Edoxaban Impurity C (HCl) CAS: 1243308-37-3
Catalog Number | XD93702 |
Product Name | Edoxaban Impurity C (HCl) |
CAS | 1243308-37-3 |
Molecular Formula | C9H10Cl2N2O3 |
Molecular Weight | 265.09 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
Edoxaban Impurity C (HCl) is a chemical compound that has specific applications in the pharmaceutical industry. It is an impurity that is typically found in edoxaban, a medication used to prevent stroke and blood clots in individuals with atrial fibrillation.The presence of Impurity C (HCl) in edoxaban can have implications on its quality, purity, and effectiveness. Therefore, it is essential to understand and control the levels of this impurity during the manufacturing process of edoxaban.In pharmaceutical manufacturing, impurities can arise from various sources, such as starting materials, reagents, synthesis intermediates, or degradation of the active pharmaceutical ingredient (API) during storage or processing. Impurities may have different chemical properties and structures compared to the API, which might impact the safety and efficacy of the final medication.The identification and quantification of impurities, including Edoxaban Impurity C (HCl), are crucial steps in ensuring the quality and purity of edoxaban. Regulatory guidelines dictate acceptable limits for impurities in pharmaceuticals, and manufacturers must comply with these standards to provide safe and effective medications to patients.Analytical methods, such as high-performance liquid chromatography (HPLC), can be employed to detect and quantify Impurity C (HCl) in edoxaban samples. These methods involve separating the impurity from the API and other components in the sample and measuring the amount present. By monitoring and controlling the levels of Impurity C (HCl), pharmaceutical manufacturers can ensure that the edoxaban being produced meets regulatory requirements and is safe for patients' use.Additionally, understanding the nature and properties of Edoxaban Impurity C (HCl) can aid in the development of strategies to minimize its formation during the synthesis of edoxaban. This can involve process optimization, selection of appropriate starting materials, and modification of reaction conditions to reduce impurity formation.Overall, Edoxaban Impurity C (HCl) is an impurity found in edoxaban that requires careful monitoring and control during its manufacturing process. By effectively managing and minimizing the levels of this impurity, pharmaceutical companies can ensure that edoxaban meets the required quality standards and provides maximum safety and efficacy to patients using this medication.