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Supelco

Conjugated (9Z,11E)-Linoleic acid

analytical standard

Sinônimo(s):

(9Z,11E)-9,11-Octadecadienoic acid, 9Z,11E-CLA, Bovinic acid, Linoleic acid (9-cis, 11-trans)

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About This Item

Fórmula empírica (Notação de Hill):
C18H32O2
Número CAS:
Peso molecular:
280.45
Número MDL:
Código UNSPSC:
85151701
ID de substância PubChem:
NACRES:
NA.24

fonte biológica

synthetic

Nível de qualidade

grau

analytical standard

Ensaio

≥96.0% (HPLC)

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

índice de refração

n20/D 1.478-1.483

Formato

neat

grupo funcional

carboxylic acid

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

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-

chave InChI

JBYXPOFIGCOSSB-GOJKSUSPSA-N

Descrição geral

Conjugated Linoleic acid is a naturally occurring fatty acid. It has anti-cancer, anti-atherogenic and anti-diabetic properties. 9Z,11E is a geometric isomer which belongs to linoleate group.

Aplicação

It was may be used for HPLC-ESI-MS/MS analysis to quantify and also structural analysis of nitrated species of CLA.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Embalagem

Bottomless glass bottle. Contents are inside inserted fused cone.

Produtos recomendados

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.

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves


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Conjugated linoleic acid is a preferential substrate for fatty acid nitration.
Bonacci G
The Journal of Biological Chemistry, 287(53), 44071-44082 (2012)
Yu Y, Correll PH, Vanden Heuvel JP
Biochimica et Biophysica Acta, 1581(3), 89-99 (2002)
Sanjay Basak et al.
Biochimica et biophysica acta, 1831(4), 834-843 (2013-01-29)
A number of studies have been carried out to examine the biological function of conjugated linoleic acid (CLA) and its potential health benefits. However, not much is known about how CLA isomers mediate their effect on angiogenesis and vascularization during
José M Pestana et al.
Meat science, 90(3), 819-827 (2011-12-03)
The influence of slaughter season and muscle type on the detailed fatty acid composition, including conjugated linoleic acid isomers, and contents of total cholesterol and lipid-soluble antioxidant vitamins (α-tocopherol and β-carotene) in Mirandesa-PDO veal was assessed. Mirandesa purebred calves (n=29)
Elena Giordano et al.
Nutrition research (New York, N.Y.), 31(11), 855-862 (2011-11-29)
Conjugated linoleic acid (CLA) is a polyunsaturated fatty acid that has numerous biologic activities. Previous studies in rodents demonstrated that chronic intake of CLA t10,c12 or CLA c9,t11 isomers perturbs the metabolism of retinoids (vitamin A and its derivatives). Specifically

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