Properties
Description
Iodoacetate-mannose conjugates incorporate halogenated acetyl groups covalently bonded to carbohydrate structures, enabling thiol-selective alkylation reactions alongside sugar-mediated biological interactions.
Source
Chemical synthesis
Functional Group
Iodoacetate
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
Mannose-iodoacetate can be used for its potential to alkylate cysteine residues in site-directed protein modification research.