For research use only. Not for therapeutic Use.
Catalog Number | R061648 |
CAS Number | 2566-97-4 |
Synonyms | (9E,12E)-9,12-Octadecadienoic acid, methyl ester; (E,E)-9,12-Octadecadienoic acid, methyl ester; Linolelaidic acid, methyl ester; (9E,12E)-9,12-Octadecadienoic acid methyl ester; (E,E)-9,12-Octadecadienoic acid methyl ester; Methyl (9E,12E)-octadecad |
Molecular Formula | C19H34O2 |
Purity | ≥95% |
Storage | -80°C |
IUPAC Name | methyl (9E,12E)-octadeca-9,12-dienoate |
InChI | 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+ |
InChIKey | WTTJVINHCBCLGX-ZDVGBALWSA-N |
SMILES | CCCCCC=CCC=CCCCCCCCC(=O)OC |
Reference | <br>1. A. Lanser et al. “Metabolism of Linoleate versus Linoelaidate in the Laying Hen” Lipids, vol. 13 pp. 103-109, 1978<br>2. A. Christy “Thermally Induced Isomerization of Trilinolein and Trilinoelaidin at 250 _C: Analysis of Products by Gas Chromatography and InfraredSpectroscopy” Lipids, vol. 44 pp. 1105-1112, 2009<br>3. H.-H. Lo et al. “In vitro activation of mouse skin protein kinase C by fatty acids and their hydroxylated metabolites” Lipids, vol. 29 pp. 547-553, 1994<br>4. D. Zapolska-Downar et al. “Trans Fatty Acids Induce Apoptosis in Human Endothelial Cells” Journal of Physiology and Pharmacology, vol. 56 pp. 611-625, 2005</br></br></br></br> |