140670-40-2 Usage
Description
(4Z,7Z,10Z,13Z,16Z,19Z)-Docosa-4,7,10,13,16,19-hexaenoic acid 2,3-dihydroxy-propyl ester is a chemical compound that is an ester form of docosahexaenoic acid (DHA), an omega-3 fatty acid known for its numerous health benefits, particularly for brain and heart health. This specific ester form of DHA possesses potential antioxidant, anti-inflammatory, and neuroprotective properties, making it a valuable compound for various applications in the health and wellness industry.
Uses
Used in Dietary Supplements:
(4Z,7Z,10Z,13Z,16Z,19Z)-Docosa-4,7,10,13,16,19-hexaenoic acid 2,3-dihydroxy-propyl ester is used as a dietary supplement for its health benefits, particularly in supporting brain and heart health. The ester form enhances bioavailability and absorption, making it an effective source of DHA for consumers.
Used in Pharmaceutical Ingredients:
In the pharmaceutical industry, (4Z,7Z,10Z,13Z,16Z,19Z)-Docosa-4,7,10,13,16,19-hexaenoic acid 2,3-dihydroxy-propyl ester is used as an ingredient in the development of medications targeting various health conditions. Its antioxidant, anti-inflammatory, and neuroprotective properties make it a promising candidate for therapeutic applications.
Used in Skincare and Personal Care Products:
(4Z,7Z,10Z,13Z,16Z,19Z)-Docosa-4,7,10,13,16,19-hexaenoic acid 2,3-dihydroxy-propyl ester is used as a component in skincare and personal care products due to its potential antioxidant and anti-inflammatory properties. It may contribute to the development of products aimed at improving skin health and reducing inflammation.
Used in the Health and Wellness Industry:
Overall, (4Z,7Z,10Z,13Z,16Z,19Z)-Docosa-4,7,10,13,16,19-hexaenoic acid 2,3-dihydroxy-propyl ester is used across various sectors within the health and wellness industry for its potential to support brain, heart, and skin health, as well as its antioxidant and anti-inflammatory properties.
Check Digit Verification of cas no
The CAS Registry Mumber 140670-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,6,7 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 140670-40:
(8*1)+(7*4)+(6*0)+(5*6)+(4*7)+(3*0)+(2*4)+(1*0)=102
102 % 10 = 2
So 140670-40-2 is a valid CAS Registry Number.
140670-40-2Relevant articles and documents
One-pot synthesis of polyunsaturated fatty acid amides with anti-proliferative properties
Tremblay, Hugo,St-Georges, Catherine,Legault, Marc-Andr,Morin, Caroline,Fortin, Samuel,Marsault, Eric
, p. 5635 - 5638 (2015/01/09)
A one-pot environmentally friendly transamidation of ω-3 fatty acid ethyl esters to amides and mono- or diacylglycerols was investigated via the use of a polymer-supported lipase. The method was used to synthesize a library of fatty acid monoglyceryl esters and amides. These new derivatives were found to have potent growth inhibition effects against A549 lung cancer cells.
COMPOSITIONS COMPRISING POLYUNSATURATED FATTY ACID MONOGLYCERIDES OR DERIVATIVES THEREOF AND USES THEREOF
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Page/Page column 27, (2008/12/07)
There are provided various compounds and compositions comprising polyunsaturated fatty acid monoglycerides and derivatives thereof. These compounds and compositions can be useful as cancer chemopreventive agents. They can also be useful for enhancing solubility of various active agents and enhancing their bioavailability.
Synthesis of Triacylglycerol from Polyunsaturated Fatty Acid by Immobilized Lipase
Kosugi, Yoshitsugu,Azuma, Naoki
, p. 1397 - 1403 (2007/10/02)
More than 95percent of polyunsaturated acid (PUFA) was converted to triacylglycerol by immobilized lipase from Candida antarctica or Rhizomucor miehei.The esterification was carried out at 50-60 deg C with shaking and dehydration for 24 h.The substrates consisted of glycerol and free fatty acid or ethyl esters of the fatty acid at a 1:3 molar ratio.The docosahexaenoic acid (DHA) or eicosapentaenoic acid (EPA) in the substrate polymerized during the reaction, and they required 5-10percent more than the stoichiometric amount to compensate for the PUFA loss.On the contrary, ethyl esters of DHA and EPA were not polymerized.Pure tridocosahexaenoyl, trieicosapentaenoyl and triarachidonoyl glycerol were isolated after passing the product through a basic aluminum oxide column.Industrial feasibility of this process was discussed for the ethyl ester as substrate. KEY WORDS: Docosahexaenoic acid, docosahexaenoyl ethyl ester, eicosapentaenoic acid, immobilized lipase, lipase, polyunsaturated fatty acid, triacylglycerol, triarachidonoyl glycerol, tridocosahexaenoyl glycerol, trieicosapentaenoyl glycerol.
