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From Self-sufficiency
- ...J. Bacteriol.|volume=172|pages=5650–5654}}</ref> This is because charged amines interact with negative charges on the cell membrane, and can cause leakage26 KB (3,675 words) - 10:11, 20 September 2010
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- ...s in the manufacture of precursors to [[polyurethane]]. Like most volatile amines, it possesses the somewhat unpleasant odour of rotten fish. It ignites read ...e]]s such as aniline are, in general, much weaker bases than [[aliphatic]] amines because of the electron-withdrawing effect of the phenyl group. Aniline rea14 KB (2,008 words) - 13:10, 20 September 2010
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- ...due to oxidized impurities.<ref name=Ullmann>P. F. Vogt, J. J. Gerulis, “Amines, Aromatic” in Ullmann’s Encyclopedia of Industrial Chemistry 2005, Wile [[Category:Aromatic amines]]4 KB (509 words) - 13:11, 20 September 2010
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- ...ties in common with other aryl (often incorrectly referred to as aromatic) amines. Due to the amino group bonded to the aromatic ring, the toluidines are [[ [[Category:Aromatic amines]]4 KB (551 words) - 13:11, 20 September 2010
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- Aromatic amines, when protonated, usually have lower pKa's (are more acidic) than their non [[Category:Aromatic amines]]1 KB (181 words) - 13:12, 20 September 2010
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- ...y amine]]; by the condensation of ''para''-aminoazo compounds with primary amines, and by the action of ''para''-nitrosodialkylanilines with secondary [[base [[Category:Aromatic amines]]5 KB (638 words) - 13:12, 20 September 2010
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