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se as an essence of apples, one part of this valerianate of amyloxide is dissolved in 6 or 8 parts of alcohol. * * * * * VOLATILE OIL OF GAULTHERIA PROCUMBENS. BY W. BASTICK. The chemical history of this oil is one of great importance and interest, affording, as it does, one of the examples where the progress of modern chemistry has succeeded in producing artificially a complex organic body, previously only known as the result of vital force. This volatile oil is obtained from the winter-green, an American shrub of the heath family, by distillation. When this plant is distilled, at first an oil passes over which consists of C_{10}H_{8}, but when the temperature reaches 464 deg. Fahr., a pure oil distils into the receiver. Therefore the essential oil of this plant, like many others, consists of two portions--one a hydro-carbon, and the other an oxygenated compound; this latter is the chief constituent of the oil, and that which is of so much chemical interest, from the fact that it has been artificially prepared. It is termed, when thus prepared, the spiroylate of the oxide of methyl, and is obtained when two parts of wood spirit, one and a half parts of spiroylic acid, and one part of sulphuric acid are distilled together. It is a colorless liquid, of an agreeable aromatic odor and taste; it dissolves slightly in water, but in all proportions in ether and alcohol; it boils between 411 deg. and 435 deg. Fahr., and has a specific gravity of 1.173. This compound expels carbonic acid from its combinations, and forms a series of salts, which contain one atom of base and one atom of spiroylate of the oxide of methyl. It behaves therefore as a conjugate acid. Its formula is C_{14}H_{5}O_{5} + C_{2}H_{3}O. The spiroylic acid may be separated from the natural oil by treating it with a concentrated solution of caustic potash at a temperature of 113 deg. Fahr., when wood spirit is formed and evaporates, and the solution contains the spiroylate of potash, from which, when decomposed with sulphuric acid, the spiroylic acid separates and subsides in the fluid. Spiroylic acid is also formed by the oxidation of spiroyligenic acid, and when saligenin, salicin, courmacin, or indigo, is heated with caustic potash. * * * * * ON THE APPLICATION OF ORGANIC CHEMISTRY TO PERFUMERY. BY DR. A.W. HOFMANN, _Professor to the Royal College of Chemistry, Londo
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