Phenazine-1,6-diol
95%
- Product Code: 39048
CAS:
69-48-7
| Molecular Weight: | 212.2041 g./mol | Molecular Formula: | C₁₂H₈N₂O₂ |
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| EC Number: | MDL Number: | MFCD01708477 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Phenazine-1,6-diol is primarily utilized in the field of biochemistry and microbiology due to its redox-active properties. It serves as a crucial component in the study of electron transfer processes, often employed as a redox mediator in microbial fuel cells to enhance electron transfer efficiency between microorganisms and electrodes. Additionally, it is investigated for its potential antimicrobial activity, making it a candidate for developing new antibacterial agents. Its ability to generate reactive oxygen species also positions it as a useful tool in oxidative stress research, particularly in understanding cellular damage and defense mechanisms. Furthermore, it finds application in synthetic chemistry as a building block for the preparation of more complex phenazine derivatives, which are explored for their diverse biological activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,301.00 |
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Phenazine-1,6-diol
Phenazine-1,6-diol is primarily utilized in the field of biochemistry and microbiology due to its redox-active properties. It serves as a crucial component in the study of electron transfer processes, often employed as a redox mediator in microbial fuel cells to enhance electron transfer efficiency between microorganisms and electrodes. Additionally, it is investigated for its potential antimicrobial activity, making it a candidate for developing new antibacterial agents. Its ability to generate reactive oxygen species also positions it as a useful tool in oxidative stress research, particularly in understanding cellular damage and defense mechanisms. Furthermore, it finds application in synthetic chemistry as a building block for the preparation of more complex phenazine derivatives, which are explored for their diverse biological activities.
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