Levofloxacin Reference Standard (CAS 100986-85-4) and Impurity Standards

Levofloxacin, a crucial broad-spectrum antibiotic, is increasingly asserting its indispensable role in healthcare. This active pharmaceutical ingredient (API) demonstrates activity against both Gram-positive and Gram-negative strains and is a bactericidal antibiotic used in the treatment of various infections. It is the levo isomer of racemic ofloxacin. To ensure the absolute therapeutic efficacy and safety of the drug, strict quality control through Levofloxacin reference standards (CAS 100986-85-4) and Levofloxacin impurity standards is extremely essential. This article will introduce a reliable solution for providing reference standards and impurity standards that meet the most stringent requirements of the pharmaceutical industry.

Detailed information about Levofloxacin Reference Standard:

• Chemical Name: Levofloxacin
• CAS Number: 100986-85-4
• Molecular Formula: C18H20FN3O4
• Molecular Weight: 361.37
• Synonyms: (−)-Ofloxacin; (S)-9-fluoro-2,3-dihydro-3-methyl-10-(4-methylpiperazin-1-yl)-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic Acid; (S)-9-Fluoro-2,3-dihydro-3-methyl-10-(4-methylpiperazin-1-yl)-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic Acid
• Classification: Aromatics, heterocycles, pharmaceutical standards, intermediates, Fine Chemicals, sulfur and selenium compounds
• Form: Pale yellow powder
• Storage Conditions: 2-8°C (refrigerator)

The Importance of Levofloxacin Reference and Impurity Standards

In pharmaceutical manufacturing and testing, quality control is a crucial factor in ensuring the safety, efficacy, and regulatory compliance of products. For Levofloxacin, the use of pharmaceutical reference standards and Levofloxacin impurity standards plays an extremely important role in many aspects:

• Qualitative and Quantitative Analysis: Levofloxacin reference standard (CAS 100986-85-4) helps accurately determine the content of Levofloxacin in the final product, ensuring correct dosage and therapeutic effectiveness.
• Purity Control: Levofloxacin impurity standards 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 drug quality and safety.
• Research and Development (R&D): Reference and impurity standards support the active ingredient synthesis process, formula optimization, and stability testing of Levofloxacin under various conditions.
• Ensuring Compliance with International Pharmacopoeias: The use of pharmacopoeial reference and impurity standards is a mandatory requirement for pharmaceutical manufacturers to comply with strict industry regulations, thereby ensuring that products are permitted for global market circulation.

Reliable Source for Levofloxacin Reference Standards and Levofloxacin Impurity Standards

We are proud to be a trusted provider of high-quality Levofloxacin reference standards (CAS 100986-85-4) and Levofloxacin impurity standards, fully meeting the stringent requirements of the pharmaceutical industry. Our product catalog includes Levofloxacin reference standards, and pharmacopoeial and non-pharmacopoeial impurities, as well as stable isotopes. Specifically:

• Levofloxacin Reference Standard: The purest active ingredient form to be used as a primary reference standard.
• Pharmacopoeial impurities of Levofloxacin: Including impurities listed and controlled according to international pharmacopoeias.
• Non-pharmacopoeial impurities of Levofloxacin: Other impurities that may arise but are not yet officially listed in pharmacopoeias, still requiring control to ensure product safety.
• Stable isotopes of Levofloxacin: Isotopic versions of Levofloxacin used in in-depth research, mass spectrometry analysis, and bioavailability testing.

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• Optimal storage and transportation: Products are stored under ideal conditions (2-8°C) and transported under standard conditions to maintain the best quality from our warehouse to the customer’s hands.

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