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128 These results indicate that the genuine oil consists almost wholly of triglycerides of lauric, chaulmoogric, and linolic acids, whilst the doubtful oil is a mixture of tri- and diglycerides.

On neutralising the oil with alcoholic potash and adding a dilute solution of calcium, magnesium, or zinc chloride, the corresponding metallic salt of "gynocardic acid " is precipitated. Calcium and magnesium " gynocardates " are white crystalline substances slightly soluble in boiling water and most soluble in bailing alcohol, whilst zinc "gynocardate " is white and crystalline, insoluble in water and only very sparingly soluble in boiling alcohol, 10 drops of the genuine oil stirred with 1 drop of sulphuric acid gave a yellow coloration, changing rapidly to reddish-brown and finally to dirty brown, whilst the doubtful oil gave similar colour changes, but the final coloration was olive-green, this reaction being also given by the fatty acids from both oils and by chaulmoogra fat.— J. Oh. I. Nov. 15, 1915.

But in the American Journal of Pharmacy, for 1915 (pp. 493 — 500), Mr. Frederick B. Power severely criticises the above paper.

He emphasizes the statement that chaulmoogra (Taraktogenos) oil and gynocardia oil are totally unlike, both in their physical characters and chem. compn. Along with data establishing the authenticity of his oils, Mr. Power gives the following : Physical characters : (1) chaulmoogra oil : soft solid at ordinary temp., m. 22-3°, d25 0.951 and d45  0.940, [a]D15°+52.0°, acid value 23.9, sapon. value 213.0, I value 103.2. (2) Gynocardia oil : pale yellow liquid at ordinary temps., odor resembling that of linseed oil, d25 0.925, acid value 4.90, sapon. value 197.0. I value 152.8. Chemical composition : (1) chaulmoogra oil : (from the seeds of Taraktogenos Kurzii, King), optically active, consists, to a large extent, of the glyceryl esters of optically active acids of an entirety new type, represented by the general formula CnH2n—4O2, having a cyclic structure. The acid present in the largest proportion possesses the formula C18H32O2, m. 68°, [a]D+56° , and has been designated chaulmoogric acid, while a lower homolog, C16H28O2 , m. 60°, [a]D+68°, has been termed hydnocarpic acid, on account of having first been isolated from a hydnocarpus oil {J. Chem. Soc. 87, 888 (1905)). Both of these acids are beautifully cryst. substances, from which a number of derivs. have been prepd., and their constitution has also been definitely established (C. A. 1, 1561, 2114). Inasmuch as acids of the above described type had hitherto not been known to occur in a fatty oil, they have been classified by Lewkowitsch (" Chemical Technology and Analysis of Oils, Fats and Waxes") under the heading of "the chaulmoogric acid series." Chaulmoogra oil contains, furthermore, a relatively small proportion of palmitic acid and a phytosterol. (2) Gynocardia oil (from the seeds of Gynocardia odorata, R. Br.) is completely devoid of optical activity, contains none of the members of the chaulmoogric acid series, and has been shown to consist of the glyceryl esters of the following acids : (cf. J. Chem. Soc. 87, 896-900 (1905) ; (1) linolic acid, or isomerides of the same series, constituting the largest proportion