Therapeutic Uses
Anti-Asthma / COPD
Storage Condition
Store at refrigerator (2-8ยฐC) for long term storage
Synonyms
Budesonide acetaldehyde acetal (epimers) (USP)
Application Notes
Useful research chemical for a range of applications
Hazard Compound
Yes -Refer MSDS for accurate information
Budesonide EP Impurity B is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
Refund Policy
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Budesonide EP Impurity B usage and description
Budesonide EP Impurity B is a chemical compound that is commonly used as an analytical reference standard in the pharmaceutical industry. It is a degradation product of Budesonide, a corticosteroid medication used to treat asthma, allergic rhinitis, and inflammatory bowel disease. Budesonide EP Impurity B is a derivative of 16ฮฑ-hydroxyprednisolone, which is a synthetic glucocorticoid that has been shown to have anti-inflammatory and immunosuppressive properties.
The chemical formula of Budesonide EP Impurity B is C21H26O6, and it has a molecular weight of 386.43 g/mol. It is a white to off-white crystalline powder that is soluble in organic solvents such as methanol and ethanol. The compound is stable under normal storage conditions, but it may degrade over time if exposed to light or heat.
Budesonide EP Impurity B is primarily used as a reference standard for the identification and quantification of impurities in Budesonide formulations. It is also used in the development and validation of analytical methods for the quality control of Budesonide products. The compound is typically analyzed using high-performance liquid chromatography (HPLC) or gas chromatography (GC) techniques.
In summary, Budesonide EP Impurity B is a useful analytical reference standard in the pharmaceutical industry that plays an important role in ensuring the quality and safety of Budesonide products.
