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Details

Stereochemistry RACEMIC
Molecular Formula C18H36O3
Molecular Weight 300.4766
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 12-HYDROXYSTEARIC ACID

SMILES

CCCCCCC(O)CCCCCCCCCCC(O)=O

InChI

InChIKey=ULQISTXYYBZJSJ-UHFFFAOYSA-N
InChI=1S/C18H36O3/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)

HIDE SMILES / InChI
Molecular Formula C18H36O3
Molecular Weight 300.4766
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

2007
239
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

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 Mon Mar 31 19:26:53 GMT 2025
Edited
by admin
on Mon Mar 31 19:26:53 GMT 2025
Record UNII
933ANU3H2S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HYDROXYSTEARIC ACID
INCI  
INCI  
Preferred Name English
12-HYDROXYSTEARIC ACID
USP-RS  
Systematic Name English
OCTADECANOIC ACID, 12-HYDROXY-
Common Name English
12-HYDROXYOCTADECANOIC ACID [HSDB]
Common Name English
DL-12-HYDROXYOCTADECANOIC ACID
Common Name English
NSC-2385
Code English
12-HYDROXYSTEARATE
Common Name English
12-HYDROXYOCTADECANOIC ACID
HSDB  
Systematic Name English
CASID HSA
Brand Name English
12-HYDROXYSTEARIC ACID [USP-RS]
Common Name English
STEARIC ACID, 12-HYDROXY-
Common Name English
Code System Code Type Description
RXCUI
1368629
Created by admin on Mon Mar 31 19:26:53 GMT 2025 , Edited by admin on Mon Mar 31 19:26:53 GMT 2025
ALTERNATIVE
NSC
2385
Created by admin on Mon Mar 31 19:26:53 GMT 2025 , Edited by admin on Mon Mar 31 19:26:53 GMT 2025
PRIMARY
CHEBI
85208
Created by admin on Mon Mar 31 19:26:53 GMT 2025 , Edited by admin on Mon Mar 31 19:26:53 GMT 2025
PRIMARY
PUBCHEM
7789
Created by admin on Mon Mar 31 19:26:53 GMT 2025 , Edited by admin on Mon Mar 31 19:26:53 GMT 2025
PRIMARY
EVMPD
SUB68871
Created by admin on Mon Mar 31 19:26:53 GMT 2025 , Edited by admin on Mon Mar 31 19:26:53 GMT 2025
PRIMARY
RXCUI
1370462
Created by admin on Mon Mar 31 19:26:53 GMT 2025 , Edited by admin on Mon Mar 31 19:26:53 GMT 2025
PRIMARY
EPA CompTox
DTXSID8026725
Created by admin on Mon Mar 31 19:26:53 GMT 2025 , Edited by admin on Mon Mar 31 19:26:53 GMT 2025
PRIMARY
CAS
106-14-9
Created by admin on Mon Mar 31 19:26:53 GMT 2025 , Edited by admin on Mon Mar 31 19:26:53 GMT 2025
PRIMARY
SMS_ID
100000134913
Created by admin on Mon Mar 31 19:26:53 GMT 2025 , Edited by admin on Mon Mar 31 19:26:53 GMT 2025
PRIMARY
RXCUI
1368628
Created by admin on Mon Mar 31 19:26:53 GMT 2025 , Edited by admin on Mon Mar 31 19:26:53 GMT 2025
PRIMARY RxNorm
HSDB
5368
Created by admin on Mon Mar 31 19:26:53 GMT 2025 , Edited by admin on Mon Mar 31 19:26:53 GMT 2025
PRIMARY
DAILYMED
933ANU3H2S
Created by admin on Mon Mar 31 19:26:53 GMT 2025 , Edited by admin on Mon Mar 31 19:26:53 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-366-1
Created by admin on Mon Mar 31 19:26:53 GMT 2025 , Edited by admin on Mon Mar 31 19:26:53 GMT 2025
PRIMARY
RS_ITEM_NUM
1331008
Created by admin on Mon Mar 31 19:26:53 GMT 2025 , Edited by admin on Mon Mar 31 19:26:53 GMT 2025
PRIMARY
CHEBI
24747
Created by admin on Mon Mar 31 19:26:53 GMT 2025 , Edited by admin on Mon Mar 31 19:26:53 GMT 2025
PRIMARY
CHEBI
84201
Created by admin on Mon Mar 31 19:26:53 GMT 2025 , Edited by admin on Mon Mar 31 19:26:53 GMT 2025
PRIMARY
FDA UNII
933ANU3H2S
Created by admin on Mon Mar 31 19:26:53 GMT 2025 , Edited by admin on Mon Mar 31 19:26:53 GMT 2025
PRIMARY
Related Record Type Details
Structure of MAGNESIUM 12-HYDROXYSTEARATE
SALT/SOLVATE -> PARENT
Structure of SODIUM HYDROXYSTEARATE
SALT/SOLVATE -> PARENT
Structure of POTASSIUM HYDROXYSTEARATE
SALT/SOLVATE -> PARENT
NIH
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