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Zabofloxacin CAS NO 219680-11-2
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CAS No.:219680-11-2
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Zabofloxacin CAS NO 219680-11-2 is a novel broad-spectrum fluoroquinolone antibiotic developed for its potent activity against respiratory pathogens, including drug-resistant strains. Its primary value lies in its enhanced efficacy against quinolone-resistant bacteria, offering a critical therapeutic option in the global fight against antimicrobial resistance. This advanced pharmaceutical intermediate is essential for research institutions, contract development and manufacturing organizations (CDMOs), and pharmaceutical companies developing next-generation antibacterial treatments.
Application
- Pharmaceutical Active Ingredient (API): Serves as the core active component in the formulation of finished antibiotic drugs.
- Antimicrobial Research: Used in preclinical and clinical research to study efficacy against Gram-positive and Gram-negative bacteria, particularly those causing respiratory tract infections.
- Drug Development: A key intermediate for pharmaceutical companies developing new fluoroquinolone-based therapies with improved safety and resistance profiles.
- Reference Standard: Employed as a high-purity analytical standard in quality control laboratories for method development and validation.
- Combinatorial Chemistry: Utilized in research to create novel analogs and derivatives for structure-activity relationship (SAR) studies.
Basic Information
| Product Name | Zabofloxacin |
| CAS No. | 219680-11-2 |
| Molecular Formula | C₁₉H₂₁FN₄O₄ |
| Molecular Weight | 388.39 g/mol |
| Synonyms | DW-224a; Zabofloxacin hydrochloride; (3S)-9-Fluoro-3-methyl-10-(4-methylpiperazin-1-yl)-7-oxo-2,3-dihydro-7H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid; DW224a; ACT-387042; Zabofloxacin (base) |
| EINECS | Contact for details |
Quality Control
Our Zabofloxacin 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 stringent specifications for pharmaceutical R&D use. Certificates of Analysis (COA) documenting all test results are provided to guarantee traceability and batch-to-batch consistency.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption, which may affect stability and purity.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (IR) | Conforms to reference spectrum |
| Identification (HPLC) | Retention time corresponds to reference standard |
| Assay (HPLC) | ≥98.0% |
| Related Substances (HPLC) | Total impurities ≤2.0% Any single unknown impurity ≤0.5% |
| 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.
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