Linoleic acid methyl ester,
|Related Categories||Aloe Vera, Biochemicals and Reagents, Cell Biology, Esters, Fatty Acids and conjugates,|
|bp||192 °C/4 mmHg(lit.)|
|density||0.889 g/mL at 25 °C(lit.)|
1, 5, 10, 25 g in glass bottle
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 1.
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.
Methyl linoleate, non-conjugated, is more easily oxidized than conjugated methyl linoleate 2.
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UVA photoirradiation of nitro-polycyclic aromatic hydrocarbons-induction of reactive oxygen species and formation of lipid peroxides. Xia Q, Yin JJ, Zhao Y, et al. Int. J. Environ. Res. Public Health 10(3), 1062-84, (2013)
Ozone-induced dissociation of conjugated lipids reveals significant reaction rate enhancements and characteristic odd-electron product ions. Pham HT, Maccarone AT, Campbell JL, et al. J. Am. Soc. Mass Spectrom. 24(2), 286-96, (2013)
Synthesis of glycosyl ferulate derivatives by amine-promoted glycosylation with regioselective hydrolysis using Novozym 435 and evaluation of their antioxidant properties. Shimotori Y, Tsutano K, Soga K, et al. Carbohydr. Res. 359, 11-7, (2012)
A detailed identification study on high-temperature degradation products of oleic and linoleic acid methyl esters by GC-MS and GC-FTIR. Berdeaux O, Fontagné S, Sémon E, et al. Chem. Phys. Lipids 165(3), 338-47, (2012)
Dichloro-4-quinolinol-3-carboxylic acid: synthesis and antioxidant abilities to scavenge radicals and to protect methyl linoleate and DNA. Li GX, Liu ZQ, and Luo XY Eur. J. Med. Chem. 45(5), 1821-7, (2010)
Synthesis of acyl arbutin by an immobilized lipase and its suppressive ability against lipid oxidation in a bulk system and O/W emulsion. Nagai M, Watanabe Y, and Nomura M Biosci. Biotechnol. Biochem. 73(11), 2501-5, (2009)
Betacyanins as phenol antioxidants. Chemistry and mechanistic aspects of the lipoperoxyl radical-scavenging activity in solution and liposomes. Tesoriere L, Allegra M, Gentile C, et al. Free Radic. Res. 43(8), 706-17, (2009)
Catalytic epoxidation of a technical mixture of methyl oleate and methyl linoleate in ionic liquids using MoO(O2)2.2QOH (QOH = 8-quinilinol) as catalyst and NaHCO3 as co-catalyst. Cai SF, Wang LS, and Fan CL Molecules 14(8), 2935-46, (2009)
FT-NMR 1 (1), 989:B / IR-Spectra (2), 336:C / IR-Spectra (3), 379:H / RegBook 1 (1), 723:N / Sigma FT-IR 1 (1), 1415:A / Structure Index 1, 110:D:8 / Vapor Phase 3, 686:B
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