Sofosbuvir impurity F
≥97%
- Product Code: 102558
CAS:
1337482-17-3
| Molecular Weight: | 798.6900000000001 g./mol | Molecular Formula: | C₃₄H₄₅FN₄O₁₃P₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
Sofosbuvir Impurity F plays a critical role in the pharmaceutical industry, particularly in the development and quality control of Sofosbuvir, a key antiviral medication used to treat hepatitis C. This impurity is closely monitored during the drug manufacturing process to ensure the final product meets stringent regulatory standards for safety and efficacy. By analyzing and controlling the levels of Sofosbuvir Impurity F, manufacturers can maintain the purity of the active pharmaceutical ingredient (API), which is essential for the drug's therapeutic performance. Additionally, understanding the behavior and characteristics of this impurity helps in optimizing synthesis processes, reducing potential side effects, and ensuring compliance with global pharmaceutical guidelines. Its study also aids in the development of robust analytical methods for impurity profiling, which is vital for batch-to-batch consistency and patient safety.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.001 | 10-20 days | ฿180,000.00 |
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-
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| 0.005 | 10-20 days | ฿420,000.00 |
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|
Sofosbuvir impurity F
Sofosbuvir Impurity F plays a critical role in the pharmaceutical industry, particularly in the development and quality control of Sofosbuvir, a key antiviral medication used to treat hepatitis C. This impurity is closely monitored during the drug manufacturing process to ensure the final product meets stringent regulatory standards for safety and efficacy. By analyzing and controlling the levels of Sofosbuvir Impurity F, manufacturers can maintain the purity of the active pharmaceutical ingredient (API), which is essential for the drug's therapeutic performance. Additionally, understanding the behavior and characteristics of this impurity helps in optimizing synthesis processes, reducing potential side effects, and ensuring compliance with global pharmaceutical guidelines. Its study also aids in the development of robust analytical methods for impurity profiling, which is vital for batch-to-batch consistency and patient safety.
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