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Details

Stereochemistry ACHIRAL
Molecular Formula C6H7NO
Molecular Weight 109.1259
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of M-AMINOPHENOL

SMILES

NC1=CC(O)=CC=C1

InChI

InChIKey=CWLKGDAVCFYWJK-UHFFFAOYSA-N
InChI=1S/C6H7NO/c7-5-2-1-3-6(8)4-5/h1-4,8H,7H2

HIDE SMILES / InChI

Molecular Formula C6H7NO
Molecular Weight 109.1259
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Spectrophotometric determination of folic acid in pharmaceutical preparations by coupling reactions with iminodibenzyl or 3-aminophenol or sodium molybdate-pyrocatechol.
2002 Aug 15
An ultrastuctural study of hair fiber damage and restoration following treatment with permanent hair dye.
2002 Feb
Growth phase dependent substrate utilization by Pseudomonas strain PH1.
2002 Nov-Dec
3-Aminophenol as a novel coupling agent for the spectrophotometric determination of sulfonamide derivatives.
2003 Dec
Higher susceptibility of newborn than young rats to 3-methylphenol.
2003 May
A general and high yielding fragment coupling synthesis of heteroatom-bridged calixarenes and the unprecedented examples of calixarene cavity fine-tuned by bridging heteroatoms.
2004 Dec 1
Quantitative determination of p-aminosalicylic acid and its degradation product m-aminophenol in pellets by ion-pair high-performance liquid chromatography applying the monolithic Chromolith Speedrod RP-18e column.
2004 Jan
Toxic effects of aminophenols on aquatic life using the zebrafish embryo test and the comet assay.
2004 Oct
Charge redistribution on electronic excitation. Dipole moments of cis- and trans-3-aminophenol in their S(0) and S(1) electronic states.
2004 Sep 15
'Green' methodology for efficient and selective benzoylation of nucleosides using benzoyl cyanide in an ionic liquid.
2005 Jul 15
Prediction of genotoxicity of chemical compounds by statistical learning methods.
2005 Jun
[Extraction of nitrobenzene and its metabolite 3-aminohydroxybenzene from water solutions].
2006 Jan-Feb
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006 Nov
ESR studies of poly(aniline-co-m-aminophenol) in the solid state and nonaqueous solution.
2007 Jun 28
Quinoxaline-3-amino-phenol-water (2/1/2).
2008 Apr 23
Development and in vitro Evaluation of Enteric Coated Multiparticulate System for Resistant Tuberculosis.
2008 Jul-Aug
Characterization of an AM404 analogue, N-(3-hydroxyphenyl)arachidonoylamide, as a substrate and inactivator of prostaglandin endoperoxide synthase.
2009 Dec 29
Surface chemistry, porous texture, and morphology of N-doped carbon xerogels.
2009 Jan 6
Metabolite screening of aromatic amine hair dyes using in vitro hepatic models.
2009 Nov
A new on-line solid phase extraction high performance liquid chromatography tandem mass spectrometry method to study the sun light photodegradation of mono-chloroanilines in river water.
2010 May 14
Prediction of the contact sensitizing potential of chemicals using analysis of gene expression changes in human THP-1 monocytes.
2010 Nov 10
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:50:42 GMT 2023
Edited
by admin
on Fri Dec 15 16:50:42 GMT 2023
Record UNII
L3WTS6QT82
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
M-AMINOPHENOL
INCI   MI   USP-RS  
INCI  
Official Name English
NSC-1546
Code English
C.I. 76545
Common Name English
3-AMINOPHENOL
HSDB  
Systematic Name English
M-AMINOPHENOL [INCI]
Common Name English
PHENOL, 3-AMINO-
Systematic Name English
M-AMINOPHENOL [USP-RS]
Common Name English
3-HYDROXYANILINE
Systematic Name English
RODOL EG
Brand Name English
M-AMINOPHENOL [MI]
Common Name English
ORISTAR APH3
Brand Name English
3-AMINOPHENOL [HSDB]
Common Name English
COVASTYLE MAP
Brand Name English
M-HYDROXYAMINOBENZENE
Systematic Name English
COLOREX MAP
Brand Name English
JAROCOL MAP
Brand Name English
MESALAZINE IMPURITY B [EP IMPURITY]
Common Name English
CI 76545
Common Name English
Code System Code Type Description
NSC
1546
Created by admin on Fri Dec 15 16:50:42 GMT 2023 , Edited by admin on Fri Dec 15 16:50:42 GMT 2023
PRIMARY
RXCUI
1435285
Created by admin on Fri Dec 15 16:50:42 GMT 2023 , Edited by admin on Fri Dec 15 16:50:42 GMT 2023
PRIMARY RxNorm
ECHA (EC/EINECS)
209-711-2
Created by admin on Fri Dec 15 16:50:42 GMT 2023 , Edited by admin on Fri Dec 15 16:50:42 GMT 2023
PRIMARY
MESH
C055528
Created by admin on Fri Dec 15 16:50:42 GMT 2023 , Edited by admin on Fri Dec 15 16:50:42 GMT 2023
PRIMARY
EPA CompTox
DTXSID3024497
Created by admin on Fri Dec 15 16:50:42 GMT 2023 , Edited by admin on Fri Dec 15 16:50:42 GMT 2023
PRIMARY
PUBCHEM
11568
Created by admin on Fri Dec 15 16:50:42 GMT 2023 , Edited by admin on Fri Dec 15 16:50:42 GMT 2023
PRIMARY
SMS_ID
100000159522
Created by admin on Fri Dec 15 16:50:42 GMT 2023 , Edited by admin on Fri Dec 15 16:50:42 GMT 2023
PRIMARY
CHEBI
28924
Created by admin on Fri Dec 15 16:50:42 GMT 2023 , Edited by admin on Fri Dec 15 16:50:42 GMT 2023
PRIMARY
CAS
591-27-5
Created by admin on Fri Dec 15 16:50:42 GMT 2023 , Edited by admin on Fri Dec 15 16:50:42 GMT 2023
PRIMARY
MERCK INDEX
m1726
Created by admin on Fri Dec 15 16:50:42 GMT 2023 , Edited by admin on Fri Dec 15 16:50:42 GMT 2023
PRIMARY Merck Index
FDA UNII
L3WTS6QT82
Created by admin on Fri Dec 15 16:50:42 GMT 2023 , Edited by admin on Fri Dec 15 16:50:42 GMT 2023
PRIMARY
RS_ITEM_NUM
1026004
Created by admin on Fri Dec 15 16:50:42 GMT 2023 , Edited by admin on Fri Dec 15 16:50:42 GMT 2023
PRIMARY
DAILYMED
L3WTS6QT82
Created by admin on Fri Dec 15 16:50:42 GMT 2023 , Edited by admin on Fri Dec 15 16:50:42 GMT 2023
PRIMARY
HSDB
2586
Created by admin on Fri Dec 15 16:50:42 GMT 2023 , Edited by admin on Fri Dec 15 16:50:42 GMT 2023
PRIMARY
EVMPD
SUB169708
Created by admin on Fri Dec 15 16:50:42 GMT 2023 , Edited by admin on Fri Dec 15 16:50:42 GMT 2023
PRIMARY
WIKIPEDIA
3-AMINOPHENOL
Created by admin on Fri Dec 15 16:50:42 GMT 2023 , Edited by admin on Fri Dec 15 16:50:42 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP