share

Ciprofloxacin Hydrochloride CAS NO 86483-48-9


Unit Price:

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.

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.