Description

Enoxacin Gluconate is a fluoroquinolone antibiotic salt, synthesized from enoxacin and gluconic acid to enhance solubility and bioavailability. This compound is critical for the development of advanced antibacterial formulations, offering broad-spectrum activity against a wide range of Gram-positive and Gram-negative pathogens. It is primarily utilized by pharmaceutical manufacturers and research institutions in the production of ophthalmic solutions, injectable antibiotics, and other therapeutic agents requiring high-purity active pharmaceutical ingredients (APIs).

Application

• Pharmaceutical API: Serves as a key active ingredient in the formulation of antibacterial medications, particularly for ophthalmic and injectable products.
• Veterinary Medicine: Used in the development of antibacterial treatments for livestock and companion animals.
• Research & Development: A vital reference standard and intermediate in microbiological research and the synthesis of novel quinolone derivatives.
• Antibacterial Formulations: Incorporated into topical creams, gels, and solutions for the treatment of skin and soft tissue infections.
• Clinical Diagnostics: Employed in susceptibility testing and as a component in culture media for microbiological assays.

Basic Information

Product Name	Enoxacin Gluconate
CAS No.	104142-71-4
Molecular Formula	C19H24FN3O3 • C6H12O7
Molecular Weight	585.55 g/mol
Synonyms	Enoxacin Gluconate Salt; Enoxacin D-gluconate; 1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-1,8-naphthyridine-3-carboxylic acid compound with D-gluconic acid; AT-2266 Gluconate; CI-919 Gluconate; Flumark Gluconate; Enoxacin (Gluconate); Enoxacin Gluconic acid salt
EINECS	Contact for details

Quality Control

Our Enoxacin Gluconate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, identification by IR and NMR spectroscopy, and stringent control of residual solvents and related substances. We provide Certificates of Analysis (COA) with each shipment, ensuring traceability and compliance with cGMP and ICH Q7 guidelines for active pharmaceutical ingredients.

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 powder
Identification (IR)	Conforms to reference standard
Identification (HPLC)	Retention time matches reference
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 5.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Residual Solvents (GC)	Complies with ICH Q3C
Heavy Metals	≤ 20 ppm
Microbial Limits	Complies with Ph. Eur. 2.6.12/2.6.13

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