An aromatic organic base, C9 H7 N, having a pungent tarlike odor, synthesized or obtained from coal tar, and used as a food preservative and in making antiseptics, drugs, and dyes.
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A colorless, liquid compound, C9H7N, obtained by the destructive distillation of bones, coal tar, and various alkaloids, or by synthesis: it is used in making antiseptics, dyes, etc. and as a solvent.
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Any of various derivatives of quinoline.
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An aromatic organic base, C9 H7 N, having a pungent tarlike odor, synthesized or obtained from coal tar, and used as a food preservative and in making antiseptics, drugs, and dyes.
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An aromatic organic liquid having a pungent, tarlike odor. Quinoline is a base and is obtained from coal tar or is synthesized. It is used as a food preservative and in making antiseptics and dyes. Chemical formula:C9H7N.
This compound condenses in alkaline solution with compounds containing the grouping - CH 2 - CO - to form quinoline or its derivatives; thus, with acetaldehyde it forms quinoline, and with acetone, a-methyl quinoline.
Marckwald (Ann., 93, 74, 331; 1894, 79, 14) has supported this formula from considerations based on the syntheses of the quinoline ring.
Similarly a CH group may be replaced by a nitrogen atom with the production of compounds of similar stability; thus benzene gives pyridine, naphthalene gives quinoline and isoquinoline; anthracene gives acridine and a and 3 anthrapyridines.
Naphthyridines and naphthinolines result from the condensation of two pryridine and two quinoline nuclei respectively; and quino-quinolines are unsymmetrical naphthyridine nuclei condensed with a benzene nucleus.
It combines with alkaline chlorides - potassium, rubidium and caesium - to form crystalline plumbichlorides; it also forms a crystalline compound with quinoline.