share

Gatifloxacin Nicotinate CAS NO 316819-35-9


Unit Price:

CAS No.:316819-35-9

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Gatifloxacin Nicotinate CAS NO 316819-35-9 is a pharmaceutical-grade salt form of the broad-spectrum fluoroquinolone antibiotic, gatifloxacin. This compound is valued for its enhanced stability and solubility profile, which is critical for precise formulation in advanced medicinal products. It is primarily required by manufacturers in the pharmaceutical and research sectors for the development and production of potent antibacterial agents.

Application

  • Active Pharmaceutical Ingredient (API) Synthesis: Serves as a key intermediate or the final active substance in the manufacture of antibacterial medications.
  • Ophthalmic Solution Formulation: Used in the production of sterile eye drops for treating bacterial conjunctivitis and other ocular infections.
  • Veterinary Pharmaceutical Production: Incorporated into formulations for treating bacterial infections in animals.
  • Research & Development: Employed in biochemical and microbiological research to study quinolone mechanisms of action and resistance.
  • Reference Standard: Utilized as a high-purity analytical standard in quality control laboratories for HPLC and other assay methods.

Basic Information

Product Name Gatifloxacin Nicotinate
CAS No. 316819-35-9
Molecular Formula C24H24FN3O6
Molecular Weight 469.46 g/mol
Synonyms Gatifloxacin Nicotinate; Gatifloxacin Nicotinate Salt; 1-Cyclopropyl-6-fluoro-8-methoxy-7-(3-methylpiperazin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid compound with pyridine-3-carboxylic acid (1:1); AM-1155 Nicotinate; BMS-206584-01; Gatifloxacin Mononicotinate; (±)-Gatifloxacin Nicotinate
EINECS Contact for details

Quality Control

Our Gatifloxacin Nicotinate is manufactured under strict quality systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling via HPLC, to ensure it meets stringent pharmaceutical standards. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance.

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 dry environment to prevent moisture absorption, which can affect stability and potency.

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) ≤ 1.0%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 20 ppm
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 0.5%

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.