t-Butoxycarbonyl-PEG3-NHS ester has a t-Boc protecting group and an NHS ester moiety. The t-butyl group can be deprotected under acidic conditions. NHS ester can react specifically and efficiently with primary amines such as the side chain of lysine residues or aminosilane-coated surfaces at neutral or slightly basic conditions to form a covalent bond. The hydrophilic PEG linker increases the water solubility of the compound in aqueous media.
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