923842

Alginate Aldehyde

35% aldehyde content, medium viscosity

• Synonyme(s) : Alginate aldehyde, Oxidized alginate
• Formule linéaire : (C₆H₇NaO₆)_n(C₆H₃NaO₆)_m
• Code UNSPSC : 12352201
• Nomenclature NACRES : NA.23

Propriétés

• Niveau de qualité: 100
• Description: Degree of functionalization: 30-40%
• Forme: powder
• Résistance de la couche: 15.6m Ω/sq (25 mum after curing at 150 Celsius for 5 min on glass)
• Couleur: white to off-white
• Adéquation: conforms to structure for NMR
• Température de stockage: 2-8°C
• Chaîne SMILES: CO[C@H]1[C@@H](O)[C@H](O)[C@H](O/C(C=O)=C\C([O-])=O)O[C@@H]1C([O-])=O.OC2[C@H](OC(O)C=O)[C@@H](C([O-])=O)O[C@@H](OC)[C@H]2O

Description

Application

Alginate is an anionic polysaccharide that is widely used in pharmaceutical and biomedical applications due to its non-animal origin, low toxicity, biocompatibility, and biodegradability[1]. Alginate hydrogels are commonly used to fabricate tissue engineering scaffolds[3], bioinks for 3D bioprinting[2][4], and nanocarriers for drug &gene;delivery.

Alginate is commonly crosslinked into a hydrogel via ionic-crosslinking with divalent cations (e.g., Ca²⁺). To prevent matrix degradation, alginate can be functionalized with reactive groups that can be chemically crosslinked, such as aldehydes.[5] Aldehyde- functionalized alginate can be used to prepare hydrogels by reaction with amine groups, such as gelatin through Schiff-base reaction to form a chemical hydrogel. This material can be used in a variety of biomedical applications such as the delivery of drugs, cells, or biomolecules in different tissues, wound healing, and muscle and bone tissue engineering. [6]

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable