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o-Toluidine (ortho-toluidine) is an organic compound with the chemical formula CH 3 C 6 H 4 NH 2. It is the most important of the three isomeric toluidines . It is a colorless liquid although commercial samples are often yellowish.
The toluidines are poorly soluble in pure water but dissolve well in acidic water due to formation of ammonium salts, as usual for organic amines. ortho- and meta-toluidines are viscous liquids, but para-toluidine is a flaky solid. This difference is related to the fact that the p-toluidine molecules are more symmetrical.
2-Tolidine (orthotolidine, o-tolidine; not to be confused with o-toluidine) is an organic compound with the chemical formula (C 6 H 4 (CH 3)NH 2) 2. Several isomers are known; the 3-tolidine derivative is also important commercially. It is a colorless compound although commercial samples are often colored. It is slightly soluble in water.
Tobacco, oral use of smokeless products – Tobacco smoke – Tobacco smoke (Primary) – Tobramycin sulfate: 49842-07-1 Toluene: 108-88-3 Toluene diisocyanate: 26471-62-5 o-Toluidine: 95-53-4 o-Toluidine hydrochloride: 636-21-5 Topiramate: 97240-79-4 Toxaphene (Polychlorinated camphenes) 8001-35-2 Fusarium toxins – Treosulfan: 299-75-2 ...
Preparations of this chemical may be named as a hydrochloride (e.g. "3-chloro-p-toluidine hydrochloride", CPTH), indicating that hydrochloric acid has been used to neutralize the molecule to a salt in which the amine group is protonated and a chloride counterion is present; otherwise the free base is indicated.
Mauveine is a mixture of four related aromatic compounds differing in number and placement of methyl groups.Its organic synthesis involves dissolving aniline, p-toluidine, and o-toluidine in sulfuric acid and water in a roughly 1:1:2 ratio, then adding potassium dichromate.
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It is pale yellow liquid that crystallizes in two forms, called α (−9.27 °C) and β (−3.17 °C). It is mainly a precursor to o-toluidine, which is an intermediate in the production of various dyes. [4]