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Details

Stereochemistry ACHIRAL
Molecular Formula C8H8O2
Molecular Weight 136.1479
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HYDROXYACETOPHENONE

SMILES

CC(=O)C1=CC=C(O)C=C1

InChI

InChIKey=TXFPEBPIARQUIG-UHFFFAOYSA-N
InChI=1S/C8H8O2/c1-6(9)7-2-4-8(10)5-3-7/h2-5,10H,1H3

HIDE SMILES / InChI

Molecular Formula C8H8O2
Molecular Weight 136.1479
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Novel pathway for bacterial metabolism of bisphenol A. Rearrangements and stilbene cleavage in bisphenol A metabolism.
1994 Mar 11
[Constituents of Liguliria vellerea (Franch.) Hand-Mazz].
2001 Dec
4-Hydroxyacetophenone monooxygenase from Pseudomonas fluorescens ACB. A novel flavoprotein catalyzing Baeyer-Villiger oxidation of aromatic compounds.
2001 May
Xenoestrogens in the River Elbe and its tributaries.
2003
Potential inhibitors from wet oxidation of wheat straw and their effect on ethanol production of Saccharomyces cerevisiae: wet oxidation and fermentation by yeast.
2003 Mar 20
Inhibiting activities of the secondary metabolites of Phlomis brunneogaleata against parasitic protozoa and plasmodial enoyl-ACP Reductase, a crucial enzyme in fatty acid biosynthesis.
2004 Aug
The Hotdog fold: wrapping up a superfamily of thioesterases and dehydratases.
2004 Aug 12
Extraction of p-hydroxyacetophenone and catechin from Norway spruce needles. Comparison of different extraction solvents.
2005 Jun
Theoretical study of the o-OH participation in catechol ester ammonolysis.
2005 Mar 7
Chemical composition of propolis from Canada, its antiradical activity and plant origin.
2005 Oct
Time-resolved resonance Raman and density functional theory study of the deprotonation reaction of the triplet state of p-hydroxyacetophenone in water solution.
2005 Oct 28
Enhancement of alcohol dehydrogenase activity in vitro by acetylsalicylic acid.
2005 Oct 31
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006 Nov
A theoretical investigation of P-hydroxyphenacyl caged phototrigger compounds: how water induces the photodeprotection and subsequent rearrangement reactions.
2007 Oct 11
Controlling accumulation of fermentation inhibitors in biorefinery recycle water using microbial fuel cells.
2009 Apr 1
Divergent chemical cues elicit seed collecting by ants in an obligate multi-species mutualism in lowland Amazonia.
2010 Dec 30
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:52:37 GMT 2025
Edited
by admin
on Mon Mar 31 17:52:37 GMT 2025
Record UNII
G1L3HT4CMH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HYDROXYACETOPHENONE
INCI  
Official Name English
4-HYDROXYACETOPHENONE
FHFI  
Preferred Name English
4-HYDROXYACETOPHENONE [FHFI]
Common Name English
P-HYDROXYACETOPHENONE
Common Name English
P-HYDROXYPHENYL METHYL KETONE
Common Name English
NSC-3698
Code English
4'-HYDROXY ACETOPHENONE
Systematic Name English
ETHANONE, 1-(4-HYDROXYPHENYL)-
Systematic Name English
FEMA NO. 4330
Code English
PARACETAMOL IMPURITY E [EP IMPURITY]
Common Name English
4-HYDROXY ACETOPHENONE
Common Name English
4'-HYDROXYACETOPHENONE
Systematic Name English
1-(4-HYDROXYPHENYL)ETHAN-1-ONE
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION 4-HYDROXYACETOPHENONE
Created by admin on Mon Mar 31 17:52:37 GMT 2025 , Edited by admin on Mon Mar 31 17:52:37 GMT 2025
Code System Code Type Description
ECHA (EC/EINECS)
202-802-8
Created by admin on Mon Mar 31 17:52:37 GMT 2025 , Edited by admin on Mon Mar 31 17:52:37 GMT 2025
PRIMARY
MESH
C031335
Created by admin on Mon Mar 31 17:52:37 GMT 2025 , Edited by admin on Mon Mar 31 17:52:37 GMT 2025
PRIMARY
EPA CompTox
DTXSID0029133
Created by admin on Mon Mar 31 17:52:37 GMT 2025 , Edited by admin on Mon Mar 31 17:52:37 GMT 2025
PRIMARY
PUBCHEM
7469
Created by admin on Mon Mar 31 17:52:37 GMT 2025 , Edited by admin on Mon Mar 31 17:52:37 GMT 2025
PRIMARY
DAILYMED
G1L3HT4CMH
Created by admin on Mon Mar 31 17:52:37 GMT 2025 , Edited by admin on Mon Mar 31 17:52:37 GMT 2025
PRIMARY
CAS
99-93-4
Created by admin on Mon Mar 31 17:52:37 GMT 2025 , Edited by admin on Mon Mar 31 17:52:37 GMT 2025
PRIMARY
FDA UNII
G1L3HT4CMH
Created by admin on Mon Mar 31 17:52:37 GMT 2025 , Edited by admin on Mon Mar 31 17:52:37 GMT 2025
PRIMARY
CHEBI
28032
Created by admin on Mon Mar 31 17:52:37 GMT 2025 , Edited by admin on Mon Mar 31 17:52:37 GMT 2025
PRIMARY
NSC
3698
Created by admin on Mon Mar 31 17:52:37 GMT 2025 , Edited by admin on Mon Mar 31 17:52:37 GMT 2025
PRIMARY
RXCUI
1541733
Created by admin on Mon Mar 31 17:52:37 GMT 2025 , Edited by admin on Mon Mar 31 17:52:37 GMT 2025
PRIMARY RxNorm
JECFA MONOGRAPH
2018
Created by admin on Mon Mar 31 17:52:37 GMT 2025 , Edited by admin on Mon Mar 31 17:52:37 GMT 2025
PRIMARY
WIKIPEDIA
Piceol
Created by admin on Mon Mar 31 17:52:37 GMT 2025 , Edited by admin on Mon Mar 31 17:52:37 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> METABOLITE
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP