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Diphenylamine is an organic compound with the formula (C 6 H 5) 2 NH. The compound is a derivative of aniline , consisting of an amine bound to two phenyl groups. The compound is a colorless solid, but commercial samples are often yellow due to oxidized impurities. [ 5 ]
4-Aminodiphenylamine is a diphenylamine with an additional amine substituent. This dimer of aniline has various industrial uses, including as a hair dye ingredient, but also has raised concerns about toxicity by skin contact. [1] It is also a starting material for the synthesis of 6PPD, an antiozonant for various rubber products. [2]
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The main structure of chemical names according to IUPAC nomenclature. The International Union of Pure and Applied Chemistry (IUPAC) has published four sets of rules to standardize chemical nomenclature. There are two main areas: IUPAC nomenclature of inorganic chemistry (Red Book) IUPAC nomenclature of organic chemistry (Blue Book)
To avoid long and tedious names in normal communication, the official IUPAC naming recommendations are not always followed in practice, except when it is necessary to give an unambiguous and absolute definition to a compound. IUPAC names can sometimes be simpler than older names, as with ethanol, instead of ethyl alcohol. For relatively simple ...
Preferred IUPAC name. 4,4′-Methylenedianiline. Other names MDA . dadpm 4,4′-Diaminodiphenylmethane 4,4′-Methylenebisbenzenamine para,para′-Diaminodiphenylmethane
2-Nitrodiphenylamine is an organic chemical with the formula C 6 H 5 NHC 6 H 4 NO 2.It is a nitrated derivative of diphenylamine.It is a red solid, usually found in form of flakes or powder.
Triphenylamine is an organic compound with formula (C 6 H 5) 3 N. In contrast to most amines, triphenylamine is nonbasic.At room temperature it appears as a colorless crystalline solid, with monoclinic structure.