| Identification | Back Directory | [Name]
10E,12Z-octadecadienoic acid | [CAS]
2420-56-6 | [Synonyms]
T10C12 Cla
10E,Z12-CLA
10E,12Z-CLA
CLA 10TR,12C
10-TRANS, 12-CIS CLA
Acifluorfen Impurity 8
(10E,12Z)-Linoleic Acid
TRANS-10,CIS-12LINOLEICACID
10TR-12C-OCTADECADIENOIC ACID
10,12-Conjugated linoleic acid
Conjugated linoleic acid FFA80
10(E),12(Z)-OCTADECADIENOIC ACID
LINOLEIC ACID (10-TRANS, 12-CIS)
Conjugated linoleic acid (CLA) EE
10(E),12(Z)-ConjugatedLinoleicAci
Conjugated linoleic acid (CLA) FFA
CLA (Conjugated Linoleic Acid) Oil
CONJUGATED LINOLEIC ACID (10E,12Z)
CONJUGATED (10E,12Z)-LINOLEIC ACID
TRANS-10,CIS-12-OCTADECADIENOICACID
Conjugated linoleic acid—80% (CLA)
2420-56-6 Conjugated linoleic acid
Octadecadienoic acid(10E,12Z)(C18:2)
10(E),12(Z)-Conjugated Linoleic Acid
(10E,12Z)-Octadeca-9,12-dienoic acid
(10E,12Z)-10,12-OCTADECADIENOIC ACID
10TRANS,12-CIS-CONJUGATEDLINOLEICACID
TRANS-10,CIS-12CONJUGATEDLINOLEICACID
(10E,12Z)-Octadeca-10,12-dienoic acid
10,12-Octadecadienoic acid, (10E,12Z)-
CONJUGATED LINOLEIC ACID(CLA-TG, EE FFA)
trans-10, cis-12 Conjugate linoleic acid
10-TRANS,12-CIS-18:2CONJUGATEDLINOLEICACID
10-trans,12-cis-Octadecadienoic acid (10tr)
Conjugated (E10,Z12)-Linoleic acid Solution
10,12-Octadecadienoicacid, (10E,12Z)- (9CI)
Conjugated (10E,12Z)-Linoleic acid solution
DELTA 10 TRANS DELTA 12 CIS OCTADECADIENOIC ACID
(10E,12Z)-10,12-Octadecadienoic acid, 10E,Z12-CLA, Linoleic acid (10-trans, 12-cis) | [EINECS(EC#)]
607-342-5 | [Molecular Formula]
C18H32O2 | [MDL Number]
MFCD02259040 | [MOL File]
2420-56-6.mol | [Molecular Weight]
280.45 |
| Chemical Properties | Back Directory | [Boiling point ]
377.7±11.0 °C(Predicted) | [density ]
0.911±0.06 g/cm3(Predicted) | [Fp ]
14℃ | [storage temp. ]
−20°C | [solubility ]
Chloroform (Slightly), Dichloromethane (Slightly), DMSO, Methanol (Slightly) | [form ]
Oil | [pka]
4.78±0.10(Predicted) | [color ]
Colourless | [biological source]
synthetic | [Stability:]
Light Sensitive |
| Hazard Information | Back Directory | [Description]
Conjugated linoleic acid (CLA) refers to a family of 8 geometric isomers of linoleic acid in which the two double bonds are contiguous. (The predominant form of linoleic acid in nature, 18:ω6, has double bonds at 9 and 12, interrupted by a methylene carbon.) CLA is found in both meat and dairy products, but it is not found to any significant degree in plants. The predominant isomer of CLA in animal tissue is 9Z,11E; smaller amounts of 10E,12Z also occur. Various antioxidant and antitumor activities have been attributed to CLA or its downstream metabolites.1 Reported health benefits of dietary supplementation with CLA have been attributed variously to competitive inhibition of Δ6-desaturase and/or PPARγ activation.2 [Matreya, LLC. Catalog No. 1249] | [Uses]
10-trans,12-cis-Linoleic Acid?is an isomer of Linoleic Acid (L467495). Linoleic Acid is a dietary unsaturated fatty acid, which increases the expression of adhesion molecules and attenuates Endothelial cell function. Linoleic Acid is anti-inflammatory, acne reductive, and moisture retentive when applied topically on the skin. It is popular in the beauty products industry because of its beneficial properties on the skin. | [Definition]
ChEBI: (10E,12Z)-octadecadienoic acid is an octadeca-10,12-dienoic acid having (10E,12Z)-configuration. It is a conjugate acid of a (10E,12Z)-octadecadienoate. | [IC 50]
PPARα | [References]
[1] RONALDO OLIVEIRA. Fatty Acid Profile of Milk and Cheese from Dairy Cows Supplemented a Diet with Palm Kernel Cake.[J]. Molecules, 2015, 20 8: 15434-15448. DOI: 10.3390/molecules200815434
[2] S Y MOYA-CAMARENA. Conjugated linoleic acid is a potent naturally occurring ligand and activator of PPARalpha.[J]. Journal of Lipid Research, 1999, 40 8: 1426-1433.
[3] YEONHWA PARK . Inhibition of hepatic stearoyl-CoA desaturase activity by trans-10,cis-12 conjugated linoleic acid and its derivatives[J]. Biochimica et biophysica acta. Molecular and cell biology of lipids, 2000, 1486 2: Pages 285-292. DOI: 10.1016/s1388-1981(00)00074-3
[4] ILANA PLATT Ahmed E S. Effects of 9cis,11trans and 10trans,12cis CLA on osteoclast formation and activity from human CD14+ monocytes.[J]. Lipids in Health and Disease, 2009, 8: 15. DOI: 10.1186/1476-511x-8-15
[5] KUI-JIN KIM. ATF3 Mediates Anti-Cancer Activity of Trans-10, cis-12-Conjugated Linoleic Acid in Human Colon Cancer Cells.[J]. Biomolecules & Therapeutics, 2015, 23 2: 134-140. DOI: 10.4062/biomolther.2014.107
[6] EDURNE SIMóN. trans-10,cis-12 Conjugated linoleic acid prevents adiposity but not insulin resistance induced by an atherogenic diet in hamsters[J]. Journal of Nutritional Biochemistry, 2006, 17 2: Pages 126-131. DOI: 10.1016/j.jnutbio.2005.06.001 |
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