Description

Flurbiprofen is a potent non-steroidal anti-inflammatory drug (NSAID) belonging to the phenylalkanoic acid class, widely recognized for its anti-inflammatory, analgesic, and antipyretic properties. Its primary commercial value lies in its effectiveness as an active pharmaceutical ingredient (API) for the formulation of prescription and over-the-counter medications. This compound is essential for pharmaceutical manufacturers and research institutions developing treatments for conditions such as rheumatoid arthritis, osteoarthritis, and postoperative pain management.

Application

• Pharmaceutical API: Primary use as the active ingredient in oral tablets, capsules, and topical formulations for pain and inflammation relief.
• Ophthalmic Solutions: Used in the formulation of eye drops for the inhibition of intraoperative miosis during cataract surgery.
• Analgesic Preparations: Key component in medications designed for the management of mild to moderate pain, including dental pain and dysmenorrhea.
• Anti-inflammatory Drugs: Formulation of drugs targeting chronic inflammatory conditions like rheumatoid arthritis and ankylosing spondylitis.
• Veterinary Medicine: Application in veterinary pharmaceuticals for the management of pain and inflammation in animals.
• Research & Development: Serves as a reference standard and a key intermediate in pharmacological and biochemical research exploring COX enzyme inhibition.

Basic Information

Item	Details
Product Name	Flurbiprofen
CAS No.	81937-33-9
Molecular Formula	C15H13FO2
Molecular Weight	244.26 g/mol
Synonyms	(±)-2-Fluoro-α-methyl-4-biphenylacetic acid; (±)-Flurbiprofen; Ansaid; Froben; Cebutid; Flugalin; 2-(2-Fluoro-4-biphenylyl)propionic acid; 2-Fluoro-α-methyl-4-biphenylacetic acid; 3-Fluoro-4-phenylhydratropic acid
EINECS	Contact for details

Quality Control

Our Flurbiprofen is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards, typically exceeding 99.0%, and complies with major pharmacopoeial specifications such as USP and EP. A detailed Certificate of Analysis (COA), confirming identity, purity, and impurity profiles via methods like HPLC and IR spectroscopy, is provided with every shipment to guarantee batch-to-batch consistency and regulatory compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Keep away from heat, open flames, and incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to standard
Assay (HPLC)	≥ 99.0%
Related Substances (HPLC)	Total impurities ≤ 0.5% Any individual impurity ≤ 0.1%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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