EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

methyl ricinoleate
9-octadecenoic acid, 12-hydroxy-, methyl ester, (R-(Z))- (9CI)

Supplier Sponsors

CAS Number: 141-24-2Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:205-472-3
FDA UNII: 90FDR3O96Y
Nikkaji Web:J427.132G
Beilstein Number:6132055
MDL:MFCD00046712
XlogP3-AA:6.10 (est)
Molecular Weight:312.49352000
Formula:C19 H36 O3
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:emollients
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
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Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
FDA Mainterm (IAUFC):141-24-2 ; METHYL RICINOLEATE
 
Physical Properties:
Assay: 92.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 411.00 to 413.00 °C. @ 760.00 mm Hg (est)
Flash Point: 310.00 °F. TCC ( 154.60 °C. ) (est)
logP (o/w): 6.205 (est)
Soluble in:
 alcohol
 water, 0.09867 mg/L @ 25 °C (est)
Insoluble in:
 water
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: skin conditioning
skin conditioning - emollient
 
Suppliers:
Acme Synthetic Chemicals
Methyl Ricinoleate Min. 85% Ricinoleate by GC
Santa Cruz Biotechnology
For experimental / research use only.
Ricinoleic Acid methyl ester >99%
Sigma-Aldrich: Sigma
For experimental / research use only.
Methyl ricinoleate ≥99% (GC)
TCI AMERICA
For experimental / research use only.
Methyl Ricinoleate >75.0%(GC)
 
Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
emollients
Recommendation for methyl ricinoleate usage levels up to:
 not for fragrance use.
 
Recommendation for methyl ricinoleate flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):141-24-2
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :5364698
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
methyl (Z)-12-hydroxyoctadec-9-enoate
Chemidplus:0000141242
 
References:
 methyl (Z)-12-hydroxyoctadec-9-enoate
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:141-24-2
Pubchem (cid):5364698
Pubchem (sid):134975256
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
FDA Indirect Additives used in Food Contact Substances:View
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2918.19.9000
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
 emollients
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
 castor oil acid, methyl ester
 flexricin P-1
12-hydroxy-9-octadecenoic acid methyl ester
 methyl (9Z)-12-hydroxy-9-octadecenoate
 methyl (Z)-12-hydroxyoctadec-9-enoate
 methyl 12-hydroxy-9-octadecenoate
9-octadecenoic acid, 12-hydroxy-, methyl ester
9-octadecenoic acid, 12-hydroxy-, methyl ester, (9Z,12R)-
9-octadecenoic acid, 12-hydroxy-, methyl ester, (R-(Z))- (9CI)
9-octadecenoic acid, 12-hydroxy-, methyl ester, (Z)-
 ricinoleic acid methyl ester
 ricinoleic acid, methyl ester
 

Articles:

PubMed:Synthesis and evaluation of antioxidant and antifungal activities of novel ricinoleate-based lipoconjugates of phenolic acids.
PubMed:Methyl ricinoleate as platform chemical for simultaneous production of fine chemicals and polymer precursors.
PubMed:Integration of gas chromatography mass spectrometry methods for differentiating ricin preparation methods.
PubMed:Fed-batch versus batch cultures of Yarrowia lipolytica for γ-decalactone production from methyl ricinoleate.
PubMed:Expression of POX2 gene and disruption of POX3 genes in the industrial Yarrowia lipolytica on the γ-decalactone production.
PubMed:Estolides synthesis catalyzed by immobilized lipases.
PubMed:Metathesis of fatty acid ester derivatives in 1,1-dialkyl and 1,2,3-trialkyl imidazolium type ionic liquids.
PubMed:Oil-in-water emulsions characterization by laser granulometry and impact on γ-decalactone production in Yarrowia lipolytica.
PubMed:A design-of-experiments approach for the optimization and understanding of the cross-metathesis reaction of methyl ricinoleate with methyl acrylate.
PubMed:Poly (ricinoleic acid) based novel thermosetting elastomer.
PubMed:Final report on the safety assessment of Ricinus Communis (Castor) Seed Oil, Hydrogenated Castor Oil, Glyceryl Ricinoleate, Glyceryl Ricinoleate SE, Ricinoleic Acid, Potassium Ricinoleate, Sodium Ricinoleate, Zinc Ricinoleate, Cetyl Ricinoleate, Ethyl Ricinoleate, Glycol Ricinoleate, Isopropyl Ricinoleate, Methyl Ricinoleate, and Octyldodecyl Ricinoleate.
PubMed:Decalactone production by Yarrowia lipolytica under increased O2 transfer rates.
PubMed:Metabolism of fatty acid in yeast: characterisation of beta-oxidation and ultrastructural changes in the genus Sporidiobolus sp. cultivated on ricinoleic acid methyl ester.
PubMed:Surface properties of Yarrowia lipolytica and their relevance to gamma-decalactone formation from methyl ricinoleate.
PubMed:Phospholipase-mediated preparation of 1-ricinoleoyl-2-acyl-sn-glycero-3-phosphocholine from soya and egg phosphatidylcholine.
PubMed:Deuterium NMR used to indicate a common mechanism for the biosynthesis of ricinoleic acid by Ricinus communis and Claviceps purpurea.
PubMed:Synthesis of novel tri- and tetrasubstituted C18 furan fatty esters.
PubMed:Lipase-catalyzed methanolysis of triricinolein in organic solvent to produce 1,2(2,3)-diricinolein.
PubMed:Catabolism of hydroxyacids and biotechnological production of lactones by Yarrowia lipolytica.
PubMed:Increased electron donor and electron acceptor characters enhance the adhesion between oil droplets and cells of Yarrowia lipolytica as evaluated by a new cytometric assay.
PubMed:Role of beta-oxidation enzymes in gamma-decalactone production by the yeast Yarrowia lipolytica.
PubMed:Metabolism of 1-acyl-2-oleoyl-sn-glycero-3-phosphoethanolamine in castor oil biosynthesis.
PubMed:Metabolism of ricinoleic acid into gamma-decalactone: beta-oxidation and long chain acyl intermediates of ricinoleic acid in the genus Sporidiobolus sp.
PubMed:Medium-size droplets of methyl ricinoleate are reduced by cell-surface activity in the gamma-decalactone production by Yarrowia lipolytica.
PubMed:Involvement of acyl coenzyme A oxidase isozymes in biotransformation of methyl ricinoleate into gamma-decalactone by Yarrowia lipolytica.
PubMed:In situ detoxification of the fermentation medium during gamma-decalactone production with the yeast sporidiobolus salmonicolor
PubMed:Fatty acid accumulation in the yeast Sporidiobolus salmonicolor during batch production of gamma-decalactone.
PubMed:Detection of ergot (Claviceps purpurea) in a dairy feed component by gas chromatography and mass spectrometry.
PubMed:Ultrasound-assisted synthesis of santalbic acid and a study of triacylglycerol species in Santalum album (Linn.) seed oil.
PubMed:Nuclear magnetic resonance spectroscopic analysis of homoallylic and bis homoallylic substituted methyl fatty ester derivatives.
PubMed:Bioconversion of methyl ricinoleate to 4-hydroxy-decanoic acid and to gamma-decalactone by yeasts of the genus Candida.
PubMed:Ultrasound in fatty acid chemistry: synthesis of a 1-pyrroline fatty acid ester isomer from methyl ricinoleate.
PubMed:Preparation and properties of gem-dichlorocyclopropane derivatives of long-chain fatty esters.
PubMed:Fluorescence formation from the interaction of DNA with lipid oxidation degradation products.
PubMed:NMR chemical shift reagents in structural determination of lipid derivatives. 3. Methyl ricinoleate and methyl 12-hydroxystearate.
PubMed:The GLC and TLC resolution of diastereoisomeric polyhydroxystearates and assignment of configurations.
 
Notes:
None found
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