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Details

Stereochemistry ACHIRAL
Molecular Formula C9H12O
Molecular Weight 136.191
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-ISOPROPYLPHENOL

SMILES

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

InChI

InChIKey=YQUQWHNMBPIWGK-UHFFFAOYSA-N
InChI=1S/C9H12O/c1-7(2)8-3-5-9(10)6-4-8/h3-7,10H,1-2H3

HIDE SMILES / InChI

Molecular Formula C9H12O
Molecular Weight 136.191
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Characterization of rabbit UDP-glucuronosyltransferase UGT1A7: tertiary amine glucuronidation is catalyzed by UGT1A7 and UGT1A4.
1997 Aug 15
A lipoxygenase inhibitor from Aspergillus niger.
2002 Mar
Photodegradation mechanism for bisphenol A at the TiO2/H2O interfaces.
2003 Aug
Aquatic toxicity of four alkylphenols (3-tert-butylphenol, 2-isopropylphenol, 3-isopropylphenol, and 4-isopropylphenol) and their binary mixtures to microbes, invertebrates, and fish.
2004 Feb
Photochemical transformations of tetrabromobisphenol A and related phenols in water.
2004 Jan
Characterization of new bisphenol a metabolites produced by CD1 mice liver microsomes and S9 fractions.
2004 Jul 28
Photodegradation of bisphenol-A with TiO2 immobilized on the glass tubes including the UV light lamps.
2004 Sep
Genotoxicity evaluation of electromagnetic fields generated by 835-MHz mobile phone frequency band.
2005 Apr
Cooperative h-bonds of macromolecules. 1. Binding of low-molecular-weight ligands to polymers.
2005 Jul 21
Biodegradation of phenolic environmental pollutants by a surfactant-laccase complex in organic media.
2005 Jun
Effect of metal chlorides on thermal degradation of (waste) polycarbonate.
2006
Aerobic and anaerobic biodegradation of phenol derivatives in various paddy soils.
2006 Aug 31
Dose-dependent influence of barbiturates but not of propofol on human leukocyte phagocytosis of viable Staphylococcus aureus.
2006 Feb
A novel sulfotransferase abundantly expressed in the dauer larvae of Caenorhabditis elegans.
2006 Mar
Anaerobic biodegradation of 4-alkylphenols in a paddy soil microcosm supplemented with nitrate.
2007 Aug
Anaerobic co-metabolic oxidation of 4-alkylphenols with medium-length or long alkyl chains by Thauera sp., strain R5.
2007 Jul
ipso-substitution: a general biochemical and biodegradation mechanism to cleave alpha-quaternary alkylphenols and bisphenol A.
2007 Sep
Direct evidence revealing structural elements essential for the high binding ability of bisphenol A to human estrogen-related receptor-gamma.
2008 Jan
The aqueous degradation of bisphenol A and steroid estrogens by ferrate.
2008 Jan
Isolation and characterization of a novel 2-sec-butylphenol-degrading bacterium Pseudomonas sp. strain MS-1.
2010 Apr
Modeling of ultrasonic degradation of non-volatile organic compounds by Langmuir-type kinetics.
2010 Jun
The mouse eugenol odorant receptor: structural and functional plasticity of a broadly tuned odorant binding pocket.
2011 Feb 8
Bioactivation of bisphenol A and its analogs (BPF, BPAF, BPZ and DMBPA) in human liver microsomes.
2013 Jun
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:25:27 UTC 2023
Edited
by admin
on Sat Dec 16 08:25:27 UTC 2023
Record UNII
9F59JOO816
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
P-ISOPROPYLPHENOL
Common Name English
ISOPROPYLPHENOL, P-
Common Name English
4-(1-METHYLETHYL)PHENOL
Systematic Name English
NSC-1888
Code English
PHENOL, 4-(1-METHYLETHYL)-
Systematic Name English
AUSTRALOL
Brand Name English
1-HYDROXY-4-ISOPROPYLBENZENE
Systematic Name English
P-CUMENOL
Common Name English
4-ISOPROPYLPHENOL
Systematic Name English
PRODOX 133
Brand Name English
4-(PROPAN-2-YL)PHENOL
Systematic Name English
PROPOFOL IMPURITY H [EP IMPURITY]
Common Name English
Code System Code Type Description
CHEBI
167172
Created by admin on Sat Dec 16 08:25:28 UTC 2023 , Edited by admin on Sat Dec 16 08:25:28 UTC 2023
PRIMARY
FDA UNII
9F59JOO816
Created by admin on Sat Dec 16 08:25:28 UTC 2023 , Edited by admin on Sat Dec 16 08:25:28 UTC 2023
PRIMARY
EPA CompTox
DTXSID5042299
Created by admin on Sat Dec 16 08:25:28 UTC 2023 , Edited by admin on Sat Dec 16 08:25:28 UTC 2023
PRIMARY
CAS
99-89-8
Created by admin on Sat Dec 16 08:25:28 UTC 2023 , Edited by admin on Sat Dec 16 08:25:28 UTC 2023
PRIMARY
NSC
1888
Created by admin on Sat Dec 16 08:25:28 UTC 2023 , Edited by admin on Sat Dec 16 08:25:28 UTC 2023
PRIMARY
ECHA (EC/EINECS)
202-798-8
Created by admin on Sat Dec 16 08:25:28 UTC 2023 , Edited by admin on Sat Dec 16 08:25:28 UTC 2023
PRIMARY
PUBCHEM
7465
Created by admin on Sat Dec 16 08:25:28 UTC 2023 , Edited by admin on Sat Dec 16 08:25:28 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
UNSPECIFIED
EP