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INDOLE , or BENioPYRR0I., CBH,N, a substance first prepared by A . Baeyer in 1868 . It may be synthetically obtained by distilling oxindole (C8H8NO) withSee also: zinc dust; by See also: heating orthonitrocinnamic acid with potash and iron filings; by the reduction of indigo blue; by the See also: action of sodium ethylate on orthoaminochlorstyrene; by boiling-aniline with dichloracetaldehyde; by the dry See also: distillation of ortho-tolyloxamic acid; by heating aniline with dichloracetal; by distilling a mixture of calcium
See also: INDORE
formate and calcium anilidoacetate; and by heating pyruvic acid phenyl See also: hydrazone with anhydrous zinc chloride
.
It is also formed in the pancreatic See also: fermentation of albumen, and, in small quantities, by passing the vapours of mono- and dialkylanilines through a red-hot See also: tube
.
It crystallizes in shining leaflets, which melt at 52° C. and See also: boil at 245° C
.
(with decomposition), and is volatile in a current of steam
.
It is a feeble See also: base, and gives a See also: cherry-red coloration with a See also: pine shaving
.
Many derivatives of indole are known
.
B-methyl indol or skatole occurs in human faeces
.
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