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Structure of 332064-94-5
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Fmoc-R-3-amino-5-hexynic acid features a terminal alkyne group flanked by a protected amine and a robust Fmoc handle, enabling efficient solid-phase peptide synthesis. This orthogonal functionality facilitates site-specific conjugation via copper-catalyzed azide-alkyne cycloaddition, delivering stable triazoles for bioconjugation applications.
Fmoc-R-3-amino-5-hexynic acid serves as a versatile building block for the synthesis of peptidomimetics and bioconjugates, enabling efficient CuAAC click chemistry via its terminal alkyne group. The Fmoc-protected amine facilitates standard solid-phase peptide synthesis, while the carboxylic acid functionality supports direct coupling or derivatization. Its stability under routine bench conditions and compatibility with orthogonal functional groups make it ideal for modular assembly of complex molecular architectures.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P501
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Lot numbers can be found on the outside label of a product: