68797-35-3 Usage
Description
Dipotassium glycyrrhizinate, a derivative of licorice, is a compound known for its anti-irritant, calming, and soothing properties. It is widely recognized for its ability to reduce skin redness and inflammation, making it a valuable ingredient in skincare products, particularly for sensitive and oily skin types.
Uses
Used in Skincare Products:
Dipotassium glycyrrhizinate is used as an active ingredient for its anti-inflammatory and anti-irritant properties, helping to reduce skin redness and inflammation in sensitive skin products.
Used in Pharmaceutical Industry:
Dipotassium glycyrrhizinate is used as an enhancer for improving the dissolution property of amphotericin B (AMB) and increasing the bioavailability of the drug incorporated in suppositories, thereby improving the efficacy of the medication.
Check Digit Verification of cas no
The CAS Registry Mumber 68797-35-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,7,9 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 68797-35:
(7*6)+(6*8)+(5*7)+(4*9)+(3*7)+(2*3)+(1*5)=193
193 % 10 = 3
So 68797-35-3 is a valid CAS Registry Number.
InChI:InChI=1/C42H62O16.2K/c1-37(2)21-8-11-42(7)31(20(43)16-18-19-17-39(4,36(53)54)13-12-38(19,3)14-15-41(18,42)6)40(21,5)10-9-22(37)55-35-30(26(47)25(46)29(57-35)33(51)52)58-34-27(48)23(44)24(45)28(56-34)32(49)50;;/h16,19,21-31,34-35,44-48H,8-15,17H2,1-7H3,(H,49,50)(H,51,52)(H,53,54);;/q;2*+1/p-2/t19-,21-,22-,23-,24-,25-,26-,27+,28-,29-,30+,31+,34-,35-,38+,39-,40-,41+,42+;;/m0../s1
68797-35-3Relevant articles and documents
TRANSFORMATIONS OF GLYCYRRHIZIC ACID. III.* SYNTHESIS OF NEW GLYCOPEPTIDES CONTAINING METHYL ESTERS OF AMINO ACIDS
Baltina, L. A.,Tolstikov, G. A.
, p. 1115 - 1120 (2007/10/02)
A new selective method has been proposed for the preparation of glycopeptides of β-glycyrrhizic acid (I) containing fragments of methyl esters of amino acids by reacting tris-N-hydroxysuccinimidic ester of a glycoside, obtained in situ using N,N'-dicyclohexylcarbodiimide, with hydrochlorides of methyl esters of amino acids or dipeptides in the presence of triethylamine.
