Description

Zaltoprofen is a non-steroidal anti-inflammatory drug (NSAID) belonging to the propionic acid derivative class, recognized by the CAS registry number 89482-01-9. This compound is valued for its potent anti-inflammatory, analgesic, and antipyretic properties, making it a key active pharmaceutical ingredient (API) for targeted therapeutic formulations. It is primarily required by pharmaceutical manufacturers and research institutions engaged in the development of advanced pain management and anti-inflammatory medications.

Application

• Pharmaceutical API: Primary use as the active ingredient in prescription and over-the-counter anti-inflammatory and analgesic drug formulations.
• Analgesic Development: Research and production of medications for the relief of mild to moderate pain, including post-operative and musculoskeletal pain.
• Anti-inflammatory Therapeutics: Formulation of drugs aimed at reducing inflammation associated with conditions like arthritis, tendinitis, and bursitis.
• Antipyretic Medications: Component in fever-reducing pharmaceutical products.
• Clinical Research: Used as a reference standard or active compound in pharmacological studies and clinical trials.
• Veterinary Medicine: Potential application in developing anti-inflammatory treatments for animals.

Basic Information

Product Name	Zaltoprofen
CAS No.	89482-01-9
Molecular Formula	C17H14O3S
Molecular Weight	298.36 g/mol
Synonyms	Zaltoprofen; 2-(10,11-Dihydro-10-oxodibenzo[b,f]thiepin-2-yl)propionic Acid; Soleton; Zepolas; M-5011; Peon; UNII-0PIA0B1C4U; 0PIA0B1C4U
EINECS	Contact for details

Quality Control

Our Zaltoprofen 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 identification, assay, and impurity profiling via HPLC and other pharmacopeial methods. A Certificate of Analysis (COA) detailing purity, related substances, residual solvents, and other critical parameters is provided with every shipment to guarantee traceability and 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 (typically 15-25°C). Keep the container tightly sealed to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Related Substances (HPLC)	Total impurities ≤ 1.0% Any single impurity ≤ 0.5%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Residual Solvents (GC)	Complies with ICH Q3C guidelines

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