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Product Name: | Lenalidomide Impurity 23 | CAS No: | 827026-45-9 |
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M.W: | 289.24 | MF: | C13H11N3O5 |
Appearance: | White Powder | Purity: | 95+ |
EINECS No: | 1592732-453-0 | Storage: | 5-25°C |
Highlight: | White Powder Lenalidomide Impurity 23,95 Lenalidomide Impurity 23,CAS 827026-45-9 Lenalidomide Impurity 23 |
Product Description
White Powder Lenalidomide Impurity 23 CAS 827026-45-9 95+
Name: Lenalidomide Impurity 23
CAS NO: 827026-45-9
M.W: 289.24
Appearance: White Powder
Purity: 95+
Synonyms: Lenalidomide Impurity 23
Application
Lenalidomide Impurity 23, as a specific impurity found in the production or purification process of Lenalidomide, does not have a direct application in clinical settings or as a therapeutic agent. The focus on impurities in drug manufacturing is primarily to ensure the purity, safety, and efficacy of the final drug product.
The presence of impurities, including Lenalidomide Impurity 23, can potentially affect the stability, solubility, and biological activity of the drug. Therefore, rigorous quality control measures are taken to minimize the levels of these impurities during the manufacturing process.
Researchers and manufacturers monitor and control the levels of impurities like Lenalidomide Impurity 23 to comply with regulatory requirements and ensure the consistency and reliability of the drug product. This involves the use of analytical techniques to detect and quantify impurities, as well as the optimization of manufacturing processes to reduce their formation.
While Lenalidomide Impurity 23 itself does not have a specific application, its presence and control are crucial in the overall drug development and production process. By ensuring the purity of Lenalidomide, manufacturers can provide patients with a safe and effective treatment option for various malignancies.
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