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Structure of 202207-78-1
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tert-Butyl (2-aminoethyl)(methyl)carbamate hydrochloride delivers a protected amine handle for peptide synthesis and bioconjugation. This bench-stable, moisture-tolerant derivative features a tertiary butyl carbamate group that enables selective deprotection under mild acidic conditions. The pendant primary amine supports efficient coupling reactions, while the hydrochloride salt enhances solubility in aqueous and polar organic media.
tert-Butyl (2-aminoethyl)(methyl)carbamate hydrochloride serves as a protected derivative of 2-aminoethylmethylamine, offering bench-stable handling and improved solubility in organic media. It functions as a versatile building block in peptide synthesis and medicinal chemistry, enabling selective introduction of aminoalkyl side chains. The tert-butyl carbamate group is compatible with standard deprotection protocols, while the methylamino functionality supports further functionalization via coupling reactions or cyclization pathways.
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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: