GoGuides Verified Text
INDOLE
SHA-256 integrity check: match
Source
Encyclopaedia Britannica (1911) / britannica_1911
License
public_domain
Chunk ID
1911:indole:8c5d1e7c73e7
Section
Hash Algorithm
sha256
Stored Hash
b5f4f9d1ee55736a5582d000ba4582130fcdb7d295114356d691c5ceca142ced
Computed Hash
b5f4f9d1ee55736a5582d000ba4582130fcdb7d295114356d691c5ceca142ced
Normalizer
ggnorm 1.0
Observed
2026-02-08 18:43:10
Source URL
Verified Text
indole, or benzopyrrol, c8h7n, a substance first prepared by a. baeyer in 1868. it may be synthetically obtained by distilling oxindole (c8h8no) with zinc dust; by heating ortho-nitrocinnamic acid with potash and iron filings; by the reduction of indigo blue; by the action of sodium ethylate on ortho-aminochlorstyrene; by boiling aniline with dichloracetaldehyde; by the dry distillation of ortho-tolyloxamic acid; by heating aniline with dichloracetal; by distilling a mixture of calcium formate and calcium anilidoacetate; and by heating pyruvic acid phenyl hydrazone with anhydrous zinc chloride. it is also formed in the pancreatic fermentation of albumen, and, in small quantities, by passing the vapours of mono- and dialkyl-anilines through a red-hot tube. it crystallizes in shining leaflets, which melt at 52° c. and boil at 245° c. (with decomposition), and is volatile in a current of steam. it is a feeble base, and gives a cherry-red coloration with a pine shaving. many derivatives of indole are known. b-methylindol or skatole occurs in human faeces.