544-57-0 Usage
Description
2-HYDROXYTETRACOSANOIC ACID, also known as lignoceric acid with a 2-hydroxy substituent, is a very long-chain hydroxy fatty acid derived from lignoceric acid. It possesses unique structural properties that make it suitable for various applications across different industries.
Uses
Used in Pharmaceutical Industry:
2-HYDROXYTETRACOSANOIC ACID is used as an active pharmaceutical ingredient for its potential therapeutic effects. 2-HYDROXYTETRACOSANOIC ACID's unique structure allows it to interact with specific biological targets, making it a promising candidate for the development of new drugs.
Used in Cosmetic Industry:
In the cosmetic industry, 2-HYDROXYTETRACOSANOIC ACID is used as an ingredient in skincare and hair care products for its moisturizing and emollient properties. Its long-chain structure enables it to penetrate and nourish the skin, providing hydration and improving skin texture.
Used in Chemical Industry:
2-HYDROXYTETRACOSANOIC ACID is used as a raw material in the synthesis of various chemicals and materials, such as surfactants, lubricants, and polymers. Its unique hydroxyl group allows for further chemical modifications, expanding its potential applications in the chemical industry.
Used in Research and Development:
2-HYDROXYTETRACOSANOIC ACID serves as a valuable compound for research purposes, particularly in the fields of biochemistry, pharmacology, and materials science. Its unique structure and properties make it an interesting subject for studying the effects of hydroxyl substitution on the properties and functions of long-chain fatty acids.
Used in Nutritional Supplements:
As a component of nutritional supplements, 2-HYDROXYTETRACOSANOIC ACID may provide health benefits due to its potential role in energy metabolism and its ability to support cellular functions. Its long-chain structure and hydroxyl group may contribute to its bioavailability and efficacy as a dietary supplement.
Check Digit Verification of cas no
The CAS Registry Mumber 544-57-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 544-57:
(5*5)+(4*4)+(3*4)+(2*5)+(1*7)=70
70 % 10 = 0
So 544-57-0 is a valid CAS Registry Number.
InChI:InChI=1/C24H48O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23(25)24(26)27/h23,25H,2-22H2,1H3,(H,26,27)
544-57-0Relevant articles and documents
Synthesis and absolute configuration of 6-hydroxylated new ceramides in human skin, ceramides B, 4, 7 and 8
Masuda, Yui,Mori, Kenji
, p. 4789 - 4800 (2005)
6R-Configuration was assigned to three new ceramides isolated from human skin such as ceramide B [1, (2S,3R,4E,6R)-6-hydroxy-N-(30′- hydroxytriacontanoyl)-4-sphingenine], ceramide 8 [2, (2S,3R,4E,6R)-6-hydroxy-N- (tetracosanoyl)-4-sphingenine] and ceramide 4 {3, (2S,3R,4E,6R)-6-hydroxy-N- [(30′-linoleoyloxy)triacontanoyl]-4-sphingenine}. (6R,2′ R)-Configuration was given to another ceramide in human skin, ceramide 7 [4, (2S,3R,4E,6R,2′ R)-6-hydroxy-N-(2′-hydroxytetracosanoyl)-4- sphingenine]. These assignments were made possible by enzymatic preparation of the enantiomers of 1-pentadecyn-3-ol and those of 2-hydroxytetracosanoic acid. Wiley-VCH Verlag GmbH & Co. KGaA, 2005.
Selective N-acylation of amino alcohols
-
, (2008/06/13)
The present invention provides an efficient method for the production of N-acyl amino alcohols via the selective acylation of the free amines of amino alcohols by reacting with an organic acid or a salt thereof with an alkyl sulfonyl chloride or an alkyl phenyl sulfonyl chloride, in an organic solvent and in the presence of an organic base, to form the corresponding mixed anhydride, followed by reacting the mixed anhydride with an amino alcohol or a salt thereof to form the corresponding N-acyl amino alcohol.
