Description

Prulifloxacin CAS NO 123447-62-1 is a synthetic broad-spectrum fluoroquinolone antibiotic, valued for its potent antibacterial activity against a wide range of Gram-positive and Gram-negative pathogens. Its primary commercial significance lies in its role as a key active pharmaceutical ingredient (API) for the formulation of advanced antibacterial medications. This compound is essential for pharmaceutical manufacturers and research institutions focused on developing treatments for bacterial infections.

Application

• Primary use as an Active Pharmaceutical Ingredient (API) in the manufacture of antibacterial drugs.
• Formulation of oral dosage forms, such as tablets and capsules, for systemic antibiotic therapy.
• Research and development of new antibacterial agents and combination therapies.
• Reference standard for analytical testing and quality control in pharmaceutical laboratories.
• Intermediate in the synthesis of more complex fluoroquinolone derivatives.

Basic Information

Item	Detail
Product Name	Prulifloxacin
CAS No.	123447-62-1
Molecular Formula	C21H20FN3O6S
Molecular Weight	461.46 g/mol
Synonyms	NM441; Prulifloxacinum; UNII-4Q7P6S71QO; 6-Fluoro-1-methyl-7-[4-(5-methyl-2-oxo-1,3-dioxolen-4-yl)methyl-1-piperazinyl]-4-oxo-1,4-dihydro[1,3]thiazeto[3,2-a]quinoline-3-carboxylic acid; AF 3013; (RS)-Prulifloxacin; (±)-Prulifloxacin
EINECS	Contact for details

Quality Control

Our Prulifloxacin is manufactured under strict quality management systems to ensure it meets the high standards required for pharmaceutical use. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling. A Certificate of Analysis (COA) documenting compliance with relevant specifications is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Keep the container tightly sealed in a dry environment to maintain stability.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Related Substances (HPLC)	Total impurities ≤ 2.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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