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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
Divergent chemical cues elicit seed collecting by ants in an obligate multi-species mutualism in lowland Amazonia.
2010-12-30
Studies on the chemical constituents of Anabasis aphylla L.
2010-12
Investigating the coenzyme specificity of phenylacetone monooxygenase from Thermobifida fusca.
2010-11
Photophysics and photodeprotection reactions of p-methoxyphenacyl phototriggers: an ultrafast and nanosecond time-resolved spectroscopic and density functional theory study.
2010-09-03
(E)-1-[4-(Prop-2-yn-1-yl-oxy)phen-yl]-3-(3,4,5-trimeth-oxy-phen-yl)prop-2-en-1-one.
2010-08-11
Chemical constituents of Saxifraga stolonifera (L.) Meeb.
2010-06
Select acetophenones modulate flagellar motility in chlamydomonas.
2010-03
Mast cell-dependent allergic responses are inhibited by ethanolic extract of adlay (Coix lachryma-jobi L. var. ma-yuen Stapf) testa.
2010-02-24
Structure-toxicity relationship of phenolic analogs as anti-melanoma agents: an enzyme directed prodrug approach.
2010-02-12
General reaction conditions for the palladium-catalyzed vinylation of aryl chlorides with potassium alkenyltrifluoroborates.
2009-11-06
[Phenolic compounds from Galium aparine var. tenerum].
2009-07
(E)-3-[4-(Hex-yloxy)phen-yl]-1-(4-hydroxy-phen-yl)prop-2-en-1-one.
2009-05-29
Analysis of proteins with the 'hot dog' fold: prediction of function and identification of catalytic residues of hypothetical proteins.
2009-05-28
(E)-3-[4-(Dec-yloxy)phen-yl]-1-(4-hydroxy-phen-yl)prop-2-en-1-one.
2009-04-22
Controlling accumulation of fermentation inhibitors in biorefinery recycle water using microbial fuel cells.
2009-04-01
Palladium-catalyzed cross-coupling reactions of potassium alkenyltrifluoroborates with organic halides in aqueous media.
2009-03-20
(E)-N'-[1-(4-Hydroxy-phen-yl)ethyl-idene]-2-(quinolin-8-yl-oxy)acetohydrazide methanol solvate.
2009-02-28
[Determination of four acetophenones in Radix Cynanchi bungei by high performance liquid chromatography-photodiode array detection].
2009-01
Free radical scavengers and antioxidants from Tagetes mendocina.
2008-11-13
[Studies on chemical constituents of aerial parts of Ammopiptanthus mongolicus].
2008-10
Simultaneous determination of 13 bioactive compounds in Herba Artemisiae Scopariae (Yin Chen) from different harvest seasons by HPLC-DAD.
2008-08-05
Cytotoxic constituents from the bark of Salix hulteni.
2008-08
Anaerobic degradation of p-ethylphenol by "Aromatoleum aromaticum" strain EbN1: pathway, regulation, and involved proteins.
2008-08
[Studies on chemical constituents of Saussurea laniceps].
2008-05
Fluorinated photoremovable protecting groups: the influence of fluoro substituents on the photo-Favorskii rearrangement.
2008-05
Ultrasonic cavitation applied to the treatment of bisphenol A. Effect of sonochemical parameters and analysis of BPA by-products.
2008-04
The photo-Favorskii reaction of p-hydroxyphenacyl compounds is initiated by water-assisted, adiabatic extrusion of a triplet biradical.
2008-03-19
(4-Formyl-2-methoxy-phenolato)tris-(2-methyl-2-phenyl-prop-yl)tin(IV).
2008-02-06
Efficient microbial degradation of bisphenol A in the presence of activated carbon.
2008-02
Structures of dimeric dihydrodiol dehydrogenase apoenzyme and inhibitor complex: probing the subunit interface with site-directed mutagenesis.
2008-01-01
Synthesis of 1-Aryl-3-phenethylamino-1-propanone hydrochlorides as possible potent cytotoxic agents.
2007-12-12
Interference by Mes [2-(4-morpholino)ethanesulfonic acid] and related buffers with phenolic oxidation by peroxidase.
2007-11-01
A theoretical investigation of P-hydroxyphenacyl caged phototrigger compounds: how water induces the photodeprotection and subsequent rearrangement reactions.
2007-10-11
Exudation of allelopathic substances in buckwheat (Fagopyrum esculentum Moench).
2007-08-08
Anaerobic co-metabolic oxidation of 4-alkylphenols with medium-length or long alkyl chains by Thauera sp., strain R5.
2007-07
Optimization of phenolic compounds analysis by capillary electrophoresis.
2007-06-15
Chemical constituents of cape aloe and their synergistic growth-inhibiting effect on Ehrlich ascites tumor cells.
2007-05
Simultaneous determination of p-hydroxyacetophenone, chlorogenic acid, and caffeic acid in Herba Artemisiae Scopariae by capillary electrophoresis with electrochemical detection.
2007-05
Degradation of bisphenol A by Bacillus pumilus isolated from kimchi, a traditionally fermented food.
2007-01
Biodegradation of bisphenol A and related compounds by Sphingomonas sp. strain BP-7 isolated from seawater.
2007-01
Resolution of chiral phosphate, phosphonate, and phosphinate esters by an enantioselective enzyme library.
2006-12-13
A theoretical investigation of p-hydroxyphenacyl caged phototrigger compounds: an examination of the excited state photochemistry of p-hydroxyphenacyl acetate.
2006-11-16
4-Hydroxyacetophenone-induced choleresis in rats is mediated by the Mrp2-dependent biliary secretion of its glucuronide conjugate.
2006-11
Separation and determination of trace amounts of zinc, lead, cadmium and mercury in tap and Qaroun lake water using polyurethane foam functionalized with 4-hydroxytoluene and 4-hydroxyacetophenone.
2006-10-10
Differential effects of hydroxyacetophenone analogues on the transcytotic vesicular pathway in rat liver.
2006-10-10
Inhibition of respiratory burst in human neutrophils and lipoxygenase enzyme by compounds from Haloxylon griffithii.
2006-10
Ethnopharmacological evaluation of radal (leaves of Lomatia hirsuta) and isolation of 2-methoxyjuglone.
2006-08-31
Chemical composition of propolis from Canada, its antiradical activity and plant origin.
2006-05-20
New multi-1,2,3-selenadiazole aromatic derivatives.
2005-09-30
Novel pathway for bacterial metabolism of bisphenol A. Rearrangements and stilbene cleavage in bisphenol A metabolism.
1994-03-11
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