Bisoprolol Standard (CAS 66722-44-9) and Impurities: Key Elements in Pharmaceutical Testing

Bisoprolol, a beta-blocker, is increasingly proving its indispensable role in the medical field. It is used to treat several cardiovascular diseases. Bisoprolol was discovered in 1976 and began to be used in medicine in 1986. To ensure the treatment efficacy and absolute safety of the drug, strict quality control through Bisoprolol standards (CAS 66722-44-9) and Bisoprolol impurities is extremely essential. This article will delve into the importance of Bisoprolol standards and impurities and introduce a solution for providing reputable standards and impurities that meet the most stringent standards of the pharmaceutical industry.

Detailed Information on Bisoprolol Standard

• Chemical Name: Bisoprolol
• CAS Number: 66722-44-9
• Molecular Formula: C₁₈H₃₁NO₄
• Molecular Weight: 325.44
• Synonym: Bisoprolol Fumarate
• Appearance: White to off-white solid
• Storage Condition: 2-8°C (refrigerator)

Outstanding Importance of Bisoprolol Standards and Impurities

In the field of pharmaceutical production and testing, quality control is a key factor in ensuring the safety, efficacy, and legal compliance of the product. For Bisoprolol, the use of pharmaceutical standards and Bisoprolol impurities plays a crucial role in many aspects:

• Qualitative and Quantitative Analysis: Bisoprolol Standard (CAS 66722-44-9) helps accurately determine the Bisoprolol content in the final product, ensuring the correct dosage and treatment efficacy.
• Purity Control: Bisoprolol impurities help assess the presence and content of impurities that may arise during synthesis or storage. Impurity control is mandatory to prevent unwanted substances from affecting the quality and safety of the drug.
• Research and Development (R&D): Standards and impurities support the process of active substance synthesis, formula optimization, and stability testing of Bisoprolol under various conditions.
• Ensuring Compliance with International Pharmacopoeia: The use of standards and impurities according to the pharmacopoeia is mandatory for pharmaceutical manufacturers to comply with the strict regulations of the industry, thereby ensuring that the product is allowed to circulate in the global market.

Reliable Source for Bisoprolol Standards and Impurities

We are proud to be a reputable supplier of high-quality Bisoprolol standards (CAS 66722-44-9) and Bisoprolol impurities, fully meeting the stringent requirements of the pharmaceutical industry. Our product portfolio includes Bisoprolol reference standards, pharmacopoeial and non-pharmacopoeial impurities, as well as stable isotopes. Specifically:

• Bisoprolol Standard
• Bisoprolol Pharmacopoeial Impurities: Including impurities listed and controlled according to international pharmacopoeias.
• Bisoprolol Non-Pharmacopoeial Impurities: Other impurities that may arise but are not officially listed in the pharmacopoeia, still need to be controlled to ensure product safety.
• Bisoprolol Stable Isotopes: Isotopic versions of Bisoprolol used in in-depth research, mass spectrometry analysis, and bioavailability testing.

Benefits of choosing our products:

• Guaranteed Quality: All standards and impurities are rigorously tested, ensuring the highest purity and accuracy, accompanied by a complete Certificate of Analysis (CoA).
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• Compliance with International Standards: Our products meet and exceed international standards, making it easy for customers to comply with regulations.
• Fast Delivery: With readily available inventory, we commit to fast delivery, ensuring your production and testing processes are not interrupted.
• In-depth Technical Support: Our team of experienced experts is always ready to provide dedicated technical advice and support, ensuring customers use the product most effectively.
• Optimal Storage and Transportation: Products are stored under ideal conditions (2-8°C) and transported under standard conditions to maintain the best quality from warehouse to customer.

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Investing in high-quality Bisoprolol standards (CAS 66722-44-9) and Bisoprolol impurities is not only a mandatory requirement but also a key factor in ensuring the safety and efficacy of your pharmaceutical products. Let us be your trusted partner in your quality control journey.

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