- Diphenylamine is a secondary aromatic amine that is derived from aniline1. It is used as an industrial antioxidant, dye mordant and reagent21. It is also used in agriculture as a fungicide and antihelmintic2. Diphenylamine can be used to make Dische's diphenylamine reagent, which is a colorimetric method for measuring DNA concentration31. The reagent turns blue when heated with DNA, and the intensity of the color indicates the amount of DNA3.Learn more:✕This summary was generated using AI based on multiple online sources. To view the original source information, use the "Learn more" links.Diphenylamine, a secondary aromatic amine, is an N -substituted derivative of aniline. Application Diphenylamine may be used in the preparation of diphenylamine reagent, which is employed for the quantitative estimation of nucleic acid (DNA) from various biological sources by colorimetric method.www.sigmaaldrich.com/US/en/product/SIAL/112763Diphenylamine is widely used as an industrial antioxidant, dye mordant and reagent and is also employed in agriculture as a fungicide and antihelmintic.en.wikipedia.org/wiki/DiphenylamineDische's diphenylamine reagent consists of diphenylamine, glacial acetic acid, sulfuric acid, and ethanol. When heated with DNA, it turns blue in the presence of DNA. A more intense blue color indicates a greater concentration of DNA. Mechanism The acid converts deoxyribose to a molecule that binds with diphenylamine to form a blue substance.en.wikipedia.org/wiki/Dische_test
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Diphenylamine - Wikipedia
Diphenylamine is manufactured by the thermal deamination of aniline over oxide catalysts: 2 C6H5NH2 → (C6H5)2NH + NH3 It is a weak base, with a Kb of 10 . With strong acids, it forms salts. For example, treatment with sulfuric acid gives the bisulfate [(C6H5)2NH2] [HSO4] as a white or yellowish powder … See more
Diphenylamine was discovered by A. W. Hofmann in 1864 amongst the products of dry distillation of aniline dyes; it was first purposefully synthesized through deamination of a mix … See more
Diphenylamine is considered practically insoluble according to the 2014 MSDS. It exhibits very low persistence in direct water See more
Europe
The EC set maximum residue levels for diphenylamine in 2005. (Annex II and Part B of Annex III to Regulation (EC) No 396/2005). … See moreTesting for DNA
The Dische test uses diphenylamine to test for DNA, and can be used to distinguish DNA from … See moreIn animal experiments diphenylamine was rapidly and completely absorbed after ingestion by mouth. It underwent metabolism to sulfonyl and glucuronyl conjugates and was rapidly excreted mainly via urine. Acute oral and dermal toxicity were low. … See more
• International Chemical Safety Card 0466
• NIOSH Pocket Guide to Chemical Hazards. "#0240". National Institute for Occupational Safety and Health (NIOSH). See moreWikipedia text under CC-BY-SA license Diphenylamine ACS reagent, = 99 122-39-4 - MilliporeSigma
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Diphenylamine | C6H5NHC6H5 | CID 11487 - PubChem
Diphenylamine is an aromatic amine containing two phenyl substituents. It has been used as a fungicide for the treatment of superficial scald in apples and pears, but is no longer approved for this purpose within the European Union.
Diphenylamine ReagentPlus , 99 122-39-4 - MilliporeSigma
Qualitative Nitrate Detection for Toxicity Potential
Diphenylamine CAS 122-39-4 | 820528 - Merck
Diphenylamine, BAKER ANALYZED® ACS, J.T.Baker® - VWR
Diphenylamine puriss. p.a., redox indicator, ACS reagent, reag. Ph.
Diphenylamine, ACS Grade, LabChem™ - Fisher Sci
Diphenylamine, ACS reagent, Thermo Scientific Chemicals
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