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CAFFEINE, or THEINE (1.3.7 trimethyl 2 . 6 dioxypurin) , C$ His N4 02 . H ? O, a substance found in the leaves and beans of the See also: coffee See also: tree, in See also: tea, in See also: Paraguay tea, and in small quantities in See also: cocoa and in the See also: kola See also: nut
.
It may be extracted from tea or coffee by boiling with See also: water, the dissolved See also: tannin precipitated by basic See also: lead acetate, the solution filtered, excess of lead precipitated by sulphuretted hydrogen and the filtered liquid then evaporated to See also: crystallization; or, tea is boiled with water, and the whole then evaporated to a syrup, which is mixed with slaked lime, evaporated to dryness on the water-See also: bath and extracted with See also: chloroform (P
.
Cazeneuve, Bull. de la See also: soc. chim. de See also: Paris, 1876-1877, 27, p
.
199)
.
Synthetically it may be prepared by the methylation of See also: silver theobromine and silver theophyllin or by boiling heteroxanthine with methyl iodide and potash
.
E
.
Fischer and L
.
Ach (Berichte, 1895, 28, p
.
3135) have synthesized it from dimethyl alloxan, whilst W
.
Traube (Berichte, 1900, 33, p
.
3435) has obtained it from 1 . 3 diamethyl 4 . 5 diamino 2.6 dioxypyrimidine . On the constitution of caffeine see BURIN and also E . Fischer (Annalen, 1882, 215, p . 253) . Caffeine crystallizes in long silky needles, which are slightly soluble in cold water . It becomes anhydrous at ro0° C. and melts at 234° to 23 5° C . It has a faint bitter taste and gives salts withSee also: mineral acids
.
On oxidation with nitric acid caffeine gives cholesterophane (dimethyl parabanic acid), but if chlorine water be used as the oxidant, then it yields monomethyl See also: urea and dimethyl alloxan (E
.
Fischer)
.
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