Properties
Description
Hydrazide-chondroitin sulfate aldehyde-reactive derivative is generated through carbohydrazide modification, enabling Schiff base formation with ketone or aldehyde groups.
Glycan Name
Chondroitin sulfate
Glycan Structure
The glycan structure of chondroitin sulfate (CS) is a sulfated glycosaminoglycan (GAG) composed of repeating disaccharide units. Each unit consists of:
N-acetyl-D-galactosamine (GalNAc) (β1→4 linked)
D-glucuronic acid (GlcA) (β1→88 linked)
Source
Chemical synthesis
Functional Group
Hydrazide
Impurities
No visible impurities to the naked eye.
Solubility
This product is soluble in most organic solvents, such as DCM, DMF, DMSO, and THF, and exhibits excellent solubility in water.
Identity
Confirmed by NMR.
Applications
Chondroitin sulfate-hydrazide can be used for its potential to engineer epoxide groups for ring-opening reactions with nucleophiles.
