Description

Tosufloxacin p-Toluenesulfonate Hydrate CAS NO 1400591-39-0 is a fluoroquinolone antibiotic salt form, specifically designed to enhance the stability and handling properties of the active pharmaceutical ingredient. This compound is critical for ensuring consistent potency and efficacy in pharmaceutical formulations. It is primarily required by manufacturers in the pharmaceutical and biotechnology sectors for the research, development, and production of advanced antibacterial agents.

Application

• Pharmaceutical Intermediate: Serves as a key raw material in the synthesis of final dosage forms of the antibiotic Tosufloxacin.
• Antibacterial Drug Development: Used in R&D for creating new formulations targeting a broad spectrum of bacterial infections.
• Reference Standard: Employed as a high-purity standard in analytical laboratories for quality control and method validation.
• Active Pharmaceutical Ingredient (API) Manufacturing: A crucial component in the production chain for finished antibiotic drugs.
• Veterinary Medicine: Potential application in the development of antibacterial treatments for animal health.
• Microbiological Research: Utilized in academic and industrial research to study bacterial resistance mechanisms and drug efficacy.

Basic Information

Product Name	Tosufloxacin p-Toluenesulfonate Hydrate
CAS No.	1400591-39-0
Molecular Formula	C26H25F3N4O7S
Molecular Weight	594.56 g/mol
Synonyms	Tosufloxacin Tosylate Hydrate; Tosufloxacin p-Toluenesulfonate Monohydrate; (1S,5R,6S)-6-Fluoro-1-methyl-7-[(3S,4S)-3-methyl-1-piperazinyl]-4-oxo-1H,4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylic acid 4-methylbenzenesulfonate hydrate; T-3262 Tosylate Hydrate; Ozex Tosylate; Tosufloxacin Tosylate; 1H,4H-[1,3]Thiazeto[3,2-a]quinoline-3-carboxylic acid, 6-fluoro-1-methyl-7-(3-methyl-1-piperazinyl)-4-oxo-, (3S-cis)-, 4-methylbenzenesulfonate, hydrate (1:1:1)
EINECS	Contact for details

Quality Control

Our Tosufloxacin p-Toluenesulfonate Hydrate is manufactured under strict quality systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, to ensure it meets stringent specifications for pharmaceutical use. Certificates of Analysis (COA) detailing all test results are provided to guarantee traceability and compliance with relevant industry standards.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a low-humidity environment to prevent moisture absorption and degradation.

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% (on anhydrous basis)
Water Content (KF)	3.0% - 6.0%
Related Substances (HPLC)	Total impurities ≤2.0% Any single impurity ≤0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Heavy Metals	≤20 ppm

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