6129-13-1

Usage

Uses

Used in Pharmaceutical Industry:
(2S)-3-O-Octadecylglycerol is used as an emollient and skin-conditioning agent for its ability to soften and smooth the skin, providing a moisturizing effect.
Used in Cosmetic Industry:
(2S)-3-O-Octadecylglycerol is used as an emollient and skin-conditioning agent in cosmetic products to improve skin texture and hydration, offering a smooth and supple appearance.

Upstream product

• 64-17-5 ethanol 
• 29909-06-6 1-hydroxy-3-octadecyloxy-propan-2-one 

Downstream Products

• 83526-55-0 (R)-1-O-octadecyl-3-(p-toluenesulfonyl)-glycerol 
• 629-93-6 n-iodooctadecane 
• 143996-89-8 1-O-octadecyl-3-O-p-methoxybenzyl-sn-glycerol 
• 113597-35-6 (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (R)-1-octadecyloxymethyl-2-((R)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-ethyl ester 
• 83526-72-1 3-O-Acetyl-1-O-octadecyl-sn-glycerin 
• 593-45-3 octadecane 
• 112-92-5 1-octadecanol 
• 74389-69-8 1-O-octadecyl-2-acetyl-sn-glycero-3-phosphocholine 
• 80483-86-9 2-O-Benzyl-1-O-octadecyl-sn-glycero-3-phosphorylcholin 
• 74430-89-0 Lyso-platelet-activating factor (C₁₈) 
• 105415-93-8 (R)-2-benzyloxy-3-octadecyloxypropyl 2-(N-methylpyrrolidinio)ethyl phosphate 
• 105435-57-2 (R)-2-benzyloxy-3-octadecyloxypropyl 2-(diethylmethylammonio)ethyl phosphate 

Relevant academic research and scientific papers

A kinetic study of the lipase-catalyzed ethanolysis of two short-chain triradylglycerols: Alkylglycerols vs. triacylglycerols

Lipase-catalyzed ethanolysis of two short-chain triradylglycerols, namely tributyrin and 2,3-dibutyroil-1-O-alkylglycerols, have been studied. Much faster rate of reaction for the ethanolysis of tributyrin than that of 2,3-dibutyroil-1-O-alkylglycerols was attained. A kinetic model for the rate of release of ethyl butyrate and for the inactivation of the lipase has been also studied. The parameter corresponding to the release of ethyl butyrate was one order of magnitude higher for ethanolysis of tributyrin than the corresponding of 2,3-dibutyroil-1-O-alkylglycerols.On the contrary, the stability of Novozym 435 during ethanolysis of 2,3-dibutyroil-1-O-alkylglycerols was higher than the corresponding of tributyrin.At the reaction conditions under study, both ethanolysis reactions take place with high selectivity and yield monoesterified alkylglycerols and sn-2 monobutyrin as the main acylglycerols in the reaction mixtures.

Synthesis and Ruthenium-Catalyzed Enantioselective Hydrogenation of 3-O-Substituted 1,3-dihydroxypropan-2-ones

A number of 3-O-substituted 1,3-dihydroxypropan-2-ones have been synthesized in view of their potential use as prochiral precursors of optically active glycerols.Indeed, the oxo-ethers have been reduced to the corresponding 3-O-substituted glycerols via c