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Structure of 1221722-25-3
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2-Amino-N-(prop-2-yn-1-yl)acetamide hydrochloride features a reactive alkyne handle and a primary amine group, enabling efficient bioconjugation and click chemistry applications. This bench-stable derivative delivers reliable performance in peptide labeling, probe synthesis, and targeted delivery systems under standard conditions.
2-Amino-N-(prop-2-yn-1-yl)acetamide hydrochloride serves as a versatile building block for bioactive molecule synthesis, enabling efficient access to amide-linked scaffolds via standard coupling protocols. The terminal alkyne functionality facilitates CuAAC click chemistry, while the amino and acetamide groups offer orthogonal reactivity for further derivatization. Bench-stable and readily purified by recrystallization, it functions reliably in peptide and heterocyclic synthesis workflows.
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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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: