Wednesday, May 25, 2016

Elaidic acid - Wikipedia, the free encyclopedia

Elaidic acid

From Wikipedia, the free encyclopedia
Jump to:navigation, search
Elaidic acid
Elaidic-acid-2D-skeletal-reverse.png
Elaidic-acid-from-xtal-3D-balls.png
Elaidic-acid-from-xtal-3D-vdW.png
Names
IUPAC name
(E)-octadec-9-enoic acid
Identifiers
CAS Number
112-79-8 YesY
ChEBICHEBI:27997 YesY
ChEMBLChEMBL460657 YesY
ChemSpider553123 YesY
DrugBankDB04224 YesY
Jmol 3D modelInteractive image
KEGGC01712 YesY
PubChem637517
Properties
Chemical formula
C18H34O2
Molar mass282.46 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Elaidic acid is the major trans fat found in hydrogenated vegetable oils and occurs in small amounts in caprine and bovine milk (very roughly 0.1% of the fatty acids) [1] and some meats. It is the trans isomer of oleic acid. The name of the elaidinization reaction comes from elaidic acid.

Elaidic acid increases plasma CETP activity which lowers HDL cholesterol.[2]

See Also

  • Oleic acid

References

  1. ^ Alonso L, Fontecha J, Lozada L, Fraga MJ, Juárez M (1999). "Fatty acid composition of caprine milk: major, branched-chain, and trans fatty acids". J. Dairy Sci. 82 (5): 87884. doi:10.3168/jds.S0022-0302(99)75306-3. PMID 10342226. 
  2. ^ Abbey M, Nestel PJ (1994). "Plasma cholesteryl ester transfer protein activity is increased when trans-elaidic acid is substituted for cis-oleic acid in the diet". Atherosclerosis 106 (1): 99107. doi:10.1016/0021-9150(94)90086-8. PMID 8018112. 
Retrieved from "https://en.wikipedia.org/w/index.php?title=Elaidic_acid&oldid=670380803"

No comments:

Post a Comment