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Structure of 874831-66-0
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tert-Butyl 4-(methylamino)butylcarbamate features a protected amine handle ideal for peptide synthesis and bioconjugation. The tert-butyl carbamate group enables selective deprotection under mild acidic conditions, while the primary methylaminoalkyl side chain offers a reactive site for coupling. This stable, bench-ready reagent integrates seamlessly into diverse molecular architectures.
tert-Butyl 4-(methylamino)butylcarbamate serves as a versatile bifunctional building block in medicinal chemistry, enabling the synthesis of bioactive amines and heterocyclic scaffolds. The tert-butyl carbamate (Boc) group provides stable protection under basic conditions and mild acidic deprotection, while the primary amine functionality facilitates conjugation reactions. Its methylamino substituent enhances solubility and metabolic stability in downstream analogs, making it ideal for iterative synthesis workflows requiring orthogonal functionalization.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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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: