P-METHYLAMINOPHENOL

Details

Stereochemistry	ACHIRAL
Molecular Formula	C7H9NO
Molecular Weight	123.1525
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CNC1=CC=C(O)C=C1

InChI

InChIKey=ZFIQGRISGKSVAG-UHFFFAOYSA-N

InChI=1S/C7H9NO/c1-8-6-2-4-7(9)5-3-6/h2-5,8-9H,1H3

HIDE SMILES / InChI

Molecular Formula	C7H9NO
Molecular Weight	123.1525
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
Population-based in vitro hazard and concentration-response assessment of chemicals: the 1000 genomes high-throughput screening study.	2015-05	25622337
The intra- and inter-laboratory reproducibility and predictivity of the KeratinoSens assay to predict skin sensitizers in vitro: results of a ring-study in five laboratories.	2011-04	21195160
A new in vitro method for identifying chemical sensitizers combining peptide binding with ARE/EpRE-mediated gene expression in human skin cells.	2010-09	20491607
Formation of a quinoneimine intermediate of 4-fluoro-N-methylaniline by FMO1: carbon oxidation plus defluorination.	2010-05-17	20369854
Metabolite screening of aromatic amine hair dyes using in vitro hepatic models.	2009-11	19845432
Biodegradation of crystal violet by a Shewanella sp. NTOU1.	2008-08	18582917
Antioxidant and anticancer activities of novel p-alkylaminophenols and p-acylaminophenols (aminophenol analogues).	2006-09-01	16725328
Spectrophotometric determination of certain cephalosporins in pure form and in pharmaceutical formulations.	2004-10	15350919
Optimized and validated spectrophotometric methods for the determination of nicorandil in drug formulations and biological fluids.	2004-07	15231427
Enhancement of antioxidant activity of p-alkylaminophenols by alkyl chain elongation.	2003-07-31	12837535
Two simple methods for the estimation of albendazole and its dosage forms using chloramine-T.	2003-07	12818692
Biological activity of p-methylaminophenol, an essential structural component of N-(4-hydroxyphenyl)retinamide, fenretinide.	2002-11	12417027
H2O2/TiO2 photocatalytic oxidation of metol. Identification of intermediates and reaction pathways.	2002-08	12230204
Spectrophotometric method for the determination of nifedipine with 4-(methylamino)phenol and potassium dichromate.	2002-06	12088057
Contact anaphylaxis due to para-aminophenol and para-methylaminophenol in hair dye.	2001-12	11846755
Catalytic spectrophotometric determination of vanadium in seawaters based on the bromate oxidative coupling reaction of metol and 2,3,4-trihydroxybenzoic acid.	2001-06	11707949
Is benzoquinone the prohapten in cross-sensitivity among aminobenzene compounds?	1998-12	9874021

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:11:34 GMT 2025` Edited by `admin` on `Mon Mar 31 19:11:34 GMT 2025`
Record UNII	11W1883EFB
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

N-METHYL-4-AMINOPHENOL

Preferred Name

English

P-METHYLAMINOPHENOL

Official Name

English

N-METHYL-P-AMINOPHENOL

Common Name

English

N-METHYL-P-HYDROXYANILINE

Common Name

English

PHENOL, P-(METHYLAMINO)-

Common Name

English

4-(METHYLAMINO)PHENOL

Systematic Name

English

N-METHYL-4-HYDROXYANILINE

Systematic Name

English

P-(METHYLAMINO)PHENOL

Common Name

English

N-METHYL-4-AMINOPHENOL [HSDB]

Common Name

English

4-HYDROXY-N-METHYLANILINE

Systematic Name

English

NSC-7311

Code

English

PARAMETHYLAMINOPHENOL

Systematic Name

English

P-HYDROXY-N-METHYLANILINE

Common Name

English

PHENOL, 4-(METHYLAMINO)-

Systematic Name

English

Code System Code Type Description

CAS

150-75-4