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Details

Stereochemistry ACHIRAL
Molecular Formula C16H13N
Molecular Weight 219.2811
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-PHENYL-2-NAPHTHYLAMINE

SMILES

N(C1=CC=CC=C1)C2=CC=C3C=CC=CC3=C2

InChI

InChIKey=KEQFTVQCIQJIQW-UHFFFAOYSA-N
InChI=1S/C16H13N/c1-2-8-15(9-3-1)17-16-11-10-13-6-4-5-7-14(13)12-16/h1-12,17H

HIDE SMILES / InChI

Molecular Formula C16H13N
Molecular Weight 219.2811
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Effects of copper sulfate, hydrogen peroxide and N-phenyl-2-naphthylamine on oxidative stress and the expression of genes involved photosynthesis and microcystin disposition in Microcystis aeruginosa.
2010-09-01
Effect-directed analysis of sediment-associated algal toxicants at selected hot spots in the river Elbe basin with a special focus on bioaccessibility.
2009-07
Allelochemical stress causes oxidative damage and inhibition of photosynthesis in Chlorella vulgaris.
2009-04
Bladder cancer risks in workers manufacturing chemicals for the rubber industry.
2008-10
Percutaneous absorption of aromatic amines - a contribution for human health risk assessment.
2008-06
[Status of trace organic pollution in the network water came from Huangpu River].
2008-03
Julichrome Q6 glucuronide, a monomeric subunit of the julimycin B-I complex from a terrestrial Streptomyces sp.
2007-10
Flow cytometry as a tool to study phytotoxic modes of action.
2007-02
Dephenylation of the rubber chemical N-phenyl-2-naphthylamine to carcinogenic 2-naphthylamine: a classical problem revisited.
2007
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
On the mode of action of N-phenyl-2-naphthylamine in plants.
2006-10-01
Antifungal and new metabolites of Myrothecium sp. Z16, a fungus associated with white croaker Argyrosomus argentatus.
2006
A novel alkaloid from Mitrephora maingayi.
2005-06
Spectrofluorimetric determination of phenyl-beta-naphthylamine used as rubber antioxidant.
2005-04
[Chemical constituents from marine alga Chaetomorpha basiretorsa].
2005-03
What contributes to the combined effect of a complex mixture?
2004-12-01
Effects of solvent on the fluorescence of 2-anilinonaphthalene.
2004-07
Derivative spectrophotometry in the determination of phenyl-beta-naphthylamine used as an antioxidant in rubber mixtures.
2002-09
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:36:38 GMT 2025
Edited
by admin
on Mon Mar 31 20:36:38 GMT 2025
Record UNII
456KT854AJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-PHENYL-2-NAPHTHYLAMINE
Systematic Name English
AGERITE POWDER
Preferred Name English
N-PHENYLNAPHTHALEN-2-AMINE
Systematic Name English
2-(N-PHENYLAMINO)NAPHTHALENE
Systematic Name English
2-NAPHTHYLPHENYLAMINE
Systematic Name English
ANTIOXIDANT 116
Brand Name English
2-NAPHTHALENAMINE, N-PHENYL-
Systematic Name English
PHENYL-(BETA)-NAPHTHYLAMINE
Common Name English
NEOZONE D
Brand Name English
N-PHENYL-.BETA.-NAPHTHYLAMINE
Systematic Name English
2-NAPHTHYLAMINE, N-PHENYL- [HSDB]
Common Name English
NSC-37151
Code English
2-ANILINONAPHTHALENE
Systematic Name English
N-PHENYL-2-NAPHTHYLAMINE [IARC]
Common Name English
Classification Tree Code System Code
CFR 21 CFR 176.170
Created by admin on Mon Mar 31 20:36:38 GMT 2025 , Edited by admin on Mon Mar 31 20:36:38 GMT 2025
Code System Code Type Description
MESH
C011948
Created by admin on Mon Mar 31 20:36:38 GMT 2025 , Edited by admin on Mon Mar 31 20:36:38 GMT 2025
PRIMARY
NSC
37151
Created by admin on Mon Mar 31 20:36:38 GMT 2025 , Edited by admin on Mon Mar 31 20:36:38 GMT 2025
PRIMARY
PUBCHEM
8679
Created by admin on Mon Mar 31 20:36:38 GMT 2025 , Edited by admin on Mon Mar 31 20:36:38 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-223-9
Created by admin on Mon Mar 31 20:36:38 GMT 2025 , Edited by admin on Mon Mar 31 20:36:38 GMT 2025
PRIMARY
EPA CompTox
DTXSID4021131
Created by admin on Mon Mar 31 20:36:38 GMT 2025 , Edited by admin on Mon Mar 31 20:36:38 GMT 2025
PRIMARY
CAS
135-88-6
Created by admin on Mon Mar 31 20:36:38 GMT 2025 , Edited by admin on Mon Mar 31 20:36:38 GMT 2025
PRIMARY
HSDB
2888
Created by admin on Mon Mar 31 20:36:38 GMT 2025 , Edited by admin on Mon Mar 31 20:36:38 GMT 2025
PRIMARY
FDA UNII
456KT854AJ
Created by admin on Mon Mar 31 20:36:38 GMT 2025 , Edited by admin on Mon Mar 31 20:36:38 GMT 2025
PRIMARY