Description

Ibufenac is a non-steroidal anti-inflammatory drug (NSAID) belonging to the arylacetic acid class, known for its potent analgesic and antipyretic properties. Its primary value lies in its role as a key pharmaceutical intermediate for the synthesis of more advanced therapeutic agents. This compound is essential for manufacturers and research institutions in the pharmaceutical and fine chemical sectors focused on developing new anti-inflammatory medications.

Application

• Pharmaceutical Intermediate: Primary use in the synthesis of proprietary NSAID drugs and related therapeutic compounds.
• Research & Development: Critical reference standard and building block in medicinal chemistry for exploring new anti-inflammatory pathways.
• Active Pharmaceutical Ingredient (API) Manufacturing: Serves as a direct precursor in the production scale-up of specific ibuprofen-related APIs.
• Biochemical Research: Used in studies investigating cyclooxygenase (COX) enzyme inhibition mechanisms.
• Veterinary Medicine: Potential application in formulating anti-inflammatory treatments for animal health.

Basic Information

Product Name	Ibufenac
CAS No.	1553-60-2
Molecular Formula	C12H16O2
Molecular Weight	192.26 g/mol
Synonyms	4-Isobutylphenylacetic acid; p-Isobutylphenylacetic acid; Ibufenacum; IBPA; (±)-2-(4-Isobutylphenyl)acetic acid; NSC 256952; RD 11654; BRN 2048061
EINECS	Contact for details

Quality Control

Our Ibufenac is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. We provide comprehensive Certificates of Analysis (COA) for each lot, detailing key parameters such as assay, related substances, and residual solvents. Our quality commitment aligns with cGMP guidelines for pharmaceutical intermediates, ensuring reliability for your critical synthesis processes.

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). Keep away from strong oxidizing agents and bases.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.0%
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.