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Fenoprofen Sodium (500 Mg) CAS NO 66424-46-2


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CAS No.:66424-46-2

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Fenoprofen Sodium (500 Mg) is the sodium salt form of the non-steroidal anti-inflammatory drug (NSAID) fenoprofen. This compound is a critical active pharmaceutical ingredient (API) valued for its potent anti-inflammatory, analgesic, and antipyretic properties. It is primarily required by pharmaceutical manufacturers for the formulation of solid and liquid dosage forms targeting pain and inflammation management. The product is supplied as a high-purity material suitable for pharmaceutical development and manufacturing.

Application

  • Pharmaceutical API: Primary use as the active ingredient in prescription and generic drug formulations.
  • Analgesic Tablets/Capsules: Formulation of oral solid dosage forms for the relief of mild to moderate pain.
  • Anti-inflammatory Medications: Manufacturing of drugs indicated for conditions like osteoarthritis and rheumatoid arthritis.
  • Drug Substance Intermediates: Serving as a key starting material or intermediate in further synthetic processes for novel drug candidates.
  • Clinical Trial Materials: Supply of GMP-grade material for preclinical research and clinical trial batches.
  • Reference Standard: Use as a high-purity chemical standard for analytical method development and quality control testing in laboratories.

Basic Information

Product Name Fenoprofen Sodium (500 Mg)
CAS No. 66424-46-2
Molecular Formula C15H13NaO3
Molecular Weight 264.25 g/mol
Synonyms Fenoprofen Sodium Salt; Fenopron Sodium; (±)-2-(3-Phenoxyphenyl)propionic acid sodium salt; DL-Fenoprofen Sodium; NSC 339539; Fenoprofen Na; Sodium Fenoprofen
EINECS Contact for details

Quality Control

Our Fenoprofen Sodium is manufactured and tested under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. Certificates of Analysis (COA) detailing purity, identity, and impurity profiles are provided with every shipment. We can supply material compliant with various pharmacopeial standards, including in-house specifications tailored to customer requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation. Keep away from incompatible materials.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference standard
Identification (HPLC) Retention time matches reference standard
Assay (HPLC) 98.0% - 102.0% (on anhydrous basis)
Water Content (KF) ≤ 5.0%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 20 ppm
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 0.5%

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

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