LONDON. Chemical Society, December 19, 1889.—Dr. W. J. Russell, F.R. S., in the chair.—The following papers were read:—Frangulin, by Prof. T. E. Thorpe, F.R.S., and Mr. H. H. Robinson. The authors prepared the glucoside frangulin from the bark of the alder buckthorn (Rhamnus frangula), and find its formula to be C22H22O9. On hydrolysis it yields a yellow product, C15H10O5, which agrees in its properties with emodin, and a sugar which has the power of reducing Fehling's solution, and is not identical with dextrose.—Arabinon, the saccharon of arabinose, by Mr. C. O'Sullivan, F. R. S. The substance having an optical activity “well above [a]i = 140,” obtained by the author by the hydrolysis of arabic acid, and described under the name of a-arabinose (Chem. Soc. Trans., 1884, 55), yields arabinose on hydrolysis, and appears to bear to this carbohydrate a relation similar to that which saccharon (cane sugar) bears to dextrose: the author therefore terms it arabinon. It has the formula C10H18O9, and on hydrolysis gives a yield of arabinose agreeing very closely with that required by the equation C10H18O9 + H2O = 2C5H10O5. As yet it has not been obtained in a crystalline state; it has a specific rotatory power of [a]D I98°˙8, and 100 parts have the same cuprie reducing power as 58˙8 parts of dextrose.—On the identity of cerebrose and galactose, by Mr. H. T. Brown, F.R.S., and Dr. G. H. Morris. The authors give the results of an examination of a specimen of cerebrose, prepared from phrenosin, which was placed in their hands early in 1888 by Dr. Thudichum, who first isolated and crystallized this substance. They show that its specific rotatory power, cupric reducing power, and molecular weight as determined by Raoult's method, are identical with those of galactose, thus confirming the recent work of Thierfelder, Zeit. Physiol. Chem., 14, 209) who has proved the sugar produced by the action of acid on cerebrin to be identical with galactose. In the discussion which followed the reading of the paper, Dr. Thudichum said that phrenosin, C41H79NO8, consisted of the sugar now shown to be identical with galactose, C6H12O6, of neurostearic acid, C18H36O2, an isomeride of stearic acid, fusing at 84°, and of sphingosine, an alkaloid of the formula C17H35NO2. Some human brains contained as much as 4 per cent. of phrenosin in addition to other glucosides. The crystallized sugar (galactose) from phrenosin was always accompanied by an almost equal weight of uncrystallizable sugar, of which the nature was not yet ascertained.—The action of chloroform and alcoholic potash on hydrazines, Part 3, by Dr. S. Ruhemann. The products formed by the action of chloroform and alcoholic potash on hydrazines are to be regarded as derivatives of tetrazine,; and in the present communication the author describes the di-paratolyl,-orthotolyl, and -pseudocumyl derivatives of this base (cf. Chem. Soc. Trans., 1889, 242).