Levetiracetam Reference Standard (CAS 102767-28-2) and Impurities: Key Factors in Pharmaceutical Testing

Levetiracetam, a widely used anti-epileptic drug, is a leading medication for the treatment of epilepsy. It is used as a monotherapy or in combination to control partial-onset seizures, myoclonic seizures, and primary generalized tonic-clonic seizures. Levetiracetam was approved for medical use in the US in 1999 and has since become a critical choice due to its efficacy and favorable safety profile. To ensure the treatment efficacy and absolute safety of the drug, strict quality control through Levetiracetam reference standards (CAS 102767-28-2) and Levetiracetam impurities is extremely essential. This article will delve into the importance of Levetiracetam reference standards and impurities and introduce a reliable solution for supplying reference standards and impurities that meet the most stringent standards of the pharmaceutical industry.

Detailed Information on Levetiracetam Reference Standard

• Chemical Name: Levetiracetam
• CAS Number: 102767-28-2
• Molecular Formula: C8H14N2O2
• Molecular Weight: 170.21
• Appearance: Crystalline powder or almost white powder
• Storage Condition: 2-8°C (refrigerator)

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

• Qualitative and Quantitative Analysis: Levetiracetam Reference Standard (CAS 102767-28-2) helps accurately determine the Levetiracetam content in the final product, ensuring the correct dosage and treatment efficacy.
• Purity Control: Levetiracetam 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): Reference standards and impurities support the process of active substance synthesis, formula optimization, and stability testing of Levetiracetam under various conditions.
• Ensuring Compliance with International Pharmacopoeia: The use of reference standards and impurities according to the pharmacopoeia is mandatory for pharmaceutical manufacturers to comply with the industry’s stringent regulations, thus ensuring that the product is allowed to circulate in the global market.

Reliable Source for Levetiracetam Reference Standards and Impurities

We are proud to be a reliable supplier of high-quality Levetiracetam reference standards (CAS 102767-28-2) and Levetiracetam impurities, fully meeting the stringent requirements of the pharmaceutical industry. Our product portfolio includes Levetiracetam reference standards, pharmacopoeial and non-pharmacopoeial impurities, and stable isotopes. Specifically:

• Levetiracetam Reference Standard
• Levetiracetam Pharmacopoeial Impurities: Includes impurities listed and controlled according to international pharmacopoeias.
• Levetiracetam 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.
• Levetiracetam Stable Isotopes: Isotopic versions of Levetiracetam used in in-depth research, mass spectrometry analysis, and bioavailability testing.

Benefits of choosing our products:

• Guaranteed Quality: All reference standards and impurities are rigorously tested to ensure 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, helping customers easily comply with regulations.
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• 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 transported under standard conditions to maintain the best quality from warehouse to customer.

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Investing in high-quality Levetiracetam Reference Standard (CAS 102767-28-2) and Levetiracetam 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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