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

Approval Year

2007
205
PubMed

PubMed

TitleDatePubMed
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
Properties of polyethylene glycol 660 12-hydroxy stearate at a triglyceride/water interface.
2002 Aug 21
Preparation of monodisperse, fluorescent PMMA-latex colloids by dispersion polymerization.
2002 Jan 15
Parenteral emulsions stabilized with a mixture of phospholipids and PEG-660-12-hydroxy-stearate: evaluation of accelerated and long-term stability.
2002 Sep
Effect of hydroxyl group position and system parameters on the features of hydroxystearic Acid monolayers.
2004 Aug 31
Effect of fatty acids on the membrane potential of an alkaliphilic bacillus.
2004 Mar
Cutin and suberin monomers are membrane perturbants.
2004 Mar 15
Synthesis of new sugar-based surfactants and evaluation of their hemolytic activities.
2006 Apr 28
Novel lipid system forming hollow microtubes at high yields and concentration.
2006 Mar 28
Gelled polymerizable microemulsions. 1. Phase behavior.
2007 Jul 3
Interactions of novel, nonhemolytic surfactants with phospholipid vesicles.
2007 Jun 19
Marine actinomycetes: a new source of compounds against the human malaria parasite.
2008 Jun 4
Detailed structural elucidation of polyesters and acrylates using Fourier transform mass spectrometry.
2008 Oct
Low molecular mass organogelator based gel electrolyte with effective charge transport property for long-term stable quasi-solid-state dye-sensitized solar cells.
2008 Oct 16
Physicochemical properties, pharmacokinetics, and pharmacodynamics of a reformulated microemulsion propofol in rats.
2008 Sep
Nanoengineering of a biocompatible organogel by thermal processing.
2009 Apr 16
Rheological characterization of a new type of colloidal dispersion based on nanoparticles of gelled oil.
2009 Aug 13
Solvent-modulated nucleation and crystallization kinetics of 12-hydroxystearic acid: a nonisothermal approach.
2009 Aug 4
Robust organogels from nitrogen-containing derivatives of (R)-12-hydroxystearic acid as gelators: comparisons with gels from stearic acid derivatives.
2009 Aug 4
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 Dec 7
12-Hydroxystearic acid lipid tubes under various experimental conditions.
2010 Jan 1
Formulation and evaluation of an alternative triglyceride-free propofol microemulsion.
2010 Sep
Structural relationships in 2,3-bis-n-decyloxyanthracene and 12-hydroxystearic acid molecular gels and aerogels processed in supercritical CO(2).
2010 Sep 9
Patents

Patents

06100226
2
20070181041
2
JP2002060558A
5
JP2003113015A
2
JP2003261773A
2
JP2004115395A
2
JP2005213356A
2
JP2007231273A
2
JP2008031012A
2
JP2008156471A
2
JP2009126858A
2
JP2009242272A
2
JP2011195426A
2
JP2012012463A
2
JP2834816B2
2
JPH00370796A
2
JPH02264712A
2
JPH04108711A
4
JPH0416231A
2
JPH04168143A
2
JPH05170620A
2
JPH05320617A
2
JPH0578673A
2
JPH07223931A
2
JPH07270288A
2
JPH08157864A
3
JPH0847635A
2
JPH0859914A
2
JPH0948962A
2
JPH0959140A
2
JPH11290669A
2
JPH11302682A
2
JPH1171479A
2
JPS05989398A
2
JPS5515406A
2
JPS5579314A
2
JPS56103273A
2
JPS58157880A
2
JPS58219299A
2
JPS59139135A
3
JPS61139396A
2
JPS62172531A
2
Substance Class Chemical
Created
by admin
on Sat Dec 16 01:48:50 GMT 2023
Edited
by admin
on Sat Dec 16 01:48:50 GMT 2023
Record UNII
41MQN4869V
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SODIUM HYDROXYSTEARATE
INCI  
INCI  
Official Name English
OCTADECANOIC ACID, 12-HYDROXY-, SODIUM SALT (1:1)
Common Name English
12-HYDROXYSTEARIC ACID, SODIUM SALT
Common Name English
SODIUM HYDROXYSTEARATE [INCI]
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 Sat Dec 16 01:48:50 GMT 2023 , Edited by admin on Sat Dec 16 01:48:50 GMT 2023
PRIMARY
PUBCHEM
23686579
Created by admin on Sat Dec 16 01:48:50 GMT 2023 , Edited by admin on Sat Dec 16 01:48:50 GMT 2023
PRIMARY
FDA UNII
41MQN4869V
Created by admin on Sat Dec 16 01:48:50 GMT 2023 , Edited by admin on Sat Dec 16 01:48:50 GMT 2023
PRIMARY
EPA CompTox
DTXSID30884592
Created by admin on Sat Dec 16 01:48:50 GMT 2023 , Edited by admin on Sat Dec 16 01:48:50 GMT 2023
PRIMARY
CAS
13329-67-4
Created by admin on Sat Dec 16 01:48:50 GMT 2023 , Edited by admin on Sat Dec 16 01:48:50 GMT 2023
PRIMARY
Related Record Type Details
Structure of 12-HYDROXYSTEARIC ACID
PARENT -> SALT/SOLVATE
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