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Details

Stereochemistry ACHIRAL
Molecular Formula C6H6N2O3
Molecular Weight 154.1234
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-AMINO-4-NITROPHENOL

SMILES

NC1=CC(=CC=C1O)[N+]([O-])=O

InChI

InChIKey=VLZVIIYRNMWPSN-UHFFFAOYSA-N
InChI=1S/C6H6N2O3/c7-5-3-4(8(10)11)1-2-6(5)9/h1-3,9H,7H2

HIDE SMILES / InChI

Molecular Formula C6H6N2O3
Molecular Weight 154.1234
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
2-Amino-4-nitro-phenol monohydrate.
2010-09-11
Final report on the safety assessment of amino nitrophenols as used in hair dyes.
2010-01-21
(E)-2-[(2-Hydr-oxy-5-nitro-phen-yl)iminiometh-yl]phenolate.
2009-02-11
(E)-2-[(2-Hydr-oxy-5-nitro-phen-yl)iminiometh-yl]-4-nitro-phenolate.
2009-01-14
Synthesis, IR, UV/vis-, (1)H NMR and DFT study of chelatophore functionalized 1,3-benzoxazinone spiropyrans.
2008-12-01
Vibrational spectroscopic studies and ab initio calculations of 5-nitro-2-(p-fluorophenyl)benzoxazole.
2008-11-15
LC-MS-MS analysis of 2,4-dinitrophenol and its phase I and II metabolites in a case of fatal poisoning.
2007-03-29
Interactions between nitrate assimilation and 2,4-dinitrophenol cometabolism in Rhodobacter capsulatus E1F1.
2006-07
Synthesis, anti-inflammatory and analgesic activities evaluation of some mono, bi and tricyclic pyrimidine derivatives.
2005-11-15
Peroxidase-catalyzed co-oxidation of 3,3',5,5'-tetramethylbenzidine in the presence of substituted phenols and their polydisulfides.
2004-01
[Determination of 2.4-dinitrophenol, its basic metabolite and 4-oxide diphenyl in biological materials].
2003-07-05
Continuous biotransformation and removal of nitrophenols under denitrifying conditions.
2003-07
[Extraction of 2-amino-4-nitrophenol and 4-phenylphenol from aqueous solutions].
2003-01-09
Separation and determination of nitrobenzenes by micellar electrokinetic chromatography and high-performance liquid chromatography.
2002-12-06
Vibrational analysis of substituted phenols: part II. Transferability of valence force constants.
2002-12
Effects of alternative carbon sources on biological transformation of nitrophenols.
2002
Biotransformation of nitrophenols in upflow anaerobic sludge blanket reactors.
2001-12
Peroxidase-catalyzed co-oxidation of 3,3',5,5'-tetramethylbenzidine with 2-amino-4-nitrophenol, 4,4'-dihydroxydiphenylsulfone, and their polydisulfides in aqueous and micellar media.
2001-06
Initiation and inhibition of free radical processes in H2O2-metmyoglobin (methemoglobin)-2,2'-azino-bis-(3-ethylbenzthiazoline-6-sulfonic acid) systems.
2001-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:44:51 GMT 2025
Edited
by admin
on Mon Mar 31 20:44:51 GMT 2025
Record UNII
G501UCI6T9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RODOL 42
Preferred Name English
2-AMINO-4-NITROPHENOL
HSDB   INCI  
INCI  
Official Name English
1-AMINO-2-HYDROXY-5-NITROBENZENE
Systematic Name English
PHENOL, 2-AMINO-4-NITRO-
Systematic Name English
2-HYDROXY-5-NITROANILINE
Systematic Name English
2-AMINO-4-NITROPHENOL [HSDB]
Common Name English
NSC-4664
Code English
5-NITRO-2-HYDROXYANILINE
Systematic Name English
4-NITRO-2-AMINO-1-HYDROXYBENZENE
Systematic Name English
2-AMINO-4-NITROPHENOL [IARC]
Common Name English
1-HYDROXY-2-AMINO-4-NITROBENZENE
Systematic Name English
C.I. 76530
Code English
P-NITRO-O-AMINOPHENOL
Common Name English
AMINO-4-NITROPHENOL, 2-
Systematic Name English
4-NITRO-2-AMINOPHENOL
Systematic Name English
Code System Code Type Description
HSDB
4165
Created by admin on Mon Mar 31 20:44:51 GMT 2025 , Edited by admin on Mon Mar 31 20:44:51 GMT 2025
PRIMARY
PUBCHEM
3613389
Created by admin on Mon Mar 31 20:44:51 GMT 2025 , Edited by admin on Mon Mar 31 20:44:51 GMT 2025
PRIMARY
EPA CompTox
DTXSID6020062
Created by admin on Mon Mar 31 20:44:51 GMT 2025 , Edited by admin on Mon Mar 31 20:44:51 GMT 2025
PRIMARY
NSC
4664
Created by admin on Mon Mar 31 20:44:51 GMT 2025 , Edited by admin on Mon Mar 31 20:44:51 GMT 2025
PRIMARY
FDA UNII
G501UCI6T9
Created by admin on Mon Mar 31 20:44:51 GMT 2025 , Edited by admin on Mon Mar 31 20:44:51 GMT 2025
PRIMARY
CAS
99-57-0
Created by admin on Mon Mar 31 20:44:51 GMT 2025 , Edited by admin on Mon Mar 31 20:44:51 GMT 2025
PRIMARY
MESH
C036645
Created by admin on Mon Mar 31 20:44:51 GMT 2025 , Edited by admin on Mon Mar 31 20:44:51 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-767-9
Created by admin on Mon Mar 31 20:44:51 GMT 2025 , Edited by admin on Mon Mar 31 20:44:51 GMT 2025
PRIMARY