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Etodolac CAS NO 41340-25-4


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CAS No.:41340-25-4

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Etodolac is a non-steroidal anti-inflammatory drug (NSAID) belonging to the pyranocarboxylic acid class, widely recognized for its potent analgesic and anti-inflammatory properties. Its primary commercial value lies in its selective inhibition of the COX-2 enzyme, which offers a favorable therapeutic profile for managing pain and inflammation. This active pharmaceutical ingredient (API) is essential for manufacturers in the pharmaceutical industry, specifically for the production of oral solid dosage forms such as tablets and capsules.

Application

  • Pharmaceutical API: Primary use as the active ingredient in prescription medications for the treatment of osteoarthritis and rheumatoid arthritis.
  • Analgesic Formulations: Incorporated into drug products designed for the management of acute and chronic pain.
  • Anti-inflammatory Medications: Used in formulations targeting the reduction of inflammation and associated symptoms.
  • Generic Drug Manufacturing: Serves as a critical component for companies producing bioequivalent generic versions of branded etodolac products.
  • Clinical Research: Supplied as a reference standard or raw material for pharmacological studies and new drug development.
  • Veterinary Pharmaceuticals: Potential application in veterinary medicine for pain management in animals, subject to regulatory approval.

Basic Information

Product Name Etodolac
CAS No. 41340-25-4
Molecular Formula C17H21NO3
Molecular Weight 287.35 g/mol
Synonyms 1,8-Diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid; Etodolic Acid; Lodine (Trade Name); Ultradol; AY-24236; RS-37619; (±)-Etodolac
EINECS 255-323-6

Quality Control

Our Etodolac is manufactured under strict quality management systems to ensure it meets the rigorous standards required for pharmaceutical applications. Each batch is subjected to comprehensive analytical testing, including identification, assay, and impurity profiling, to confirm compliance with relevant pharmacopeial monographs such as USP and EP. A detailed Certificate of Analysis (COA), providing full traceability and test results, is supplied 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). The product is hygroscopic (moisture-sensitive); therefore, the container must be kept tightly sealed after each use to minimize exposure to atmospheric humidity.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms
Identification (HPLC) Conforms
Assay (HPLC) 98.5% - 101.0%
Loss on Drying ≤ 0.5%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 20 ppm
Related Substances (HPLC) Individual impurity: ≤ 0.5% Total impurities: ≤ 1.5%
Particle Size Contact for details

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

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