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Structure of 5968-21-8
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1-Chloropropan-2-amine hydrochloride offers a reactive chloroalkyl handle for nucleophilic substitution, enabling efficient conjugation in peptide synthesis and bioconjugation workflows. This bench-stable salt features enhanced solubility in aqueous and polar organic media, facilitating use under standard conditions. The pendant amine group provides a site for further functionalization.
1-Chloropropan-2-amine hydrochloride serves as a versatile building block in medicinal chemistry, enabling efficient synthesis of β-amino alcohol motifs and nitrogen-containing heterocycles. Its bench-stable hydrochloride salt form facilitates handling and purification, while the chloro group supports nucleophilic substitution reactions for downstream functionalization. Widely used in peptide and small-molecule scaffold elaboration, it functions effectively in standard amine coupling and cyclization protocols.
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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-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: