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Product Name: | Regorafenib Impurity 45 | CAS No: | 39893-50-0 |
---|---|---|---|
M.W: | 221.56 | MF: | C8H3ClF3NO |
Appearance: | White Powder | Purity: | 95+ |
EINECS No: | - | Storage: | 5-25°C |
Product Description
White Powder Regorafenib Impurity 45 CAS 39893-50-0 95+
Name: Regorafenib Impurity 45
CAS NO: 39893-50-0
M.W: 377.4
Appearance: White Powder
Purity: 95+
Synonyms: Regorafenib Impurity 45
Application
"Regorafenib Impurity 45" typically refers to a trace impurity that may arise during the manufacturing process of the drug Regorafenib. In drug development and production, the control of impurities is crucial as they can potentially have adverse effects on the safety, effectiveness, and stability of the medication.
When it comes to the specific "application" of "Regorafenib Impurity 45," it is not a typical term used in this context. Impurities are not intended for any specific application but rather need to be controlled and reduced to safe levels. In drug research and quality control, researchers strive to identify and quantify various impurities to ensure the quality and safety of the final product.
If the mention of "Regorafenib Impurity 45" appears in research literature or quality control reports, it may be used to describe the nature, origin, detection methods, and control strategies for that specific impurity. Such information is essential for drug manufacturers to maintain the stability and consistency of their production processes while satisfying regulatory requirements for drug safety and purity.
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