share

Fenoprofen Calcium CAS NO 34597-40-5


Unit Price:

CAS No.:34597-40-5

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Fenoprofen Calcium is a non-steroidal anti-inflammatory drug (NSAID) belonging to the propionic acid derivative class. Its primary value lies in its potent analgesic and anti-inflammatory properties, making it a critical active pharmaceutical ingredient (API) for therapeutic formulations. This compound is essential for pharmaceutical manufacturers developing prescription medications to manage pain and inflammation associated with conditions like arthritis and other musculoskeletal disorders.

Application

  • Primary use as an Active Pharmaceutical Ingredient (API) in the manufacture of prescription analgesic and anti-inflammatory medications.
  • Formulation of oral solid dosage forms, including tablets and capsules, for the management of mild to moderate pain.
  • Key component in drugs prescribed for the symptomatic relief of rheumatoid arthritis and osteoarthritis.
  • Used in pharmaceutical R&D for developing new drug delivery systems and combination therapies.
  • Reference standard in analytical laboratories for quality control and method development (HPLC, spectroscopy).

Basic Information

Product Name Fenoprofen Calcium
CAS No. 34597-40-5
Molecular Formula C30H22CaO6 • 2H2O
Molecular Weight 558.59 g/mol (Dihydrate)
Synonyms Fenoprofen Calcium Salt; Fenoprofen Calcium Dihydrate; (±)-Fenoprofen Calcium; DL-Fenoprofen Calcium; 2-(3-Phenoxyphenyl)propionic Acid Calcium Salt; Nalfon® (Brand Name); Propionic acid, 2-(3-phenoxyphenyl)-, calcium salt (2:1); Calcium bis(2-(3-phenoxyphenyl)propionate)
EINECS Contact for details

Quality Control

Our Fenoprofen Calcium is manufactured under strict quality management systems, targeting compliance with major pharmacopoeial standards such as USP and EP. Every batch undergoes comprehensive analytical testing including identification, assay, impurity profiling, and residual solvent analysis to ensure it meets stringent pharmaceutical-grade specifications. A detailed Certificate of Analysis (COA) is provided with each shipment to guarantee traceability and quality assurance.

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). 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 standard
Identification (Calcium) Conforms to standard
Assay (HPLC) 98.0% - 102.0% (on anhydrous basis)
Water Content (KF) 5.0% - 7.0% (Dihydrate)
Related Substances (HPLC) Individual impurity ≤ 0.5%; Total impurities ≤ 1.5%
Heavy Metals ≤ 20 ppm
Residue on Ignition ≤ 0.1%
Microbial Limits Meets USP <61> and <62> requirements

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

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.