Description

Flunoxaprofen is a non-steroidal anti-inflammatory drug (NSAID) belonging to the propionic acid derivative class. It is valued for its potent anti-inflammatory, analgesic, and antipyretic properties, making it a key intermediate in advanced pharmaceutical synthesis. This compound is primarily required by manufacturers in the pharmaceutical industry for the research, development, and production of novel therapeutic formulations.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of final active pharmaceutical ingredients (APIs) with anti-inflammatory action.
• Research & Development: Used in preclinical and clinical research to study new drug delivery systems and efficacy profiles for inflammatory conditions.
• Analytical Reference Standard: Serves as a high-purity standard in quality control laboratories for HPLC, LC-MS, and other analytical method development and validation.
• Veterinary Medicine: Potential application in developing anti-inflammatory treatments for animal healthcare.

Basic Information

Product Name	Flunoxaprofen
CAS No.	66934-18-7
Molecular Formula	C15H12FNO3
Molecular Weight	273.26 g/mol
Synonyms	Flunoxaprofen; 2-(4-Fluorophenyl)-α-methyl-5-benzoxazoleacetic acid; 5-Benzoxazoleacetic acid, 2-(4-fluorophenyl)-α-methyl-; CGP 28238; (±)-Flunoxaprofen; UNII-9T1415R4EL
EINECS	Contact for details

Quality Control

Our Flunoxaprofen is manufactured under strict quality management systems. Every batch undergoes rigorous analytical testing to ensure identity, purity, and consistency, meeting high standards for pharmaceutical intermediates. A comprehensive Certificate of Analysis (COA) detailing purity, impurities, and physical characteristics is provided with each shipment to support your quality assurance protocols.

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). Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Loss on Drying	≤0.5%
Residue on Ignition	≤0.1%

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