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Details

Stereochemistry RACEMIC
Molecular Formula C18H35O3.Na
Molecular Weight 322.4585
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SODIUM HYDROXYSTEARATE

SMILES

[Na+].CCCCCCC(O)CCCCCCCCCCC([O-])=O

InChI

InChIKey=NTVDGBKMGBRCKB-UHFFFAOYSA-M
InChI=1S/C18H36O3.Na/c1-2-3-4-11-14-17(19)15-12-9-7-5-6-8-10-13-16-18(20)21;/h17,19H,2-16H2,1H3,(H,20,21);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula C18H35O3
Molecular Weight 299.4687
Charge -1
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

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
Revisiting the synthesis of a well-known comb-graft copolymer stabilizer and its application to the dispersion polymerization of poly(methyl methacrylate) in organic media.
2010-12-07
Structural relationships in 2,3-bis-n-decyloxyanthracene and 12-hydroxystearic acid molecular gels and aerogels processed in supercritical CO(2).
2010-09-09
Formulation and evaluation of an alternative triglyceride-free propofol microemulsion.
2010-09
Preparation and evaluation of microporous organogel scaffolds for cell viability and proliferation.
2010-08-01
Characterization of organogel as a novel oral controlled release formulation for lipophilic compounds.
2010-03-30
12-Hydroxystearic acid lipid tubes under various experimental conditions.
2010-01-01
Allergic contact dermatitis from 12-hydroxystearic Acid and hydrogenated castor oil.
2009-12-05
Rheological characterization of a new type of colloidal dispersion based on nanoparticles of gelled oil.
2009-08-13
Solvent-modulated nucleation and crystallization kinetics of 12-hydroxystearic acid: a nonisothermal approach.
2009-08-04
Robust organogels from nitrogen-containing derivatives of (R)-12-hydroxystearic acid as gelators: comparisons with gels from stearic acid derivatives.
2009-08-04
Nanoengineering of a biocompatible organogel by thermal processing.
2009-04-16
Low molecular mass organogelator based gel electrolyte with effective charge transport property for long-term stable quasi-solid-state dye-sensitized solar cells.
2008-10-16
Detailed structural elucidation of polyesters and acrylates using Fourier transform mass spectrometry.
2008-10
Physicochemical properties, pharmacokinetics, and pharmacodynamics of a reformulated microemulsion propofol in rats.
2008-09
Marine actinomycetes: a new source of compounds against the human malaria parasite.
2008-06-04
Gelled polymerizable microemulsions. 1. Phase behavior.
2007-07-03
Interactions of novel, nonhemolytic surfactants with phospholipid vesicles.
2007-06-19
Synthesis of new sugar-based surfactants and evaluation of their hemolytic activities.
2006-04-28
Novel lipid system forming hollow microtubes at high yields and concentration.
2006-03-28
Effect of hydroxyl group position and system parameters on the features of hydroxystearic Acid monolayers.
2004-08-31
Cutin and suberin monomers are membrane perturbants.
2004-03-15
Effect of fatty acids on the membrane potential of an alkaliphilic bacillus.
2004-03
Parenteral emulsions stabilized with a mixture of phospholipids and PEG-660-12-hydroxy-stearate: evaluation of accelerated and long-term stability.
2002-09
Properties of polyethylene glycol 660 12-hydroxy stearate at a triglyceride/water interface.
2002-08-21
Preparation of monodisperse, fluorescent PMMA-latex colloids by dispersion polymerization.
2002-01-15
Production of gamma-lactones by the brown-rot basidiomycete Piptoporus soloniensis.
2002
Improvement of the bioavailability of colchicine in rats by co-administration of D-alpha-tocopherol polyethylene glycol 1000 succinate and a polyethoxylated derivative of 12-hydroxy-stearic acid.
2002
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:01:04 GMT 2025
Edited
by admin
on Mon Mar 31 21:01:04 GMT 2025
Record UNII
41MQN4869V
Record Status Validated (UNII)
Record Version
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Name Type Language
SODIUM HYDROXYSTEARATE
INCI  
INCI  
Official Name English
12-HYDROXYSTEARIC ACID, SODIUM SALT
Preferred Name English
OCTADECANOIC ACID, 12-HYDROXY-, SODIUM SALT (1:1)
Common Name English
OCTADECANOIC ACID, 12-HYDROXY-, MONOSODIUM SALT
Common Name English
(±)-SODIUM HYDROXYSTEARATE
Systematic Name English
SODIUM HYDROXYSTEARATE, (±)-
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
236-374-9
Created by admin on Mon Mar 31 21:01:04 GMT 2025 , Edited by admin on Mon Mar 31 21:01:04 GMT 2025
PRIMARY
PUBCHEM
23686579
Created by admin on Mon Mar 31 21:01:04 GMT 2025 , Edited by admin on Mon Mar 31 21:01:04 GMT 2025
PRIMARY
FDA UNII
41MQN4869V
Created by admin on Mon Mar 31 21:01:04 GMT 2025 , Edited by admin on Mon Mar 31 21:01:04 GMT 2025
PRIMARY
EPA CompTox
DTXSID30884592
Created by admin on Mon Mar 31 21:01:04 GMT 2025 , Edited by admin on Mon Mar 31 21:01:04 GMT 2025
PRIMARY
CAS
13329-67-4
Created by admin on Mon Mar 31 21:01:04 GMT 2025 , Edited by admin on Mon Mar 31 21:01:04 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE