13296-76-9 Usage
Uses
Used in Pharmaceutical Industry:
Octadeca-9-cis, 11-trans, 13-trans-trienoic acid is used as an active pharmaceutical ingredient for its potential therapeutic effects. The specific arrangement of double bonds in this molecule may contribute to its bioactivity and interactions with biological targets, making it a candidate for the development of new drugs.
Used in Cosmetic Industry:
In the cosmetic industry, octadeca-9-cis, 11-trans, 13-trans-trienoic acid is used as an ingredient in skincare and hair care products due to its potential moisturizing and anti-inflammatory properties. The conjugated double bonds may help improve skin hydration and reduce inflammation, leading to healthier and more radiant skin and hair.
Used in Nutritional Supplements:
Octadeca-9-cis, 11-trans, 13-trans-trienoic acid is used as a component in nutritional supplements for its potential health benefits. The unique fatty acid structure may provide specific nutritional advantages, such as supporting heart health and reducing inflammation in the body.
Used in Research and Development:
In the field of research and development, octadeca-9-cis, 11-trans, 13-trans-trienoic acid serves as a valuable compound for studying the effects of conjugated double bonds on biological systems. This knowledge can be applied to the development of new drugs, materials, and technologies with improved properties and functions.
Check Digit Verification of cas no
The CAS Registry Mumber 13296-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,9 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13296-76:
(7*1)+(6*3)+(5*2)+(4*9)+(3*6)+(2*7)+(1*6)=109
109 % 10 = 9
So 13296-76-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h5-10H,2-4,11-17H2,1H3,(H,19,20)/b6-5-,8-7+,10-9+
13296-76-9Relevant academic research and scientific papers
NEW CONJUGATED LINOLENIC ACIDS AND METHODS FOR COMMERCIAL PREPARATION AND PURIFICATION
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Page 17-18, (2008/06/13)
A method for the preparation and purification of conjugated linolenic acids is described. The method comprises blending a mixture of vegetable oils and or fats including various concentrations of alpha or gamma and or both linolenic acids with a base. The method transforms approximately over two thirds of α-linolenic acid (9Z,12Z,15Z-octadecatrienoic acid) into 9Z,11E,15Z-octadecatrienoic acid and 9Z,13E,15Z-octadecatrienoic acid. The method also transforms gamma-linolenic acid (6Z,9Z,12Z-octadecatrienoic acid) into 6Z,8E,15Z-octadeccatrienoic acid and 6Z,10E,12Z-octadecatrienoic acid. In all cases, geometrical isomers and fully conjugated isomers are also produced.
Stereoselective Synthesis of Octadeacpolyenoic Esters as an Insecticide
Tsuboi, Sadao,Wu, Xue Han,Maeda, Seiji,Ono, Shinichiro,Kuroda, Akihisha,et al.
, p. 1103 - 1108 (2007/10/02)
Octadecapolyenoic acid derivatives such as (+/-)-t-butyl coriolate, α-eleostearic acid, t-butyl punicate, and t-butyl (9Z,11E)-13-hydroxy-9,11-octadien-15-ynoate were synthesized starting from oleic acid with high stereoselectivity and their insecticidal
STEREOSELECTIVE PREPARATION OF 1-CHLORO-(E,E)-1,3-DIENES. APPLICATION TO THE SYNTHESIS OF METHYL ELEOSTEARATE.
Ratovelomanana, Victorin,Linstrumelle, Gerard
, p. 6001 - 6004 (2007/10/02)
The nickel (or palladium) catalyzed reaction of alkenylalanes with (E)-dichloroethylene affords 1-chloro-(E,E)-1,3-dienes under mild conditions.The syntheses of methyl α-eleostearate which is reported to be a feeding deterrent for the boll weevil on cotto
