926167
Chitosan glycidyl methacrylate
Degree of methacrylation ~20%
Synonym(s):
Chitosan acrylate, Chitosan methacrylate, Methacrylate grafted chitosan, Methyl methacrylate modified chitosan
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About This Item
Linear Formula:
(C13H21NO7)n (C8H13NO5)m
UNSPSC Code:
12352201
NACRES:
NA.23
Recommended Products
Quality Level
storage temp.
2-8°C
SMILES string
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
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.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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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
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
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