N-Cyclohexyl-N'-phenyl-p-phenylenediamine | C18H22N2
N-Cyclohexyl-N'-phenyl-p-phenylenediamine | C18H22N2 | CID 92093 - structure, chemical names, physical and chemical properties, classification, patents, literature
Substance Name: N-Cyclohexyl-N'-phenyl-1,4-phenylenediamine
101-87-1 - ZRMMVODKVLXCBB-UHFFFAOYSA-N - N-Cyclohexyl-N'-phenyl-1,4-phenylenediamine - Similar structures search, synonyms, formulas, resource links, and other chemical information. Skip Navigation U.S. National Library of Medicine
MSDS p-Phenylenediamine, N-phenyl-N'-cyclohexyl- CAS 101-87-1 MSDS * N
cas registry number : 101-87-1 beilstein reference no. : 1978859 reference : 4-13-00-00116 (beilstein handbook reference) last updated : 199710 data items cited : 7 molecular formula : c18-h22-n2 molecular weight : 266.42 wiswesser line notation : l6tj amr dmr compound descriptor : primary irritant
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The N-Phenyl-N'-cyclohexyl-p-phenylenediamine with CAS registry number of 101-87-1 is also known as N-Cyclohexyl-N'-phenyl-p-phenylenediamine. The IUPAC name is 1-N-Cyclohexyl-4-N-phenylbenzene-1,4-diamine. It belongs to product categories of Industrial/Fine Chemicals. Its EINECS registry number is 202-984-9.
N,N'-DIPHENYL-P-PHENYLENEDIAMINE (ANTIOXIDANT DPPD)
N,N'-Diphenyl-p-phenylenediamine is used as an antioxidant and/or stabilizer for rubber, petroleum oils and feedstuffs. It is also used as a polymerization inhibitor and a retardant against copper degradation.It is a chemical intermediate to make dyes, drugs, plastics and detergent additives.
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Butylated hydroxytoluene (BHT) is a common example of hindered phenolic antioxidant. The reaction order in SN1 mechanism is 3° > 2° > 1° > CH 3 (no S N 1) so, tertiary butyl groups are substituted in phenolic antioxidant compounds. Primary antioxidants are free radical scavengers which combine with peroxy radicals and break autocatalytic cycle.