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Ciprofloxacin Hydrochloride CAS NO 86483-48-9
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CAS No.:86483-48-9
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Ciprofloxacin Hydrochloride is the hydrochloride salt form of a broad-spectrum fluoroquinolone antibiotic. This compound is a critical active pharmaceutical ingredient (API) valued for its potent bactericidal activity against a wide range of Gram-positive and Gram-negative pathogens. It is essential for pharmaceutical manufacturers producing oral and injectable antibiotic formulations. Our high-purity grade ensures reliability for demanding synthesis and formulation processes.
Application
- Pharmaceutical API: Primary use as the active ingredient in the manufacture of finished antibiotic dosage forms, including tablets, capsules, and sterile injectables.
- Veterinary Medicine: Formulation of antibacterial treatments for livestock, poultry, and companion animals.
- Research & Development: Serves as a key reference standard and starting material in microbiological research and the development of new antimicrobial agents.
- Intermediate Synthesis: Used in the chemical synthesis of more complex fluoroquinolone derivatives and prodrugs.
Basic Information
| Product Name | Ciprofloxacin Hydrochloride |
| CAS No. | 86483-48-9 |
| Molecular Formula | C17H18FN3O3 • HCl • H2O |
| Molecular Weight | 385.82 g/mol (monohydrate) |
| Synonyms | 1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid hydrochloride monohydrate; Ciprofloxacin HCl; Ciprofloxacin Hydrochloride Monohydrate; Bay q 3939; Ciprofloxacin Hydrochloride Hydrate; Cipro HC; (+-)-1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid hydrochloride monohydrate |
| EINECS | Contact for details |
Quality Control
Our Ciprofloxacin Hydrochloride is manufactured under strict quality management systems. It undergoes rigorous analytical testing to meet or exceed relevant pharmacopoeial standards such as USP, EP, and BP. Each batch is supplied with a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles to ensure compliance for pharmaceutical applications.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation.
Specification
| Item | Specification |
|---|---|
| Appearance | White to slightly yellow, crystalline powder |
| Identification (IR) | Conforms |
| Identification (HPLC) | Conforms |
| Assay (HPLC) | 98.5% - 101.0% (on anhydrous basis) |
| Water Content (KF) | 4.5% - 6.5% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 20 ppm |
| Related Substances (HPLC) | Individual impurity ≤ 0.5%; Total impurities ≤ 1.5% |
| Microbial Enumeration | Meets EP/USP requirements |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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