For chemists and quality control professionals in the pharmaceutical industry, a deep understanding of chemical intermediates is fundamental. Lomefloxacin hydrochloride, a key fluoroquinolone antibiotic precursor, requires meticulous attention to its chemical profile to ensure its suitability for pharmaceutical applications. This article explores the critical chemical specifications of Lomefloxacin hydrochloride and the significance of sourcing it from reputable manufacturers, particularly those in China known for their adherence to quality and compliance.

The chemical name, Lomefloxacin hydrochloride, associated with CAS number 98079-52-8, points to a molecule with specific structural and functional characteristics. Its appearance is typically described as a white or almost white crystalline powder, a visual indicator of its purity. However, the true measure of its quality lies in its assay, which for pharmaceutical applications, often needs to be a minimum of 99.5%. This high purity level is essential to prevent the introduction of unwanted impurities into the final drug product, which could compromise its efficacy or patient safety.

The Importance of Certifications and Standards

When sourcing Lomefloxacin hydrochloride, particularly for global markets, verifying the manufacturer's certifications and adherence to international standards is crucial. Companies that are GMP (Good Manufacturing Practice) and SGS certified demonstrate a commitment to robust quality management systems throughout their production processes. GMP ensures that products are consistently produced and controlled according to quality standards appropriate for their intended use, while SGS certification often involves independent auditing and verification of product quality and safety.

Moreover, compliance with pharmacopoeial standards such as USP (United States Pharmacopeia), BP (British Pharmacopoeia), EP (European Pharmacopoeia), and FCC (Food Chemicals Codex) is a non-negotiable aspect for pharmaceutical intermediates. These standards provide detailed specifications for identity, strength, quality, and purity, ensuring that the intermediate is suitable for incorporation into pharmaceutical formulations that will be used by patients. Sourcing Lomefloxacin hydrochloride that meets these diverse standards simplifies the regulatory approval process for the final drug product.

Sourcing Strategies: Competitive Pricing and Online Support

For many pharmaceutical companies, the decision to buy Lomefloxacin hydrochloride from China is driven by a combination of quality and cost-effectiveness. Chinese manufacturers have become key players in the global chemical supply chain, often offering competitive pricing due to efficient production methods and economies of scale. However, it is vital to partner with suppliers who not only offer attractive prices but also prioritize transparency in their quality documentation and offer reliable online purchase support. This support can range from readily available technical data sheets (TDS) and safety data sheets (SDS) to responsive customer service for inquiries and order processing.

In conclusion, the chemical integrity of Lomefloxacin hydrochloride is paramount for its use as a pharmaceutical intermediate. By focusing on suppliers with high purity levels, GMP and SGS certifications, and adherence to USP, BP, EP, and FCC standards, pharmaceutical professionals can ensure the quality and reliability of their drug development processes. The accessibility and competitive pricing from China, coupled with robust online support, make it a strategic sourcing location for this essential compound.