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Structure of 144222-23-1
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tert-Butyl (4-aminobutyl)(methyl)carbamate features a protected primary amine handle ideal for bioconjugation workflows. The tert-butyl carbamate group enables orthogonal deprotection under mild acidic conditions, while the pendant amino functionality supports coupling reactions with activated esters or aldehydes. This bifunctional scaffold integrates seamlessly into peptide and oligonucleotide synthesis, offering enhanced solubility and stability during purification steps.
tert-Butyl (4-aminobutyl)(methyl)carbamate serves as a versatile protected amine building block, enabling efficient access to polyamine scaffolds and bioactive heterocycles. The tert-butyl carbamate (Boc) group provides excellent bench stability and orthogonal deprotection under mild acidic conditions, while the primary amine and methylated secondary amine functionalities allow for sequential functionalization. This compound facilitates diverse transformations in peptide extension, macrocyclization, and medicinal chemistry campaigns.
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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: