81281-22-3 Usage
Chemical class
Glycosides
Structure
Glycerol derivative with two tetradecyl groups attached to the first and second carbon atoms, and a glucose molecule attached to the third carbon atom of the glycerol backbone.
Amphiphilic nature
Capable of interacting with both water and oil.
Surfactant properties
Useful for emulsifying, solubilizing, and foaming in various skincare and haircare products.
Applications
a. Cosmetic and personal care products
b. Potential applications in pharmaceuticals and biotechnology
Role in pharmaceuticals and biotechnology
Ability to modify the solubility and bioavailability of drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 81281-22-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,8 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 81281-22:
(7*8)+(6*1)+(5*2)+(4*8)+(3*1)+(2*2)+(1*2)=113
113 % 10 = 3
So 81281-22-3 is a valid CAS Registry Number.
InChI:InChI=1/C37H74O8/c1-4-7-9-11-13-15-17-19-21-23-25-27-30-43-36(40)34(39)33(32-38)45-35(42-29-6-3)37(36,41)44-31-28-26-24-22-20-18-16-14-12-10-8-5-2/h33-35,38-41H,4-32H2,1-3H3/t33-,34-,35+,36-,37-/m1/s1
81281-22-3Relevant articles and documents
Synthesis of 3-O-Glycosyl-1,2-di-O-tetradecyl-sn-glycerol
Ogawa, Tomoya,Beppu, Kazuo
, p. 255 - 262 (2007/10/02)
Ten diether type monoglycosyl and glycobiosyl glycerolipids, including 3-O-(4-O-β-D-galactopyranosyl-β-D-glucopyranosyl)-1,2-di-O-n-tetradecyl-sn-glycerol, a synthetic analogue of lactosyl ceramide, were synthesized and their stereochemistry was assigned
