Description

Garenoxacin Mesylate is the mesylate salt form of a potent third-generation fluoroquinolone antibiotic. This high-purity active pharmaceutical ingredient (API) is critical for the development and formulation of advanced antibacterial therapeutics. It is primarily utilized by pharmaceutical manufacturers and research institutions engaged in combating resistant bacterial infections. The compound is supplied under stringent quality control to ensure reliability for sensitive pharmaceutical applications.

Application

• Pharmaceutical API: Primary use as the active ingredient in the formulation of antibacterial injectable drugs and oral dosage forms.
• Antibacterial Drug Development: Serves as a key intermediate in R&D for novel broad-spectrum antibiotics targeting resistant pathogens.
• Clinical Research Material: Used in preclinical and clinical studies to evaluate efficacy, pharmacokinetics, and safety profiles.
• Reference Standard: Employed as a high-purity analytical standard in quality control laboratories for method development and validation.
• Veterinary Pharmaceutical Research: Investigated for potential applications in treating bacterial infections in animals.

Basic Information

Product Name	Garenoxacin Mesylate
CAS No.	223652-82-2
Molecular Formula	C₁₇H₂₀FN₃O₄ • CH₄O₃S
Molecular Weight	437.43 g/mol
Synonyms	Garenoxacin methanesulfonate; BMS-284756 mesylate; T-3811ME; (+-)-1-Cyclopropyl-8-(difluoromethoxy)-7-[(1R)-1-methyl-2,3-dihydro-1H-5-isoindolyl]-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid methanesulfonate; 1-Cyclopropyl-6-fluoro-8-methoxy-7-[(4aS,7aS)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid methanesulfonate; AM-1155 mesylate
EINECS	Contact for details

Quality Control

Our Garenoxacin Mesylate is manufactured and tested under a quality management system to ensure it meets the stringent requirements for pharmaceutical use. Each batch is analyzed for identity, purity, and impurities using validated methods such as HPLC, NMR, and mass spectrometry. A comprehensive Certificate of Analysis (COA) detailing all test results against established specifications is provided with every shipment. We can support development with material meeting various pharmacopeial standards.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept under dry conditions to maintain stability and purity.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0% (on anhydrous basis)
Water Content (KF)	≤2.0%
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.