Sodium Hyaluronate - Ph.Eur. , CAS No.9067-32-7

CAS: 9067-32-7 Cat. No.: S774025 Fórmula: (C₁₄H₂₁NaNO₁₁)n   Número CE: 618-620-0

GRADE & PURITY Ph.Eur.

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Visão geral

Hyaluronic acid is the main component of connective tissues such as intercellular matrix, vitreous humor, and synovial fluid in the human body. It plays an important physiological role in water retention, maintaining extracellular space, regulating osmotic pressure, lubrication, and promoting cell repair in the body. Hyaluronic acid molecules contain a large number of carboxyl and hydroxyl groups, which form hydrogen bonds within and between molecules in aqueous solutions, giving them strong water retention properties and the ability to bind to over 400 times their own amount of water; At higher concentrations, the complex tertiary network structure formed by intermolecular interactions exhibits significant viscoelasticity in its aqueous solution. Hyaluronic acid, as the main component of the intercellular matrix, directly participates in the regulation of electrolyte exchange inside and outside the cell, playing a filtering role in physical and molecular information. Large molecule hyaluronic acid has inhibitory effects on cell movement, proliferation, differentiation, and phagocytic function, while small molecule hyaluronic acid has promoting effects. Hyaluronic acid has unique physicochemical properties and physiological functions, and has been widely used in medicine

Specifications

Especificações e pureza

Ph.Eur.

Condições de armazenamento de armazenamento

Store at -20°C,Argon charged

Enviado em

Ice chest + Ice pads

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Grau

Ph.Eur.

Nomes e identificadores

Sorrisos canónicos

CC(=O)NC1CC(C(OC1OC2C(C(C(OC2C(=O)[O-])O)O)O)CO)O.[Na+]

InChIKey

MAKUBRYLFHZREJ-JWBQXVCJSA-M

INCHI

1S/C14H23NO11.Na/c1-4(17)15-5-2-6(18)7(3-16)24-14(5)26-10-8(19)9(20)13(23)25-11(10)12(21)22;/h5-11,13-14,16,18-20,23H,2-3H2,1H3,(H,15,17)(H,21,22);/q;+1/p-1/t5-,6+,7-,8-,9-,10+,11+,13-,14+;/m1./s1

SMILES isoméricas

CC(=O)N[C@@H]1C[C@@H]([C@H](O[C@H]1O[C@H]2[C@@H]([C@H]([C@@H](O[C@@H]2C(=O)[O-])O)O)O)CO)O.[Na+]

WGK Alemanha

3

RTECS

MT7250000

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Sugar acids and derivatives
          • Level6 Glucuronic acid derivatives

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Sugar acids and derivatives
• Direct Parent: Glucuronic acid derivatives
• Alternative Parents: Disaccharides Oxanes Pyrans Acetamides Secondary alcohols Carboxylic acid salts Secondary carboxylic acid amides Hemiacetals Polyols Acetals Oxacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Hydrocarbon derivatives Organic oxides Organic sodium salts Organic zwitterions Organonitrogen compounds Carbonyl compounds Organopnictogen compounds Primary alcohols
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Glucuronic acid or derivatives - Disaccharide - Oxane - Pyran - Acetamide - Carboxamide group - Carboxylic acid salt - Hemiacetal - Secondary alcohol - Secondary carboxylic acid amide - Acetal - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Monocarboxylic acid or derivatives - Organic alkali metal salt - Polyol - Organoheterocyclic compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Alcohol - Organopnictogen compound - Primary alcohol - Organic sodium salt - Organic salt - Organic zwitterion - Aliphatic heteromonocyclic compound
• Descrição: This compound belongs to the class of organic compounds known as glucuronic acid derivatives. These are compounds containing a glucuronic acid moiety (or a derivative), which consists of a glucose moiety with the C6 carbon oxidized to a carboxylic acid.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propriedades químicas e físicas

• Sensibilidade: Moisture sensitive