62262

Ethyl linoleate

technical, ≥65% (GC)

• Sinónimos: Linoleic acid ethyl ester
• Fórmula lineal: CH₃(CH₂)₃(CH₂CH=CH)₂(CH₂)₇COOC₂H₅
• Número de CAS: 544-35-4
• Peso molecular: 308.50
• Beilstein/REAXYS Number: 1727827
• EC Number: 208-868-4
• MDL number: MFCD00009535
• UNSPSC Code: 12352100
• PubChem Substance ID: 57651879
• NACRES: NA.22

Propiedades

• grade: technical
• Quality Level: 100
• concentration: ≥65% (GC)
• refractive index: n20/D 1.455 (lit.); n20/D 1.455
• bp: 224 °C/17 mmHg (lit.)
• density: 0.876 g/mL at 25 °C (lit.)
• functional group: ester
• SMILES string: CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC
• InChI: 1S/C20H36O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22-4-2/h8-9,11-12H,3-7,10,13-19H2,1-2H3/b9-8-,12-11-
• InChI key: FMMOOAYVCKXGMF-MURFETPASA-N

Descripción

General description

Ethyl linoleate can undergo auto-oxidation in the presence of the catalyst manganese(II)acetylacetonate.

Application

Ethyl linoleate can be used as a drying agent for alkyd paints. It can also form N²,3-ethenoguanine via reaction with deoxyguanosine.

Biochem/physiol Actions

Ethyl linoleate solated from Oxalis triangularis inhibits forskolin-induced melanogenesis and tyrosinase activity in mouse B16 melanoma cells . This anti-melanogenic effect is mediated by inhibiting cAMP production.

Información de seguridad

• Storage Class: 10 - Combustible liquids
• wgk_germany: WGK 1
• flash_point_f: 235.4 °F - closed cup
• flash_point_c: 113 °C - closed cup
• ppe: Eyeshields, Gloves