20294-76-2 Usage
Description
Octadecane-1,2-diol, also known as Glycerol, is a glycol that is octadecane bearing two hydroxy substituents located at positions 1 and 2. It is a versatile compound with various applications across different industries due to its unique chemical properties.
Uses
Used in Cosmetics Industry:
Octadecane-1,2-diol is used as a moisturizing agent for its ability to retain moisture and improve skin hydration. It helps maintain the skin's natural barrier and provides a smooth texture.
Used in Pharmaceutical Industry:
Octadecane-1,2-diol is used as a pharmaceutical excipient for its solubilizing properties, which aid in the formulation of various drugs and medications. It enhances the bioavailability and stability of active ingredients.
Used in Food Industry:
Octadecane-1,2-diol is used as an additive for its emulsifying and stabilizing properties, which help maintain the consistency and texture of various food products.
Used in Lubricants Industry:
Octadecane-1,2-diol is used as a lubricant for its ability to reduce friction and wear in mechanical applications, improving the performance and lifespan of machinery.
Used in Polymer Industry:
Octadecane-1,2-diol is used as a monomer in the synthesis of various polymers, contributing to the development of new materials with specific properties for different applications.
Used in Energy Storage:
Octadecane-1,2-diol is used as an additive in the development of advanced energy storage systems, such as lithium-ion batteries, due to its ability to improve the performance and safety of these systems.
Check Digit Verification of cas no
The CAS Registry Mumber 20294-76-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,9 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20294-76:
(7*2)+(6*0)+(5*2)+(4*9)+(3*4)+(2*7)+(1*6)=92
92 % 10 = 2
So 20294-76-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H38O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-18(20)17-19/h18-20H,2-17H2,1H3
20294-76-2Relevant articles and documents
Triflic acid catalyzed oxidative lactonization and diacetoxylation of alkenes using peroxyacids as oxidants
Kang, Yan-Biao,Gade, Lutz H.
experimental part, p. 1610 - 1615 (2012/04/04)
A clean and efficient diacetoxylation reaction of alkenes catalyzed by triflic acid using commercially available peroxyacids as the oxidants has been developed. This method was also applied in oxidative lactonizations of unsaturated carboxylic acids in good to high yields.
Structure-activity relationship of α-galactosylceramides against b16- bearing mice
Morita,Motoki,Akimoto,Natori,Sakai,Sawa,Yamaji,Koezuka,Kobayashi,Fukushima
, p. 2176 - 2187 (2007/10/02)
Agelasphin-9b, (2S,3S,4R)-1-O-(α-D-galactopyranosyl)-16-methyl-2-[N- ((R)-2-hydroxytetracosanoyl)-amino]-1,3,4-heptadecanetriol, is a potent antitumor agent isolated from the marine sponge Agelas mauritianus. Various analogues of agelasphin-9b (a lead compound) were synthesized, and the relationship between their structures and biological activities was examined using several assay systems. From the results, KRN7000, (2S,3S,4R)-1-O-(α- D-galactopyranosyl)-2-(N-hexacosanoylamino)-1,3,4-octadecanetriol, was selected as a candidate for clinical application.
