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Structure of 263162-13-6
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Tert-butyl (2-((2-aminoethyl)(methyl)amino)ethyl)carbamate features a bifunctional amine handle with tunable basicity, enabling efficient conjugation in bioconjugation workflows. The tert-butyl carbamate group provides robust protection under standard conditions while allowing facile deprotection. This scaffold integrates seamlessly into peptide and oligonucleotide synthesis applications.
Tert-butyl (2-((2-aminoethyl)(methyl)amino)ethyl)carbamate serves as a versatile bifunctional protecting group reagent, enabling selective amino protection in peptide synthesis and late-stage functionalization. Its tert-butyl carbamate moiety offers excellent bench stability and mild acid-labile deprotection, while the pendant primary amine facilitates conjugation or further derivatization. Functions effectively in aqueous and organic media with high compatibility across standard coupling protocols.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: