L1876

Methyl linoleate

≥98% (GC)

• Synonyme(s) : cis,cis-9,12-octadécadiénoate de méthyle, Ester méthylique d’acide linoléique
• Formule linéaire : CH₃(CH₂)₃(CH₂CH=CH)₂(CH₂)₇CO₂CH₃
• Numéro CAS: 112-63-0
• Poids moléculaire : 294.47
• UNSPSC Code: 12352211
• NACRES: NA.25
• PubChem Substance ID: 24896293
• EC Number: 203-993-0
• Beilstein/REAXYS Number: 1727614
• MDL number: MFCD00009534

Propriétés

• Quality Segment: 200
• assay: ≥98% (GC)
• form: liquid
• refractive index: n20/D 1.462 (lit.)
• bp: 192 °C/4 mmHg (lit.)
• mp: −35 °C (lit.)
• density: 0.889 g/mL at 25 °C (lit.)
• functional group: ester
• lipid type: omega FAs
• shipped in: ambient
• storage temp.: −20°C
• SMILES string: CCCCC\C=C/C\C=C/CCCCCCCC(=O)OC
• InChI: 1S/C19H34O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-2/h7-8,10-11H,3-6,9,12-18H2,1-2H3/b8-7-,11-10-
• InChI key: WTTJVINHCBCLGX-NQLNTKRDSA-N

Description

General description

Methyl linoleate, non-conjugated, is more easily oxidized than conjugated methyl linoleate .

Application

The oxidation of methyl linoleate in organic solution and phosphatidylcholine (PC) in liposomal membranes induced by an azo initiator has often been used as a model for lipid peroxidation in vivo .

Biochem/physiol Actions

Methyl linoleate may be used as a model compound in oxidation/peroxidation assays to evaluate the anti-peroxidation activity of fullerenes, ellagitannins and other natural products.

Informations sur la sécurité

• Classe de stockage: 10 - Combustible liquids
• wgk: WGK 1
• ppe: Eyeshields, Gloves
• flash_point_f: 338.0 °F - closed cup - (own results)
• flash_point_c: 170 °C - closed cup - (own results)