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Structure of 52815-19-7
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Boc-3-aminobutanoic acid features a tert-butoxycarbonyl-protected amine group flanked by a carboxylic acid, enabling direct incorporation into peptide chains or conjugation workflows. The stable Boc moiety facilitates selective deprotection under mild acidic conditions, while the aliphatic backbone supports efficient coupling reactions in solid-phase synthesis.
3-((tert-Butoxycarbonyl)amino)butanoic acid serves as a versatile building block in peptide synthesis and medicinal chemistry, enabling efficient incorporation of γ-amino acid motifs. The Boc-protected amine and carboxylic acid functionalities offer orthogonal reactivity, facilitating sequential coupling reactions with high stability under standard conditions. Its bench-stable nature and ease of purification support scalable synthesis workflows and direct use in constructing bioactive heterocycles and peptidomimetics.
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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: