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...[[azo compound|diazo]] [[dye]]s, [[nitroso compound]]s, and other organic compounds; in dyeing and printing textile fabrics and bleaching fibers; in [[photogra Sodium nitrite is used to convert [[amine]]s into diazo compounds. The synthetic utility of such a reaction is to render the amino group labi

...oxicology Program]</ref> and so it has been largely replaced by less toxic compounds. It is similar to [[benzidine]].

...s a known human [[carcinogen]] and has largely been replaced by less toxic compounds. 2-Naphthylamine is prepared by heating 2-[[naphthol]] with [[ammonium]] [[

...line is a starting material for the synthesis of [[Para Red]], the first [[Azo dye]]:<ref>{{cite book [[Category:Nitro compounds]]

It is used as a chemical intermediate for [[azo coupling]] component 17 and the dyes disperse yellow 5 and acid blue 29. T [[Category:Nitro compounds]]

...n]] is the major form of metabolism in humans,<ref name = jps /> and the [[azo]] ring is usually not cleaved.<ref name = jps /> On the order of 65% of an ...]].<ref>http://emedicine.medscape.com/article/778670-treatment</ref> Other azo dyes, which were previously used in textiles, printing, and plastic manufac

[[Category:Azo compounds]]

...astome]]rs. 2-Tolidine is an intermediate for the production of soluble [[azo dye]]s and insoluble pigments used particularly in the textile, leather and