506-21-8 Usage
Uses
Used in the Food Industry:
Linoelaidic acid is used as an ingredient in the food industry for the production of partially hydrogenated oils. These oils are valued for their stability, flavor, and texture, making them suitable for various culinary applications, such as frying and baking.
Used in the Chemical Industry:
Linoelaidic acid can be utilized as a raw material in the chemical industry for the synthesis of various compounds and materials. Its unique structural properties, including the presence of trans double bonds, make it a valuable component in the development of new products and technologies.
Used in the Pharmaceutical Industry:
Linoelaidic acid may have potential applications in the pharmaceutical industry, particularly in the development of drugs targeting specific biological pathways. Its unique chemical structure could be exploited to design novel therapeutic agents with improved efficacy and selectivity.
Used in the Cosmetics Industry:
In the cosmetics industry, linoelic acid could be employed as an ingredient in the formulation of various products, such as creams, lotions, and moisturizers. Its properties may contribute to improved skin hydration, texture, and overall appearance.
Used in the Biodiesel Industry:
Linoelaidic acid can be used as a component in the production of biodiesel, a renewable and environmentally friendly alternative to traditional fossil fuels. Its presence in partially hydrogenated oils makes it a suitable candidate for blending with other biofuels to improve their performance and reduce emissions.
Check Digit Verification of cas no
The CAS Registry Mumber 506-21-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 506-21:
(5*5)+(4*0)+(3*6)+(2*2)+(1*1)=48
48 % 10 = 8
So 506-21-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h6-7,9-10H,2-5,8,11-17H2,1H3,(H,19,20)/b7-6-,10-9-
506-21-8Relevant academic research and scientific papers
Method of producing dicarboxylic acids
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Page/Page column 11; 13; 17-18, (2009/05/29)
A method of producing dicarboxylic acids (e.g., α,ω dicarboxylic acids) by reacting a compound having a terminal COOH (e.g., unsaturated fatty acid such as oleic acid) and containing at least one carbon-carbon double bond with a second generation Grubbs catalyst in the absence of solvent to produce dicarboxylic acids. The method is conducted in an inert atmosphere (e.g., argon, nitrogen). The process also works well with mixed unsaturated fatty acids obtained from soybean, rapeseed, tall, and linseed oils.
