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Diphenylamine

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diphenylamine [dī¦fen·əl′am‚ēn]
(organic chemistry)
(C6H5)2NH Colorless leaflets, sparingly soluble in water; melting point 54°C; used as an additive in propellants to increase the storage life by neutralizing the acid products formed upon decomposition of the nitrocellulose. Also known as phenylaniline.

Diphenylamine 

an aromatic amine, C6H5NHC6H5; colorless crystals that darken upon exposure to light and have a slight characteristic odor. Melting point, 54°C; boiling point, 302°C. It is insoluble in water but soluble in most organic solvents. In industry, it is made by heating aniline, C6H5NH2, with aniline hydrochloride at 200°-230°C. It is used to make dyes and numerous organic intermediates (acridine, carbazole, and others), for stabilizing cellulose nitrate powders, and in colorimetric determination of some oxidizing agents (for example, nitric and nitrous acids).



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Most early propellant powders were stabilized with diphenylamine or ethyl centralite.
And on CA-stored Red Delicious and Granny Smith apples, 1-MCP treatments effectively prevented scald without diphenylamine.
There is (49 wt%) Estane, a eutectic mixture of bis(2,2-dinitropropyl) acetal and bis(2,2-dinitropropyl) formal [abbreviated BDNPA-F] (49 wt%), and a free radical inhibitor (either diphenylamine (DPA) or Irganox 1010) (2 wt%).
 
 
 
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