3-(2-azidoethyl)-3-(but-3-yn-1-yl)-3H-diazirine
95%
- Product Code: 191719
CAS:
1450754-42-3
| Molecular Weight: | 163.18 g./mol | Molecular Formula: | C₇H₉N₅ |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | 2-8°C |
Product Description:
Used primarily in photoaffinity labeling studies, this compound enables the covalent crosslinking of biomolecules upon UV irradiation. The diazirine group generates highly reactive carbenes that insert into nearby C–H, N–H, or O–H bonds, allowing researchers to capture transient interactions between proteins, nucleic acids, or ligands. The azide and alkyne functionalities support downstream conjugation via click chemistry, facilitating detection, purification, or immobilization of labeled targets. Its bifunctional design makes it valuable in chemical biology for mapping molecular interactions and studying biological pathways in complex environments.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 G | 10-20 days | ฿16,560.00 |
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| 0.250 G | 10-20 days | ฿32,160.00 |
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| 1.000 G | 10-20 days | ฿85,000.00 |
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3-(2-azidoethyl)-3-(but-3-yn-1-yl)-3H-diazirine
Used primarily in photoaffinity labeling studies, this compound enables the covalent crosslinking of biomolecules upon UV irradiation. The diazirine group generates highly reactive carbenes that insert into nearby C–H, N–H, or O–H bonds, allowing researchers to capture transient interactions between proteins, nucleic acids, or ligands. The azide and alkyne functionalities support downstream conjugation via click chemistry, facilitating detection, purification, or immobilization of labeled targets. Its bifunctional design makes it valuable in chemical biology for mapping molecular interactions and studying biological pathways in complex environments.
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