Carboxymethyl chito...

Carboxymethyl chitosan 83512-85-0
Carboxymethyl chitosan 83512-85-0
Carboxymethyl chitosan 83512-85-0
Carboxymethyl chitosan 83512-85-0
Carboxymethyl chitosan 83512-85-0

Carboxymethyl chitosan 83512-85-0

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83512-85-0 Carboxymethyl chitosan 83512-85-0 Carboxymethyl chitosan 83512-85-0 Carboxymethyl chitosan

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Product Name: Carboxymethyl chitosan
Synonyms: CARBOXYMETHYL CHITOSAN;N-Carboxymethylchitosan;CARBOXYMETHL CHITOSAN;Chitosan, N-(carboxymethyl);CarboxylMethyl Chitosan
CAS: 83512-85-0
MF: C20H37N3O14
MW: 543.51948
EINECS: 695-802-6
Product Categories: Dextrins、Sugar & Carbohydrates
Mol File: 83512-85-0.mol

Carboxymethyl chitosan Usage And Synthesis
Application
Carboxymethyl chitosan is a biocompatible and biodegradable material that is suitable for various applications such as sustained or controlled release drug delivery, pH-responsive drug delivery, gene delivery as permeation enhancer, Carboxymethyl chitosan is a coating material on nanocarriers.

Chitosan VS Carboxymethyl Chitosan
Compared to chitosan, Carboxymethyl chitosan not only can be applied in wider pH ranges of water since its higher stability, but also has a higher hydrophilicity . The larger specific surface area, a multitude of functional groups and higher hydrophilicity of Carboxymethyl chitosan are expected to play an essential role in more efficiently coordinating with mental oxide and flocculate solrelieving tickle. Carboxymethyl chitosan is an amphoteric poly-saccharide that possesses pH-sensitive property, since it bears both acidic (-COOH) and basic groups (-NH2).

Preparation
Carboxymethyl chitosan can be obtained by direct alkylation of chitosan. The Carboxymethyl chitosan achieved can be in many types: N-carboxymethyl chitosan (N-CMCS), O-carboxymethyl chitosan (O-CMCS), N,O-carboxymethyl chitosan (N,O-CMCS) and N,N-carboxymethyl chitosan (N,N-CMCS). Different reaction conditions will result in the N vs. O selectivity and different degree of substitution (DS). Carboxymethyl chitosan possesses high viscosity, large hydrodynamic volume, film- and gel-forming capabilities together with the other useful properties, such as biocompatibility, biodegradation, biological activity and low toxicity, all of which make it an attractive option in connection with its use in foods and cosmetics.

Chemical Properties Forms gel with water, lower degree of substitution than 5-00936

Details:

Product Name: Carboxymethyl chitosan
Synonyms: CARBOXYMETHYL CHITOSAN;N-Carboxymethylchitosan;CARBOXYMETHL CHITOSAN;Chitosan, N-(carboxymethyl);CarboxylMethyl Chitosan
CAS: 83512-85-0
MF: C20H37N3O14
MW: 543.51948
EINECS: 695-802-6
Product Categories: Dextrins、Sugar & Carbohydrates
Mol File: 83512-85-0.mol

Carboxymethyl chitosan Usage And Synthesis
Application
Carboxymethyl chitosan is a biocompatible and biodegradable material that is suitable for various applications such as sustained or controlled release drug delivery, pH-responsive drug delivery, gene delivery as permeation enhancer, Carboxymethyl chitosan is a coating material on nanocarriers.

Chitosan VS Carboxymethyl Chitosan
Compared to chitosan, Carboxymethyl chitosan not only can be applied in wider pH ranges of water since its higher stability, but also has a higher hydrophilicity . The larger specific surface area, a multitude of functional groups and higher hydrophilicity of Carboxymethyl chitosan are expected to play an essential role in more efficiently coordinating with mental oxide and flocculate solrelieving tickle. Carboxymethyl chitosan is an amphoteric poly-saccharide that possesses pH-sensitive property, since it bears both acidic (-COOH) and basic groups (-NH2).

Preparation
Carboxymethyl chitosan can be obtained by direct alkylation of chitosan. The Carboxymethyl chitosan achieved can be in many types: N-carboxymethyl chitosan (N-CMCS), O-carboxymethyl chitosan (O-CMCS), N,O-carboxymethyl chitosan (N,O-CMCS) and N,N-carboxymethyl chitosan (N,N-CMCS). Different reaction conditions will result in the N vs. O selectivity and different degree of substitution (DS). Carboxymethyl chitosan possesses high viscosity, large hydrodynamic volume, film- and gel-forming capabilities together with the other useful properties, such as biocompatibility, biodegradation, biological activity and low toxicity, all of which make it an attractive option in connection with its use in foods and cosmetics.

Chemical Properties Forms gel with water, lower degree of substitution than 5-00936

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