Description
Application
Diphenylamine can undergo palladium-catalyzed intramolecular cyclization to form carbazole. It may also be used as a starting material in the synthesis of triphenylamine.
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.
Specifications

General

Web Name Suffix OverrideACS reagent grade, ≥99%
NACRESNA.21
PubChem Substance ID24854569
UNSPSC Code12352100
EC Number204-539-4
MDL numberMFCD00003014
Beilstein/REAXYS Number508755
InChI keyDMBHHRLKUKUOEG-UHFFFAOYSA-N
InChI1S/C12H11N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10,13H
SMILES stringN(c1ccccc1)c2ccccc2
gradeACS reagent
vapor density5.82 (vs air)
vapor pressure1 mmHg ( 108 °C)
assay≥99%
autoignition temp.1175 °F
ign. residue≤0.03%
bp302 °C (lit.)
mp50-53 °C (lit.)
solubilityalcohol: passes test
anion tracesnitrate (NO3-): passes test
suitabilitypasses test for sensitivity to nitrate
Quality Level200
Gene Informationhuman ... UGT1A4(54657)
Merck 242586-100G Diphenylamine | IRIGHT