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Details

Stereochemistry ACHIRAL
Molecular Formula C7H5O3.Na
Molecular Weight 160.1026
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SODIUM PARABEN

SMILES

[Na+].OC1=CC=C(C=C1)C([O-])=O

InChI

InChIKey=ZLVSYODPTJZFMK-UHFFFAOYSA-M
InChI=1S/C7H6O3.Na/c8-6-3-1-5(2-4-6)7(9)10;/h1-4,8H,(H,9,10);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C7H5O3
Molecular Weight 137.1128
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Pneumocystis carinii synthesizes four ubiquinone homologs: inhibition by atovaquone and bupravaquone but not by stigmatellin.
2001
Anaerobic degradation of aromatic compounds coupled to Fe(III) reduction by Ferroglobus placidus.
2001 Apr
The influence of type and quantity of model drug on the extrusion/spheronization of mixtures with microcrystalline cellulose. I. Extrusion parameters.
2001 Apr 17
Purification and properties of p-hydroxybenzoate hydroxylases from Rhodococcus strains.
2001 Aug
Methodological setup to study allelochemical translocation in radish seedlings.
2001 Aug
Comamonas testosteroni BR6020 possesses a single genetic locus for extradiol cleavage of protocatechuate.
2001 Aug
The crystal structure of chorismate lyase shows a new fold and a tightly retained product.
2001 Aug 15
Non-ionic micellar affinity capillary electrophoresis for analysis of interactions between micelles and drugs.
2001 Feb
Synthesis, characterization and in vitro degradation of a new family of alternate poly(ester-anhydrides) based on aliphatic and aromatic diacids.
2001 Feb
Comparison of the degradation of p-hydroxybenzoic acid in aqueous solution by several oxidation processes.
2001 Feb
Analysis of the pobA and pobR genes controlling expression of p-hydroxybenzoate hydroxylase in Azotobacter chroococcum.
2001 Feb 7
Quantitative and qualitative precision improvements by effective mobility-scale data transformation in capillary electrophoresis analysis.
2001 Jan
A rate-limiting conformational change of the flavin in p-hydroxybenzoate hydroxylase is necessary for ligand exchange and catalysis: studies with 8-mercapto- and 8-hydroxy-flavins.
2001 Jan 30
Polyacrylamides as hydrophilic selectors in non-aqueous capillary electrophoresis.
2001 Jan 5
Influence of nutritional and environmental factors on polysaccharide production by Azotobacter vinelandii cultured on 4-hydroxybenzoic acid.
2001 Jul
Rerouting the plant phenylpropanoid pathway by expression of a novel bacterial enoyl-CoA hydratase/lyase enzyme function.
2001 Jul
Selective and quantitative analysis of 4-hydroxybenzoate preservatives by microemulsion electrokinetic chromatography.
2001 Jul 27
Synergistic interactions of multiple mutations on catalysis during the hydroxylation reaction of p-hydroxybenzoate hydroxylase: studies of the Lys297Met, Asn300Asp, and Tyr385Phe mutants reconstituted with 8-Cl-flavin.
2001 Jul 31
Determination of organic acids of low molecular weight and phosphate in soil by capillary electrophoresis.
2001 Jul-Aug
Regulation of the p-hydroxybenzoic acid hydroxylase gene (pobA) in plant-growth-promoting Pseudomonas putida WCS358.
2001 Jun
Kinetics of the reaction between ozone and phenolic acids present in agro-industrial wastewaters.
2001 Mar
Monitoring of Lactobacillus fermentation process by using ion chromatography with a series piezoelectric quartz crystal detector.
2001 Mar 1
Separation of a phenol carboxylating organism from a two-member, strict anaerobic co-culture.
2001 May
The ZbYME2 gene from the food spoilage yeast Zygosaccharomyces bailii confers not only YME2 functions in Saccharomyces cerevisiae, but also the capacity for catabolism of sorbate and benzoate, two major weak organic acid preservatives.
2001 Nov
Monitoring of reactive oxygen species production after traumatic brain injury in rats with microdialysis and the 4-hydroxybenzoic acid trapping method.
2001 Nov
Effects of the nitrone radical scavengers PBN and S-PBN on in vivo trapping of reactive oxygen species after traumatic brain injury in rats.
2001 Nov
Kinetic model for phenolic compound oxidation by Fenton's reagent.
2001 Oct
Fast homogeneous assay for plasma procarboxypeptidase U.
2001 Sep
Ubiquinone biosynthesis in microorganisms.
2001 Sep 25
Why phenolic acids are unlikely primary allelochemicals in rice.
2002 Jan
4-Hydroxybenzoate uptake in Klebsiella planticola strain DSZ1 is driven by DeltapH.
2002 Jan
The activity of Arabidopsis glycosyltransferases toward salicylic acid, 4-hydroxybenzoic acid, and other benzoates.
2002 Jan 4
Multiple operons connected with catabolism of aromatic compounds in Acinetobacter sp. strain ADP1 are under carbon catabolite repression.
2002 Jul
An in vitro hydroxyl radical generation assay for microdialysis sampling calibration.
2002 Jul 1
Enhanced detection and characterization of protocatechuate 3,4-dioxygenase in Acinetobacter lwoffii K24 by proteomics using a column separation.
2002 Jul 26
Agastinol and agastenol, novel lignans from Agastache rugosa and their evaluation in an apoptosis inhibition assay.
2002 Mar
Novel fluorometric assay for hydroxyl radical prevention capacity using fluorescein as the probe.
2002 May 8
On the application of 4-hydroxybenzoic acid as a trapping agent to study hydroxyl radical generation during cerebral ischemia and reperfusion.
2002 May-Jun
Physiology of exopolysaccharide production by Azotobacter vinelandii from 4-hydroxybenzoic acid.
2002 Sep
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:46:19 GMT 2023
Edited
by admin
on Fri Dec 15 19:46:19 GMT 2023
Record UNII
V6102T509B
Record Status Validated (UNII)
Record Version
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Name Type Language
SODIUM PARABEN
INCI  
INCI  
Official Name English
P-HYDROXYBENZOIC ACID MONOSODIUM SALT
Common Name English
BENZOIC ACID, 4-HYDROXY-, SODIUM SALT (1:1)
Common Name English
SODIUM PARABEN [INCI]
Common Name English
SODIUM P-HYDROXYBENZOATE
Common Name English
BENZOIC ACID, 4-HYDROXY-, MONOSODIUM SALT
Common Name English
SODIUM 4-HYDROXYBENZOIC ACID
Systematic Name English
BENZOIC ACID, P-HYDROXY-, MONOSODIUM SALT
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
204-051-1
Created by admin on Fri Dec 15 19:46:19 GMT 2023 , Edited by admin on Fri Dec 15 19:46:19 GMT 2023
PRIMARY
FDA UNII
V6102T509B
Created by admin on Fri Dec 15 19:46:19 GMT 2023 , Edited by admin on Fri Dec 15 19:46:19 GMT 2023
PRIMARY
EPA CompTox
DTXSID3059426
Created by admin on Fri Dec 15 19:46:19 GMT 2023 , Edited by admin on Fri Dec 15 19:46:19 GMT 2023
PRIMARY
PUBCHEM
16219477
Created by admin on Fri Dec 15 19:46:19 GMT 2023 , Edited by admin on Fri Dec 15 19:46:19 GMT 2023
PRIMARY
CAS
114-63-6
Created by admin on Fri Dec 15 19:46:19 GMT 2023 , Edited by admin on Fri Dec 15 19:46:19 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE