tert-butyl N-[(3H-diazirin-3-yl)methyl]-N-(prop-2-yn-1-yl)carbamate

Reagent Code: #216108
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CAS Number 2825012-63-1

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.24 g/mol
Formula C₁₀H₁₅N₃O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a photoactivatable crosslinking agent in biochemical research. Its main application lies in photoaffinity labeling, where it helps identify molecular interactions between proteins, ligands, and nucleic acids. Upon UV irradiation, the diazirine group generates highly reactive carbenes that form covalent bonds with nearby molecules, capturing transient or weak interactions. The alkyne group enables downstream detection or purification via click chemistry, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC). This dual functionality makes it valuable for studying protein-protein interactions, mapping binding sites, and probing cellular pathways in complex biological systems.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿19,000.00
tert-butyl N-[(3H-diazirin-3-yl)methyl]-N-(prop-2-yn-1-yl)carbamate
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Used primarily as a photoactivatable crosslinking agent in biochemical research. Its main application lies in photoaffinity labeling, where it helps identify molecular interactions between proteins, ligands, and nucleic acids. Upon UV irradiation, the diazirine group generates highly reactive carbenes that form covalent bonds with nearby molecules, capturing transient or weak interactions. The alkyne group enables downstream detection or purification via click chemistry, such as copper-catalyzed azide-al

Used primarily as a photoactivatable crosslinking agent in biochemical research. Its main application lies in photoaffinity labeling, where it helps identify molecular interactions between proteins, ligands, and nucleic acids. Upon UV irradiation, the diazirine group generates highly reactive carbenes that form covalent bonds with nearby molecules, capturing transient or weak interactions. The alkyne group enables downstream detection or purification via click chemistry, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC). This dual functionality makes it valuable for studying protein-protein interactions, mapping binding sites, and probing cellular pathways in complex biological systems.

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