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Levosimendan Impurity 1 is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard in the quality control of Levosimendan drug products. Levosimendan is a calcium sensitizer that enhances cardiac contractility and lowers cardiac filling pressures, making it useful in the treatment of acute and chronic heart failure.
Levosimendan Impurity 1 is a synthetic compound that is closely related to Levosimendan and is a known impurity that can be found in Levosimendan drug products. It is important to ensure that the levels of this impurity are within acceptable limits as high levels of impurities can affect the quality, safety, and efficacy of the drug product.
The chemical information of Levosimendan Impurity 1 includes its molecular formula, which is C14H18N2O2, and its molecular weight, which is 254.31 g/mol. It has a melting point of 178-182°C and a purity of at least 98%.
In terms of usage, Levosimendan Impurity 1 is typically used as a reference standard in the analytical testing of Levosimendan drug products. This includes methods such as high-performance liquid chromatography (HPLC) and gas chromatography (GC). The impurity is used as a benchmark to ensure that the drug product is of high quality and free from impurities that can affect its safety and efficacy.
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