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28874-51-3

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28874-51-3 Usage

Uses

sodium PCA (Ajidew NaPCA, Nalidone) is a high-performance humectant given its moisture-binding ability. Sodium PCA is a component of the skin’s natural moisturizing factor. For cosmetic use, it is derived from amino acids. It is considered a noncomedogenic, non-allergenic raw material recommended for dry, delicate, and sensitive skins.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 28874-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,8,7 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 28874-51:
(7*2)+(6*8)+(5*8)+(4*7)+(3*4)+(2*5)+(1*1)=153
153 % 10 = 3
So 28874-51-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H7NO3.Na/c7-4-2-1-3(6-4)5(8)9;/h3H,1-2H2,(H,6,7)(H,8,9);/q;+1/p-1/t3-;/m0./s1

28874-51-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Sodium L-pyroglutamate

1.2 Other means of identification

Product number -
Other names sodium 5-oxo-L-prolinate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:28874-51-3 SDS

28874-51-3Synthetic route

monosodium glutamate
142-47-2

monosodium glutamate

sodium L-pyroglutamate
28874-51-3

sodium L-pyroglutamate

Conditions
ConditionsYield
In water at 180℃; for 2h;
sodium L-pyroglutamate
28874-51-3

sodium L-pyroglutamate

zinc pidolate

zinc pidolate

Conditions
ConditionsYield
With nitric acid; zinc(II) sulfate In water at 20℃; for 0.5h; pH=3.7 - 5.2;
sodium L-pyroglutamate
28874-51-3

sodium L-pyroglutamate

Succinimide
123-56-8

Succinimide

Conditions
ConditionsYield
With ammonium peroxydisulfate; silver nitrate In water at 20℃; for 2h;

28874-51-3Downstream Products

28874-51-3Relevant articles and documents

Zinc pyrrolidonecarboxylate dihydrate and method of producing the same

-

Page/Page column 7, 8, (2008/06/13)

The present invention aims at providing a convenient method of producing zinc pyrrolidonecarboxylate dihydrate, which is an industrially useful compound, with high optical purity, a higher yield, and better dissolution property. The present invention also provides a convenient method of producing zinc pyrrolidonecarboxylate dihydrate with higher optical purity, a higher yield, and better solution property by adding a zinc salt to an aqueous medium containing a salt of pyrrolidonecarboxylic acid as a starting material and separating a crystal from the aqueous medium at a specific pH.

Metal Binding by Amino Acids: Preparation and Crystal Structures of Lithium, Sodium, and Potassium Hydrogen Bis-L-pyroglutamate

Kumberger, Otto,Riede, Juergen,Schmidbaur, Hubert

, p. 1829 - 1834 (2007/10/02)

Lithium, sodium and potassium bis-L-pyroglutamate , , and , respectively, have been prepared by reaction of aqueous solutions of the metal hydroxides with L-pyroglutamic acid in the molar ratio 1:2, or in methanol.Crystalline samples of the salts could be obtained by slow evaporation of solutions of the salts in methanol.In the solid state, Li(L-pGlu)(L-pGluH) adopts a chain structure with the lithium atoms arranged in double strands.Adjacent metal centers are bridged by the carboxylate groups of the L-pGlu- ligands.The L-pGluH ligands are attached to the metal centers through the amide oxygen atoms.Na(L-pGlu)(L-pGluH) forms a three-dimensional coordination polymer with two half-occupied sodium positions, one L-pGlu- and one L-GluH ligand in the asymmetric unit.The carboxyl and carboxylate groups of the L-pGluH and the L-pGlu- ligands are bridging the sodium centers, giving rise to eight-membered rings, which consist of two sodium atoms, a carboxyl and a carboxylate group.The hydrogen atoms of the carboxyl group of the L-pGluH ligands are involved in strong hydrogen bonds between a carboxyl and an adjacent carboxylate oxygen atom.K(L-pGlu)(L-pGluH) adopts a layer structure with strands of potassium atoms.The metal centers are connected through bridging carboxyl and carboxylate groups of the L-pGluH and L-pGlu- ligands, respectively.The structure features eight-membered ring units comparable to those observed for Na(L-pGlu)(L-pGluH), again with the hydrogen atom of the carboxyl group engaged in a strong transannular hydrogen bond.The amide oxygen atoms of the L-pGlu- and the L-pGluH ligands are coordinated to the metal centers of adjacent coordination chains.The results of 1H- and 13C-NMR investigations of aqueous solutions of the compounds indicate extensive electrolytic dissociation in diluted solutions. Key Words: Hydrogen bis-L-pyroglutamates, lithium, sodium, potassium / Pyroglutamate coordination and conformation

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