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Product Name: | Levosimendan Impurity 35 | CAS No: | 1630760-90-5 |
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M.W: | 222.67 | MF: | C11H11ClN2O |
Appearance: | White Powder | Purity: | 95+ |
EINECS No: | - | Storage: | 5-25°C |
Product Description
White Powder Levosimendan Impurity 35 CAS 1630760-90-5 95+
Name: Levosimendan Impurity 35
CAS NO: 1630760-90-5
M.W: 222.67
Appearance: White Powder
Purity: 95+
Synonyms: Levosimendan Impurity 35
Application
The specific applications of Levosimendan Impurity 35 are not well-defined as it typically refers to a specific chemical impurity rather than a standalone compound or product. Levosimendan Impurity 35 could be one of the impurities generated during the synthesis or production of Levosimendan, a positive inotropic agent primarily used in the treatment of heart failure.
However, impurities like Levosimendan Impurity 35 are typically not used for pharmacological or biological applications as they may not possess the therapeutic activity or safety profile required for drugs. The presence of impurities needs to be controlled during drug manufacturing to ensure the quality and safety of the medication.
In drug development and production, the study and control of impurities are crucial. These impurities can potentially affect the stability, safety, and efficacy of drugs. Therefore, research on impurities may involve understanding their chemical properties, sources, concentrations in the drug product, and their impact on the quality and safety of the medication.
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