Properties
Description
Thiolated hyaluronic acid derivatives (hyaluronate-SH) incorporate sulfhydryl groups directly onto the polysaccharide backbone, enabling redox-responsive material formulations.
Glycan Structure
The glycan structure of hyaluronate (hyaluronic acid, HA) is a linear, non-sulfated glycosaminoglycan composed of repeating disaccharide units.
Source
Chemical synthesis
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
Hyaluronate-SH plays a key role in facilitating crosslinking in bioink formulations for 3D bioprinting applications.