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| | 4-(N-Maleimido)benzophenone Basic information |
| | 4-(N-Maleimido)benzophenone Chemical Properties |
| Melting point | 155-157°C | | Boiling point | 472.9±28.0 °C(Predicted) | | density | 1.330±0.06 g/cm3(Predicted) | | storage temp. | 2-8°C | | solubility | chloroform: 50 mg/mL | | form | Solid | | pka | -3.80±0.20(Predicted) | | color | Light Beige |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | HS Code | 29251900 |
| | 4-(N-Maleimido)benzophenone Usage And Synthesis |
| Chemical Properties | Light Beige Solid | | Uses | 4-(N-Maleimido)benzophenone can be used as a sulfhydryl reactive heterobifunctional photocrosslinking reagent. It generates photoactivatable conjugates from thiols | | Uses | A heterobifunctional cross-linking reagent containing a sulfhydryl-specific group and a photo-active group. Typically, coupled initially by thioether to molecule containing free sulfhydryl buffered at pH 6.8 (6.5-7.0). Second bonding occurs during UV irradiation (250 nm) via diradical excited state. Benzophenones demonstrate greater specificity for C-H insertion and are more stable in water than analogous reagents. In general they are more efficient in attachment because they may be repeatedly irradiated; however, a more intense irradiation may be required. The benzophenone is not sensitive to | | Uses | Maleimide-containing benzophenone as photoinitiator | | reaction suitability | reagent type: cross-linking reagent |
| | 4-(N-Maleimido)benzophenone Preparation Products And Raw materials |
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