Description

Zoliprofen is a non-steroidal anti-inflammatory drug (NSAID) belonging to the arylpropionic acid class, recognized by the CAS registry number 56355-17-0. This compound is valued for its potent anti-inflammatory, analgesic, and antipyretic properties, making it a key intermediate in advanced pharmaceutical research and development. It is primarily required by pharmaceutical manufacturers and research institutions engaged in the synthesis of novel therapeutic agents for pain and inflammation management.

Application

• Pharmaceutical intermediate for the synthesis of novel NSAID (Non-Steroidal Anti-Inflammatory Drug) formulations.
• Active Pharmaceutical Ingredient (API) research and development for pain management therapies.
• Reference standard in analytical laboratories for quality control and method validation.
• Biochemical research to study cyclooxygenase (COX) enzyme inhibition mechanisms.
• Preclinical studies for evaluating pharmacokinetics and metabolic pathways.
• Development of combination drug therapies targeting chronic inflammatory conditions.

Basic Information

Product Name	Zoliprofen
CAS No.	56355-17-0
Molecular Formula	C15H12O3
Molecular Weight	240.26 g/mol
Synonyms	2-(4-Chlorophenyl)-α-methyl-5-benzoxazoleacetic acid; Zoliprofenum; Zoliprofene; UNII-6B6T0309QO; 5-Benzoxazoleacetic acid, 2-(4-chlorophenyl)-α-methyl-; α-Methyl-2-(4-chlorophenyl)-5-benzoxazoleacetic acid
EINECS	Contact for details

Quality Control

Our Zoliprofen is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency, meeting the stringent requirements for pharmaceutical intermediates. Certificates of Analysis (COA) detailing specifications and test results are provided with every shipment.

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 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 ≤ 1.5% Any single impurity ≤ 0.5%
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.