Rumenic acid: Difference between revisions
Appearance
Content deleted Content added
Tom.Reding (talk | contribs) m →top: CS1 maintenance: vauthors/veditors or enumerate multiple authors/editors; WP:GenFixes on, using AWB |
m add template |
||
Line 56: | Line 56: | ||
==References== |
==References== |
||
{{Reflist}} |
{{Reflist}} |
||
{{Fatty acids}} |
|||
{{DEFAULTSORT:Rumenic Acid}} |
{{DEFAULTSORT:Rumenic Acid}} |
Revision as of 08:22, 16 October 2019
Names | |
---|---|
IUPAC name
(9Z,11E)-Octadeca-9,11-dienoic acid
| |
Other names
Bovinic acid; C9-T11 acid
| |
Identifiers | |
3D model (JSmol)
|
|
ChEBI | |
ChemSpider | |
KEGG | |
PubChem CID
|
|
CompTox Dashboard (EPA)
|
|
| |
| |
Properties | |
C18H32O2 | |
Molar mass | 280.452 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Rumenic acid, also known as bovinic acid, is a conjugated linoleic acid (CLA) found in the fat of ruminants and in dairy products. It is an omega-7 trans fat. Its lipid shorthand name is cis-9, trans-11 18:2 acid. The name was proposed by Kramer et al. in 1998.[1] It is formed along with vaccenic acid by biohydrogenation of dietary polyunsaturated fatty acids in the rumen.[2] It can be considered as the principal dietary form, accounting for as much as 85-90% of the total CLA content in dairy products.[3]
References
- ^ Kramer J, Parodi P, Jensen R, Mossoba M, Yurawecz M, Adlof R (1998). "Rumenic acid: a proposed common name for the major conjugated linoleic acid isomer found in natural products". Lipids. 33 (8): 835. doi:10.1007/s11745-998-0279-6. PMID 9727617.
- ^ F. Destaillats; E. Buyukpamukcu; P.-A. Golay; F. Dionisi; F. Giuffrida (2005). "Letter to the Editor: Vaccenic and Rumenic Acids, A Distinct Feature of Ruminant Fats". Journal of Dairy Science. 88 (449): 449. doi:10.3168/jds.S0022-0302(05)72705-3.
{{cite journal}}
: Unknown parameter|last-author-amp=
ignored (|name-list-style=
suggested) (help) - ^ Cyberlipid. "Polyenoic Fatty Acids". Retrieved 2007-01-17.