trans,trans-9,11-Octadecadienoicacid Chemical Properties

storage temp. 

-20°C

solubility 

Chloroform, Dichloromethane, Ethyl Acetate, Hexane

color 

White

biological source

synthetic

InChI

InChI=1S/C18H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h7-10H,2-6,11-17H2,1H3,(H,19,20)/b8-7+,10-9+

InChIKey

JBYXPOFIGCOSSB-XBLVEGMJSA-N

SMILES

C(O)(=O)CCCCCCC/C=C/C=C/CCCCCC

Safety Information

WGK Germany 

3

trans,trans-9,11-Octadecadienoicacid Usage And Synthesis

Description

9(E),11(E)-Conjugated linoleic acid (9(E),11(E)-CLA) refers to a family of 8 geometric isomers of linoleic acid in which the two double bonds are contiguous. 9(E),11(E)-CLA is the 9,11 all-trans isomer of linoleic acid. CLA was originally identified in ground beef, but it is also present in a variety of dairy products. CLA is effective at reducing mammary tumors in rats at levels as low as 0.1% by weight of their diet. [Matreya, LLC. Catalog No. 1181]

Uses

(9E,?11E)?-9,?11-?Octadecadienoic Acid is a by product during the synthesis of Rumenic Acid (R701590), a trans fatty acid that may potentially reduce the risk of cancer and cardiovascular diseases. It may also prevent disease processes that lead to chronic inflammation, atherosclerosis, and diabetes.

Definition

ChEBI: 9E,11E-octadecadienoic acid is an octadeca-9,11-dienoic acid having 9-trans,11-trans-stereochemistry. It has a role as an apoptosis inducer, an antineoplastic agent, an anti-inflammatory agent, an antiatherogenic agent, a bacterial xenobiotic metabolite and a human metabolite.

References

[1] Conjugated-linoleic-acid[J]. Reactions Weekly, 2021, 28 1: 137-137. DOI: 10.1007/s40278-021-06458-4

trans,trans-9,11-Octadecadienoicacid(544-71-8)Related Product Information

• Docosahexaenoic Acid
• Lauric acid
• Lecithin
• ISOVALERAMIDE
• APIGENIN-6-ARABINOSIDE-8-GLUCOSIDE
• ZIP
• Taurine
• Stearic acid
• RICE BRAN OIL
• 10E,12Z-octadecadienoic acid
• SUNFLOWER SEED OIL
• Citric acid
• CLA