20590-32-3 Usage
Chemical Properties
Mead acid, also referred to as eicosatrienoic acid, is chemically a carboxylic acid with a 20-carbon chain and three methyleneinterrupted cis double bonds. The first double bond is located at the ninth carbon from the omega end. In physiological literature, it is given the name 20:3(n-9) b. Mead acid can form various hydroxy (HETE) and hydoperoxy (HpETE) products .
Uses
Mead Acid (20:3, n-9) is a precursor in biosynthesis of prostaglandins, thromboxanes and leukotrienes - anti-inflammatory.
Definition
ChEBI: An icosatrienoic acid with three cis-double bonds at positions 5, 8 and 11.
Check Digit Verification of cas no
The CAS Registry Mumber 20590-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,5,9 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20590-32:
(7*2)+(6*0)+(5*5)+(4*9)+(3*0)+(2*3)+(1*2)=83
83 % 10 = 3
So 20590-32-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H34O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h9-10,12-13,15-16H,2-8,11,14,17-19H2,1H3,(H,21,22)/b10-9-,13-12-,16-15-
20590-32-3Relevant academic research and scientific papers
Functional acylglycerides
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, (2008/06/13)
The present invention relates to the field of human and animal nutrition, and in particular to certain novel compositions of conjugated linoleic acids (CLA). In particular, the present invention relates certain isomers of conjugated linoleic acids at eith
Triglyceride and composition comprising the same
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, (2008/06/13)
The present invention provides a novel triglyceride and a composition containing that novel triglyceride having a triglyceride structure of the human breast milk type, which triglyceride has a saturated fatty acid having 16-18 carbon atoms at the position 2, at the position 1 and/or 3; which is and at least one ω6, ω9 or ω3 unsaturated fatty acid manufactured by subjecting a glyceride in which a saturated fatty acid having 16 to 18 carbon atoms is bonded at position 2 to transesterification using a lipase and a ω6, ω9 or ω3-unsaturated fatty acid.
