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Details

Stereochemistry ACHIRAL
Molecular Formula C12H9O.Na
Molecular Weight 192.189
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-PHENYLPHENOL SODIUM

SMILES

[Na+].[O-]C1=CC=C(C=C1)C2=CC=CC=C2

InChI

InChIKey=PJOIPAGEBPZNSD-UHFFFAOYSA-M
InChI=1S/C12H10O.Na/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10;/h1-9,13H;/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula C12H9O
Molecular Weight 169.1993
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula Na
Molecular Weight 22.98976928
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Preparation and properties of the specific anti-influenza virus transfer factor.
2010-09-13
Placental transfer of conjugated bisphenol A and subsequent reactivation in the rat fetus.
2010-09
3-Ethyl-sulfanyl-2,5-diphenyl-1-benzofuran.
2010-07-21
Variable products in dielectric-barrier discharge assisted benzene oxidation.
2010-06-15
Occurrence and sources of selected phenolic endocrine disruptors in Ria de Aveiro, Portugal.
2010-05
Biphenyl-4-yl 2,2,2-trichloro-ethyl sulfate.
2010-04-14
Inhibition of three algae species using chemicals released from barley straw.
2010-04-01
2-(4-Chloro-phen-yl)-3-methyl-sulfanyl-5-phenyl-1-benzofuran.
2010-03-13
In vitro profiling of endocrine disrupting effects of phenols.
2010-02
3-Ethyl-sulfanyl-2-(4-fluoro-phen-yl)-5-phenyl-1-benzofuran.
2010-01-13
The evaluation of benzene and phenol biodegradation kinetics by applying non-structured models.
2010
2-(4-Fluoro-phen-yl)-3-methyl-sulfanyl-5-phenyl-1-benzofuran.
2009-10-17
Evaluation of skin diseases and disorders in photographers.
2009-08
4-(4-Nitro-phenoxy)biphen-yl.
2009-03-06
Mass flows of endocrine disruptors in the Glatt River during varying weather conditions.
2009-03
Bisphenol A at low nanomolar doses confers chemoresistance in estrogen receptor-alpha-positive and -negative breast cancer cells.
2009-02
Photodecomposition profiles of beta-bond cleavage of phenylphenacyl derivatives in the higher triplet excited states during stepwise two-color two-laser flash photolysis.
2008-11-13
Modeling pi-pi interactions with the effective fragment potential method: the benzene dimer and substituents.
2008-06-12
Stepwise two-color laser photolysis studies of alpha-cleavage in highly excited triplet states of alpha-acyl-4-phenylphenols.
2008-06
[GC-FTIR analysis of structural isomers from hydrogenation products of p-phenylphenol].
2008-04
4-Alkylphenols and related chemicals show similar effect on the function of human and rat estrogen receptor alpha in reporter gene assay.
2008-03
Changes of multiple biotransformation phase I and phase II enzyme activities in human fetal adrenals during fetal development.
2008-02
Endocrine-disrupting potential of bisphenol A, bisphenol A dimethacrylate, 4-n-nonylphenol, and 4-n-octylphenol in vitro: new data and a brief review.
2007-12
Unique bisphenol A transcriptome in prostate cancer: novel effects on ERbeta expression that correspond to androgen receptor mutation status.
2007-11
Self-assembled monolayers: influence of complementarity between chemisorbed and crystallizing molecules in polymorph selection.
2007-09-01
Crystal structure of a cyclomaltoheptaose-4-hydroxybiphenyl inclusion complex.
2007-08-13
Qualitative analysis of phenols and alcohols in complex samples after derivatization to esters of ferrocene carboxylic acid by gas chromatography with mass spectrometric detection.
2007-07-20
Structure control for fine tuning fluorescence emission from side-chain azobenzene polymers.
2007-06-14
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Detection of androgenic activity in emissions from diesel fuel and biomass combustion.
2006-08
Oxidative ring cleavage of low chlorinated biphenyl derivatives by fungi leads to the formation of chlorinated lactone derivatives.
2006-07
Cleaning validation 1: development and validation of a chromatographic method for the detection of traces of LpHse detergent.
2006-05-03
Mediator-assisted laccase-catalyzed oxidation of 4-hydroxybiphenyl.
2006-05
Estrogenic activities of chemicals related to food contact plastics and rubbers tested by the yeast two-hybrid assay.
2006-04
Effect of side group chemistry on the properties of biodegradable L-alanine cosubstituted polyphosphazenes.
2006-03
Estrogen-like properties of fluorotelomer alcohols as revealed by mcf-7 breast cancer cell proliferation.
2006-01
Phosphate removal from the returned liquor of municipal wastewater treatment plant using iron-reducing bacteria.
2005
Metabolism of aromatic hydrocarbons by the filamentous fungus Cyclothyrium sp.
2004-11
Simultaneous expression of guinea pig UDP-glucuronosyltransferase 2B21 (UGT2B21) and 2B22 in COS-7 cells enhances UGT2B21-catalyzed chloramphenicol glucuronidation.
2004-10
Oxidation of phenolic compounds by peroxidase in the presence of soluble polymers.
2004-09
Substituent effects in pi-pi interactions: sandwich and T-shaped configurations.
2004-06-23
Photocatalytic one-electron oxidation of biphenyl derivatives strongly coupled with the TiO2 surface.
2004-03-30
Factors affecting the oxidative activity of laccase towards biphenyl derivatives in homogeneous aqueous-organic systems.
2004
Formation of a structurally novel, serial diglucuronide of 4-hydroxybiphenyl by further glucuronidation of a monoglucuronide in dog liver microsomes.
2002
Characterization of rabbit UDP-glucuronosyltransferase UGT1A7: tertiary amine glucuronidation is catalyzed by UGT1A7 and UGT1A4.
1997-08-15
Cloning and expression of a rat liver phenobarbital-inducible UDP-glucuronosyltransferase (2B12) with specificity for monoterpenoid alcohols.
1995-10-01
Stable expression of a human liver UDP-glucuronosyltransferase (UGT2B15) with activity toward steroid and xenobiotic substrates.
1994-09-01
A recombinant phenobarbital-inducible rat liver UDP-glucuronosyltransferase (UDP-glucuronosyltransferase 2B1) stably expressed in V79 cells catalyzes the glucuronidation of morphine, phenols, and carboxylic acids.
1994-01
Characterization of a cloned human dihydrotestosterone/androstanediol UDP-glucuronosyltransferase and its comparison to other steroid isoforms.
1993-10-12
cDNA cloning and expression of two new members of the human liver UDP-glucuronosyltransferase 2B subfamily.
1993-07-15
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:51:25 GMT 2025
Edited
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on Mon Mar 31 22:51:25 GMT 2025
Record UNII
5RZN7161MJ
Record Status Validated (UNII)
Record Version
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Name Type Language
P-PHENYLPHENOL SODIUM
Common Name English
4-BIPHENYLOL, SODIUM SALT
Preferred Name English
SODIUM P-PHENYLPHENOXIDE
Common Name English
(1,1'-BIPHENYL)-4-OL, SODIUM SALT
Systematic Name English
(1,1'-BIPHENYL)-4-OL, SODIUM SALT (1:1)
Systematic Name English
SODIUM, (4-BIPHENYLYLOXY)-
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 64117
Created by admin on Mon Mar 31 22:51:25 GMT 2025 , Edited by admin on Mon Mar 31 22:51:25 GMT 2025
Code System Code Type Description
PUBCHEM
23678870
Created by admin on Mon Mar 31 22:51:25 GMT 2025 , Edited by admin on Mon Mar 31 22:51:25 GMT 2025
PRIMARY
FDA UNII
5RZN7161MJ
Created by admin on Mon Mar 31 22:51:25 GMT 2025 , Edited by admin on Mon Mar 31 22:51:25 GMT 2025
PRIMARY
CAS
3645-61-2
Created by admin on Mon Mar 31 22:51:25 GMT 2025 , Edited by admin on Mon Mar 31 22:51:25 GMT 2025
PRIMARY
EPA CompTox
DTXSID20890581
Created by admin on Mon Mar 31 22:51:25 GMT 2025 , Edited by admin on Mon Mar 31 22:51:25 GMT 2025
PRIMARY