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Product Name: | Levosimendan Impurity | CAS No: | 1630760-89-2 |
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M.W: | 188.23 | MF: | C11H12N2O |
Appearance: | White Powder | Purity: | 95+ |
EINECS No: | - | Storage: | 5-25°C |
Product Description
White Powder Levosimendan Impurity CAS 1630760-89-2 Purity 95+
Name: Levosimendan Impurity
CAS NO: 1630760-89-2
M.W: 298.3
Appearance: White Powder
Purity: 95+
Synonyms: Levosimendan Impurity
Application
Drug Research and Development: Studying Levosimendan Impurity can assist in optimizing drug synthesis routes, minimizing impurity formation, and enhancing drug purity. Additionally, understanding the structure and properties of impurities can provide valuable insights for drug structure design and optimization.
Quality Control: Monitoring and controlling Levosimendan Impurity during production is crucial for ensuring the quality and safety of the final drug product. Rigorous impurity control can promptly identify potential production issues, ensuring product quality and stability.
Stability Studies: Examining the stability and degradation pathways of Levosimendan Impurity under various conditions can predict the stability of the drug during storage and use. This information is essential for determining appropriate storage conditions and setting expiration dates.
Safety Assessment: Although Levosimendan Impurity may not possess therapeutic activity, its presence could pose potential risks to human health. Therefore, thorough safety assessments of impurities are a crucial part of the drug development process. In-depth studies of impurities can provide robust support for drug safety evaluations.
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Small package(1g, 25g, 1Kg, 25Kg) can be shipped by Express. (DHL, FedEx, EMS, etc.)
Large package(100kg and more than100Kg) can be transported by Air or Sea.
All transportation is in accordance with the customer's needs.
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