Description

Furcloprofen is a non-steroidal anti-inflammatory drug (NSAID) belonging to the arylpropionic acid class, known for its potent analgesic and anti-inflammatory properties. This compound is a critical active pharmaceutical ingredient (API) for the development and manufacturing of effective pain management medications. It is primarily utilized by pharmaceutical manufacturers and research institutions engaged in the production of anti-inflammatory and analgesic formulations, as well as in advanced pharmacological research.

Application

• Pharmaceutical API: Primary use as the active ingredient in prescription and over-the-counter (OTC) analgesic and anti-inflammatory drugs.
• Anti-inflammatory Formulations: Used in the development of topical creams, gels, and oral tablets for treating conditions like arthritis, muscle pain, and post-operative inflammation.
• Analgesic Drug Development: Serves as a key compound in R&D for new pain relief medications targeting COX enzyme inhibition.
• Veterinary Medicine: Applied in formulations for managing pain and inflammation in animals.
• Biochemical Research: Used as a reference standard and probe in pharmacological studies to understand NSAID mechanisms and pathways.
• Generic Drug Manufacturing: Essential for producing cost-effective generic versions of furcloprofen-based medications for global markets.

Basic Information

Product Name	Furcloprofen
CAS No.	58012-63-8
Molecular Formula	C15H12ClFO2
Molecular Weight	278.71 g/mol
Synonyms	2-Fluoro-α-methyl-4-biphenylacetic acid; 2-(4-Chlorophenyl)-3-fluoro-α-methylbenzenacetic acid; (±)-2-(2-Fluoro-4-biphenylyl)propionic acid; Furbiprofen (common misspelling); NSC 339024; FURCLOPROFEN; U-27182
EINECS	Contact for details

Quality Control

Our Furcloprofen is manufactured under strict quality management systems to ensure it meets the high standards required for pharmaceutical applications. Each batch undergoes comprehensive analytical testing, including identity confirmation, purity assay, and impurity profiling via advanced techniques like HPLC and GC. Certificates of Analysis (COA) are provided with every shipment, detailing full compliance with in-house specifications that align with ICH guidelines. We support audits and can provide documentation for regulatory submissions.

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 the container tightly sealed to protect from moisture. Store away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
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%
Heavy Metals	≤ 20 ppm
Sulfated Ash	≤ 0.1%

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