148691-24-1 Usage
Description
(Z,Z,Z,Z,Z)-icosa-5,8,11,14,17-pentaenoic acid 2-((Z)-octadec-9-enoyloxy)-1-((Z)-octadec-9-enoyloxymethyl)ethyl ester is a complex ester compound characterized by a long carbon chain with multiple double bonds, indicating its classification as a polyunsaturated fatty acid. (Z,Z,Z,Z,Z)-icosa-5,8,11,14,17-pentaenoic acid 2-((Z)-octadec-9-enoyloxy)-1-((Z)-octadec-9-enoyloxymethyl)ethyl ester is formed through a reaction between an acid and an alcohol, featuring two long alkyl chains attached to the ester group. The presence of these double bonds suggests potential health benefits when consumed in moderation, although further research is necessary to fully comprehend its properties and possible applications.
Uses
Used in Pharmaceutical Industry:
(Z,Z,Z,Z,Z)-icosa-5,8,11,14,17-pentaenoic acid 2-((Z)-octadec-9-enoyloxy)-1-((Z)-octadec-9-enoyloxymethyl)ethyl ester is used as an active pharmaceutical ingredient for its potential health benefits due to its polyunsaturated fatty acid nature. It may be utilized in the development of medications targeting various health conditions related to inflammation, cardiovascular health, and other areas where polyunsaturated fatty acids are known to play a beneficial role.
Used in Nutritional Supplements:
In the nutritional supplement industry, (Z,Z,Z,Z,Z)-icosa-5,8,11,14,17-pentaenoic acid 2-((Z)-octadec-9-enoyloxy)-1-((Z)-octadec-9-enoyloxymethyl)ethyl ester could be used as an additive for products aimed at promoting heart health and reducing inflammation. Its polyunsaturated fatty acid composition may contribute to the overall health benefits of these supplements.
Used in Research and Development:
(Z,Z,Z,Z,Z)-icosa-5,8,11,14,17-pentaenoic acid 2-((Z)-octadec-9-enoyloxy)-1-((Z)-octadec-9-enoyloxymethyl)ethyl ester is used as a subject of study in research and development for its unique chemical structure and potential applications in various scientific fields. This may include exploring its properties, understanding its interactions with biological systems, and identifying new uses in medicine, nutrition, or other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 148691-24-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,6,9 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 148691-24:
(8*1)+(7*4)+(6*8)+(5*6)+(4*9)+(3*1)+(2*2)+(1*4)=161
161 % 10 = 1
So 148691-24-1 is a valid CAS Registry Number.
148691-24-1Relevant articles and documents
Rapid access to structured triacylglycerols acylated with n-3 polyunsaturated fatty acids for nutritional applications
Vaique, Emilie,Guy, Alexandre,Couedelo, Leslie,Gosse, Isabelle,Durand, Thierry,Cansell, Maud,Pinet, Sandra
experimental part, p. 8872 - 8879 (2011/01/04)
In order to better understand the metabolic fate of n-3 polyunsaturated fatty acids (PUFAs), an efficient access to symmetrical and unsymmetrical triacylglycerols (TGs), esterified with PUFAs, with known high purity, is required. In this context, we optimized the esterification of a mixture of glycerols protected as dioxane and dioxolane with PUFAs. The kinetics of this reaction depends on various factors, such as the fatty acid chain length and the stereochemistry of the dioxane. Then, one-pot acetal hydrolysis and esterification of hydroxyl groups led to the desired structured TGs without either double bond isomerization or acyl migration (except when symmetrical TGs are acylated with long-chain saturated fatty acids in external positions). PUFAs location on the glycerol backbone was assayed by NMR, HPLC and pancreatic lipase hydrolysis.
