Therapeutic Uses
Anti-Hypertensives
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
N-Benzyl Carvedilol; Carvedilol Related Compound C
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 90%
Hazard Compound
No -Refer MSDS for accurate information
Carvedilol EP Impurity C is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
Refund Policy
We are committed to offering products of the highest quality in order to meet the needs of our customers, and have elaborate systems in
place to ensure that material specifications, their certification and all handling and storage conditions are communicated at the time of
material handover.
We have invested in the highest quality packaging materials and use international logistics partners to service our customers. While all
possible precautions have been taken to deliver the required product(s), there may be some rare situations when our product does not
meet your requirements. Should that arise, please contact us with your concerns and we will endeavour to address them on a priority
basis. If there is no other option, we will either replace your product(s) or issue a refund or account credit, whichever you prefer.
If there is an issue with one or more of our products, our policy is that it must be reported to us within 45 days of your receiving shipment.
While we will always address product issues after the 45 day return window has passed, we cannot issue a refund or account credit. As
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Carvedilol EP Impurity C usage and description
Carvedilol Impurity C is a chemical compound that is typically used as a reference standard for the identification and quantification of impurities in Carvedilol drug substance and drug product. Carvedilol is a beta-blocker medication that is used to treat heart failure, hypertension and other cardiovascular conditions. This impurity is a byproduct that is formed during the synthesis of Carvedilol, and its presence can impact the purity and potency of the drug.
In terms of chemical information, Carvedilol Impurity C is also known as 2,3-dihydro-3-(phenylmethylene)-2-oxo-1H-indole-5-sulfonic acid. It is a white to off-white crystalline powder with a molecular formula of C15H11NO4S and a molecular weight of 307.32 g/mol. The compound is soluble in water and methanol, and its purity is typically measured using high-performance liquid chromatography (HPLC) or gas chromatography (GC).
Overall, Carvedilol Impurity C plays a crucial role in ensuring the quality and safety of Carvedilol-based medications. By accurately identifying and measuring this impurity, manufacturers can ensure that their products meet regulatory standards and deliver the intended therapeutic benefits to patients.
