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Structure of 165391-09-3
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tert-Butyl (2-(2-aminoethoxy)ethyl)carbamate hydrochloride delivers a protected amine handle for peptide and oligonucleotide synthesis. This bench-stable, moisture-tolerant derivative features a cleavable carbamate linkage that enables selective deprotection under mild acidic conditions, streamlining conjugation workflows in chemical biology and medicinal chemistry applications.
tert-Butyl (2-(2-aminoethoxy)ethyl)carbamate hydrochloride serves as a stable, bench-ready precursor for the introduction of aminoalkoxy functionalities. It facilitates efficient amine incorporation in peptide conjugation and heterocyclic synthesis, offering excellent solubility and compatibility with standard coupling conditions. The protected amine functionality enables selective deprotection under mild acidic conditions, supporting iterative synthesis workflows in medicinal chemistry and API development.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: