502-73-8 Usage
Description
16-Hentriacontanone is a dialkyl ketone derived from hentriacontane, with the hydrogens at position 16 replaced by an oxo group. This organic compound is characterized by its unique chemical structure and properties, which may have potential applications in various industries.
Uses
Used in Chemical Industry:
16-Hentriacontanone is used as a chemical intermediate for the synthesis of various compounds due to its unique ketone functional group, which can be utilized in a range of chemical reactions.
Used in Pharmaceutical Industry:
16-Hentriacontanone is used as a starting material for the development of new pharmaceutical compounds, potentially targeting specific diseases or conditions. Its unique structure may offer novel therapeutic opportunities.
Used in Cosmetics Industry:
16-Hentriacontanone may be used as an ingredient in the formulation of cosmetics, such as fragrances or skincare products, due to its specific chemical properties that could contribute to the product's efficacy or stability.
Used in Research and Development:
16-Hentriacontanone serves as a valuable compound for research purposes, particularly in the study of organic chemistry, molecular structure, and the development of new synthetic methods or applications.
Check Digit Verification of cas no
The CAS Registry Mumber 502-73-8 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 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 502-73:
(5*5)+(4*0)+(3*2)+(2*7)+(1*3)=48
48 % 10 = 8
So 502-73-8 is a valid CAS Registry Number.
InChI:InChI=1/C31H62O/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31(32)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-30H2,1-2H3
502-73-8Relevant articles and documents
Physico-chemical studies on calcium soaps
Mehrotra, K. N.,Upadhyaya, S. K.
, p. 625 - 627 (1987)
Calcium soaps were prepared by the metathesis of the corresponding potassium soap with an aqueous solution of calcium acetate.The IR results showed that the fatty acids exist in a dimeric structure as a result of hydrogen bonding between the carbonyl groups of two acid molecules, whereas calcium palmitate has an ionic character.The X-ray analysis indicated that the zig-zag chains of the fatty acid radical constituent of the soap molecules extend straigthforward on both sides of each basal plane and that the molecular axes of the soaps are slightly inclined to the basal plane.The thermal decomposition of calcium palmitate was found to be kinetically of zero order and the energy of activation for the decomposition was in the region of 3 KJ/mole.
METHOD FOR PRODUCING HIGHER LINEAR FATTY ACIDS OR ESTERS
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Page/Page column 32-33, (2021/11/26)
The present invention relates to a method of producing linear fatty acids comprising 7 to 28 carbon atoms or esters thereof using a combined biotechnological and chemical method. In particular, the present invention relates to a method of producing dodecanoic acid (i.e. lauric acid), via higher alkanones, preferably 6-undecanone.
PROCESS FOR PRODUCING RENEWABLE PRODUCTS
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Page/Page column 22-23, (2020/07/21)
The present invention relates to a method for producing renewable ketones, paraffin waxes, base oil components and alkenes from a feedstock of biological origin, wherein the method includes ketonisation of esters of fatty acids and monohydric alcohols wherein the alcohols have carbon chain length of two or more.