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Structure of 4332-45-0
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This triazole-functionalized carboxylic acid integrates readily into click chemistry workflows, offering a stable, bioorthogonal handle for conjugation. The 1,2,3-triazole moiety provides enhanced metabolic stability and facilitates efficient copper-catalyzed or strain-promoted coupling reactions.
3-(1H-1,2,3-Triazol-1-yl)propanoic acid serves as a versatile building block in click chemistry and bioconjugation workflows. The triazole moiety provides metabolic stability and hydrogen-bonding capacity, while the terminal carboxylic acid enables facile derivatization via amide coupling or esterification. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for synthesizing peptide conjugates, macrocyclic scaffolds, and functionalized polymers in medicinal chemistry and materials science applications.
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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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: