14435-34-8 Usage
Uses
Used in Cosmetics and Pharmaceuticals:
2-Octadecenoic acid methyl ester is used as a solvent, emulsifier, and lubricant in the manufacturing of cosmetics and pharmaceuticals. Its ability to dissolve and stabilize various ingredients makes it an essential component in the formulation of these products.
Used in Industrial Applications:
In the industrial sector, 2-Octadecenoic acid methyl ester serves as a lubricant and emulsifier, contributing to the production of a variety of products. Its properties allow it to improve the performance and efficiency of industrial processes.
Used as a Flavoring Agent and Food Additive:
2-Octadecenoic acid methyl ester is utilized as a flavoring agent and food additive in the production of processed foods. Its mild and pleasant odor enhances the taste and aroma of various food items.
Used in Biofuel Production:
Due to its renewable and biodegradable nature, 2-Octadecenoic acid methyl ester has potential applications as a biofuel. It can be used as an alternative energy source, reducing reliance on fossil fuels and promoting environmental sustainability.
Check Digit Verification of cas no
The CAS Registry Mumber 14435-34-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,3 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14435-34:
(7*1)+(6*4)+(5*4)+(4*3)+(3*5)+(2*3)+(1*4)=88
88 % 10 = 8
So 14435-34-8 is a valid CAS Registry Number.
14435-34-8Relevant academic research and scientific papers
PROCESS FOR THE ISOMERISATION OF SUBSTITUTED ALKENES
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Page/Page column 6-8, (2013/03/26)
The invention relates to a process for the isomerization of unsaturated fatty acids or esters or amides thereof, said process comprising reacting: (a) an unsaturated fatty acid or ester or amide thereof; (b) a source of Pd; (c) a bidentate diphosphine of formula I, R1R2 > P1-R-P2 a lower alcohol; and (e) an acid co-catalyst, under conditions for isomerization to take place. The process is particularly advantageous for the isomerization of substituted alkenes harbouring a hydroxy group when the desired end product has a keto group, such as ricinoleic acid or ester thereof.
