Description

Flurbiprofen Axetil is a potent non-steroidal anti-inflammatory drug (NSAID) prodrug, specifically designed for enhanced delivery and efficacy. This compound is of significant commercial interest for its targeted therapeutic action and improved pharmacokinetic profile compared to its parent molecule. It is primarily required by pharmaceutical manufacturers and research institutions engaged in the development of advanced analgesic and anti-inflammatory formulations.

Application

• Pharmaceutical Active Ingredient (API): Core component in the manufacture of injectable and topical analgesic medications.
• Post-Operative Pain Management: Formulated for intravenous administration to control acute pain following surgical procedures.
• Anti-inflammatory Formulations: Used in developing treatments for conditions involving inflammation and swelling.
• Research & Development: Serves as a critical reference standard and intermediate in pharmacological studies and new drug development.
• Controlled-Release Drug Delivery Systems: Utilized in advanced drug delivery platforms designed for sustained release and targeted action.

Basic Information

Product Name	Flurbiprofen Axetil
CAS No.	91503-79-6
Molecular Formula	C19H18FO4
Molecular Weight	338.34 g/mol
Synonyms	Flurbiprofen Axetil; Flurbiprofen 1-Acetoxyethyl Ester; (±)-2-Fluoro-α-methyl-4-biphenylacetic Acid 1-Acetoxyethyl Ester; (RS)-2-(2-Fluoro-4-biphenylyl)propionic Acid 1-Acetoxyethyl Ester; Axetil Flurbiprofen; Lipfen; Ropion; S-5960-A
EINECS	Contact for details

Quality Control

Our Flurbiprofen Axetil is manufactured under strict quality systems to ensure it meets the high standards required for pharmaceutical intermediates and APIs. Quality is assured through comprehensive analytical testing, including HPLC, IR, and residual solvent analysis. A Certificate of Analysis (COA) is provided with each batch, detailing purity, identity, and impurity profiles to support regulatory submissions and quality assurance protocols.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to maintain stability and potency.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.0% Any single impurity ≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%

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