Enrofloxacin, identified by the Chemical Abstracts Service (CAS) number 93106-60-6, stands as a vital raw material in the pharmaceutical industry, particularly within the veterinary sector. As a member of the fluoroquinolone class of antibiotics, it is widely recognized for its efficacy in treating a broad spectrum of bacterial infections in animals. The availability of high-quality Enrofloxacin powder is crucial for the production of effective veterinary medicines.

This essential active pharmaceutical ingredient (API) is typically presented as a white or off-white solid powder. Its quality is paramount, adhering to stringent international pharmaceutical standards such as GMP, USP, EP, and BP. Meeting these benchmarks ensures the purity, potency, and consistency required for pharmaceutical manufacturing processes. A high-grade Enrofloxacin raw material will exhibit specific physical and chemical properties, including precise melting points, low levels of water content, and minimal residual impurities.

The pharmaceutical utility of Enrofloxacin CAS 93106-60-6 is rooted in its mechanism of action, which involves inhibiting bacterial DNA gyrase and topoisomerase IV, enzymes essential for bacterial DNA replication, transcription, repair, and recombination. This leads to rapid bacterial cell death, making it an effective tool against various pathogens responsible for respiratory, urinary tract, and skin infections in livestock and pets. The demand for this reliable antibiotic necessitates a consistent supply of the raw material meeting high purity standards.

Quality control is a critical aspect of producing pharmaceutical-grade Enrofloxacin powder. Comprehensive testing, including identification tests (like IR and HPLC), solubility checks, and assays for purity and related substances, ensures that each batch conforms to established specifications. Batches often demonstrate assay results exceeding 99%, validating their suitability for demanding pharmaceutical applications. Furthermore, control over particle size is often a specified standard, impacting the compound's processing characteristics and ultimately the quality of the final dosage form.

Proper storage of Enrofloxacin raw material is also vital to maintain its integrity and shelf life. It must be preserved in tight, light-resistant containers and kept in a cool place to prevent degradation and maintain its chemical stability. Adherence to these storage guidelines is essential for both the manufacturer and the end-use pharmaceutical formulator.

Sourcing high-purity Enrofloxacin CAS 93106-60-6 powder requires partnering with a reliable supplier dedicated to quality and compliance. Companies seeking to buy or purchase this critical API need transparent information regarding product specifications, quality documentation like Certificates of Analysis, and regulatory support. Discussions regarding the price and minimum order quantities are standard steps in the procurement process for this valuable raw material.

In summary, Enrofloxacin raw material powder is an indispensable ingredient in the veterinary pharmaceutical landscape. Its high purity, adherence to rigorous quality standards, and broad-spectrum antibacterial activity make it a preferred choice for treating bacterial infections. For companies looking to secure a supply of this essential API, understanding its properties, quality requirements, and sourcing from reputable partners are key. NINGBO INNO PHARMCHEM CO.,LTD. is proud to provide information on high-quality pharmaceutical raw materials like Enrofloxacin.