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Candesartan Standard (CAS 139481-59-7) and Impurities: Key Factors in Pharmaceutical Testing

Candesartan, an angiotensin II receptor blocker, is increasingly affirming its indispensable role in the healthcare field. It is used to treat several cardiovascular diseases. Candesartan was discovered in 1982 and began to be used medically in 1990. To ensure the treatment efficacy and absolute safety of the drug, strict quality control through Candesartan standards (CAS 139481-59-7) and Candesartan impurities is extremely essential. This article will delve into the importance of Candesartan standards and impurities and introduce a solution for supplying reputable standards and impurities that meet the most stringent standards of the pharmaceutical industry.

Detailed Information on Candesartan Standard

• Chemical Name: Candesartan
• CAS Number: 139481-59-7
• Molecular Formula: C₂₄H₂₀N₆O₃
• Molecular Weight: 440.45
• Synonym: Candesartan M1
• Appearance: White to off-white solid
• Storage Condition: 2-8°C (refrigerator)

Outstanding Importance of Candesartan 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 Candesartan, the use of pharmaceutical standards and Candesartan impurities plays a crucial role in many aspects:

• Qualitative and Quantitative Analysis: Candesartan Standard (CAS 139481-59-7) helps accurately determine the amount of Candesartan in the final product, ensuring the correct dosage and treatment efficacy.
• Purity Control: Candesartan impurities help assess the presence and amount 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 Candesartan under different conditions.
• Ensuring Compliance with International Pharmacopoeia: The use of standards and impurities according to the pharmacopoeia is a mandatory requirement 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 Candesartan Standards and Impurities

We are proud to be a reputable supplier of high-quality Candesartan standards (CAS 139481-59-7) and Candesartan impurities, fully meeting the stringent requirements of the pharmaceutical industry. Our product catalog includes Candesartan reference standards, pharmacopoeial and non-pharmacopoeial impurities, as well as stable isotopes. Specifically:

• Candesartan Standard
• Pharmacopoeial Impurities of Candesartan: Includes impurities listed and controlled according to international pharmacopoeias.
• Non-Pharmacopoeial Impurities of Candesartan: Other impurities that may arise but are not officially listed in the pharmacopoeia, still need to be controlled to ensure product safety.
• Stable Isotopes of Candesartan: Isotopic versions of Candesartan 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).
• Diverse Product Range: Meets all needs from research, development to production and quality control in pharmaceutical laboratories.
• Compliance with International Standards: Our products meet and exceed international standards, making it easier 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 products most effectively.
• Optimal Storage and Transportation: Products are stored under ideal conditions (2-8°C) and shipped under standard conditions to maintain the best quality from warehouse to customer.

Contact Us Now to Enhance Your Pharmaceutical Quality

Investing in high-quality Candesartan standards (CAS 139481-59-7) and Candesartan impurities is not only a mandatory requirement but also a key factor in ensuring the safety and efficacy of pharmaceutical products. Let us be your trusted partner in your quality control journey.

Contact us now for a quote and detailed advice on standards and Candesartan impurities – a reliable solution for all pharmaceutical laboratories and businesses.
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