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Structure of 1056024-94-2
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N3-PEG3-CH2CH2COOH features a triazole-linked PEG3 spacer terminating in a carboxylic acid group, enabling site-specific conjugation via amine coupling. This bifunctional reagent combines enhanced stability with efficient bioconjugation, ideal for labeling proteins, peptides, or biomolecules under physiological conditions.
N3-PEG3-CH2CH2COOH serves as a versatile bifunctional linker for bioconjugation and peptide synthesis, combining the robustness of a triazole-forming azide group with a C-terminal carboxylic acid for amide bond formation. The three-ethylene glycol spacer enhances solubility and reduces non-specific binding, while the aliphatic tether ensures minimal steric interference. This reagent enables efficient site-specific conjugation in aqueous environments, facilitating the construction of protein-drug conjugates, PEGylated peptides, and functionalized biomaterials.
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Lot numbers can be found on the outside label of a product: