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Structure of 850080-13-6
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This azide-functionalized ester integrates a pyrrolidinone core with a long aliphatic chain, enabling site-specific conjugation in bioorthogonal labeling. The 11-azidoundecanoate moiety delivers enhanced solubility and stability under standard conditions, while the dioxopyrrolidine ring provides controlled reactivity. Designed for efficient coupling in peptide and polymer modification workflows.
2,5-Dioxo-1-pyrrolidinyl 11-azidoundecanoate serves as a versatile bifunctional building block for conjugate addition and strain-promoted azide-alkyne cycloaddition (SPAAC) reactions. The pyrrolidinone carbonyl enables efficient Michael addition with nucleophiles, while the terminal azide group facilitates bioorthogonal ligation. Its stability under ambient conditions and compatibility with diverse functional groups make it well-suited for modular synthesis of peptide-protein conjugates and polymer-drug architectures.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: