2-(3-Methyl-3H-diazirin-3-yl)ethanol

≥95%

Reagent Code: #208935
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CAS Number 25055-82-7

science Other reagents with same CAS 25055-82-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 100.12 g/mol
Formula C₄H₈N₂O
badge Registry Numbers
MDL Number MFCD22683730
thermostat Physical Properties
Boiling Point 133.2±32.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, stored in inert gas from light

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 enables the covalent bonding of ligands to their target proteins upon UV irradiation. This allows researchers to study protein-ligand interactions, map binding sites, and identify unknown receptor subunits. The hydroxyl group provides a convenient handle for chemical modification, making it useful in synthesizing probes and tagged molecules for affinity purification or detection. Due to its ability to generate reactive carbenes upon photolysis, it forms stable covalent bonds with nearby biomolecules, offering high spatial and temporal control in complex biological systems.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,100.00
inventory 250mg
10-20 days ฿6,900.00
2-(3-Methyl-3H-diazirin-3-yl)ethanol
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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 enables the covalent bonding of ligands to their target proteins upon UV irradiation. This allows researchers to study protein-ligand interactions, map binding sites, and identify unknown receptor subunits. The hydroxyl group provides a convenient handle for chemical modification, making it useful in synthesizing probes and tagged molecules f

Used primarily as a photoactivatable crosslinking agent in biochemical and molecular biology research. Its main application lies in photoaffinity labeling, where it enables the covalent bonding of ligands to their target proteins upon UV irradiation. This allows researchers to study protein-ligand interactions, map binding sites, and identify unknown receptor subunits. The hydroxyl group provides a convenient handle for chemical modification, making it useful in synthesizing probes and tagged molecules for affinity purification or detection. Due to its ability to generate reactive carbenes upon photolysis, it forms stable covalent bonds with nearby biomolecules, offering high spatial and temporal control in complex biological systems.

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