56219-06-8 Usage
Description
Myristoleic Acid Methyl Ester, also known as Methyl Myristoleate, is the methyl ester of myristoleic acid (cis-tetradec-9-enoic acid). It is a colorless liquid that is insoluble in water but soluble in alcohol and ether. Myristoleic Acid Methyl Ester is combustible and has been found to have cytotoxic properties, inducing apoptosis and necrosis in cells.
Uses
Used in Medical Research:
Myristoleic Acid Methyl Ester is used as a cytotoxic inducer of apoptosis and necrosis for medical research purposes. Its ability to induce cell death makes it a valuable compound for studying various diseases and potential treatments.
Used in Organic Synthesis:
Methyl Myristoleate can be used as a reagent or intermediate in organic synthesis, contributing to the development of new chemical compounds and materials.
Used in Pharmaceutical Industry:
Given its cytotoxic properties, Myristoleic Acid Methyl Ester may also be utilized in the pharmaceutical industry for the development of drugs targeting specific diseases, particularly those involving abnormal cell growth or cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 56219-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,1 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56219-06:
(7*5)+(6*6)+(5*2)+(4*1)+(3*9)+(2*0)+(1*6)=118
118 % 10 = 8
So 56219-06-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H28O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15(16)17-2/h6-7H,3-5,8-14H2,1-2H3/b7-6-
56219-06-8Relevant articles and documents
DIRECT METHOD AND REAGENT KITS FOR FATTY ACID ESTER SYNTHESIS
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Page/Page column 18; 21-22; 29, (2008/12/07)
Provided are efficient, cost-effective and water tolerant methods (e.g., single-vial methods) for preparing fatty acid esters from organic matter, comprising: obtaining organic matter comprising at least one fat substituent, contacting the organic matter in a reaction mixture with a basic solution under conditions suitable to provide for hydrolytic release of monomeric fatty acids from the at least one fat substituent to provide a base-treated reaction mixture, and esterifying the monomeric fatty acids of the base-treated reaction mixture by acidification of the reaction mixture and treating in the presence of an organic alcohol to provide fatty acid esters. The methods optionally further comprise, prior to esterifying, neutralizing the base-treated reaction mixture to provide for neutralized fatty acids, separating the neutralized fatty acids from the neutralized reaction mixture, and dissolving the separated fatty acids in the esterification reaction mixture. Also provided are related methods and kits for fat analysis.
