Description

Enrofloxain Hydrochloride is a synthetic fluoroquinolone antibiotic, widely recognized for its potent broad-spectrum antibacterial activity. This high-purity active pharmaceutical ingredient (API) is critical for ensuring the efficacy and safety of veterinary and pharmaceutical formulations. It is primarily utilized by manufacturers in the animal health, pharmaceutical, and research sectors for developing treatments against susceptible bacterial infections.

Application

• Veterinary Pharmaceutical Formulations: Primary use in injectable solutions, oral suspensions, and tablets for the treatment of bacterial infections in livestock, poultry, and companion animals.
• Aquaculture Treatments: Used in medicated feeds or water treatments to control bacterial diseases in fish and shrimp farming operations.
• Pharmaceutical Intermediates: Serves as a key chemical intermediate in the synthesis of other advanced fluoroquinolone derivatives.
• Research & Development: Employed in microbiological research, antimicrobial susceptibility testing, and the development of new therapeutic agents.
• Feed Additive Premixes: Incorporated into specialized premixes for prophylactic or therapeutic use in animal nutrition.

Basic Information

Product Name	Enrofloxain Hydrochloride
CAS No.	93106-59-3
Molecular Formula	C19H23ClFN3O3 • HCl
Molecular Weight	424.31 g/mol (Free base: 359.81)
Synonyms	Enrofloxacin Hydrochloride; Enrofloxacin HCl; Baytril (Hydrochloride form); 1-Cyclopropyl-7-(4-ethylpiperazin-1-yl)-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid hydrochloride; ENRO-HCl; ENF HCl; CI-914 Hydrochloride; Ethyl Ciprofloxacin Hydrochloride
EINECS	Contact for details

Quality Control

Our Enrofloxain Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. Certificates of Analysis (COA) detailing purity, identity, and impurity profiles are provided with every shipment. We can supply material compliant with various pharmacopeial standards upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept under dry conditions to prevent 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% - 102.0% (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%
Microbial Limits	Meets standard requirements

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