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Structure of 210345-86-1
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(R)-2-(Aminomethyl)-3-methylbutanoic acid features a chiral α-amino acid scaffold with a branched alkyl side chain, delivering enhanced metabolic stability and favorable solubility for peptide conjugation. This stereodefined building block integrates efficiently into bioactive peptide architectures, enabling precise control over conformation and receptor interaction in drug discovery applications.
(R)-2-(Aminomethyl)-3-methylbutanoic acid serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of bioactive molecules through standard amide and ester formation. Its well-defined stereochemistry and bench-stable carboxylic acid functionality facilitate straightforward derivatization, purification, and incorporation into peptidomimetics or drug candidates requiring branched aliphatic side chains.
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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: