Azobenzene-3,3'-dicarboxylic Acid
97%
- Product Code: 95109
CAS:
621-18-1
| Molecular Weight: | 270.24 g./mol | Molecular Formula: | C₁₄H₁₀N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03844759 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
Azobenzene-3,3'-dicarboxylic acid is primarily used in the development of photoswitchable materials due to its ability to undergo reversible trans-cis isomerization upon exposure to light. This property makes it valuable in the field of smart materials, where it can be incorporated into polymers, gels, or surfaces to create light-responsive systems. It is also employed in the design of molecular machines and nanoscale devices, where its light-induced structural changes can be harnessed for controlled motion or function. Additionally, it serves as a building block in supramolecular chemistry for constructing dynamic, light-triggered assemblies. Its applications extend to photopharmacology, where it can be used to develop light-activated drugs for precise therapeutic control.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light yellow to Amber to Dark green powder to crystaline |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | £28.95 |
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| 1.000 | 10-20 days | £92.28 |
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Azobenzene-3,3'-dicarboxylic Acid
Azobenzene-3,3'-dicarboxylic acid is primarily used in the development of photoswitchable materials due to its ability to undergo reversible trans-cis isomerization upon exposure to light. This property makes it valuable in the field of smart materials, where it can be incorporated into polymers, gels, or surfaces to create light-responsive systems. It is also employed in the design of molecular machines and nanoscale devices, where its light-induced structural changes can be harnessed for controlled motion or function. Additionally, it serves as a building block in supramolecular chemistry for constructing dynamic, light-triggered assemblies. Its applications extend to photopharmacology, where it can be used to develop light-activated drugs for precise therapeutic control.
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