methyl-9,12-octadecadienoate

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methyl linolelaidate

CAS: 2462-85-3 C19 H34 O2 MW: 294.47838000
All Ingredients Aromatic Ingredients CAS Numbers EINECS Numbers Found in Nature

Identification

Namemethyl-9,12-octadecadienoate
IUPACmethyl (9E,12E)-octadeca-9,12-dienoate
CAS Number2462-85-3
EINECS219-560-4
FDA UNIIJRB7ACQ5NW
Molecular FormulaC19 H34 O2
Molecular Weight294.47838000
MDL NumberMFCD00069997
Nikkaji NumberJ47.156I
Beilstein1727615

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Soluble in water, 0.01981 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for methyl-9,12-octadecadienoate usage levels up tonot for fragrance use.
Recommendation for methyl-9,12-octadecadienoate flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

cynara cardunculus flower

Synonyms

methyl (9E,12E)-octadeca-9,12-dienoate methyl linolelaidate methyl octadeca-9,12-dienoate methyloctadeca-9,12-dienoate PubMed: Selective oxidation reactions of natural compounds with hydrogen peroxide mediated by methyltrioxorhenium. PubMed: Biosynthesis of linoleic acid in Tyrophagus mites (Acarina: Acaridae). PubMed: Reaction products of [60]fullerene during the autoxidation of methyl linoleate in bulk phase. PubMed: Proportion of geometrical hydroperoxide isomers generated by radical oxidation of methyl linoleate in homogeneous solution and in aqueous emulsion. PubMed: Neighboring methoxyl participation in the acid catalyzed methoxylation of methylene-interrupted fatty acids. PubMed: Linoleate hydroperoxides are cleaved heterolytically into aldehydes by a Lewis acid in aprotic solvent.