monia to an aqueous solution, a flocculent matter is precipitated. This abundant amorphous mass, either an alkaloid or not, — it is certainly far from being simply morphine, — remains in solution if the liquid contains a little alcohol ; one-third alcohol of the volume of the aqueous filtrate is quite sufficient for the purpose. Yet of no less importance is the action of the ether. It not only prevents the narcotine from being thrown down together with the morphine, but ether greatly promotes the formation of distinct and pure crystals of morphine. This alkaloid evidently separates very readily from a liquid saturated with ether. No further mention is made in the above considerations of narcotine. Should its amount also be estimated in the official drug ? I think not. The action assigned to narcotine by the physiological experiments appears to be not considerable at all. Should it, however, become desirable to estimate it, it would probably be a good plan to extract the opium first by water and then by acetic acid. The narcotine is present chiefly in the free state, as it is not really an alkaloid ; it is therefore not, or not entirely, removed by water. With acetic acid, as well as with other acids, narcotine forms not well defined salts ; the acids are simply solvents, from which it again separates as soon as the acid is neutralized. This is accomplished with carbonate of calcium. By shaking an acetic solution of narcotine and morphine with that car¬ bonate, narcotine is precipitated ; not so the morphine. I have not, however, more exactly investigated this method, practical pharmacy, to which the present paper is devoted, being not strictly interested in the matter. I believe that the above method for the estimation of morphine very well answers for pharmaceutical purposes. I shall be glad if the criticisms which it may meet with lead to some further progress in the question under notice. Mr. Draper passed a warm eulogium on the paper which he said was characterized by great lucidity. Mr. Naylor said it was not his experience that mor¬ phia existed in the form of sulphate of morphia, unless the paper referred to the Turkey opium. If morphia was dialysed the sulphate of morphia would undergo no decomposition whatever. If it was carefully examined by the microscope the sulphate of morphia could be readily seen, and so also could the crystals of the meconate of morphia if it was evaporated at a low heat. If meconate of morphia was heated at a high temperature it would split up. His objection to the process was that no very special provision in the process — as part of the process — was made for separating narcotine. The process to which they had just listened was identical with the beautiful pro¬ cess of Yvon published in the Journal de Pharmacie et de Chimie, only if his memory served him correctly the pro¬ portions of spirit and ether were a little different. Mr. Williams viewed it as a slow process compared with others. Professor Attfield admitted that it was a slow pro¬ cess, but easy. The President said Professor Fliickiger deserved their thanks for his paper, and the Conference accorded him that compliment. Place of Meeting in 1880. Mr. N. M. Grose (Swansea), introduced by the Presi¬ dent, said he was deputed by the druggists of Swansea to convey to the British Pharmaceutical Conference a hearty invitation to visit the town in 1880, and if the association did them the honour to accept the invitation they would do all in their power to render their sojourn in Swansea agreeable. 256 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. (September 27, 1879 Professor Attfield moved that the best thanks of the meeting be accorded to the chemists of Swansea, so ably- represented by Mr. Grose, and that their invitation be accepted. . . Mr. Reynolds seconded the motion and, adverting to the admirable way in which Sheffield had received the pharmacists, said Yorkshire felt proud of Sheffield for the way in which it had entertained the Conference. The motion was then carried. Election of Officers. A ballot for the President and Officers for the ensuing year was then taken, with the following result : • President. W. Southall, F.L.S., Birmingham. Vice-Presidents. N. M. Grose, Swansea. R. Reynolds, F.C.S., Leeds. G. W. Sandford, Pres. Ph. Soc. of G. B., London. W. Ward, E.C.S., Sheffield. Treasurer. C. Ekin, F.C.S., Bath. General Secretaries. Professor Attfield, F.C.S., London. F. Baden Benger, F.C.S., Manchester. Local Secretary. J. Hughes, Swansea. Other Members of Executive Committee. M. Carteighe, F.C.S., London. T. Greenish, F.C.S., London. H. W. Maleham, Sheffield. A. H. Mason, F.C.S., Liverpool. C. Symes, Ph.D., Liverpool. J. C. Thresh, F.C.S., Buxton. W. A. Tilden, D.Sc., F.C.S., Clifton. C. Umney, F.C.S., London. J. T. Williams, Swansea. Auditors. G. Ellinor, Sheffield. J. Lloyd, Swansea. Thanks to the Local Committee, etc. Mr. Williams moved — “That the cordial thanks of the non-resident mem¬ bers of the British Pharmaceutical Conference be given to the Local Committee, and the other Sheffield members, and especially to Mr. Maleham, Mr. Ward, Mr. Ellinor, Mr. Learoyd and Mr. Cub- ley for the very successful manner in which they had conducted the arrangements of the meeting.” He said Mr. Reynolds had stated that Yorkshire felt proud of Sheffield for the way in which it had entertained the Conference, and if Sheffield had satisfied Yorkshire he felt that the rest of the country must be satisfied. Mr. Draper seconded the motion and referred to their cordial reception and the pains the Local Committee had taken in showing the pharmacists the various manufac¬ tories for which the town was famous. The motion was carried unanimously. Mr. Ward, in acknowledging the compliment, said it had afforded him extreme pleasure to see the Conference in Sheffield, but he must in justice say that nearly the whole of the work had devolved upon Mr. Maleham. If the as¬ sociation were gratified the Local Committee were satis¬ fied, and if they were gratified the Local Committee were satisfied. Mr. Maleham said he was glad to have an opportunity of expressing his gratification at the kind manner in which the services of the Local Committee had been acknow¬ ledged by their guests. He deprecated the idea that he had done all the work, and said he had been ably sup¬ ported by the Local Committee and Mr. Learoyd, the assistant secretary. Mr. Learoyd and Mr. Ellinor also acknowledged the compliment on behalf of the Local Committee. Professor Tichborne moved the following resolu¬ tion : — “That the members of the British Pharmaceutical Conference, assembled in Sheffield, desire to express their best thanks to Messrs. John Brown and Co., Limited, and Messrs. Brown, Bayley and Dixon, for having thrown open their most interesting works, and also to the managers of departments and others whose courtesy and attention so enhanced the plea¬ sure of the visit.” Mr. T. E. Abraham seconded the motion, which was carried. Mr. Foster moved the following resolution : — “That the best thanks of the Conference be conveyed to Messrs. John Round and Son, Messrs Joseph Rodgers and Son, and Messrs. Walker and Hall, who have so kindly afforded members the privilege of visiting their works.” Mr. Walter Hills seconded the motion, which was carried. Thanks to the President. Mr. Sumner moved — “ That the best thanks of the Conference be given to the President for the able manner in wkich he has conducted the business of the meeting.'” He said he was delighted at the ability shown by the young members of the Conference, and that their papers showed that they were making progress beyond their predecessors. He did not see why such should not be the case, for they should live on the experience of the past, and the practice of the present. Mr. Radley, as the senior member of the trade in Sheffield, seconded the resolution, and referred to the efforts of the President in the promotion of pharmacy. The motion was carried with acclamation. The President, in acknowledging the compliment, said he was afraid his friends sadly overrated his efforts as President. It must not be forgotten that he followed a long list of distinguished men, from whose example he had had large opportunities for learning his duties; moreover the kind consideration he had received from every individual who had attended the meeting had rendered his task so easy that his own share of the merit of having presided with some success was very small indeed. He confessed to some feeling of regret at relinquishing his highly honourable post, but had the satisfaction of knowing that it would pass into the hands of a very able man, one whose scientific qualifications would certainly very much exalt its dignity. The Resignation of Professor Attfield. The President said although the positive proceedings of the Conference had now concluded, there was just one matter he should like to introduce to their notice. The opinion had been expressed in the Executive Committee at its sitting that afternoon, that the members of the Conference generally would probably wish that some permanent record of their obligation to Professor Attfield should be presented to him, now that he found it neces¬ sary to resign the post of Honorary Secretary. The Committee had accordingly prepared a resolution, which would now be submitted for the approval of those pre¬ sent. “ 1. That under the circumstance of Dr. Attfield’s announced retirement from the post he now occupies, it is desirable to institute some permanent recogni- September 27, 1879 ] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 257 tion of the invaluable services to the Conference rendered by Professor Attfield as its Senior General Honorary Secretary since its establishment sixteen years ago. “ 2. That the gentlemen present form themselves into a Provisional Committee to give effect to this resolu¬ tion, with power to add to their number. “ 3. That Mr. Carteighe be appointed Honorary Secre¬ tary pro tern, to the above Committee.” The Conference then broke up. Iparliamcntarg and Uaa |3rocmtiitgs. Prosecution for Sale of Adulterated Cream of Tartar. At the Chertsey Petty Sessions on Wednesday, Sep¬ tember 24, before W. C. Scott, Esq., chairman, B. L. Lewis, Esq., W. F. Harrison, Esq., Baron G. de Worms, H. Yool, Esq., and T. W. Weeding, Esq., Mr. George Boyce was summoned for selling to one Frank Walters a certain drug, to wit, 2 ounces of cream of tartar, to his prejudice, on the 19 th of August. Mr. A. Haynes appeared for the defendant. Police-constable Waters said: On the 19th of August h»e went to Mr. Boyce’s shop under instructions from Superintendent Bungard and asked for 2 ounces of cream of tartar and was served by Mr. Clark, the assistant. He paid 4 cl. for it. After receiving the cream of tartar he told the assistant it would be handed over to Super¬ intendent Bungard, who would take it next day to Guy’s Hospital to be analysed. Witness asked him if he would like to keep a portion of it. The assistant said that he did not wish to do so. Witness then sealed it up in his presence and twenty minutes later handed it over to Superintendent Bungard. Cross-examined by Mr. Haynes : He bought some quinine wine and other articles at the same time that he purchased the cream of tartar. He asked the assistant to take a portion of each of the articles that he purchased, but the assistant declined. Superintendent Bungard said: On the 19th of August he received 2 ounces of cream of tartar from last witness and on the 21st took it to Guy’s Hospital. He produced Dr. Stevenson’s certificate, which stated the cream of tartar to contain 11*7 of tartrate of lime and *6 of sul¬ phate of baryta, and that the foreign ingredients were insoluble and not injurious to health. Cross-examinined by Mr. Haynes : The other articles purchased were sent to the analyst and reported to be genuine. This wras the case for the prosecution. Mr. Haynes then addressed the Bench. He said that for the last sixty years Mr. Boyce and his father before him had been chemists in the town, and always had the very highest character for selling the best and choicest articles, and never before had they had the least word of complaint. The charge that he had to answer that day was that Mr. Boyce sold an article that was not of the required quality. He could only have wished that Dr. Stevenson had been present, because he could then have asked him questions that would have put a proper com¬ plexion on the case. However, he had practical and scientific witnesses present who would inform the Bench as to the manufacture of cream of tartar, and it would be shown that *no adulteration in the sense of the word had taken place, and moreover Dr. Stevenson’s certificate showed that it was not injurious to health, and was, therefore, not prejudicial to the purchaser. Cream of tartar was manufactured in France and Spain and other wine-growing countries, and he could prove that it could not possibly be made without tartrate of lime, as through the processes it underwent such was incidental to its manufacture, and was, in fact, part and parcel of the drug. Mr. Hodgkinson, of whom the articles were pur¬ chased, would produce some cream of tartar in its crude state and inform them how it was manufactured. He would also tell them that Mr. Boyce always bought drugs of the very best quality and paid the very best price for them, and, in fact, such evidence would be given as he. thought would completely exonerate his client. He then called — Mr. William Hodgkinson, of the firm of Hodgkinson. and Co., Aldersgate Sti-eet, who said that defendant and his father before him had been customers of his firm for many years. Mr. Boyce was very particular, and was always supplied with the very best drugs. The cream of tartar which was the subject of the present case he had reasons to know came from Messrs. Hodgkinson’s stores. Cream of tartar was sent to this country from Spain and France and came in a state that was known as argol, and was consigned from the brokers to the manufacturers. The argol was generally taken from the docks by the= grinders. The cream of tartar in question came into the market in the usual way and was ground by Messrs, Stafford, Allen and Sons, who returned it to his firm and they sent it out as it w*as purchased. Messrs. Allen and Sons were the only grinders of the drug. The article sent to Mr. Boyce was the very finest that could be obtained. Argol, or cream of tartar, was the natural product of the fermentation of the juice of the grapes. It was impossible to have cream of tartar without tartrate of lime, and he was informed from the best authority that it was generally found in quantities of from 10 to 20 per cent., and the lowest he ever heard of was 7 per cent. He recognized the sample of cream of tartar produced from its very fine grinding. It could not be obtained finer. He could not account for the very small amount of baryta being with the drug, but had seen it with cream of tartar before. Mr Edward llansome Allen, of City Road, London, said his firm received a delivery order to obtain the cream of tartar in its crude state. It w*as then ground and sent to Messrs. Hodgkinson, and nothing was added to it. Mr. George Boyce said he purchased the drug of Messrs. Hodgkinson and sold it as he received it. He believed it was the best quality that he could possibly buy. Dr. Benjamin Horatio Paul, I’h.D., F.C.S., and Editor of the Pharmaceutical Journal, said the term “ cream of tartar ” was, according to the British Pharmacopoeia, a. synonym for acid tartrate of potash. The article referred to was the medicinal form of acid tartrate of potash and that met with in commerce. It consisted essentially of the compound of tartaric acid with potash, together with some varying proportion of tartrate of lime, which was inci¬ dental to the manufacture of cream of tartar in the usual way. The presence of tartrate of lime in cream of tartai* Avas indicated by the British Pharmacopoeia. Sulphate of baryta was an extraneous impurity, but it was scarcely conceivable that so small a proportion as that indicated by the analyst’s certificate could have been intentionally added as an adulteration. The only other possible expla¬ nation of its presence was accidental admixture; but it was an inert substance not injurious to health, and the trifling amount present did not sensibly affect the medi¬ cinal efficacy of the cream of tartar or its intrinsic value. The Chairman said the Bench were unanimous in dismissing the case. Death from Opium Eating. On Tuesday, September 23, Mr. D. Wightman held an inquest in Sheffield, on the body of Sydney Barnes, 50 years of age, painter. The evidence was to the effect that for the last two years the deceased had suffered from ‘‘painter’s cholic,” and in consequence had lost the use of one of his arms. Some time last week he fell from the top of a vine house at Sharrow, and broke his ribs. A 258 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [September 27, 1879. year or two ago he was in the habit of taking quantities of opium, but he had not done so latterly as far as his wife knew. On Saturday night he went to Mr. Ward's shop, on Sheffield Moor, and bought two separate penny¬ worths of opium, stating that he wanted the drug to relieve the pains in his side, caused by broken ribs. He returned home, and shortly after dinner on the following day he took the opium, except a small quantity, which his wife destroyed. In the evening he went to bed and slept soundly until Monday morning, after which time he remained in a drowsy state up to his death. On Sunday lie told his wife he intended to go to the Hospital next day to see what was amiss with his side. It was explained that the deceased had taken about one scruple and a half of opium, equal to 720 drops of ordinary laudanum. Mr. F. A. Willington, surgeon, said he saw the deceased for the first time shortly before three o’clock on Monday afternoon. He was then insensible, and evidently dying. He applied the usual remedies, but death ensued, caused by an overdose of opium. The Coroner remarked that the man, in his opinion, had died from an overdose of opium. It had transpired that he had been in the habit of taking it regularly on previous occasions, and all the symptoms explained by the surgeon indicated poisoning by opium. The deceased had taken much more opium than a surgeon would have advised him to take. The quantity was sufficient to have poisoned all the persons in the room. The jury returned a verdict of “Death from taking an overdose of opium for the purpose of relieving pain, brought on by a recent accident.” — Sheffield Daily Times. Hftemottawta. In order to assist as much as possible our younger brethren, for whose sake partly this column was established, considerable latitude is allowed, according to promise, in the propounding of supposed difficulties. But the right will be exercised of excluding too trivial questions, or re¬ petitions of those that have been previously discussed in principle. And we would suggest that those who meet w'ith difficulties should before sending them search previous numbers of the Journal to see if they can obtain the re¬ quired information. [339]. I think “Minor” ought to use Acid. Nitric. Dil. [340]. In answer to “Inquirer’s ” note, I have used at times a little glycerine to rub down the sulph. iodid. when making ung. sulph. iodid. ; by this means he will produce an ointment slightly lighter in appearance, but a much more satisfactory preparation. Thomas E. Chadwick. [341]. Calx Hydrarg. Alba is white precipitate. Manchester. W. Wilkinson. [341]. Calx Hydrargyri Alba was the term by which the present Hydrargyrum Ammoniatum was known in the old London Pharmacopoeia (1788), and therefore Ung. Hyd. Ammon., B.P., should have been dispensed. W. F. Norman. [341]. Unguentum Calcis Hydrargyri Albse, vel Un- guentum Hydrargyri Ammonio-Chloridi (Pharmacopoeia Londiniensis, 1788) : — Take of — Ammonio-Chloride of Mercury . . 2 drachms . Lard . 3 ounces. Add the ammonio-chloride of mercury to the lard, and rub them together. Norwich. W. S. Corder. [3421 The official Ung. Plumbi Subacet. Co., in¬ variably assumes a streaked orange colour soon after it is made, but it rapidly becomes rancid and the colour dis¬ appears. The orange tint is probably due to the separation of an oxide of lead and the disappearance of the colour to decomposition of the oxide by the fatty acids present in the rancid ointment. Neither coloration nor rancidity appears if vaseline be substituted for the oil and wax, which alteration will possibly be made in the formula when we have a new Pharmacopoeia. R. II. Parker. [342]. I should be glad if some reader would reply to the query of “An Apprentice ” in the Journal of Sep. 6, with regard to ung. plumbi subacet. co. I made a little and found it turned the pale orange colour he describes, and attributed it to the fact that the liq. plumbi was an imperfect solvent, it having deposited a good deal of plumbi carb. in the bottle, and the camphor acting upon it turned the oxyacetate into litharge again, and hence the colour. Again I made some with a perfectly fresh solution and, as “ An Apprentice ” says, followed the instructions implicitly, and I find after four or five days that has turned the same. I cannot find any allusion to the cause in any work that I have referred to. And as it is an ointment not unfrequently ordered in prescriptions, it is of great importance that it should be sent out so that the patient should not be surprised to find an orange coloured oint¬ ment after a few days. Alchemist. [343]. R Acet. Scilla . ^iss. Spt. Chloroformi . q.s. Sacc. Ust . q.s. Aqua . ad §ij. A teaspoonful every two or three hours. How should the above be dispensed ? Was I right in putting in 3ss spt. chlorof., and 6 minims sac. ust. ? [344]. Will a reader of the Journal say how he would dispense, or of what strength he would make the following solution? — Solutio Cheltenham Salts. 1 Tinct. Zingib. . . 3*1 f §xij • Tinct. Card. Co . 3*1 ) A wineglassful every third morning in half a tumbler¬ ful of warm water. Dispenser. gtoks anti Queries. [624]. COLOUR OF CLOTH.— Pure nitric acid is used to test the durability of the colour in cloth. The test depends on the length of time it takes to destroy the colouring matter. W. Fowler. [625]. ANILINE COPYING INK.— Could any reader oblige me with a formula for making copying ink (aniline) for the gelatine letter press? By so doing he would greatly oblige. Qilero. [626]. CLEANSING OF OLD COINS.— Will any reader of the J ournal kindly furnish me with a formula of a solution for cleansing old coins by simply immersing them? Thos. F. Elton. September 27, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 259 Registration of Chemists’ Assistants as bona fide Dentists. Sir, — Having read four letters in reply to mine, I can see but one, F. W. S., who sees the question as regards the regis¬ tration of assistants in the right light. The legislators of the Dental Act were perfectly willing to recognize existing rights, but not to bring to life rights that had never existed at all, or to induce any person to register himself as a matter of convenience with the view of taking up dentistry at some future time and thus save himself the necessary education and examination. Nothing was said about preventing chemists or their assistants from extracting teeth (which is the least important part of a dentist’s business), and it was not necessary to register in order to continue to do so, and to say the least it is contrary to the laws of common morality for a person not a dentist to register as being in bona fide practice as such. “ Lower Molar” says he wrote to Mr. Miller asking if it was necessary to register as a dentist in order to extract teeth, and that he received the declaration papers in reply, etc., etc. I must call his atten¬ tion to the fact that it is not the duty of the registrar to answer inquires or to determine who is legally entitled to register, and that everyone is allowed to fill up the papers a3 his conscience will allow him, and that on payment of the fee his name is placed on the register conditionally, i.e. that his claim will bear investigation. Of course on the publication of the register the Dental Association will take up the matter of illegal registrations, or why should section xxxv. be inserted at all ? If bond fide chemists and dentists, or even chemists who without assuming the title of dentist merely performed the operation of extraction, have registered as being in bond fide practice as dentists, it must surely be allowed that that does not constitute a right for their apprentices and assistants to do the same ; the Act was for the protection of the public, and not to raise up an army of ignorant impostors who have sprung into life as dental practitioners during the passing of the Act, to the detri¬ ment of the public and degradation of the legitimate pro¬ fession. “Manager” must have a very poor idea of dental operations when he asserts that they can be performed as ably by dabblers in the art as by any professional dentist who has devoted all hi3 attention to the sp6cialite. I should like to to see very much the chemist’s assistant who could put in really reliable gold and amalgam fillings, fill root canals, cap exposed pulps, etc. The old proverb that a “ Jack of all trades is generally master of none” is very applicable to the above, and a Ph. C., dental surgeon, etc., must have as many irons in the fire as he can keep warm. J. J. Musgrave. Sir,— The writers of the letters relating to the Dental Practitioners Bill in your last issue appear to have all taken up arms rather hastily against Mr. Musgrave. “Lower Molar” certainly may be in the right in con¬ sidering himself a dentist from the mere fact of extracting teeth, but the question is still an open one as to whether when the weeding out of the Dental Register takes place those whose only claim towards registering themselves con¬ sists in the fact of their extracting teeth will be considered dentists by the Medical Council, should information be made against them. The declaration may be made, the fee may be received, but the whole responsibility of such declaration rests upon the person who makes it. Evidently clause xxxv. wras inserted from a certain foresight pos¬ sessed by promoters of the Bill. The spirit of the law will be frustrated perhaps by many ; anyhow, Mr. Musgrave gives a friendly warning, to the effect that should the spirit of the Act, which the words bond fide convey, be carried out, many who are now on the register may possibly find their names erased in future (even if not in the present) edition of the Dental Register, Holders of the certificate must remember that the register alone will be legal evidence. The spirit of the Act appears to have been to protect those men who before its passing had been bond fide engaged as dentists, and had called themselves such before the public. My only object in writing is to uphold Mr. Musgrave’s action in writing his letter, and to suggest that those who took up arms against him should wait until they see whether there were any cause for so doing. Mr. Musgrave’s opponents appear to have spoken with the dictum of both judge and jury in the matter, so they have hardly a right to be so harsh on him, who as they say, holds simply a brief. After all the only thing to be done is to wait and see. It is said that “the wicked fleeth when no man pursueth.” George Ernest Clarke, Surgeon-Dentist. Woodbridge. The Health of the Drug Trade. Sir, — Mr. J. K. Nicol, in the Journal of 'the 6th’ inst., calls attention to the circumstance that a large percentage of chemists die at a very early age, and speculates as to the cause. To satisfy myself that the average age was less than it ought to be, 1 have gone over the Journal obituaries for three years, 18/5-6, 1876-7, 1877-8, and I find that the average is fifty. This is certainly not very encouraging for the rising race of pharmacists. And now, what are the causes of this early mortality ?' It seems to me that there are three things to be taken into consideration in accounting for it. These are : — (1) Con¬ finement, on account of the length of business hours. (2) The strain upon the mind which is inseparable from the proper conduct of a chemist’s business. (3) The highly polluted atmosphere of the shops. A chemist’s business is, I should say, the most confining business under the sun. In a small business, where the proprietor cannot afford to keep an assistant regularly, he is frequently several weeks at a time without being away from liis shop. People do not always expect to find a physician or surgeon at home, but they never for a moment entertain the idea of not finding a chemist ready at any time to answer his bell, and supply sixpennyworth of physic. And take the case of assistants. In England, where the situations are indoor, an assistant’s life partakes very much of the nature of that of a domestic servant ; perhaps two hours twice a week, at night, are allowed for recreation. In Scotland the situations are outdoor, and most of the places close at 8 p.m., and as few of the shops have night bells — perhaps one in each district of the town — the greater number of the assistants are free every night after that hour. This would seem better. In reality it is not so. In order, I suppose, that the outdoor assistants should have no advantage over their indoor fellows in their chance of longevity, it is generally the case that they have to get their tea after 8 o’clock. In a few humane places arrange¬ ments exist for the assistants either to get out for half an hour to tea, or to have it on the premises. These places, however, are very few. It is needless for me to do more than refer to the injurious effects upon the health of so long a fast between dinner and tea, and the taking of tea at so late an hour. In English situations the hours are longer, but meals are had regularly. In Scotch situations the hours are shorter, but meals are had irregularly. Which is the better ? To my mind there is little to choose in either. The practice of pharmacy requires great care and atten¬ tion. The strain upon the mental faculties of those engaged in a busy shop is consequently very great, and when continued during such a length of time must of neces¬ sity be exhausting. There are other businesses in which a concentration of attention, equal to that in ours, is required; but I am not aware of any in which it has to be kept up for the same length of time. And, finally, there is the polluted atmosphere. Chemists do not feel the smell of their shops, because they have become accustomed to it. There are few, however, of their customers who do not feel what they call the ‘ ‘ physicky ” smell always present. Hydrochloric acid vapour, free chlorine, fumes of nitric and sulphurous acids, ammonia, and carbonic acid gas, not to sjjeak of an occasional wliiff of bromine, make a nice addition to the already not over pure air of a town. To be confined for twelve hours a day in a compound atmosphere of this kind can scarcely be con¬ ducive to good health. People say w*e cannot readily catch infection, because the germs of contagious diseases find the atmosphere of our shops fatal to them. This may be true, but to escape contagion only to share the fate of the germs is not much for which to be thankful. It is time that attention should be directed to the un¬ healthy nature of our business, apart from long hours. 260 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [ September 27, 13:9. Instead of having long hours we ought to have exceptionally short ones. No doubt the claims of the public must be attended to. I do not, however, think that the public, exacting though it be, desires that the members of one class should sacrifice their lives to save those of the members of another class. A free discussion of the subject may initiate a disposition on the part of employers to favour shorter hours of business, or, at least, the concession of more time for inhaling fresh air to their assistants. I am strongly of opinion that a reduction in the hours of business would be a very effectual means of raising the standard of the drug trade. The pre¬ sent hours are in their effects very demoralizing. Edinburgh. Junius. Sir, — Like your correspondent, Mr. Nicol, the undue mortality in our trade has been matter for reflection with me for years. I commenced at one time tabulating the deaths recorded in your own and other journals, with the view of instituting a comparison with the average general mortality, but finding that the ages were frequently omitted, I gave up the attempt. Speaking from an experience of twenty years, I do not for one moment think that (special manufactures apart) there is anything in the atmosphere of the ordinary chemist’s shop prejudicial to health. The cause is to be found almost solely in our own individual habits. In a business full of constant anxieties, we volun¬ tarily keep too long hours — we voluntarily allow ourselves too little outdoor recreation. If our aim is merely through this business to obtain a social competency, it is yet highly necessary, but if passing beyond this, we are also striving for mental cultivation, it is yet more imperative that Ave allow nothing to defraud us of our chances of re-oxygenation. We voluntarily keep too long hours — voluntarily I ad¬ visedly said — we are not bound to keep our shutters down until the last possible customer has appeared. If medicine is really wanted there is not much fear of patients dying for lack of ringing the druggist’s bell, while with the shop open unnecessarily late, for one application that is really pressing there may be dozens of the most trivial character. From the nature of our calling the public justly expect us to cheerfully attend to their true wants at whatever hours they may arise; but for that very reason they should be considerate of us in not infringing upon our ordinary leisure times unnecessarily. The public require educating in this respect. It would be the dawn of a new era with us were we to arrive at a general understanding to adopt hours akin to those in other callings, and to levy a mild percentage upon all business effected after the shop was closed. Let each pharmacist thus arrange for himself, and for those in his employ, some respite for breathing time, and we shall soon hear less of undue mortality in our ranks. One of the greatest obstacles, often, to improvement in this direction is, singularly enough, the solitary chemist, — he who has neither assistant nor apprentice. His neighbours are all willing to close, but “ Why should I shut up?” argues he. “I shall have no peace, the bell will ring, and I may as well be in my shop as in my back room.” Such a one should remember that none of us liveth to himself, that although he may not feel himself at liberty to leave his premises, he should surely hesitate before in effect compelling everyone else in the trade in the town also to remain at home. Now that there is such a call for educated pharmacists, it is more than ever necessary that for the production of the mens sana in corpora sano the requisite leisure should be afforded. Cambridge. J. T. Sir, — The letters of your correspondents on the health of the drug trade would have been of more value if they had supplied authentic figures, either from the Registrar- General’s report, or other sources, from which the longevity in our trade might have been compared with that in others. No opinion on such a subject can be worth anything unless it is based upon deductions drawn from correct statistics. Such statistics I am unable to supply, but the following figures, taken from obituaries printed in the Pharmaceutical Journal during the years 1377, 1878, and 1879, may interest your readers: — Two hundred deaths gave an average length of life of 51'8 years. Four lives exceeded eighty, and were eighty, one, eighty-three, eighty-six, and eighty-seven respectively. The shortest life recorded was twenty-one years. A percentage gave the following results : — 18* 99 thirty and forty. 195 „ 99 forty and fifty. 19'5 „ 99 fifty and sixty. 225 „ 99 sixty and seventy. 11*5 „ 99 seventy and eighty. 2* 99 eighty and ninety. My obituaries were all exhausted, or I should have extended these figures, and so made the statistics reliable. It should be mentioned that nearly all the deaths were of chemists in business for themselves. Denmark Hill. Thos. Henry Powell. Essence of Ginger. Sir, — I think that if Mr. Baildon will be at the trouble of again agitating his essence of ginger with silica (in very fine powder) and filtering, that it will become clear. I recently prepared some and found that upon first filtration it was opalescent, but refiltration has made it perfectly bright. With regard to the alleged misprint, there is no mistake, but perhaps it would have been better to have said ‘ * until nothing further is precipitated.” Upon first addition of the lime the tincture becomes very dark coloured; when more is added a somewhat bulky precipitate speedily falls and the solution becomes of a “rich yellow colour,” but is much paler than when the first portion of the lime has been added. The proportions of the various resins differ so much in different specimens of ginger, that a little judgment is required in addition of lime, etc. John C. Thresh. Nitrate of Pilocarpine. Sir, — From the misinterpretation of my remarks on the solubility of the above (p. 240 last week), Mr. Gerrard can¬ not have read my statement (p. 215, Pharm. Journ. 1879) carefully. W. Martindale. Erratum. — In Mr. Fletcher’s paper on “ Citrate of Iron and Quinine,” page 228, line 25 from top, for (2 673x0'86) read (2'673x30'86). “ Bonus” is recommended to make his wants known by means of an advertisement. J. H. Dingier. — Hypericum androscemum. H. Cocks. — The effect of the addition of sodium hyposul¬ phite is well known, but the resulting product can no longer be correctly designated a preparation of iodine. F. A. Barrow. — Syrup of Gentian (Codex). — Gentian Root, 100 grams ; Roiling Water, 1000 grams ; White Sugar, q.s. Pour the boiling water on the gentian, infuse for six hours in a closed vessel, strain and press. Add the sugar in the proportion of 190 parts to 100 parts of the in¬ fusion, and make a syrup by simple solution in a covered water-bath. A. H. Pope. — See the section on crystallography in Fownes’s ‘ Manual of Chemistry,’ vol. i., or the more ex¬ tended treatise in Watt’s £ Dictionary.’ “ Alterative ” is recommended to communicate the cir¬ cumstances to the Secretary of the local Association. “Army Compounder.” — The principle which should be followed in making up mixtures containing resinous tinctures has been explained on several occasions recently. See, for instance, vol. ix., pp. 528 and 529. W. B. Southgate. — The following recipe for “Pick-me- up” has already been given in the present series of this Journal : — Cardamons, 5 parts ; Caraways, 2 ; Cochineal, 2 ; Cinnamon, 10 ; Raisins, 80 ; Orange Peel, 56 : Ginger, 14 ; Gentian Root, 3; Woimwood, 2; Quassia, 1; Alcohol, ('838) 750; AVater, 750. Macerate for fourteen days, filter, and add syrup 200 parts. Communications, Letters, etc., have been received from Messrs. Wetzel, Wilkinson, Clarke, Wershoven, Musgrave, Postans, J. Griffith, Mushens, Turner, Howe, Catechu, Yerus, Student, Junior, Omnes Moriemur, Chemist, Gaul, An Emigrant, A Sawney, G. H. L. ctober 4, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 261 NOTES ON SOME JAPANESE DRUGS. BY E. M. HOLMES, F.L.S., Curator of the Museum of the Pharmaceutical Society. (Concluded from page 203.) FRUITS AND SEEDS. Kotree see (18): — Coriandrum sativum, L. The Japanese coriander seed does not differ in any respect from that of English commerce. Mahno dah-rah-gay (19) : — Datura alba, Nees.; Nees. in Linn. Tran. 17, p. 73; D. Stramonium , Thunb., FI. Jap. p. 91. Syn. Man-to-lo-hwa, Dr. Porter Smith, Mat. Med. Chin. p. 83 ; Chosenasa-gao, So mokou Zoussetz, vol. iii. fol. 55 ; Mandara-reuge, Phonzou Zoufou, vol. xxiii. fol. 20. These fruits are rather smaller than those of D. Stramonium, more globular, with shorter spines, the base of the spines being markedly striated. The specimens have evidently been gathered and dried before ripe, the seeds not being mature. Datura alba differs from Stramonium in its ovate downy leaves. It is used by the natives of India for poisoning, and professional poisons are often called dhatureas, on account of the use made of this drug. See ‘Pharm. India,’ pp. 175, 460. Meh-no-me (60) Prunus Armeniaca, L. (Apricot kernels). Syn. Kjoo, Kara momu, Ansu, Ksempf. Amoen. p. 798, Thunb. FI. Jap. p. 200. These seeds correspond well with specimens of P. Armeniaca in the Indian collection. The endo- carps, which are sparingly present, are quite smooth. The kernels are cordate, ovate, and about half an inch long and rather less in width, and two lines in thickness. The taste resembles that of a bitter almond. Apricot kernels are known to yield an excellent oil, nearly, if not quite, equal to almond oil, but to what medicinal use the Japanese put these kernels, I have not been able to ascertain. Oo-bei (35) : — Amygdalus nana, L. Syn. Prunus Mume, Sieb. et Zucc., FI. Jap. I. p. 29; Bai, Thunberg, FI. Jap. p. 199; Ume and Umebos, Kiempf. Amoen, p. 799; Mume, Momi, Fr. et Sav. vol. i. p. 117. This drug consists of the dried unripe fruits. In appearance they resemble small prunes, but are very dry and hard. They have apparently been dried at a high temperature, since the kernels have a roasted taste and dark-brown colour internally. The endocarp or stone is half to three-quarters of an inch long and about half an inch wide, and one- third to half an inch thick. It is perforated with small holes like that of the almond. The taste of the sarcocarp, or fleshy part, is intensely sour. The Japanese character, Bei, pronounced in Chi¬ nese Mei, is a generic term for any kind of plum, and is sometimes applied to other fruits. See Porter Smith, ( Mat. Med. Chin.’ p. 174. The fruits, preserved in dregs of Sacki or Japanese beer, are said by Koempfer to be exported to India and China. According to Siebold andZuccarini (l. c., p. 30, 31) Amygdalus nana is much cultivated in Japan and was probably introduced from China. The same authors give a long and interesting account of the Third Series, No. 484. uses of this plant. It is a shrub or small tree from 12 to 20 feet feet in height, flowering early in February, and is one of the plants which the Japanese cultivate extensively in the form of minia¬ ture trees. The flowering branches are used to de¬ corate the dwellings of the Japanese and the altars of their idols to indicate the approach of spring. The acid juice of the unripe fruits is used as a cooling drink in various fevers, for when ripe the taste is insipid. The acid juice is also used in the prepara¬ tion of the delicate pink rouge from safflower. Ren-nikh (51) : — Nelumbium speciosum, Willd. Syn. Nymplicea Nelumbo, L. ; Thunb. FI. Jap. p, 223; Lien-gau, Porter Smith, Chin. Mat. Med, p. 139, sub Lotus ; Ren, Hatsis ; Koempf, Amoen. p. 880; Hasu, Hachisu, So rnokou Zoussetz, vol. x. fol. 9 ; Phonzou Zoufou, vol. xxxiv. fol 9. This drug consists of the dark grey oval carpels,, about five-eighths of an inch long, and one-third of an inch in diameter. The shell is moderately thinr but very hard, and encloses a sweet white starchy kernel. They are used in Cochin China, according; to Loureiro (FI. Cochin Chin. p. 341), both in foocL and medicine, in the latter for diarrhcea, etc. A long and interesting account of the uses of various parts- of the plant is given by Dr. Porter Smith, in his 1 Materia Medica of China.’ The Japanese character Ren is identical with the' Chinese one for Lien, and means a river, the term nikh, meaning meat or food. The name “river- meat ” is probably given on account of the kernels of the seeds being eaten. iK - Sai hee (9) : — Citrus bigaradia , var. trifolia, Thunb. El. Jap. 294. Syn. Ssi vidgo Karatats Banna Gees, Ksempf. Amccn. p. 801 with fig. ; Ko kits, Phonzou Zoufou, vol. lxxxvii. fol. 8. This drug consists of the thin peel of a small orange about the size of the mandarin variety, which has the bitter flavour of the Seville orange. The peel has been removed entire by making four ver¬ tical slits in the peel nearly to the base of the orange and then pulling it off in one piece. The Japanese characters above translated Sai-hee, are in Chinese pronounced Hiang-pi, Sai meaning green, and hee, peel or rind. This name is probably given on account of its being gathered before the fruit is ripe. The rind, mixed with'that of other species, is made, according to Ktempfer, into a celebrated medicine called Ki-koku, a name also applied to the fruit. Sang-shih see (36) : — Gardenia fiorida, L. Syn. Shan-chi-tsze, Porter Smith, Chinese Mat.- Med. p. 101 ; San che, Hanbury, Science Papers, p. 241, fig. 7 ; Kutsi jinasi, Fr. et Sav. vol. ir p. 207 ; Sansisi, Misuktjinasi, Thunb. FI. Jap,- p. 109; Kutsjinas, Ksempf. Amoen. p. 808. This fruit appears to belong to more than one species, but the larger proportion consists of the kind represented under fig. 7 in Hanbury’s ‘ Science Papers,’ p. 241. The fruits are about an inch or more long, three-eighths of an inch in diameter, bright brown colour, with six longitudinal narrow wings, and contain numerous seeds rather smaller and wider than linseed, bound together into a mass by a dried yellow pulp. 262 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 4 is79. According to Mayer, the yellow colour of the pulp is due to a body named crocine, which appears to be identical with the polychroite of saffron. In China these fruits are supposed to possess emetic, stimulant and diuretic properties. A full account of the drug is given by Hanbury. The Japanese character for Sang- shih-see is identical with the Chinese one, although there is a slight difference in the pronunciation. The Gardenia from which these fruits are probably obtained is a native of woody places in Japan, flowering in J une and J uly, but is often used to form hedges in the gardens of the nobility. The fruits are also used as a dye. Sekkee-doo hee (24) : — Punica Granatum. L. Syn. Shiuli-p‘i, Porter Smith, Chin. Mat. Med. p. 176; Dsjakurgo or Sakuro, Ksempf. Amoen. p. 800; Thunb. FI. Jap. p. 199. This is the rind of the fruit dried. From its small size it would appear to be obtained from immature fruits. The pomegranate is stated by Ksempfer to be rare in Japan and to produce an inferior fruit with a rather disagreeable taste, but Thunberg remarks that it is common about Kosedo. Sho-ee-koh (39) : — Foeniculum vulgare. Syn. Sen-rio; Kure no Nomo, Thunb. FI. Jap. p. 120. This is a small variety of fennel seed with a taste at first strongly resembling that of anise. The large vittse, few in number, at once distinguish it from that fruit. Shiku-sha (5) : A Ipinia japonica , Miq. Prol. p. 304. Syn. Giobba japonica , Thunb. FI. Jap. p. 23 ; Hana-miyo-ga, So rnokou Zouss. vol. i. fig. 10; San Dsjoka, Jamma Mjogo, Ksempf. Amoen. p. 827 ; Phonzou Zoufou, vol. 10, fig. 5, Fr. et Sav. vol. ii. pt. 1, p. 20. These are the seeds of a species of Alpinia, a few of the small fruits being mixed with it. The fruits, which are about the size of a large pea, but rather oval than spherical in outline, have a thin wrinkled pale-brown papery pericarp containing 3 to 8 trian¬ gular pyramidal seeds. The seeds are pale exter¬ nally with a thin silvery coat, and have a faintly aromatic taste, but no pungency. These characters distinguish them from the fruits of A. galanga which are similar in appearance, but more oblong, and the seeds are remarkably pungent. This plant grows in damp shady places near lakes, etc., and the fruit is ripe in December and January. It is often cultivated in Japan. Tau ning (62) : — Amy g dolus Persica. Syn. Too, Momu, Ksempf. Amoen. p. 798, 'jThunb. FI. Jap. p. 199, Tau-jin, P. Smith, Chin. Mat. Med. 169. These kernels are mixed with a few fragments of the endocarp, which is undoubtedly that of a small form of peach, Tau signifying a peach, and ning, ker¬ nels. In Chinese the last word is pronounced “jin.” Thunberg enumerates several varieties of the peach as follows: Ke momu, with downy acute fruits ; Katu isi momu, with red glabrous, round fruits ; Kito momu, with red double flower ; Sato momu, with white simple flower. In Japan the peach blossoms in March and April. _ In China the kernels are used for coughs, blood diseases, amenorrlioea and worms. From the list of Japanese drugs now concluded, it will be observed that there is a great similarity between the materia rnedica of China and Japan, an exchange of drugs evidently taking place between the two countries. Of the fifty-nine drugs here described, twenty-seven are apparently peculiar to Japan, and twenty-two others are common to China as well, while ten are well known in all civilized countries. The last include white hellebore root, zedoary root, mallow root, mallow leaves, elder flowers, burdock seed, pomegranate peel, orange peel, fennel seed, and coriander seed. Several in common use in this country are represented in Japan by analogous drugs, viz., Colchicum by the roots of FritiUaria Thunbergii and Pinellia tuberifera ; Tritir cum repens by the root of Eulalia japonica ; pulsa- tilla by Anemone cernua root ; valerian by Patrinia scabioscefolia ; gentian root by Gentiana Buergeri ; peppermint by Japanese peppermint ; cliirata by Pleurogyne rotata ; and rue by Eooclia rutcecarpa. Of Indian drugs Datura alba and Cassia Tora are used in Japan, while Coptis Tecta and Datura alba find a substitute in the roots of C. anemoncef olia. The influence of western civilization appears to have already had an effect on the materia rnedica of Japan ; this is noticeable in the absence of any of the disgusting animal remedies used by the Chinese from the specimens sent over to this country. Hardly any of the Japanese drugs are altogether without sensible properties, either mucilaginous, tonic, astringent, aromatic or acrid, some of them being equal in power to analogous European remedies, and a few others, such as aconite root and valerian root, de¬ cidedly superior to the corresponding European drugs. SUPPOSED IDENTITY OF COLUMBIN AND LIMONIN.* BY E. PATTERNO AND A. OGLIALORO. Schmidt ( Annalen , 41, 338) considered that limonin was identical with the columbin extracted from Colombo root by Wittstock (ibid., 19, 298) ; and as the authors found much difficulty in preparing limonin in quantity from the seeds of the lemon and orange, whilst columbin could be obtained with comparative ease, they determined to examine into the question of the supposed identity of the two substances. The yield of limonin is but small, only 80 grams of the impure substance having been obtained from 15,000 grams of the seeds. It crystallizes in beautiful lustrous plates, and has the characters ascribed to it by Schmidt, except that it melts at 275° and not at 244° : moreover, it not only dissolves in potash without alteration, but also in baryta water, forming a kind of salt, which is not decomposed by carbonic anhy¬ dride. The formula which agrees best with the analytical results is C26H30O8; this requires C = 66’38 ; H = 6‘38. When Colombo root is extracted with ether and the solution is evaporated, a crystalline residue is obtained which, after beiDg washed with a little cold ether to remove fatty matters, etc., is treated with boiling alcohol : on cooling, the solution deposits colourless prismatic crystals, which melt at 182°, and have all the properties of Wittstock’s colombin. The results of the elementary analysis agree with the formula C2xH2907, which requires C = 65-28; H = 5'69. When the residue which is left after the separation of the columbin, and is almost insoluble in alcohol, is crys¬ tallized from boiling glacial acetic acid, it yields a second substance, having a melting point of 218 — 220°. Both this compound and Wittstock’s columbin are therefore quite distinct from limonin. * From the Gazzetta chimica italiana, 9, 64—67. Reprinted from the Journal of the Chemical Society. Oeto-er 4, i8?9.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 263 ®he flmmaqutual JamjimL - ♦ - SATURDAY , OCTOBER 4 , 1879. Communications for the Editorial department of this Journal, books for review, etc., should be addressed to the Editor, 17, Bloomsbury Square. Instructions from Members and Associates respecting the transmission of the Journal should be sent to Mr. Elias Bremridge, Secretary, 17, Bloomsbury Square, W.C. A dvertisements, and payments for Copies of the Journal, Messrs. Churchill, New Burlington Street, London, W. Envelopes indorsed “ Pharm. Journ .” _ THE ADMISSION OF WOMEN AS MEMBERS OF THE PHARMACEUTICAL SOCIETY. In the history of pharmaceutical affairs the first of October, 1879, will in future be memorable in that relation as the occasion when British pharma¬ cists were relieved from the anomalous necessity of regarding their better halves as inferior to them¬ selves. The persons most interested in this event have special reason to be thankful to the mover and seconder of the motion in their behalf for having at the earliest moment of the present session pressed forward the decision of the question whether women should be admitted to membership of the Society; for if it had been left for the following meeting of Council this achievement of petticoat emancipation would have been uncomfortably associated with the anniversary of another attempt to bring about social revolution. And considering how nearly opinions are balanced in regard to the desirability of admitting women into the Society it is, we think, at least fortunate for the protegees of Mr. Hampson I and Mr. Woolley that the advocacy of their case on the 5th of November has not afforded opponents an opportunity of instituting comparisons between their endeavours and those of Guy Fawkes and his col¬ leagues. For our own part we think that the movers of the resolution by which the petticoat has ceased to be a garb of disability for membership of the Phar¬ maceutical Society, and by which the admission of eligible persons into that body will no longer be regulated by circumstances over which the can¬ didates have no control, may well be congratulated for having, by their success, done away with an obvious inconsistency. From the time when the word “ person ” was, in point of law, decided to apply to women as well as men, the prosecution of the business of pharmacy under the terms of the Act of Parliament became by law as freely open to women as it had formerly been by usage, and although under the older regime, while submission to tests of qualification was voluntary, there might have been sound reason for declining to admit women as members of the Pharmaceutical Society, it is now very difficult, if not impossible, to say why women who have satisfied the requirements of the law in proving their eligibility to practise phar¬ macy should be refused participation in such benefits as appertain to membership of the Society. From a purely pharmaceutical point of view therefore, it may be regarded as matter for regret that any ob¬ jection had ever been raised to the election of women as members, and we think that the very general support of Mr. Hamfson’s motion by the members of Council may be taken as expressing that view of the subject. But the decision of the question from this point of view excluded from consideration most, if not all, of the arguments by which the election of female members @f the Pharmaceutical Society was opposed. In the Council, at least, that opposition was not based upon narrow-minded feelings of jealousy, or of disrespect for women, any more than it was upon an assumption that they were incompetent to per¬ form the duties of the pharmacist ; but it was mainly out of consideration for what was held to be due to women in their social relations that the unfitness of some portions of the pharmacist’s duty was urged as a reason for not admitting women as members of the Society. Their election into the body was held to be an encouragement for women to take up the business ; it was opposed on the ground that it was an undesirable encouragement. This has always been the principle upon which Mr. Sandford has opposed the election of female members of the Society, and consistently with these views he has now, as Pre¬ sident of the Society, recorded his vote against Mr. Hampson’s proposition. There is, however, an absence of common ground upon which these opposite views respecting the election of female members can be considered together in such a manner that the acceptance of the one would involve the rejection of the other, and consequently we must infer that the altered direction of the votes given on the present occasion is due to the consideration of the question from a more special point of view than was formerty the case when Mr. Sandford’s opinions were more generally supported. The desirability of putting an end to the agitation of this question also seems to have weighed with much effect in determining the votes of some members of the Council. Incidentally the discussion of this matter suggests some important considerations as to the propriety of forcing to the issue of a vote a question upon which there are such opposite opinions. The fact that on two occasions the votes at general meetings of the Society were so evenly divided is scarcely a satis¬ factory ground for insisting upon the question being disposed of by the Council one way or the other. If those experiences pointed to anything they seem to favour the conservative course of keep¬ ing things as they were. Fortunately the admis¬ sion of women as members of the Society is not calculated to affect very seriously the interests of other members, and there is consequently less reason for dissatisfaction with the settlement of the question by a narrow majority. But 264 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 4, 1879 there are other subjects in regard to which we can conceive that either section of the equally divided pharmaceutical body would strenuously object to the decision of a question by so narrow a majority as that which has until the present occasion obtained in voting upon the female question either in tho Council or at a general meeting. However, it is far from being our desire to dis¬ parage on these or any other grounds the successful championship of the ladies by Mr. Hampson and Mr. Woolley, on the contrary, we congratulate Miss Clarke and Miss Minshull upon their election as members of the Society, and we congratulate the Society itself upon the removal of a restriction that was regarded as a grievance by those against whom it operated, with the result of stimulating an agita¬ tion which engaged more time and energy than the intrinsic merit of the question at issue really justified. IRREGULAR SALE OF POISONS. The intimation furnished by Mr. Flux at the hearing of the recent case of prosecution for illegal sale of poison, that any person might be the prose¬ cutor in cases of irregular practice of this kind, has been very soon acted upon by the Chemists and Drug¬ gists’ Trade Association. As will be seen from the report of legal proceedings at page 278, three such cases have been tried at Blackburn, Liverpool, and Birmingham, in all of which persons were charged, under the 17th section of the Pharmacy Act, 1868, with selling poison insufficiently labelled. In all of the cases the offence was virtually admitted by the defendants, and they were subjected to the pay¬ ment of fines ranging from ten to twenty shillings and costs. These eases will serve to bring before the minds of magistrates the fact that the provisions of the Pharmacy Act for the safety of the public are being systematically disregarded by a great number of persons throughout the county trading as oil and colour merchants, grocers, drysalters and patent medicine dealers. A great number of the poisons contained in the schedule to the Act are thus supplied to the public without bearing any of those precau¬ tionary protections against accident or misuse which the Legislature has indicated to be necessary. This fact has been emphatically pointed out by the jury in the late inquest at Newhaven (see p. 279), and the opinion had very properly been expressed by them that the preparation and sale of medicines containing dangerous ingredients should be restricted to duly qualified persons. The mere word “ poison ” written upon or placed as a printed label upon packets of such articles is not sufficient to satisfy the requirements of the Act, and hence persons selling poisons in this way are liable under the 17th section to a penalty of £5 and costs. Even if, in such cases as we have mentioned, the word poison, as well as the name of the poison, together with the name and address of the seller, were placed upon the packet or bottle containing the poison, and the provisions of the Act were complied with so far as the 17th section is concerned, persons selling poison in this way would be further liable to a penalty for breach of the law under the 15th section of the Pharmacy Act. In the Horsington case the defendant pleaded as a defence that the laudanum he sold bore a patent medicine stamp, and it is well known that in some places the use of the stamp in this way is supposed to be a protection against liability under the Phar¬ macy Act. That it is not of such virtue to the unregistered vendors of poison is, however, beyond question, and we are glad to find action is being taken with the view of making these circumstances known to magistrates and the police as well as to the persons engaged in the irregular trade by which the public safety is imperilled and the business of the legally qualified chemist and druggist unfairly interfered with. DEATH OF DR. MOHR AND M. POGGIALE. With much regret we have to make known the death of Dr. Friederich Mohr at the age of 72. Originally a pharmacist at Coblentz, and since 1864 the Professor of Pharmacy at the University of Bonn, Dr. Mohr has established a world-wide reputation for his scientific acquirements and as author of several valuable works connected with chemistry, physics and geology. One of these, on practical pharmacy, is well known in this country in the form of a translation, edited by Professor Redwood ; another, on volumetric analysis, has been made familiar to English chemists by the valuable labour bestowed upon it by Mr. Sutton, of Norwich. We hope shortly to be able to furnish our readers with some further account of the life of this remarkable man. The October number of the Journal de Pharmacia et de Chimie also contains an announcement of the death of an active member of its editorial staff, M. Poggiale, and the discourses pronounced at his funeral by representatives from the various bodies to which he belonged. M. Antoine-Baudoin Poggiale was born in 1808, and his first memoir, published in 1834, was devoted to proving that the “ parigline ” of Palotta, the “ smilacine ” of Folchi, the “ salseparine ” of Tubeuf and the “ parillinic acid ” of Batka, were one and the same immediate principle. Amongst his subsequent works may be mentioned his treatise on Volumetric Analysis. M. Poggiale had filled the office of President of the Paris Society of Pharmacy and was a member of the Academy of Medicine. Among the scientific works announced to be pub¬ lished during the coming season by Messrs. Mac¬ millan and Co. is a “new and thoroughly revised edition” of Fluckiger and Hanbury’s ‘Pharma- cographia. October 4, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 265 Sanctions 0f f jtotfftg* MEETING OF THE COUNCIL. Wednesday, October 1, 1879. MR. GEORGE WEBB SANDFORD, PRESIDENT. MR. GEORGE FREDERICK SCHACHT, VICE-PRESIDENT. Present — Messrs. Atkins, Bottle, Churchill, Frazer, Gostling, Greenish, Hampson, Hills, Mackay, Richard¬ son, Rimmington, Robbins, Savage, Shaw, Squire, Symes, Williams and Woolley. The minutes of the previous meeting were read and | confirmed. Weights and Measures. The President stated that on the day following the last Council meeting he had received the following letter from the Privy Council office : — “ Board of Trade, “ (Standards Department), “ 7, Old Palace Yard, S.W., “ 3rd September, 1879. “Weights and Measures Act, 1878. “ Sir, — I am directed by the Board of Trade to acknow¬ ledge your letter of 27th ult. on the subject of verifying and stamping apothecaries’ weights and measures. “ In reply, I am to point out that the local authorities named in the above Act are charged with the duty of inspecting, verifying, and stamping all weights and mea¬ sures used in the trade, and that this Board are not authorized to interfere therein. “ I am also to add that, if the Pharmaceutical Society will depute someone to call on Mr. Chaney at the Stand¬ ards Office, 7, Old Palace Yard, that officer will be glad to give him any information that may be in his power with reference to the above Act. “ I am, sir, “ Your obedient servant, “ Henry G. Calcraft. “ G. W. Sandford, Esq., ‘ ‘ President of the “Pharmaceutical Society of Great Britain, “ 17, Bloomsbury Square, W.C.” In accordance with this communication he had waited on Mr. Chaney, and the result of the interview had been that he had received the following information: — No order had yet been issued] as to the verifying of glass measures, and it had not yet been decided to issue any respecting them; if determined on it would probably only refer to the top line of graduation, and not to the sub¬ divisions. For the present chemists need fear no inter¬ ference from local inspectors, because they were not in possession of the standards, and would not be for three months to come. With regard to the idea which some persons entertained that weights or measures could only be used in the district in which they had been stamped, Mr. Chaney said this was altogether a mistake. A weight or measure stamped in one district was good in every j district. Mr. Rimmington said it was very desirable that what the President had stated should be generally known. Mr. Richardson had always understood that the standards in each district were regulated by the standard in London. With reference to the glass measures, he did not quite understand whether they were to go on under the old system or to wait. The President said that at present they must go on; they could not get them verified by the local inspectors. Mr. Richardson said nothing varied more than glass measures. When could they have them stamped ? The President said certainly not for two or three months, because the inspectors would not have any standards by which to try them. Mr. Shaw said he understood it was competent for any one to send his glass measures to the stamping office to be verified, and that Mr. Greenish had already sent three or four dozen, which had been verified and a mark placed upon them. The President said he could only repeat that at present no inspector had in his possession the standards by which he could verify glass measures. The Vice-President said it was very important that it should be generally known to chemists that any in¬ spector who required a chemist to have his measuies verified was for the present exceeding his authority. The Chemists’ Ball. It was unanimously resolved that an application from Mr. Arthur L. Savory, asking permission to use a room on the Society’s premises, fora meeting to make arrange¬ ments for the Chemists’ Ball, be acceded to. Local Secretary. Mr. Sharp was unanimously elected Local Secretary for Sunderland in place of Mr Nicholson deceased. Elections. member. Pharmaceutical Chemist. The following, having passed the Major examination and having tendered his subscription for the current year, was elected a Member of the Society : — Grimble, Alfred . Boston. ASSOCIATES. The following, having passed the Minor examination and tendered or paid as Apprentices or Students their subscriptions for the current year, were elected “Asso¬ ciates” of the Society: — Goodall, Thomas Torby . Derby. Wilks, Charles Frederick . York. APPRENTICES OR STUDENTS. The following, hating passed the Preliminary examina¬ tion and tendered their subscriptions for the current year, were elected “ Apprentices or Students ” of the Society : — Rowntree, Alfred Henry . Manchester. Timm, Edmund . ..Goole. It was proposed by Mr. Hampson, and seconded by Mr. Woolley — “That the following Pharmaceutical Chemists, having tendered their subscriptions for the current year, be elected Members of the Society : — Clarke, Isabella Skinner . London. Minshull, Rose Coombes . London. Mr. Hampson, in moving this resolution, said he was very glad to see that the ladies had again applied for membership. Two or three years ago, this question had been, he thought, unwisely relegated to the annual meeting, but since then there had been two or three elections of Council, and they were now, he contended, perfectly entitled to interpret the Act of Parliament according to the best of their ability. He believed the two ladies in question, having passed the requisite exami¬ nations and become registered, were without any doubt eligible according to the Act of Parliament to become members. They had conformed to everything which the Act required, and he thought the duty of the Council was to elect eligible persons irrespective of anything else. He had been told more than once that it was a matter of option with the Council, but he could not see it in that light. The duty of the Council was not to make the law, but to carry out the law ; and it seemed to him somewhat impertinent to say, ‘Because you are a woman, although you have gained admission to the rights of pharmacy under the Act of Parliament, when you apply under another por¬ tion of the Act of Parliament to become a member of the Society, you shall be refused.’ This refusal had con¬ tinued to take place for several years, but he took his stand on this point that the Council could not say that 266 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. October 4, i87». one portion of the Act of Parliament was a public matter, and another was a private matter. Some members had taken this ground, but he altogether refused to accept it, because the operations of the Society were carried on by the members of the Society, and the members were for the most part elected because they were pharmaceutical chemists or chemists and druggists before the passing of the Act, and it seemed to him that to put any stumbling block in the way of carrying out the Act of Parliament was illegal. If the members of the Council refused to admit eligible persons to membership of the Society because of their own private convictions or sentimental views, they were overriding the Act of Parliament and neglecting their duty as a Council. But apart from the legal aspect, he would say that it appeared somewhat ungenerous, he would almost say unmanly, to continue this persistent refusal. Surely there could be no harm in admitting as members those who had satisfied the examiners ; on the contrary, they would do the Society honour by admit¬ ting to its ranks properly qualified lady members. Besides, by a refusal these ladies were also denied the privileges of using the library and museum, the title of member¬ ship, which in some parts of the kingdom was considered of great value, and the J ournal. He did hope that this question would now be taken out of the hands of the annual meeting, where it ought never to have been placed. It was part of the executive duty of the Council to elect all eligible persons, irrespective of their sex. It would be as reasonable to ask what church they attended as to inquire as to the sex of eligible persons who applied for admission, and he hoped the matter would now be settled by carrying out the Act in its entirety. Mr. Woolley seconded the motion, and endorsed everything which Mr. Hampson had said. He should be sorry for the Pharmaceutical Council to be the last to grant a request, the justice of which was obvious, and which must, ultimately, inevitably be granted. Body after body was granting to women what was their un¬ doubted right, and he did trust the Pharmaceutical Council would not be left in the unenviable position of being the last to recognize it. Mr Williams said he intended to support the motion. He had watched the proceedings of two general meetings in which this question had been agitated, and he should be very sorry that such a question should again be dis¬ cussed by the general body. The necessity for such discussion no longer existed, for on two occasions the meetings were so evenly divided that it was a mere toss up which opinion should be followed. Taking it in its broader sense and seeing that these pharmaceutical che¬ mists had applied for membership, he could see no reason why the fact of their being ladies should prevent their being elected. He thought the question had now come back to the Council for decision, and it was time it was finally set at rest. He should vote for the motion on that ground, and also because he agreed with Mr. Hamp¬ son that there was no real reason why they should not be elected. Mr. Atkins intended to support the motion, though he demurred to the remark that the question ought never to have been referred to the annual meeting. He was very glad it had been so referred, for he did not think it would have been well to attempt an organic change without feeling the pulse of the constituency. He was, however, quite convinced that it was un¬ desirable to remit it still further. Having tested the opinion of the members twice, the Council had done all it was bound to do, and he believed its con¬ stituents would be thankful to have the question taken out of the arena of unprofitable discussion. It was un¬ necessary to go over again the abstract arguments, and he hoped the question had now been removed from the ground of controversy altogether. Mr. Savage was very glad to have so far a unanimous expression of opinion as to the desirability of admitting these ladies to the Society. He had always held that they had a right to be admitted, and he felt more than ever the importance of saving any further discussion of the question. The admission of all who had distinguished themselves in the examinations was, he thought, desirable, and he thought it was very much to the credit of these ladies that they had had the moral courage and per¬ severance to go successfully through the ordeal. The President said as he still adhered to the view he had always held, he must correct Mr. Savage as to the opinion of the Council being unanimous. He had always voted against the admission of ladies and should continue to do so. Mr. Hampson said the Council ought to carry out the laws, but if it were to carry them out without judgment, they would be utterly useless. Then again, Mr. Hampson said that the members carried on the business; but if so, they had the vote of the members against the admission of ladies. Mr. Hampson : By a majority of one or two. The President said never mind what the majority was, it was a majority, and having sent this question to the members for decision, he held that the Council was to a great extent bound by their decision. Mr. Hampson had said the members of the Council had withheld from ladies certain privileges, but they were only privileges which belonged to members of the Society, not privileges which conferred any rights in respect of trading. He need not say anything further, because his views were well known. Mr. Mackay said that in these days of wars arid rumours of wars, he felt disposed to be a man of peace. Although he had his own ideas with regard to the admis¬ sion of ladies to membership, he could not hide from himself that there had been an immense deal of agitation about it, and unless it were settled to-day there would probably be a great deal more ; he was therefore disposed to settle the matter by voting for the admission of ladies. Mr. Frazer said he rejoiced at the conversion of some of the members, and he trusted the matter would now be settled. Mr. Richardson heartily supported the motion. He looked upon pharmacy as a suitable occupation for women, especially in villages and small towns, and their reception as members would give an impetus to women to become pharmacists. He hoped the President would withdraw his opposition, and that the vote, would be unanimous. Mr. Bottle said he should vote for the motion, not with a view of conceding to ladies what Mr. Hampson asserted was their right, but as a matter of courtesy, which he thought they had well earned by passing the examinations, and also with a view of bringing about a peaceful termination to a question which had formed a bone of contention for some years. A prolonged agitation would be infinitely worse than admitting even a dozen women into the Society. Mr. Shaw said he had always supported the admission of ladies, and he was delighted to find such a large number of conversions to the proposition now made. He regretted that the matter had ever been remitted to the annual meeting, and he would remind gentlemen that during the discussions on the Pharmacy Act it was distinctly stated that all persons passing the examination, or persons who became pharmaceutical chemists, should be eligible to become members of the Society. That was held out to everyone, and as ladies were not excepted, they had certainly a right to be admitted. Mr. Greenish said he should vote for the motion as a simple act of justice to those who had qualified them¬ selves by passing the examination and who had been left out in the cold for a long time. Mr. Hills said he also intended to record his vote in favour of the motion. Mr. Robbins said he had brought forward a motion last year to endeavour to settle this question by an appeal to the members, on which he had been outvoted. The matter had oome before the Council several times October 4, 187b]. THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS 267 and he thought the members were all getting tired of it. To avoid further agitation, and to settle the question, he thought the Council were now prepared to give an almost unanimous vote in favour of the admission of ladies. The motion was then put and carried, the President being the only dissentient. Mr. Bottle asked what would be the position of these ladies in case they changed their names. The President thought the Married Women’s Property Act would reserve to the ladies their right of membership. Two persons were restored to their former status in the Society, upon payment of the current year’s subscription and a fine. Additions to the Register. The Secretary reported that — John Cammack, Benington, near Boston; William Clarke Edmonds, Rawmarsh, Yorks; Frederick Ellis, 25, Cleveland Road, Downham Road, Islington, N.j Frederick John Sicre, 33, Molyneaux Road, Farn- worth Street, Everton, Liverpool ; and William Henry Thomas, 94, Victoria Street, Dowlais ; having made statutory declarations that they were in business before the passing of the Pharmacy Act, 1868, and their declarations having been duly supported by medical practitioners, their names have been placed on the register. Reports op Committees. The President said that the Solicitor had been re¬ quested to attend at half past twelve, and he would therefore ask the Council to take the General Purposes Committee’s report first, as it was on matters arising out of that report the Solicitor’s opinion was required. The Council would of course go into committee to discuss these matters. Mr. Symes said, in case a resolution was passed in regard to reporting the proceedings in committee, he could fancy it quite possible the Council might be in a dilemma as to what might be reported. He would suggest that the best mode of carrying out the resolution which was carried at his suggestion at the last meeting but one, would be, that the Council when in committee should frame a report which should be presented to the Council on resuming, and published. That was a parlia¬ mentary method of proceeding, and he merely rose to call general attention to that fact, so that when the Council went into committee the members should know what they were going into committee upon and should be in a position to frame a report of the proceedings to be presented to the Council on resuming. Mr. Shaw said he was not present when the resolution referred to was passed, but he had read the report with interest. It struck him that the resolution would not amount to anything, and he found that, in answer to an inquiry, Mr. Symes explained that what had been optional in former times would now become compulsory. If he understood Mr. Symes’ s present proposal aright, it was this, that when the Council went into committee notes were to be taken, and when the discussion came to a close it was to be put to the members, and a decision come to as to what report should be published. This would be a most difficult thing to carry out, for imme¬ diately the Committee had closed one discussion it would have to open another as to what should be reported. Such a system would entirely destroy freedom of discussion. It had hitherto been left to the discretion of the profes¬ sional reporter, who was constantly called upon to exer¬ cise his judgment in such matters, and he should recom¬ mend that the same course be followed in future, it being, of course, understood that the reporter would omit all personal matters and details of pending legal proceedings. Mr. Hampson supported Mr. Symes’s view. The reso¬ lution he brought forward some time ago was for the purpose of having a report of what took place in com¬ mittee which would give satisfaction to the outsiders, and do no harm to the interests of the Society. It appeared to him that the best pei'son to take the report would be the reporter himself ; but it would necessarily be brief, and he thought it should be handed to the Committee, who should decide whether it was a faithful report and suitable for publication. The President having read the resolution referred to, Mr. Richardson said he feared that if Mr. Symes’s proposal were adopted the members of Council would be there for a week. He thought the matter might safely be left to the President, the Secretary, and the reporter. He had been connected with a public body for nearly nine years, and he thought it would be much better if every report from a Committee were rendered in a form in which it could be published in the Journal and dis¬ cussed in open Council. The President said the Council had a good deal of business to do, and he must ask Mr. Symes to give notice of a motion if he had anything definite to propose, other¬ wise they must proceed with the report of the Committee. GENERAL PURPOSES. The report of this Committee was then read. It consisted principally of correspondence with the Solicitor, with regard to sundry legal matters in which he had been instructed to take proceedings. There was also correspondence with the Secretary relating to alleged infringements of the Pharmacy Act, in regard to some of which the Committee recommended that pro¬ ceedings should be taken. It also recommended that a grant of £35 be made to the Manchester Chemists and Druggists’ Association, to partly defray the expenses of lectures on Chemistry, Materia Medica and Qualitative Analysis at the Manchester School of Pharmacy. The Council then went into committee to consider the report and to confer with the Solicitor on certain points therein contained. In the course of the conversation the Solicitor stated that he had just received a communication saying that — Daniel Tudor Williams, of Aberdare, who had been sued in the county court for a penalty for infringement of the Pharmacy Act, 1868, had paid the amount claimed, with costs, into court.* On resuming, the report and recommendations of the Committee were unanimously received and adopted. Mr. Churchill stated that he had just received a telegram from the Secretary of the Chemists and Druggists’ Trade Association saying that in one' of the cases which had been before the Committee, the Trade Association had prosecuted, and the defendent had been fined £1 and costs. Mr. Richardson thought it would lead to confusion if both bodies undertook the prosecution of offenders. The President said that anyone could institute pro¬ ceedings under the 17th section ; the Society did not generally prosecute under that section, which constituted a police offence. The Council again went into committee to consider the opinion just given by the Solicitor with regard to a certain case which had been submitted to him, but after some discussion it was ordered to stand over to next month, the Secretary in the meantime to obtain fuller information. The Council then resumed. FINANCE. The report of this Committee included a recommenda¬ tion that sundry accounts be paid. It also stated that the Committee had considered the question referred to it by the Council, with regard to the payment of annual subscriptions to local secretaries, and was of opinion that * It will be remembered that Mr. Williams’s name was removed from the Register some time ago. 268 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. October 4, 1879 it would not be wise to alter the existing regulations, excepting in the form of letter sent to members who had not paid by March 31st, an amended form being submitted. The report and recommendations were received and adopted. LIBRARY, MUSEUM AND LABORATORY. This Committee reported that a prosecution having been instituted against a member of the Society for the sale of cream of tartar alleged to be adulterated, the case had been under its consideration, and that as cream of tartar of commerce invariably contained a portion of tartrate of lime, it was deemed desirable that the Solicitor of the Society should watch the case at the time of the hearing. That he had been instructed to do so, and the magistrates had dismissed the summons.* Mr. Woolley asked if the defendant received his costs. The President said he could not answer that question. Mr. Woolley said there was a case near Manchester, in which the analyst gave an opinion that proved to be totally erroneous with regard to a certain drug, and there costs were awarded against him. Honest tradesmen ought not to be subjected to this kind of persecution and have to bear the costs into the bargain. The President said there had been another prosecu¬ tion for the sale of cream of tartar in the same county, and no doubt by the same analyst, which the magistrates had dismissed without calling for any defence. The report was received and adopted. benevolent fund. The report of this Committee included a recommenda¬ tion of the following grants: — £15 to the widow of a registered chemist and druggist, aged 60. Applicant had a grant of £10 in Pebruary, 1877. £15 to a member, aged 59, suffering from ill-health. He had a grant of £20 in August, 1878. £10 to a former member, unable to work from sick¬ ness, who has had three previous grants. £10 to a registered chemist and druggist, formerly in business, who has had two previous grants. £10 to a registered chemist and druggist, who has also had two previous grants. £5 to another registered chemist and druggist, aged 61, an unsuccessful candidate for an annuity last year, and who has had two previous grants. £10 to a female registered chemist and druggist, who has had three previous grants. One other application was ordered to stand over for further inquiries. The Secretary had reported that there are now twenty- nine annuitants on the Fund, and given particulai-s of the age and date of election of each. The Committee having considered the financial position of the fund, was of opinion that it was expedient to elect three pensioners, and recommended that the election be held on Friday, December 19. Mr. Williams said the Committee only proposed to elect three annuitants, but there were nine candidates, and several other worthy, objects could easily have been added to the list, but the Committee was really aground for want of funds. In fact it was running some risk in proposing to elect three, for in all probability the means would be exhausted by the end of the year. If the sub¬ scriptions were more general from those who now did not subscribe at all, there would be abundance of funds not only for three, but for the whole nine. He trusted that their friends in the country would see this, and recog¬ nizing that it was not a matter of disputed politics, but of genuine benevolence, would endeavour to give some¬ thing, however small, to assist the fund. Mr. Rimmington drew attention to the case of one of the annuitants whose conduct had on a former occasion been the subject of inquiry, and suggested that it would be well to remove him and put a better man in his place. * This case was reported in the Journal of September 27. Mr. Williams said this could hardly be done offhand without due notice and consideration. Mr. Bottle hoped the Council would feel that it was in a position to elect three annuitants, and he was sorry it could not be more. But he had felt on the previous evening when the Committee considered the matter that he could not go to the extent of proposing four, since the balance sheet showed that it was doubtful on which side the balance would be at the end of the year ; but there would certainly be no surplus for investment. It was true that in the coming year some deaths might occur, but, on the other hand, as the annuitants became older they were entitled to larger pensions, and there were constantly more claims for casual relief. He therefore hoped that all who were able to contribute to the fund would assist in doing the large amount of good which the Benevolent Fund was calculated and he hoped for many years wTould continue to do. The report and recomendations were unanimously adopted. Mr. Shaw gave notice that he should next month bring forward a motion for the purpose of preventing canvas¬ sing cards and circulars being issued by candidates. The Pharmaceutical Conference at Hanover. Mr. Greenish stated that, with Dr. Paul and Mr Passmore he had attended the meeting of the German Pharmaceutical Association held in Hanover the first week in September. As on the former occasion in Coblentz, they were very cordially welcomed, and at the dinner the toast of the Foreign Guests had been received with considerable enthusiasm. There had also been placed at the disposal of each of them a guide to Hanover and its surroundings, also tickets of admission to the Pharmaceutical Exhibition and other places of interest in and about Hanover. Some specimens of new preparations shown in the exhibition had been promised for the Society’s Museum. The apparatus, which formed an important part of the exhibition, was mainly composed of modifications of that of Beindorff, so well known in German pharmacies. There was also exhibited by a firm in Berlin a polarimeter very efficient, and at a moderate price, and a microscope of a construc¬ tion that possessed some advantages over those in general use in this country ; both of these there was some proba¬ bility of being able show at one of the Evening Meetings of this Society. He should be glad to see some of their colleagues in Germany return the visit on one of our festive occasions in England. He had much pleasure in moving — “That a vote of thanks be presented to the President of the German Pharmaceutical Association and the Local Committee at Hanover for their cordial recep¬ tion of English visitors at the meeting of their Asso¬ ciation.” The motion was seconded and carried unanimously. PHARMACEUTICAL MEETING. Wednesday , October 1, 1879. The first evening meeting of the session took place on Wednesday, October 1, the chair being taken by the President of the Society at halt-past eight. The minutes of the last meeting were read and confirmed. The President, having expressed his pleasure at seeing so large a gathering on the opening night of the session, called on Professor Redwood to present his — ' Report on the Chemistry and Pharmacy Class* Professor Redwood said the business of the even¬ ing being of a somewhat varied character, and the actors who were to take part in the proceedings October 4, 1879.3 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 269 ; [ ! being numerous, it was necessary, or at least desir¬ able, that those who had merely formal duties to perform should be as brief as was consistent with setting forth the merits of those whom they had to introduce to the notice of the meeting. In reference to the examinations he might state that in his class and also in that of his colleague, Professor Bentley, who he regretted to say was unable to be present that evening, there had been three separate exami¬ nations. In the first place there were two examina¬ tions for those students who had studied five months, namely, one at the end of March, and one at the end of July. On these examinations a bronze medal was awarded and certificates of merit, the latter being only given to those students who obtained an equal number of marks to those who at the ten months’ examination obtained a certificate of honour. The certificate of merit therefore in this case was really of greater value than the certificate of merit in the ten months’ examination. As the result of the examination in March he found that there were five gentlemen in his class who received certain indications of merit; at the head of these was a gentlemen who would be found to figure also in subsequent examinations, one whose name could not fail to be familiar to them, namely, Mr. Mackay, of Edinburgh, — not a member of the family of Mack ay’s which they were most familiar with, but still it was satisfactory to know that talent was not confined to that one family. There were four other gentle¬ men, whose names appear below, all of whom ob¬ tained 75 per cent, of the highest number of marks which could be given, and they were all entitled to certificates of merit. In the July examination some of these gentlemen again appeared. Those who had previously obtained honours as five months’ students could not compete on that occasion in the five months’ examination; but there were again five gentlemen who obtained distinction, the bronze medal being awarded to Thomas Horton. In July also there was the examination for those who had been studying ten months, and those who had not been studying so long were eligible to compete, and occasionally did so, but it could not be expected that they would often succeed in competition with those who had been studying for double the length of time. Here again the silver medal was awarded to Mr. Mackay. As he mentioned the names of the other successful competitors, Professor Redwood said he desired to add one remark, namely, that it was a feature in these examinations of late years that a larger number of students had competed than was formerly the case, and further, that a larger propor¬ tion of those who had competed had proved success¬ ful in the competition. This was a highly satisfactory feature, inasmuch as it seemed to indicate that the students now obtained a more thorough preliminary education before they came to that school; they were better prepared, and were therefore more generally successful than was the case several years ago. The following is a list of the students in this class to whom prizes have been awarded : — Five Months’ Cookses. Bronze Medal Certificates of Merit FIRST COURSE. . James B. Lillie Mackay. Frank Harris Alcock. Beresford Fred. Harold . -J Maudson. Edward Jarrett Eaton. (.James Henry Allan. SECOND COURSE. Bronze Medal Certificates of Merit ...Thomas Horton. ( Henry William Drew. 1 William Herbert Hyatt. ) George Wale. ( William Inchle Gulliver. Ten Months’ Session. Silver Medal . James B. Lillie Mackay» ! Thomas Horton. Edward Jarrett Eaton. J ames Henry Allan, j Frank Harris Alcock. . \ Henry William Drew. The following were the questions for the examina¬ tions : — FIRST COURSE. BRONZE MEDAL. Certificates of Merit Hours 10 till 2. 1. Define the meaning of the terms matter, force and inertia. 2. What is the meaning of the term weight ? 3. What is the weight of a pint of rectified spirit, B. P. ? 4. What marked distinctions are there between gaseous diffusion and liquid diffusion ? 5. Briefly explain the undulatory or wave theory of light. 6. Describe the normal composition and characters of crystallized carbonate of potassium, and also of the car¬ bonate of potash of the Pharmacopoeia. 7. Give the composition of oxide of zinc, and describe the methods by which it may be produced. 8. In what state is bismuth principally found in nature ? What is its melting point, and what appearance does the metal present when a mass of it, after being melted, and then cooled, is broken ? 9. Give the respective compositions of the lowest and highest oxides of antimony, and describe the processes by which they may be obtained. 10. Give the respective compositions of glucose, alcohol, aldehyde, acetic acid, and acetone, and explain how these are or may be related to each other. SECOND COURSE. BRONZE MEDAL. Hours 10 till 2. 1. Describe the method of taking the specific gravity of calomel and also that of wax. 2. Explain the meaning of the term “allotropy.” 3. What is the meaning of the terms “ specific heat ” and “ latent heat ? ” 4. Describe the essential characters of an emulsion. 5. Describe ozone and peroxide of hydrogen, their properties and the method of producing them. 6. Describe phosphorus, its production from natural sources, its allotropic conditions, and its properties. 7. What is the natural source of cadmium, how is it isolated, and what are its properties ? 8. Describe acetic acid, its production in various ways, and the relation it bears to alcohol. SESSIONAL COURSE. SILVER MEDAL. Hours — 10 till 1, and from 2 till 5. 1. What is the weight of a pint of distilled water, and what is the specific gravity of a liquid, a pint of which weighs 9625 grains? 2. What are respectively the specific heats of water, oil, and mercury? 3. What is the velocity with which a body falls to the earth through a vacuum, at the latitude of London, in the first, second, and third second of time ? 4. Describe the principle of the action of the siphon. 5. What is the law relating to the rate of diffusion among gases ? 6. In what way does the density of a gas into which diffusion takes place affect the result? 7. Describe the production of chloride of magnesium and also of chloride of aluminium. 270 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 4, is79 8. What is the composition, and the assumed constitu¬ tion of borax, and how is the borax of commerce usually prepared ? 9. What are the chemical charges that occur in the conversion of barley into malt? 10. Describe the production of lactic and butyric acid. 11. Describe the production of artificial urea, and point out the relation it bears to cyanogen. Report on the Practical Chemistry Class. Professor Attfield being next called upon, said he was much pleased to see such a large number of old students present, and no doubt his colleagues who lectured in that hall would be very glad il they could see such a muster every day in the session. He appeared there in two capacities, as professor and as examiner. As professor he had given in his report to the Council in the usual way at the end of the session, and that report he now held in his hand. He would not read the whole of it, but might say formally that the number of students was 75, the average period of work by each was six months, and the number of hours occupied in work daily during that period was three and a half. As compared with the previous session the number of pupils was the same, the average number of months’ work was rather greater, but the number of hours worked daily was decidedly less, hence neither this nor, indeed, the previous one compared favourably with former sessions. Out of the 75 pupils only 5 attended for purposes other than those connected with phar¬ macy, whilst there were three ladies working at practical chemistry for the requirements of the medical profession. He might add with regard to the lady students that he saw no reason whatever why ladies should not work at practical chemistry in the Pharmaceutical Society’s laboratories. With regard to the general work of the session, he had only to say that they had had what might be called a quiet session. They had got on remarkably well together throughout. The class consisted of gentle¬ men, and without exception they were men who had come to be prepared not so much for examination as for the general work of life. He trusted they were not disappointed. As examiner, he had to report that at the end of the session he held an examination for the Council prizes, when the student who ob¬ tained the highest number of marks was Mr. Frank Harris Alcock. He obtained 81 out of 100 marks, and hence took the silver medal. The second, Mr. F. W. Warrick, and third, Mr. R. J. Price, obtained 76 and 75 per cent, of marks respectively, and were awarded bronze medals, and then came five gentle¬ men whose numbers carried Council certificates. Nine other competitors obtained less than 60 marks, so that there were 17 in all, a good proportion of the whole number of students. This was the result of his examination, extending over two days, but he had also been teacher of these men, and had one way or other examined them for more than two hundred days during the session. He had thus gained so good a knowledge of the relative positions of these seventeen men that he was able to say that two who did not even obtain the mini¬ mum number of marks qualifying for a certificate of merit were as good men as those who had obtained marks qualifying them for medals. The sound, and he thought safe deduction, was that even a two days’ examination conducted by a professor in the subject was an inefficient test of competency, but he would not be so disloyal to the School or the Society, to say nothing of himself, as thus to criti¬ cize his own action as an examiner, unless he were prepared with a remedy. The remedy he suggested was to let the professors’ periodical examinations throughout the session count in the adjudication of position at the end of the session. It would be scarcely right, having said thus much about the two gentlemen who did not succeed, if he were not to add that in one of the two cases he knew why the competitor did not obtain a higher place, and in the other case he believed he knew the reason. In the one case the man was ill, and in the other case he thought lie had good evidence that instead of analysing a certain solution which hml been given to him, the man took up the wrong vessel and analysed something which had not been given to him. It was well known that he had great sym¬ pathy with men who failed at all kinds of examina¬ tions, because he knew it was not always their fault. Whether they failed because of such an accident as he had described or because they did not happen to be very well, or because they happened to have been educated at a school like his own, where the students were not so much prepared for examination as for the battle of life, and consequently, he was sorry to say, sometimes did not do very well at examinations; whatever the causes were, he had great sympathy with disappointed candidates, and he hoped this little suggestion with regard to his own work would have attention. The method might be carried further and deeper if the Council thought fit ; if so, he was sure that a large number of good men would cease to suffer from failure at examinations. The following is a list of students in this class to whom prizes have been awarded : — Silver Meclal . Bronze Medals Certificates of Merit ...Frank Harris Alcock. j Fredk. W almsley W arriclc \ Robert John Price, f Edward J arrett Eaton. | James B. Lillie Mack ay. q W illiam Inchle Gulliver. | Beresf ord F. H . Maudson. L Thomas Horton. The following were the questions for the exami¬ nation : — July 21 st and 22nd, 1879. Hours 10 to 5 each day. [Books and Memoranda permitted.) Standard number of Marks, 100. FIRST DAY. 1. The “solution” given to you may contain any of the ordinary metallic salts used in medicine ; analyse it, and state the result. 2. Is there any common poison in the “ vomit” placed before you ? SECOND DAY. 3. Examine the specimens of epsom salt, iodide of potassium, sulphate of quinia and distilled water supplied to you, and report on their quality. 4. How much nitrate of silver is present in one fluid ounce of the “ lotion ” given to you ? Note. — Manipulation as well as results will be scru¬ tinized. Report upon the Botany and Materia Medica Class. The President then, in the absence of Professor r Bentley, presented the report which that gentleman had sent in. He first read a letter which Professor Bentley had addressed to him, explaining that his October 4, i«79.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 271 1' ! official duties at King’s College, as Dean of the Medical Faculty, would prevent his being present that evening, and saying liow deeply lie re¬ gretted being deprived of the pleasure of meeting liis old students on that occasion as he had been accustomed to do for so many years. The Pro¬ fessor’s report stated that in the first course exami¬ nation he liadl9 candidates, the average marks being exceedingly good, some exceptionally so ; the three first obtained respectively 90, 80 and 77 tier cent., and 2 more 76 and 75. In the second course there were 6 candidates, 3 being specially worthy of dis¬ tinction, who obtained respectively 92, 82 and 75 marks. At the terminal sessional examination there were 14 candidates, the majority of whom passed through it very creditably, and the first three ob¬ tained exceptionally high marks. The following is a list of the students in this class to whom prizes have been awarded : — SECOND COURSE. RRONZE MEDAL. Hours from 10 till 1. 1. Describe the internal structure of an acrogenous or acotyledonous stem. 2. Define the following terms as applied to leaves : — Primordial, connate, decussate, equitant, crenate, serrate, lanceolate, obcordate, pinnate, and pinnatifid. 3. Describe the parts of a carpel ; and explain the terms simple and compound pistil, apocarpous and syn- carpous. 4. What are the botanical and geographical sources of sumbul ? Describe its general and chemical characters, and mention its official preparations. 5. What are the common adulterants of scammony, and how may they be detected ? 6. What do you understand by a balsam ? Describe the botanical source, collection, preparation and general and chemical characters of balsam of Peru, and mention any official preparation into which it enters as a con¬ stituent. Five Months’ Courses. Bronze Medal . Certificates of Merit FIRST COURSE. . James B. Lillie Mackay. I Fred. Wm. Ed. Shrivell. 1 Frank Harris Alcock. . . I James Edward Williams. ( Edward Jarrett Eaton. SECOND COURSE. Bronze Medal . Certificates of Merit .Thomas Horton. Henry William Drew. William Inchle Gulliver. Ten Months’ Session. Silver Medal . Certificates of Honour Certificates of Merit ...James B. Lillie Mackay. 1 Thomas Horton. ) Frank Harris Alcock. I Henry William Drew. ( Edward Jarrett Eaton. James Edward Williams. William Inchle Gulliver, j Fred. Wm. Ed. Shrivell. ] J ames Henry Allan. Percival C. Powrie. Isaac Leach. • The following were the questions for the examina¬ tions : — FIRST COURSE. BRONZE MEDAL. Hours from 10 till 1. 1. Describe the structure of a seed; and define the terms dicotyledonous, monocotyledonous, and acotyle¬ donous. 2. Describe the characters of ( a ) ordinary woody tissue ; ( b ) disc-bearing woody tissue ; (c) liber tissue ; and mention the plants and parts of plants where they are respectively found. 3. Describe the structure of a leaf-bud. Define the following: — Herb, spine, runner, rhizome, corm, bulb, tubercule and tuber. 4. What are the botanical and geographical sources of Alexandrian and East Indian sennas ? Describe their general and chemical characters and enumerate their official preparations. 5. What are the botanical and geographical sources of the official ipecacuanha ? Describe its general and che¬ mical characters, and show how it may be distinguished from the varieties of ipecacuanha known- as striated and undulated. 6. What are the botanical and geographical sources of asafeetida. How may it be distinguished from the other official gum resins of the Umbellifene, and what are its official preparations ? TEN MONTHS’ SESSION. SILVER MEDAL. Hours from 10 till 1. Botany. 1. Describe the structure of epidermal tissue. 2. Define the following : — Amentum, capitulum, cyme, thalamus, receptacle, disk, involucre, cupule, spathe, monoecious, dioecious, and corona. 3. Describe the several kinds of placentation, and give illustrations of natural orders in which they may re¬ spectively be found. 4. What is the nature of the fruit ? Explain the com¬ position of the following fruits : — Apple, strawberry, rose, acorn, fig, and pine-apple. 5. Distinguish the Composite from the Dipsacaceae ; and the Labiatse from the Scrophulariaceae and Bora- ginaceas. 6. Give the essential characters of the following natural orders : — Ranunculacese, Leguminosse, Umbellifene, Or- chidacese, Iridacese, and Liliacese. Materia Medica. Hours from 2 till 5. 1. Describe the general and chemical characters of Senega root. Mention the. roots which have been found mixed with it, and the means of distinguishing them. 2. What are the botanical and geographical sources of Ammoniacum ? Describe its general characters, the mode in which it is obtained, and its composition ; and , mention its official preparations. 3. How would you distinguish the official jalap resin from the resins of Tampico Jalap, Scammony, and Guaiacum. 4. What are the supposed botanical sources of the official Rhubarb root ? Describe its general and che¬ mical characters, and show how it may be distinguished from English Rhubarb root. 5. Describe the characters of the flowers of Anthemis nobilis ; and state how they may be distinguished from those of Matricaria Parthenium. 6. Describe the physical and chemical characters of Croton Seeds. Mention the differences between East Indian and English Croton oil, and give the dose and official preparations of Croton oil. Report on the Botanical Prize. The President read Professor Bentley’s report on the Herbarium competition. There were four collections submitted, the first of which was admir¬ able in every respect and included 800 specimens. For this he recommended that a silver medal should « be awarded to Mr. Thos. F. Perkins. The second, by Mr. Walker, which contained 600 specimens, was also highly to be commended, and eminently 272 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 4, 1&79 deserved the bronze medal ; and the third by Mr. Norman deserved a certificate of merit. The following were the awards : — Silver Medal . Thos. Frampton Perkins. Bronze Medal . Charles Walker. Certificate of Merit . William Francis Norman. The Council Examination Prizes. Mr. Southall, being next called upon to report on the examination for the Pereira medal and other Council examination prizes, said he appeared in a position very different from that of the gentlemen who had already addressed the meeting, inasmuch as he and his colleague, Mr. Moss, had had no opportunity of seeing and conversing with the students whose work they had examined, as the Professors had, but simply knew them by the mottoes attached to their papers. The examinations had been gone through in a satis¬ factory manner, showing that the competitors had paid great attention to their studies. The following are the names of the persons to whom the prizes have been awarded : — Pereira Medal ( silver ) ; and Books value £5, presented by Mr. T. II. Hills. Frank Harris Alcock. Pharmaceutical Society's Medal ( silver ) ; and Books value £3, presented by Mr. T. H. Hills. Marshall Leigh. Pharmaceutical Society's Medal ( bronze ) ; and books value [£2, presented by Mr. T. H. Hills. Henry Allen. The following were the questions for this exami¬ nation : — Chemistry. Time 10 to 1. Five only of the following questions must be at¬ tempted : — 1. Catalysis, Eremacausis, Fermentation, Putrefaction. Define these terms and give an instance in which each is correctly applied. 2. How would you perform the analysis of glass ? 3. What is a graphic formula ? Give such formulas of Phosphoric Anhydride and Acetic Acid. 4. Give reasons for representing Ferric Chloride as Fe2 Cl6, and not Fe Cl3, and Tartaric Acid as H2 C4 H4 06, and not HC2 H2 03. 5. What is an Alcohol, an Olefine , a Ketone , a Glycol, a Chlorhydrin, a Nitrile ? Give an example of each with formula. 6. What is the construction of Nicol’s prism ? De¬ scribe the effect produced upon a ray of light directed through its length. State also how light transmitted by one prism is affected by a second according to the re¬ lative positions of the two. Botany. Time allowed : Three hours. In framing answers Candidates should not enlarge upon the questions, but should confine themselves to giving, as briefly and clearly as they can, the information required. 1. Expain the processes of assimilation and metastasis in the living plant. 2. Describe the organs termed elaters and their func¬ tion, and mention the natural orders in which they occur. 3. Describe any special provisions you may be ac¬ quainted with for the fertilization of Orchids. 4. What are proliferous flowers, and what organs of plants are occasionally viviparous, giving examples of each ? Materia Medica. 1. Describe Myrrh, its chemical composition, the lo¬ calities whence it is imported, and the history of its use. 2. Give any information you may possess respecting the cultivation of Cinchona in India, and name the most valuable species and varieties. 3. What are Hermodactyls ? 4. What is Gurjun Balsam, and what is it remarkable for ? The President then presented the various prizes and certificates to the successful competitors, after which he called upon Mr. Taylor to state the result of the examination for The Jacob Bell Memorial Scholarship. Mr. Taylor said he had now for four years shared the duty of conducting this examination and he must again express, as he did last year, his surprise and disappointment that these prizes received so little attention and attracted so few competitors. Last year Mr. Williams, the then President, drew forcible attention to the value of these scholarships, in the hope that more would be induced to compete for them, but this year the number was one less than last. When it was considered that these scholarships were worth nearly all the other prizes put together, and that there were only eleven com¬ petitors, it could not but occasion a feeling of surprise as well as regret. Of these eleven, eight were from London and oneeachfrom Nottingham, Brighton and Manchester. The successful candidates were Mr. Wm. Elborne and Mr. John Thomas. These gentlemen acquitted themselves so well, and their testimonials from previous employers were so good, that his colleague and himself had no difficulty in submitting their names to the Council. He trusted they would avail themselves of the privileges they had obtained, and if they made as good use of them as previous Bell Scholars had done, they would become accomplished and useful members of society and reflect credit not only on the Society but on the name of the distinguished man in whose name these scholarships were founded. He could not sit down without saying that the third candidate, who took the motto Labor omina vincit, did his work so well, that he hoped, if eligible, he would try again. Bat no doubt there were dozens of young men now engaged in pharmacy, who could pass an equally good, if not better examination than those who had now succeeded, and considering that the scholar¬ ships were worth £30 each in money, together with free education and all the privileges the Society could afford, it was really astonishing that so few should compete for them. The President, after presenting the Bell Scholars with the books given by Mr. Hills, said he hoped that both the successful and unsuccessful competitors for the prizes which had just been distributed would be encouraged to renew their studies with zeal, and so prepare themselves, as Professor Attfield had expressed it, for the battle of life. They must remember that their education did not end here, and he hoped they would so extend it as to become ornaments both to society in general and to that Society in particular. They would be looked to for the future prosperity and honour of the Society. Those who had obtained the scholarships he would earnestly exhort to look at the bright example of their predecessors, and a very bright example was now be.fore them in Dr. Tilden, one of the earliest Bell Scholars; who had already greatly distinguished October 4, 1879.J THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 273 himself, and promised to distinguish himself still more. Let them as far as lay in their power follow in such footsteps. The successful candidates for these scholarships were ; — William Elborne and John Thomas. The questions set for this examination were as follows : — Time allowed : Three hours (12 to 3). LATIN. Translate into English : — 1. Turn vero omne mihi visum considere in ignis Ilium, et ex imo verti Neptunia Troja : Ac veluti, summis antiquam in montibus ornum Quum, ferro accisam crebisque bipennibus, instant Eruere agricolse certatim ; ilia usque minatur, Et, tremefacta comam concusso vertice, nutat ; Volneribus donee paullatim evicta supremum Congemuit, traxitque, jugis avolsa, ruin am. Descendo, ac, ducente deo, flammam inter et hostis Expedior : dant tela locum, flammseque recedunt. 2. In Extractis prseparandis, nisi aliter indicatum sit, humorem balneo aquoso in patina quamprimum consume, sub finem assidue spathd, movens, donee crassitudo sit ad pilulas fingendas idonea. Grammatical questions on the above : — 3. Parse visum, verti, veluti, ornum, accisam, instant, tremefacta, concusso. 4. Explain the cases of ignis, ferro, agricolce, volneribus. ENGLISH. 1. Parse fully : — The real strength and security of governments in these days lie in public opinion formed and enlightened by free discussion. 2. Write a short essay on Peace. ARITHMETIC. 1. Simplify 2^ + 721 + 316^ + 2-875. 2. A person sold '15 of an estate to one person and then jy of the remainder to another person. What part of the estate did he still retain ? 3. If 9 men or 15 women, working 10 hours a day could reap a field in 8 days 6 hours, in how many days of 10 L hours each could 10 men and 12 women reap a field one-fourth larger ? 4. Express a gallon in litres, and a kilometre in yards. FRENCH AND GERMAN.* Translate into English : — Plusieurs furent pris, blesses, ou tues, ou entraines loin du roi par la foule qui se jetait sur eux: il ne restait que cinq hommes auprbs de Charles : il avait tue plus de douze ennemis de sa main, sans avoir regu une seule blessure par ce bonheur inexprimable qui jusqu’alors l’avait accompagn£ partout, et sur lequel il compta toujours. Enfin un colonel nomme Dardof se fait jour k travers des Calmouks avec seulement une compagnie de son regiment : il arrive a temps pour d^gager le roi. And : — Il s’est efforce de connaltre Dieu, que par sa grandeur est inconnu aux hommes, et de connaltre l’homme, qui par sa vanity, est inconnu h, lui-mOme. Or : — Er starb endlich auf einer italieaischen Reise in der Stadt Mantua, im drei uml siebeuzigsten Jahre seines Lebens, und im Vollgenuss seines Iiuhms, nachdem er hatte besessendas Vertrauen seines Kouigs vierzig Jahre ununterbrochen. * The candidate is at liberty to choose either Freuch or German, and is not required to show a knowledge of both. And : — Nach Frankreich zogen zwei Grenadier, Die waren in Russland gefangen, Und als sie kamen ins deutsche Quartier, Sie liessen die Kopfe hangen. CHEMISTRY, PHARMACY, AND BOTANY. Time allowed : Two hours (4 to 6). 1. Describe the process for the manufacture of com¬ mercial oil of vitriol. What is Nordkausen sulphuric acid, and how can it be prepared ? 2. Acidum liydrochloricum, B.P.,has a specific gravity 1’16, and contains 31 ’8 per cent, by weight, of hydro¬ chloric acid gas. How many fluid ounces of the B.P. acid can theoretically be prepared by the decomposition of one pound of pure chloride of sodium by means of sulphuric acid ? 3. Give the official process for making ferri phosphas, with any remarks you may consider suitable. 4. State what you know concerning rectified spirit and proof spirit. How can a spirit 60° over prottf be reduced to proof spirit ? Name a few tinctures made with rectified spirit, and give reasons for its employment in those tinctures. 5. Give the Pharmacopoeial process for making injectio morphise hypodermica, suppositoria morphia}, tinctura opii and syrupus papaveris. 6. What is thistledown ? Describe the inflorescence of the oat. 7. Give an account of the germination of an almond, and describe the tissues of which the bark of an exo¬ genous stem is composed. The President then called upon Dr. Tilden to deliver the — Inaugural Sessional Address. Ladies and Gentlemen, — The Council of the Pharmaceutical Society of Great Britain has done me the honour to request that I would address a few words to the assembled students on this interesting anniversary. Those who have preceded me in this position upon corre¬ sponding occasions have been, every one of them, men older in years than myself, of wider knowledge and experience, and above all distinguished practi¬ tioners of pharmacy; but, I think the Council did wisely to engage, once in a way, the services of one who, whilst retaining distinct and pleasurable re¬ collections of his association with pharmaceutical students, has in the course of events so far severed connection with the pharmaceutical body that he can look upon their proceedings from the standpoint of an outsider. Notwithstanding misgivings as to my individual fitness for the post, I did not hesitate to accept the invitation of the Council, because I was anxious to testify to all my good friends here my reciprocatiou of the kind feelings which led to the proposal. I had no better way of expressing my thanks than to accede to the request. We are met together, as every one present is aware, for the express purpose of doing honour to the students attending the courses of instruction in this institution. In the name of the Council, the Pro¬ fessors and Officers of the Society, I have first of all to express to those students who have just received their prizes at the hands of the President, most hearty congratulations upon the success with which their labours have been crowned, and to wish them prosperity in the career upon which they are now about to enter. Gentlemen, you are justly proud of the honours which are the reward of your industry. You are justly gratified at the approbation of your friends. You have listened, I doubt not, with 274 THE r H ARMACEUT1CAI , JOURNAL AND TRANSACTIONS. [Obtober 4, 1^7?. quickened pulse to the praises pronounced by your professors. You have received the applause of this great meeting. I am sure that the memory of these things will abide by you, and when, in future years, some of you may appear as spectators at a renewal of this scene to celebrate the successes of those who will come after you, you will all feel stirred, as we do to night, with a sympathetic triumph. There is another class of students, for the moment less distinguished, but in general equally deserving of respect. I mean the students who have not re¬ ceived prizes — to whom, I feel also, every one present will desire that I should say a few words of encouragement. Do not despair, my friends, because you have no trophies to carry away with you. If you have worked steadily, with an honest desire to learn, you have gained that which will serve you more use¬ fully in the battle of life than prize-books or certificates. You carry with you the recollection of conflicts with self, of struggles against difficulties apparently insuperable, of encounters with tempta¬ tion in which you have come off victorious, and these experiences, added to even a moderate amount of professional knowledge, will make good and useful citizens of you. But my belief is that we may anticipate something even better than this. When I look back through the prize-lists of past years, I see there many names that have since become dis¬ tinguished in the ranks of pharmacy, and when I remember that in the competition for prizes there is often but a small, and sometimes a scarcely dis¬ cernible difference between the merits of the best man, who gets the prize, and the second best man, who does not get it, I feel satisfied that of the majority of the students of this institution we have not heard the last when they take their leave of the place. But I must not forget, gentlemen, to urge upon you all, whether prize-takers or not, the importance of seriously and systematically continuing your studies. I do not mean to say that I would advise everyone to go on working away at the whole range of subjects to which your attention has been directed in your progress through this school. It is now the time when each of you may follow the bent of his own inclination. I do not say I hope you will choose chemistry or botany or therapeutics, or any other branch of science in particular, but I am myself deeply impressed with the necessity for a reasonable interest, call it a “ hobby” if you like, to every reasonable man. And I ask you to take my word for it there is no prophylactic so potent, no remedy so sure, against the inevitable weariness which sooner or later overtakes the mere idler or seeker after pleasure. Some of you probably think you have learnt a great deal since you came here, ltelatively to your former state of ignorance that is no doubt true, but after all what you now know by comparison with what you have yet learn is a mole-hill to a moun¬ tain. Do not suppose I wish to disparage. This is merely the condition of everyone in this room, pro¬ fessors (if they will forgive my saying so) and all, and the wisest man is he who recognizes this some- what humiliating fact the soonest, and does his best to add to his little heap. What is the use of all this ? I will tell you pre¬ sently some of the so-called practical uses, but in the meantime I want just to remind you that increased knowledge will give you a treasure which, in one way at least, is better even than a good balance at the bank. It will give you self-respect. I do not mean conceit, that peculiar and special vice of half- educated people. I mean by self-respect that kind of self-knowledge which enables a man to estimate his own powers at their true value, avoiding, on the one hand, exaggerated distrust on the score of defects perceived and, on the other hand, undue exaltation by reason of conscious ability. But I would impress upon you young pharmacists the importance of finding your “hobby,” if possible, in your business. If you make your business the real occupation of your life it will certainly yield you a harvest not merely of internal satisfaction, a reward rich enough in itself, but tangible advantages such as commend themselves to the commercial mind are equally certain to accrue. This is true of every calling in life. It is almost a truism. But in its special application to pharmacy I want to speak a few words. The old-fashioned pharmacist, repre¬ sented in my memory by the late Henry Deane, was a man with a soul, but not above his business. I know that, happily, some of the race remain. Such a man knows the contents of every bottle and drawer in his shop, not merely in regard to cost and retail price, but the entire history and precise quality of each particular sample. He buys no concentrated abominations whilst the roses, long innocent of any tint but brown, moulder in their dusty corner. His aromatic waters are distilled and have no acquaintance with calcined magnesia. He has his own views on the proper season for the preparation of liquor taraxaci and makes it with his own hands. He knows what medicinal plants grow in his own neighbourhood, and he prefers to make his own extracts of henbane and conium. I spare you the rest. You know how much more I might say, but if you have any doubt whether this kind of thing pays look round at any such men you can find and judge for yourselves of their prosperity. But there is another aspect of the same question. Some years ago a remarkable paper was read at the Pharmaceutical Conference by Mr. Joseph Ince. Everyone present will understand that I refer to the essay on “ Pharmaceutical Ethics.” In that paper Mr. Ince did not hesitate to declare unre¬ servedly that “ pharmacy is a trade,” and in a meet¬ ing which included many of the most able, and not a few of the most influential of living pharmacists, there was no dissentient from that view of the matter. So far as I am able to judge, and in spite of Acts of Parliament since devised to regulate the practice of pharmacy, the occupation of the phar¬ macist is not materially changed since 1866. But it appears to my humble judgment that this dictum of Mr. Ince’s, whilst absolutely and literally true, does not cover the whole of the facts of the case. The pharmacist is a tradesman, but interwoven with his trade is a multifarious system of transactions in¬ volving the employment of knowledge and skill, gathered through the somewhat prolonged course of training, which at present culminates in the exami¬ nations of this Society. And it is a question in my mind whether the ideal pharmacist ought to be purely a tradesman. When the time comes, as I believe it will come, and perhaps very soon, the pharmacist who desires to do so will be in a position to make his election , between a kind of business represented by the shop October 4, 1879 ] THE PHARMACEUTICAL JODRNaL AND TRANSACTIONS. 275 s I on the one hand, the mere drug store bringing ac¬ cording to the accounts of the grumblers neither honour nor profit ; and on the other hand a calling in which he will have due exercise for what pro¬ fessional skill he may possess and gather his income somewhat in accordance with the customs prevailing in other professions. But this will not be done by railing at the law, the public, or the doctors. A young man having passed his examination, whether it is the Minor or the Major, is not entitled on that account to regard himself as an unrecognized and unrewarded benefactor of the human race. He has sulfered all this toil and expense, not I apprehend for the good of mankind, but because he knows there is at the end of it a monopoly, such as it is, of a certain calling reserved for him by the law. I know the reply which is almost upon the lips of some of my hearers. Look at the state of trade, look at the cheap drapers and grocers, who destroy all one’s profit, and then the co-operative stores ! Let us look at this calmly for a few minutes. So far and so long as the pharmacist is a trader, he must take with other traders the chances of competition and the stores, and he must submit to the neglect of what is called “ society.” I know not what may be the end of all this, and I question whether in this room there is a prophet who is qualified so far to prophesy. But it is perfectly clear to my mind that no amount of remonstrance, be it never so reasonable, no amount of reproach, be it never so vehement, will prevent the public from supplying themselves in any way which the fashion of the moment renders the most acceptable. It appears to me that the pharmacist will be more likely to improve his position by stedfastly pro¬ moting the cause of higher education, and by main¬ taining an attitude of dignity in that professional citadel in which he cannot be assailed, and into which, sooner or later, I believe he will not only be obliged to retreat, but will find it his best interest to do so. In plain English what does all this mean? I figure to myself a time when the pharmacist will leave to his neighbour, the grocer, the sale of such commodities as starch, mustard, pepper, cigars, British wines, aerated waters, quack medicines, and all such trumpery ; when he will no longer dispute with the hairdresser the trade in toothbrushes, pomade, and shaving soap, and will no longer think it necessary to deck his pharmacy with glittering smelling bottles or chest protectors in bright array ; when the plate glass front shall disappear from without, and the counter with at least half the mysterious, and often meaningless, gold labels from within. But I know that all this sounds unpractical, if not impossible. I admit that it is very largely so at the present moment, but not, I venture to think, in the immediate future. I am aware that after taking away from the pharmacist the whole or nearly the whole of his trade, the residue of pure pharmacy and dispensing practice remaining over would, in too many cases, be sadly unproductive of income. Although these should undoubtedly constitute the chief avocation of the pharmacist, yet I may be permitted to remind you that the chemist and druggist and the pharmaceutical chemist have contrived to secure to themselves the patent of a title which Sir Humphry Davy himself, unless he happened to be on the pharmaceutical register, would not now be suffered to use unchallenged. Does not this suggest something? It point?, I think, unmistakably to a development which the pharmacist, with due qualifications, has within his reach. Who so well fitted as he, by his special training, to become the public adviser upon all questions connected with sanitary affairs, to inves¬ tigate cases of poisoning or adulteration? What is there to prevent him from in time supplanting the half-informed medical officer of health, and the too often incompetent public analyst ! If he wishes to get a further stamp put upon his qualifications, either for his own gratification or for the satis¬ faction of his clients, there is the Institute of Chemistry realy to examine him. I should be taxing your patience too severely if I were to attempt to enter into further detail upon this topic which, however, appears to me to be worthy the deliberate and serious consideration of all phar¬ macists, but more especially of you students who are about to commence your professional career. I do not say you are driven to anything of the kind I have endeavoured feebly to picture. If you prefer it, or find it advantageous in the pursuit of that indispensable commodity, a sufficient income, or for other reasons find no escape from the pre¬ valent form of general business, no one can question your right to do as you think fit ; but I ask you as reasonable men whether you can be j ustly surprised that a generally ignorant, always unreasoning ami careless public, should fail to appreciate at their due value professional services performed, and profes¬ sional opinions pronounced behind a barricade of little articles that would find their appropriate place in an Italian warehouse or a fancy bazaar. But my task is only half accomplished. I should be neglecting a most important part of my duty if I omitted to address myself to those who are- about to commence or to continue their studies to-morrow. There is but one golden rule for the student, and that is, learn all you can and learn it thoroughly. Some there may be here who feel disposed to question the utility of all this chemistry and botany that the pharmaceutical student is now expected to learn. I can only assure you that if you will but wait patiently you will discover in time a practical application for every scrap that you can gather of this seemingly superfluous knowledge, and wish you had more. When it was my fortune to have to do with pharmaceutical students they were invariably most earnest, painstaking and in¬ dustrious, and I have no doubt that these qualities still form their most prominent characteristics. They were, however, liable to one or two little weaknesses which I dare scarcely hope have since disappeared. My attention was very frequently drawn in those days to a disposition to regard every question from the so-called practical point of view, a certain degree of restlessness being too often mani¬ fest when anything like general theoretical questions came to be discussed, unless they happened to bear in the most direct and unmistakable manner upon some subject of every day life. I do not mean to imply that this is a peculiarity of pharmacists or of pharmaceutical students, but merely that they arc not free from this which is the characteristic error of most practical men. I remember a speaker upon some occasion, I cannot now remember the who, when or where, took upon himself to declare that there was no such thing as 'pharni'iceutioai chemistry. Such an expression sounds a little startling, but the 276 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 4, 1879. meaning of the speaker was probably this, that the broad principles of science remain the same no matter what application yon propose to make of them, and that without a knowledge of these prin¬ ciples you may know the whole of materia medica from beginning to end and yet be absolutely igno¬ rant of chemistry ; you may be familiar with the name and even with the aspect of every ilower of the field and have no claim to be considered a botanist. Science does not consist in mere manual dexterity, neither does it consist in a knowledge of any number of hard names. One of the most serious consequences of neglecting all but what lies close at hand is this, that whilst you may learn to perform with the most punctilious accuracy all kinds of individual operations, you remain almost as incapable as ever of coping with any unexpected difficulty, and you are quite unable to assist in making the advances which pharmacy, in common with every other human art, must continue to make if it is to survive1 There is just one other topic, in conclusion, to which I must advert. We have all heard a great deal in this room and elsewhere about that ugly word “cram.” Now whilst I sympathize with nearly all that has been said and written upon the subject, and whilst I deplore the existence of a system so de¬ structive, I think there has been just sufficient am¬ biguity in the use of the term to make some students feel the denunciations rather too wholesale and some¬ what indiscriminate. There are two sorts of “ cram.” The one is both foolish and dishonest. But although, I suppose, we must admit that it is sometimes practised by candidates for pharmaceutical examinations, I have so much confidence in the skill and experience of our Board of Examiners, that I do not believe the system meets with greater success here than at other institutions, or even so great. I need not enter now into details because the subject has been discussed over and over again ad nauseam. But I would just suggest to those young men who propose to devote that portion of their time which should be spent in the acquisition of knowledge to the invention of schemes for cheating the examiners, that it will be to their own interest to credit the examiners with just a little common sense as well as knowledge of their business, or they may find out to their disap¬ pointment that the Board is not made up, as they fondly suppose, of a pack of idiots like themselves. The legitimate process,- on the other hand, is that kind of cramming to which every student must resort if he wishes to pass a given examination safely and honourably. This process consists in nothing less than learning very thoroughly the subjects in which he is to be examined, and for the time, no others. It seems to me unreasonable to complain of a student because he declines to make the attempt to study the whole of a text-book, of botany for example, when the board before whom he is to present himself for examination has pre¬ viously announced that it intends to examine him in a portion only of that subject. It may fairly be assumed that the limit has not been fixed without due deliberation, and if the student honestly sets to work at the task assigned, that is all that can be expected of him. One cannot be said to know a subject well unless he is prepared to answer clearly and intelligently any reasonable questions that may be put to him in that subject, and therefore the most mportant thing to aim at is precision, without which a great deal of knowledge may become worse than useless for the purposes of examination, and let me add of practical life. From all which you will perceive that I am one of those persons who, whilst recognizing the possible harm that may befall that rare phenomenon, the extraordinary genius, by reason of the existence of the examination system, yet hold the opinion that in the influence of the system upon the cause of education the good decidedly predominates. To candidates for examination let me add one hint. Supposing the student to have attained to an accurate knowledge of the subject, or that part of it in which he is to be examined, what reasonable grounds ca there be for that excessive nervousness displayed by some candidates ? If I were an ex¬ aminer, a candidate in this condition would excite my suspicions at once. I should either suppose the nervousness assumed, with the object of deceiving me, or I should credit him with a knowledge of de¬ fects apparent to his own consciousness, though hidden from mine. And now, Gentlemen, I need not detain you any longer. You are about to enter upon a period in your career, at once the most interesting and the most delightful. One word of caution. You all start off, I know, with a great stock of resolutions and good intentions. Take care they are not all wasted at the outset. In commencing an ascent the experienced mountaineer will start soberly, and pur¬ sue, at a steady pace, the path previously determined upon. The unskilful only tries short cuts, exhausts himself by spurts, or loiters, with the notion that it will be time enough to make up lost ground later in the day. Be advised in time. You have in your professors experienced and able guides. Follow them, act upon their instructions as to your journey, and do not be lured from the open path by people who tempt you with vain promises to relieve you of your labour. We who have climbed the same heights will watch your progress with unfailing interest. We know what are the difficulties you are likely to encounter and how they are to be sur¬ mounted. But we know, also, that the labour must be your own. The President proposed a vote of thanks to Dr. Tilden for the admirable and practical address which he had just given. While it contained excellent advice to the younger members of the meeting, he was quite sure there was no one present, even as old as himself, who would not be benefited by a careful consideration of it. The Vice-President said such a resolution really required no seconder, but he hoped he might be excused if he added a word or two, for two reasons. In the first place, they would wish to express in the most emphatic way their appreciation of Dr. Tilden ’s kindness, and therefore, perhaps, it would be appro¬ priate that he, in his official position as Vice-President, should second the vote of thanks. Secondly, he was probably better acquainted than many present with Dr. Tilden’s claims to their gratitude. Dr. Tilden had for several years occupied a very important scientific position in the locality with which he was himself con¬ nected, and consequently he knew the work Dr. Tilden had been doing there, and the high position he had taken. Under such circumstances it might not un¬ reasonably have happened that Dr. Tilden might have forsaken pharmacy altogether ; but that was October i, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 2 77 not so. In his own endeavours to advance scientific tific pharmacy he had constantly received the greatest possible assistance from Dr. Tilden, who had helped forward the work with his large knowledge and high scientific attainments in a manner which no other gentleman could possibly have done. There¬ fore, when that gentleman now came forward to de¬ liver his address to the students who were aiming to sustain pharmacy in its highest role they must not regard it as a spasmodic effort on his part, but as the last of a long series of acts all tending in the same direction. The motion having been carried by acclamation — Dr. Tilden said it had given him great pleasure to appear there on that occasion, and he esteemed it an honour to receive the invitation of the Council. They would easily understand that he might have acquitted himself better if he had been called upon at a somewhat earlier date, because, coming tenth or twelfth in a succession of men who had occupied a similar position, it became increasingly difficult every year to say anything worthy the acceptance of the meeting. A.nd when it was remembered that the best men were always selected first, it would be seen that those who came later had an additional difficulty to contend with. There were probably many parts of his address which might require further elaboration and explanation than he had been able to give, in order to make his meaning accept¬ able to members of the Society, and he felt that he had to some extent taken a liberty in attempting to express himself on some of the topics on which he had touched, but he hoped that any imperfections of that kind would be excused, for his intentions cer¬ tainly were of the best. The meeting then adjourned to Wednesday, November 5. fktrmnqal ©raiusautions. LIVERPOOL CHEMISTS’ ASSOCIATION. The Annual Meeting of the thirtieth session of this Association was held in the Royal Institution, September 25, 1879. The president, Mr. T. Fell Abraham, in the chair. The minutes of the last general meeting were read and confirmed. The donations to the library were duly acknowledged. The following annual report of the coun¬ cil and the treasurer’s financial statement, which showed a balance in hand of £13 15s. 3d., were read. Annual Report. “ In presenting the Annual Report of the Thirtieth Session of the Liverpool Chemists’ Association, your Council has pleasure in observing the renewed energy and increased scope of usefulness which characterize the pro¬ ceedings of the session now closing. “ Twenty-four new members and thirteen associates were elected during the past session, fourteen members and four associates have retired from various causes, leaving the number at present on the list 172 — consisting of 17 honorary members, 130 members, and 25 associates. “ There were eleven general meetings held during the session, the time of each being fully occupied with papers of chemical, pharmaceutical, or general scientific interest, whilst many important subjects were discussed under the head of miscellaneous communications. “There has been a marked improvement in the attendance of members and associates at the meetings. This, comibned with a more general activity, appears to your Council a very encouraging sign. The Council is glad also to report that your fourteenth Conversazione proved itself a very successful and enjoyable entertainment, whilst financially it yielded a credit balance to the general fund. The Asso¬ ciation is indebted to the several members who rendered their services, to the exhibitors of the numerous objects of interest, and in particular to Mr. Edward Davies, F.C.S., F.I.C., for his exceedingly interesting lecture on ‘ Phos¬ phorescence and Fluorescence.’ “ The Association, as in the previous year, took part in the holding of the Second Associated Soiree of the Literary, Scientific, and Art Societies of Liverpool, and is indebted to Mr. Davies on that occasion also for the delivery of an entertaining and appreciated lecture. “ The School of Pharmacy was provided with courses of lectures on Chemistry by Mr. Thomas Williams, F.C.S. ; Botany, by Dr. Shearer; and Materia Medica, by Dr. Carter. Eight pharmaceutical students attended the Chemistry Class, and, at the close, an examination was held, under the superintendence of the President. The questions were kindly supplied by Professor Attfield, who also adjudicated the answers, deciding in favour of Mr. John Albert Jones, who will this evening be awarded the President’s prize. “ The syllabus for the forthcoming Chemistry Classes has been already issued. The lectures on Materia Medica and Botany will be announced in due course. “ Several donations of books and pamphlets have been added to the Library during the session, and some periodicals and journals have been bound. Various specimens have also been contributed to the Museum, including a complete series illustrative of sugar refining, from Mr. J. T. Armstrong, F.C.S. The re-arrangement of the contents of the Museum has made some progress. The issue of books from the Library amounted to 445 volumes, in addition to references. “ Invitation having been received to send delegates to the British Pharmaceutical Conference, held at Sheffield, the President, Vice-President, Treasurer, and Mr. A. H. Mason, F.C.S., were appointed and attended. “ The ballot at the concluding general meeting for the appointment of President for the thirty-first session resulted in the election of Mr. Charles Symes, Ph.D. “ Mr. Armstrong having resigned his seat on the Council in consequence of removal from the neighbour¬ hood, Mr. Thomas Garside, F.C.S., was elected in his place. “ The following members of Council retire by rotation, and are eligible for re-election : — Messrs. T. F. Abraham, E. Davies, T. Garside, and T. Williams.” It was moved by the president, seconded by Mr. E. F. Morton, and carried unanimously, that “The reports as read be adopted and together with the list of members and abstract of proceedings of the past session be printed and circulated among the members.” It was proposed by Mr. J oseph Hallawell seconded by Mr. A. Watt, F.C.S., F.I.C., and carried unanimously, that “The best thanks of the meeting be given to the donors to the Library and Museum, to the authors of papers and to the exhibitors of apparatus, etc., during the past session.” It was proposed by Mr. T. H. Johnson, F.C.S., F.I.C., seconded by Mr. Henry Burroughs, and carried unani¬ mously, that “The best thanks of this meeting be given to the officers and council for their services during the past session.” The president’s prize of books offered to the student in the chemistry class who should pass the best written examination was produced, having been awarded on Pro¬ fessor Attfield’s adjudication to Mr. John Albert Jones. The meeting then proceeded to the election of four mem¬ bers of council. Messrs. Edward Davies, F.C.S., F. I.C., Thomas Garside, F.C.S., Alexander Watt, F.C.S., F.I.C., and Thomas Williams, F.C.S., were declared duly elceted. 278 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 4, 187P. favlianifiitarg and Jfaui ^rocmlings. Prosecutions under the 17th Section of the Pharmacy Act, 1868. At the Blackburn Borough Police Court, on Friday, September 26, 1879, before Messrs. E. Wharton (chair¬ man) and W. Hopwood, Stephen Green, drysalter and patent medicine vendor, appeared in answer to a sum¬ mons charging him with unlawfully selling poison. Mr. Henry Glaisyer, solicitor, Birmingham, appeared in support of the summons, being instructed by the Che¬ mists and Druggists’ Trade Association of Great Britain. He said the summons was issued by Mr. William Frederic Haydon, the Secretary of the Association, under the pro¬ visions of the 17th section of the Pharmacy Act, 1868, which said — “It shall be unlawful to sell any poison either by wholesale or by retail unless the box, bottle, parcel, wrapper or cover in which such poison is con¬ tained be distinctly labelled with the name of the article and the word ‘ poison,’ and with the name and address of the seller of the poison ; and any person selling poison otherwise than is herein provided shall upon a summary conviction before two justices of the peace in England be liable to a penalty not exceeding £5 for the first offence, and for the purposes of this section the person on whose behalf any sale is made out, an apprentice or servant, shall be deemed the seller.” Mr. Haydon came to Black¬ burn on .the 30th of July last, and visited the defendant’s shop in Bolton Hoad and purchased a pennyworth of oxalic acid, a pennyworth of white precipitate powder^ or ammoniated mercury, and a packet of rat poison, con¬ taining strychnine, all of them being poisons mentioned in the schedule to the Act and subject to its provisions. It was proposed to proceed only in one of these cases, that of the oxalic acid. The label on the packet con¬ tained only the word “ poison,” and therefore there were two particulars in which the statute had not been complied with. The name of the poison was not mentioned, and the name and addi*ess of the seller of the poison was not stated. The defendant was not a chemist, and was therefore unqualified to sell poison at all. A penalty is provided by the statute for selling poisons by unauthorized per¬ sons. but such penalty was not recoverable before the magistrates, and the defendant was charged on that occasion with having infringed the statute by not having labelled the packet in accordance with the provisions of the 17th section. Mr. Glaisyer, in continuation, drew attention to the fact that the business belonged to the defendant beyond a doubt, for his name appeared on a board over the door, and he had also paid rates in respect of the premises. The provisions of this statute were necessary in order to protect the public and afford a ready means of tracing where poison was obtained in cases where it was subsequently improperly used. The defendant pleaded guilty, and said he was sorry for doing wrong. He had been in the trade twelve years. The Chairman: You must have known you were doing wrong. Mr. Glaisyer : I may state for the information of the Bench that in consequence of the sale of poison being made in this way so frequently, the present proceedings have been instituted in order to make known the pro¬ visions of the statute. The Chairman (to the defendant) : This is the first case of this description that we have had in this court, and we shall be content if you pay a fine of 20s. and the costs. You are liable to a fine of £5 and costs. At the Liverpool Borough Police Court on Saturday, September 27, 1879, before Messrs. Henry Hugh Hornby and Edward Browne, justices of the peace, Mr. Bichard Bowland Minton and others, trading as K. B. Minton and Co., appeared in answer to a summons charging them that they did on the 6th day of August last, at the borough of Liverpool, unlawfully sell to William Frederic Haydon, at 135, St. James’s Street, certain poison, to wit, oxalic acid, in a certain packet, the cover of which packet did not set forth the name of the article or the name or address of the sellers of the same, con¬ trary to the provisions of the 17th section of the Act, 31 and 32 Viet., cap. 121. Mr. Henry Glaisyer, solicitor, of Birmingham, instructed by the Chemists aud Druggists’ Trade As¬ sociation, appeared in support of the summons. The defendant appeared in person. Mr. Glaisyer, in opening the case, said that the defendants were the partners in the firm of Messrs. B. B. Minton and Co. They carried on an extensive business in this town, at Cheapside, and other establishments, as oil and colour merchants. The summons, as in the previous case, was issued under the provisions of the Pharmacy Act, 1868, 31 and 32 Viet., cap. 121, sec. 17, which he read . The facts of the case were shortly these : — Mr. Haydon, the secretary of the Chemists and Druggists’ Trade As¬ sociation, came to Liverpool on the 5th of August, and visited the defendant’s shop, 135, St. James’s Street, and there he purchased a pennyworth of oxalic acid, which is one of the poisons mentioned in the schedule to the statute. There was no label placed on the packet, but the word “ poison ” was written on it. There were therefore two particulars in which the section of the Act had not been complied with. There was no doubt the business belonged to Messrs. Minton and Company. Their name appeared on brass plates attached to the windows of the shop, and also on many articles in the shop, and in addition they were rated for the premises and had paid rates due in respect of them. Mr. Hornby: You say the word “ poison ” was written on the packet ? Mr. Glaisyer : The word “ poison ” was written on the packet, but not the other particulars. Mr. Goodwin, who appeared for defendant, said he did not dispute that defendant sold this article ; but it was a long time ago. Mr. Stubbs : What you have to say is in mitigation. Mr. Goodwin : We only wish to say it is not an article we generally keep ; we did not know in fact that it was in the shop. A young man got it to oblige a few cus¬ tomers. It is used by dyers principally, and is sold in very small quantities. It is quite an omission that the young man has not put a proper label on the wrapper. William Frederic Haydon, called, sworn, and examined, gave evidence bearing out the opening statement by Mr. Glaisyer. Mr. Goodwin: As one of the principals I might as well say we admit we are guilty in this matter. But really we were not aware the acid was being sold. We leave ourselves entirely in your hands. We will take care that in future nothing of the kind shall occur. I have no doubt we have transgressed the law. Mr. Hornby : The defendants are fined 10s. and costs. At the Birmingham Police Court, on Wednesday, October 1, 1879, before Messrs. Balph Heaton and Henry Wiggin, Joseph Guest Earp, oil and colour merchant, 22, Cheapside, Birmingham, was summoned by the Chemists and Druggists’ Trade Association of Great Britain, for a contravention of the 17th section of the Pharmacy Act, 1868, “by selling certain poison, to wit, oxalic acid, in a certain packet, the cover of which packet did not set forth the name of the article, or the name or address of the seller of the same, contrary to the statute in such case made and provided.” Mi\ Glaisyer appeared in this case, instructed by the Chemists and Druggists’ Trade Association of Great Britain, the information being laid by the secretary, Mr. W. F. Haydon. Mr. Glaisyer said the summons was issued under the provisions of the Pharmacy Act, 1868, 31 and 32 Viet., cap. 121, sec. 17 (as in the previous cases). The facts October 4, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 279 I of the case were shortly these: — Mr. Haydon visited the defendant’s shop, 22, Cheapside, Birmingham, on the 8th of August last, and there he purchased a pennyw orth of oxalic acid, which is one of the poisons mentioned in the schedule to the statute. The label placed on the packet contained the word “ poison ” only. There were therefore two particulars in which the section of the Act has not been complied with. There was no doubt the business belonged to Mr. Earp. His name appeared over the shop door, and in addition he was rated for the premises. The defendant : No doubt about it. Mr. Glaisyer: I am instructed to press for a heavy penalty, Mr. Haydon having in June, 1877, two years since, purchased poisons from the defendant, who was at that time warned that he was acting illegally. A month after that purchase, Mr. Haydon was told by an assistant of the defendant that Mr. Earp only sold poisons to persons he knew. In August last defendant sold the poison with which he was now charged. William Frederic Haydon, called and sworn, deposed to the above facts. In reply to a question, Mr. Haydon said that in J une, 1877, he purchased from the defendant oxalic acid and red oxide of mercury, both poisons scheduled under the Pharmacy Act, and this being so far as he was aware, the defendant’s first offence he reported the purchases to the Secretary and Registrar of the Pharmaceutical Society of Great Britain. He now produced a letter, dated July 5, 1877, which he received from the Secretary and Registrar of that Society, stating that he had written to the defendant giving him notice that if he continued to infringe the provisions of the Pharmacy Act, legal proceedings would be taken against him without further notice. In July of the same year, witness went to the defendant’s shop and again endeavoured to purchase oxalic acid, but was told by the assistant that they had ceased to sell poisons except to persons they knew as customers. The defendant : I have never been warned. The magistrates’ clerk to Mr. Haydon : The letter you have produced is not admissible as evidence that the defendant has been previously cautioned. The defendant : My foreman has omitted to put the name of the article and my name and address on the packet. We sell oxalic aoid to boot makers, and for cleaning brass. The magistrates’ clerk to Mr. Haydon : Have you cautioned the defendant yourself ? Mr. Haydon : I have not. Mr. Heaton, addressing defendant : You have not conformed to the Act of Parliament. It requires that you should put the name of the poison upon the packet, also your own name and address. Had it been clearly proved that you had been cautioned previously, we should have inflicted the full fine. You must, however, pay 20s. and costs. The Sale op “ Fever Powders.” On Tuesday, September 30, the Deputy Coroner for East Sussex (Mr. J. E. Fullagar) held an adjourned inquest at the Bridge Hotel, Newhaven, on the body of Elizabeth Ellen Young, a little girl aged four years and eleven months, who was supposed to have died under suspicious circumstances. - Mr. Edward Henry Moore deposed that he was the public analyst for the county of Sussex. He received from P. S. Renville a packet containing twelve powders. They bore a label, indicating that they were “ Welch’s Fever Powders,” and professing to be prepared by Henry Moon, Trafalgar Street, Brighton. They were in six sets of two powders each, professing to be suitable for different ages of children, and there was a blank space on the labels for the age to be filled in. The different sets were for cases of children from six to eight years of age, four to six years, three to four years, two to three years, one to two years, and four to seven months. He had made an analysis of the powder, and had found that the composition was entirely sugar and calomel. He had further assured himself of the absence of those mineral poisons which, from their appearance, would be likely to be mistaken for calomel, viz., antimony, arsenic, a possible impurity of calomel, and bichloride of mercury. Taking the powders generally, the proportion of calomel was 1 to 3 grains. The difference in the weight of the powders, as presumably for the same age, was in eight cases out of ten exceedingly marked. In the two powders for children from three to four years of age there was a difference of weight of three-quarters of a grain, representing a variation of one-quarter of a grain of calomel. 1 he variation averaged in the eight powders from 12 to 25 per cent. In all cases of variation the proportion of calomel to sugar was fairly sustained. In the two powders for four to six years there was a varia¬ tion of half a grain, one weighing 4^ grains (Lj grain calomel), and the other 5 grains (Ingrain calomelf. The greatest difference was noticeable in the powders for children of from six to eight years, where there was a variation of 1 grain in weight. The two powders, one to two years, and the two from four to seven months were identical in weight. The first representing 4 grains to each powder, consequently containing If grain of calomel, and. the latter containing 27V grains of calomel. The powders from three to four contained If grain of calomel. Calomel was a difficult powder to mix with nice accuracy owing to its extreme weight as compared with its usual excipient. The difference of the weight of some of the powders was to such extent as to be sugges¬ tive to measuring rather than weighing. In his opinion the powders were imperfectly described as “ Fever Pow¬ ders,” and the use of calomel would be prejudicial in a case like the present. Police Sergeant Renville stated that he purchased twelve powders at Mr. Samuel Sargeant’s shop, on Tuesday evening last. Mr. Sargeant served him himself. The six sets, for different ages of children, were kept in six different boxes, which bore a label outside stating the age of the child for which the powder was intended. The packets containing the powder were all alike, and there was a blank space for the age to be filled in. Mr. Sar¬ geant filled in the ages on the twelve packets in witness’s presence. He sent them to Mr. Moore. Mr. T. M. Cann stated that he had made a post-mortem examination of the deceased, and found that death was due to inflammation of the bowels. A powder containing one and three quarter grains of calomel would tend to aggravate the symptoms instead of relieving them. That amount of calomel would not necessarily be too much for a child if it was administered by a medical man for certain diseases, but it was a highly injurious medicine for general distribution. In cases like the present it would increase the inflammation, but it would not be possible to ascertain where the natural inflammation left off, and the inflammation caused by calomel commenced. The powders were very improperly described as fever powders, for although calomel might be useful in certain special instances, it would be injurious in the great majority of fevers. This concluded the evidence, and the Deputy- Coroner then summed up, remarking that one good result of the inquest would be that parents would be warned against buying a powder which they might imagine to be a cooling or aperient medicine, but which in reality con¬ tained a very dangerous ingredient. In this case it had not been proved that death was caused through the taking the powder, especially as evidence had been given showing that a portion of the medicine was vomited, but at the same time these so-called fever powders were being extensively used, and might produce very injurious effects. Apart from the dangerous nature of the powder itself, he considered that the packets were sold in a manner which 280 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 1 [October i, 1879. might very easily lead to a serious blunder. The en¬ velopes containing powder of different strengths were precisely alike, and it would be a very easy mistake to sell them out of the wrong box, or to get the packets in the different boxes confused. If the jury were of opinion that death could not be traced to anything else but natural causes, it would rest with them, if they thought fit to do so, to append a rider expressing their opinion concerning the indiscriminate sale of dangerous medicines. After some consideration, the jury returned a verdict of “Death from natural causes,” and added the following rider : — “ The evidence discloses that a medicine fit only for skilled application is being indiscriminately sold and administered by incompetent persons, and the jury are of opinion that the sale and preparation of medicines con¬ taining dangerous ingredients should be restricted to duly qualified persons, and the active ingredient of such medicines should be stated on the wrapper in which the medicine is contained.” — Brighton Gazette. Trading by Government Clerks. Sir, — I am sorry to see that the retail traders in London have again been making themselves ridiculous by holding a meeting in Exeter Hall. They seem to have attempted to make capital out of the presence of a provincial mayor, who expressed disappointment at the smallness of the number of representatives. I know nothing of that gen¬ tleman’s social status at home, but I suspect that he felt anything but flattered with the society in which he found himself in Exeter Hall. From the small number who attended it seemed to be inferred that retail traders are lukewarm as to the effect upon their businesses by competition with trading establish¬ ments conducted by the clerks in the service of the govern¬ ment. The fact is they feel the grievance very keenly, but they have no power at the present to grapple with it. As a body they are men of sense and judgment and bear their grievance quietly rather than mix themselves up with such as gave evidence before the Royal Commission or those who constituted the conference at Exeter Hall. I have watched the progress of the stores with some in¬ terest and I have observed with regret the ill-judged action taken by a certain class of retailers to counteract their progress. I admit the perfect freedom of every one to pur¬ chase hi3 requirements in any market which may be most to his fancy and I think no one denies the right of fair and legitimate competition in business which gives stimulus to enterprise, and at the same time offers every facility for enabling the public to spend their money to the best ad¬ vantage. As regards the establishment of trading concerns con¬ ducted by the clerks in the employ of the government I maintain without fear of contradiction that the system is an illegitimate and dishonorable innovation upon the vested interests of a very large and important section of the tax- paying community, a system altogether uncalled for by the requirements of the public and utterly unjustifiable, as it aims to subvert interests which are national and to set up no compensating interests in their stead. Government clerks, ■whether active or pensioned, are in every sense of the word the servants and dependents of the public; al¬ though they are not under the immediate control of the public, their salaries and pensions are paid out of the earn¬ ings of the public through those whom the latter entrust with the custody of their welfare. As such the clerks in the employ of the government have neither legal nor moral right to do anything detrimental to the interests of any portion of the community. What would be thought of an individual taking service under another and taking advan¬ tage of some hitch in his contract to use the advantages of his position for his own benefit and to the detriment of his employer. Yet the government clerks now engaged upon the stores are in exactly the same position. They may be under no contract prohibiting them from such proceedings, but that arises only from the fact of such restrictions not having been previously required. Circumstances alter cases and what would be considered actionable at, if not punishable by law in an individual, seems to be justified in this case by the social status of those engaged in it. I cannot but feel surprised at the keen patronage bestowed upon the stores by many landed proprietors and clergymen of the Church of England, although I must admit there are many exceptions. I see landed proprietors and clergymen whose rents and tithes are realized in the neighbouring market towns spend as little of their money as possible in those towns, but supply their establishments from the stores, although their predecessors and even they themselves at one time seemed to have no idea of spending their money except in their own neighbourhood. Of course every one is perfectly at liberty to spend his money where he thinks- proper, but I would ask such if that is an equitable appli¬ cation of the principle “ live and let live.” I have also’ been surprised at the favourable attention bestowed upon the stores by professional men such asjawyers and doctors. Now these gentlemen as a rule are dependent for their incomes upon the personal feeling of the community around them, and yet I know several who are stealthily keeping their household from the stores. It is not difficult to bring such gentlemen to their bearings, as tradesmen clients have only to transfer their patronage to such as spend their money at home. I have seen the principle applied in two cases with electrical effect ; one had the chagrin of seeing a younger rival pocket an account of close upon fifty pounds which he would have received himself, but for the careful housekeeping of his good lady, and 1 saw another visibly cringe under the same process from a like cause ; few can afford to lose practice any more than traders can afford to lose business. In my day the best feeling existed amongst the town tradesmen towards the county families and the feeling was reciprocated ; now I am sorry to see that a stand-off feeling is gaining ground and that owing to nothing which has- taken place between them, but from the habit of the latter to take advantage of the illegitimate system of trading in¬ augurated by the clerks in the government offices. Now, sir, it is admitted that the antagonism of class against class in the case of capital and labour is a national misfortune. Is it desirable then that division should be still further increased by setting the middle and upper classes against each other, and that at the instigation of a small body who were unknown and possessed no influence until they com¬ menced their system of trading and gave it influence by combining with it a state title? The clerks in the government offices have a perfect right to co-operate in supplying themselves with the necessaries of life, but they have no right whatever to extend their operations beyond their own immediate class as they are now doing. They are not only supplying their own wants, but they are increasing their salaries by taking advantage of facilities which were never intended for such a purpose and at the expense of a class who are heavily taxed to support the expenses of the state, part of which, no matter what proportion, are the salaries and pensions of active and retired clerks in the employ of the state. Promoters of stores may say what they like about the small percentage of the business of the country which they do, but that is not the point. The question to be decided is, Are the clerks in the government offices to be allowed to receive salaries at the expense of the public and at the same time to be allowed to embark in business to the detriment of those out of whose earnings their salaries are paid?. I think that the subject only requires to be brought fairly before the government and the system can admit of no defence. To those who are already so engaged I would give a certain time, say three years, either to withdraw their connection or to resign the service of the state, al¬ though they have no claim to consideration on account of vested interests. The remedy is in the hands of the retail traders'; a general election is close at hand and they have sufficient influence to demand the support of a measure for such a purpose. A LOOKER-ON. Communications, Letters, etc., have been received from Messrs. Leslie, Moscrop, Rogers, Siebold, Brayshay, Hall, Need, Shillcock, Tanner, Evans, Burrell, Rusticus, Ele¬ vator, Ph. Chemist and Dentist, Nostrum, Ink, Chemist and Dentist, Analyst for the County of Surrey, Student, Eboracum, Potassium, X. Y. Z., A. B., F. W. S. G., J. S., R. W., H. P. October 11, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 281 NOTES ON INDIAN DRUGS. BY W. DYMOCK. (Continued from page 123.) Ophioxylon Serpentinum, Linn., Apocyne.®. — The root. Vernacular : Chota-chand (Hind.) ; Chan¬ dra (Beng.) ; Harkai (Bomb.) ; Patalagandhi (Tel.). History , Uses, etc. — This shrub is mentioned in Sanskrit works under the name of sarpagandha. The Hindus use the root as a febrifuge and as an antidote to the bites of poisonous reptiles ; also in dysentery and other painful affections of the in¬ testinal canal. By some it is supposed to cause uterine contraction, and promote the expulsion of the foetus. Ainslie gives the following account of it : “ Tsjovanna amelpodi is the name given on the Malabar coast (‘ Rheede Mai./ vi., 81, t. 47) to a plant the bitter root of which is supposed to have sovereign virtues in cases of snake bites and scorpion stings ; it is ordered in decoction to the extent of a pint in twenty-four hours, and the powder is applied, ex¬ ternally, to the injured part. The plant is the radix mustela of Rumphius (‘ Amb.’ vii., 29, t. 16). The Javanese class it among their anthelmintics, and give it the name of puli pandak. It may be found noticed both by Burman, in his ‘ Thesaur. Zeylan.’ (t. 64), and Garcia ab Horto (‘ Hist. Aromat.’) ; the latter recommends it as stomachic. Rumphius speaks of it as an antidote to poisons, and Bontius, in his ‘ Hist. Mat. Med. Ind.’ tells us that it cures fever ” (‘Mat. Ind.’ ii., 441). In the Pharmacopoeia of India its use in labours to increase uterine contraction is noticed, upon the authority of Dr. Pulney Andy, but we have no evi¬ dence of its efficacy in such cases. In Bombay most of the labourers who come from the Southern Concon keep a small supply of the root, which they value as a remedy in dysentery and other painful affections of the intestines. * Description. — Root crooked, tapering from half an inch in diameter downwards. Bark soft, corky, marked by longitudinal fissures, light brown ; wood brittle, showing rings and medullary rays, visible to the naked eye. Taste very bitter ; odour of the fresh root acrid. Microscopic structure. — The suber upon transverse section presents the appearance of a piece of honey¬ comb, viz., alternate rows of long tubular cells and compressed scales. The inner portion of the bark consists of a delicate parenchyma, loaded with starch, and traversed by indistinct medullary rays. The wood is remarkably starchy. The root is not an article of commerce. The Allamanda Aubletii (Cathartica, Linn.), Apocyne®, is said to have been introduced into India from Brazil by the Portuguese. It has become quite naturalized, and in some places has run wild. Though not used in India, it has a medicinal reputation, the leaves being considered a valuable cathartic in moderate doses, especially in the cure of painter’s colic ; in overdoses it is said to be violently emetic and purgative. Ainslie has a short notice of the plant, and mentions its use at Surinam by the Dutch as a cathartic. It is a beautiful climbing shrub, very common in Bombay gardens. The leaves are elliptic, lanceolate, and arranged in fours round the stem on very short petioles. The flowers are large, yellow, Third Series, No. 485. and funnel shaped, and are borne at the ends of the branches. It has no native name, but the gardeners call it peula, which simply means yellow. Carissa corundas, Linn., Apocyne®. The root. Vernacular : Karonda, Karaunda (Hind ) ; Karwand Karinda (Bomb) ; Karamcha (Beng.) ; Kalaka (Tam.). History, Uses, etc. — This very common shrub, called in Sanskrit, karamardaka, is remarkable for its white jasmine-like flowers, which have a powerful odour, and for its purple-black fruit, which, unripe, is so much used by Europeans for preserving. The natives also use the unripe fruit for pickling. It is described in native works on materia medica as astringent, and the ripe fruit as cooling, acid, and useful in bilious conditions. The root has a reputation as a bitter stomachic, but I have no experience of its use. Description.— Roots long, brown and scabrous; wood very close grained and tough. The greater part of the bark consists of enormous stony cells, often more than an inch in length, flat, and closely packed together, forming a network round the wood, through the interstices of which the soft parenchyma comes in contact with the cambium layer. The odour of the root is disagreeable, and the taste acrid and slightly bitter. The fruit in size, shape, colour, and taste is not unlike a damson. Strychnos potatorum, Linn.fil., Loganiace®. The seeds. Vernacular : N irmali (Hind., Beng., Bomb.) ; Tetran-Kottai (Tam.). History, Uses, etc. — This seed, in Sanskrit kataka or ambuprasada, has been in use in India from the earliest ages for the purpose of clearing muddy water. It is mentioned by Susruta in his chapter on water. One of the seeds is usually rubbed hard for a short time round the inside of the earthen pot, into which the water is afterwards poured and left to settle ; the impurities subside and the water re¬ mains clear and tasteless. Medicinally nirmali rubbed down with honey and camphor is applied to the eyes to strengthen the sight and prevent lacryma- tion, it is also Used in ulceration of the cornea and purulent discharge from the conjunctiva (Confer. Chakradatta). Mahometan writers tell us that itis cold and dry and that when applied externally to the abdomen it relieves colic; they also notice its use to strengthen the sight, and as a remedy in snake-bite. The author of the ‘ Taleef-i-shareefee’ recommends it in irritation of the urinary organs and gonorrhoea. He directs four of the seeds to be powdered and mixed with a little curd of milk, to be tied up in a piece of cloth and steeped in water during the night. The infusion is to be taken in the morning. Ainslie says, “The fruit, though when very young it is made into a preserve and eaten, is reckoned, in ts mature state, amongst the emetics of the Tamool doctors in Southern India ; given in powder in the quantity of about half a teaspoonful.” The clearing nut has a place in the secondary list of the Pharma¬ copoeia of India, and is there said to be used as a remedy in diabetes on the authority of Kirkpatrick A suggestion is also made that the nut would be of use if supplied to troops marching in the rainy season, when little but muddy water can be procured. Dr. Pereira ( Pharmaceutical Journal, 1850, vol. ix.. p. 478) suggests that the property of clearing water 282 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 11, 1879. possessed by these seeds depends upon the albumen and casein which they contain. If the seeds be sliced and digested in water, they yield a thick mucilaginous liquid, which when boiled, yields a coagulum (albumen), and by subsequent addition of acetic acid, it furnishes a further coagulum (casein) (Confer. ‘Phar. of India,’ p. 146). Description. — The seed is nearly orbicular button¬ shaped, about h an inch in diameter and \ inch thick; round the border is a slightly prominent ridge, which makes the junction of the two portions of albumen constituting the bulk of the seed. At one point a slight irregularity of the ridge marks the situation of the radicle; from this runs a faintly pro¬ jecting line to the umbelicus, which is central and well marked ; a hardly perceptible depression marks the opposite side of the seed. The integuments are yellowish grey and covered with fine silky hairs. The albumen homy but not quite so hard as that of nux vomica. The embryo consists of a club-shaped radicle and two delicate heart-shaped cotyledons. The albumen is tasteless. Microscopic structure. — The hairs have a similar structure to those of nux vomica, and show the same play of colours with polarized light. Strychnos colubrina, Linn., Loganiacea:. The root ami ivood. Vernacular : Naga-musadi (Tel.) ; Modira-coniram (Mai.) ; Kuchila-lata (Hind., Beng.) ; Goagari-lakri (Bomb.). History, Uses , etc. — This scandent strychnos is supposed to be the arbor ligni colubrini of Rum- phius, who states that it is used in J ava as a febrifuge and anthelmintic and also externally in certain skin diseases. Horsfield notices its use in cutaneous affections and to alleviate the pain and swelling from confluent smallpox. Ainslie says that it is the dund-ul-sini of Avicenna ; but this I think must be incorrect, as dund is the name given in Arabic works for Croton tiglium. Virey,inhis£Histoire Naturelledes Medicaments,’ p. 191, informs us thatbois de coulenore in an overdose occasions tremors and vomiting, but mentions at the same time, that in smaller doses it may be considered as a useful vermifuge, and be givtfn also with advantage in obstinate quartan agues. Guibourt considers that S. colubrina yields the true lignum colubrinum, or pao de cobra of the Portuguese, but he is unable to decide whether the wood usually found in commerce is produced by this tree or by S. nux vomica. (Confer. Guibourt, ‘Hist. Nat.’ ed 1869, vol. ii., p. 527.) Lts claims as an antiperiodic have been examined by Dr. Berdenis Van Berkelow (Schmidt’s ‘ Jahrbucher,’ May 24, 1866, and ‘Brit, and For. Med. Chir. Rev.,’ April ,1867, p. 527.) ; and after a trial with it in twenty-two cases, quartan and tertian, he reports favourably of its action, and con¬ siders that from its cheapness it may advantageously be used as a febrifuge. In Bombay shops, two kinds of lignum colubrinum (goagurree-lakri) are met with ; the genuine and least common is the wood of 8. colubrina the other that of S. nux vomica; both are much used by the Hindus on account of their tonic properties in dyspepsia and malarious affections. In the dyspepsia of vegetarians preparations contain¬ ing strychnia are particularly efficacious. I usually prescribe the extract of nux vomica in half grain doses and find that it has all the virtues of the lignum colubrinum. Description. — The smaller branches with the bark on, form the goagurree-lakri of the shops. The general structure of the bark resembles that of nux vomica, but it is of a rusty colour, and the small warts upon it instead of being pale are of a bright rusty brown. The pieces of wood vary in size and length, and are much more knotty and crooked than those of nux vomica. The texture of the wood is also closer, harder, and of a deeper colour ; when touched with nitric acid it turns of a reddish orange. Microscopic structure. — The bark is thicker than that of nux vomica, but resembles it in structure, with the exception that the zone of stone-cells is wider and more irregular, and the cells themselves are bright yellow, and larger. (See microscopic structure of nux vomica bark). PlIYLLANTHUS NIRURI, Linn., PHYLLANTHUS URIN¬ ARIA, Linn, EupiiorbiacE/E. The plants. Ver¬ nacular: — (P. niruri), Jaramla (Hinch), Bhui- amla, (Beng.), Bhui-aunla (Bomb.), Kizhkay- nelli (Tam.), P. urinaria bears the same names with the addition of the adjective red. History, Uses, etc. — These plants are common weeds which appear in the rainy season. The name bhumyamlaki, which occurs in Sanskrit works, is probably applicable to both. Hindu physicians consider P. niruri to be deobstruent, diuretic and healing ; they prescribe the dried plant in powder or decoction in jaundice. The dose of the powder is about a teaspoonful. Meer Muhammad Husain in his ‘Makhzan’ tells us that the milky juice of P. niruri is a good application to offensive sores and that a poultice of the leaves with salt cures scabby affections of the skin ; without salt it may be applied to bruises, etc. From Ainslie we learn that these two plants are the Herbce niceroris alba and rubra of Rumphius, and that an infusion of the leaves of P. niruri with fenugreek seed is considered a valuable remedy in chronic dysentery; also that the leaves are a good stomachic bitter. In Bombay P. niruri is used as a diuretic in gonorrhoea and acidity of the urine. Description. — P. niruri, annual, erect-branched ; branches herbaceous, ascending, floriferous ; branch- lets filiform ; leaves elliptic, mucronate, entire, glabrous ; male and female flowers in separate axils, male on the lower ones ; dehiscence of anthers transverse, glands in the female bifid and trifid ; capsule globose, smooth, two seeds in each cell ; seeds triangular (‘ Bombay Flora ’). P. urinaria. — Root ; generally annual, though in some soils bi- and even perennial. Stem erect, striated, of a pale reddish colour. Branches several, ascending, striated from the insertions of the stipules. Leaves scattered, spreading, pinnate, from one to two inches long, flower bearing. Leaflets alternate, linear, oblong, entire, smooth, three-fourths of an inch long, and one-fourth broad. Petioles com¬ pressed, somewhat triangular. Stipules of the petioles three-fold, acute, membranaceous ; those of the leaflets two, lateral. Male flowers, exterior leaflets axillary, two to three, subsessile. Calyx, nec¬ tary and stamens as in P. niruri. Female flowers, lower leaflet axillary, solitary, sessile. Calyx and nectary as in the male. Capsule scabrous, three-celled, six-valved. Seeds two in each cell, transversely striated on the outside. It is immediately dis¬ tinguished from P. niruri by its sessile flowers and scabrous capsules (Roxb.). (To be continued). October li, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS 283 THE DIGESTIVE FERMENT OF CARICA PAPAYA.* BY A. WURTZ AND E. BOUCHUT. The analyses of Vauquelin and the observations o^ Cossigny, Bajon, Endlicher, Peclcholt, Roy, and Mon* corvo, concerning the digestive action of the juice of the papaya, induced one of the authors to obtain some of this product from America, and submit it to a number of experiments which have been carried out during two years in the H6pital des Enfants Malades. These have been recently completed from a chemical point of view in the laboratory of the Faculty of Medicine. The liquid juice which flows from incisions made in the tree is neutral and milky. It coagulates immediately and separates into two parts, a kind of insoluble or slightly soluble pulp, and a colourless and limpid serum. Juice which had been sent to the authors had undergone alteration which was manifested by a putrid odour. In this the butyric ferment was discovered. In order to protect the juice from this change some was sent mixed with sugared water or glycerine and aromatized with some drops of oil of peppermint. In this state it appeared as a thick milky liquid, without any odour suggesting fermentation. Put into contact with raw meat, fibrin, boiled white of egg or gluten it attacked and softened them after a few minutes, and eventually dissolved them after a digestion of some hours at 40° C. Milk is coagu¬ lated at first and the precipitated casein is afterwards dissolved. The false membranes of croup, removed by tracheotomy, and worms, such as ascarides and tseniae, are attacked and digested in a few hours. Without doubt this juice contains a digestive ferment analogous to that which is secreted by the carnivorous plants, Nepenthes, Drosera, and Darlingtonia , to which Messrs. Darwin and Hooker have called attention. It is known that Messrs. Gorup-Besanez and Will have separated from this juice a kind of vegetable pepsin. The following is a description of the experiments made to recognize the nature and mode of action of the digestive ferment which exists in the Carica Papaya, and which appears to be more active than that secreted by the above-mentioned plants : — (1). The milky liquid described above was thrown upon a filter and the gelatinous precipitate washed several times with distilled water. The solution, with the wash waters added to it, was reduced to a small volume in a vacuum, then mixed with ten times its volume of absolute alcohol. A white precipitate was formed which was left in contact with the alcohol during twenty-four hours, then collected on a filter and dried in a vacuum. There was thus obtained a white amorphous matter that was entirely and easily soluble in water. The aqueous solution was again precipitated with alcohol, and the new precipi¬ tate, washed with absolute alcohol, was dried in a vacuum. In this state, the product obtained appeared under the form of a white amorphous powder, completely soluble in water, a property that indicates the absence of vegetable albumen, coagulable by alcohol. According to a preliminary analysis, this body, which is a ferment, contains 10‘6 per cent, of nitrogen. Its concentrated aqueous solution possesses a slightly astrin¬ gent taste, becomes slightly turbid upon boiling, gives with alcohol an abundant precipitate and is precipitated by nitric acid, an excess of which dissolves the precipitate, forming a yellow liquid. Acetate of lead and tannin form with it abundant precipitates. 0 J gram of ferment, precipitated once by alcohol, was dissolved in 50 c.c. of distilled water, and the neutral solution digested at 40° C. with 10 grams of moist fibrin. At the end of ten hours the fibrin was dissolved except a residue weighing 1*5 gram in the moist state. 0*1 gram of ferment precipitated once by alcohol, was dissolved in 50 c.c. of water, and the solution, rendered slightly alkaline by caustic potash, was digested at 40° C. * Read before the French Academy of {Sciences, Aug. 26, 1879 ( Comptes Rendus , vol, lxxxix., p. 425). with 10 grams of moist fibrin. At the end of ten hours the fibrin was dissolved, except a residue of dyspeptone. The filtered liquid, slightly alkaline, gave a precipitate with acetic acid; it was also precipitated by nitric acid and became turbid upon boiling. The conversion into peptone was not complete. 0T5 gram of ferment, precipitated once by alcohol, was added to 10 grams of moist fibrin reduced to a thick jelly with 75 c.c. of water acidulated by of hydro¬ chloric acid. This jelly, heated in a stove to 40° C., liquefied in a quarter of an hour. At the end of two hours the whole was reduced to a turbid liquid. The finely divided precipitate remained in suspension in the liquor and presented ’the appearance of dyspeptone of fibrin. Its weight was T8 gram in the moist state and 0'48 gram when dry. The filtered liquid gave a preci¬ pitate with nitric acid. 0*1 gram of ferment, precipitated twice by alcohol, was added to 20 grams of moist fibrin and 150 c.c. of water and the whole heated in a stove to 40° C. during twenty- four hours. At the end of that time the fibrin was dissolved, except a residue weighing 2*5 grams in the moist state. The digestion was not prolonged because the liquor manifested signs of putrefaction. The filtered solution was coagulable by heat and precipitable by nitric acid. In this experiment, made with a neutral liquid, as in that which was made with one slightly alkaline, the fibrin dissolved without swelling. The flocks at first softened, preserving their form and volume, and were disintegrated by dissolving ; there remained a I’esidue of dyspeptone. It results from the preceding experiments that the nitrogenous matter precipitable by alcohol from the aqueous juice of the papaya possesses the property of dissolving large quantities of fibrin, and is distinguished from pepsine by the character that it dissolves fibrin, not only in the presence of a small quantity of acid, but even in a neutral or slightly alkaline medium. This ferment the authors designate under the name of “ papaine.” (2). The carefully washed pulp from which the aqueous liquid containing the papaine had been separated was submitted to long washings with distilled water. These wash waters, having been evaporated in a stove at 40° G. and reduced to a small volume, gave with alcohol a pre¬ cipitate that dissolved fibrin under the same conditions as the papaine precipitated directly from the aqueous juice. This experience gave rise to the thought that the soluble ferment might have its origin in the action of water upon the pulp, which itself has very decided digestive pro¬ perties, and which possesses, even after long washing, a slightly acid reaction. However, this point is reserved, for the pulp to which it refers is difficult to wash and only yields to water very slowly the soluble ferment it retains. It is besides very aqueous : 54 grams of this pulp left upon evaporation only2-5 grams of a solid residue having a gummy appearance. 20 grams of this pulp, well washed with water and containing 0*9 gram of^dry substance, were put to digest, at 40° C., with 56 grams of moist fibrin and 200 c.c. of water. The digestion was prolonged during forty-eight hours, some drops of prussic acid being added to prevent putrefaction. The fibrin was completely dissolved : the weight of insoluble residue was inferior to that of the pulp introduced. 10 grams of well washed pulp (leaving after drying 0‘ 43 gram of solid matter) were digested at 40° C. with 17 grams of moist fibrin and 50 c.c. of water, with the addi¬ tion of one drop of hydrocyanic acid. The whole was dissolved at the end of twenty hours, save a residue weighing 3 grams in the moist state, or 0*71 gram after desiccation. The filtered liquid gave no precipitate with nitrio acid. In these last experiments there was not only solution of the fibrin but transformation into peptone, i.e., com¬ plete digestion. The filtered liquid, having been con- 284 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 11, 1 8; ». centrated in a stove, gave with alcohol an abundant precipitate, which collected at the bottom of the vessel in clots of gummy appearance and presenting all the cha¬ racters of peptone of fibrin. It was entirely dissolved in water, and the aqueous solution was not coagulated by heat; it gave no precipitate either with nitric acid or with ferrocyanide of potassium added to acetic acid. Heated with an excess of nitric acid, it gave a yellow liquor (xanthoproteic acid). With acetate of lead it gave a slight turbidity, with tannin an abundant precipitate. Diluted with water it gave with picric acid a yellow pre¬ cipitate soluble in an excess of peptone and in a great excess of water or picric acid. This is, according to M. Henninger, a very delicate reaction of fibrin peptone. The alcoholic liquors from which the papa’ine had been precipitated were distilled in vacuo at a low temperature and put into contact with fibrin and water. The fibrin was not dissolved; the ferment had been entirely preci¬ pitated by the alcohol. It results from these experiments that Carica Papaya contains an energetic digestive ferment that can be easily isolated. THE ACTION OF HEAT IN VACUO ON METALS.* BY T. A. EDISON. In the course of my experiments on electric lighting I have developed some striking phenomena arising from the heating of metals by flames and by the electric current, especially wires of platinum, and platinum alloyed with iridium. These experiments are in progress. The first fact observed was that platinum lost weight when heated in a flame of hydrogen, that the metal coloured the flame green, and that these two results con¬ tinued until the whole of the platinum in contact with the flame had disappeared. A platinum wire four- thousandths of a inch in diameter, and weighing 306 mgrms., was bunched together and suspended in a hydro¬ gen flame. It lost weight at the rate of a fraction less than 1 mgrm. per hour as long as it was suspended in the flame. When a platinum wire is stretched between two clamping posts, and arranged to pass through a hydrogen flame, it is coloured a light green ; but when the tempera¬ ture of the wire is raised above that of the flame, by passing a current through it, the flame is coloured a deep green. To ascertain the diminution in the weight of a platinum wire when heated by the electric current, I placed between two clamping posts a wire five-thousandths of an inch in diameter, and weighing 266 mgrms. This wire, after it was brought to incandescence for twenty minutes by the current, lost 1 mgrm. The same wire was then raised to incandescence ; for twenty minutes it gave a loss of 3 mgrms. Afterwards it was kept incan¬ descent for one hour and ten minutes, at which time it weighed 258 mgrms. — a total loss of 8 mgrms. Another wire, weighing 343 mgrms., was kept moderately incan¬ descent for nine consecutive hours, after which it weighed 301 mgrms., showing a total loss of 42 mgrms. A plati¬ num wire twenty-thousandths of an inch in diameter was wound in the form of a spiral one-eighth of an inch in diameter and one-half an inch in length. The two ends of the spiral were secured to clamping posts, and the whole apparatus was covered with a glass shade 2^ inches in diameter and 3 inches high. Upon bringing the spiral to incandescence for twenty minutes that part of the globe in line with the sides of the spiral became slightly darkened ; in five hours the deposit became so thick that the incandescent spiral could not be seen through the deposit. This film, which was most perfect, consisted of platinum, and I have no doubt but that large plates of glass might be coated economically by placing them on each side of a large sheet of platinum, kept incandescent by the electric current. This loss in weight, together # Paper read before the American Association for the Advancement of Science ; Saratoga Meeting. with the deposit upon the glass, presented a very serious obstacle to the use of metallic wires for giving light by incandescence, but this was easily surmounted after the cause was ascertained. I coated the wire forming the spiral with the oxide of magnesium, by dusting upon it finely powrdered acetate of magnesium : while incan¬ descent the salt was decomposed by the heat, and there remained a strongly adherent coating of the oxide. This spiral so coated was covered with a glass shade, and brought to incandescence for several minutes ; but instead of a deposit of platinum upon the glass, there was a deposit of the oxide of magnesia. From this and other experiments I became convinced that this effect was due to the washing action of the air upon the spiral ; that the loss of weight in and the coloration of the hydrogen flame were also due to the wearing away of the surface of the platinum by the attrition produced by the impact of the stream of gases upon the highly incandescent surface, and not to volatilization, as commonly understood ; and I venture to say, although I have not tried the experi¬ ment, that metallic sodium cannot be volatilized in high vacua by the heat derived from incandescent platinum ; any effect that may be produced will be due to the wash¬ ing action of the residual air. After the experiment last described I placed the spiral of platinum in the receiver of a common air-pump, and arranged it in such a manner that the current could pass through it, while the receiver was exhausted. At a pressure of 2 millimetres the spiral was kept at incandescence for two hours before the deposit was sufficient to become visible. In another experiment, at a higher exhaustion, it required five hours before a deposit became visible. In a sealed glass bulb, exhausted by a Sprengel pump to a point where a quarter of an inch spark from an induction-coil would not pass between points 1 millimetre apart, was placed a spiral, the con¬ necting wires passing through the glass. This spiral has been kept at the most dazzling incandescence for hours without the slightest deposit becoming visible. I will now describe other and far more important phenomena observed in my experiments. If a short length of platinum wire one-thousandth of a inch in diameter be held in the flame of a Bunsen burner, at some part it will fuse, and a piece of the wire will be bent at an angle by the action of the globule of melted platinum ; in some cases there are several globules formed simultaneously, and the wire assumes a zigzag shape. With a wire four-thousandths of an inch in diameter this effect does not take place, as the temperature cannot be raised to equal that of the smaller wire, owing to the increased radiating surface and mass. After heating, if the wire be examined under a microscope, that part of the surface which has been incandescent will be found covered with innumerable cracks. If the wire be placed between clamping posts, and heated to incandescence for twenty minutes, by the passage of an electric current, the cracks will be so enlarged as to be seen with the naked eye ; the wire, under the microscope, presents a shrunken appearance, and is full of deep cracks. If the current is continued for several hours these effects will so increase that the wire will fall to peices. This disintegration has been noticed in platina long subjected to the action of a flame by Prof. John W. Draper. The failure of the process of lighting invented by the French chemist, Tessie du Motay, who raised sheets of platinum to incandescence by introducing them into a hydrogen flame, was due -to the rapid disintegration of the metal. I have ascertained the cause of this phenomenon, and have succeeded in eliminating that which produces it, and in doing so have produced a metal in a state hitherto unknown, and which is absolutely stable at a temperature where nearly all substances melt or are consumed ; a metal which, although originally soft and pliable, becomes as homogeneous as glass and as rigid as steel. When wound in the form of a spiral it is as springy and elastic when at the most dazzling incandescence as when cold, and cannot be annealed by any process now commonly known, for the October 11, It r9.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS 285 cause of this shrinking and cracking of the wire is due entirely to the expansion of the air in the mechanical and physical pores of the platinum, and the contraction upon the escape of the air. Platinum as sold in com¬ merce may be compared to sandstone, in which the whole is made of a great number of particles with many air spaces. The sandstone upon melting becomes homo¬ geneous and no air spaces exist. With platinum or any metal the air spaces may be eliminated and the metal made homogeneous by a very simple process. This process I will now describe. I had made a large number of platinum spirals, all of the same size and from the same quality of wire ; each spiral presented to the air a radiating surface of three-sixteenths of an inch ; five of these were brought by the electric current up to the melting-point, the light was measured by a photometer, and the average light was equal to four standard candles for each spiral just at the melting-point. One of the same kind of spirals was placed in the receiver of an air-pump, and the air exhausted to 2 millimetres ; a weak current was then passed through the wire, to slightly warm it for the purpose of assisting the passage of the air from the pores of the metal into the vacuum. The temperature of the wire was gradually augmented, at intervals of ten minutes, until it became red. The object of slowly increasing the temperature was to allow the air to pass out gradually and not explosively. Afterward the current was increased at- intervals of fifteen minutes. Before each increase in the current the wire was allowed to cool, and the contraction and expansion at these high temperatures caused the wire to weld together at the points previously containing air. In one hour and forty minutes this spiral had reached such a temperature with¬ out melting that it was giving a light of twenty-five standard candles, whereas it would undoubtedly have melted before it gave a light of five candles had it not been put through the above process. Several more spirals were afterwards tried, with the same result. One spiral, which had been brought to these high temperatures more slowly, gave a light equal to thirty standard candles. In the open air this spiral gave nearly the same light, although it required more current to keep it at the same temperature. Upon examination of these spirals, which had passed through the vacuum process, by the aid of a microscope, no cracks were visible ; the wire had become as white as silver, and had a polish which could not be given it by any other means. The wire had a less dia¬ meter than before treatment, and it was exceedingly difficult to melt in the oxy-hydrogen flame. As compared with untreated platinum, it was found that it was as hard as the steel wire used in pianos, and that it could not be annealed at any temperature. My experiments with many metals treated by this pro¬ cess have proved to my satisfaction, and I have no hesita¬ tion in stating that what is known as annealing of metals to make them soft and pliable is nothing more than the cracking of the metal. In every case where a hard drawn wire had been annealed a powerful microscope revealed myriads of cracks in the metal. Since the experiments of which I have just spoken I have, by the aid of Sprengel mercury pumps, produced higher exhaustion, and have, by consuming five hours in excluding the air from the wire and intermitting the current a great number of times, succeeded in obtaining a light of eight standard candles from a spiral of wire with a total radiating surface of l-32nd of an inch, or a surface about equal to one grain of buckwheat. With spirals of this small size which have not passed through the process, the average amount of light given out before melting is less that one standard candle. Thus I am enabled, by the increased capacity of platinum, to withstand high temperatures, to employ small radiating surfaces, and thus reduce the energy required for candle light. I can now obtain eight separate jets, each giving out an absolutely steady light, | and each equal to sixteen standard candles, or a total of 128- candles, by the expenditure of 30,000 foot-pounds of energy, or less than one horse-power. As a matter of curiosity I have made spirals of other metals, and excluded the air from them in the manner stated. Com¬ mon iron wire may be made to give a light greater than platinum not heated. The iron becomes as hard as steel, and just as elastic. Nickel is far more refractory than iron. Steel wire used in pianos becomes decarbonized, but remains hard, and becomes the colour of silver. Aluminium melts only at a white heat. In conclusion, it may be interesting to state that the melting-point of many oxides is dependent on the manner of applying the heat ; for instance, pure oxide of zirco¬ nium does not fuse in the flame of the oxy-hydrogen blow-pipe, while it melts like wax and conducts electricity when on an incandescent platinum spiral which is at a far lower temperature ; on the other hand oxide of alu¬ minum easily melts in the oxy-hydrogen flame, while it only vitrifies on the platinum spiral. PILL COATING.* BY ROBERT H. DIMOCK. Pills without coat are, when freshly made, undoubtedly most active, but if kept for any length of time, grow hard and more or less insoluble. Mr. H. M. Wilder’s recommendation to keep them in mass and make them as required (as in the case of blue mass, and directed by the British Pharmacopoeia) is a good suggestion, but some inconveniences are connected with it which interfere with its general adoption. Inclosing or coating the mass, when freshly made in the form in which the pills are to be taken, and thus preventing drying and hardening, is an improvement ; and when we not only preserve the pills from deterioration through atmospheric influences, but also improve the appearance and conceal the taste, it would seem as though we had reached perfection. Still, there remains an opportunity for experiment to fill a want felt at the prescription counter ; we need a coating which can be applied to the fresh pill as soon as formed, and which will dry sufficiently in a few minutes to permit the pill being placed in a box. I hope to supply that need, in this paper, and think the process will enable any pharmacist to coat all the pills he dispenses with a permanent soluble coating. Sugar, as a coating, is very beautiful in appearance, and pills so coated are fairly active, when well made ; but the use of sugar-coated pills compels the druggist to depend upon the wholesale manufacturer, as with no means or machines can he coat, on a small scale, pills 'with sugar to compare in appearance with those in the market. The necessity for drying the pills, to prevent the discoloration of the sugar and allow perfect adherence of coating, and the time required to bake on the coating, removes sugar, when used alone, from those materials which may be employed at the prescription counter with economy of time. It seems hardly necessary to speak of resinous coatings, as apart from the insolubility of the resin the same dry, hard pill is needed as in the case of sugar. Dipping in gum, or sugar solution, and then rolling in either powdered starch, slippery elm, French chalk, etc., fails to produce a coating which I would take much pride in; the pill dries slowly, and when dispensed in an excess of powder without drying, complaints are raised that the coating adheres to the fingers or to the patient’s mouth, and that the pill tastes very bad. When thoroughly dry, I find these coatings very insoluble, more so than at first I would have thought possible. A mass for coating, composed of flaxseed, Irish moss and sugar (as recommended in the Druggists' Circular ) was tried, but was found to harden slowly and to mould easily, but to be very soluble. Gelatin has given me * From the American Journal of Pharmacy, September, 1879. 286 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October li, 187#. the best satisfaction, and more closely approaches, I think, what we want in a quick yet efficient coating, as pills can be coated while soft, the coating hardens quickly, is elegant in appearance and does not require much skill in applying. Among the disadvantages in its use should be mentioned insolubility of coating, if the gelatin has not been carefully selected ; moulding, if the coating is too thick ; stickiness of coating, from careless¬ ness about concentration of solution ; the time required and the trouble in handling the pills on needles ; inability to keep the mass ready for use, owing to decomposition, and the injury caused by successive heatings. Moulding of the gelatin, both in solution and on the pill, will be, to a certain extent, remedied by the addition of 10 grains salicylic acid in solution with 8 grains borax to 1 ounce gelatin and ^ ounce water. If the water- bath is made properly shallow, time will be saved in melting ; but the injury caused by heating the mass many times can only be obviated, I think, by using the solution described below. The time occupied in the hardening of the coat sufficiently for placing the pills in a box is not under fifteen minutes in the most favourable dry and cool weather, while in mine it will average ten minutes. Of the different kinds of coatings having gelatins for their base, Garod's consists of gelatin, 5 oz ; gum arabic, 3 oz. ; sugar, 2 oz. ; water, q. s. ; it does not harden as quickly as gelatin alone, and has not as bright and fine an appearance, but is very soluble. It has probably been suggested by the composition used for capsules. The coating most satisfactory to me, perhaps because originating with me, is made as follows : — Take of — Gelatin . 3vj Acid Acetic, No. 8 . f?i 5vj Spirit of Nitrons Ether . f 3j Granulated Gum Arabic . 5j Oil of Gaultheria . tn,y Dissolve the gelatin and gum in the acetic acid with the aid of a water-bath, then add the other ingredients, and mix. If the coating solution is to be used with needles alone, substitute for the gum two drachms more of gelatin. Keep securely corked in a wide mouth bottle. Make the pill mass a very little softer than ordinarily ; use as little powder as possible in rolling out ; when the mass is nearly brought to the proper length for cutting, lay a thread long enough to reach over the sides of the machine before the pill mass, then roll to the proper length and form pills by the machine. With some masses it may be necessary to cut with a sharp knife a slit in the top of the roll, then lay the thread in the slit and close by rolling. If the mass is of proper consistency and the machine handled right, every pill will be nicely formed and all connected by the thread. Then take hold of each end of the string of pills, shake off powder if there is any adhering, dip in the coating solution and twirl as though it was a toy buzz- wheel, which will throw off excess of coating ; then hang up by placing pins through each end of the thread and then into wood, and expose to as cool a draught of air as possible. When hard enough to place in the box, cut the thread close to each pill with a pair of scissors or sharp knife, thus leaving no hole in the coating ; the little piece of thread in each pill in length equal to the diameter of the pill should do no harm. Pills can be coated in this way, I think, in less time than by any other method. They compare favourably in appearance, solubility, etc., with pills coated with any other substance, or with the same substance in any other and longer way. With sufficient practice, every pill can be caught on the thread and neatly rolled without touching with the fingers ; twenty-four pills, or more, according to the size of the machine, can thus be coated as easily as one by the needle, as ordinarily used, and as a matter of course they dry quicker, as in coating with the needle the last pill coated will not be hard when the first is ready for the box. Even if at first only half the number of pills adhere on the thread, they may be coated as easily as one, and the remainder can be coated on the needles until the manipulator improves. Some of the advantages of this coating are that it is always ready for use — and thus injury caused by repeated heating is prevented — it does not mould or decompose, it drys or hardens quickly, can be applied to pills as soon as made, and when applied is more soluble than, gelatin alone. I would say, in conclusion, that I have been able by practice to make the thread work successfully on my machine, but there is, perhaps, enough of trouble in learning how, to make it doubtful that this method will be of general use ; still it is an idea which is freely given for what it may be worth. The coating may not be entirely new to others, but it is to me, and, as far as has been possible, I have reviewed the pharmaceutical literature on this subject. It may be capable of improve¬ ment ; and for such purpose, and for a trial of what I believe to be its advantages over other coatings, it is now placed before the profession. CALCIUM PHOSPHITE.* BY R. ROTHER. When sugar is added to saturation to a solution of calcium hypophosphite, the latter is precipitated. This fact is not generally known, and hence it is highly probable that a dense syrup of the mixed hypophosphites. contains little if any of the calcium salt. Therefore, only a moderately thin syrup is certain of representing the requisite amount of calcium as one of the components of the compound syrup of the hypophosphites. In the presence of iron a precipitate also forms, but the propor¬ tion of sugar has apparently no share in this change. The statement is circulated, but it is not clear on what authority, that ferric hypophosphite, when contained in such a syrup, easily reverts to the ferrous form by reason of the reducing action of the hypophosphorous acid. In view of this supposition, it was proposed to substitute the very soluble ferrous salt for the uncertain and diffi¬ cultly soluble ferric hypophosphite. This compound syrup is not, however, much in vogue. The writer once prepared such a syrup, but found, contrary to expectation, that the ferrous salt readily oxidized, even in the presence of sugar forming the dark green and very soluble ferroic (ferro-ferric) hypophosphite. Now, if the ferric salt suffered a reduction, it seems that this intermediate ferric compound would result without yielding a preci¬ pitate, unless the latter were occasioned by the generated phosphoric acid as calcium phosphate. The fact is, that ferric hypophosphite occurs in several modifications, of which the crystalline variety is next to insoluble in hypophosphorous acid, and hence it is this compound which deposits from the syrup. Having on hand a quan¬ tity of this sediment, the writer attempted to regenerate it by reducing it to the ferrous condition by the inter¬ vention of sulphurous acid. This treatment, however, resulted in an altogether unexpected reaction, wherein the sulphurous acid was decomposed into sulphuric acid, sulphur and oxygen ; the latter, reacting upon the hypo¬ phosphorous acid of the sediment, converted it into* phosphorous acid. The same result was obtained by mixing sulphurous and hypophosphorous acids together. In moderate concentration the precipitation of sulphur was instantaneous, but in dilute solutions this was pre¬ ceded by a transient yellow coloration of the liquid. When solutions of calcium hypophosphite and sodium sulphite are mixed calcium sulphite is precipitated. Th*e addition of chlorhydric acid to this mixture redissolves * From the Pharmacist for August, 1879. October 1M879]. THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS.' 287 the calcium sulphite ; but no further reaction sets in until both the hypophosphorous and sulphurous acids are entirely freed by the addition of enough chlorhydric acid. The evidence of the resumption of change appears in the production of the deep yellow solution above mentioned ; this persists for about five minutes, more or less, accord¬ ing to the degree of concentration, and is then followed by a copious deposit of sulphur, mixed with calcium sulphate. The yellow coloration is by no means due to nascent sulphur in solution. It is caused by the inter¬ mediate formation of hyposulphurous acid, H2S02 (not the thiosulphuric acid, H2S203, formerly called hypo- sulphurous). The decomposition of the sulphurous acid is complete in six or eight hours. The solution, after filtering off the sulphur, is but mildly acid, and yields, on the addition of ammonia, a crystalline precipitate of calcium phosphite. This precipitate, however, contains less than half of the phosphorous acid generated, owing to the fact that hypophosphorous acid is monobasic, whilst phosphorous acid is dibasic, and also that a small loss of calcium is incurred as sulphate. Therefore, the liquid filtered from the calcium phosphite, on being treated with calcium chloride, gives »n additional precipitate of calcium phosphite. But if the liquid filtered from the sulphur be treated with calcium carbonate, a much larger amount of calcium phosphite is thrown down than with ammonia. If after several hours the mixture is filtered, and to the neutral filtrate calcium chloride be added, a further precipitation of calcium phosphite takes place. The addition of a very little ammonia to the precipitate, with calcium chloride, always causes this to become more distinctly crystalline and to subside more rapidly. The calcium phosphite is most speedily and conveniently washed by decantation. Calcium phosphite is a white crystalline powder, which, when heated in a test tube, evolves spontaneously in¬ flammable hydric phosphide, accompanied by slight de¬ tonations. When raised to a certain temperature it suddenly becomes incandescent for a moment and then leaves a residue of calcium phosphate. When 60 grains of calcium hypophosphite are converted into phosphite by the addition of 180 grains of sodium sulphite, 120 grains of chlorhydric acid and 4 fluid ounces of water, filtration after a lapse of six or eight hours, exposure of the filtrate to dissipate excess of sulphurous oxide and final addition of ammonia, the yield is only 4075 grains ; but the amount of phosphorous acid pre¬ sent is sufficient to produce 97 '4 grains of the salt, as follows : — CaH4(P02)2 + 02 — CaH4(P03)o, or CaHP03 + H,POo, and CaH4(F02)2! (170) : CaHP03OH2, (138)::60?48-£ and as the quantity of calcium contained in the hypo- phosphite, as seen from the above, is only half enough to neutralize the phosphorous acid, giving theoretically but 487 grains of the phosphite, it is evident that the intro¬ duction of the requisite amount of calcium will afford double this, or 97’4 grains. The difference between 487 and 4075 grains is loss attributable to calcium sulphate and solubility of the phosphite. It appears that no phosphoric acid is generated, as decomposition of the precipitate with oxalic acid and treatment of the filtrate with ammonio-magnesian sulphate fails to give the characteristic precipitate. SPECIFIC GRAVITIES OF FATS, RESINS, ETC.* BY DR. H. HAGER. The author first describes a simple method for deter¬ mining these specific gravities . This consists in melting the respective fat, dropping it into a flat-bottomed vessel containing alcohol, in such a manner that the point from which the drops are allowed to fall is not over three centimetres distant from the surface of the alcohol, and that each drop be allowed to fall on a different spot. The fat globules thus deposited at the bottom are then removed to a liquid, consisting of either alcohol, water or glycerin, or mixtures of these, until after careful stirring and reduction or increase of the density, by the addition of one or another of the above liquids, the fat globules are held in equilibrium in any part of the liquid. The specific gravity of the latter is then determined, and this is, of course, at the same time the specific gravity of the fat. The author then gives a list of specific gravities, which is here reproduced : — Sp. gr. at 15—16* C. Butter Eat, clarified by settling , . 0*938 - 0*940 „ „ several months old . . 0*936 - 0*937 Artificial Butter . 0*924 - 0*930 Hog’s Lard, fresh . 0*931 - 0*932 „ „ old . 0*940-0*942 Beef Tallow . 0*925 - 0*929 Sheep’s Tallow . 0*937 — 0*040 Beef and Sheep’s Tallow, mixed 1 :1 . 0*936 — 0*938 Butter of Cacao, fresh . 0*950 - 0*952 „ „ very old .... 0*945-0*946 „ and Beef Tallow, mixed 1:1 . . 0*938— 0*939 Expressed Oil of Nutmegs .... 1*016 — 1*018 „ „ „ extracted with carbon disulphide . 1*014 — 1*015 Expressed Oil of Nutmegs, adulterated with fatty acids . 1*010-1*011 Expressed Oil of Nutmegs, crystal¬ line . 0*965-0*966 Stearic Acid, melted and in drops. . 0*964 „ „ crystalline . 0*967 — 0*969 Wax, yellow . 0*959 — 0*962 „ African . . 0*960 „ yellow and resin, mixed 1:1 . . 0*973 — 0*976 ,, „ and paraffin, mixed 1:1 . 0*916 — 0*919 „ „ „ yellow ceresin, mixed 2:1 . 0*942-0*943 Ceresin, yellow . 0*925—0*928 Wax, Japan . 0*977—0*978 „ „ very old . 0*968—0*970 ,, white, very old and true . . . 0*963—0*964 „ „ new . 0*916 — 0*925 „ „ „ and stearic acid, mixed 1:1 . . 0*945 Wax, sp. gr. 0*963 and stearic acid, sp. gr. 0*963 mixed 1:1 . 0*975 Ceresin, very white, pure . 0*905 - 0*908 „ white . 0*923 — 0*924 Araucaria Wax . 0*990 Resin (fr. pine), yellow transparent . 1*083- 1*084 „ whitish, opaque . 1*044—1*047 „ very dark colophony .... 1*100 Shellac, light coloured . 1*113 — 1*114 „ darker . 1*123 „ bleached . 0*965 — 0*968 Dammar, old. . . 1*075 Copal, East Indian . 1*063 — 1*070 „ West Indian . 1*070—1*800 „ very old . 1*054-1*055 Benzoin, Siam . 1*235 „ Penang . 1*145—1*155 „ Borneo . 1*165-1*170 Guaiac Resin, pure . 1*236 - 1*237 Amber . 1*074—1*094 Sandarac . 1*038 — 1*044 Mastic . 1*056-1*060 Balsam of Tolu, old brittle . . . . 1*231-1*232 (Kamala . 1*115— 1*120) (Lycopodium . 1*016 — 1*020) * Pharm. Centrcilh., 1879, 132. Remedies, September, 1879. Reprinted from New Many of these figures may be used as criteria for dis- , tinguishing the various bodies. 288 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 11, 1879 RADIANT MATTER. * BT WILLIAM CROOKES, F.R.S. To throw light on the title of this lecture I must go back more than sixty years — to 1816. Paraday, then a mere student and ardent experimentalist, was twenty- four years old, and at this early period of his career he delivered a series of lectures on the General Properties of Matter, and one of them bore the remarkable title, On Radiant Matter . The great philosopher’s notes of this lecture are to be found in Dr. Bence J ones’s ‘ Life and Letters of Faraday,’ and I will here quote a passage in which he first employs the expression Radiant Matter “ If we conceive a change as far beyond vaporization as that is above fluidity, and then take into account also the proportional increased extent of alteration as the changes rise, we shall perhaps, if we can form any conception at all, not fall far short o Radiant Matter ; and as in the last conversion many qualities were lost, so here also many more would disappear.” Faraday was evidently engrossed with this far-reaching speculation, for three years later — in 1819 — we find him bringing fresh evidence and argument to strengthen his startling hypothesis. His notes are now more extended, and they show that in the intervening three years he had thought much and deeply on this higher form of matter. He first points out that matter may be classed into four states — solid, liquid, gaseous, and radiant — these modifica¬ tions depending upon differences in their several essential properties. He admits that the existence of Radiant Matter is as yet unproved, and then proceeds, in a series of ingenious analogical arguments, to show the probability of its existence.^ If, in the beginning of this century, we had asked/ What is a Gas ? the answer then would have been that it is matter, expanded and rarefied to such an extent as to be impalpable, save when set in violent motion ; invisible, incapable of assuming or of being reduced into any definite form like solids, or of forming drops like liquids ; * A lecture delivered to the British Association for the Advancement of Science, at Sheffield, Friday, August 22, 1879. .... I may now notice a curious progression in physical properties accompanying changes of form, and which is perhaps sufficient to induce, in the inventive and sanguine philosopher, a considerable degree of belief in the associa¬ tion of the radiant form with the others in the set of changes I have mentioned 1 “As we ascend from the solid to the fluid and gaseous states, physical properties diminish in number and variety, each state losing some of those which belonged to the preceding state. When solids are converted into fluids, all the varieties of hardness and softness are necessarily lost. Crystalline and other shapes are destroyed. Opacity and colour frequently give way to a colourless trans¬ parency, and a general mobility of particles is con¬ ferred. “Passing onward to the gaseous state, still more of the evident characters of bodies are annihilated. The immense differences in their weight almost disappear; the remains of difference in colour that were left, are lost. Transparency becomes universal, and they are all elastic. They now form but one set of substances, and the varieties of density, hard¬ ness, opacity, colour, elasticity and form, which render the number of solids and fluids almost infinite, are now supplied by a few slight variations in weight, and some unimportant shades of colour. “ To those, therefore, who admit the radiant form of matter, no difficulty exists in the simplicity of the properties it possesses, but rather an argument in their favour. These persons show you a gradual resignation of properties in the matter we can appreciate as the matter ascends in the scale - of forms, and they would be surprised if that effect were to cease at the gaseous state. They point out the greater exer¬ tions which Nature makes at each step of the change, and think that, consistently, it ought to be greatest in the passage from the gaseous to the radiant form.” — ‘ Life and Letters of Faraday,’ vol. i., p. 308. always ready to expand where no resistance is offered, and to contract on being subj ected to pressure. Sixty years ago such were the chief attributes assigned to gases. Modem research, however, has greatly enlarged and modified our views on the constitution of these elastic fluids. Gases are now considered to be composed of an almost infinite number of small particles or molecules, which are con¬ stantly moving in every direction with velocities of all conceivable magnitudes. As these molecules are exceed¬ ingly numerous, it follows that no molecule can move far in any direction without coming in contact with some other molecule. But if we exhaust the air or gas con¬ tained in a closed vessel, the number of molecules becomes diminished, and the distance through which any one of them can move without coming in contact with another is increased, the length of the mean free path being inversely proportional to the number of molecules present. The further this process is carried the longer becomes the average distance a molecule can travel before entering into collision ; or, in other words, the longer its mean free path, the more the physical properties of the gas or air are modified. Thus, at a certain point, the phenomena of the radiometer become possible, and on pushing the rarefaction still further, i.e., decreasing the number of molecules in a given space and lengthening their mean free path, the experimental results are obtainable to which I am now about to call your attention. So distinct are these phenomena from anything which occurs in air or gas at the ordinary tension, that we are led to assume that we are here brought face to face with Matter in a Fourth state or condition, a condition as far removed from the state of gas as a gas is from a liquid. Mean Free Path. Radiant Matter. I have long believed that a well-known appearance ob¬ served in vacuum tubes is closely related to the phenomena of the mean free path of the molecules. When the negative pole is examined while the discharge from an induction- coil is passing through an exhausted tube, a dark space is seen to surround it. This dark space is found to increase and diminish as the vacuum is varied, in the same way that the mean free path of the molecules lengthens and contracts. As the one is perceived by the mind’s eye to get greater, so the other is seen by the bodily eye to increase in size ; and if the vacuum is insufficient to permit much play of the molecules before they enter into collision, the passage of electricity shows that the “dark space” has shrunk to small dimensions. We naturally infer that the dark space is the mean free path of the molecules of the residual gas, an inference confirmed by experiment. I will endeavour to render this “ dark space ” visible to all present. Here is a tube (Fig. 1), having a pole in the centre in the form of a metal disk, and other poles at eacft end. The centre pole is made negative, and the two end poles connected together are made the positive terminal. The dark space will be in the centre. When the exhaus¬ tion is not very great the dark space extends only a little October 11, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 289 on each side of the negative pole in the centre. When the exhaustion is good, as in the tube before you, and I turn on the coil, the dark space is seen to extend for about an inch on each side of the pole. Here, then, we see the induction spark actually illuminating the lines of molecular pressure caused by the excitement of the negative pole. The thickness of this dark space is the measure of the mean free path between successive collisions of the molecules of the residual gas. The extra velocity with which the nega¬ tively electrified molecules rebound from the excited pole keeps back the more slowly moving molecules which are advancing towards that pole. A conflict occurs at the boundary of the dark space, where the luminous margin bears witness to the energy of the discharge. Therefore the residual gas — or, as I prefer to call it, the gaseous residue — within the dark space is in an entirely different state to that of the r.-sidual gas in vessels at a lower degree of exhaustion. To quote the words of our last year’s President, in his Address at Dublin : — “In the exhausted column we have a vehicle for electricity not constant like an ordinary conductor, but itself modified by the passage of the discharge, and per¬ haps subject to laws differing materially from those which it obeys at atmospheric pressure.” In the vessels with the lower degree of exhaustion, the length of the mean free path of the molecules is exceed¬ ingly small as compared with the dimensions of the bulb, and the properties belonging to the ordinary gaseous state of matter, depending upon constant collisions, can be observed. But in the phenomena now about to be examined, so high is the exhaustion carried that the dark space around the negative pole has widened out till it entirely fills the tube. By great rarefaction the mean free path has become so long that the hits in a given time in comparison to the misses may be disregarded, and the average molecule is now allowed to obey its own motions or laws without interference. The mean free path, in fact, is comparable to the dimensions of the vessel, and we have no longer to deal with a continuous portion of matter, as would be the case were the tubes less highly exhausted, but we must here con¬ template the molecules individually. In these highly exhausted vessels the molecules of the gaseous residue are able to dart across the tube with com¬ paratively few collisions, and radiating from the pole with enormous velocity, they assume properties so novel and so characteristic as to entirely justify the application of the term borrowed from Faraday, that of Radiant Matter. Radiant Matter exerts powerful Phosphoro genic Action where it strikes. I have mentioned that the Radiant Matter within the dark space excites luminosity where its velocity is arrested by residual gas outside the dark space. But if no residual gas is left, the molecules will have their velocity arrested by the sides of the glass ; and here we come to the first and one of the most noteworthy properties of Radiant Matter discharged from the negative pole — its power of exciting phos¬ phorescence when it strikes against solid matter. The number of bodies which respond luminously to this molecular bombardment is very great, and the re¬ sulting colours are of every variety. G-lass, for instance, is highly phosphorescent when exposed to a stream of Radiant Matter. Here (Fig. 2) are three bulbs composed of different glass ; one is uranium glass (a), which phos¬ phoresces of a dark green colour ; another is English glass (5), which phosphoresces of a blue colour ; and the third (c) is soft G-rman elass — of which most of the Fig. 2. apparatus before you is made — which phosphoresces of a bright apple-green. My earlier experiments were almost entirely carried on by the aid of the phosphorescence which glass takes up when it is under the influence of the radiant discharge ; but many other substances possess this phosphorescent power in a still higher degree than glass. For instance, here is some of the luminous sulphide of calcium prepared according to M. Ed. Becquerel’s description. When the sulphide is exposed to light — even candlelight — it phos¬ phoresces for hours with a bluish white colour. It is, however, much more strongly phosphorescent to the molecular discharge in a good vacuum, as you will see when I pass the discharge through this tube. Other substances besides English, German, and uranium glass, and Becquerel’s luminous sulphides, are also phos¬ phorescent. The rare mineral Phenakite (aluminate of glucinum) phosphoresces blue ; the mineral Spodumene (a silicate of aluminium and lithium) phosphoresces a rich golden yellow ; the emerald gives out a crimson light. But without exception, the diamond is the most sensitive substance I have yet met for ready and brilliant phos¬ phorescence. Here is a very curious fluorescent diamond, green by daylight, colourless by candlelight. It is mounted in the centre of an exhausted bulb (Fig. 3), and the molecu¬ Fig. 3. lar discharge will be directed on it from below upwards. On darkening the room you see the diamond shines with as much light as a candle, phosphorescing of a bright green. 290 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October n, JS79 Next to the diamond the ruby is one of the most remarkable stones for phosphorescing. In this tube (Fig. 4) is a fine collection of ruby pebbles. As soon as the induc¬ tion spark is turned on you will see these rubies shining I have here a tube (Fig. 5) which will serve to illustrate the dependence of the phosphorescence of the glass on the degree of exhaustion. The two poles are at a and b, and at the end (c) is a small supplementary tube Fig. 4. with a brilliant rich red tone, as if they were glowing hot. It scarcely matters what colour the ruby is, to begin with. In this tube of natural rubies there are stones of all colours — the deep red and also the pale pink ruby. There are some so pale as to be almost colourless, and some of the highly-prized tint of pigeon’s blood ; but under the impact of Radiant Matter they all phosphoresce with about the same colour. Now the ruby is nothing but crystallized alumina with a little colouring-matter. In a paper by Ed. Becquerel,* published twenty years ago, he describes the appearance- of alumina as glowing with a rich red colour in the phos- phoroscope. Here is some precipitated alumina prepared in the most careful manner. It has been heated to whiteness, and you see it also glows under the molecular discharge with the same rich red colour. The spectrum of the red light emitted by these varieties of alumina is the same as described by Becquerel twenty years ago. There is one intense red line, a little below the fixed line B in the spectrum, having a wave-length of about 6S95. There is a continuous spectrum beginning at about B, and a few fainter lines beyond it, but they are so faint in comparison with this red line that they may be neglected. This line is easily seen by examining with a small pocket spectroscope the light reflected from a good ruby. There is one particular degree of exhaustion more favourable than any other for the development of the properties of Radiant Matter which are now under exa¬ mination. Roughly speaking it may be put at the millionth of an atmosphere.^ At this degree of exhaus¬ tion the phosphorescence is very strong, and after that it begins to diminish until the spark refuses to pass.* * Annales de Chimie et de Physique, 3rd series, vol. lvii., p. 50, J859. t TO millionth of an atmosphere = 0'00076 milm. 1315789 millionths of an atmosphere — TO milm. 1,000,000' „ „ „ — 760'0 milms. „ ,, „ ,, —1 atmosphere. X Nearly 100 years ago Mr. Wm. Morgan communicated to the Royal Society a Paper entitled “ Electrical Experi¬ ments made to ascertain the Non-conducting Power of a Perfect Vacuum, &c.” The following extracts from this Paper, which was published in the ‘ Phil. Trans.’ for 1785 vol. lxxv., p. 272), will be read with interest : — “ A mercurial gage about 15 inches long, carefully and accurately boiled till every particle of air was expelled from the inside, was coated with tin-foil 5 inches down from its sealed end, and being inverted into mercury through a per¬ foration in the brass cap which covered the mouth of the cistern ; the whole was cemented together, and the air was exhausted from the inside of the cistern through a valve in the brass cap, which producing a perfect vacuum in the gage formed an instrument peculiarly well adapted for experi- Fig. 5. connected with the other by a narrow aperture, and containing solid caustic potash. The tube has been exhausted to a very high point, and the potash heated so as to drive off moisture and injure the vacuum. Exhaustion has then been re-commenced, and the alter¬ nate heating and exhaustion repeated until the tube has been brought to the state in which it now appears before you. When the induction spark is first turned on nothing is visible — the vacuum is so high that the tube is non-conducting. I now warm the potash slightly and liberate a trace of aqueous vapour. Instantly conduction commences and the green phosphorescence flashes out along the length of the tube. I continue the heat, so as to drive off more gas from the potash. The green gets fainter, and now a wave of cloudy luminosity sweeps over the tube, and stratifications appear, which rapidly get narrower, until the spark passes along the tube in the form of a narrow purple line. I take the lamp away, and allow the potash to cool ; as it cools, the aqueous vapour, which the heat had driven off, is re-ab¬ sorbed. The purple line broadens out, and breaks up into* fine stratifications ; these get wider and travel towards the potash tube. Now a wave of green light appears on the glass at the other end, sweeping on and driving the last pale stratification into the potash ; and now the tube glows over its whole length with the green phosphores¬ cence. I might keep it before you, and show the green growing fainter and the vacuum becoming non-conduct¬ ing ; but I should detain you too long, as time is required for the absorption of the last traces of vapour by the potash, and I must pass on to the next subject. ments of this kind. Things being thus adjusted (a smal wire having been previously fixed on the inside of the cistern to form a communication between the brass cap and the mercury, into which the gage was inverted) the coated end was applied to the conductor of an electrical machine, and notwithstanding every effort, neither the smallest ray of light, nor the slightest charge, could ever be procured in this exhausted gage.” •‘If the mercury in the gage be imperfectly boiled, the experiment will not succeed ; but the colour of the electric light, which in air rarefied by an exhauster is always violet or purple, appears in this case of a beautiful green, and, what is very curious, the degree of the air’s rarefaction may be nearly determined by this means ; for I have known instances, during the course of these experiments, where a. small particle of air having found its way into the tube, the electric light became visible, and as usual of a green colour ; but the charge being often repeated, the gage has at length cracked at its sealed end, and in consequence the external air, by being admitted into the inside, has gradually produced a change in the electric light from green to blue, from blue to indigo, and so on to violet and purple, till the medium has at length become so dense as no longer to be a> conductor of electricity. I think there can be little doubt, from the above experiments, of the non-conducting power of a perfect vacuum.” ‘ ‘ This seems to prove that there is a limit even in the rarefaction of air, which sets bounds to its conducting power ; or, in other words, that the particles of air may be so far separated from each other as no longer to be able to transmit the electric fluid ; that if they are brought within a certain distance of each other, their conducting power begins, and continually increases till their approach also arrives at its limit.” (To be continued.) October 11, 1879.] THE PHABMaCEUTICAL JOURNAL AND TRANSACTIONS. 291 gth« §hai|maqutual Jflupal. - «. - SATURDAY, OCTOBER 11, 1879. Communications for the Editorial department of this Journal , books for review , etc., should be addressed to the Editor, 17, Bloomsbury Square. Instructions from Members and Associates respecting the transmission of the Journal should be sent to Mr. Elias Bremridge, Secretary, 17, Bloomsbury Square, W.C. Advertisements, and payments for Copies of the Journal, Messrs. Churchill, New Burlington Street, London , W. Envelopes indorsed “ Pharm. Journ .” REGISTRATION UNDER THE DENTAL ACT. The letter which, appeared in this J ournal some weeks since from Mr. Musgrave, was not, in our opinion, either timely or judicious; but, having regard to the character of affording full opportunity for the expression of opinion, which we seek to merit by the insertion of letters in our correspondence columns, we allowed that influence to overrule the disposition to treat the letter in question as unsuit¬ able for publication. As might naturally be expected the appearance of Mr. Musgrave’s letter has induced a number of correspondents to enter the lists with him for the purpose of controverting the opinions he has put forward. The publication of the letters which appear in the present number of the Journal has been unavoidably postponed, and since they were in type we have received many others, but as they are all very much to the same effect as those which have been published, it is unnecessary to occupy more space by inserting them also. As regards the most prominent topic of Mr. Mus¬ grave’s letter, viz., the claim of chemists’ assistants to registration as dentists, we confess to having some considerable difficulty in coming to a decided con¬ clusion whether or not chemists’ assistants should be included among those who constitute the third class of persons described in the Act as entitled to regis¬ tration under it. So far as concerns the present question, the persons who are there mentioned are such as were at the passing of the Act bond fide engaged in the practice of dentistry or dental surgery in conjunction with pharmacy. It may be con¬ tended that the common sense no less than the strict legal interpretation of those words should have reference only to those who were thus engaged in practice on their own account, and that con¬ sequently persons acting merely in the capacity of assistants to chemists and druggists who were engaged in the practice of dentistry would not be included in the terms .of the Act and would not have the same right to registration as their em¬ ployers. Certainly if this view of the matter were allowed to govern the admission to the Dental Register some very grave injustice would be done to many. It is quite conceivable that a chemist’s assistant or apprentice may have acquired by appli¬ cation and experience in the dental operations that are usually performed by chemists, such skill and competence as to make him fit for registration in accordance with the spirit of the Act. As possessing the ability requisite for doing dental work, it would be a very hard case if such a person were denied registration upon the ground that his practice had not been bond fide because it had been carried on for someone else and not solely on his own account. The hardship of such a case would be the greater, since the Dental Act does not contain any definite provision for admitting persons to registration by means of a modified examination, such as that pro¬ vided to meet the case of chemists’ assistants at the passing of the Pharmacy Act. One of our corre¬ spondents, writing from the same point of view as Mr. Musgrave, lays great stress upon the significance of the term “ bond fidef as being well understood by lawyers as one that, far from being lax or ambiguous, sweeps away all ambiguity. W e fail altogether to ap¬ preciate in this way the import of the words “ bond fide ” as used in the Act, but on the contrary are dis • posed to regard these very words as constituting the difficulty to be encountered in reading the Act. The man who has by study and experience become skilful in the performance of dental operations and has carried them out successfully, as well as to the satis¬ faction of those operated upon, may well be said to have been “ bond fide ” engaged in the practice of dentistry. Whether he did this as a chemist in busi¬ ness on his own account, or whether he did it only as a pupil or assistant, does not much matter so far as the common sense view of the matter is concerned; nor do we think it much matters in regard to the true object and aim of the Dental Act. We believe from what has been stated by some of our correspondents that many chemists’ assistants who have had training and experience in dentistry in the way above mentioned, have sought and ob¬ tained registration under the Dental Act. Mr. Musgrave* s own inquiries have resulted in estab¬ lishing the same fact. Of course we cannot under¬ take to say that in all cases the grounds upon which such registration was obtained were what they should have been, nor is it our business to attempt this ; the settlement of any question that may be raised in regard to that point is in the hands of the Medical Council, by which body it will doubtless be conducted with just regard to all the circum¬ stances of the case, rather than with the object of giving undue support to any attempted establish¬ ment of a monopoly in dental practice. Meanwhile we would suggest to ardent reformers like Mr. Musgrave that it is somewhat premature to talk and write so emphatically about “fraudulent registrations” and to flourish in such an aggressive manner the red flag of the 35th or penal clause of the Dental Act. We fully sympathize with them in their desire to make the practice of dentistry respectable by confining it to those who possess the requisite skill ; it is but the other day such an 292 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October ll, 1879 undertaking was entered upon by our own body, and it would be ungenerous if we did not accord to dental reformers the same encouragement which pharmacists have been glad to receive from medical men. But these endeavours to effect reform must not be carried out with a high-handed disregard of antecedent condi¬ tions and their consequences. The first great work of the dental reformers is not to set Up a graven image as the ideal standard to which all dentists must con¬ form and to insist upon the immediate sacrifice of all that do not so. This achievement may be left for the dentistry of the future and present labour must be devoted to the making of a register. We cannot expect nor do we think dental reformers can hope that this will easily be made a satisfactory roll of persons entitled, in every sense of the word, to practise dentistry. It is in other ranks than those of chemists and druggists that are to be found the practitioners who have brought discredit upon the dental branch of the medical profession, and this is so well known that we are at a loss to understand the bitterness with which the dental practice of chemists has been fixed upon as a thing to denounce, and if possible to suppress. Until dental practice shall have become, under the judicious administration of the Dental Act, a' much better regulated occupation than it has been, we do not think there is much probability that Mr. Musgrave’s idea of a dentist will correspond with more than a very small number of the registered persons who are legally qualified to practise dentistry and entitled to recover fees for so doing. We fully admit that from an ideal point of view the dentist should have been engaged in every branch of the dental art, able to undertake any operation and do any mechanical work that may be required for the mouth by the public ; but there is no immediate prospect of the dental register being wholly occupied by such men. They must long be content to rank on a legal equality with many inferiors, just as the more accomplished pharmacist is still constrained to accept the legal level prescribed by the Pharmacy Act and trust to individual excellence for gaining greater recognition than that standard of qualifica¬ tion will afford. As regards the general public and the existing order of things Mr. Musgrave’s dentist is to a great extent, if not entirely, the dentist of the future, and as regards the dental practice of chemists, there is not a shadow of reason for accepting his definition of what a dentist should be in the eye of the law. He speaks of chemists that have been pointed out to him who have never done any dental operation beyond extracting a tooth, and he adds that they probably never saw the inside of a dental laboratory, know absolutely nothing of “ dentistry ” in his sense of the term, and he urges this is inconsistent with the fact that they are registered as having being in bond fide practice as dentists. We do not desire to question the good faith with which Mr. Musgrave puts forward this argument as an objection to the legal recognition of the chemist as a dental prac¬ titioner, and would only point out its fallacious nature by reference to the circumstance that drawing teeth is pretty well the extent to which dentistry has been practised by chemists, or to which they are generally called upon to practise dentistry. It was upon this ground that the Council of the Pharmaceutical Society applied for and obtained the insertion of a clause to enable chemists to continue as they had done mainly the extraction of teeth and some other operations of dentistry. But for that clause a chemist who drew teeth would have been to that extent practising as a dentist and by holding himself out as doing so by means of a notification on his window he would have been liable to a penalty. In one and the same breath Mr. Musgrave expresses his contempt for this limited exercise of dentistry, and yet grudges the chemist the regis¬ tration by which he is enabled to practise it lawfully. This seems to us unreasonable. The very limitation of the chemist’s dental practice which he despises should be a reason for inducing him not to treat the tooth-drawing chemist as an opponent or a rival. At the same time drawing a tooth is a dental operation, and as the chemist who does it practises dentistry it seems irrational to leave him outside the operation of the Act by which it is sought to improve dental practice generally. We understand the Dental Register has now been published and that the public, no less than the medical and pharmaceutical communities, will be able to know who is legally qualified to practise dentistry. That numerous amendments will have to be made necessitating the early publication of a new edition may be taken as certain, and if we may ac¬ cept the intimation of some of our correspondents, the British Dental Association will soon be busy in its search for defective titles. That this should be done we admit is right ; but judging from the spirit mani¬ fested in some of the letters we have received, it will not be at all less right to suggest that this work of purging the register should be conducted with dis¬ cretion and justice, under the guidance of common sense rather than of high-flown ideas, and above all without a feeling of animosity against those members of the pharmaceutical body who have been brought into legal confraternity with dental practitioners more generally and exclusively engaged in the prac¬ tice of dentistry. The occasion of the retirement of Mr. G. S. Pedler, of Fleet Street, from the Court of Common Council of the City of London has furnished an opportunity to some of his fellow-citizens to show their appreciation of the services he has rendered to the ward and city generally during a period of upwards of forty years. The testimonial, which was presented on Monday week, took the form of a silver tea and coffee service and salver and a framed address, and was accompanied by a handsomely set gold ring for Mrs. Pedler. October 11, 1 879. j THE PHARMACEUTICAL joctrnal and transactions. Z9S $ro»ittj[ial Sfransadtons. MANCHESTER CHEMISTS AND DRUGGISTS’ ASSOCIATION AND SCHOOL OF PHARMACY. On Friday evening, September 26, a large number of pharmacists, assistants and apprentices, assembled at the Memorial Hall, Manchester, to hear a lecture on “ Phar¬ maceutical Education,” delivered by Mr. L. Siebold, F.C.S., under the auspices of the Manchester Chemists and Druggists’ Association; Mr. G. S. Woolley presided. Mr. Siebold, addressing himself chiefly to the younger members of the trade, who were present in large numbers, strongly urged upon them the necessity of making an early beginning with their scientific studies. He regarded their apprenticeship as pre-eminently the period for ac¬ quiring a sound fundamental knowledge of their calling, which they would then be in the best position to augment during their subsequent career, to their own immense advantage, and to the benefit of all they were called upon to serve. It was a mistake to suppose that their ap¬ prenticeship ought to be devoted solely to the acquisition of a practical knowledge of the trade, and that their scientific education should be reserved for a later period. Their practical training, no doubt was a most essential element, the importance of which he would be the last to underrate; but he did not see how it could be efficiently acquired without its being associated with a sufficient amount of scientific knowledge te impart life, thought, and intelligence to their daily work. Their practical and theoretical studies ought to be carried on together, and if this was judiciously and conscientiously done during a period in which learning was easier than ever afterwards, they would find themselves in a position when old enough to present themselves for the compulsory examination to satisfy all demands without any previous resort to cram, and by further exertions, under the guidance of com¬ petent and conscientious teachers, to obtain that higher distinction, which, he hoped, it would be the wish of most of them to attain. It was to him a matter of surprise that the apprentices in the larger towns, where courses of lectures were provided for their benefit, were so slow in availing themselves of the opportunities thus offered, and offered on terms which were certainly within the reach of the poorest of them. They would be in a position to attend such courses of instruction for several sessions during their apprenticeship, and if they were to do this, and to supplement the efforts of their teachers by a moderate amount of home work, they would obtain in a proper systematic manner an amount of knowledge which would benefit them for ever afterwards, and which would make their Minor examination a longed-for instead of a dreaded event. If it was then their intention to set apart an entire session for the acquisition of higher attainments, and for this purpose to enter the Pharma¬ ceutical Society’s school in London, as he most strongly recommended them to do, they would find their previous efforts still further rewarded, as the benefit they would derive from the great opportunities there afforded to them would be incomparably greater than if they entered un¬ provided with a sound foundation of knowledge. As it was, the majority of apprentices wasted much of their valuable time without any serious effort in a scientific direction, implicitly trusting to some future cramming process to make up for all. This process, however, de¬ spite all assurances and announcements to the contrary, failed in very many cases altogether, while where it succeeded in passing a man through the examination, it yet left him without the real knowledge required for the efficient discharge of his duties. He (Mr. Siebold) had the greatest faith in knowledge slowly and systematically acquired ; such knowledge was permanent, and could be employed with advantage in the pursuit of one’s calling. If, however, the earlier opportunity of the pharmacist had been neglected, and he had to face the necessity of gaining rapidly knowledge which would much better have been acquired by degrees, then it was all the more important that such a student should seek the aid of able and conscientious teachers, and avoid the unscrupulous crammer. There was this great distinction between learning and cramming, that the former process leads to a proper understanding of the facts committed to memory, enabling the student to make use of such facts for deduc¬ ing other facts yet unknown to him, and to augment his store of knowledge, not merely by further additions from without, but also by his own reasoning and reflection ; while the process of cramming (in the objectionable sense of the term) conveys to the students mere facts without any intelligible conception of their true meaning and the uses to which they may be applied. Such a system was intended not to impart real knowledge, but to get ignorant men through their examination ; but he (Mr. Siebold) believed that in most cases it would fail to accomplish even that. He was quite aware of the fact that many passed their examinations after such a course of cramming ; but he felt sure that in the great majority of such cases the success was due to previous honest efforts on the part of the candidates, and that the pro¬ cess would utterly fail with actual beginners. To those who did not wish to learn, but whose sole aim it was to endeavour by a show of sham knowledge to impose upon examiners— to those he had not a word to say. He trusted, however, that there would be an ever increasing number of young pharmacists anxious to obtain a sound scientific training, which he regarded as the surest means of winning for them the respect of professional men, and of raising them to a higher place in the social scale. At the conclusion of the lecture, The Chairman, in moving a vote of thanks to the lecturer, noticed with great satisfaction amongst the audience the large proportion of young men. He sug¬ gested to such of the latter as were engaged in study, that they might derive considerable inexpensive recreation from the formation of materia medica and botanical collections and the practice of qualitative analysis during a portion of their leisure time. Mr. J. B. Payne seconded the resolution. He had listened to Mr. Siebold ’s remarks with great interest and very much pleasure. With reference to one of the re¬ marks made by the lecturer at the commencement of his paper, in which he said that it was the duty of every employer to see that the apprentice committed to his care devoted some portion of his time to study, and which statement he cordially endorsed, Mr. Siebold did not tell them how that was to be accomplished in the case of those youths who showed themselves unwilling. He had had experience of both classes, those anxious to receive every assistance they could get, and those who utterly set it aside, and he must confess his inability to deal with the latter class. It was often a consideration with young men how to obtain possession of text-books and works of reference, and he took this opportunity of reminding those present that the Manchester Association had a good library, and that any youth on taking a note from his employer, who was a member of the Association, could have books for use at home by applying for them. He was sure also that the Council would whenever re¬ quisite be glad to make additions to the library, provided good use were made of the books. Mr. Bostock, in supporting the motion, paid a tribute of respect to Mr. Siebold for his earnestness and en¬ thusiasm in instructing his pupils. The lecturer briefly acknowledged the thanks of the meeting, and the proceedings terminated. ©bihtarg. Notice has been received of the death of the following: — On the 30th of August, 1879, Mr. John Jackson, Chemist and Druggist, Northampton Street, Leicester. Aged 73 years. 594 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. LOctober 11, W« On the 3rd of October, at Shanghai, China, of cholera, Mr. William Arthur Thirlby, Pharmaceutical Chemist, formerly of Ashby- de-la-Zouch. Aged 27 years. Mr. Thirlby had been a Member of the Pharmaceutical Society since 1874. On the 7th of October, 1879, Mr. Thomas Croskell Blaymire, Chemist and Druggist, St. Ann’s Square, Manchester. Aged 25 years. Mr. Croskell had been an Associate of the Pharmaceutical Society since 1871. BOOKS, PAMPHLETS, ETC., RECEIVED. Hospital Formulary and Posological Table for the Use of the Department of Public Charities and Cor¬ rection of the City of New York. New York. 1879. From Mr. C. Rice. Elements of Modern Chemistry. By Adolphe Wurtz. Translated and Edited from the Fourth French Edition by W. H. Greene, M.D., etc. London and Philadelphia. J. B. Lippincott and Co. 1879. From the Publishers. Sispnising Uftemoipmda. In order to assist as much as possible our younger brethren, for whose sake partly this column was established, considerable latitude is allowed, according to promise, in the propounding of supposed difficulties. But the right will be exercised of excluding too trivial questions, or re¬ petitions of those that have been previously discussed in principle. And we would suggest that those who meet with difficulties should before sending them search previous numbers of the Journal to see if they can obtain the re¬ quired information. [345]. Ought the following injection to be filtered or a “shake the bottle” label put on? — R Zinci Sulphatis . grs. v. Liq. Plumbi Subacetatis . 3j* Aquae . 3vj. Misce. For injection. Assistant. [346]. When pigment, iodi. is ordered which should be sent out, the tincture or liniment of iodine ? “Juvenis.” [347] . I have had euonymin from several good wholesale houses. That which I get in Scotland is always distinctly green in colour, whereas that from London is as invariably a distinct brown, with slightly greenish tinge. Will some competent person kindly say which is as it should be, and by what tests it may be recognized ? Glasgow. Euryowie. [348] . I had the following prescription handed meto-day. Will some of your correspondents give their opinion as to how it should be dispensed ? Is the top ingredient meant for Ferri Am. Cit? — ft. Ferri Ammoniae Sulph . 3j* Syrupi Flor. Aurant . 3V* Aquae Destil . ad gviij. Cap ^ ter die. Perhaps I may say I could not see the prescriber. Mag. Carb. [349]. The following prescription was presented to me a few days ago. Would some of your numerous readers inform me as to the best mode of dispensing it ? — ft 01. Copaibae . . ntij. Magnesiae Ust . gr. ij. Gum. Acaciae . gr.j. M. Ft. pil. Mitte tales xxxvi. Sig. Three pills to be taken thrice a day. Junior. [350]. How should the following be dispensed, and what appearance should it present? — ft Chloral Hydrat . gr. xx. Pulv. Camphor . gr. v. Syr. Tolut . 3j- Aq . adgj. M. ft. haust. Statim sd. Tyro. [351]. ft Sodae Bicarb . gr. x. Pulv. Calumb . gr. x. „ Zingib . gr. v. M. Ft. pulv. j. capt. ter die. ft Potass Bromid . ^ss. Acid. Tartaric . ^iv. Aquae . ad t^vj. A tablespoonful three times daily with one of the powders previously dissolved in two-tablespoonfuls of water, whilst effervescing. Ought the mixture to be clear? It has been sent out turbid and bright, and with a heavy deposit (Pot. Bitart.), and still the patient is not happy. “ Country.” [352]. ft Liq. Strychniae . . . . . . . HI xxiv. Ferri et Ammon. Cit . . . . . 3iss. Potass. Bromidi . . . .... Zb Magnes. Sulphatis . . .... 3ij- Aquae Flor. Aurantii . . 3vj- M. Ft. mist. The above produced a turbid mixture which was brought back by the patient the following day, who assured me that at Lucerne it had been dispensed a bright red and perfectly clear solution; moreover her physician had particularly requested to be allowed to see the first bottle before any was taken and expressed his surprise to find that it had been so scientifically dispensed. I made up another bottle in the presence of the lady, reversing the order in which I had mixed it the previous day, but with no better result. Afterwards I made several small quantities varying the modus operandi in every conceivable way, and testing the neutrality of the magnes. sulph., but without the success of my confrere at Lucerne. I would add that this is the second phar¬ macy in Paris in which it has been dispensed with a like result, and should be glad if some of your readers would explain the method of mixing, so as to obtain a perfectly clear and bright red mixture. Paris. O. Rogers. [353]. The following prescription was brought to me the other day and I had to make ten dozen of the pills. Should be glad to hear the opinion of some your corre¬ spondents on the best method of manipulation, and allow¬ ing for the difference in price of Howard’s Quinine here (18s. 6d.) what they would consider a fair price to charge per doz. : — ft Quinae. Disulph., Hwd’s . 3V* Acid. Sulph. Dil . ttlxx. Pulv. Phosphori . gr. iss. Strychnine Sulph . gr. iss. M. s. a. Ft. massa et divid. in pilul. LX. (in fob auro involv.). After finishing, the pills were of a large size but not larger than an ordinary six grains pill. Orange, N. S. W. J. S. [354]. Should this ft Potassii Iodidi Ferri Tart. Aquae . . . M. mixture be clear or turbid ? — . ^ss. . 7>ij. ad £viij. T. Brayshay. October 11, 1879 ] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS, 295 [355]. Can a powder be made with these ingredients? — ft Pulv. Sodse Phosphat . giij. Pulv. Zingiberis . 3ij. Potass. Citratis . Jiv. M. Ft. pulv. T. Brayshay. [356]. ft Castile Soap . 3j- Camphor . 3iij- Opium . Jiij. Flowers of Benjamin . Oil of Aniseed . . 3^j- Ft. mass. Can any reader of the Journal inform me the best mode of forming this into a nice mass ? It was presented to me the other day. After I got them mixed up (with¬ out the oil of aniseed), they turned to be as soft as treacle. A Student. Jtotqs attd (fumes. [625]. ANILINE COPYING INK.— Dissolve a few grains of methyl aniline violet in methylated spirit (as little as possible), then dilute with about five or six times as much water, and add few drops of mucilage to make it a proper consistency for writing with. J. Need. [626]. TINCT. KINO. — Will some reader kindly state the best method of filtering tincture of kino ? By means of filtering paper the process is exceedingly slow. A better method will greatly oblige Minor. [627]. JAPAN. — Can some reader give me a good receipt for best black japan which shall not turn opales¬ cent with a bluish or greenish tinge on being varnished ? M. P. S. [628]. STAINS FROM COCOA.— Would any of the readers of the Journal state their opinion as to the best mode of removing stains caused by cocoa on china, linen, etc.? Ignoramus. [629]. ROOKE’S GOLDEN OINTMENT.— Would any correspondent kindly oblige me with the recipe for making Dr. Rooke’s Golden Ointment, as given by him some years ago? Inquirer. [630]. FERROUS OXALATE FOR PHOTO¬ GRAPHIC PURPOSES. — Could some one through the medium of the Journal inform me how ferrous oxalate, suitable for photographic purposes, is prepared? Hibernia. [631]. FRENCH SALVE. — Can any correspondent kindly inform me what is the formula for “ French Salve,” and if not, where the preparation can be obtained? It is used for scurvy. Gaul. ^or^sgoml^nr^ *#* No notice can be taken of anonymous communica¬ tions. Whatever is intended for insertion must be authenti¬ cated by the name and address of the writer; not necessarily for publication , but as a guarantee of good faith. Dental Registration. Sir, — Having read with much interest the letters appear¬ ing in your columns about dental registration, I cannot refrain from adding a few remarks. I think we shall all agree with Mr. Musgrave in doubting whether chemists’ assistants or apprentices had any legal right to register, though if like “Lower Molar ” they wrote to Mr. Miller asking the question and received the form of declara¬ tion in reply, we can hardly accuse them of a breach of common morality in thus registering, and that having been done, it would be rather unwise, despite Mr. Musgrave’s solemn warning, to withdraw their names until the matter is legally decided. Having had the advantage of a three years’ dental training under an L.D.S., I can understand Mr. Musgrave’s an¬ noyance at seeing hundreds of men now legally entitled to claim all the advantages of the dentist with so little of the expense or trouble of a dental education, but the Act being now passed which renders their position perfectly legal, it would be better to recognize it with a good grace than show any perhaps natural jealousy. All will agree with Mr. Musgrave that the Act was for the protection of the public ; but how little he thinks of that when he says he would leave the operation of extraction, which he calls the least important part of the dentist’s busi¬ ness, to the unregistered (dentally) chemist or his assist¬ ant, while he would reserve for the dentist the less surgical but more remunerative department of putting in reliable gold stoppings, etc. I fear the public if they could speak on the matter would hardly appreciate Mr. Musgrave’s kind consideration for them, but would prefer rather to be protected from the man who by a clumsy extraction fractures the tooth or the alveolus and causes them weeks of intense pain, than from him who puts in a gold stopping which proves unreliable. In poor neighbourhoods, where the chemist and dentist generally does the most practice, the finer branches of the dental art (gold stopping, exposed pulp capping, etc.), are seldom or never required, the patients could not pay for even if they could understand the advantages of them ; with them, if the tooth aches they go to the dentist with the firm determination of having it out, and they would have no faith in the man who recommexded any other treatment. Mr. Musgrave may have his own definition of a dentist, but let me say that with the great majority of the public the extraction of the tooth is considered the primary and most important branch of the dental art, and if asked to describe their dentist they would say “ the man who pulls out their teeth.” The chemist and dentist as a rule does not pretend to practise every branch of dentistry ; if he has the knowledge he has not the time for it, but generally confines himself to the surgical part (extracting, stopping, scaling, etc.), getting the mechanical (artificial teeth, etc.) made for him by some working dentist, and Mr. Musgrave can hardly be astonished when he finds men who successfully perform most of the operations of dental surgery politely spoken of by the “ professional dentist” as “ dabblers in the art.” Unfortunately we have not all received Mr. Musgrave’s kind advice in the spirit in which he says it was intended, and I am sure we shall all cordially hope that for the future he will have so much to do warming his irons in bis own fire as to have no time for thrusting any into ours. A. P. Penrose, Pli. C. and Dentist. Amwell Street E.C. Sir, — Mr. J. J. Musgrave in the Journal for September 27th, writes that the extraction of teeth is the least import¬ ant part of a dentist’s business. In a lucrative sense it may be so, in a surgical and there¬ fore dangerous sense it certainly is not so, and as regards skill I venture to think it requires to the full quite as much as that department of dentistry known as mechanical. Something of the importance of purely surgical dentistry may be gathered from the reports of cases treated at the National Dental Hospital ; thus for August 1st to August 31st, out of 1426 operations 995 are for extractions, 262 for stoppings, 119 for advice and scaling. I quote from the British Journal of Dental Science, September 15th. York. _ Elevator. Sir, — Neither Mr. Musgrave nor Mr. Clarke appears to be very certain on the points at issue, as to whether a chemist performing the simple extraction could claim to be put on the register; they evidently regard it as very questionable. Mr. Clarke speaks about the -weeding out of the Dental Register by order of the Medical Council. I have never understood the Act gives them authority to demand legal evidence of fitness, else what is the declaration form for? 296 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 1 1, 1879. A weak point in that to my idea is the absence of a credible witness. My opinion is that a chemist actually in business performing the simple extraction before the passing of the Dentists’ Act could legally claim to be registered, although perhaps not compelled to do so. I fail to see how either as* sistants or apprentices could conscientiously fill up the declaration form, however highly qualified they might be. It seems to me that a Dentists’ Defence Association would be more likely to prosecute a chemist who was not on the register for extracting a tooth, rather than one who only performed the simple extraction, and had registered as a precautionary measure. Respecting the capabilities of dentists, my experience is decidedly in favour of the chemist-dentist. I find as a rule they give more time and attention to their work, and in consequence the result is more satisfactory to the patient. Walworth. F. W. S. Cream of Tartar. Sir, — In commenting upon a prosecution for the sale of impure cream of tartar at Chertsey, you state that I totally ignored the fact that tartrate of lime is a natural ingredient of cream of tartar. So far is this from being the case that I have invariably stated on my certificates given under the Sale of Food and Drags Act, that a given sample of cream of tartar was a “good,” “ fair,” or “ inferior” specimen of cream of tartar (according to its quality), when the article consisted of acid tartrate of potash and tartrate of lime only. In no such case has a prosecution been instituted on my certificate. I must, however, point out that the B.P. in its description of cream of tartar gives a formula and a quantitative test, which distinctly contemplate an article which cannot contain more than a trace of lime salt. Some months ago, I directed the attention of the sur¬ viving editor of the B.P., to the fact that the B.P. article was an impossible cream of tartar ; and 1 also brought the matter under the notice of some of the leading firms in the drug trade. Notwithstanding your strictures, I think that when a sample of cream of tartar contains a baryta salt, it is in¬ cumbent on the wholesale firm supplying the article to give some explanation of the presence of such impurity, other than mere accident. From the county of Surrey alone, I have, during the last three months, received seventeen samples of cream of tartar. Of these, no less than seven, or 41 per cent, contained sulphate of baryta in quantities varying from g to 4g per cent. In other respects, the articles were of a very varied quality, and they were obtained from diverse sources — grocers as well as chemists and druggists. Surely some member of the drug trade can enlighten your readers as to the cause of this admixture. The Analyst for the County of Surrey. Sir, — I have read with much interest the report of the prosecution for the sale of cream of tartar at Chertsey, and also your leading article on the same subject. I shall be glad if you can spare me space for the following remarks. It appears from the certificate of the analyst that the sample in question contained 11'7 per cent, of tartrate of lime and 0’6 per cent, of sulphate of baryta, and the case appears to have been dismissed chiefly owing to the evidence of Mr. William Hodgkinson that the above proportion of tartrate of lime was not abnormal. This witness stated that he had never heard of a sample of cream of tartar containing less than 7 per cent, of tartrate of lime, and that the usual proportion was from 10 to 20 per cent. Mr. Hodgkinson’s experience in cream of tartar seems to have been exceedingly unfortunate, and he cannot have gone very deeply into the matter or he would have found that the best authorities, Pereira among others, give amounts of tartrate of lime compared with which the minimum proportion he has heard of seems excessive. According to R. Warington, a high authority on this subject, the proportion of tartaric acid existing as neutral tartrates in refined tartars varies from to 7 percent. Taking these amounts as calcium tartrate, we may say that the proportion, of that salt existing in cream of tartar is from 2 0 to 8’8 per cent. In my capacity of public analyst, I have recently received from inspectors fourteen samples of cream of tartar, which have been considered genuine (in addition to an adulterated sample to be referred to subsequently). These were not all obtained in the same town or at places in the same neighbourhood, but at various small towns and villages in Derbyshire and the West Riding of Yorkshire, and their purchase has extended over some ten months. As one of the tests of purity I am in the habit of igniting a known weight of the sample, boiling the residue with water, filter¬ ing and again igniting the residue. This last product, when moistened with carbonate of ammonium, in the case of a pure sample, consists essentially of carbonate of calcium. It dissolves with effervescence in hydrochloric acid, leaving the faintest trace of residue. Evidently its amount repre¬ sents the calcium in the original sample, and if its weight be multiplied by the factor 1‘88, we obtain a very fair estimate of the proportion of calcium tartrate originally existing in the sample. Now in the fourteen samples referred to, the higheit percentage of “insoluble ash” ( = carbonate of calcium) found was 6'46 per cent., the next being 6 '36, and no other above 4 '68. The lowest amount was 2'60, and the mean of the whole fourteen was exactly 4 per cent. Multiplying these numbers by 1"88 we fiild that the highest amount of tartrate of lime met with was 12‘14 per cent., the lowest 4'89, and the mean 7*52. Hence it appears that so far from commercial cream of tartar con¬ taining an average of 10 to 20 per cent, of tartrate of lime, as stated in evidence by Mr. Hodgkinson, in this part of the country at any rate the articles sold contain an average of only 7 or 8 per cent., and hence the cream of tartar commonly sold by country druggists and shopkeepers is equal in purity to the best specimen Mr. Hodgkinson ever heard of and is twice as pure as that commonly sold by his firm. It appears to me that if it be admitted that cream of tartar is a preparation obtained by boiling crude tartar or argol in water, filtering, and crystallizing the salt from the clear liquid, the tartrate of calcium ought not to be present in more than a certain proportion, although it is true that it is far more soluble in solution of bitartrate of potassium than in pure water. But it does not follow that because a high percentage of tartrate of calcium is present, that it is necessarily a legiti¬ mate constituent of the article. Any proportion beyond that readily soluble in boiling water cannot be regarded as proper. Now 20 parts of boiling water are amply sufficient to effect the solution of bitartrate of potassium, and any tartrate of calcium not soluble in this amount must be re¬ garded with suspicion. Now, in the case of the two samples yielding 6'46, and 6'36 per cent, of “insoluble ash,” I ascertained the amount of matter left on boiling the original sample with water, and found 3'15 and 3'35 per cent, respectively. These residues were soluble in hydro¬ chloric acid, and, as far as my notes go, appear to have consisted of calcium tartrate. Hence if 3'15 be subtracted from 12T4 per cent., the total amount of calcium tartrate present, we have a residue of 9 per cent, legitimately present as a soluble constituent of the cream of tartar. This shows a close coincidence with Warington’s highest result. 1 am not prepared to stick at a difference of 1 or 2 per cent in the proportion of tartrate of lime, but when Mr. Hodgkinson states that 20 per cent, is a common and legitimate proportion, I would ask whether such samples are comnletely soluble in 20 times their weight of boiling water, and, if not, what right he has to regard them as genuine creams of tartar? (N.B. — Bitartrate of potassium i3 soluble in 15 parts of boiling water.) But it may be asked, how does the excessive proportion of tartrate of lime get into the samples ? In the case of crude tartars it is well known to be due to the addition of plaster to the wine, but this is not an explanation of an excessive amount in cream of tartar. In all probability such high amounts as are present in the samples known to Mr. Hodgkinsop are due to adulteration of the specimens with compounds of calcium. Sophistication by chloride of calcium is said to have occurred, and there are authentic cases of adulteration by chalk and marble. In a cream of tartar sold near Pontefract, I recently found 20 per cent, of sulphate of calcium (probably as plaster of paris), and 2'3 per cent, of sulphate of barium. Of course, on treating such a sample with water a large quantity of calcium tar¬ trate is formed. Hence it is clear that before we regard unusual proportions of tartrate of lime as normal, we must be quite sure that it is not a product of the decomposition of the tartrate of potassium with some adulterant. October 11, 1879.3 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 297 How the barium sulphate occasionally gets into cream of tartar, — as in the sample which has called forth this letter —I am at a loss to imagine. It occurs too frequently for its presence to be the result of accident, as suggested by one of the witnesses for the defence. In a case at Huddersfield it was found in the form of crystalline heavy spar. Can any of your readers explain the occurrence of this curious im¬ purity? Sheffield. Alfred H. Allen. Sir, — With the view of preventing other pharmacists from occupying the unfortunate and unenviable position of Mi*. Boyce, at Chertsey, whose case was reported in last week’s Journal, and with whom I am sure we ought all to deeply sympathize, I should like to mention a simple and easy test whereby all may assure themselves of the com¬ parative purity of this article when they receive it into stock. About 1 grain of the suspected sample should be shaken. in a test tube with 6 or 8 c.c. of a 5 per cent, so¬ lution)' | potassic hydrate (the liquor potassae of the official strength, provided it be free from lime, will answer every purpose) ; if the sample entirely dissolves barium sulphate is absent. The solution will, however, contain the calcium tartrate if any be present (and all samples of cream of tartar contain it to a greater or lesser degree), but on heat¬ ing the solution to boiling, the calcium salt, being insoluble in hot solution of potash, will be thrown down, and its amount may be judged of comparatively by the bulk it occupies.* On cooling the solution the precipitate is again dissolved, so that for the purpose of comparing a number of samples I would recommend that after being well boiled they ba kept hot in a water-bath, when, having been all allowed an equal time to settle, and using tubes of the same size, no difficulty will be found in estimating the com¬ parative contamination. I merely put this forward as a rough test, and one which every pharmacist can quickly and easily employ. Of course, if it be wished to determine the actual amount of calcium tartrate present it will be necessary to take a weighed sample, incinerate and treat the residue with HC1, filter and add NH40 and (NH4)2C204; the precipitated CaC.,04 may then be dried at 100° C. and weighed or ignited and weighed as CaC03 ; in either case its calculation into tartrate will be an easy matter. It is unfortunate that the B.P., which should be our unfailing guide in this matter, is rather vague and am¬ biguous. We are told that cream of tartar, potassae tartras acida and potassae bitartras are synonymous, and that it is “ an acid salt obtained from the crude tartar” (this crude tartar being evidently something quite distinct from cream of tartar). Among the characters and tests given is one which it has been stated provides for the presence of tartrate of lime. This runs as follows : “ Heated in a crucible it evolves inflammable gas and the odour of burnt sugar, and leaves a black residue. This effervesces with diluted hydrochloric acid and forms a solution which .... when neutralized with ammonia is rendered slightly turbid by oxalic acid.” It certainly does provide for a trace of tartrate of lime, but I think it will be admitted by those who know what a delicate test for lime oxalic acid is that the presence of only 1 or 2 per cent, would give something more than a slight turbidity when treated as above. But admitting for the sake of argument, that the presence of calcium tartrate is provided for by that test, what is the meaning of the next one ? “ 188 grains heated to redness till gas ceases to be evolved leave an alkaline residue which requires for exact neutralization 1000 grain measures of the volumetric solution of oxalic acid.” If it means anything it is that the sample shall contain 100 per cent. KHC4H406 or absolute purity, and herein lies what I consider to be a contradiction. That cream of tartar does contain tartrate of lime is the experience of every one who has ever had to do with the examination of it, but that it should contain it in anything more than a trace I am by no means ready to admit. So far as my experience goes I have found samples * This is substantially the test I recommended when discussing this subject before the Liverpool Chemists’ Association in November, 1877, and will be found with other remarks at p. 467, vol. viii., 3rd series, and I then ventured to predict that some unfortunate pharmacist would suffer prosecution for this impurity, and at the same time urged upon chemists the necessity of examining their stocks. to contain from 3 to 7 per cent., never so much as stated in your report last week, viz., 11*7. If crude tartar is taken and ground and sold as cream of tartar, one can understand this large percentage, and this being the case it would be interesting to know how much tartrate of lime cream of Tartar might contain and yet be still cream ©f tartar. It has been a matter of some surprise to me that this article ha3 not been selected by the zealous public analysts before now, and should some wholesale house consider it worth while to supply its customers with an article gua¬ ranteed to within, say, 5 per cent, of impurity, I have no doubt its efforts would be duly appreciated by pharmacists generally. With regard to the presence of barium sulphate in the small quantity usually found, it cannot be looked upon as an intentional admixture, and the source of its contamination may possibly be from the stones in grinding 137a, Aldersgate Street, E.C. Alfred E. Tanner. The Admission of Women as Members of the Pharmaceutical Society. Sir, — I am one of those who consider the Council of the Pharmaceutical Society to be a representative body, and hence open to criticism by their electors ; and I therefore Venture to trespass upon your columns in order to express an adverse judgment upon the conduct of some of their number whom I voted for at the l.tst election, trusting that they will take my remarks in the friendly spirit in which they are written. I shall not mention any names; but, sir, some of us who have advocated on principle the undesir¬ ability of the female (pharmaceutical) franchise will share the evident astonishment of some of our opponents at the “sudden conversion” of some in whom we had confidence at the last election as sound upon this question— a confi¬ dence supported by their speeches in and out of Council up to so late a date as the last Annual Meeting of the Pharma¬ ceutical Society. What, then, has occurred between that time and the recent meeting of the Council to alter the opinion of these gentlemen on so important a question? There may, of course, be reasons not expressed in their speeches of Wednesday last; but, if so, I think we are en¬ titled to know them, and the reasons there expressed for a charge they must really excuse my characterizing as shallow in the extreme. I admit, sir, that it requires rather more courage to oppose two individual cases of application for membership than it does to advocate the broader question of the undesirability of the female franchise ; and I feel quite to unite in the con¬ gratulations expressed in your leading article for this week, to these ladies upon the removal of a supposed grievance. But, sir, will it stop here? And will not the recent action of the Council weaken their own hands or those of some future-elected body in refusing admission to further appli¬ cation for membership from others of the fair sex, without drawing invidious distinctions ? I am one of those who are sometimes accused of advocating a policy of “peace at any price,” but not, sir, at the sacrifice of principle, and the action of some of these veteran Councillors reminds one too much of the conduct of the unjust judge in the parable (vide Luke xviii., 4 and 5), with this important difference that they were right in principle at the outset where he was wrong. Our venerable President seems to be the only man among them who holds to the courage of his convictions. Scarborough. Chas. Fryer. Sir, — I was very much surprised to see by the Pharma¬ ceutical Journal of Saturday last, that the Council at its meeting on Wednesday, had granted membership of the Society to two women, especially after having referred the question to the Annual Meeting, and that meeting had on two occasions voted by a small majority against their ad¬ mission. True, the majority was small, still it was a majority, and I do not think the Council have acted wisely in thus ignoring the decision of the members. If the Council did not mean to abide by the decision of the members they ought not to have sent the question to the General Meeting. Probably the fact of the matter is that the Council were tired of the question, and (knowing it would in all proba¬ bility be brought forward again at the next General Meet¬ ing) admitted the ladies rather than have any more trouble 298 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 11, 1379, about it, notwithstanding the ladie3 have on two occasions been rejected by a General Meeting of the Members. London, W. C. E. P. The Competition op Co-operative Societies. Sir, — Will you kindly afford me space in your columns for a few remarks on our position as druggists with regard to the competition of the co-operative societies ? The competition of these societies to which we, in common with others, are exposed, and by which we are in many cases injured, makes it necessary that every means should be tried to lessen the evil. A great variety of suggestions have been made with this end in view, but the objection that has been fatal to most of them has been that they were impracticable. The evil still continues, and though in course of time I do not doubt that it will be greatly lessened, at present it rather grows than diminishes. In combating this injurious competition the druggist finds himself somewhat handicapped ; he does not stand on the same vantage ground possessed by those who deal in articles of food or clothing ; he cannot in the case of the majority of articles in which he deals, by reducing the price offer an inducement to increased consumption. But I think he would by adopting more fully the leading principle of these societies, viz., cash payments, find himself in a better position to compete with them. There are certain practical difficulties in the way, which will occur to most ; smallness of many of the transactions, for instance; but these would not, I think, prevent the general adoption of the system. There are very many articles in which the druggist deals which it would be easy to arrange for sale at two prices, viz., a cash and a credit price, — patent medicines, for instance. The customer would reap an advantage and the druggist would have the money in his desk to trade with instead of having it out at his customer’s without interest; he would also have done something towards removing the manifest inj ustice under which the cash customer suffers in being called upon to pay as much for his purchase as the man does who has it booked for a twelvemonth or more. A great many of the articles in which the druggist deals might be listed without diffi¬ culty at cash and credit prices, and the adoption of the principle of distinguishing between the cash and the credit customer would, I feel sure, benefit both buyer and seller, and be the introduction of a sound principle into trade. The druggist could not supply medicines or dispense pre¬ scriptions at the prices charged at the “ stores,” nor should he attempt to do so. It is this part of his business that requires special qualification and is entitled to special remuneration ; but even here the public would appreciate a move in the direction I have indicated, and with a difference between the cash and the credit price would be willing to pay something for the positive advantages offered by a personally conducted pharmacy as compared with the divided responsibility of the drug department of a general store. I merely wish in this letter to bring the general question before your readers. The system may be carried out into practice by individuals, but I think it would be better if it became the subject of discussion among druggists generally, perhaps first through the pages of your Journal. By this means valuable opinions and much useful information may be obtained as to its probable working both generally and in particular localities. It is of no use to indulge in violent diatribes against co-operative stores, however satisfactory it may be to one’s feelings to do so. Altered conditions of society and an overgrown credit system have produced them, and they can only be effectually checked by a return to sounder principles of trade. Iv. K. The Health oe the Drug Trade. Sir, — An interesting and important discussion has begun in your columns on the above subject, which would need to be handled with great caution. There is nothing so common as to draw sweeping conclusions from imperfect data, and I would warn your correspondents against making too hasty deductions from the meagre collection of facts at our command. The statistics gleaned from the obituary of the J ournal for three or four years will not j ustify any conclusion as to the healthfulness or unhealthfulness of our business through¬ out the United Kingdom. A satisfactory solution of the question can be determined only by a careful collection of facts gathered from a very large area. Speaking from my own experience and observation, extending over a period of more than forty years, I would decidedly deny that our business is more unwholesome than any other shop-keeping occupation. In my time I have had between fifty and sixty assistants and apprentices, and I do not remember a single instance of a breakdown traceable to the nature of our calling. On the contrary, boys somewhat delicate, have- come to me who, under the invigorating influence of regular hours, and the frequent use of a sixteen pound pestle, de¬ veloped into strong, active fellows. It is nonsense to say our well-known and gratefully-appreciated shop smell is unwholesome ; as well say the blended odours of a flower garden will shorten life. Of course a dirty, ill-kept drug¬ gist’s shop, where the inmates inhale nothing but a “villainous compound” of unsavoury smells, can neither conduce to comfort nor health ; but that may be said of any place similarly circumstanced. If a druggist’s shop be properly ventilated and kept clean, and he himself be regular in taking out-door walking exer¬ cise, eschewing late hours and the use of tobacco in any shape, and as he sights forty or fifty years of age, using the milder stimulants, such as beer or wine moderately, I have no doubt his life will be of average duration and as enjoy¬ able as that of any occupation. But our young men when they elect to follow pharmacy must not expect to go through life in a Pullman’s car ; like the rest of us, they must rough it in some shape, and as a result they will in due time exhibit the manly attributes of self-reliance and self-respect, and I hope men of experience who may have been soured by circumstances entirely unconnected with the business, will not darken the prospects of our young men by their gloomy and illogical deductions. Montrose. Geo. Burrell. Sir, — I have read with much interest the correspondence appearing lately in your columns regarding the causes of the comparatively high percentage of mortality among chemists. The remarks made on the subject by “ Sandford,” in a recent issue, are very much to the point, and de¬ serve careful perusal by every pharmacist who regards his health as something worth taking care of. A badly venti¬ lated shop, the air in which has become impregnated with a heterogeneous mixture of foul odours and noxious gases, and where fresh air only admitted when the door is opened by customers entering and leaving, is not likely to produce an atmosphere best suited for respiratory purposes, during the greater part of the day. Undoubtedly impure air, coupled with insufficient bodily exercise, is a very important factor in bringing about the early fatal consummation so devoutly to be deplored. Another reason hinted at by Mr. Nicol in drawing attention to the subject is also deserving of notice. It is the heavy strain which is daily imposed upon the mental faculties of the pharmacist by the peculiar nature of his occupation. The continual dispensing and handing of drugs, many of them demanding the concentration of all his faculties, and taxing his utmost ingenuity in their manipu¬ lation, impose a tax upon the brain, which, slowly it may be, but all too surely nevertheless, reacts unfavourably on the physical constitution. The remedy in both instances is obvious. Let every possible means be employed to keep the air inside the shop pure and unadulterated, and instead of remaining on the rack for the space of ten and eleven hours out of the twenty- four, as is almost universally the case at present, let the number be reduced to nine at the very utmost. I have for a good many years been a strong advocate in favour of shorter hours being adopted by our profession, and have never yet discovered a single satisfactory reason why they should not be adopted. The petty jealousies and bad feeling which exist among ourselves are almost the only obstacles in the way of progress in this much desiderated direction, and so long as these obstacles remain, the present long hours system must remain also, and the high rate of mortality among chemists obtain as it has obtained in the past. Edinburgh. Omnes Moriemur. Sir, — On reading Mr. Nicol’s remarks on the early death of chemists, and also the other correspondents on the subject, . I felt a desire to make a few remarks. No doubt the locality October ii, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 299 in cities have much to do with our health, but I think our mode of living has more to do with the longevity of our lives than situation. As an instance, one chemist in this town carried on his business in a dense and low locality, and was never out of his shop from early dawn till very late at night ; he is now retired, and if living he must be over -eighty. Myself I am always at my post from soon till late, and have not been a day out of my shop for nearly twenty years, have never a day of sickness, and am now sixty-two years of age. Of course I always have plenty of air, both by door open, and also fanlight, and in winter very seldom close the door unless extremely cold. I think by constantly harping on the short lives of chemists, parties will imagine the calling is unhealthy for a young man. “ Nothing of the sort;” essential cleanliness and the requisites for inducing health are all that are required to prolong our lives to the “allotted span.” Verus. Sir, — I notice a letter in the Journal of Saturday, September 6, by J. K. Nicol, regarding the health of the drug trade, in which he states that nearly 80 per cent, of chemists and druggists die at an early age. _ Should this statement be correct it calls for serious con¬ sideration. Impure air and close confinement are?seemingly the two great evils. We find a great many assistants with limited means starting business on their own account, and having recourse to long hours and assiduous attention to work to eke out a livelihood, and thereby utterly destroying their own con¬ stitution. I would therefore suggest as reasonable business hours from 8 a.m. till 7 p.m., and should these hours be strictly kept sufficient time would be allowed for recreation, and doubtless the percentage of premature deaths would gradu¬ ally decrease. T. S. W. How to Reduce our Death Rate. Sir, — Allow me to throw out a few simple remarks on this subject. That our death rate is high, we can all easily believe, and we can as easily understand the reasons. Whether the percentage of those who die in their prime be quite up to what Mr. Nicol has found it, -we may not be able exactly to determine ; but certain enough it must be deplorably high. The reasons for it are plain, and the chief ones are these three : The comparatively stagnant nature of our work ; the undoubtedly bad air we breathe, and, worst of all, the general long hours of the trade. If we are to reduce our high death rate, the great thing we .must aim at is shorter hours, or more recreation and rest in one way or another. The nearer we can get, in fact, to that golden rule of eight hours to work, eight to play, and eight to sleep, the happier will our lives be, the lower our death rate. What each of us seems to be driving at in this go-ahead age is ever making a good business, — making money. In our zeal for these we forget health, or we give it but a third place in our thoughts. This must not be if we are to live longer lives. The order must be health, first, business, second, money, third. But the question will be asked, “ How can chemists act up to this rule of eight hours to work, or where is the ordinary chemist who can carry it out?” I confess he is a rara avis, and in my travels of a dozen years, I have only met with two who had the good •sense and courage to do it. One was a chemist in a small provincial town, the other was the chief of a large establish¬ ment in an important manufacturing town. I had noticed that the former took a great deal of recreation, and one day, about six years ago, I asked him how he was able to do it. He replied that he had simply made it a rule, almost from the first year he went into business, that he should not work more than eight hours a day on the average. He had stuck to this rule up to that time, and, I believe, he doe3 so still. He did not work exactly eight hours each day, but between frequent holidays and short hours while he was at business, he made certain that his average was not more than that for each day of the year. It may be asked, and liow did his business fare? He had always an assistant who was left in charge to do the best he could, and when the chemist J returned from a holiday, the assistant got out to have his turn. He was always sure of getting more recreation time than the most of such assistants get. In this way did this small chemist enjoy life, and keep himself healthy, while he also gave the health of his assist¬ ant a due amount of consideration, and in this way he also kept his business going at a fair pace. No doubt, had he stuck as closely to it as most chemists on his level do, he might now have had a better business, and a little more money saved for his old age (that i3 if he had lived to see it) ; but was it not wiser of him to enjoy life as he went along, to keep himself healthy, and to be content with a smaller business ? I have always thought this man one of the most sensible chemists I ever met, and he certainly was one of the jolliest and healthiest. This, then, is one good model for chemists to go by, and it is happily one from the humble rank. The other I referred to was a noble specimen in every sense of the word. He had, I believe, made it a rule during the most of his business life of nearly fifty years, to work only about eight hours a day, going to business at 10 a.m., and leaving at 5 or 6 in the evening. He lived in vigorous health almost to the last week of his life, and died beyond the three score and ten, leaving a large business and a large fortune. He also thought of his assist¬ ants, the hours for ten out of twelve of them being from 10 a.m. to 8 p.m., with a break of three quarters of an hour for dinner. This made the day’s work fully nine hours, but as each assistant got a fortnight’s holiday in the year, that reduced the average day’s work to little over eight hours, which was all that could be desired. This man was one of Nature’s noblemen. Chemists may be divided into three classes. First, those who are not able to keep an assistant and who can do little more than make a liviag ; second, those who keep from one to four assistants and who make an income of from £300 to £600 a year ; third, those who are able to employ half a dozen assistants or more and whose income is beyond £600. It is, no doubt, the first class who do most to swell up our high death rate. We have pity for these men in their lives and we regret their fate if they go to the ground in their prime on account of the confined life they have led. I would, I think, prefer the life of Mr. Barnaby ’sniggers, for in all likelihood they would have the free pure air to breathe and work in and companions to toil beside, which would do much to brighten and lengthen life, slave life though it might be called. I would, however, recommend the chemists of this class, who must remain in the business they have chosen, to live as carefully, economically and contentedly as they can, doing their best to improve their condition ; and wherever it can be done, let them shorten the day’s work by an hour or two. Let them take what little exercise and recreation they can ; a day or two, or a week or two occasionally in the country, according as their circumstances will admit, by getting a temporary assistant to take charge. They should see well to the proper ven¬ tilating of their shops. A current of air should always, if possible, be allowed to go right through the shop during the night, especially in winter time, when the air must be foul with the burning gas and closed doors. Rather let a fanlight remain open that might allow a burglar to get in, than entirely shut up that vicious air, to have to go into it again in the morning ; for the burglar, if he go in, can at best but steal away a few shillings or pounds, while the other will assuredly steal a few years of life. As men of this class have so little exercise, they should, during winter, wear a good layer of lamb’s wool from neck to toe, which will help greatly to keep heat in and cold out, and it will enable them to do with less gas stove or fire heat. This is an important matter though it may be lightly thought of ; and those who want proof of it will find it in Combe’s ‘ Constitution of Man,’ in which work many other valuable hints may be got for the preservation of life. Hufeland’s ‘Art of Prolonging Life,’ is another book from which many good hints may be got. It would be well for chemists who aspire to long lives to give a little more attention to such books as these and less to their chemistries. The second class of chemists can have almost no excuse if they do not keep near to this rule of the three eight hours. Instead of admiring men of this class for their industrious ways, or, in other words, for making slaves of themselves to business, we should look upon them with contempt. If such men die in their prime, we should have little sympathy for them ; we should rather be thankful they have gone, o 300 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 11, 1379. that others like them, -working as they done, may take warning and do otherwise. Little requires to be said about the chemists of the third or highest class. If any of them die in their prime, we know well what we should style them. It is to this class we look for the example of shorter hours, and it is very gratifying indeed to notice that some of the principal Lon¬ don houses are closing much earlier than they did a few years ago. Assistants in these houses, I have also observed remain much longer, and work more contentedly than they did when the hours were longer. One word to assistants: They must not imagine that they are to do nothing and masters all to bring about this short hour system, and to reduce this high death rate. They must make up their minds to take a moderate salary for a situation in which the hours will be short, and be certain to ask for the highest where the hours are long. Shorter hours throughout the trade, and a lower death rate we certainly will have as we get more enlightened. Chemists will not always be suchfoois as to sell their lives at such a rate for the mere glory of business or money ; a happy and healthy long life they will look to first. There are signs of better times coming, now that the doors of some good west end houses begin to close at 7 o’clock ; but if SO per cent, are still dying in their prime, we may well raise a cry for the rest to lower their hours as far and as fast as they can, and let it ring right down to the poorest of the line. A Sawney. Nitrate of Pilocarpine. Sir, — I acknowledge to have overlooked part of Mr. Mar- tindale’s remarks at the Sheffield Conference on the purifi¬ cation of nitrate of pilocarpine ; therefore, I will set aside my letter published in tli9 Journal on September 20, and start afresh with a desire to be strictly accurate and give credit to whom it is due. The process spoken of by Mr. Martindale was first made public by M. Petit, in the Repertoire de Phcirmacie, for August 25, 1S77, and no matter how long previously Mr. Martindale may have used the same process, he must know he is not justified in claiming it as his own discovery two years after its publication by another. The merit of the process is due to M. Petit and to him it must be given. University College Hospital. A. W. Gerrard. Gelatinization of Tincture of Kino. Sir, — In respect to Mr. Bamford’s remarks, and those of others, on the difficulty of keeping this fractious tincture from “jellying,” it is a curious fact that during my forty years’ experience with drugs, etc., I have always found the above tincture very difficult to keep, but I have now in my posses¬ sion some obtained from Messrs. Evans, Sons, and Co. five or six years ago, and still it is as good as ever. The bottle has been several times opened, it is placed behind others, and is perhaps shifted and dusted every week, and it is as perfect and liquid as the day it was made. How it is I cannot pretend to say, but it is the only tincture of kino that I have seen in my forty years’ experience that has not “jellied.” Catechu. Tincture of the Resin of Podophtllum Peltatum. Sir, — This tincture is now ordered a good deal, and in the absence of an official fornmla we would take the liberty of suggesting that the following strength should be ob¬ served : — Podophyllin (Resin) gr. j. Alcohol . -\i. M. Fifteen minims will thus represent one-fourth of a grain of the resin, and this when taken on lump sugar is quite a nice dose. Only this morning a medical man was inquiring the usual strength of the tincture, and although we believe many houses prepare it of the strength indicated, yet we have found that others make it widely different, and as the drug is an active one it is of considerable importance. 35, Baker Street, W. Young and Postans. Pharmacy in the Transvaal. Sir, — Can any of your readers kindly favour us with any information respecting pharmacy in the Transvaal, the num¬ ber of chemists, prices obtained, and mode of doing business ? Are examinations compulsory, or is there any association whatever of chemists and druggists? How are assistants paid, and what are the hours of business ? Any information respecting our profession either in Natal or New Zealand will greatly oblige. An Emigrant. “ Epsilon ” (who should have sent his name and address). — There are two alternate whorls, which really answer to the calyx and corolla, but in consequence of their being btoh of the same colour are termed the perianth. “ Epipactis.” — If you send such plants to the Journal Department, after you have yourself done what you can towards naming them, we shall be willing to help you. The works mentioned are of about equal authority. 31. P. S. — We understand that the firm in question has recently promised to discontinue the use of the title. In- formation respecting the sale of vermin killer containing strychnia by unregistered persons should be forwarded to the Registrar. F. H. Fairweather. — (1) Hypnum tamariscinum. (2) Hypnum triquetrum. (3) Hypnum loreum. ( 4 ) Neckera complanata. (5) Ramalina calicaris. (6). Usnea fiorida. W. H. — See the paper on “ Pills and Pill Coatings,” by Dr. Symes, in vol. viii. of the present series of this Journal, p. 461. Several other papers on the same subject may be found by reference to the Index. There is also one in the present number. “ Acid.” — The addition of borax with and without glycerine and other salts, to promote the solubility of salicylic acid has been recommended, but probably in all these cases new compounds are formed not possessing properties identical with the original one. See Pharm. Journal [3], vol. vii., pp. 103 and 429. A. B. — We do not quite understand your question, as tincture of iodine is itself of a red-brown colour. X. Y. Z. is recommended to communicate with the officer appointed by the local authority under the Explosives Act. “Orchid.” — Spiranthes autumnalis. J. H. Dingle. — (1) Scirpus palustris. (2) Senebiera Coronopus. (3) Silene maritima. (4) Arenaria serpyU lifolia. “ Framnus.” — (1) Poa annua. (2) Folium perenne. “French.” — An advertisement in one of the French pharmaceutical journals would probably secure what you require. “ Lindum ” is referred to the rule respecting anonymous communications. “ Medical ” should address his question to the Secretary of the Royal College of Surgeons. “ Bill.” — W e are not acquainted with a mineral answer¬ ing to your description. “ Sarniensis ” should examine the Calendar of the University of London or apply to the Registrar of that institution. “ Fons et Origo.” — “Crabs’-eyes ” are concretions of car¬ bonate and phosphate of lime found in the craw fish when about to cast its shell. They were formerly used as an ab¬ sorbent and antacid remedy. 31. Leigh. — The Secretary of the Institute of Chemistry, Mr. C. E. Groves, Somerset House Terrace, W.C. B. J. Kent. — A copy of the Pharmaceutical Journal con¬ taining all the information yet published on the subject has been forwarded to you. Erratum. — On p. 265, col. ii., line 31, in the list of Associates elected, for “ Goodall, Thomas Torby, Derby,” read “ Goodall, Thomas Sorby, Derby.” Communications, Letters, etc., have been received from Messrs. Pollard, Swenden, Young, Turner, Edwards, Law- on, Thresh, Quince Sulph., Theta, Epsilon, C.E.P. October 18, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 301 ACONITUM HETEROPHYLLUM, WALL.* * * * BY DR. M. DUNIN Y. WASOWICZ. Some years ago the attention of European phy¬ sicians resident in India was directed to a nodular root which was known to the natives under the names, “ utees,” “ atees ” and “ atis,” and was used in fevers on account of its antiperiodic effects. Closer examination showed that although the name utees ” was also applied to several other drugs, for instance, the root of Convallaria Polygonatum , Solomon’s seal root, or a tasteless and inert root considered to belong to Asparagus sarmentosus, f and in Kunawar to the root of A conitum Napellus,% which is there eaten on account of its tonic effects, still this name was principally to be understood as referring to that species of aconite which Wallich called Aconitum heterophyllum. This root is said to have no poisonous properties, § and to be, in fact, a very valuable remedy for intermittent and other fevers. It is administered in ordinary intermittent fever in the form of powder in doses of 20 grains and as a simple tonic in doses of 5 to 10 grains three times a day.|| No information respecting this drug is extant, although, according to O’Shaughnessy,!' it has long been famous among Indian drugs on account of its tonic effects. Professor Yon Schroff, sen.,** * * §§ was the first to com¬ municate some cursory observations upon this drug in 1866, which were supplemented in 1871 by Schroff, jun.,tf in regard to its pharmacognosy. Professor Fluckiger, in ‘ Pharmacograpliia,’ made known that Broughton had succeeded in obtaining from the root an alkaloid which he had not closely examined. Upon the basis of a platinum salt analysis Broughton assigned to it the empirical formula C40H74N2O4, and he called it “atisine.” In the same year Broughton published a note on this drug in which he stated that the amount of alkaloid was exceedingly small and that the hydrochlorate was the easiest preparation to obtain. At the end of the year, T. B. Groves, in preparing aconitine nitrate from German Aconitum Napellus, found that after separating that salt crystals were formed in the mother liquor differing in form from aconitine nitrate and not poisonous. On the basis of polari¬ zation experiments and similarity of reactions he came to the conclusion that these crystals contained a base identical with the atisine obtained by Broughton.JJ At the time Hanbury expressed a doubt as to the identity of the two substances and shortly afterwards§§ C. R. A. Wright showed that Groves’ inactive base more probably had the formula C31H45NO10, or C30H45NO10, than that of Broughton’s atisine. Subsequently, Professor Fluckiger succeeded in obtaining a quantity of this root and he entrusted to me the examination of it. Aconitum heterophyllum , Wallich, grows in the mild districts of the Western Himalayas, in Simla, * Archiv. der Pharmacie, vol. xi., p. 193. f Pharm. Journ. (1875), p, 181. £ Hooker and Thomson, ‘ Flor. Ind.’ (1855), p. 58. S ‘ Pharmacopoeia of India ’ (1868), p. 434. II ‘ Pharmacographia,’ p. 15. If ‘Bengal Dispensatory’ (1842), p. 167. ** ‘ W ochenblatt der k. k. Gesell. d. Aeiize,’ Yienna (1866), p. 165. tt ‘ Beitrag zur Kenfcniss d. Aconits v. Dr. C. Y. Schroff jun. Yienna, 1871, p. 65. || Pharm. Journ. [31, vol. v., p. 170. §§ Pharm. Journ. [3], vol. vi., p. 189. Third Series, No. 486. Kashmir and Kumaon, at a height of 8300 to 13,300 feet above the sea level. The finest and largest samples grow upon the mountains Clioor, Shalma and Kadarkantar. The plant is from 1 to 3 feet high, with heart-shaped, acute, indistinctly 5-lobed, Fig. 1. — Leaf. or sometimes incised, radiate -veined, leathery leaves? and racemes of large dirty yellow purple-veined or entirely blue flowers arranged in a panicle. The calyx is furnished with a semicircular ascending pubescent helmet ; the spur is ovate and obtuse ; the limb long and bent downwards ; the stamens are arrow-shaped and winged ; the five carpels and the bracts roundish or rather long. O Fig. 2. — A blue flower. Fig. 3. — Two upper petals, with anthers and follicles. The roots, which are only to be found in Indian bazaars, are ovoid, longish or turnip-shaped tubers, almost always somewhat flattened at the upper end, but generally conical at the lower extremity and only seldom sharp-pointed. Some few of the tubers are stalk-shaped (fig. 7 a to g). They are closely but irregularly covered with scars of lateral roots and here and there small remains of leaves are to 302 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October is, 1 879. be found at the upper end of some roots. Externally the roots are pale yellowish grey, in some parts Fig. 5. — Seel. Fig. 4. — Capsule. Fig. 6. — Portion of the stalk with tuberous roots. almost white, with numerous longitudinal wrinkles, and at the upper end from two to five transverse wrinkles, though only in some of the roots. In some cases there is a furrow or channel-shaped de¬ pression extending the whole length of the root. The roots are from inch to 3 inches long. The thickest diameter is from \ inch to nearly an inch, and they weigh from 7 grains upwards, the weight of most of the tubers varying between 38 and 90 grains. The fracture is almost even ; within the tubers are clear white. The taste is mealy, somewhat mucila¬ ginous and bitter, without any biting or acrid after¬ taste. Digested in cold water for some hours the tubers swell up and after perfect drying become hard and horny. This is also the case when they are digested with hot water. Under the microscope the pure white transverse section presents an almost uniform tissue, intersected with from three to seven rather yellowish coloured irregular bundles of vessels, situated in a scattered manner and enclosing an apparently large meditul- lium. Concentrated sulphuric acid colours the sec¬ tional surface reddish ; solution of iodine in iodide of potassium colours it at first violet and then a dirty bluish black. Millon’s reagent colours it only slightly reddish, and perchloride of iron does not alter it at all. Thin fragments, perfectly freed from starch by treatment with dilute acids and careful washing, give with alkaline solution of cupric tartrate, or with Millon’s reagent, no reaction to indicate the presence of solid protein substances. Fig. 7 a to (j.— Roots, natural size. Under the micro¬ scope the outer rind of the roots appears to be formed of four or five or six rows of somewhat rounded tabular cells crowded together and having their walls slightly brown - coloured. Next to this comes a rind consisting of five to twelve rows of elon¬ gated collenchyma- tous cells of uniform size and slightly thickened. This rind is separated from the rest of the tissue by a distinctly yellow-coloured zone. The cells of this zone are thin- walled and distinguished only by the yellow colour from those of the central por¬ tion of the root. The latter are rounded slightly thickened polyhedral cells of a parenchymatous nature of which the whole general mass of the tissue is formed. In this tissue there are gener¬ ally very irregularly distributed vascular bundles, to the number of three or seven, which seldom consist of single vessels, but more frequently of three to nine, arranged in rows or groups. The latter are mostly scalariform, less frequently spiral, and their walls are yellowish, but much lighter coloured than those of the yellow zone. Round these vascular bundles the cells of the principal tissue are the smallest. These bundles surround a medilullium, which is almost always in the centre of the trans¬ verse section, but is not so big as it appears under the microscope. It consists also of rounded poly¬ hedral cells, having only very small intercellular spaces and exceeding in size three or four times those of the principal tissue. The form of this tissue, consisting of large cells, varies very much; some¬ times it is triangular, sometimes square, sometimes aacircle or almost an ellipse, according to the number and situation of the vascular bundles above men¬ tioned. Among the many transverse sections that I have examined from different parts of the root, by far the most of them presented the appearance shown in fig. 8. At the upper part of the root, where it Octobers, 1879 ] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 303 iiiiiMBtkiMaB is almost always flattened, tlie transverse section also presents such an appearance as is especially to be seen in the large-celled parenchymatous tissue. A closed cambium-ring was not to he detected either in the upper parts or at the ends of the roots. To- Fig. 8. — Transverse section of middle of root. wards the conicaLsliaped end of the root the trans¬ verse section appears regularly arranged, and in almost all the sections presented the appearance shown in fig. 9. In the longitudinal section the Fig. 9. — Transverse section towards end of root. vascular bundles, or more correctly the single vessels, extend from the scars of the staik to the opposite pointed end of the root; and though bent and curved, are always separate, and never anastomosing, and only here and there extending into a lateral root. Some vessels originate first in the centre of the root, as shown in fig. 10 a. The lateral roots, so far as I could judge from their remains, have a comparatively thicker rind, consisting of longitudinally extended cells, which are rounded at [both the narrow ends. The yellow zone appears distinctly also, as in the principal root, and separates the rind from the other tissues. This, as well as the vessels and the parenchymatous tissue, are formed in the same way as the corresponding parts of the prin¬ cipal root ; but frequently the central tissue is not Fig. 10. — Longitudinal section : a, vessels originating almost in the middle of the root. visible. Its place is then occupied by a bundle of seven to sixteen vessels. Frequently it is also com¬ paratively very elongated longitudinally, and bounded by two vascular bundles which consist of several rows of vessels. Stony cells are altogether wanting both in the principal and the lateral roots. The contents of all the parenchymatous cells (with the exception of the empty collenchymatous rind cells) consist of single, simple or compound, or merely aggregated starch granules. The number of the parts of the granules amounts to from two to seven, more frequently from two to W <9 0 9 'J* three. The appearance of the starch granules resembles sometimes the starch of Phaseolus and sometimes that of Col- chicum (fig. 11). Some /^S of them closely resemble Ss- ' the 4-par tite granules of Starch grains. Crocus starch. They are comparatively small, about 15 to 18 m.m. at the most, and always somewhat larger than the granules of Aconitum Napellus. The starch granules of the principal are always bigger than those of the lateral roots. (To be continued.) Fig. 11. PRELIMINARY NOTICE ON TEUCRIUM FRUTICANS* BY A. OGLIALORO. This labiate plant, which is employed as a febrifuge, is called “olivetta” by the Italian peasants, from the resemblance of its leaves in colour to those of the wild olive. The fresh plant collected in June soon after flowering gave no essential oil when distilled with water ; it was therefore dried in the sunshine, and treated with boiling alcohol in a continuous displacement apparatus for two days. On cooling, the extract deposited a deep green granular pasty substance. The partly exhausted plant was then treated for other two days with fresh spirit, and on cooling, a nearly colourless crystalline sub¬ stance was deposited from the solution. _ * From the Gazsetta chimica itaMana, 8, 440 — 446. Reprinted from the Journal of the Chemical Society. 304 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 1 3, is;s. The green deposit from the first extract consists of two substances mixed with a large quantity of chlorophyll. When treated with boiling alcohol, a white crystalline substance is left undissolved, identical with the crystalline deposit from the second extract. The other compound, which is readily soluble in hot alcohol and in benzene, can only be freed from chlorophyll with difficulty. It is a nearly white somewhat soft substance, insoluble in water, and melting at about 80 — 85°. As it does not crystallize, and constant analytical results could not be ob¬ tained, the author is inclined to consider it as a mixture. Teucrin. — The nearly colourless crystalline substance obtained from T. fruticans dissolves but very sparingly in any of the ordinary solvents, with the exceptitSh of glacial acetic acid, which affords the best means of purifying it. It crystallizes in slender prisms of a yellowish colour, which melt at 228 — 230° with decomposition. The results of the analyses accord best with the formula C2iH240h, but the author reserves his opinion on this subject until he has more thoroughly investigated the nature of the substance. Teucrin is decomposed when heated with dilute nitric acid, leaving a residue of a red colour; on cooling, the solution deposits yellow crystals, which may be purified by recrystallization from boiling water. The new substance is thus obtained in long silky prisms (m.p. 180°) of a golden colour. It is of an acid nature, and yields a silver salt, rather soluble in water, but which is thrown down in splendid golden-yellow plates on adding alcohol or ether to a mixture of the ammonium salt with silver nitrate. The analysis of the acid itself and that of the silver salt points to the formula C8Hs03 for the acid, which is that of hydroxytoluic acid ; its fusion point also is nearly the same as that of Fittica’s /3-hydroxytoluic acid ( Ber ., 7, 927). The nitric acid mother liquors, from which this acid crystallizes, contain oxalic and tartaric acids, indicating that the substance is a glucoside. Teucrin is decomposed when boiled with dilute sulphuric acid, leaving a yellow residue of an acid nature, the quantity of which was too small to establish its identity with the acid obtained by the action of nitric acid ; the solution contains a substance of the nature of glucose, so that there can be no doubt that teucrin is a glucoside. Three 0'5 gram doses of teucrin administered to a dog caused a lowering of the temperature of the animal. STATICE CAROLINIAN A.* BY EUGENE L. REED, PH.G. Marsh rosemary is considered by Nutall, Torrey and other botanists as a mere variety of Statice limonium, of Europe, while others regard it a distinct species. It is indigenous to the Atlantic coast of the United States, and has a perennial root, sending up annually tufts of leaves, which are obovateor cuneiform, entire, mucronate, smooth and on long foot stalks. They differ from the leaves of S. limonium in being flat on the margin, while the latter are undulated. The flower-stem is round and smooth, from a few inches to a foot or more in length, sending off near its summit numerous subdividing branches, which terminate in spikes, and form altogether a loose panicle. The flowers are small, bluish-purple, erect, upon one side only of the common peduncle, with a mucronate, scaly bract at the base of each, a five-angled, five-toothed caylx, and spatulate obtuse petals. The meadows in the vicinity of Atlantic City are made beauti¬ ful by the marsh rosemary when in flower. The delicate bluish-purple of its blossoms, which appear in August and September, produce a pleasant relief to the eye from the varying shades of green of the salt grases. It is the forerunner of the bright yellow' and crimson tints of the pickle-weed, which later in the fall gives to the meadows such richness of colour. The marsh rosemary, or meadow lavender, is highly prized by those who collect grasses to ornament their homes in winter, and is placed above picture frames and in bouquets as one of their most attractive features. The root collected in October pos- * From the American Journal of Pharmacy, Sept., 1879. sesses medicinal properties in a higher degree than tha^ collected later in the season. It is large and spindle- shaped, branched, fleshy, compact, rough and of a purplish- brown colour. Its length depends upon the nature of the soil, which varies from dark muddy to light sandy in numerous localities over the meadows. If found in sandy soil, the root is short and of a branching character, while that obtained from muddy soil is long, straight and less branching. It is bitter and very astringent to the taste, and in the fresh state is without odour, but a decoction kept in a warm place for several days ferments and has a molasses-like odour. The fresh root is tough and not easily bruised except after the addition of a little alcohol. The tincture obtained with a mixture of one part of alcohol and two parts of water yielded a precipitate with acetate of lead, the filtrate from which contained sugar, gum and ex¬ tractive matter. The precipitate was dissolved in alcohol, the solution decomposed by sulphuretted hydrogen, and the filtrate evaporated ; it yielded 17| per cent, of residue, consisting chiefly of tannin, which gives a greenish- black colour with solution of chloride of iron. Statice is powerfully astringent. In domestic practice it is freely used in some parts of the coast line as a remedy for diarrhoea and dysenteiy, to restrain morbid discharges from mucous surfaces, as a gargle in sore throat and aphthous condition of the mouth and fauces, and as a styptic in passive hemorrhages. If it were necessary to pay the cost of importation, statice would probably be held in as high estimation by the medical profession as kino and catechu. It can be tinctured and employed for all the purposes for which these popular remedies are given ; it may also be given in decoction or infusion. Its abundance and valuable properties should cause it to be brought before the medical profession and to be more generally used. CHLOROFORM AS AN ANESTHETIC.* BY J. REGNAULD. The purity of chloroform for anaesthetical purposes being very important, the following simple tests are re¬ commended by the author. If chloroform is dropped on paper and allowed to eva¬ porate, the last portion on being inhaled has a character¬ istic pleasant smell, and leaves the paper perfectly dry and odourless; impure chloroform however possesses a dis¬ agreeable irritating odour, which it imparts to the paper. Pure chloroform does not redden blue litmus or give even a cloudiness with silver nitrate. If it should do either, it contains hydrochloric acid or the products of decomposition of some other chlorides. Pure chloroform remains perfectly colourless when boiled with potash; the presence of aldehyde causes a brown coloration. When shaken with concentrated sulphuric acid and allowed to stand for half an hour, the two liquids should separate into two colourless layers. The presence of alcoholic chlorides produces a brown coloration. The purity of chloroform may be judged by its constant boiling point, GO'S0. Impure chloroform may boil above or below according to the impurities it contains. The sp. gr. of chloroform can hardly be used as a criterion of its purity, since its determination has been attended with conflicting results. Liebig has found the sp. gr. of pure chloroform to be 1‘48 at 18°. Souberain shows that this number is too low, the sp. gr. at 12° being P496. Again, Remys [Arch. Pharm. [3], 5, 31) points out that the sp. gr. of pure chloroform is 1'5 at 15°, and moreover the presence of -gfe of alcohol lowers the sp. gr. '002. The purity of chloroform may to a certain extent be judged by the complete insolubility of Hofmann’s violet in it : if it contains a trace of alcohol, the solution is coloured a beautiful purple. * From the J. Pharm. [4], 29, 402 — 405. Reprinted from the Journal of the Chemical Society , September, 1879. October IS, 1870.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 305 Sfa §kpaquiital Joitijim! SATURDAY, OCTOBER 18, 1879. THE “ SODA WATER ” OF COMMERCE. The weakness that is indicated by the popular application to anything of the term. “ milk and water,’’ seems to be still the prevailing characteristic of the proceedings of public analysts, and almost in¬ voluntarily they appear to be influenced by some verbal connection between the articles which first engaged their attention as a body and those which they from time to time undertake to inquire into now. From the milk of the cow they went on to il milk of sulphur,” and from that have since ad¬ vanced to “cream of tartar,” as though subject to some kind of fascination. Though to a great extent the examination of water is outside the duty of a public analyst, the kind of aerated water known as “ soda water,” and commonly used as a beverage, has on several occasions been taken as the material for investigation and last week the Newport magistrates were occupied in hearing a case of prosecution under the Food and Drugs Act arising out of this exercise of the public analyst’s skill. The case we refer to is fully reported at page 312 of the present number of the Journal, and it was based upon the certificate and evidence of the New¬ port public analyst to the effect that a certain article called “ soda water,” supplied by Mr. Davis, a chemist, of Newport, was not of the quality and nature required by the purchaser, inasmuch as it did not contain bicarbonate of soda. According to that official, water charged with carbonic acid would not have the effect of neutralizing acidity in the stomach in the same manner that the soda water of the British Pharmacopoeia would do, and apparently under the belief that soda water was drunk only by persons afflicted with acidity in the stomach, the Newport analyst followed the example of many of his brethren in arriving at the conclusion that the British Pharmacopoeia furnished a standard for the composition of soda water, — that if it did not contain in the half pint 15 grains of carbonate of soda it was not of the nature and quality of “ soda water.” In some form or other this mischievous delusion of regarding the British Pharmacopoeia as a standard for the nature and quality of articles of ordinary daily consumption, has misled many public analysts, and has been a source of considerable unnecessary vexation to individual traders. We have on various occasions endeavoured to impress upon the minds of these official analysts that the British Pharmacopoeia relates, like the Pharmacopoeia of any other country, solely to the composition and strength of articles to be used as medicines, that it is intended simply to afford to the members of the medical profession and those engaged in the preparation of medicines, one uniform standard and guide, whereby the nature and composition of substances to be used in medicine may be ascertained and determined. In certain of the cases of prosecution where the public analyst has sought to make the British Pharmacopoeia the standard by which to gauge the nature and quality of articles that it does not in fact refer to, the soundness of the principle we have sought to impress on the con¬ sideration of public analysts has been repeatedly endorsed by the magistrates or judges before whom the cases have been tried. But still the endeavour goes on to treat the chemist and druggist as though he never sold anything but physic, and hence we have such prosecutions got up as the one just disposed of at Newport. Fortunately for Mr. Davis some of the magistrates before whom the case was brought were in the habit of drinking “ soda water.” They seem also to have had such a knowledge of the virtues of bicar¬ bonate of soda and such a wise regard for the soundness of their internal economy, that they took care the soda water they drank contained no soda at all, and would not drink it if they knew it con¬ tained any soda. That is to say they would not think of drinking as a daily beverage the effervescing solution of soda of the British Pharmacopoeia, not¬ withstanding the fact that this preparation may be very beneficial for persons with acidity in the stomach. In short, they drew a distinction between medicinal soda water and that ordinarily used as a beverage. Upon this ground they dismissed the summons, but as is usual, they refused to allow costs to the defendant, since the prosecution, how¬ ever mistaken, was undertaken for the public benefit. For our own part we regret that the defence of this case was not based upon an outspoken assertion of the principle by which the magistrates were spontaneously guided in deciding it, for in our opinion there is ample reason for the opinion that “ soda water ” for ordinary drinking purposes is far better when made, as it generally is, by merely charging pure water with carbonic acid gas, than it would be if it contained some bicarbonate of soda. CHEMISTS’ ASSISTANTS’ ASSOCIATION. On Wednesday next, the 22nd inst, the Chemists’ Assistants’ Association will hold a Conversazione at St. James’s Hall (Regent Street entrance), at which all interested in pharmacy are invited to be present. There will be an exhibition of microscopes, spectro¬ scopes and other scientific apparatus of general interest, as well as the performance of a musical programme. Tickets (to admit lady and gentleman) may be obtained by letter from the Hon. Sec., 32a, George Street, Hanover Square, W. THE HOWARD MEDAL. The subject chosen by the Statistical Society for the Howard Medal to be awarded in November, 1880, is “ The Oriental Plague in its Social, Econo¬ mical, Political and International Relations ; special reference being made to the labours of Howard on the subject.” This prize was instituted in the year 1873, the centenary of the appointment of John Howard as High Sheriff of the county of Bedford. It consists of a bronze medal, and is adjudged by the Council of the Statistical Society for the best essay on some subject in Social Statistics. On this occasion a sum of i>20 will be given in addition. The competing essays must be sent in on or before the 20th of June, 1880, and should not exceed in length 150 pages of the Journal of the Statistical Society. 306 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 18, |)rooitt([ial ©ransantions. LIVERPOOL CHEMISTS’ ASSOCIATION. The first general meeting of the thirty-first session was held at the Royal Institution on Thursday evening, October 9. The President, Dr. Charles Symes, in the chair. The minutes of the previous meeting having been read and confirmed, Mr. J. McCaig was elected a member ; Messrs. T. Blyton, H. Edwards, J. Hallawell, A. Hughes and P. C. Williams were elected associates. The President then delivered his inaugural address. Inaugural Address. After an interval of five years you have again done me the honour of electing me your President. When some few months since I consented to act in tbis capacity, my official duties were fewer than they now are, otherwise I might justly have hesitated in taking this further re¬ sponsibility ; nevertheless, seeing that those who have most to do, do the most, I am hopeful that with the support which I can fully rely on from the Council and from the members generally we shall have a successful session. This society has now an established position, a history extending over nearly one-third of a century, a dignity to maintain, a useful work to perform. It is a proverb of antiquity that “ no man lives unto himself,” and what is true of the individual is equally so of the body corporate. As individual members of this society we have helped to swell its numbers and have contributed to its funds ; but we have done more, we have entered a brotherhood where the common weal should be our first thought, we have virtually pledged ourselves (one and all) to contribute to the common fund of information, to impart as well as to receive, to cull from our every day experience, from the work or reflections of our leisure, something, however small, which will help to add interest and profit to our evening meetings. As a society we represent the progress and interests of chemistry and pharmacy in this town and neighbourhood, and have our relations to the other scientific societies which meet in this institution and elsewhere. We are one (and I venture to think not the least important) of the societies established throughout the country for the fostering and development of these sciences, so that it requires but a moment’s reflection to see how great is our joint respon¬ sibility, how necessary for us to maintain in its integrity the work of the founders and of those who have reared and brought the society to maturity. Passing from the society itself to the branches of science which it repre¬ sents, and the relation of these to the numerous other branches, the mind of the most profound thinker is unable to grapple with the whole of the facts, deductions and theories which rise up before it, some real and substantial, others semi-ideal, some with so much of truth about them that they cannot be lightly dispensed with, others having barely a claim to recognition. A connecting thought here, a missing link there, this clear exposition, that conflicting evidence, passing from arguments of solidity through the various grades of attenuation to the most ideal theories of the imagination. An interminable network of ramifications embracing all, from the commonplace things of every day life to the borders of infinity. But if the gravest philosopher is incapable of grasping the whole of this and of arriving at satisfactory generalizations, can it be expected that we, men of average minds and capabilities, shall be able to deal with them ? Presumably not, but you will agree with me that it is well that we should dip sufficiently deeply into these things to enable us to realize the earnestness and reality of life and to penetrate beyond the mere surface of existence. This probably will be best accomplished by limiting our sphere of inquiry and regarding more especially the chemist and pharmacist, and his environment, not in the broadest possible acceptation of the term ; but con¬ templating more especially his surroundings, the accom¬ plishments of the present and the work of the immediate- future. Next to what Carlyle calls “the vestural tissue,” around the chemist are his chemicals, balances, burettes, beakers, to an almost endless list ; his laboratory. Around the pharmacist his measures, mortars, medicines, an ever increasing multitude ; his pharmacy. These are the surroundings within which he, as a rule, gains ex¬ perience and acquires the means by which he is sustained and enabled to impart energy to the mind, that mind by which he is or should be judged as regards his social position and capabilities for usefulness to mankind. It is not however the mere possession of, but the prac¬ tical application of knowledge which determines the environment outside that already mentioned, and che¬ mistry provides abundant scope for this, seeing that it is at the very foundation of our knowledge of things. Professor Allman, in his recent’presidential address to the British Association, pointed to the conclusions of Max Schultze, which are now generally accepted as being cor¬ rect, viz., “ that the same protoplasm lies at the base of all the phenomena of life, whether in the animal or veget¬ able kingdom,” and further, that although in all prob¬ ability chemically the same, it differs in some unknown physical property. Here, then, chemistry is called on to decide a most important question, a fundamental principle in biology, and this single illustration will suffice to show the importance of and necessity for exactness in the results of its operations. Great as this exactness already is, workers in this field are constantly aiming at new or im¬ proved methods for the acquirement of greater accuracy, and while this work is steadily progressive, the facts or subject matter of chemistry remain constant and immu¬ table to all time. Not so the theories by which these facts are explained ; within comparatively few years these have undergone a complete revolution, and the student who twenty years ago took special pains to ground his knowledge thoroughly in the principles on which chemical phenomena were generalized, has, if desirous of keeping pace with the times, been compelled to unlearn and con¬ sider erroneous much of what he then regarded as incon¬ trovertible fact, and to begin de novo to acquire the modern system. The work of the professional chemist is not materially affected by these theoretical considerations, but inasmuch as he seldom enters this profession simply on account of the amount of remuneration it yields, but rather because his taste lies in this direction ; because he takes pleasure in his occupation, and delights in unravelling these mysteries surrounding the primary and complex condi¬ tions of matter, he will be induced at every step to go beyond the mere requirements of his work. Chemical occupation has considerably increased in modern times ; within a comparatively short period a small army of public analysts has been created, which, with its vassals, is pledged to guard the public against the baneful influ¬ ences of adulteration, a very desirable object and one in which undoubted good has already been accomplished. That some unqualified, over officious and even unprincipled men should have entered the ranks is not at all surprising, seeing that the demand sprang suddenly into existence without the years of necessary preparation for supplying it efficiently, but the position is becoming elevated and the evil which has existed in some localities (happily not in ours) viz., where the public analyst has been a terror equally to the unjust and the just, will doubtless soon cease; a consummation greatly to be desired and by none more so than by the conscientious and efficient mem¬ bers of the body. In addition to the various chemical works throughout the country there are many manufac¬ tures, the conduct of which involves some chemical knowledge, and in some instances this is sufficient to justify the employment of one or more chemists on the premises. This is a growing occupation for chemists and one which must necessarily increase in direct proportion to the enlightenment of the age. I have in my mind at October 18, 1879], THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS.' 307 the present moment one or two large manufacturing firms who, to my personal knowledge, by using their laboratories as guides in their operations, are enabled even in these trying times to compete successfully with what would otherwise be overwhelming competition. Belonging to this department of technical chemistry are certain manu¬ factures in which huge chemical processes are involved. Those of us who attended the recent meeting of the British Pharmaceutical Conference at Sheffield had an opportunity of witnessing one of these in the Bessemer process of manufacturing steel, the grandeur of which produced an effect on the minds of many which will not readily be effaced. The Hollway process of rapid oxida¬ tion and the use of sulphides as fuel is of so recent a date as to be scarcely perfected, at least as regards working details, but it is a grand conception, the ultimate effects of which cannot at present be estimated. Ores so poor as not to be worth working on account of the cost of the fuel which would be consumed, are by this process made to produce their own fuel and can be worked at a profit. These are two instances of applied chemistry, but many others might be quoted if time permitted. Beyond this we have the more attenuated environment of chemical physics, in which we gradually pass from experimental demonstration to deductions, theories and hypotheses ; here rapid strid«s have been made during the last few years, and still there is room for work. Quite recently we were startled by the announcement that oxygen, hydrogen and nitrogen had been liquefied ; but the other day it was more than hinted that chlorine had been dissociated, and now Mr. Crooks opens up a new field of inquiry into the chemistry of “radiant matter.” So far he finds that even in this attenuated condition the molecules retain their chemical charac¬ teristics ; if, however, the character of the molecules can be modified by physical influences, or if it is possible for the atom to exist in a free and uncombined state, it seems probable that the most favourable condition for such existence will be found in this direction. Having thus gone over in outline some of the sur¬ roundings of the chemist as a professional and scientific man, let us contemplate shortly but more especially the environment of the pharmacist. I have already men¬ tioned the close proximity of the pharmacy, its medicinal contents and the instruments and utensils by which the latter is dispensed ; but seeing that drugs, etc., have t© undergo selection and certain processes of manufacture before they are fitted for use in the pharmacy, some amount of skill is required to enable the operator to accomplish these things satisfactorily. But compara¬ tively few years since only one school of pharmacy (to the best of my knowledge) existed in this country, now there are probably a score or more. Books and other facilities for education have been multiplied, all of which are, or should be, healthy signs ; and I think it cannot be denied that the pharmacist of to-day is a decidedly more accomplished man in his calling than he was even twenty years ago. But whether pharmaceutical education has kept pace with the provisions made for it is somewhat doubtful ; if young men trust too much to the “ short outs ” so temptingly provided and neglect systematic training and home study, the knowledge gained will be exceedingly evanescent and will be of little real use to them ; it might perhaps suffice to enable them to pass an examination or two, but it should be borne in mind that examinations are not the aim and end of our existence, they are but the portals through which it is necessary to pass in order to enter into the real business of life, first as assistant and then as principal, during which transition views of things often undergo considerable modification. The chemistry of the pharmaceutical laboratory is not so •exhaustive as that previously referred to; many of its operations are mechanical and can be performed in detail by less skilled labour, but that both knowledge and judgment of no mean order are involved in the direction of these, no one with personal experience in the matter will doubt. But chemistry does not stand alone; some knowledge of botany, a sound knowledge of materia medica and of the various operations and requirements embraced by the broad and comprehensive term of phar¬ macy are absolutely necessary, and if these are faithfully acquired it is not at all surprising that those who conduct a business involving proficiency in such sciences should lay claim to a professional status. Many, however, find it impossible or inexpedient to conduct their business on a purely professional basis ; hence we have the existing state of things well known amongst us, viz., pharmacy as a combination of profession and trade. The social position of the pharmacist has been so recently and so ably dealt with by the President of the Conference that very little from me on this point will suffice. There can be no doubt but the public regard pharmacy as something above an ordinary trade, and the pharmacist as a man of superior intelligence; but he is a shopkeeper, and with the superficial portion of society this militates considerably against him. Yet if my experience is worth anything, it indicates that those who have the most substantial claims to position themselves, readily accord to us our proper status. Still, an anomaly does exist, and this social environment of the pharmacist is a problem not easily solved. It has occurred to me in this relation, as it probably has to others, that there is something in a name, and if we, after continental fashion, were to educate ourselves and the public to speak of our places of business as Phar¬ macies, and to regard our charges for dispensing — -however small or large — in the light of fees or payment for pro¬ fessional work — which they really are, and added to this, if we put forth a general effort to improve the tone of our business, we shall have done, not all, but something toward the accomplishment of our aim, which must necessarily be a work of time. Progress will of course be less rapid in times of general depression than it would in those of prosperity, and far as I am from believing in the perpetuity of “bad times,” if only half one hears is true, it would be useless denying their existence at present. But as a picture cannot consist entirely of background and shadows, but must have its high lights and half tones, so the evil cannot exist without some attendant good; the refining process rarely fails to pro¬ duce better metal, and I believe these trying times have their salutary influences, inasmuch as they are calculated to stimulate our capabilities, to test the strength of our mental resources and to develop our best energies. Our latent powers are doubtless greater than we should ever be aware of but for the necessity which calls them into action, and if we add to these fortitude and patience, there can be no doubt but the end will be worthy the means. The present time is one in which we should most thoroughly appreciate an association like this, which brings us together for friendly intercourse, for mutual help by the exchange of ideas, tending to render more perfect the sciences we profess, and to make us better capable in our respective spheres of serving our day and generation, so that when called on to give place to others, we may leave Chemistry and Pharmacy some¬ thing better than we found them. There is much un¬ cultivated ground to work ; much that remains to be done. Truly, at first sight, it appears as though every atom of the universe, every molecule of which it is built up had been twisted and turned by scientists in every conceivable or possible direction ; but going somewhat more deeply into our subject we find that so vast is the prospect which opens up before us that we are overcome by the contemplation of how little it is possible for one individual in a lifetime to accomplish. The amount of partially developed ideas and unfinished work by which we are surrounded is very considerable ; versatility of talent and the wide range of operations seem to tempt workers to pass on to new subjects and new inquiries, and to leave the old ones with still much to be done for their completion. 308 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 18, 18 79 There are still many vacant places in the tables of homologous substances. Synthesis of the alkaloids is merely commenced, inasmuch as with only two or three has it been accomplished. Not until within a few weeks since were we furnished with reliable information on the chemistry of so common a substance as ginger. Perusal of the blue list published by the British Phar¬ maceutical Conference, and of the list of queries given by the American Pharmaceutical Association, at once suggests the incompleteness of our knowledge in many chemical subjects and pharmaceutical processes, and re¬ minds us that there is more work than there are workers. Gentlemen, let us, as members of this Association, resolve that during the present session we will do some¬ thing toward working out the numerous problems which lie around us for solution, and so contribute something to the common stock of chemical and pharmaceutical knowledge. One word to the students now entering on a new session, and I have done. Let your work be thorough. You have examinations to pass and must of necessity work in a direction to acquire the requisite education ; but if you work solely for this, with no higher or broader aim, then, however successful you may be in passing, you utterly fail to accomplish the object for which examina¬ tions exist. It is not by spasmodic efforts, but by per¬ sistent study — Nulla dies sine lined- -that you can gather in a rich harvest of knowledge and thereby gain the approval of your own consciences and are enabled more thoroughly to serve the interests of your fellow men. A cordial and unanimous vote of thanks, proposed by Mr. R. Sumner, seconded by Mr. Davies and supported by Mr. Mason, having been accorded Dr. Symes for his able and instructive address, the meeting terminated. CHEMISTS AND DRUGGISTS’ TRADE ASSO¬ CIATION OF GREAT BRITAIN. A meeting of the Law and Parliamentary Committee of the Association was held at the office of the Association, 23, Burlington Chambers, New Street, Birmingham, on October 8, 1879, at 1 p.m., Mr. Thomas Barclay, President, in the chair. Present — Messrs. Andrews (London), Churchill (Birmingham), Cross (Shrewsbury), Hampson (London), Holdsworth (Birmingham), Jones (Leamington), Symes (Liverpool) and the Solicitor of the Association. The minutes of the previous meeting of the Committee were read and confirmed. The Secretary said that in compliance with the in¬ structions of the Committee he had issued circulars to influential members of the trade asking for well- authenticated instances in which fatal results had followed the sale of scheduled poisons under cover of the patent medicine stamp, with a view to obtain information and suggestions that would prove to the satisfaction of the Legislature that the present system of unregistered persons vending poisons under cover of the patent medi¬ cine stamp was dangerous to the general public. A large number of replies to this circular were laid on the table, and extracts from some read. The President said the Committee at its last meeting spent a considerable amount of time in endeavouring to devise some means of carrying out the wishes of the Executive in procuring information to aid them in dealing with that question. As had been seen from the minutes of that meeting, several suggestions had been considered, and a resolution passed instructing the secretary to issue a circular. They had to consider whether the replies to that circular contained adequate information or whether it would be advisable to adopt other means to that end. Mr. Hampson said they had heard in one of the letters read by the Secretary a statement to the effect that it made little difference who sold patent medicines con¬ taining poisons, as they were not supposed to know the contents of such medicines. Such remarks had from time to time been applied to poisons sold uncovered by the stamp, but he was of opinion that it did make a con¬ siderable difference in whose hands the sale of such poisons was placed. He believed that the fact of the public being compelled to go to particular shops for the purchase of poisons was in itself an advantage to the trade. The public knew that they must go to registered persons to obtain poisons ; if those poisons were obtainable at every shop they would be ranked with groceries and such like goods. It was thought wise — the Legislature thought it wise — to restrict the sale of certain poisons to registered persons, and he failed to see any distinction, or any very important distinction, between the sale of poisons covered by the patent medicine stamp and the same poisons sold uncovered by the stamp. He con¬ sidered that the sale of all scheduled poisons covered or uncovered by the stamp should be restricted to chemists and druggists, and he thought the efforts of the Associa¬ tion should be directed to that end, and that it was their duty to aid the Executive in accomplishing that object. Mr. Symes said he supported Mr. Hampson’s views; it was an opinion he had long held. If the sale of patent medicines containing scheduled poisons were placed in their hands exclusively, it would, to a certain extent, increase their responsibilities, but he thought in the present state of affairs they must be prepared to accept those increased responsibilities. The President said it had been already decided by the Executive to endeavour to restrict the sale of poisons under cover of the patent medicine stamp to chemists and druggists. After further discussion it was unanimously resolved : — “ That the Secretary be empowered to take such steps as he deems expedient, by conference or otherwise, to collect information and suggestions on the sale of patent medi¬ cines, with a view to bring about modifications in the Pharmacy Act, 1868, to restrict the sale of scheduled poisons under cover of the patent medicine stamp to registered chemists and druggists.” The case of a member of the Association, against whom proceedings had been taken under the Sale of Food and Drugs Act, for the sale of soda water, was discussed at considerable length, and after mature deliberation, it was unanimously resolved : — “ That the Solicitor be instructed to defend a member of the Association prosecuted for the sale of soda water, under the Sale of Food and Drugs Act, and to employ the services of Professor Attfield and Mr. Stoddart.” The Secretary reported that in compliance with a resolution passed by the Committee at its last meeting, he had taken out summonses against three illegal traders for infringements of the 17th section of the Pharmacy Act, 1868, and that a fine was in each case imposed by the magistrates. He said they would probably have observed from a leader in the last number of the Phar¬ maceutical Journal that the Editor attributed that action on the part of the A ssociation to an intimation furnished by the Solicitor of the Pharmaceutical Society at the hearing of a recent case of prosecution under the same section of the Act, undertaken by order of the Pharma¬ ceutical Council. The Editor had, he presumed, forgotten that the Association carried to a successful issue three cases, proceedings in which were taken under that section so long ago as June, 1877. The Secretary further reported having forwarded to the Secretary and Registrar of the Pharmaceutical So¬ ciety particulars of eight cases of infringements of the provisions of the 15th section of the Pharmacy Act, in which he had collected evidence. Communications were read from the Secretary and Registrar of that Society acknowledging the receipt of that letter, and detailing the course he had adopted in dealing with each particular case. A letter was read from a member of the Association stating that there were ten or twelve illegal dealers m © October 18, 1379.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 309 poisons carrying on business in and around the town in which he resided. It was unanimously resolved : — “ That the Secretary be instructed to take proceedings from time to time against illegal traders under the 17th section of the Pharmacy Act, 1868, in such cases as in his opinion, and that of the Solicitor, it is expedient.” EDINBURGH CHEMISTS’ ASSISTANTS’ ASSOCIATION. The first meeting of the second session of the above Association was held in the rooms of the Pharmaceutical Society (North British Branch), 119a, George Street, on Wednesday evening, October 8. The minutes of the final meeting of last session having been read and adopted, The President, Mr. D. McLaren, proceeded to read the opening address. In thanking the members of the Association for the honour they had conferred upon him in electing him as their President, he assured them of his willingness to do his utmost in furthering the interests of the Association ; but remarked that it was the exertion of individuals alone which would constitute the sine qua non in carrying out that end. In referring to the re¬ lationship existing between the medical profession and -chemists, he argued that while it was the care of the physician to ascertain the nature and seat of disease and to prescribe the appropriate remedies, it was the province of the chemist to collect, compound and dispense these remedies. While the exercise of the duties of a physician demanded a much higher standard of qualification than was requisite to the discharge of the duties of a chemist, yet the application of much care and dexterity, as well as a considerable acquaintance with scientific knowledge, was demanded of him also. In speaking on the subject of counter prescribing, he discountenanced the practice of chemists assuming to themselves on all occasions the responsibility of properly qualified practitioners, but maintained that on many occasions, and more especially where the poorer classes were concerned, it was necessary, if not incumbent, upon the chemist to give advice in the treatment of minor ailments. Admitting that there was thus a tendency on the part of the chemist to encroach upon the rights of the doctors, yet the keeping of an open shop by doctors, was, he affirmed, no less an encroachment on the rights of the chemist. After briefly noticing the various essays to be delivered during the session, as stated in the syllabus, he expressed his opinion that members would derive not only much pleasure, but also valuable information from their attendance on these meetings. At the close of the address, a discussion was entered into as to the best means to be adopted for the shortening of business hours in those shops which remained open later than 8 p.m. A Committee, consisting of the Presi¬ dent, Vice-President, Secretary and Treasurer, was finally appointed with powers to take such steps in the matter as might be thought desirable. A very cordial vote of thanks was awarded to the President for his interesting and instructive address, to which, having briefly replied, the meeting was brought to a close. proceedings of J^cienti/i^ Societies. AMERICAN PHARMACEUTICAL ASSO¬ CIATION.* The twenty-seventh annual meeting of this Association was called to order in the Supreme Court Room, in the city of Indianapolis, Ind., on Tuesday, September 9, at 3 p.m., by its President, Mr. George J. Luhn, of Charles¬ ton, S. C. President Luhn read the annual address which is * Abstract of the report in the Druggists’ Circular and Chemical Gazette, October, 1879. usually expected from the retiring President. The address was replete with information as to the work, objects, and success of the Association in the past, as also the present attainments of pharmacy, made necessary through the working of the laws relative to pharmacy in many of the States, and the examinations of the Boards of Pharmacy under these laws. This advance is being greatly aided by the formation of State Pharmaceutical Boards, and of these several have been established during the past year. Allusion was made to the work of the officers, as also the several committees authorized by the Association. Among the other subjects commented upon were the time at which the meeting was held, the finances of the Association, and the centennial fund. The President advised that the meetings should be held earlier in the year ; when in the Southern States, it should be as early as April or May, and when in more northern latitudes, not later than August. Regarding the finances, he named some plans for the relief of the debt the Society owed, and said that definite measures should be adopted at this meeting for that purpose. The centennial fund, which had now held over for two years, had made slow progress, as but one-third of the necessary amount had as yet been collected. At the conclusion of the address it was, on motion, referred to a committee. The Committee of Credentials reported that they had received the credentials of delegates of various associa- tions. Invitations to attend the meetings of this body were extended by the Business Committee, on behalf of the Association, to the following : — The Governor and State Officers, Judges of the Supreme Court, Mayor, Medical College of Indiana, Central College of Physicians and Surgeons, and the Marion County Society of Micro- scopists. The names of fifty-four persons were read, and of these fifty-two were elected, two names being withdrawn for the present. At subsequent sessions, other members were elected, including the two names temporarily withdrawn, making eighty-five new members elected at this meeting. Some discussion arose as to qualifications for member¬ ship, as to time of service in the business, and the following resolution was offered by E. H. Sargent, of Chicago : — ri That a committee of three be appointed to report at our next session what changes may be desirable in our bye-laws to make definite and uniform the ballot¬ ing for members, and also to report on the requisite qualifications of candidates for membership in this Association.” The Chairman of the Executive Committee, Mr. G. W. Kennedy, read his report. The main facts may be briefly stated as follows : — Total number of members at present, 1106. This is a decrease from last year, as the number of members elected at Atlanta in November last was exceeded by the number lost by various causes, of which 8 were by death, 13 by resignation, and 61 from other causes ; total 82. The report was ac¬ cepted and directed to be published. The delegates present then named one from each dele¬ gation, and to this the President added five others, and these gentlemen were constituted the Committee to Nominate Officers for the ensuing year. The President appointed a Committee on Exhibits ; and, after this, the Secretary called the roll of members present. The Association then adjourned until 9 o’clock Wed¬ nesday morning. SECOND SESSION. The meeting was called to order shortly after 9 o’clock, when the Secretary read the minutes. T. Roberts Baker, of Richmond, Va., then read the report of the Nominating Committee ; immediately after which followed the election of all the gentlemen named by the Committee. The principal officers were as follows : — President, George W. Sloan, Indianapolis ; 310 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 18, 1S79. First Vice-President, T. Roberts Baker, Richmond, Va. ; Second Vice-President, Joseph L. Lemberger, Lebanon, Pa. ; Third Vice-President, Philip C. Candidus, Mobile, Ala. ; Treasurer, C. A. Tufts, Dover, N. H. ; Permanent Secretary, John M. Maisch, Philadelphia, Pa. ; Reporter on the Progress of Pharmacy, C. Lewis Diehl, Louis¬ ville, Ky. The Committees appointed included the Executive Committee, Committee on Drug Market, Committee on Papers and Queries, Business Committee, Committee on Prize Essays and Committee on Legislation. The retiring President then introduced Mr. G. W. Sloan, of Indianapolis, the new President, who briefly acknowledged the honour conferred upon him. Prof. Maisch then read his report as Permanent Secretary. The topics discussed were mainly the ex¬ penses incurred in publication of proceedings, and suggestions as to where in future there might be some retrenchments as to expenses, as also how it might be possible to increase the income. Alluding to the delay in issuing the last volume of proceedings, it was stated that it was due in part to the delay in obtaining the wood-cuts to illustrate the work as desired. The total expenses of issuing the volume were 3,823.42 dollars. The expenses of various years were compared, showing that, considering the increased volume of the proceedings, it has cost the Association much less, proportionately, than in the past six years. Although the organization is practically in debt, the Reporter did not favour an assessment, but rather decreased expenses and an effort to largely increase the membership. A resolution was passed some years ago that the subscription to the various papers and periodicals received for the Reporter on the 1 Progress of Pharmacy” is thought to be an unnecessary tax on the body, and it was suggested that it be left discretionary with the Executive Committee and the Permanent Secretary. It was also suggested that in localities where more than three or four members reside, authorized agents of this Association be appointed to extend its interests. The report was accepted, and subsequently referred to committee. The Treasurer, Charles A. Tufts, M.D., of Dover, N. H., then read his report. The total receipts for the year are 4,849.12 dollars; the disbursements were 4,730.45 dollars, and a cash balance on hand of 980.98 dollars. This balance of cash on hand represents in part dues of members paid in recently, while there are some heavy bills still due for the publishing of last year’s volume. The Association has actually incurred expenses in the past more rapidly than it has provided ways and means for their payment. * The report was received and referred to an Auditing Committee, named by the chair. After some considerable discussion relative to the finances, and the two reports just read, it was, on motion, referred to a Special Committee appointed by the chair. The subject of the Centennial Fund was brought to the notice of the members, and on motion of Prof. Diehl, the chair named three members to act with the Chairman of the Executive Committee to endeavour to secure the balance of the amount necessary. The Committee appointed at the previous session to suggest such revision of the bye-laws as might be thought desirable relating to membership and election of new members, made a report recommending alterations in the bye-laws, adding to the duties of the Executive Com¬ mittee, by requiring that the names of candidates shall be read at one session and balloted for at the next session, and that a vote of two-thirds shall elect ; the Executive Committee to hear and decide upon any objections that may be offered to any name presented ; and no names to be balloted for until they have been approved by the Committee. The Committee suggested the advisability of so changing the bye-laws that all matters relating strictly to business be brought before a Business Council, and thus devote much more time to the reading and dis¬ cussion of papers than is now possible under the present rules. The consideration of the proposed changes was laid over till the next session, when the resolutions offered by the Committee were adopted, and the necessary altera¬ tions of the bye-laws will be made in accordance there¬ with. It was stated by the President that it was now in order to receive suggestions as to where the next annual meeting should be held. Prof. Maisch read an invitation signed by the drug¬ gists of Kansas City, Mo., and Prof. Bedford read an invitation signed by the druggists resident at Saratoga Springs, N. Y., as also one signed by the proprietors of the several mineral springs of Saratoga. Prof. C. L. Diehl then read the introductory to his report on the progress of pharmacy. The Association adjourned shortly after the reading of the introductory of this report. THIRD SESSION — WEDNESDAY AFTERNOON. Soon after 3 o’clock the meeting was called to order by the President, the minutes of the previous session read,, and then, in accordance with a motion previously offered. Prof. Remington was named as the reader for the Asso¬ ciation. Prof. Maisch read the report of the Committee on Legislation. The principal new facts related to the minor modification of the law of New Jersey, and the fact that a law has been enacted which relates to the sale of medicines and poisons in King’s County, N. Y. The remaining portion of the afternoon was occupied by the reading of scientific papers, after which the meeting adjourned until Thursday morning at 9 o’clock. FOURTH SESSION — THURSDAY MORNING. The Association was called to order at 9.30 by the President, Mr. George W. Sloan. The Committee appointed to examine the reports of the Secretary and Treasurer, with a view to ascertain what changes may be recommended for the advantage of the Association, reported the following recommenda¬ tions : — 1. That local agents be appointed in all places where more than three members reside. 2. That delegates from the various bodies be in future required to pay initiation fees. 3. That the volume of proceedings he reduced in size, as the judgment of the Executive Committee may determine. 4. That the Secretary be empowered to sell such of the pamphlets which are used for the Committee on the Progress of Pharmacy, as in his judgment are of ne further use. 5. That the Treasurer present annually a tabulated statement of all receipts and expenditures. 6. That the fiscal year begin with January 1, instead of September 1. The report, after a very brief explanation, was adopted, and Prof. Remington was requested to alter the bye-laws accordingly. In the absence of Mr. Charles Rice, the Chairman of the Committee on the Revision of the U. S. Pharmaco¬ poeia, Prof. Diehl, one of the Committee, read the introductory report offered by Mr. Rice. The report was a very voluminous one, and well represents the untiring industry of the Chairman of the Committee and his efficient co-labourers. The desire of the Association, as expressed in the resolution by which this Committee was reconstructed in 1877, was that at the present meeting the Committee should have their report completed and ready to present at the meeting of the Pharmacopoeial Convention in May next. This October 18, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 311 seems to be an absolute impossibility ; the most that can be hoped for is to publish as much as can be prepared by that time. The various members of the Committee have taken up departments of the work, and others have aided liberally in giving valuable time for careful experi¬ ments. FIFTH SESSION — THURSDAY AFTERNOON. The Association met at 3 p.m. The Business Committee then called up an amendment to the constitution proposed by Mr. J oseph T. Remington to strike out the words “ the United States,” and insert in place thereof “ America,” so as to make the sentence read as follows : — “ Its aim shall be to unite the educated and reputable Pharmaceutists and Druggists of America in the following objects.” This was, with a brief ex¬ planation and discussion, adopted. SIXTH SESSION — FRIDAY MORNING. The meeting was called to order, and the usual business disposed of. The President returned his thanks to the Association for their consideration, and then put the motion that the Association do now adjourn, to convene in Saratoga Springs, N. Y., on the second Tuesday (the 14th) of September, 1880, at 3 o’clock, which was adopted. The following papers in replies to queries were read during the intervals of business : — Eriodictyon Californicum is receiving attention for its action in lung diseases and bronchial affections. What is its therapeutical value, and to what is its activity due ? Make a chemical examination of it. By Charles Mohr. The writer made a very full examination of the plant, and the action of the various solvents in regard to the amount and quality of extractive matter. The properties are believed to be due chiefly to the resinous matter, which is best extracted by alcohol, to which it yields nearly 11 per cent, of its weight. It yields an ethereal extract of 15 per cent, and an aqueous of 19 per cent., but that which is taken up by alcohol seems more satis¬ factorily medicinal in its character. Its apparent action is as an astringent and tonic to the bronchial tubes, but as a remedial agent in consumption the author thinks it no better than many other panaceas whose uselessness was long ago proved. Fluid Extract and Syrup of SeneJca. — Should it not be prepared with an alkaline menstruum ? By George W. Kennedy. The writer stated that for the past seven years he had used an alkaline menstruum in making both the fluid extract and syrup of seneka, and has never during that time noticed a single instance of gelatinization, and in but very few instances any precipitate whatever. It also furnishes handsome and brighter looking preparations, and is apparently more acrid and stronger. For 16 troy ounces of seneka root 3 fluid drachms of aq. ammonia are sufficient, and this amount is added to two pints of dilute alcohol. The finely ground drug is prepared for percolation, and after the first 12 ounces of percolate have been obtained, the percolation is continued to exhaustion. The second percolate is evaporated to 3J ounces, to which is added £ ounce of alcohol, and this is added to the reserved percolate of 12 fluid ounces. In making syrup of seneka, this alkaline liquid is used, but otherwise the process o? the Pharmacopoeia is followed. Mr. S. Campbell thought a stronger alcoholic men¬ struum with glycerine answered as well. Mr. Lloyd spoke of the fact that seneka root yields both salicylic acid and oil of wintergreen under certain conditions, though in very small quantity. Can any of the Decoctions or Infusions of the United States Pharmacopoeia be satisfactorily prepared from the Fluid Extracts of the United States Pharmacopoeia, and in what particulars do they differ from infusions and decoc¬ tions prepared in the prescribed manner ? By William Saunders. This paper gave many detailed experiments, and the results of preparing infusions and decoctions from fluid extracts. In the author’s opinion when the fluid extracts are made with a menstruum of dilute alcohol, they may readily and satisfactorilybe used to prepare both of the above weaker remedies ; but when the solvent used is stronger alcohol, and this be diluted with water to make it the same strength as an infusion or decoction, the general result is a persistent cloudiness or milky appearance, rendering it objectionable in dispensing. The affinity of Glycerin for water is well known : to what extent will officinal glycerin attract moisture on being exposed to a damp atmosphere? By George W. Kennedy. The author exposed to the atmosphere of a damp cellar, glycerin of specific gravity l-23 and 1*26 in vessels of broad shape, also in narrow mouth bottles, weighing the vessels at frequent intervals. In the first ten days the vessels of broad, open space had absorbed 4 per cent, of moisture, and this had continued until, at the end of ten months, the increase had amounted in the glycerin of 1 '23 sp. gr., to 55^ per cent., and in the denser variety to 57^ per cent. Revision of the u. s. pharmacopoeia. Several papers were presented on this subject. The introductory by Mr. Charles Rice was an admirable review of the subject, discussing the work already done and in process, and alluding to the changes in the character of the work itself. The proposition of the committee is to arrange the contents in alphabetical order, without any regard to the present division into materia medica and preparations ; to do away with any mention of weights, substituting parts by weight , arrang¬ ing these in the simplest ratios possible. In preparing medicated waters, precipitated phosphate of calcium is proposed in place of carbonate of magnesia, for the purpose of diffusing volatile oils and similar materials for better solution in water. Prof. J. P. Remington presented a very full report upon the tinctures, giving detailed formulas, some in¬ volving modifications, but all arranged upon the plan of simplifying processes as much as possible. The paper was accompanied by numerous specimens of tinctures made as proposed, as also by the residues of the exhausted drugs. PHARMACEUTICAL EXHIBITION. Masonic Hall, situated on the opposite side of the street from the Supreme Court Room, was the place selected for the exhibition of articles connected with pharmaceutical interests. The large room was literally crowded to repletion with beautiful products of the art of the chemist, pharmaceutist, manufacturer, artizan and perfumer ; and in many cases the crude materials from which they are prepared. CHEMISTS’ ASSISTANTS’ ASSOCIATION. A meeting of the above Association was held at George Street, Hanover Square, on Wednesday evening, October 8. The inaugural address was read by the President (Mr. F. W. Branson), who after alluding to the rise and pro¬ gress of the Association and the large increase of new members, touched upon several topics of general interest, and concluded by noticing how useful a large and varied source of knowledge was to the pharmacist, and recom¬ mending as recreative studies a more intimate acquaint¬ ance with the vague separation of the animal and vegetable kingdoms and geology, which especially recommended itself by being a healthy as well as a scientific study. 312 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October is 1879 A vote of thanks to Mr. Branson was proposed by Mr. Snow, and seconded by Mr. Naylor. Mr. Ernest Cardwell, the late Honorary Secretary, was then presented with a complete set of Dickens’s Works, together with an illuminated address, as a slight token of esteem on his severing his connection with the Associa¬ tion. Mr. Branson then referred to the approaching Con¬ versazione to be held at St. James’ Hall, on Wednesday next, October 22, and expressed his opinion that it would be a great success. farnaiimitarg and 3faui Ikocecdings. The Nature and Quality of Soda Water. IMPORTANT PROSECUTION UNDER THE SALE OF FOOD AND DRUGS ACT. At the Newport (Mon.) Borougk Police Court, on October 10, 1879, before Dr. Woollett (chairman), and Messrs. Charles Lewis and Henry Phillips, Mr. Eleazer Davis, chemist and soda wMer manufacturer, of 55, Dock Street, Newport, was charged under the Sale of Food and Drugs Act, 1875, for that he did in the said borough “sell a certain article, called soda water, not of the quality and nature asked for.” Mr. Line (Deputy Town Clerk) conducted the prosecu¬ tion, and Mr. Henry Glaisyer, instructed by the Chemists and Druggists’ Trade Association of Great Britain, ap¬ peared for the defendant. Mr. Line said this was a somewhat important case, and the facts were these : — On the day in question, Septem¬ ber 15 last, the public officer went to the defendant’s shop and asked for six bottles of soda water, which were sup¬ plied to him. The ordinary course was adopted by the officer as to the division of the samples. Two of these bottles were sent to the borough analyst, whose certificate states : “I, the undersigned, public analyst for the borough of Newport, do hereby certify that I received on September 16, 1879, from Mr. T. H. Jones, a sample of soda water (bottle marked No. 125) for analysis, and have analysed the same, and declare the result of my analysis to be as follows : — I am of opinion that the same is a sample of water charged with carbonic acid gas, and I am of opinion that the said sample contained the parts as under, or the percentage of foreign ingredients as under : — Total solid residue, 14‘63 grains per gallon ; metallic impurity equiva¬ lent to grain of lead per gallon. Observations : — This sample is ordinary water charged with carbonic acid gas, and does not contain added bicarbonate of soda, and is not ‘soda water.’ The metallic impurity is not consider¬ able, but care should be taken no lead pipes or solder joints containing lead are used in the apparatus employed in the manufacture. As witness my hand September 23, 1879. (Signed) J. W. Thomas, F.C.S., Mem. Inst. Chem.” The question to be considered was whether water simply charged with carbonic acid gas and contain¬ ing no soda is soda water within the meaning of the Act. The defence would perhaps endeavour to show that this article without soda was soda water, but he sub¬ mitted that a person going to a chemist’s shop would ex¬ pect to get a different article from what he would expect to get if he asked for the same thing at a restaurant. Soda was a highly important medicine. Mr. Glaisyer: You are not going into the question of a drug, I suppose. We are not summoned on that. Mr. Line : I am not ; it is a question of a food. It is not the article of food which a person going into a che¬ mist’s shop would expect to receive when he had asked for soda water. Mr. Glaisyer : Why into a chemist’s shop ? The Chairman of the Bench : Is it an article of food ? Mr. Line : It is an article of food sold by chemists, and I submit in this case the chemist is selling as soda water a water not containing soda, and that consequently the defendant has not supplied the article asked for and expected. We do not drag this person here as an ordi¬ nary malefactor. If you hold that in getting this par¬ ticular water the inspector has obtained what he may have reasonably expected to get, then, sir, of course you will dismiss the summons ; if, however, you hold other¬ wise, I shall be satisfied with a small penalty. By the Bench: Have you selected Mr. Davis especially as being a chemist ? You seem to dwell very much on the fact of his being a chemist. Mr. Line : Soda water is, of course, a medicated water . Chairman of the Bench : Then that takes it out of the category of its being a food : you would not go to the chemist’s shop to buy a food ? Mr. Line : Chemists sell many goods that are not medi¬ cines or drugs ; for instance, pomade, tooth-powders, and such like things. By the Bench : We must shut our eyes to the fact that it is a chemist who is the defendant in this case. Mr. Glaisyer : I am very glad to hear that remark from the Bench, as it has anticipated some observations I was about to make. Thomas Henry Jones, called, sworn and examined by Mr. Line, said he was the officer appointed under the Sale of Food and Drugs Act in the borough. He went to the defendant, who is a chemist and druggist and soda water manufacturer, residing in Dock Street, on Sep¬ tember 15 last, and asked for six bottles of soda water. He told defendant the soda water was to be analysed by the public analyst, and offered to divide it into three parts, which offer was accepted. Witness handed two bottles to the defendant and took two to Mr. Thomas, the public analyst, at Cardiff, the following day. De¬ fendant said, “ This is soda water, there are about three grains to each bottle.” When he asked the defendant for soda water he expected to get water containing soda. Could not say what proportion of soda he expected to get in it. Did not expect to get a medicine of nauseous taste and highly alkaline, but should expect to get a soapy-tasting article. Knowing there were two kinds sold, he did not ask especially for any particular kind. Mr. Glaisyer: The provisions of that section of the Act which relate to the division of the sample intend, that by such division a portion of the purchase shall be retained by the defendant, another portion shall be sent to the analyst, and a third shall be retained by the pur¬ chaser, and that all these portions shall be identical in their constituents. From the division which has been made in the present case this result is impossible, because by the process which the defendant adopts in the manu¬ facture of his soda water each bottle necessarily contains a variable quantity of soda, from this simple fact, which I am prepared to prove, that the soda is introduced into each bottle separately; and consequently the only way in which the purchase in this case could be satisfactorily divided to meet the intention of the Act of Parliament would be by an actual division of each bottle of soda water. By the Bench : According to your argument it would be impossible in any case to properly divide the samples. Mr. Glaisyer : You could divide any article purchased into three parts. Chairman of the Bench : Is it a matter of fact that the soda is put into each bottle separately ? Mr. Glaisyer : Yes ; and I submit it is a point of law as to whether this sample has been properly divided or not. Mr. Line: I submit the sample has been properly divided. The section referred to is the 14th section of the Act, which is as follows : — “ The person purchasing any article with the intention of submitting the same to analysis shall, after the purchase shall have been com¬ pleted, forthwith notify to the seller or his agent selling the article his intention to have the same analysed by the October 18. 1879. j THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 313 public analyst, and shall offer to divide the article into three parts, to be then and there separated, and each part to be marked and sealed, or fastened up in such manner as its nature will permit, and shall if required to do so proceed accordingly, and shall deliver one of the parts to the seller or his agent. He shall afterwards retain one of the said parts for future comparison, and submit the third part, if he deems it right to have the article analysed, to the analyst.” Well, I say, sir, the article purchased by us consisted of six bottles. If we had made six distinct purchases, then each bottle must have been separately divided, but such was not the case. I think in this case it will be found that the only active principle in the soda water was the gas, which would have vanished had the bottles been opened. Mr. Fox (Magistrates’ Clerk) : You must assume, then, that supposing there were three grains in each of these two bottles, and none in the others, you would then have had a portion of alkali in each bottle. Mr. Line : There have been hundreds of cases in which the samples have been divided as in this case. Mr. Glaisyer : This particular point has never yet been raised. The Bench conferred and decided that the case had better go on. Mr. J. W. Thomas, called, sworn and examined by Mr. Line, said he was public analyst for the boroughs of Newport, Cardiff, and the county of Monmouthshire. On September 16 last, he received from inspector Jones two bottles of soda water, No. 125. They were sealed with ihe official seal of the borough of Newport. He took par¬ ticular notice that the rubber was not destroyed in any way ; it was moist, and the wax did not adhere to it in the slightest. Both bottles were analysed, and his cer¬ tificate referred to both. Soda water containing a rea¬ sonable amount of soda, if taken internally, would have the effect of neutralizing acidity in the stomach. Water charged with carbonic gas would not have that effect. 30 grains of soda to the pint was the Pharmacopoeia standard, and a bottle of half- pint ought to contain 15 grains. In his analyses of soda waters he found they generally contained soda. Chairman of the Bench : I must say that the soda water I generally drink contains no soda at all. Cross-examined by Mr. Glaisyer: You say Pharma¬ copoeia soda water contains 30 grains to the pint ? — That is so. But there is another kind of soda water? — Not to my knowledge. Then whenever soda water is asked for the British Pharmacopoeia preparation should be supplied ? — I didn’t say that. Then there is more than one kind of soda water? — No; I did not admit that. Will you explain your answer then ? — It depends upon the quantity of soda added ; I cannot say it differs in kind. Well, if a half -pint bottle contains 15 grains of soda, what do you say that is? — Soda water. Supposing it contains only 3 grains ? — It would still be soda water. Supposing it contained half a grain ? — Then it would probably be an impurity in the water from which the soda water was made. I may say I think the standard of the Pharmacopoeia is too high. Would not Pharmacopoeia soda water be dangerous if taken too frequently? — I cannot say. Would it not be injurious if taken in large quantities? — That is a medical question I cannot answer. You say you have examined many samples — with what result? — They contained soda — from 5 grains to 15 grains per bottle. You have never had a sample containing less than 5 grains?— No. Is the British Pharmacopoeia soda water such a pre¬ paration as the public would drink ? — It is not very palatable. Is it not very nauseous? — Well, it is not palatable. Have you had soda water submitted to you for analysis which contained, as you say this sample contained, no soda? — I have had samples submitted tome as soda water which I do not admit it to be soda water. Your certificate is an analysis of both bottles submitted to you?— Yes, taken separately, and the analyses agree in every particular. There was a trace of soda present? — No, not of added soda : it had an alkaline residue. Is the residue of all water alkaline ? — In the majority of instances it is. Have you examined Newport Waterworks water? — Yes; the residue is slightly alkaline. To what extent? — Only a very moderate trace; about the same as in this soda water. Is the alkalinity due to soda? — To a certain extent it may be. Do you know whether it is or not? — I am not abso¬ lutely certain. Do you recollect from j’our analysis of Newport water what the amount was ? — It is stated on my certificate that this soda water contained 14’63 grains of solid residue per gallon, and the town water contains from 13 to 15 grains per gallon, according to the state of the weather. Have you frequently had samples to analyse ? — No, not very frequently. There may be only 13 grains of residue per gallon? — Yes, possibly. And there may be one grain to the gallon of added matter in this soda water ? — Yes, but not of carbonate of soda. How so ? — Because I should have been able to estimate it in the residue. How did you estimate the alkalinity ? — By the standard tests. Did you test both bottles for alkali ? — I tested both residues. You say in your certificate that there was a metallic impurity amounting to one-twentieth of a grain of lead to the gallon : now would that amount be injurious to health ? — No. Perfectly innocuous ? — No, I do not say that. How do you test the water for lead ? — By sulphuretted hydrogen. How do you account for the presence of lead? — From the pipes in the manufacture. Could it not have got in in any other way? — Well, I don’t think it could. By the Bench : Do you think it is likely to have come from the apparatus? — Yes. Mr. F ox : What is the smallest quantity of bicarbonate of soda you could have traced in the soda water ? — I could readily have detected half a grain. By the Bench : Then if half a grain of soda had been added to the water of each bottle you would have detected it ? — Yes, sir. Mr. Line : That is my case. Mr. Glaisyer: The case, as far as I am prepared to carry it, is this — that soda water has been largely manu¬ factured for use as an agreeable beverage, and that as such it should be as free as possible from medicinal pro¬ perties. It is well known that the article in general use is a very different article from that prepared according to the formula of the Pharmacopoeia, and I think I shall produce evidence to prove to you that the Pharmacopoeia soda water would be injurious to health if drunk con¬ stantly. The case seems to have shaped itself simply into the questiou whether the defendant did sell soda water with or without soda, and I think I may keep the Pharmacopoeia preparation out of the question. Chairman of the Bench : Quite so ; what is soda water of commerce? Mr. Glaisyer : Then I shall call the defendant and the boy that assists him in the soda water department of his 314 THE rHAKMACEUTICAL JOURNAL AND TRANSACTIONS. lOctober is, w». trade, and they will tell you that the water is charged with carbonic acid gas, and that the soda is added to each bottle separately before being filled with aerated water. I shall call as witnesses Professor Attfield and Mr. Stod- dart, both eminent analysts, and they will both tell you that soda was present in the samples they analysed, and, therefore, you will see the force of mv objection which I previously urged as to the division of the sample, and I think in the end you will either be satisfied to dismiss the case upon the technicality I have raised —and which is really something more than a technicality in this case — or to dismiss the case upon the consideration that the defendant did actually supply the soda water of oom- merce. Mr. E. Davis, called, sworn, and examined by Mi\ Glaisyer, said : I am a chemist and druggist and a soda water manufacturer in the borough, and have been in business thirteen to fourteen years. I have manufactured soda water between four and five years. Do you make the British Pharmacopoeia preparation ? — I made it once, one bottle for my own use. Have you ever had it asked for ? — Never. What is your process of manufacture? — Whiting is placed in a leaden generator, sulphuric acid is added, and the carbonic acid gas evolved is conducted by means of pipiDg into a gasometer ; it is then pumped into a soda water machine and forced from thence through the bot¬ tling machine into the bottles. Previous to the bottles being placed in the machine for charging each bottle has a certain amount of bicarbonate of soda placed in it. Is that done under your superintendence ? — When it is not-done by myself it is done under my immediate super¬ intendence. Describe the manner in which the soda is placed in the bottles ? — Cases containing the bottles are arranged side by side along the bottling machine, the bottles are placed in rows consecutively, then the soda is added to one bottle after another. By the Bench : Is that always done? — Yes, invariably. A little soda is taken on the point of a knife and dropped into the neck of each bottle. Mr. Glaisyer: Is it not weighed ? — No. You use one make of bottles, I believe? — Yes, only one make — Codd’s patent. By the Bench: What is the smallest quantity you would put into each bottle? — Well, about If or 2 grains. Would it be more than a grain? — Yes ; I did not think it was necessary to be very distinct or definite as to the amount, so long as some was put in. Cross-examined by Mr. Line: Witness said he con¬ sidered it necessary, in order to comply with the provisions of the Act, to put some soda ih. The generator in which he made the gas was of lead. Chairman of the Bench : Then I would advise you to alter it, as lead is pretty sure to come over with the gas. Albert Harvey, examined by Mr. Glaisyer, said : I as¬ sist the defendant in his business by helping him to make soda water. I put the soda into the bottles by means of a knife, putting a little into each bottle. Professor Attfield, called, and examined by Mr. Glaisyer. What in your opinion is soda water ? — There are two kinds of soda water in trade now. There used to be three. First, medicinal soda water, and the present offi¬ cial strength of that is 15 grains of bicarbonate of soda to the bottle of half a pint, and it was this medicinal soda water that gave the name to the article. This medicinal soda water always contained carbonic acid gas, and was aerated soda water. This aerated soda water created a demand on the part of the public for “soda water” that had no “soda” in it ; created a demand for aerated water, in fact. Created a demand for aerated water which the public always continued persistently to call soda water. To meet this demand for a beverage manufacturers used commonly to make soda water, so called by the public, without any soda in it, but some manufacturers put a dash of soda in it to warrant the name. But since pro¬ secutions have been instituted about soda water nearly all, practically all, manufacturers put at least a dash of soda in it, just to warrant the name, and I may say to meet the requirements of officials under the Act. Can you say anything as to the quantity of soda to meet this? — That varies very much. By the Bench : Say how much ? — It varies from a fraction of a grain to three or four grains per bottle. This is according to my experience as an analyst, and the reason of its varying is, in my opinion, because the boys and the work-people put the soda in, as has been described in this case, rapidly instead of with care. And it is important for commercial purposes that it should be done rapidly, in which case it is impossible for such boys to be very accurate as to the amount employed, that is to say, in the cases of those makers who adopt this rough- and-ready mode of adding the soda. Mr. Glaisyer : Have you had an official sample ? — I have. This is the label of the sample which I received on October 3, and it corresponds with that of the sample produced. By the Bench: Then you have analysed one of the sealed samples ? — Yes. Mr. Glaisyer : Tell us the result of your analysis. — I found bicarbonate of soda in that bottle. And what would you term the liquid you analysed ? — There being soda there, it was of course soda water. There was enough soda to warrant the name. By the Bench : Soda in what quantity ? — It was about a quarter of a grain per bottle. By the Bench : Was it added or was it in the water used ? — I can only say from my knowledge of the waters in this district, which I believe to be mainly sandstone waters, that - By the Bench : Some water here comes from lime¬ stone ; many natural waters would contain soda in the quantity you have found, I take it ? — Some waters would contain that quantity, others contain traces only, and others really none at all ; and as such waters as are supplied to this district contain, practically, none at all, therefore, in my opinion, this quarter of a grain of soda I found was added carbonate of soda. Mr. Glaisyer : Did you examine the bottle in which the water was sent to you ? — Yes. Now how do you account for the small quantity of soda found in that bottle of water ? — On account of the rapidity of the manipulation of the work by the boy in putting the soda into the bottles, I should certainly expect the quantity to vary from, say, a £ of a grain to 3 or 4 grains. I have seen this work done by boys, and I am certain the amount of soda must almost necessarily vary in the bottles. Is it also possible for a portion of soda to be forced out after being put into the neck of the bottle ? — That ques¬ tion I have gone into, and have made experiments myself in bottling soda water from a machine. The soda dropped into one of these patent bottles falls on the glass ball — sometimes partly and sometimes mainly ; and then, when the water charged with gas is driven by the machine into the bottle, air and gas escape from the neck of the bottle, and with that air nearly always comes out some spray, and with that spray might come a certain amount of the soda. Did you make a further analysis of anything that came with the sample? — Yes. When I proceeded to open my sample I found it extremely difficult to get out the whole of the wax with which the bottle was sealed. I knew as a chemist that even if a fiftieth part of a grain of the colouring matter of the wax got into the bottle it might contaminate the water ; and, although I took especial care, I found it impossible to get all the wax out. The fact of the pressure of the glass ball acting on the centre of the indiarubber ring in the neck of the bottle caused the inner edge of that ring to curl up and I found it October is. is79. J THE PHARMACEUTICAL JOURNAL ANL TRANSACTIONS. 315 utterly impossible to get all the wax from beneath, although I myself tried with a penknife, but I found I could not do so. I then pressed down the ball and got out the liquid, and found lead therein. I immediately examined the particles of wax for lead, and there found lead in considerable quantity. By the Chairman of the Bench : Do you think the lead would get there from the lead generator? — I have examined many samples of soda water, the gas for which was made in a leaden generator. Some contained lead, others no lead. I have sometimes found that lead does come from the pipes ; at other times I have been sure it could not have come from that source. Very minute traces of lead might come over with the gas, notwith¬ standing one or two washings of the gas. I am of opinion that it is just possible for lead to be present from that '■*ause. Mr. Glaisyer : Could any other substance be used in¬ stead of lead for the generator of the gases ? — Makers of soda water apparatus are turning their attention to that subject now, but up to a short time ago lead has been almost universally used. Do you consider the lead in this sample innocuous? — Perfectly ; such a minute quantity must be. Cross-examined by Mr. Line, witness saidalarge quantity of the soda water he had examined contained only small quantities of soda, which would not practically have any effect at all, but was put in to make it the so-called “soda water” of commerce; it was the ‘fault of the public that this term is kept up. There was no question of cost in the matter. The contentions in these soda water cases were mere contentions about names. Some makers had called this beverage “ aerated water,” others carbonated water,” but the public did not take kindly to these names ; they seem to prefer their old term, “ soda water,” and it practically caused no confusion, except to officials under the Act. Mr. W. W. Stoddart, called, sworn, and examined by Mr. Glaisyer, said he was public analyst for the city of Bristol. He had had a sample of this water sent to him for analysis bearing the official seal of the borough. He found 1 and 1-10 grain of bicarbonate of soda in it. He had examined three samples of Newport water. In one he found total solids about 8 grains to the gallon, in another about 13 grains to the gallon, and in the third about 14 grains to the gallon. There was no soda in Newport water. If a quarter of a grain were found there it must have been added. He found a small trace of lead, which he thought came from the generator in which the gas was made. One-twentieth part of a grain of lead would not be serious. Mr. Line, addressing the Bench : I would call your atten¬ tion to the second section of the Act. “ The term ‘ food ’ shall include every article used for food or drink by man, other than drugs or water.” Soda water is neither a drug nor is it water, and therefore it is an article of food. Mr. Glaisyer : I admit that. Mr. Line : My point is this, that a person going into a chemist’s shop - Mr. Fox : I may say I have all my soda water from Mr. Young, a chemist, in quantities of six dozen at a time. I would not drink soda water if I knew it con¬ tained any soda. Mr. Line : I submit that a large number of persons going into a chemist’s shop for soda water would expect to get water containing soda. Chairman of the Bench : "The defence have proved that this water did contain soda. Mr. Glaisyer : I admit that it is a food, which ends that point. Mr. Line : I go still further. Mr. Glaisyer : I must protest against this. Mr. Line : I am arguing a question of law. Mr. Glaisyer: What question of law ? Mr. Fox : It is admitted on all hands this should have soda in it ; is that so or not ? Mr. Line : I say, sir, the Legislature never intended that the Act should be evaded by such a small quantity as a | grain of soda being added to each bottle on the point of a knife. Chairman of the Bench : When this Act was passed it was intended to apply to stronger drinks than soda water. Mr. Line : If £ grain only was in the water it is nothing substantial, nothing material. By the Bench: The defence have proved there is something material in the water. Chairman of the Bench : I have drunk soda water for many years, and I must say if I thought there was any quantity of soda in it I should never have drunk it. Mr. Line : It is ridiculous to argue that you can make soda water by putting ^ grain of soda into the water, or that the water contains it as a natural constituent. Mr. Fox: It makes no difference whether the soda be added, or whether it be present as a natural constituent of the water. In either pase it will be soda water. Mr. Line : Take the case of a member of the general public suffering from gout or rheumatism : he asks for soda water and expects to get some soda in it. Chairman of the Bench : Then let him ask for medici¬ nal soda water. The magistrates conferred. Chairman of the Bench : W e think this soda water was the ordinary soda water of commerce, and we shall not inflict any penalty ; in fact we dismiss the summons. Mr. Glaisyer: Do you award costs? By the Bench: This action was taken on public grounds; they are a public body who are prosecuting. No costs will be awarded. Chairman of the Bench (addressing Mr. Line) : Do you propose proceeding with the other two cases ? Mr. Line : No, sir. This case will govern the others, as the charge is the same in each instance. Deaths from Chloroform. On Monday last an inquest was held at Ashton-under- Lyne, by Mr. Price, the district coroner, on the body of a young lady named Mary Handford. The deceased had been suffering from a tumour upon her breast, and by the advice of her medical attendants, Dr. Gardiner and Mr. E. Lund, professor of surgery at Owens College, Man¬ chester, she consented to have it removed. The two gentlemen named attended at her house on Saturday for this purpose, and Dr. Gardiner administered the chloro¬ form in the form of vapour by means of an inhaler. She had inhaled the anaesthetic for only about two minutes, and had not passed into the second stage of narcosis when her pulse became feeble and she died. Both medical men had previously given it as their opinion that she was a fit subject to receive chloroform, and no blame was at¬ tributed to them by any person. The verdict was one of death by misadventure. On Wednesday, also, Dr. Hardwicke held an inquiry at the University Hotel, Grafton Street, Tottenham Court Road, as to the death of Harry Knowlton, aged six years, son of a smith, living at 61, Bemerton Street, Islington, who died in University College Hospital on Friday while under the influence of chloroform. The evidence showed that for two years past he had been under treatment in different hospitals for contraction of the sinews of the legs. On the 6th inst. he was taken to the University College Hospital. On Thursday, Mr. Marshall, the senior surgeon, performed an operation on him, and the next day it was decided that splints should be placed on his legs. Chloroform was given to the child, and he was about to be operated on when it was noticed that he had ceased to breathe. Artificial respiration was resorted to, but without success. The jury returned a verdict of “Death from misadventure.” 316 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October is. 1879. Swinging IRmoqamto:. In order to assist as much as possible our younger brethren, for whose sake partly this column was established, considerable latitude is allmved, according to promise, in the propounding of supposed difficulties. But the right will be exercisedj of excluding too trivial questions, or re¬ petitions of those that have been previously discussed in principle. And ive ivould suggest that those who meet with difficulties should before sending them search previous numbers of the Journal to see if they can obtain the re¬ quired information. [345]. I think that the injection mentioned ought to be filtered, as the precipitate (sulphate of lead) could not have been intended on the part of the prescriber. Nemo. [345]. “Assistant” should puf a “Shake the bottle” on this. J. C. [352]. I cannot understand how this recipe should pro¬ duce a turbid mixture, and do not see any particularly scientific dispensing in producing a bright red or rather a dark reddish-brown and perfectly clear solution. There is no need for any especial care in mixing, for if the in¬ gredients are all put into the bottle and the aq. aurant. added the result is just the same as if each is dissolved separately and afterwards mixed, viz., a clear dark solution. Can the difference be in the French and English ferri am. cit.? W. Wilkinson. [355]. So far as an assistant’s knowledge and experience direct me, I find no difficulty in dispensing this prescrip¬ tion, and am at a loss to discover grounds for Mr. Bray- shay’s doubts. Further than that, the salts are very deliquescent, it is a very good powder as a diuretic and aperient, and taken in doses of half to one teaspoonful. We send it out in W. M. bottles. I think Mr. Brayshay should have stated his difficulty. W. Lyle. [345]. This injection should be sent out with a “ Shake the bottle ” label on. The ingredients must be carefully rubbed up in a mortar with distilled water. St. Rule. [346]. In answer to “ Juvenis,” I beg to state that it is usual to give the tinct. iodi when pigment is ordered. Nemo. [346j. Liniment, iodi should be used. J. C. [346]. There are four formulae for pigmentum iodi in Squire’s ‘Hospital Pharmacopoeias.’ I should be inclined to use “King’s” 3j- iodin. to ^j. s. v. r. W. Wilkinson. [348]. I should use ferri ammon. cit. without troubling the prescriber, even if I knew him. It is evidently a slip of the pen. W. Wilkinson. [348]. Ferri ammoniee sulph. is iron alum, and I should think that was meant. J. C. [348]. “ Mag. Carb.” will find that it will be as well to explain his difficulty to the patient and offer to dis¬ pense it with ferri am. cit., which I have no doubt was intended by the prescriber. Nemo. [348]. The top ingredient is ferri ammonite sulph. It is a double salt, frequently used in photography, very seldom employed as a therapeutic agent, but as such it acts as a powerful astringent in uterine cases. It is sometimes difficult to get from the wholesale dealers. St. Rule. [350]. Rub the chloral and camphor together into a smooth semi-fluid paste ; rub with this 3ss. to ij. mist, acaciae, then add the syrup, and afterwards the water gradually. This produces a milky looking emulsion in which the camphor is suspended ; if the gum is not put in the camphor separates in the form of a greasy substance floating on the water. W. Wilkinson. [351]. In regard to this mixture my opinion is this, “ that it should be filtered before sending out.” Supposing the prescriber’s intention be to order hydrobromic acid, which this mixture undoubtedly represents, we have the authority of Dr. Fothergill for removing by filtration the pot. bicarb, precipitate. Wm. Lyle. [357]. The following prescription was handed to me the other day for dispensing. Will any of your correspon¬ dents inform me as to the best mode of preparing it? I digested two quantities with different pepsin of well-known makers, from ten to twelve hours each at 100° Fahr., but failed to get a clear mixture as ordered in the prescription. Perhaps some one may have had a similar prescription and was more successful in preparing it, if so will he kindly give me particulars ? New Milk . Oj. Pure Pepsine . gr. 100. Dilute Hydrochloric Acid .... hi 80. Mix and digest in a water-bath at a temperature of 100° Fahr. When the mixture has become quite clear, neutralize the acid with bicarbonate of soda. T. E. [358] . How should the following prescription be dis¬ pensed? — ft. Quiniae Sulph . gr. xxiv. Sp. Ammon. Foetid., Tinct. Aurantii . aa 3vj. Aqua . ad 3xij. Ft. mist. Take a twelfth part three times a day. Quinke Sulph. [359] . I shall feel obliged if any reader of the J our- nal will give me the correct mode of dispensing the following : — 01. Olivae . 3ij* Ext. Belladonae . 3ij* Ft. lin. I endeavoured to mix in a mortar, but finding it, as I thought, impossible, I used lin. belladonae instead. This not having the desired effect was sent back. Apprentice. [360] . ft Codeiae . gr. iij. Acid. Carbolic . . gr. \. M. Ft. pil. j. Mitte xxxvj. What is the best method of dispensing the above so as to make the pills as small as possible ? A. W. [361] . Pulv. Calaminae . . 3ias- Zinci Oxyd. . . . . 3Ls. Glycerine . . . . Sj. Liq. Carb. Deterg. . 3j. 01. Olive .... . ,')iss. Aq. Calcis . . . *7 • • . 5iJ* Aq. Rosae . . . . ad ^vj. Ft. lotion. How can I dispense this elegantly ? The way I prc- October 18, 1879 ] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 317 ceeded to do it was to rub the calamine and zinci oxyd’ together with the glycerine, then adding a little rose¬ water. I then mixed the oil and lime water, and lastly, the liq. carb. deterg. After standing a few minutes a thick white scum collects at the top, and is not dispersed by frequently shaking. It was dispensed in the same way at Apothecaries’ Hall, but two other West End houses sent it out with a sediment only at the bottom. How is it done ? C. W. Lawton. [362], Can any one supply information as to how the following should be dispensed ? It comes from the pen of Dr. A. A. Biermann, L’Hiver, San Remo, and was last dispensed in that town : — ft Acid. Muriat. Cone . 2/0 Tr. Aurantii . 18/0 M.S. 10— 15 mma. 18* 11-78. Nemo. BOOKS, PAMPHLETS, ETC., RECEIVED. A Treatise on Chemistry. By H. E. Roscoe, F.R.S., and C. ScHORl EMMER, F.R.S. Vol. II. Metals — Part II. London: Macmillan and Co. 1879. From the Publishers. Analytical Chemistry, a Series of Laboratory Exer¬ cises, constituting a Preliminary Course of Qualitative Chemical Analysis. By W. Dittmar. London and Edinburgh: W. and R. Chambers. 1879. From the Publishers. The Dentists’ Register, printed and published under the Direction of the General Council of Medical Education and Registration of the United Kingdom. London : Spottiswoode and Co. 1879. From the Registrar. [363]. A prescription of the following formula was dispensed by me the other day, and after standing forty- eight hours or so it changed from clear pale to turbid brick-red : — ft Sodse Bic . • • Dij P. Acid. Tart . • • Bb Potass. Iod . • • Potass. Brom . Tr. Aconiti . Sp. Camph., Ess. Menth. P . . f a x Aq . . ad §vj Can any one account for the difference in the mixtures ? I have kept it for weeks, and it has not changed pre¬ viously. Nemo. r? [364]. ft Acid. Phos. Dil . Glycyrrhini . Aquae . Sig. One teaspoonful every two hours. What is meant by the second article in above prescrip¬ tion? Pyrethrum. oh 6b oB- |]oh;s and Queries. [626]. In answer to Mr. Elton’s inquiry, coins can be quickly cleansed by immersion in nitric acid (fort.), then speedily washed with water. If very dirty, or corroded with verdigris, it is best to give them a rubbing with paste or with the following, which of course entails a little “ elbow grease ” and a little time : — ft Pu. Potass. Bichrom . ^ss Acid. Sulphuric., Aq. Fort. . aa. 33 Rub over, wash with water, wipe dry, polish with rotten stone or chalk. W. Lyle. [629]. This I believe to be merely the unguentum hydrargyri oxidi rubri (B.P ). St. Rule. [630]. In answer to “ Hibernia ” the following is from the ‘English Mechanic,’ and is Captain Abney’s process. To prepare the ferrous oxalate developer, make a saturated solution of neutral potassium oxalate, and in this dissolve as much ferrous oxalate as it will take up ; allow it to ■stand and pour off the clear red solution, and dilute with •one quarter its bulk of water. It should be kept in air¬ tight bottles with corks luted with paraffin. J. C. *»* No notice can he tal'en of anonymous communica¬ tions. Whatever is intended for insertion must he authenti¬ cated by the name and address of the writer; not necessarily for publication, hut as a guarantee of good faith. The Cream of Tartar of the Pharmacofceia. Sir, — In a letter from Dr. Stevenson, the analyst for the county of Surrey, and also in some other communications which appeared at the same time in your Journal, refer¬ ence is made to the description of cream of tartar as given in the Pharmacopoeia, and in the former of these it is said that my attention was some months ago directed to the fact “that the B.P. article was an impossible cream of tartar.” I have no recollection of such remark, and have been some¬ what puzzled to conceive what it should mean ; but I presume the difficulty Dr. Stevenson may have experienced in interpreting the Pharmacopoeia must have arisen from the way in which chemical names and formulae are used in that work to represent commercial articles which are rarely or never in a state of chemical purity. Thus, the name acid tartrate of potash is given to the article formerly called bitartrate of potash, but more commonly known as cream of tartar, and this is followed by a chemical formula which precisely represents what the composition of the article would be if it were chemically pure. The definition thus far is such as would be given in a purely chemical work. But the subsequent description shows that the salt is not required or expected to be chemically pure. There is certainly some appearance of inconsistency in this, and it has been suggested that chemical formulae might with advan¬ tage be omitted on account of their too great precision. The same objection, however, might be taken to the use of chemi¬ cal names. But these objections, in my opinion, are greatly outweighed by advantages which the use of known chemical names and formulae afford in defining the articles referred to. Chemical formulae are used in the Pharmacopoeia not only for explaining chemical names, but also for shortening and facilitating the description of products, while “ charac¬ ters and tests,” when these are appended, serve further to define the nature of the substances named, and often to qualify what the name and formula, if used alone, would indicate. These must, therefore, be taken altogether, the context as well as the text. In the case of cream of tartar, the lime salt, the presence of which is indicated by the test, being variable in quantity, the specified indication of it is made to refer to a minimum rather than a maximum quantity, and it is probable that the average is greater now, since plastering wines has become so largely practised, than it was twelve or thirteen years ago, when the Pharmacopoeia was constructed. Tartrate of lime has always been recognized as a legitimate, because necessary, constituent of cream of tartar, from which it could not be made perfectly free without augment¬ ing the price to an extent that would practically prohibit its use. Pereira says, “as found in commerce it usually contains from 2 to 5 per cent, of tartrate of lime, and sometimes a little sulphate of lime. . . This is of no material consequence in a medicinal point of view.” For the preseuce of sulphate of barium, I know of no legitimate excuse ; but it may possibly arise from the use, in plastering wine, of mineral matter containing both 318 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 18, 1879. barium and calcium salts. I am informed by a large Spanish wine maker that in the district in which he lives they plaster wine by the use of earth found in the locality of the vineyards, without reference to its special composi¬ tion. It is not known as gypsum, or by any name representing sulphate of calcium, but merely as an earth that answers the wine makers’ purpose. Some remarks made by Mr. Tanner on this same subject have surprised me. He thinks the description of cream of tartar in the B.P. is “ rather vague and ambiguous,” and as far as I can gather from his remarks, the ambiguity lies in the statements that cream of tartar is obtained from ‘'something quite distinct from cream of tartar,” namely the crude tartar which is deposited during the fermentation of grape juice ; that this cream of tartar when tested gives evidence of the presence of what he calls a trace of tartrate of lime, and that the ash resulting from the incineration of 1S8 grains of the salt requires for its neutralization 1000 grain measures of volumetric solution of oxalic acid. He thinks this last test would prove that the salt was a pure potash salt! and he observes, “that cream of tartar does contain tartrate of lime is the experience of every one who has ever had to do with the examination of it, but that it should contain it in anything more than a trace, I am by no means ready to admit.” He then suggests that it should be guaranteed not to contain more than 5 per cent, of im¬ purity, which may be supposed to be what he represents as a trace. Surely all this indicates ambiguity somewhere else than in the B.P. Again, I am at a loss to understand how anyone could suppose that crude tartar on being ground would form cream of tartar, or anything like it, as apparently assumed by Mr. Tanner. The cream of tartar alluded to by Mr. Hodgkinson, at the hearing of the case, was represented by Mr. Allen, the grinder, as having been obtained by a delivery order for “ cream of tartar, in its crude state,” which, of course, means the usual roughly crystallized cream of tartar, a very different thing from crude tartar or argol. October 15, 1879. T. Redwood. Cream of Tartar. Sir,— Now that the presence of a little calcium in com¬ mercial cream of tartar is being made a rock of offence by public analysts, it may not be out of place to direct attention to a point which appears to have escaped notice in the discussion which has arisen with regard to this subject. In every prosecution which has occurred the adulterant has been reported to be so much “ tartrate of lime.” Is this statement a matter of fact, or of assumption ? If the former, it is certainly a striking coincidence ; if the latter, the cream of tartar has probably been credited with nearly twice the amount of impurity which it actually contained. Cream of tartar may, and not unfrequently does contain a small proportion of sulphate of lime. If, therefore, the estimation of the calcium is made (as is frequently the case) by solution of the bitartrate in hydrochloric acid, and precipitation by alkali, the whole of the calcium will be thrown down as tartrate, and its amount consequently largely over estimated The same error would, of course, follow even if the calcium is precipitated as oxalate, and thus the presence of little more than 6 per cent, of calcium sulphate would figure in the report as 13 per cent, of “ tartrate of lime.” So seriously indeed does the presence of the former salt affect the analysis, that, according to Scheurer-Kestner, “ in the presence of calcium sulphate only an approxima¬ tion can be made of the relative amount of potassium bitartrate and calcium tartrate, and even this is not possible when the sample contains other acid substances besides tartaric acid.” For the homoeopathic proportion of baryta, it seems to me that the “yeso,” or the “Spanish earth,” previously added to the wine may fairly be held responsible. Knop and others have found barium salts in Nile mud and in the ashes of plants grown therein. The conjecture, therefore, that the presence of traces of these substances in cream of tartar may result from one or more of the elegant processes adopted by the Spanish vintner is not more wild than is the supposition that six-tenths of a per cent, of sulphate of barium is wilfully added as an adulterant by the British wholesale druggist. Holloway, N. F. W. Fletcher. The Right of Registration under the Dental Act. Sir, — I scarcely know which to despise most, the select stupidity of all dentists in the way they have conducted their affairs, or the assurance of over two thousand odd chemists. Dentists first allow every one and any one to register, and then when the opportunity is taken, roundly abuse. But be that as it may, still I am a dentist of over thirty years’ practice, yet was struck with amazement at the assertion of chemists that any man is a bond fide dentist, or was in actual practice at the passing of the Dentists Act as a dentist, who had extracted a tooth. Pray let me ask chemists to be just a trifle more consistent. Would, for instance, any man have been registered as a chemist, under the Pharmacy Act, simply and solely because he had made up a prescription ? Certainly not! But surely, sir, if a man is a dentist simply be¬ cause he has taken out a tooth, then it follows as logically that any one is a chemist because he has made up a pre¬ scription. Again there is no value in the Dentists Act or the necessity of registration, if extraction is the sole qualification of a dentist. The argument is rankly absurd on the very face of it. What then is a bond fide dentist? Why a man who can do with his hands whatever in or appertaining to dentistry he may be called upon or asked to do, viz., anything from lancing the gums to making an artificial set of teeth or palate. A dentist who cannot make a set of artificial teeth, palate, etc., with his own hands, though he can extract and fill, is not a true dentist, but a nondescript, or at the best a surgeon of a very limited order of surgery. Thus it is the ability to construct artificial teeth, palates, regulation plates with filling that constitutes a bond fide dentist ; but there is a very wide difference between all this and extraction. I know four barbers, two farriers and a butcher’s slaughterman, who are indeed first class extractors of teeth. But who would call them dentists? The truth is any simpleton can extract, that is pull, and in the majority of cases the tooth must come and without breaking. I should indeed despise my skill as a dentist if it consisted simply of extraction. Permit me, sir, to further disprove the assertion of che¬ mists, and show by their own acts and deeds, and also those of medical men, that they had no right on principle to oppose the Dentists Act, much less to register. Listen, sir. In 1814 the Medical Act came in force, but is there a word in it relative to dentists or dentistry? No ! Later on came the Pharmaceutical Act, is there a word in it relative to dentists or dentistry? No! But why not if dentistry is a branch of medicine and pharmacy, as the opposition of medical men and chemists implied ? But let us admit that dentistry is a branch of medicine and pharmacy; still how comes it that medical men after the Medical Act of 1814, and chemists after the late Pharmaceutical Act, permitted unqualified men by the hundreds to practise a branch of their several callings, if it be a branch. The truth is, not only were dentists after the passing of the Medical and Pharmaceutical Acts permitted to practise without any diplomas or qualifications whatever; but a Dentists Act was needed, years after the other two named, to legalize dentists themselves with medical men and chemists and to legalize dentistry as a profession. But surely no such Act was needed if dentistry be a branch of medicine and pharmacy. Also medical men and chemists having Acts of their own surely did not need another just to confirm a mere branch. The whole thing is highly absurd on the very face of it and proves inconfcestibly that dentistry — not the extraction of teeth, which was the actual right of both medical men and chemists — is a special and peculiar calling and has no more to do with medicine and pharmacy, or with with medical men and chemists, than electricity or photo¬ graphy, though the one is somewhat allied to medicine and the other to chemistry. In fact the very passing of the Dentists Act was proof positive that dentistry is not merely the extraction of teeth, but a profession special and distinet, or the Dentists Act never could have become law. It is sheer folly and nonsense to argue otherwise. Now the reason that it passed in the manner it did was owing to the gross incapacity, apathy, supineness and imbecility of den¬ tists themselves in general and the late Dental Reform October 18, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 319 Committee in particular. We dentists, sir, ought decidedly to take to Dr. Pangloss’s last title, viz., the A.S.S., for we have really earned it. It is also far too late to scold and whine now the die is cast, and we must grin and hear it as best we can. In America there is a matchless dental pro¬ fession, independent of medical men and chemists; in this United Kingdom it is — well a branch of medicine and pharmacy, a branch of anything in fact. In conclusion, let me humbly advise chemists, that advice is — Ne sutor ultra crepidam. Translate it, my brother chemists-dentists, and lay it to heart, for they are words of wisdom. Thus far more in sorrow than in anger that we dentists have so egregiously sold our dear profession and its independence. However, fools must pay for their folly. 185, Oxford Street, W, George Ward, S.D. „ _ Sir, — As one who has lent his aid to the passing of the Dentists Act, I beg to thank you for your timely and temperate article on “ Registration under the Dentists Act ” in your issue of the 11th. I believe I know the disposition and intentions of the promoters of this Act, and feel sure that their views are of the most liberal nature regarding the scope of registration privileges, and that nothing but the most urgent sense of duty towards the public — for whose protection the Act was primarily framed — and the dental profession will ever induce them to put the penal clause of the Act in force against anyone. I feel sure of the support of every promoter of the Dentists Act when I say that I most heartily endorse the concluding sentence of your article, and I assure you, sir, that there is no feeling of animosity existing against “those members of the pharmaceutical body who have been brought into legal confraternity” with us. It is well known to all that many of those gentlemen are much more professional in their views and conduct than many who have come upon the register with the undoubted right to call themselves dentists pure and simple. Moreover, many pharmaceutical chemists and dentists have used their interest and freely given of their means to help the passing of the Dentists Act, and I think that such men, as well as all who can establish their bona jides, would have reasonable cause of complaint if the Dentists’ Register becomes a refuge for those who cannot find a place on your own special register. I do not think that a youth who has been engaged in bottle washing and in sweeping a chemist’s shop, and who might have learned to do a little dispensing, could be con¬ sidered eligible for the Pharmaceutical Register even at the most liberal period of its existence, and I may be permitted to doubt how far the Pharmaceutical Society has not had cause to regret past liberality, though it may have been more or less due to a want of power to be more strict, You say truly that it is quite conceivable that a chemist’s assistant or _ apprentice may have acquired such skill and competence in dentistry as to make him fit to register under the Act, and in such a case you recognize a probability of hardship. I submit that it is hardly possible to frame a law which in the commencement of its operations may not inflict hardship of a limited kind. Prom the alteration of the rules of an examining body up to an Act of Parliament such always has been and will be the case, and to legislate for what is conceivable is, I think, beyond the most com¬ prehensive law-making intellect. But I would ask how far we are right in admitting this speculative ability of acquir¬ ing skill into our calculations. Such exceptional skill must be rare indeed, and the possessor, if his ambition be in that direction, will find little difficulty in attaining the position to which he aspires by means far more satisfactory than by taking advantage of a side door, supposed to have been left open by an Act of Parliament. If such skill be common, then the demands of the Pharmaceutical Society and of the Dentists Act in reference to apprenticeships are excessive, I do not speak now of Preliminary examinations, but if a youth, say a chemist’s apprentice, be able to spare so much of his time from the period during which he has to learn the nature of drugs and the business of compounding them, and all the technicalities which belong to the practice of phar¬ macy, surely both pharmacy and dentistry are much more easily acquired than some authorities would have us believe. From what I can gather, many chemists and druggists have registered from diverse motives. Some have done so not so much for the sake of practising dentistry as to avoie jury seivingand such inconveniences. Others, and thesd are mostly young men, have registered so that they may have dentistry to fall back upon should pharmacy fail them ; and others have come upon the register with a view to continue the practice of dentistry to the same limited extent as before the passing of the Act. "With regard to this last class, it is a common thing to see announcements in the shop windows of chemists and druggists, to the effect that teeth are scaled or extracted or stopped as need be. Now I am perfectly sure that the framers of the Den¬ tists Act never contemplated interfering in anyway with these most useful men. Hundreds have done so hitherto without calling themselves dentists, and there is not a word in the Dentists Act which seeks to interfere with their doing so still. I know that certain medical journals sent the chemists and druggists in force against the Dentists Bill on that ground. These journals knew how they had been embarrassed in their abortive attempts to prevent counter practice and they hoped to produce a like embar¬ rassment for the promoters of the Dentists Act, but in doing so they were only trying to serve their own end and in no way to benefit the chemists and druggists. I repeat the Dentists Act only interferes with unqualified persons using certain titles ; the chemist and druggist may extract or scale or stop teeth as heretofore, but he may not call himself a dentist. With regard to the other two classes named, I think it cruel to encourage young men to think that having the power to assume a title will ever enable them to successfully compete with the educated class of men who will arise along with them, and I can but say, regarding the third variety, that it is not fair to make the Dentists’ Register a refuge for those who are unable to place themselves elsewhere. Referring to the uncertainty of the meaning of the term bond fide, your correspondent who says it is designed to sweep away all ambiguity certainly gives the view of a very high legal authority. Whether his view be exact or no, is not for me to say. I can only as a layman repeat the opinion as laid down by those who are supposed to under¬ stand those matters. There is yet another point which is worthy of the con¬ sideration of those who may have registered on rather slender claims, viz., what is the meaning of the term “ in connection with medicine, surgery or pharmacy ? ” When a man wants to prove himself a doctor or a surgeon, he must appeal to the Medical Register, so I presume the same con¬ dition applies to one who wishes to prove himself a phar¬ macist. In conclusion, sir, I am sure that the spirit in which the expurgation of the Dental Register will be carried out will be such as to meet with your approval, and that the confidence shown in the Dental Reform Committee by a large number of most excellent men who have practised dentistry in connection with pharmacy will not have been misplaced. I trust to your kindness to give this letter a place in your Journal if you think fit, and apologize for its great length. A Member of the Dental Reform Committee. Friedrichshall Water. Sir, — We are in receipt of a communication from the secretary of the Apollinaris Company, the agents of the Hunyadi Janos Bitter Water, in which he complains that an advertisement of the Bitter Water of Friedrichshall, which appeared in the Pharmaceutical Journal of Sep¬ tember 27, contains an erroneous translation of a testimonial of Professor Virchow. We herewith send you a copy of the certificate in the German language, with the rendering which should have appeared, and side by side with it, the misleading translation, which was inserted in the advertise¬ ment columns of the Pharmaceutical Journal through an oversight on our part. German original. “Auf ihre gefiillige Mittheilung erwidere ich, dass icli das natiirliche Friedrichshaller Bitterwasser seit Dezennien kenne und anwende und dass ich die vortreffiichen Eigen- scliaften desselben nach wie vor schiitze. Es ist nicht meine 320 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 1 8, 1379. Absicht gewesen, indem icli mich liber ein anderes Bitter- wasser giinstig aussprach, dadurch das Friedrichshall er herabsetzen zu wollen, und icli tezeuge daher recht gern, dass es mir fern gelegen bat, irgend ein anderes ahnliches Wasser als das unter alien Yerhaltnissen vorzuzieliende und als das absolut beste zu empfehlen. “Berlin, 8 Juli 1879.” Rud. Yiechow. Correct Translation. “To your polite commu¬ nication, I reply that for upwards of twenty years (seit Dezennien) I have known and employed the natural Friedrichshall Bit¬ ter Water, and that now, as heretofore, I appreciate its excellent qualities. In giv¬ ing a favourable opinion of another Bitter W ater, I did not intend thereby to de¬ preciate the Friedrichshall Water, and I quite willingly affirm that it was far from me to recommend any other similar Water as that which is to be preferred under ail circumstances and as the ab¬ solutely best. “ Signed Rud. YlRCHOW “Berlin, 8 July, 1879.” Incorrect Translation. “ I have known and used the Friedrichshall Bitter Water for a long time, and experience has proved to me its mauyexcellent properties. Although I do not wish to undervalue the merits of other Bitter Waters, I feel that in justice to the Bitter Water cf Friedrichshall, I must record my opinion that it is the best and most use¬ ful of the Bitter Waters, and as such I can confidently and gladly recommend it.” We are, sir, Your obedient servants, J. and A. Churchill. Health of the Drug Trade. Sir, — I was very much struck with the correctness of the statements made by “ Junius,” and consider that we may trace with ease the apparently short life of the chemist to those three causes — confinement, want of recreation, and the vitiated atmosphere in which he lives. The greatest evil of the three i3 late closing, and one which is deserving of immediate attention. Should we not, at a time when examinations are com¬ pulsory, endeavour to raise ourselves and the business to which we belong to something better and higher than what it was before such things were thought or heard of? If chemists as a body would unanimously agree, we might without any difficulty close our respective shops at a reasonable hour, and by so doing I feel certain that it w ould tend to raise us in the estimation of the public, and be beneficial to the health of both assistant and master. At a meeting held recently in our largest town, the question was very seriously discussed as to whether they might close at 10 instead of 11 p.m. When we know that such a miserable state of affairs exists, can we reasonably wonder that we are not men of strong constitution and long lives ? Bootle. Camphora. A Simple Standard. Sir, — It may perhaps be new to the majority of your readers, as it was to myself, when the advantages of this standard were first pointed out to me by a friend, and on this ground I have taken the liberty of troubling you with my few remarks, with the hope that they may prove useful to those, who, like myself, are in the habit of dispensing from solutions of various salts. There can be no doubt whatever that in such cases where the salt does not undergo any change by being kept in solution, this practice is not only allowable, but preferable to weighing the dry salts, especially in such establishments where much dispensing is done and where time is necessarily valuable. I have usually made my solutions 5j ad 5j> and this strength answered very well in most instances, but for simplicity it is not to be compared with that which I now desire to bring before your notice, viz., 1 in 6, the advan¬ tages of which will be quite apparent on a careful examina¬ tion of the following examples : — Strength 1 in G. No. of grains No. of drachms, ordered. of solution. l grain equals *1 2 grains 9 9 •2 3 99 99 •3 10 99 9 9 1‘0 12 9 9 99 1-2 15 99 99 1-5 20 99 99 2‘0 25 99 99 2‘5 40 9 9 99 4*0 5j or 60 99 99 60 5b „ 120 99 99 12 ‘0 or 3iss „ 240 99 99 2L0,, 3iij si „ 480 99 99 43'0 „ 3yj On glancing at the above title it will be noticed that the- figures in both columns are the same, with the addition of the decimal point (•) in the second column ; thus the number of grains, ordered in a prescription, indicates the number of drachms of solution necessary to use, 10 grains requiring 10 drachm or 5j, etc. It may be thought by some, that where an odd number of grains is ordered, the calculation will be difficult, but this need not be so, if the principle of the standard be grasped. ‘1 drachm means drachm= mvj ; '2 must then = mxij; ‘5 = 538, etc. The placing of the decimal point (‘) it should be noticed is fixed by the- number of grains ordered, 10 grains requiring 1‘0 drachm or 5j- In conclusion, I trust that my endeavour to make known a simple remedy for a common want may be a sufficient excuse for me venturing to trespass so much upon your valuable space. Sunderland. Robt. H. Mushens. Tincture of Yellow Jasmin. Sir, — As the above tincture is frequently prescribed, I would respectfully ask, through the medium of the Pharma¬ ceutical .Journal, of what strength it ought to be? Every wholesale house has its “Tinct. Gelsem. Sempervirens ” (in some instances the word “Special” or the maker’s name follows), but the strength is seldom if ever given. When large doses are prescribed it is absolutely necessary that we should know whether we are on the safe side or not, in dispensing them, as the drug is comparatively little known. I think it would be a good plan if every wholesale house stated the strength of the tincture and the dose, and abolished the favourite terms which follow the name, and which frequently have to be paid extra for. Aberpawe. H. Waistell. — A recipe for stamping ink will be found on p. 80 of the present volume. G. H. Morgan. — We do not think you should assume that the statement made by your customer is correct, but should communicate with the chemist and druggist in question. B. Hardy should address his question to the editor of a. medical journal. R. Grant. — For a description of the way in which koumiss is made by the Tartars, see vol. v. of the present series, p. 325. “ Fraxinus.” — (1) Holcus mollis. (2) Festuca gigantea. (3) Dactylis glomerata. F. Gale. — Artemisia vulgaris. J. H. — The arms are the property of the Society as an incorporated body, and cannot be used legally by any in¬ dividual, “ Student .” — (1) The question of the dispensing of ‘ ‘ chloric ether ” has been fully discussed recently in the “ Dispensing Memoranda.” See vol. viii., pp. 19, 38 and 67. (2) The swelling of the pills is probably due to the decomposition of the oxide of silver. Communications, Letters, etc., have been received from Messrs. Rogers, Wills, Willmott, Deck, J. Squire, Siebold, Wilkinson, Swinn, Sub Umbra Floresco, Jek, Progress is Life, Forceps, Apprentice, T. E., R. H. R. October 25, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS'. 321 “ THE MONTH.” “ Chill October ” well deserves its name this year, the cold but delightfully bracing north-east winds having effected a marvellous change in a few days and brought autumn so suddenly upon us that flowers are disappearing from our gardens and hedges all too quickly. At the Kew Gardens several families in the Herbaceous Ground still present a sufficient number of plants in flower to illustrate their characters. Among those which still linger thus are the Leguminosce, Composites, Scrophulariaceee, Malvjccece, Polygonaceee, Boraginaceee, Linacecs, Gera- niacecc , Onagracece and Loasacece. Of medicinal plants few remain in blossom. Several varieties of tobacco, the camomile, alkanet, melilot, and most beautiful of all, the colehicum, still remain in blos¬ som. Several species of the last mentioned genus now present quite a bright appearance, while close by the rare British species, Crocus nudi/lorus, which also flowers without the leaves, is scarcely to be dis¬ tinguished by external appearance, and it is only when the inside of the flower is examined that the six stamens and the different character of the stigma is perceived. The shining black berries of the belladonna, the bright red ones of the woody night¬ shade and the prickly fruits of the tliornapple, almost alone represent the Solanaceae, just a few blossoms of Solanum nigrum, and some scattered panicles of the graceful Solanum jasminoides, being all that are left to represent this family at the present time. A species of Datura, to which the name of tliornapple in this case is most inappropriate, for the capsule is quite smooth, may now be seen in fruit. Among a few other Rosaceee, the Agrimonia odorata still remains in blossom. Although by some botanists it is distinguished as- a species, there are scarcely suffi¬ cient permanent characters by which to separate it specifically from large specimens of A. Eupatoria, the distinguishing features being that the stems are 3 or 4 feet high, the furrows on the fruit rudimen¬ tary or even quite un distinguishable, and the calyx wider at the mouth than in the other species. A. Eupatoria is occasionally used by herbalists in this country in affections of the liver, and in fact, it has had a reputation for complaints of that organ since the time of Dioscorides, who says it is “a remedy for them that have bad livers and for such as are bitten with serpents,” and as Gerarde translates it “ the leaves being stamped with old swine’s grease and applied, closeth vp vlcers that be hardly healed.” This reputation may perhaps explain a discovery recently made by Dr. Brinsley Nicholson, who, in a paper in the Medical Times and Gazette, speaks very highly of the value in scurvy and tapeworm of a plant called by the Caffres “Uhlinga,” a species of Agrimonia ( Agrimonia Eupatoria ?), which has succeeded in his hands in the latter complaint even where turpentine failed. In eighty-six cases tried by the author the remedy acted effectually as a t?enicide or tsenifuge in nearly all. The violet may almost be called an autumn as well as a spring flower, for almost every year a few blossoms may be found during the autumn where the plant grows freely, especially in sheltered spots in gardens. One of this genus has recently been ex¬ amined by Dr. J. Konig, who finds as much as 21 per cent, of zinc oxide in the ash of the plant. This plant, which is by many botanists considered to be a variety of Viola tricolor, receives its name of Viola calaminaria , from the fact that it appears to be Third Series, No. 487. restricted to soil containing zinc, and thus serves to indicate the presence of the metal in the soil, where it might not otherwise have been suspected. Sufficient attention has perhaps not been paid to the influence of the chemical constituents of soil in producing variations in plants, nor to the value of such varieties in indicating the nature of the soil. Probably many of our readers have noticed with regard to the common violet, Viola odorata, how rare it is to find plants with blue flowers on a limestone soil, the prevailing colour being white. With regard to Viola tricolor, of which Viola calaminaria is probably a variety, Sowerby’s ‘Botany’ makes the following statement: — “Some years ago a writer in the Medical Journal called attention to the heartsease as a valuable remedy for the cutaneous disease called crusta lactea in children. For this purpose half a drachm of the leaves or a handful of the fresh herb boiled in milk was to be given every night and morning and poultices made of the leaves, to be applied externally.” When distilled with water it gives a volatile oil having an odour something like peach kernels, which may be also observed on chew¬ ing a leaf or portion of the stem. The possibility of the relation of this oil to the odour of violets, might be worth investigation. An account of poisoning by fungi of a boy, three years of age, is given in the Lancet for October 11. The child had eaten some small fungi which he had gathered in Hyde Park, specimens of which were shown to the medical man by the child’s sister. The child recovered next day. As the symptoms were somewhat peculiar and the name of the fungus or fungi eaten could easily have been ascertained at the Botanical Department of the British Museum, or by application to anyone of our numerous fun- gologists, it is to be regretted that such an oppor¬ tunity of adding to our knowledge of the little- known properties of the plants of this interesting class was allowed to pass by. Four other cases of fungus poisoning during the first few days of October were admitted into Middlesex Hospital. In these cases the symptoms were those caused by a strong intoxicant, and in two cases accompanied by violent delirium. They all eventually recovered. In these cases also no mention is made of the species which produced these results. Fungi probably possess properties as dissimilar in different groups, or even in species of the same genus, as those which are found in different species of aconite among the flowering plants ; thus a species of Amanita, A . rubescens, which differs from the delete¬ rious A. muscaria in having a pale drab-coloured cap, and flesh reddening when bruised, is edible. No opportunity of ascertaining the pecularities of poison¬ ous species should, therefore, be neglected. While speaking of fungi it may be mentioned that Dr. B. Crowther, of Hobart Town, calls attention, in the Lancet, to the use of hyposulphite of sodium in zymotic diseases, and states that it is a potent remedy in certain intractable acute and chronic ulcers, whose origin and continuance seem due to some local irritant of a fungoid or bacterioid nature. He further adds, “ From the vast number and varied class of diseases over which it exercises a controlling influence, it is destined to hold the first position as a specific in our Pharmacopoeia.” It may be dded that it possesses the advantage over the bisulphite of having a less disagreeable taste. A curious illustration of the fact that all know- 322 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 25, 1879. ledge is useful at some time or other has recently occurred in the discovery of diatoms in the goose¬ berry preserve of commerce. The study of the Diatomaceoe has generally been looked upon as comparatively useless, although the beauty of the forms of these plants renders it a very delightful one. M. Ch. Menier, professor of materia medica at the School of Medicine and Pharmacy at Nantes, in examining a specimen of gooseberry preserve from Paris, recognized that its gelatinous consistence was due to algae, by finding in it a very beautiful diatom, Arachnoidiscus japonic us, which is known to occur in “Japanese isinglass.”* Probably the gelose came from the French colony of Cochin China. The colouring matter was due in part to cochineal, as determined by analysis, and in part to the petals of the Rose Tremiere (a dark-flowered variety of Althaia rosea), as indicated by the pollen grains charac¬ teristic of the Malvacece, which in consequence of the union of the petals to the androphore would be almost sure to be present. At the recent drug sales several packages of calabar beans were offered ; these have been rather scarce for some months, and as this is about the time of year when they become ripe, an abundance may soon be expected. Zanzibar aloes, having an opaque appear¬ ance like Natal aloes, but as usual packed in monkey skins, was observed. There was also a quantity of fine Jooking yellow bark, which would probably pass as Calisaya, but contains generally only traces of cinchonidineand a small percentage of quinine. Rose geranium oil from Algeria, Dalmatian insect powder, Siam benzoin in fine tears, Samovey jjook isinglass, German camomile flowers ( Matricaria ChamomiUa) and patchouli leaves were among those of less fre¬ quent occurrence. At a sale, in London, during the early part of this month, a number of small gourds of curari were exposed for'’ sale and labelled aloes ! They were tasted by several people, who fortunately, owing to its bitterness, probably ejected their saliva immediately afterwards, for had the mucous mem¬ brane of the mouth been in any case abraded, the consequences must have been disastrous. It was well for the public that the gourds were of so small size, that they would, probably in any case, have been purchased merely as curiosities. As soon as the true nature of the drug was known it was immediately withdrawn. According to Gehe’s report curari is already going out of favour owing to its want of uniformity. Some time since, M. Preyer in the endeavour to obtain an active principle of definite strength from curari, prepared a crystallized sulphate of curarin ; this substance, which was stated by the discoverer to be twenty times stronger than curari, was afterwards found by Theodor Sachsf to be composed of phosphate and carbonate of lime with a little adherent curari, sufficient only to produce a weak physiological action. There now appears a possibility of a definite principle having the properties of curari being procurable at no distant date. An important discovery has recently been made by M. Jobert, whose investigation of the source of curari was noticed in this Journal on a former occasion, J and will probably call renewed attention to the drug. He has found that Strychnos castclnce and Strychnos tori/era are by no means the * Ser. [3], vol. ix., p. 1056. f Liebig’s Annalen der Chemie, 101, n. 255. j Ser. [3], vol. viii., p. 581. ~ - : - . — . - = ^ only species which yield a poison similar to curari ; but that so far as experiments have gone, the South American species are distinguished from the Asiatic by possessing properties resembling those of curari rather than strychnia. He considers that the most active of what may be called the curari-yielding species of strychnos is S. rubiginosa, Piauhy, and the least toxic, S. triplinervia , Gaertn; indeed in so slight a degree does the latter possess toxic properties that it is employed for fevers by the natives. In another number of the same journal, MM. Couty and De Lacerda give an account of the extraction of the active constituents of the latter plant and the physiological action of the extract. They found that the extract made from the bark of stems of moderate size was more active than that of the root, and although much less powerful than curari. LI. Jobert states that the Peruvian Indians mix the juice of a menispermaceous plant which has a poisonous action on the heart with the curari, and that only the pure extract of the strychnos should therefore be used in order to obtain definite physiological results. In Strychnos tripli¬ nervia, we have, according to MM. Couty and De Lacerda, an agent which can easily be obtained of a definite strength and offers the advantages that the valuable physiological effects of curari can be obtained in a few moments and that the symptoms can be arrested at different periods as may be required. Dr. W. Murrell, in an article in the Practitioner this month, states that he has found picrotoxin afford great relief in the night-sweating of phthisis, having had only one case of failure out of twenty, and even then the remedy did some good at first. The strength of the solution used in his experiments was at first 1 part in 180, but as some of the picro¬ toxin crystallized out a solution.of 1 part in 240 of water was afterwards adopted. Of the former solution, 1 drachm in an eight-ounce bottle of water was pre¬ scribed, the dose ordered being in most cases a teaspoonful, or in other words, about one ninety- sixth of a grain. In the severe diarrhoea which often occurs in the course of the same disease, Dr. J. B. Yeo has found that the fluid extract of coto bark in doses of 5 to 8 minims, arrests or checks it even in its severest forms, and he remarks that he is quite sure that coto bark is a valuable remedy which ought rapidly to come into general use. Dr. Yeo also calls attention to the very important fact that when administered in the form of pills or with the mistura crctte, B.P., it appeared inert, and that he found a resinous element was precipitated in tough masses when the fluid extract was carelessly mixed with water, but that when given in com¬ bination with tincture of cardamoms and mucilage it was very effectual. He also makes the very pertinent observation that “this is probably the fate of many valuable medicines which appear to fail, not from want of virtue in themselves, but from want of patience and attention in their mode of adminis¬ tration.” In the Indian Medical Gazette, Mr. A. L. Deb recommends the root of Hedysarum gangeticum in dysentery. The fresh root is given three or four times a day in the form of pulp, ground down and mixed with water, to the extent of thirty or forty grains each time for adults. He considers it to stand next in value to Jxora coccinea and to be especially adapted for acute dysentery of moderate severity. October 25, 1879 ] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 323 In the United States the bark of Piscidia ery- thrina, or Jamaica Dogwood, is being tried as an anodyne and soporific. Some years ago Dr. W. Hamilton, of Plymouth, called attention in the Pharmaceutical Journal to this drug. The strength used is 4 oz. of the bark to 16 oz. of rectified spirit, and the dose taken to ease pain and procure sleep is 1 drachm for adults. Dr. L. Mann, of California, has recently been experimenting upon the Californian laurel ( Oreo - daphne Californical ) and finds that the odour of the leaves causes in some persons a severe frontal head¬ ache when they stand under a tree. Apparently this suggested a use of the remedy in nervous headache, in the treatment of which he has found the bruised leaves, used as an inhalation, very successful. The taste of the leaves is exceedingly pungent and to some persons disagreeable, and the plant seems to be one likely to possess some useful properties. The odour is said to be disliked by mosquitos and other insects. During the last few weeks ITamamelis virginica, which is well known as the chief ingredient in Pond’s Extract, has attracted some attention in the correspondence columns of the Lancet. The writers appear to be unaware that a formula for the tincture has already been published, and as uniformity in unofficial preparations is very desirable it may be useful to some of our readers to know that a formula may be found in the last edition of Squire’s 1 Companion to the Pharmacopoeia/ Medical practitioners would obtain much more satisfactory and uniform results from the use of unofficial pre¬ parations than is sometimes the case if they would indicate in their prescriptions the streugtli of tinc¬ ture intended to be' used. Dr. E. Schrader, in the Chemilcer Zeitung, describes a new method of making varnish, which consists in causing ozone to act on linseed oil, by which it is bleached and brought to the proper consistence, without the aid of fire. In the same journal, M. A. Tschirch calls attention to the fact that in almost all the bottles of magnesium sulphate and in some of calcium sulphate solutions in the laboratory of Berlin University, algse belong¬ ing to the Palmellacece and developing chlorophyll have made their appearance. Recently there was noticed in these columns an interesting announcement that Herr Ladenberg had succeeded in recombining tropic acid and tropin to form the alkaloid atropine of which they were the products of decomposition. It is now announced that a similar feat has been performed with respect to milk sugar by M. E. Demole ( Gomptes Pend., lxxix., 481). Upon treating with boiling anhydrous acetic acid the mixture of galactose and lactoglucose into which milk sugar is converted in contact with dilute acids, an octacetyle ether is formed resembling that obtained by Schutzenberger with dextroglucose. An alcoholic solution of this ether poured into baryta solution and kept for a few minutes at a temperature of 90° gives off acetic ether, and after exact neutra¬ lization with sulphuric acid, evaporation to dryness, and re-dissolving in water, is by several recrystalli¬ zations aided by alcohol obtained as a crystalline body having all the properties of sugar of milk. “Octacetic saccharose” similarly treated with alkalies is said to have yielded cane sugar, but the crystalli¬ zation was not successful. Another investigator in this direction, M. A. Michael, has effected even more interesting results in the synthesis of two glucosides and has indicated a probable method by which a large numbers of others may be produced and investigated. Of M. Michael’s two products the more interesting at present to pharmacists is undoubtedly “helicin,” a glucoside described ly Piria and produced by the action of dilute nitric acid upon salicin and reconvertible into salicin by the action of nascent hydrogen. The relation between these two glucosides is shown by the following equation : — G\;}H1807 + 0 = C13H1607 + HoO Salicin. lleliciu. The medium used by M. Michael for the introduc¬ tion of the molecule of glucose is a compound called a ietochlorliydrose obtained by the reaction of chlo¬ ride of acetyle upon glucose. Equivalent quantities of acetoclilorhydrose and salicylite of potassium were dissolved in absolute alcohol, mixed in the cold and left to stand ; there was evolution of acetic ether and formation of a precipitate of chloride of potassium, the reaction being completed in about three days. After filtration the alcohol was allowed to evaporate spontaneously, when there was left an oily substance that solidified after ten days, and which when puri¬ fied gave upon analysis the composition of helicin and was also identical in its other properties. Heli¬ cin so produced is slightly soluble in cold water, and very soluble in hot water, from which it is deposited on cooling in white arborescent crystals. Boiled with dilute sulphuric or hydrochloric acid it splits up into salicylic aldehyde and glucose, and the same decomposition is induced by the action of emulsin. The other glucoside was obtained by the reaction between acetoclilorhydrose and plienate of potassium ; it does not correspond with any known natural substance, and has been named phenol glucoside. Acetoclilorhydrose appears to be endowed with con¬ siderable powers of substitution. It acts upon levu- lose with the evolution of gaseous hydrochloric acid and acetic acid and the formation of a small quantity of crystalline matter which may prove to be dextro- levulose (cane sugar). Other compounds have also been obtained by its use that have yet to be examined and described. After a considerable amount of writing suggestive of the mythical there appears to be at last some prospect of the properties long attributed to the papaw tree undergoing scientific investigation. In the paper published in the Journal for the lltli inst. (p. 283), Messrs. Wurtz and Bouchut describe a substance having the properties of an energetic diges¬ tive ferment which they have separated by precipi¬ tating with alcohol an aqueous solution of juice from the stem of the papaw, and named “papaine.” Curiously enougli]almost simultaneously Dr . Peckliolt, of Cantagallo, Brazil, has published in the Zeitschrift of the Austrian Apotheker-Verein a long and interest¬ ing account of the Carica Papaya , in which he describes under the name of “ papayotin” a substance apparently identical with “papaine.” Dr. Peckl.olt’s researches appear to have been carried out some ten years since, and only to have been published now because of the revived interest in the subject. Not¬ withstanding Dr. Peckliolt’ s long delay in publishing, due probably to his residence in Brazil, and the fact that he disclaims any intention to claim priority, it would appear that he really is entitled to do so, since his paper appeared in the Austrian journal tor the 20th 324 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 25, is:s>. of August, whilst M. Dumas’ communication was not read in the Academy of Sciences until five days afterwards. Last month there appeared in this Journal a letter from Messrs. Baildon and Son, stating that after following out Mr. Thresh’s formula for making soluble essence of ginger (before, p. 193) they had failed to obtain a clear preparation. Mr. Thresh replied recommending a reagitation with silica and filtration. It may be useful to mention that a second letter has been received from Messrs. Baildon stating that upon carrying out the suggestion a bright preparation was the result. The wide-spread interest in this subject is illustrated by the fact that a few days since a letter was received from Jackson¬ ville, Florida, U.S., attesting the practicability of Mr. Thresh’s process. It is now officially announced that the day on which this Journal is published is to be the day upon which the India Museum will be finally closed. Whatever may have been the circumstances which have induced the authorities to take this step — whether simply in consequence of the expense, or that in addition to other causes —only regret can be expressed at such a necessity having arisen. In distributing this fine collection among other institu¬ tions no doubt care will be taken to select the most fitting recipients, and it may be hoped that a large portion of the materia medica, including the essential oils, will find its most suitable resting place in the museum of the Pharmaceutical Society. The annual report of the Director of Kew Gardens, which has just appeared, contains an unusually large amount of matter interesting from a pharma¬ ceutical point of view. This includes information concerning the introduction of Columbian barks into India, the success of cinchona cultivation in Jamaica, African dragon’s blood, lignaloes, or eagle wood, olibanum and myrrh. Extracts from this report will probably appear in future numbers of this Journal. The Dentists’ Register, which has appeared during the past month, has no doubt, ere this, been scanned through spectacles variously tinged according to the wearers’ views of what such a Register ought to contain. It appears to be carefully compiled, and is prefaced by a “ table showing the number and qualifications, with percentage of the total of persons registered.” From this it appears that the total number of names on the Dentists’ Register on the 1st of August was 5289. The Licentiates in Dental Surgery of different medical bodies who have been registered number 483. Of persons registered on their own declaration as having been in bond fide practice before the passing of the Act, 2707 have claimed to have carried on dentistry separately, 2049 in conjunction with pharmacy, 17 in conjunc¬ tion with medicine, 11 with surgery, 20 with medi¬ cine and surgery, and two with surgery and pharmacy. There have also been two persons registered as doctors of dental medicine of the University of Harvard. The third part of Dr. Dodel-Port’s valuable ( Atlas der Botanik ’ will be published in a few days. It will contain figures of Spirochcete Obermeieri, the contagium of a certain typhoid disease; also the whole development of the carbuncle fungus, Bac¬ terium anthracis , as investigated by Professor Nageli and the author of the atlas ; the development of the prothallium of the fern genus Aspidium from the spore to the formation of the embryo ; the fertiliza¬ tion of Polysiphonia subulata by the aid of animal- culae, and other recent observations of great value. Pharmacists will be glad to learn that a new and thoroughly revised edition of ‘ Pharmacographia ’ will be published .during the coming season by Messrs. Macmillan. The first edition has been out of print for some time, and much additional matter has appeared since the date of its publication wh:cli will doubtless be represented in the clear and cen - densed manner for which the work is so remarkabl e. “ A little knowledge is a dangerous thing.’’ The British Medical Journal of the 18th, in an editorial paragraph, refers to the paper of Mr. Fahnestock, on “ The Valuation of Blistering Beetles,” which was recently (vol. ix., p. 1038) reproduced in this Journal from the American Journal of Pharmacy. In doing so it credits the author of that paper with saying that the fresh powder of the “ potato beetle ” yields about 1^ per cent, of pure cantharidin, and remarks that this is a large product, and that “no doubt these pests will be increasingly used as a source of this drug.” But it further ventures to prophesy that mankind will hardly be prevailed upon to desist from vigorous efforts to exterminate the insect because it is now shown to be capable of acting effectually as a physical as well as a moral blister. Perhaps a taste of this insect’s power in the moral blister direction will be realize! by the writer if he turns to the original paper, where he will find that the author does not speak of the Colorado “ potato beetle” ( Dorypliora decemlineata), but of the potato bug ( Cantharis vittata). The power of ridicule is acknowledged, and there is no doubt it may be utilized in making impressions upon the memory. In connection with the New York College of Pharmacy there is a conversational class, in which the office of “ quiz ” is a recognized institution. Banter appears, in fact, to have been so useful in correcting errors in past sessions that the Board of Trustees have at the commencement of the present one formally appointed two gentlemen to the office of “ quiz masters.” The meeting of the American Pharmaceutical Association at Indianapolis, a report of which has appeared during the past month, seems to have been a success in point of attendance, but showed a marked falling off in the number of papers read . A large amount of time was taken up in considering the rules of the Association, whilst some reports in respect to the next edition of the United States Pharmacopoeia naturally absorbed much of the attention of the men by whom that book will have to be used when it appears. One alteration in the rules, in which the word America is substituted for United States, throws open the eligibility for mem¬ bership to Canadians, Mexicans, Chilians and citizens of other South American States. One little contretemps , whilst amusing, shows how easily the u best laid plans ” may “ gang oft agee ” on such occasions. It appears that when assembling for the “ banquet,” the Secretary, Professor Maisch, four past Presidents of the Association, and about a score of old members stood on one side to give precedence to their juniors. These flocked in in such numbers, however, that the room was filled and the doors were closed, leaving still outside the seniors, who were fain to comfort themselves at a neighbouring restaurant. As usual with the American Pharmaceutical Associa- October 25, 1879.] THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 325 tion, the reports were a good feature. In one of them Mr. H. S. Wellcome stated that he had not been able to find “ any drugs now cultivated here which were formerly obtained from foreign countries,” with perhaps the exception of valerian, now cultivated in Vermont. In another report upon the market of San Francisco, Mr. Steele gave an account of the manufactures of his section, one of the most remark¬ able among which was that of 25,000 gallons of castor oil per annum. A specimen of a new salt, salicylate of cinchonidia was exhibited by the secretary. It crystallizes in well defined prisms, is sparingly soluble in water, and dissolves freely in weak and in strong alcohol. The extent to which colour blindness is prevalent amongst railway servants has been the subject of an official inquiry in Germany. It is reported that on the State lines 1 employe in 125 is colour blind, whilst on the companies’ lines only 1 in 250 is so affected. Probably this difference in the figures is due to a difference in the standard adopted, and it is noteworthy that they approach closely to the numbers recently published by the English Board of Trade, of 1 in 230 partially affected and sent back for further trial and 1 in 150 finally rejected. According to the Pharmaceutische Zeitung fur Russland the Russian armies were well supplied with all manner of drugs during the recent war, as much as eighty waggonfuls of unused drugs having been brought back with the army from Bulgaria. Some of the quantities used by the armies on active service are given as follows : — cinchona bark, 1083 lbs. ; quinine hydrochlorate, 2358 lbs. ; quinine sulphate, 5083 lbs. ; chloroform, 3088 lbs. ; opium, 1546 lbs. ; morphia, 52 lbs. ; castor oil, 25,953 lbs. ; rhubarb, 1138 lbs. ; ipecacuanha, 1820 lbs. ; carbolic acid, 5597 lbs.; camphor, 6771 lbs. It is further stated that in the years 1877 and 1878 the medical department of the Russian war office purchased altogether 260,350 ounces of quinine sulphate and 194,700 ounces of quinine hydrochlorate at an ex¬ penditure of two and a half millions of roubles. “Physicians’ prescriptions accurately prepared” is the dispenser’s motto, but to accomplish this with neatness and facility certain requirements are almost essential in a pharmacy. The letter of Mr. Mushens in last week’s Journal, page 320, on a simple standard for solutions of salts daily and hourly re¬ quired in dispensing, directs attention to one series ; others will in due course be referred to. Opinions may differ as to the relative proportions of the salt in solution, but there can be but one opinion as regards the value of the principle, and its application may be left to the judgment of each dispenser. An “ endeavour to make known a simple remedy for a common want” needs no apology, and the readers of this Journal will be indebted to those whose efforts are successful. The first prescription requiring notice is that of No. 343, where sp. chlorof., without any quantity being given, forms part of the prescription. Judging from the size of the mixture and from its dose, that it was for a child, 3ss. sp. chlorof. would be a fair quantity. The next article sacc. ust. is only a colouring matter and must be left to the dispenser’s discretion. No. 344 contains a solution of Cheltenham salts. The writer of a prescription sometimes severely tries a dispenser’s resources. To confine a prescriber to the Pharmacopoeia would tend to check therapeutic progress, but there should be some limit to erratic prescribing. A teaspoon ful or a quarter of an ounce of Cheltenham salts is the dose recommended for occasional use; one ounce and a half, therefore, in the twelve ounce mixture would give that proportion to each dose. A dispenser is required to keep the pre¬ parations of the B.P. ready for use in his pharmacy, but the Cheltenham salts have not yet occupied that position. It may assist “Dispenser” to give him Beasley’s formula for artificial Cheltenham salts, which would be supposed to represent the saline and tonic characters of the Cheltenham waters:— Sulphate of soda 16 oz., sulphate of magnesia 8 oz., muriate of soda 1 oz., sulphate of iron 8 grs. Dis¬ solve in the smallest quantity of hot water, strain and evaporate to dryness. It is not usual to filter an injection such as No. 345, neither should a “shake the bottle” label be put on. A decomposition takes place, acetate of zinc is formed and remains dissolved, whilst sulphate of lead is pre¬ cipitated. The writer may wish the deposit to remain at the bottom of the bottle, as he does not direct it to be filtered, or he may not desire it to be used with the fluid, as would be indicated by a “shake the bottle” label. The deposit is not considered an essential part of the remedy or one that possesses any value ; the dispenser therefore has nothing to justify him in ordering the bottle to be shaken. Pigment, iodi is prescribed in No. 346, and “ Juvenis” wishes to know whether tinct. or linim. iodi should be dispensed. There is no formula for a preparation of iodine with the name pigment, iodi in the B.P., but on reference to the formula of the Throat Hospital, for pigment, iodi, the linim. iodi is directed to be used. This circumstance will be a guide to the dispenser, and a sufficient justification for the use of linim. iodi when pigment, iodi is ordered. The question No. 347 refers to the varying appear¬ ance of different samples of enonymin. For several of these remedial agents from the United States, and recently introduced into this country, there is no published form, and there being more than one maker, it is but reasonable to conclude that each has his own particular method of manufacture. On re¬ ference to some papers which have at different times appeared in this Journal on the preparation of podo- phyllin, it will be observed how the appearance of the product is affected by very slight differences in the process of deposition from its solution. From what has been stated the difficulty or rather impos¬ sibility of furnishing a safe test of quality, or a test by which one of these vegetable products, probably of a resinoid character, may be recognized must be apparent. It is difficult to say what the writer of No. 348 meant when he wrote ferri ammoniae sulph. If he cannot be referred to, the dispenser will be quite safe in using ferri ammonias sulph., a salt formerly much used in photography, but little known in medicine. The remarks of St. Rule, p. 316, are very much to the point, but he would have made them more valu¬ able if the source of the information that ferri ammoniae sulph. acts as a “ powerful astringent in uterine cases ” had been appended. It will be ob¬ served that many correspondents assume ferri am¬ moniae cit. to have been intended by the writer, but this is by no means certain. “ J. C.” states that ferri ammon. sulph. is iron alum ; this is an error, iron alum is a ferric sulphate with sulphate of ammonia or potash ; ferri ammon. sulph. is a ferrous sulphate with sulphate of ammonia. 326 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 25, 1879. The pills in prescription No. 349, may be made by the addition of a very small quantity of soap to the ingredients ordered ; with the assistance of the soap a satisfactory mass may be obtained, firm, and capable of being rolled into pills. “Junior” is re¬ ferred to remarks on the combination of similar ingredients in some of the preceding “ Months/’ The chloral hydrate and camphor in No. 350 may be so combined as to form a milky emulsion by following the directions of Mr. Wilkinson, p. 316, on this prescription. Care should be taken to rub the chloral hydrate and camphor till they become semi¬ fluid, before the addition of the mucilage, or the emulsion may be imperfect and gritty from the presence of free camphor. There will necessarily result, from the mixture of bromide of potassium and tartaric acid, ordered in No. 351, a deposit of acid tartrate of potash with a super¬ natant clear solution of hydrobromic acid. Of this decomposition the prescriber may not have been aware, or he may have been aware of the de¬ composition, but considered that on the addition of the deposited acid tartrate of potash to each dose of the sodae bicarb, in the powder, a potassic tartrate of soda would be formed ; the dispenser should there¬ fore direct the mixture to be shaken so that each dose of it may contain a definite relative quantity of the sediment. The dispenser would do well, how¬ ever, to suggest to the prescriber that a more elegant combination would result by combining the sodae bicarb, with the potass, bromid., and then putting the acid. tart, into the powder. Effervescence would equally take place and there would be little, if any, formation of acid tartrate of potash ; the result would be more elegant, and probably just that which was intended. Of course this would depend upon whether the prescriber intended to give his patient bromide of potassium or hydro¬ bromic acid. The turbidity resulting from the mixture, No. 352, is due to the presence of the magnesiae sulph. On that salt being added there is a separation of brown, flocculent matter; without it, the other ingredients may be combined so as to form a mixture free from deposit, and tolerably bright. The alkalinity or otherwise of different samples of ferri et ammoniae cit. may have a bearing on the change which with some samples certainly takes place. It is, of course, impossible to say how the mixture may have been prepared to show such different results. The prescription, No. 353, contains pulv. phos- phori, and from the dose being the same as that of the strych. sulph., it may be presumed that the amor¬ phous variety was not intended. The combination is not suitable for retaining phosphorus in an unoxi¬ dized condition; however, it should be dissolved in a little bisulphide of carbon before being mixed with the other ingredients, and then probably the best excipient will be the glycerine of tragacanth. With regard to the price, that must be left to individual judgment, its discussion is not suited for these columns. A paper on the subject of prices charged for dispensed medicines, by the late Daniel Hanbury, will be found among ‘ Science Papers ’ (p. 453), and may be read with advantage. The mixture, No. 354, will become turbid soon after being mixed, and there will be a considerable amount of deposit on standing. The powder, No. 355, becomes moist, due to the water of crystallization of the sodae phosphas. A better result would ensue if the phosphate of soda be deprived of a part of the water before being mixed with the potass, citrat.; but as written it will not retain its condition as a powder, and is not an elegant combination. The ingredients of recipe No. 356, with the ex¬ ception of the oil of aniseed, can be very well com¬ bined as a powder if each be in a dry condition, but the addition of the oil of aniseed makes the mass too soft. It is a piece of veterinary practice, and probably oil of aniseed quan. suff. would be more suitable to form the other ingredients into a manage¬ able mass. The prescription, No. 357, becomes difficult from, the remark of the writer “when the mixture has become quite clear.” The digestion of the in¬ gredients at the temperature indicated will result in a curdling of the milk, and subsequent deposit of the clot, but the supernatant liquid will not be clear except in comparison with the milk. It is probable that this is the condition it is intended the mixture should be in when adapted for neutralization by bi¬ carbonate of soda. The quinine mixture with ammonia, No. 358, is in principle similar to others which have been pre¬ viously commented on, so that “ Quiniae Sulph.” must be referred to those. Mucilage should be used as there indicated, to retain the quinine in suspension. The mixture of ol. olivae with ext. of belladonna, as in No. 359, may be satisfactorily made by rubbing the ext. bellad. with a little water, on a warm slab, to a smooth paste, gradually adding the oil. If care be taken to reduce the extract with a suitable quantity of water, an elegant ointment may be made from this prescription, but lin. bellad. should not have been used. The carbolic acid, No, 360, should be used in a crystalline state, and then there will be little or no difficulty experienced in making the pills. Reference may be made to carbolic acid in pills commented on quite recently. In the lotion, No. 361, aq. calc, and ol. olivae in equal proportions emulsify very satisfactorily, but if other water, or even more liquor calcis be added, there is a separation of some of the partially saponified oil, though on standing this is absorbed. Mr. Cair- nie’s process, in this week’s Journal, is probably the best that can be adopted. The prescription, No. 362, it is presumed, was intended to be dispensed just as written : — 2 parts by weight, acid, muriatic cone, with 18 parts tr. aurantii, 10-15 minims for a dose: the subsequent figures most probably bear reference to the date of the prescription. It is difficult to account for a change of colour in the mixture, No. 363 ; there is no reason why there should be one. Such a mixture may be dispensed with great uniformity of result. The decomposition alluded to can only be referred to impure iodide of potassium or careless dispensing. The second ingredient in No. 364 is evidently intended for glycerine ; but there would seem to have been some little confusion in the mind of the writer between the Latin of glycerine and that of liquorice. In reviewing the prescriptions referred to in this “Month,” it can scarcely be said that the inquiries are not fair and reasonable, and it will be observed that most of them owe their origin to errors or incom- patibles on the part of the writers of the several prescriptions. October 25, i . 2 drachms. . ^ drachm. . 4 pints. Can. Ph. Journ. A BRILLIANT PURPLE FOR SHOW BOTTLES. Sulphate of copper . 2 drachms. Water . . . 2 ounces. French gelatine . 1 drachm. Boiling water . 2 ounces. Solution of potassa . 2 pints. Dissolve the copper salt in the water and the gelatine in the boiling water. Mix the two solutions and add the liquor of potassa. Shake the mixture a few times during ten hours, after which decant and dilute with water. Can. Ph. Journ . October 25, i«M THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 331 llrapaqittital Joupal. - 4. - SATURDAY , OCTOBER 25, 1879. Communications for the Editorial department of this Journal , books for review, etc., should be addressed to the Editor, 17, Bloomsbury Square. Instructions from Members and Associates respecting the transmission of the Journal should be sent to Mr. Elias Bremridge, Secretary, 17, Bloomsbury Square, W.C. Advertisements, and payments for Copies of the Journal, Messrs. Churchill, New Burlington Street, London, W. Envelopes indorsed “ Pharm. Journ .” THE APPLICATION OF THE FOOD AND DRUGS ACT IN NEW DIRECTIONS. We have so often had occasion to complain of the vexatious manner in which the Sale of Food and Drugs Act has been had recourse to as a means of instituting frivolous prosecutions that it is with much satisfaction we are enabled to speak of some recent cases with approval, and also to express the opinion that if the line of action taken in those cases is fol¬ lowed up, some real service may be done in the public interest as well as in the furtherance of the objects contemplated by the Pharmacy Act. Reports of the cases we now refer to will be found in the present number of the Journal at page 336. In one of these cases a person described as a druggist, of 229, Stirling Road, Glasgow, was charged with having sold to the food inspector of the district a quantity of powders — purporting to be dispensed according to the prescription of a medical practitioner in Glasgow — that were not what was ordered by the prescriber. In the first place, we may state that the person against whom the prosecution was instituted is not upon the Register ot Chemists and Druggists of Great Britain, and that he is therefore presumably as unqualified to dispense the prescriptions of medical men as he is disentitled to use the designa¬ tion of druggist. That such was the case may be inferred from the manner in which the powders wrere prepared on account of which he has been charged with a breach of the Food and Drugs Act. The prescription ordered salicylate of soda 5 grains and pulv. ipecac, co. 6 grains, with the direction in Latin that eight such powders should be supplied. The person dispensing the prescription does not appear to have been acquainted with the usual mode of writing such directions and consequently to have divided the quantities of the ingredients ordered into eight parts, so that each of the powders was deficient in quantity to the extent of seven eighths. It is unnecessary to comment upon the nature of this proceeding from a pharmaceutical point of view, but having regard to the provisions of the 7th section of the Sale of Food and Drugs Act, that no person shall sell any compounded drug which is not tomposed of ingredients in accordance with the iemand of the purchaser, there seems to be no ques¬ tion that it involved a breach of the law, and that it rendered the seller of the powders liable to the penalty of £20 imposed by the 7th section of the Food and Drugs Act. It appears that there was no attempt at defence, and that the defendant at once pleaded guilty, and thereupon a fine of £5 was imposed by the sheriff, who remarked that though he was satisfied there was no fraudulent intention, the powder had evidently been dispensed by a person ignorant of the medical formulae used in prescriptions. The further offence of improperly using the desig¬ nation “ druggist ” is one to be dealt with under the Pharmacy Act. As this proceeding is under some pretext or other common in Glasgow this case will probably receive further notice. The other two cases were both prosecutions of grocers in Derbyshire, for the sale of an adulterated drug as it was technically stated, the article referred to being u paregoric,” that was not of the quality demanded, inasmuch as it was found on analysis to be devoid of opium, the most important ingredient of that preparation. An attempt was made to defend both cases on the ground that “paregoric” was a preparation that had no place in the British Phar¬ macopoeia, and consequently that there was no standard by which its composition should be judged of. Hence it was contended that the Court had no power to deal with the cases under the Food and Drugs Act for the deficiency, while at the same time the absence of opium from the preparation sold as “ paregoric ” protected the seller from liability to a penalty under the Pharmacy Act, 1868. The un¬ tenable nature of this defence is too apparent to require argument, and we cannot avoid expressing our deep regret at finding from the statements made that such a defence should, as it appears, have been suggested by members of the pharmaceutical body, and that such irregular sales of medicinal prepara¬ tions should have been in any way encouraged by them. Whether the term “ paregoric ” has a place in the British Pharmacopoeia or not seems to be, in our opinion, a matter of very little importance, since it is so familiarly known as being a popular synonym for the preparation that is in the Pharmacopoeia, and just as we should contend that a person asking for “ milk of sulphur ” should be supplied with the pre¬ paration that name is most frequently understood to represent, so we should contend that any person asking for “ paregoric ” ought to be supplied with a preparation containing opium. It may be that as there is now no recognition of the term “paregoric” in the British Pharmacopoeia the preparation of that article may be carried out according to various private formulae, but still in its general character it ought to conform closely to the standard of strength as a mild opiate that appertains to the Pharma¬ copoeia preparation which it represents. We think, therefore, the magistrates exercised a 332 THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. [October 25, 1879. very wise discretion in rejecting the defence offered and holding that persons who sold “paregoric” should sell what was properly to be understood by that name, and nothing else which they or the persons who supply them may imagine to answer the pur¬ poses of trade without incurring the penalties result¬ ing from infringement of the Pharmacy Act. But we cannot go the length of agreeing with the magis¬ trates’ suggestion that if the Pharmacy Act does not permit unregistered persons to sell “ paregoric ” with opium in it, they should sell an article under that name without opium in it, even under the condition of putting upon the bottle a label stating that it is “minus the opium.” Such a proceeding would be, we think, very objectionable and we should have laudanum without opium, and perhaps other potent preparations sold without the ingredient to which their medicinal as well as poisonous energy is due, and the confusion thus created between the prepara¬ tions that possessed their proper character and those that did so only in name might readily lead to the most disastrous consequences. There has been lately much dissatisfaction among members of the drug trade because of the irregular sales of medicines and drugs by grocers and other small dealers in country places, and we have reason to believe that there is too much probability that in some cases such a trade is promoted by in¬ dividuals without due regard for the general interests of the body to which they belong. Whether that trade be carried on so as to con¬ stitute a punishable breach of the Pharmacy Act, or under the belief that it can be done with impunity by making use of the patent medicine stamp, or, worse still, by selling to the public articles which have no virtue beyond assuming the names of the preparations they are pretended to be, it is certainly time that some vigorous and united action should be taken by those who have the common welfare of the business at heart with the object of putting an end to practices so detrimental to the credit of pharmacy. We regret to have to record the death, on the 16th inst., of Dr. Arthur Leared, Senior Physician of the Great Northern Hospital. It appears that only a few days previously he returned home unwell from a holiday tour, having contracted typhoid fever in Portugal. Dr. Leared on more than one occa¬ sion showed his interest in the Pharmaceutical Society by taking part in its Evening Meetings, and he also contributed an interesting collection of Morocco drugs to the Society’s Museum. The death is also announced of Mr. Alfred Henry Garrod, Fullerian Professor of Physiology at the Royal Institution, at the early age of 30 years. The deceased was a son of Dr. Alfred Baring Garrod, and had already attained a con¬ siderable prominence in the scientific world. §OTitsa:j[tion:8 of fire iljitrmaceafel $ wjielg. PRELIMINARY EXAMINATION. At a meeting of the Board of Examiners for England and Wales, held in London, on Wednesday, October 22nd, 1879, the report of the College of Preceptors on the ex¬ amination held on October 7th, was received. Three hundred and eighty-seven candidates had presented themselves for examination, of whom one hundred and eighty-three had failed. The following two hundred and four passed, and the Registrar was authorized to place their names upon the Register of Apprentices or Students : — (Arranged alphabetically). Abbott, Thomas Henry . Bradford. Akerman, John William . Bath. Allan, Alexander Fergusson ...Greenock. Allan, Charles Joseph . Tadcaster. Andrews, Walter . Winchester. Aplin, John Dare . Colyton. Amott, Daniel . Pontypridd. Baker, Alfred John E . St. Austell. Bassano, Francis William . Derby. Bay ley, Alfred Jonathan . Lancaster. Bearpark, Thomas . Leyburn. Beck, William Henry . Selby. Bell, Andrew . Dundee. Bell, John Henry . Epworth. Bell, Thomas . London. Booth, Frank . Mansfield. Boyd, Alexander . Glasgow. Bradford, Lionel Meredith . London. Brown, Fredk. Wm., jun . London. Brown, James . Ripon. Carter, Octavius . Bournemouth. Carter, William . Penzance. Chabot, Frank . London. Chadwick, John Booth . Stockport. Chamberlain, John W. West ...York. Chamberlin. Charles J ames . . . Barnsley. Chattaway, William . . Leicester. Clayton, George . Manchester. Coleman, Alfred Thomas . Leicester. Collen, William Creswell . London. Compton, Richard William ...Leicester. Cooper, Walter Temple . London. Dale, John Dickin . Stafford. Davis, Frederick . Oundle. Davis, Norman . Sunderland. Deighton, Frank . Bradford. Dinsdale, Fred . Liverpool. Dobie, Robert Douglas . Glasgow. Doubleday, Frederick Wm . Norwich. Down, Frank Walter . Sittingbourne. Downs, Herbert . Edinburgh. Dowty, William . Evesham. Dry den, Thomas . .Landore. Elliott, Horace Herbert . Stowmarket. Farquhar, Robert Forbes . Aberdeen. Felce, Albert . Norwich. Flynn, Robert Francis . Feltbam. Fodd, John William . Peebles. Fraser, Alexander Mackie . Girvan. Freeman, Frederick William. ..St Albans. Gant, Robert Richard . Norwich. Gibson, John William . Richmond, Yorks. Gilding, Matthew . Wainfleet Gilson, Charles Boulter . London. Gordon, Robert Henderson . Rosemarkie. Gray, Philip . Bristol. Greaves, William . Ironville. Gregory, George Henry . Lincoln.’ Hamilton, Francis . Glasgow. Harding, John W. Ainsworth...Macclesfield. Harries, Charles Albert ........ . Velindre. Harrison, Jeremiah . Clitheroe. October 25, 1879. j THE PHARMACEUTICAL JOURNAL AND TRANSACTIONS. 333 Harrison, John . Lincoln. Hepworth, Harry . Skipton. Hilton, Ivor Ajax Robinson . . . My erscough. Hogg, Tom . Derby. Holmes, Fred . Lincoln. Holroyd, Henry . Hingham. Holt, Clarence Dalton . Manchester. Hooper, William Henry . Okehampton. Hunter, George Ackland . London. Hutton, James Alfred . Scarborough. Irving, John Thomas . Skipton. Jack, James . Arbroath. Jacka, Vivian Tyacke . Penzance. Jaffrey, William . Logie Buchan. Jeans, Alfred . Mansfield. .Ten kin son, Arthur . London. Johnson, Arthur George . Sutton- on- Trent. Johnson, John Robert . Cambridge. Jones, Benjamin Owen . Llanidloes. Jones, Edwin Pryce . Aberdare. Jones, Ellis . Portmadoc. Jones, John . Llandovery. Jones, Johnj Wesley . Llanelly. Jones, Samuel . Llandilo. Kerr, David . Oakham. Kerr, Peter Murray . Dumfries. King, Ebenezer Thomas . Reading. Kingston, Edwin J. B . Bath. Knight, William . Chichester. Lee, Charles Henry . Melton Mowbray. Lees, James . . Manchester. Legg, James Alfred . London. Ling, Frederic George . Southampton. Livesey, William Forrest . Preston. Longtoft, William . Bedale. Lowther, Herbert Reginald . . . Birmingham. Loxton, William Arthur . Plymouth. Lyon, Herbert . Sheffield. McGeorge, David . Castle Douglas. McGuffie, William A . Stranraer. McIntosh, John . Edinburgh. Mack, William Wilson . Nottingham. Mackenzie, Alexander . Leith. Marr, Edward Albert . Newcastle-on-Tyne. Marshall, Arthur Harflete . Redhill. Martin, James . Carnoustie. Martin, John . Redruth. Martin, John Bennet . Falmouth.] May, Harry Arthur . Reading. Mays, Frank Webb . Grantham. Menhinick, Charles H. F . Stonehouse, Devon. Miller, Frederick . Strood. Miller, J ohn Priest . . N or wich. Morgan, William Thomas . Llandovery. Morrison, Clarence . Inverness. Moxon, John Lawrence . Wellingborough. Neale, Charles Swanson . Stoke-on-Trent. Neve, Annie . . London. Nichol, Anthony . Carlisle. Nichol, Henry Walter . Bedford. Noble, James . Camborne. Norman, Edwin . Ripley. Orchard, Arthur Bishop Carey..London. Owen, Evan . Weston-super-Mare. Paine, Charles . Belton. Paine, William . . . Ashton-under-Lyne. Parish, Alfred James . Kidderminster. Pearce, William Frederick . Southampton. Pollock, Arthur . Glasgow. Puckey, William . Bishops Stortford. Raff an, Robert . Buckie. Raine, Ralph William . Newcastle-on-Tyne. Reece, Richard James . London. Rees, John . . . Rhydlewis. Roberts, Lewis . Aberystwith. Roberts, Rowland . Holyhead. Robertson, Daniel . Perth. Robinson, John Colburn . London. Rose, George Ernest . Stratford-on-Avon. Rutter, Clement Thomas . Birmingham. Sanders, Ernest . Manchester. Scholes, William Isaac . Pendleton. Senior, Joseph . Castle Northwich. Shaw, John Bingley . Lincoln. Shepperley,Fredk.Montgomery.Nottingham. Shipman, Joseph James . Chesterfield. Skilling, James . Stonehouse, Devon. Skirrow, William . Bingley. Smeeton, Charles William . Leeds. Smith, George . '. . Worcester. Smith, John . Manchester. Smith, Lewis . Grassendale. Smith, Sam . . . Batley Carr. Smith, William John . Newcastle-on-Tyne: Softley, William Henry . Godaiming. Spark, Albert Edward . Kirkwall. Stark, Arthur Campbell . Norwich. Stark, John Edgar . Dumfries. Stephen, James, jun. . Gamrie. Stephenson, Thomas . Edinburgh. Stirling, George . Dunoon. Sturdy, John Robert . Lincoln. Sursham, Frederick Thomas ...London. Sutherland, David Alexander. . .Edinburgh. Sykes, Ernest John . Bath. Taggart, Robert . Glasgow. Terry, Edwin . Tadcaster. Thomas, David . . . Pontypridd. Thomas, John Griffith . Neath. Titmas, John H . Flixton. Tollitt, William . Liverpool. Tomlin, John Percy . Tunbridge Wells. Topham, Thomas . Mirfield. Trezise, George T. E . Wellingborough. Tugwell, Ernest Harry . Greenwich. Turner, George Edward . Brigg. Ward, Robert Edward . Kettering. Walker, John Frederick . Hull. Watchorn, Fredk. William . Leicester. Watkins, William James . Bath. Watson, Frederick Percy . Lincoln. Weeks, Charles Frederick . Devonport. Weighill, William Lancelot ...West Hartlepool. Welch, John Latimer . Bristol. Wharton, James . Preston. Whitfield, Allison . Sunderland. Whitton, James . Dingwall. Wilde, Frank . Andover. Wilkie, John Proudfoot . Hayfield. Williams, Arthur Gore . Llandovery. Williams, David . St. Clears. Williams, John Fox., . Gloucester. Wilson, Albert . Garstang. Winter, George Mitchell . Leicester. Wisker, Robert Hardy . York. Withers, William . West Bromwich. Woltz, Alfred Eugene . London. Wood, Alfred Lyon . Stonehaven. Wood, Arthur W. H . Ullesthorpe. Woodward, Edwin . Macclesfield. Woolley, Evan Edward . Llanidloes. Young, John . .-.Newport. Mon. The questions for examination were as follows: — Time allowed: Three hours for the three subjects. I. LATIN. 1. Translate the following passages into English: — A. Quibus rebus cognitis, cum ad has suspiciones certis- simse res accederent, quod per fines Sequanorum Helvetios traduxisset, quod obsides inter eos dandos curasset, quod ea omnia non modo injussu suo et civitatis, sed etiam inscien- tibusipsis/ecmetf, quod amagistratu Hseduorum accusare- 334 THE FHARMACEUT1CAL JOURNAL AND TRANSACTIONS. iCctober 25, w tur, satis esse causae arbitrabatur , quare in eum aut ipse animadverteret, aut civitatem animadvertere juberet. B. Haec cum pluribus verbis flens a Caesare peteret, Caesar ejus dextram prendit; consolatus rogat finem orandi faciat ; tanti ejus apud se gratiam esse ostendit, uti et rei publicae injuriam et suum dolorem ejus voluntati ac precibus condonet. Dumnorigem ad se vocat, fratrem adhibet ; quae in eo reprehendat ostendit, quae ipse intel- ligat, quae civitas guemZMr, proponit ; monet, utin reliquum tempus omnes suspiciones vitet ; preeterita se Divitiaco fratri condonare dicit. 2. Give the present, perfect, and infinitive of tlie verbs in italics. 3. Parse either “ non modo injussu suo et civitatis,” or “ consolatus rogat finem orandi faciat” 4. Compare certus, and give three adverbs formed from the superlative degree of adjectives. Decline obsides. 5. Decline, singular and plural, the pronouns ego, tu , ille, qui. II. ARITHMETIC. [The working of these examples, as well as the answers, must be written out in full.] 6. Of twenty-one people, thirteen lose £116 7s. Sd. each, and eight lose £93 05. 9 d. each. What is the average loss per man. 7. Find the weight of 5 dozen spoons, each weighing 2 oz. 4 dwt. 2 2- 8. Multiply 3t3o by 15^, and divide g3 by an