tert-butyl (3,6,9,12-tetraoxapentadec-14-yn-1-yl)carbamate

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Reagent Code: #241976
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CAS Number 1219810-90-8

science Other reagents with same CAS 1219810-90-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 331.41 g/mol
Formula C₁₆H₂₉NO₆
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a bifunctional linker in bioconjugation and pharmaceutical synthesis, particularly in the preparation of antibody-drug conjugates (ADCs) and PEGylated compounds. The tert-butyl carbamate (Boc) group provides a protected amine that can be selectively deprotected under mild acidic conditions, allowing for controlled coupling to biomolecules. The terminal alkyne enables efficient conjugation via copper-catalyzed azide-alkyne cycloaddition (CuAAC), commonly known as click chemistry, making it valuable in drug discovery, bioconjugation, and the development of diagnostic probes. Its polyether (PEG-like) spacer enhances solubility and improves pharmacokinetic properties of conjugated molecules.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,400.00
inventory 250mg
10-20 days ฿4,140.00
inventory 1g
10-20 days ฿15,600.00

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tert-butyl (3,6,9,12-tetraoxapentadec-14-yn-1-yl)carbamate
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Used as a bifunctional linker in bioconjugation and pharmaceutical synthesis, particularly in the preparation of antibody-drug conjugates (ADCs) and PEGylated compounds. The tert-butyl carbamate (Boc) group provides a protected amine that can be selectively deprotected under mild acidic conditions, allowing for controlled coupling to biomolecules. The terminal alkyne enables efficient conjugation via copper-catalyzed azide-alkyne cycloaddition (CuAAC), commonly known as click chemistry, making it valuabl

Used as a bifunctional linker in bioconjugation and pharmaceutical synthesis, particularly in the preparation of antibody-drug conjugates (ADCs) and PEGylated compounds. The tert-butyl carbamate (Boc) group provides a protected amine that can be selectively deprotected under mild acidic conditions, allowing for controlled coupling to biomolecules. The terminal alkyne enables efficient conjugation via copper-catalyzed azide-alkyne cycloaddition (CuAAC), commonly known as click chemistry, making it valuable in drug discovery, bioconjugation, and the development of diagnostic probes. Its polyether (PEG-like) spacer enhances solubility and improves pharmacokinetic properties of conjugated molecules.

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