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Aromatic amine





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Inorganic chemistry, an aromatic amine is an organic compound consisting of an aromatic ring attached to an amine. It is a broad class of compounds that encompasses anilines, but also many more complex aromatic rings and many amine substituents beyond NH2. Such compounds occur widely.[1]

Representative aromatic amines
Aromatic ring Name of parent amines Example
benzene aniline substituted anilines
phenylenediamines the antioxidant p-phenylenediamine
toluene toluidines the pharmaceutical prilocain
diaminotoluenes the hair dye ingredient 2,5-diaminotoluene
naphthalene naphthylamines the dyes Congo red and Prodan
pyridine aminopyridines the drug tenoxicam
pyrimidine aminopyrimidines the nucleobase cytosine
quinoline aminoquinolines the drug primaquine
purine aminopurines the nucleobase guanine
acridine aminoacridines fluorescent dyes

Aromatic amines are widely used as precursor to pesticides, pharmaceuticals, and dyes.

Aromatic amines in textiles

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Since August 2012, the new standard EN 14362-1:2012 Textiles - Methods for determination of certain aromatic amines derived from azo colorants - Part 1: Detection of the use of certain azo colorants accessible with and without extracting the fibres is effective. It had been officially approved by the European Committee for Standardization (CEN) and supersedes the test standards EN 14362-1: 2003 and EN 14362-2: 2003.

The standard describes a procedure to detect EU banned aromatic amines derived from azo colorants in textile fibres, including natural, man-made, regenerated, and blended fibres. The standard is also relevant for all coloured textiles, e.g. dyed, printed, and coated textiles.

See also

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References

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  1. ^ P.F. Vogt, J.J. Gerulis (2005). "Amines, Aromatic". Ullmann’s Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a02_037.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Aromatic_amine&oldid=1114410647"
 



Last edited on 6 October 2022, at 10:43  





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This page was last edited on 6 October 2022, at 10:43 (UTC).

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