Inquire About a Product| 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 |
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| Pricing: |
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| Formula: | C8H6BrN3O | ||||||||||||
| Molecular Weight: | 240.06 | ||||||||||||
| Structure: |
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| Appearance: | Light brown powder | ||||||||||||
| Category: | Affinity Chromatography | ||||||||||||
| Stability: | Stable under recommended storage conditions. | ||||||||||||
| Storage: |
Keep container tightly closed in a dry and well-ventilated place. Storage temperature: 2-8°C. |
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| 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) |
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| 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) |
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| 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 |