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Product Name: | Levosimendan Impurity 16 | CAS No: | 2290570-69-1 |
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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 16 CAS 2290570-69-1 Purity 95+
Name: Levosimendan Impurity 16
CAS NO: 2290570-69-1
M.W: 298.3
Appearance: White Powder
Purity: 95+
Synonyms: Levosimendan Impurity 16
Application
Drug Research and Development: Studying Levosimendan Impurity 16 aids in understanding the by-products and reaction mechanisms involved in the synthesis of the drug. This knowledge can optimize the synthesis route, minimize impurity formation, and enhance the purity and quality of the final drug product. Additionally, analyzing the structure and properties of the impurity can provide valuable insights for drug structure design and optimization.
Quality Control: Monitoring and controlling Levosimendan Impurity 16 during production is crucial for ensuring the quality and safety of the drug. Rigorous control of impurity levels can promptly identify potential production issues, ensuring product consistency and stability.
Stability Studies: Examining the stability and degradation pathways of Levosimendan Impurity 16 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 16 may not possess therapeutic activity, its presence could pose potential risks to human health. Therefore, a thorough safety assessment of the impurity is essential in the drug development process. Detailed studies of the impurity can provide robust support for drug safety evaluations.
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