Description

Pradofloxacin is a third-generation fluoroquinolone antibiotic specifically developed for veterinary medicine, offering broad-spectrum bactericidal activity. Its primary value lies in its enhanced potency against both Gram-positive and Gram-negative bacteria, including resistant strains, making it a critical tool in modern animal health. This compound is essential for manufacturers of veterinary pharmaceuticals, particularly for developing treatments for skin, urinary tract, and respiratory infections in companion animals and livestock. We supply high-purity Pradofloxacin CAS NO 195532-12-8 to support the production of safe and effective therapeutic solutions.

Application

• Veterinary Pharmaceutical Formulations: Primary active ingredient in injectable solutions, tablets, and topical preparations for dogs and cats.
• Companion Animal Medicine: Treatment of pyoderma, wound infections, and urinary tract infections (UTIs) in pets.
• Livestock Health Management: Used under veterinary prescription for specific bacterial diseases in cattle and swine.
• Aquaculture: Potential application in treating bacterial infections in farmed fish, subject to regional regulatory approvals.
• Research & Development: Reference standard and building block for antimicrobial research in veterinary science.
• Veterinary Compounding: Sourced by specialized pharmacies for custom medication preparations.

Basic Information

Product Name	Pradofloxacin
CAS No.	195532-12-8
Molecular Formula	C21H24F3N4O4
Molecular Weight	453.44 g/mol
Synonyms	Pradofloxacin; Veraflox; 8-Cyano-1-cyclopropyl-7-[(1S,6S)-2,8-diazabicyclo[4.3.0]non-8-yl]-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid; (1S,6S)-8-(8-Cyano-1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinyl)-2,8-diazabicyclo[4.3.0]nonane-7-carboxylic acid; BAY 35-9036; BAY Vp 2674; Pradofloxacinum
EINECS	Contact for details

Quality Control

Our Pradofloxacin is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity, suitable for pharmaceutical applications. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We adhere to relevant Good Manufacturing Practice (GMP) principles and can support regulatory documentation for veterinary drug master files (DMFs).

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation. The original container should be kept sealed when not in use.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 98.5% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Total impurities ≤ 1.5% Any single impurity ≤ 0.5%
Heavy Metals	≤ 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.