4-(3-(Trifluoromethyl)-3H-diazirin-3-yl)aniline

Reagent Code: #238998
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CAS Number 1610689-08-1

science Other reagents with same CAS 1610689-08-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.15 g/mol
Formula C₈H₆F₃N₃
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

description Product Description

Used primarily as a photoactivatable crosslinking agent in biochemical and molecular biology research. Its main application lies in photoaffinity labeling, where it helps identify and map interactions between biomolecules such as proteins, nucleic acids, and ligands. Upon exposure to UV light, the diazirine group generates highly reactive carbenes that form covalent bonds with nearby molecules, capturing transient or weak interactions that are difficult to study with other methods. The aniline moiety allows for further chemical modification, enabling conjugation to probes, tags, or functional groups for detection or purification. It is especially valuable in studying protein-protein interactions, receptor-ligand binding, and mapping binding sites in complex biological systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿24,700.00
4-(3-(Trifluoromethyl)-3H-diazirin-3-yl)aniline
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Used primarily as a photoactivatable crosslinking agent in biochemical and molecular biology research. Its main application lies in photoaffinity labeling, where it helps identify and map interactions between biomolecules such as proteins, nucleic acids, and ligands. Upon exposure to UV light, the diazirine group generates highly reactive carbenes that form covalent bonds with nearby molecules, capturing transient or weak interactions that are difficult to study with other methods. The aniline moiety all

Used primarily as a photoactivatable crosslinking agent in biochemical and molecular biology research. Its main application lies in photoaffinity labeling, where it helps identify and map interactions between biomolecules such as proteins, nucleic acids, and ligands. Upon exposure to UV light, the diazirine group generates highly reactive carbenes that form covalent bonds with nearby molecules, capturing transient or weak interactions that are difficult to study with other methods. The aniline moiety allows for further chemical modification, enabling conjugation to probes, tags, or functional groups for detection or purification. It is especially valuable in studying protein-protein interactions, receptor-ligand binding, and mapping binding sites in complex biological systems.

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