Bis(p-nitrophenyl) azidophosphonate
≥98%
- Product Code: 73567
CAS:
51250-91-0
| Molecular Weight: | 365.2 g./mol | Molecular Formula: | C₁₂H₁₈N₅O₇P |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 105-115℃ | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
Used as a photoactive crosslinking agent in biochemical research to study protein interactions and nucleic acid structures. It forms covalent bonds upon UV irradiation, enabling the identification of molecular proximities and interactions.
Applied in the development of advanced materials, particularly in creating photo-responsive polymers and coatings. Its ability to generate reactive species under light exposure makes it valuable for surface modification and patterning.
Utilized in organic synthesis as a reagent for introducing phosphonate groups into molecules, facilitating the creation of complex organic compounds with specific functionalities.
Employed in photolithography for microfabrication processes, where its light-sensitive properties are exploited to create precise patterns on substrates.
Acts as a key component in the synthesis of bioactive molecules, aiding in the development of pharmaceuticals and agrochemicals by enabling targeted modifications of molecular structures.
Used in the preparation of functionalized surfaces for biosensors, enhancing their sensitivity and specificity by allowing controlled immobilization of biomolecules.
Incorporated into the design of light-activated adhesives and sealants, providing on-demand curing capabilities for industrial applications.
Applied in the study of enzyme mechanisms, where it serves as a photoaffinity labeling agent to investigate active sites and binding interactions.
Utilized in the creation of advanced photoresists for semiconductor manufacturing, contributing to the production of high-resolution electronic components.
Employed in the development of light-triggered drug delivery systems, enabling precise control over the release of therapeutic agents in response to specific wavelengths of light.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿12,620.00 |
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Bis(p-nitrophenyl) azidophosphonate
Used as a photoactive crosslinking agent in biochemical research to study protein interactions and nucleic acid structures. It forms covalent bonds upon UV irradiation, enabling the identification of molecular proximities and interactions.
Applied in the development of advanced materials, particularly in creating photo-responsive polymers and coatings. Its ability to generate reactive species under light exposure makes it valuable for surface modification and patterning.
Utilized in organic synthesis as a reagent for introducing phosphonate groups into molecules, facilitating the creation of complex organic compounds with specific functionalities.
Employed in photolithography for microfabrication processes, where its light-sensitive properties are exploited to create precise patterns on substrates.
Acts as a key component in the synthesis of bioactive molecules, aiding in the development of pharmaceuticals and agrochemicals by enabling targeted modifications of molecular structures.
Used in the preparation of functionalized surfaces for biosensors, enhancing their sensitivity and specificity by allowing controlled immobilization of biomolecules.
Incorporated into the design of light-activated adhesives and sealants, providing on-demand curing capabilities for industrial applications.
Applied in the study of enzyme mechanisms, where it serves as a photoaffinity labeling agent to investigate active sites and binding interactions.
Utilized in the creation of advanced photoresists for semiconductor manufacturing, contributing to the production of high-resolution electronic components.
Employed in the development of light-triggered drug delivery systems, enabling precise control over the release of therapeutic agents in response to specific wavelengths of light.
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