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Merck
CN

90983

Conjugated (9E,11E)-Linoleic acid

analytical standard

Synonym(s):

(9E,11E)-9,11-Octadecadienoic acid, 9E,11E-CLA, Isolinoleic acid, Linoleic acid (9-trans, 11-trans), Mangold’s acid

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About This Item

Empirical Formula (Hill Notation):
C18H32O2
CAS Number:
544-71-8
Molecular Weight:
280.45
NACRES:
NA.24
PubChem Substance ID:
329769982
UNSPSC Code:
85151701
MDL number:
MFCD00133681

Key Documents

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InChI key

JBYXPOFIGCOSSB-XBLVEGMJSA-N

SMILES string

CCCCCC\C=C\C=C\CCCCCCCC(O)=O

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+

biological source

synthetic

grade

analytical standard

assay

≥98.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

format

neat

functional group

carboxylic acid

storage temp.

−20°C

Quality Level

100

Related Categories

General description

Conjugated (9E,11E)-linoleic acid can be obtained via hydrogenation of linoleic acid in the middle [12,13] double bond.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCP2911
BCCN5695
BCCK0335
BCCF9012
BCCB5535

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Kulp K et al.
Batters and Breadings in Food Processing, (2) (2016)
Manuela Oraldi et al.
Lipids, 48(1), 29-38 (2012-11-07)
Conjugated linoleic acid (CLA) is thought to have anti-proliferative and anti-inflammatory properties, but its effect on cancer cachexia is unknown. Two effects were here investigated: that of CLA on inflammatory mediator production in human lung cancer cells, and that of
Anne-Catherine Schneider et al.
PloS one, 7(3), e32824-e32824 (2012-03-20)
Conjugated linoleic acids (CLA), and principally c9t11 CLA, are suspected to have numerous preventive properties regarding non-infectious pathologies such as inflammatory diseases, atherosclerosis and several types of cancer. C9t11 CLA is produced in the rumen during biohydrogenation of linoleic acid
Christian Degen et al.
Biochimica et biophysica acta, 1811(12), 1070-1080 (2011-09-06)
Conjugated fatty acids (CFAs) exhibit growth inhibitory effects on colon cancer in vitro and in vivo. To investigate whether the anticancerogenic potency depends on number or configuration of the conjugated double bonds, the effect of conjugated linoleic acid (CLA; C18:2)
Ton Baars et al.
Journal of the science of food and agriculture, 92(14), 2883-2890 (2011-12-17)
Organic milk is seen as more healthy in terms of its fatty acid (FA) profile. In three on-farm crossover trials with 10-12 cows in each group, different forages were compared for their potential to improve the FA composition. Different hay
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