26247-79-0 Usage
Description
POLY-L-GLUTAMIC ACID SODIUM SALT, also known as gamma-Polyglutamic Acid Sodium Salt, is a technical-grade compound derived from the polymerization of L-glutamic acid. It is a solid substance with unique chemical properties that make it suitable for various applications, particularly in the cosmetic and pharmaceutical industries.
Uses
Used in Cosmetic Industry:
POLY-L-GLUTAMIC ACID SODIUM SALT is used as an ingredient in skincare products for its moisturizing effect, ability to enhance skin absorption, and its role in repairing damaged skin cells. Its properties contribute to the overall health and appearance of the skin, making it a valuable addition to cosmetic formulations.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, POLY-L-GLUTAMIC ACID SODIUM SALT can be utilized for its potential therapeutic applications, such as in drug delivery systems or as a component in the development of new medications. Its solid form and chemical properties may offer advantages in formulating and stabilizing pharmaceutical products.
Biochem/physiol Actions
Poly-L-glutamic acid is an anionic biocompatible polymer used in combination with cationic biopolymers such as poly-lysine to form stable time-release controlled polyelectrolyte shells to protect drug and molecular delivery structures such as protein-loaded starch microgels and nanocapsules.
Check Digit Verification of cas no
The CAS Registry Mumber 26247-79-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,2,4 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 26247-79:
(7*2)+(6*6)+(5*2)+(4*4)+(3*7)+(2*7)+(1*9)=120
120 % 10 = 0
So 26247-79-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H23N3O10/c16-7(1-4-10(19)20)13(25)17-8(2-5-11(21)22)14(26)18-9(15(27)28)3-6-12(23)24/h7-9H,1-6,16H2,(H,17,25)(H,18,26)(H,19,20)(H,21,22)(H,23,24)(H,27,28)/t7-,8-,9-/m0/s1
26247-79-0Relevant articles and documents
CAGED COMPOUND, AND MANUFACTURING METHOD AND EXPRESSION METHOD OF CAGED COMPOUND
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Paragraph 0166; 0167, (2019/03/01)
PROBLEM TO BE SOLVED: To provide a caged compound excellent in light reactivity and dark place stability, and capable of deprotection by a visible light. SOLUTION: A caged compound is represented by the following general formula (1). In the general formula (1), R1 represents a hydrogen atom, a halogen atom, an alkyl group, an aryl group, a cyano group, an alkoxy group, a hydroxy group, or an alkylamino group, R2 represents an alkyl group or a hetero atom other than a nitrogen atom, R3 represents a hydrogen atom, a halogen atom or an alkyl group, X represents a monovalent anion, Y represents a monovalent organic group, Z represents a hydrogen atom or a monovalent organic group, and a represents 0 or 1, however a represents 0 when R2 represents the hetero atom other than the nitrogen atom. SELECTED DRAWING: None COPYRIGHT: (C)2019,JPOandINPIT
Process for chemical reaction of amino acids and amides yielding selective conversion products
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Page 7-8, (2008/06/13)
The invention relates to processes for converting amino acids and amides to desirable conversion products including pyrrolidines, pyrrolidinones, and other N-substituted products. L-glutamic acid and L-pyroglutamic acid provide general reaction pathways to numerous and valuable selective conversion products with varied potential industrial uses.
