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  • ...J. Bacteriol.|volume=172|pages=5650–5654}}</ref> This is because charged amines interact with negative charges on the cell membrane, and can cause leakage
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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 rea
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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]]
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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]]
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  • Aromatic amines, when protonated, usually have lower pKa's (are more acidic) than their non [[Category:Aromatic amines]]
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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]]
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