Hazardous Substance
May cause skin irritation, serious eye irritation, and respiratory tract irritation. Handle with appropriate laboratory safety equipment.
Eyes: Flush with water for 15 minutes and seek medical attention.
Skin: Wash thoroughly with soap and water; remove contaminated clothing.
Bisoprolol EP Impurity N (CAS 1346601-75-9) is a specialized chemical entity categorized as a pharmaceutical impurity standard. It is structurally related to Bisoprolol, a widely prescribed beta-blocker used for hypertension and heart failure. In the pharmaceutical manufacturing cycle, this compound serves as a critical reference material for monitoring the purity and safety profile of active pharmaceutical ingredients (APIs).
In the Indian pharmaceutical landscape, which serves as a global hub for generic drug manufacturing, the demand for high-quality impurity standards is significant. Indian manufacturers utilize this compound to conduct rigorous stability studies and batch release testing, ensuring that their final drug products meet the stringent quality benchmarks set by international regulatory bodies like the EDQM and USFDA.
Procurement of this chemical requires careful attention to certification, specifically the availability of a Certificate of Analysis (CoA) and NMR/Mass Spectrometry data. Buyers should source from reputable suppliers who provide traceable documentation and maintain cold-chain logistics if required for long-term stability. It is recommended to verify the batch-specific purity levels against the intended analytical application before finalizing procurement.
Bisoprolol EP Impurity N pricing in India depends on grade, order quantity, and delivery location, and it moves with market conditions — so a single fixed price is rarely accurate for a specific requirement.
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Bisoprolol EP Impurity N prices in India vary by grade, order quantity and delivery location, and move with market conditions. To get the current price for your requirement, submit an enquiry on Chemical Dekho and receive verified quotes from suppliers and manufacturers within 24 hours.
No, this is an analytical reference standard intended for laboratory and research use only, not for human consumption.
Yes, all our impurity standards are supplied with a comprehensive CoA including HPLC, NMR, and Mass Spectrometry data.
For optimal stability, it should be stored at 2-8°C in a refrigerator.
Yes, it is specifically designed for use in HPLC method development and validation for Bisoprolol Fumarate.
Yes, this product is manufactured to meet the specifications defined for Bisoprolol EP Impurity N in the European Pharmacopoeia.
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