NINGBO INNO PHARMCHEM CO.,LTD. places a strong emphasis on the detailed understanding and characterization of our pharmaceutical raw materials. Enrofloxacin Lactate powder, a critical 'veterinary raw material', possesses specific chemical properties that are crucial for its successful application in veterinary medicine. For manufacturers seeking a reliable 'enrofloxacin lactate pharmaceutical intermediate', understanding these attributes is key.

Enrofloxacin Lactate typically presents as a 'white or light yellow crystalline powder'. Its molecular formula is C15H16ClN3O2, with a molecular weight of approximately 305.759. The compound's density is noted to be around 1.3±0.1 g/cm³. While its boiling point is not applicable (N/A), its melting point is also listed as N/A, which is common for complex organic compounds that may decompose before melting distinctly. This physical form is ideal for handling and incorporation into various pharmaceutical formulations.

The purity of our Enrofloxacin Lactate powder is consistently above 99%, ensuring optimal performance in therapeutic applications. Identification tests, such as the bismuth potassium iodide solution test, result in a brownish-red color, and UV absorption maximum is observed at 277nm, conforming to established standards. The product also responds to tests for Fluoride and Lactate, further validating its composition.

Stability is a critical factor for any pharmaceutical intermediate. Enrofloxacin Lactate powder is generally stable when stored correctly. The product details indicate specific parameters like Loss on Drying (≤5.0%), Residue on Ignition (≤0.2%), and a specified pH range (4.0~5.5), all of which contribute to its quality and shelf-life. These characteristics underscore why 'high purity enrofloxacin lactate' is so vital for reliable veterinary drug production.

When considering where to 'buy enrofloxacin lactate', manufacturers should prioritize suppliers like NINGBO INNO PHARMCHEM CO.,LTD. who provide comprehensive technical data. This information, including chemical properties and adherence to standards for related substances (≤2.0%), ensures that the 'veterinary antibiotic enrofloxacin lactate' will perform as expected in its intended applications.