|Related Categories||Alphabetical Index of Analytical Standards, Analytical Standards, Analytical/Chromatography, Applications, Biochemicals and Reagents,|
|packaging||ampule of 1 mL|
|concentration||10 mg/mL in methylene chloride (as total weight)|
Qualitative mixtures. Useful for establishing a retention time identification. Data sheet supplied with each ampule.
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|cis-9,cis-12,cis-15-Octadecatrienoic acid methyl ester ~ 3 % (w/w)|
|cis-9,cis-12,trans-15-Octadecatrienoic acid methyl ester ~ 7 % (w/w)|
|cis-9,trans-12,cis-15-Octadecatrienoic acid methyl ester ~ 7 % (w/w)|
|cis-9,trans-12,trans-15-Octadecatrienoic acid methyl ester ~ 15 % (w/w)|
|trans-9,cis-12,cis-15-Octadecatrienoic acid methyl ester ~ 7 % (w/w)|
|trans-9,cis-12,trans-15-Octadecatrienoic acid methyl ester ~ 15 % (w/w)|
|trans-9,trans-12,cis-15-Octadecatrienoic acid methyl ester ~ 15 % (w/w)|
|trans-9,trans-12,trans-15-Octadecatrienoic acid methyl ester ~ 30 % (w/w)|
Trans Fat Labeling Trans fats (trans unsaturated fatty acids) are fatty acids that contain at least one double bond in the trans orientation. This orientation causes carbon atoms to align in a straig...
Katherine K. Stenerson
Reporter US Volume 30.2
Keywords: Addition reactions, Capillary electrophoresis, Chromatography, Derivatizations, Digestions, Flame ionization detector, Fractionation, Gas chromatography, Hydrogenations, Ion-exchange chromatography, Methylations, PAGE, Pesticides, Separation, Solid phase extractions, Solvents, Thin layer chromatography
Combined analysis of C-18 unsaturated fatty acids using natural abundance deuterium 2D NMR spectroscopy in chiral oriented solvents. Lesot P, Baillif V, and Billault I Anal. Chem. 80(8), 2963-72, (2008)
A direct and fast method to monitor lipid oxidation progress in model fatty acid methyl esters by high-performance size-exclusion chromatography. Márquez-Ruiz G, Holgado F, García-Martínez MC, et al. J. Chromatogr. A 1165(1-2), 122-7, (2007)
Identification of 4-oxo-2-hexenal and other direct mutagens formed in model lipid peroxidation reactions as dGuo adducts. Maekawa M, Kawai K, Takahashi Y, et al. Chem. Res. Toxicol. 19(1), 130-8, (2006)
Comparative methyl linoleate and methyl linolenate oxidation in the presence of bovine serum albumin at several lipid/protein ratios. Zamora R and Hidalgo FJ J. Agric. Food Chem. 51(16), 4661-7, (2003)
Mutagenicity tests of lipid oxidation products in Salmonella typhimurium: monohydroperoxides and secondary oxidation products of methyl linoleate and methyl linolenate. MacGregor JT, Wilson RE, Neff WE, et al. Food Chem. Toxicol. 23(12), 1041-7, (1985)
The identification of the allylic nitrite and nitro derivatives of methyl linoleate and methyl linolenate by negative chemical ionization mass spectroscopy. Gallon AA and Pryor WA Lipids 28(2), 125-33, (1993)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
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