83374-51-0 Usage
Chemical structure
A chemical compound consisting of two palmityl groups attached to a glycerol backbone, with a cellobiosyl unit linked to the glycerol molecule through a (1'--3) glycosidic bond.
Surfactant and emulsifier
Commonly used in various skincare and cosmetic products for its ability to reduce surface tension and stabilize mixtures of oil and water.
Moisturizing properties
Known for its ability to help retain moisture in the skin, making it a popular ingredient in skincare products.
Enhances texture and spreadability
Improves the texture and spreadability of creams and lotions, making them easier to apply and more comfortable to use.
Non-toxic and safe for use
Generally considered safe for use in personal care and cosmetic products, as well as in the food and pharmaceutical industries.
Derived from natural sources
The palmityl groups and glycerol in the compound are derived from natural sources, making it an appealing choice for consumers who prefer natural ingredients in their products.
Check Digit Verification of cas no
The CAS Registry Mumber 83374-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,7 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 83374-51:
(7*8)+(6*3)+(5*3)+(4*7)+(3*4)+(2*5)+(1*1)=140
140 % 10 = 0
So 83374-51-0 is a valid CAS Registry Number.
InChI:InChI=1/C47H92O13/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-55-35-37(56-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2)36-57-46-44(54)42(52)45(39(34-49)59-46)60-47-43(53)41(51)40(50)38(33-48)58-47/h37-54H,3-36H2,1-2H3/t37?,38-,39-,40-,41+,42-,43-,44-,45-,46-,47+/m1/s1
83374-51-0Relevant articles and documents
AN EFFICIENT AND STEREOSELECTIVE SYNTHESIS OF 1,2-O-DIALKYL-3-O-β-D-GLYCOSYL-sn-GLYCEROLS
Six, Lambert,Ruess, Klaus-Peter,Lieflaender, Manfred
, p. 1229 - 1232 (2007/10/02)
Long chain 1,2-O-dialkyl-3-β-D-glucosyl-(maltosyl)sn-glycerols - model-compounds for glycolipids of archaebacteria - were efficiently synthetized in a stereochemically unambigous manner.