Description

Niflumicacid CAS NO 4249-00-7 is a non-steroidal anti-inflammatory drug (NSAID) belonging to the fenamate class, recognized for its potent cyclooxygenase (COX) inhibitory activity. This compound is a critical intermediate in pharmaceutical synthesis, valued for its role in developing analgesic and anti-inflammatory medications. It is primarily required by pharmaceutical R&D laboratories, fine chemical manufacturers, and academic institutions engaged in drug discovery and development.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of advanced anti-inflammatory and analgesic drug candidates.
• Biochemical Research: Used as a reference standard and tool compound in pharmacological studies targeting prostaglandin synthesis and COX enzyme pathways.
• Analytical Standard: Serves as a high-purity certified reference material (CRM) for quality control and method validation in analytical laboratories.
• Academic Research: Employed in university and institutional research for investigating NSAID mechanisms of action and structure-activity relationships (SAR).

Basic Information

Product Name	Niflumicacid
CAS No.	4249-00-7
Molecular Formula	C13H9F3N2O2
Molecular Weight	282.22 g/mol
Synonyms	2-{[3-(Trifluoromethyl)phenyl]amino}nicotinic acid; N-(3-Trifluoromethylphenyl)anthranilic acid; Fenazox; UP 83; R 368C; JDL 369; Nifluril; Niflactol; Inflaryl
EINECS	224-215-8

Quality Control

Our Niflumicacid is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing, including HPLC for purity, IR for identification, and residual solvent analysis, to ensure it meets exacting standards for research and synthesis. A detailed Certificate of Analysis (COA) with batch-specific data is provided with every shipment.

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 heat and incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥98.0%
Loss on Drying	≤0.5%
Residue on Ignition	≤0.1%
Heavy Metals	≤20 ppm
Related Substances (HPLC)	Individual impurity ≤0.5%; Total impurities ≤1.0%

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