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Structure of 1310680-18-2
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This protected amino acid derivative features a tert-butoxycarbonyl (Boc) group that enables stable incorporation into peptide synthesis workflows. The sterically hindered dimethylbutanoic acid backbone enhances solubility and reduces racemization risk during coupling. Ideal for constructing complex peptide architectures under standard conditions.
4-((tert-Butoxycarbonyl)amino)-3,3-dimethylbutanoic acid serves as a versatile building block in peptide synthesis and medicinal chemistry. The Boc-protected amine and terminal carboxylic acid enable sequential functionalization, while the sterically hindered tert-butyl group enhances stability and simplifies purification. It facilitates efficient coupling reactions and acts as a key intermediate in constructing complex scaffolds for API development.
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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: