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Structure of 54895-12-4
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This protected amino acid derivative features a tert-butoxycarbonyl (Boc) group that ensures stability and ease of handling during peptide synthesis. The 3-methylbutanoic acid backbone provides a hydrophobic, sterically hindered scaffold ideal for incorporation into complex peptide sequences. Its bench-stable nature facilitates straightforward manipulation under standard conditions.
2-((tert-Butoxycarbonyl)amino)-3-methylbutanoic acid serves as a versatile building block in peptide synthesis, enabling efficient incorporation of N-terminal amino acids with side-chain stability. The tert-butyl carbamate (Boc) group provides robust protection under acidic conditions, while the branched aliphatic chain enhances solubility and minimizes epimerization during coupling. Its well-defined reactivity facilitates straightforward deprotection and integration into complex scaffolds for medicinal chemistry applications.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: