Description

Binfloxacin CAS NO 108437-28-1 is a synthetic fluoroquinolone antibiotic compound. It is valued for its potent antibacterial activity, particularly against a broad spectrum of Gram-positive and Gram-negative pathogens. This active pharmaceutical ingredient (API) is primarily utilized in pharmaceutical research and development for creating advanced antibacterial formulations.

Application

• Primary use as an Active Pharmaceutical Ingredient (API) in the synthesis of antibacterial drugs.
• Research and development of novel veterinary medicines for treating bacterial infections in animals.
• Key intermediate in the production of ophthalmic solutions for eye infections.
• Component in pharmaceutical reference standards for quality control and analytical testing.
• Utilized in microbiological research to study bacterial resistance mechanisms.
• Potential applications in the development of topical antimicrobial creams and ointments.

Basic Information

Product Name	Binfloxacin
CAS No.	108437-28-1
Molecular Formula	C20H24FN3O4
Molecular Weight	389.42 g/mol
Synonyms	Binfloxacin; 1-Cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-(3-methyl-1-piperazinyl)-4-oxo-3-quinolinecarboxylic acid; (±)-Binfloxacin; DL-Binfloxacin; BIN 286; BIN-286; BIN286; 9-Fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid
EINECS	Contact for details

Quality Control

Our Binfloxacin is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, residual solvent analysis, and identification by IR and NMR spectroscopy, to ensure it meets high-grade pharmaceutical standards. Certificates of Analysis (COA) are provided with every shipment to guarantee traceability and compliance.

Storage

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

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%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%

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