Accéder au contenu
Merck
Toutes les photos(1)

Documents

926167

Sigma-Aldrich

Chitosan glycidyl methacrylate

Degree of methacrylation ~20%

Synonyme(s) :

Chitosan acrylate, Chitosan methacrylate, Methacrylate grafted chitosan, Methyl methacrylate modified chitosan

Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme


About This Item

Formule linéaire :
(C13H21NO7)n (C8H13NO5)m
Code UNSPSC :
12352201
Nomenclature NACRES :
NA.23

Niveau de qualité

Température de stockage

2-8°C

Chaîne SMILES 

CO[C@H]1[C@@H](O)[C@@H](N)[C@H](O[C@H]2[C@@H](O)[C@@H](NC(C)=O)[C@H](C)O[C@@H]2CO)O[C@@H]1COCC(O)COC(C(C)=C)=O

Catégories apparentées

Application

The unique physicochemical properties offer chitosan great potential in a range of biomedical applications such as tissue engineering, drug delivery vehicles, and enzyme immobilization for biosensing. Methacrylate functionalized chitosan is thermo/photo cross-linkable and used as a precursor for the fabrication of hydrogels in a wide range of biomedical applications including tissue engineering, 3D bioprinting, and drug and gene delivery. Chitosan-based material also has mucoadhesive properties and hence widely used in transmucosal therapeutics delivery.

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


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

Déjà en possession de ce produit ?

Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Shefali Jaiswal et al.
Carbohydrate polymers, 211, 109-117 (2019-03-03)
A methyl methacrylate (MMA) modified chitosan (CS) conjugate (CSMMA) has been synthesized by a green method via Michael addition reaction between CS and MMA in ethanol. The synthesized conjugate was characterized by FT-IR, 1H NMR, X-ray diffraction spectrometry and SEM
Panita Maturavongsadit et al.
ACS applied bio materials, 4(3), 2342-2353 (2022-01-12)
3D bioprinting has recently emerged as a very useful tool in tissue engineering and regenerative medicine. However, developing suitable bioinks to fabricate specific tissue constructs remains a challenging task. Herein, we report on a nanocellulose/chitosan-based bioink, which is compatible with
Farnoosh Pahlevanzadeh et al.
Materials (Basel, Switzerland), 13(11) (2020-06-18)
Chitosan (CS) has gained particular attention in biomedical applications due to its biocompatibility, antibacterial feature, and biodegradability. Hence, many studies have focused on the manufacturing of CS films, scaffolds, particulate, and inks via different production methods. Nowadays, with the possibility
Oluwadamilola M Kolawole et al.
International journal of pharmaceutics, 550(1-2), 123-129 (2018-08-22)
Chitosan is a cationic polysaccharide that exhibits mucoadhesive properties which allow it to adhere to mucosal tissues. In this work, we explored chemical modification of chitosan through its reaction with methacrylic anhydride to synthesise methacrylated derivative with the aim to
Chandra M Valmikinathan et al.
Soft matter, 8(6), 1964-1976 (2012-02-14)
Hydrogel based scaffolds for neural tissue engineering can provide appropriate physico-chemical and mechanical properties to support neurite extension and facilitate transplantation of cells by acting as 'cell delivery vehicles'. Specifically, in situ gelling systems such as photocrosslinkable hydrogels can potentially

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

Contacter notre Service technique