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Structure of 1198791-53-5
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Fmoc-D-Lys(N3)-OH is a chiral, Nα-Fmoc-protected amino acid derivative featuring a trifunctional side chain with a terminal azide group. This configuration enables site-specific conjugation via copper-catalyzed or strain-promoted azide-alkyne cycloaddition, making it ideal for bioconjugation and peptide-based drug discovery workflows. The D-stereoisomer enhances metabolic stability in biological applications.
Fmoc-D-Lys(N3)-OH serves as a key building block for the synthesis of D-amino acid-containing peptides and peptidomimetics. The azide group enables efficient copper-catalyzed or strain-promoted click chemistry, facilitating site-specific conjugation in bioconjugation and combinatorial library development. The Fmoc group provides orthogonal protection for amine functionality during solid-phase peptide synthesis, while the side-chain azide offers high stability and compatibility with standard purification methods.
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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 : 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: