Description

Furaprofen is a synthetic organic compound belonging to the class of non-steroidal anti-inflammatory drugs (NSAIDs) with a specific furan ring structure. It serves as a key pharmaceutical intermediate and a reference standard in analytical research and development. This compound is essential for manufacturers and research institutions focused on developing and quality-controlling anti-inflammatory and analgesic agents.

Application

• Pharmaceutical Intermediate: Primary use in the synthesis of advanced NSAID drug candidates and active pharmaceutical ingredients (APIs).
• Analytical Reference Standard: Serves as a high-purity standard for method development, validation, and quality control (QC) testing in pharmaceutical laboratories.
• Biochemical Research: Used in pharmacological studies to investigate mechanisms of action related to cyclooxygenase (COX) enzyme inhibition.
• Chemical Synthesis: Acts as a versatile building block for medicinal chemists to create novel derivatives with potential therapeutic activity.

Basic Information

Product Name	Furaprofen
CAS No.	67700-30-5
Molecular Formula	C15H12O3
Molecular Weight	240.26 g/mol
Synonyms	2-(4-Isobutylphenyl)propionic acid 2-furylmethyl ester; Furaprofen; Furaprofen ester; Isobutylphenylfuryl propionate; Furan-2-ylmethyl 2-(4-isobutylphenyl)propanoate; (±)-Furaprofen; α-Methyl-4-(2-methylpropyl)benzeneacetic acid 2-furanylmethyl ester
EINECS	Contact for details

Quality Control

Our Furaprofen is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, IR and NMR for structural confirmation, and residual solvent analysis. We provide Certificates of Analysis (COA) with detailed results for traceability and compliance. Specifications can meet the requirements for use as a pharmaceutical intermediate or analytical standard.

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 strong oxidizing agents and 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)	≥ 98.0%
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.