Ɑ-Propargylacetamido-ω-Iodoacetamido PEG

PEGylation reagent for "Click" Chemistry. This PEG crosslinking reagent with a terminal alkyne functionality on one chain end reacts with azides under "Click" Chemistry conditions (for example Cu (I) catalyzed alkyne-azide cycloaddition, CuAAC) to form a stable triazole link between the two reaction partners. The iodoacetamide group is known for its ability to react selectively with cysteine residues in proteins or other thiols, forming stable covalent bonds via thioether linkage. This allows for the site-specific pegylation of proteins, enabling the attachment of various functional groups on the other chain end of the PEG linker. Iodacetamide PEGs react with other nucleophiles to a significantly lesser degree.