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Structure of 129765-95-3
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This carbamate-protected amino acid derivative features a tert-butoxycarbonyl group flanking a branched aliphatic chain, enabling stable incorporation into peptide synthesis workflows. The sterically hindered methyl substitution enhances resistance to racemization during coupling reactions.
3-[[(1,1-Dimethylethoxy)carbonyl]amino]-3-methylbutanoic acid serves as a stable, bench-ready amino acid equivalent for peptide synthesis, enabling efficient incorporation of N-tert-butoxycarbonyl (Boc)-protected valine derivatives. Its sterically hindered α-carbon enhances selectivity in coupling reactions, while the Boc group offers orthogonal protection compatible with standard deprotection protocols. The molecule facilitates clean functionalization and simplifies purification in multi-step syntheses.
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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: