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Structure of 1421933-39-2
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Bromoacetamido-PEG3-NH-Boc features a reactive bromoacetamide group flanked by a triethylene glycol spacer and a Boc-protected amine. This bifunctional reagent enables site-specific conjugation in bioconjugation workflows, combining efficient nucleophilic displacement with orthogonal protection for downstream deprotection and functionalization.
Bromoacetamido-PEG3-NH-Boc serves as a versatile bifunctional linker for bioconjugation and peptide synthesis, enabling site-specific attachment via nucleophilic substitution at the bromoacetamide group. The PEG3 spacer enhances solubility and reduces steric hindrance, while the Boc-protected amine allows for subsequent deprotection and coupling. This reagent exhibits excellent bench stability and compatibility with diverse functional groups, facilitating efficient conjugation workflows in antibody-drug conjugate (ADC) development and peptidomimetic design.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: