| Product: | p-Azidophenacyl Bromide | ||||||||
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| Catalog Number: | 7039 | ||||||||
| CAS Number: | 57018-46-9 | ||||||||
| Synonyms: | 4-Azido-α-bromoacetophenone; 4’-Azido-2-bromoacetophenone; 1-(4-Azidophenyl)-2-bromoethan-1-one | ||||||||
| Pricing: |
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| Formula: | C8H6BrN3O | ||||||||
| Molecular Weight: | 240.06 | ||||||||
| Structure: |  | ||||||||
| Appearance: | Light brown powder | ||||||||
| Category: | AffinityChromatography | ||||||||
| Stability: | Stable under recommended storage conditions. | ||||||||
| Storage: | Keep container tightly closed in a dry and well-ventilated place. Storage temperature: 2-8°C. | ||||||||
| Transportation: | IATA: Hazard Class: 4.1; UN Number: UN1325; Packing Group: II; Shipping Name: Flammable solid, organic, n.o.s. (1-(4-Azidophenyl)-2-bromoethan-1-one) | ||||||||
| Literature References: | Hixson, S.H., et al., p-Azidophenacyl bromide, a versatile photolabile bifunctional reagent. Biochemistry 14, 4251, (1975); Hu D., et al., Probing the Structure of the PI-SceI-DNA Complex by Affinity Cleavage and Affinity Photocross-linking. J. Biol. Chem. 275, 2705, (2000) | ||||||||
| MSDS: | |||||||||
| Applications: | Photoactive, heterobifunctional cross-linking reagent. Typically, the initial reaction couples to sulfhydryl in the pH range 7.0-8.0. Second bonding occurs during UV irradiation (250 nm) via reactive nitrene. The latter bonding is rapid and non-specific |
