Description

Ibafloxacine is a synthetic fluoroquinolone antibiotic compound with significant antimicrobial activity. It is valued for its broad-spectrum efficacy against a range of gram-positive and gram-negative bacteria, making it a critical active pharmaceutical ingredient (API). This compound is primarily utilized by pharmaceutical manufacturers and research institutions in the development and production of veterinary and human antibacterial formulations.

Application

• Veterinary Pharmaceutical API: Core active ingredient in antibacterial medications for companion animals and livestock.
• Human Pharmaceutical Intermediates: Used in the research and synthesis of advanced fluoroquinolone-based antibiotics.
• Antimicrobial Research: Serves as a standard or test compound in microbiological and pharmacological studies.
• Formulation Development: Employed in the creation of various dosage forms such as tablets, injectables, and topical preparations.
• Reference Standard: Used in quality control laboratories for analytical method development and validation.

Basic Information

Item	Detail
Product Name	Ibafloxacine
CAS No.	91618-36-9
Molecular Formula	C19H20F3N3O3
Molecular Weight	395.38 g/mol
Synonyms	Ibafloxacin; Ibafloxacino; Ibafloxacinum; 1-Cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-[(3aS,7aS)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-4-oxo-3-quinolinecarboxylic acid; Bay Vp 2674; Bay-Vp-2674; V 2674
EINECS	Contact for details

Quality Control

Our Ibafloxacine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, assay, and impurity profile analysis by HPLC, to ensure it meets high-purity standards suitable for pharmaceutical use. Certificates of Analysis (COA) documenting full compliance with specifications are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to minimize exposure to atmospheric moisture.

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)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any individual 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.