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Details

Stereochemistry ACHIRAL
Molecular Formula C12H12N2
Molecular Weight 184.2371
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-PHENYL-P-PHENYLENEDIAMINE

SMILES

NC1=CC=C(NC2=CC=CC=C2)C=C1

InChI

InChIKey=ATGUVEKSASEFFO-UHFFFAOYSA-N
InChI=1S/C12H12N2/c13-10-6-8-12(9-7-10)14-11-4-2-1-3-5-11/h1-9,14H,13H2

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
p-Anilinoaniline enhancement of dioxin-induced CYP1A1 transcription and aryl hydrocarbon receptor occupancy of CYP1A1 promoter: role of the cell cycle.
2012-05
EPR and ENDOR spectroscopic study of the reactions of aromatic azides with gallium trichloride.
2010-11-21
Role of Mitochondrial Enzymes and Sarcoplasmic ATPase in Cardioprotection Mediated by Aqueous Extract of Desmodium gangeticum (L) DC Root on Ischemic Reperfusion Injury.
2010-11
High-affinity, non-nucleotide-derived competitive antagonists of platelet P2Y12 receptors.
2009-06-25
Skin sensitization potency and cross-reactivity of p-phenylenediamine and its derivatives evaluated by non-radioactive murine local lymph node assay and guinea-pig maximization test.
2009-04
Chemical oxidative polymerization of aminodiphenylamines.
2008-06-12
A unified description of current-voltage characteristics in organic and hybrid photovoltaics under low light intensity.
2008-05
Pi-dimer of an aniline dimer: an ESR-UV-vis spectroelectrochemical study.
2007-11-01
Detection of aniline at boron-doped diamond electrodes with cathodic stripping voltammetry.
2007-09-15
Observation of ion-transfer of photochemical reaction products of p-aminodiphenylamine across an aqueous | 1,2-dichloroethane solution interface by photo-modulation voltammetry with an ultraviolet laser.
2007-09
[The expanding role of occupational and non-occupational allergy to paraphenylenediamine].
2007
Excited state solvatochromic and prototropic behaviour of 4-aminodiphenylamine and 4,4'-diaminodiphenylamine--a comparative study by electronic spectra.
2006-06
A mild, copper catalyzed route to conducting polyaniline.
2006-03-07
In situ electrochemical ESR and voltammetric studies on the anodic oxidation of para-haloanilines in acetonitrile.
2005-06-30
Contact dermatitis in hairdressers, 10 years later: patch-test results in 300 hairdressers (1994 to 2003) and comparison with previous study.
2005-03
Structural modelling of optical and electrochemical properties of 4-aminodiphenylamines - optoelectronic studies on a polyaniline repeating unit.
2004-10
Dual fluorescent polyaniline model compounds: steric and temperature effects on excited state charge separation.
2002-07
Adsorption and kinetic studies of the intercalation of some organic compounds onto Na+-montmorillonite.
2002-01-01
Redox buffering in an electrospray ion source using a copper capillary emitter.
2001-10
Is benzoquinone the prohapten in cross-sensitivity among aminobenzene compounds?
1998-12
Patents
Name Type Language
N-PHENYL-P-PHENYLENEDIAMINE
INCI  
INCI  
Official Name English
P-AMINODIPHENYLAMINE
HSDB  
Preferred Name English
P-AMINODIPHENYLAMINE [HSDB]
Common Name English
CI-76085
Code English
N-PHENYL-P-AMINOANILINE
Common Name English
1,4-BENZENEDIAMINE, N1-PHENYL-
Systematic Name English
N,4'-BIANILINE
Systematic Name English
NSC-3401
Code English
CI 76085
Code English
RODOL GRAY B BASE
Brand Name English
N-PHENYL-1,4-BENZENEDIAMINE
Systematic Name English
Code System Code Type Description
SMS_ID
100000125957
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
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FDA UNII
007X4XXS71
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
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ECHA (EC/EINECS)
202-951-9
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
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CAS
101-54-2
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
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CHEBI
59038
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
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NSC
3401
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
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EVMPD
SUB33040
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
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WIKIPEDIA
4-Aminodiphenylamine
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
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PUBCHEM
7564
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
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EPA CompTox
DTXSID7025895
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
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HSDB
2178
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
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