Description

Ibuproxam is a non-steroidal anti-inflammatory drug (NSAID) intermediate and a derivative of ibuprofen. This compound is of significant value in pharmaceutical research and development, serving as a key precursor in the synthesis of novel anti-inflammatory agents. It is primarily required by pharmaceutical manufacturers and research institutions focused on developing new therapeutic formulations and studying the structure-activity relationships of NSAIDs.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of ibuprofen derivatives and other non-steroidal anti-inflammatory drugs (NSAIDs).
• Research & Development: Used in academic and industrial laboratories for pharmacological studies and the development of new analgesic and anti-inflammatory compounds.
• Chemical Synthesis: Serves as a starting material or intermediate in organic synthesis for creating molecules with potential therapeutic activity.
• Reference Standard: Employed as an analytical standard in quality control laboratories for method development and validation in pharmaceutical analysis.

Basic Information

Product Name	Ibuproxam
CAS No.	73826-33-2
Molecular Formula	C14H19NO2
Molecular Weight	233.31 g/mol
Synonyms	2-(4-Isobutylphenyl)propionohydroxamic acid; Ibuprofen hydroxamic acid; Ibuproxamum; NSC 339539; (RS)-2-(4-Isobutylphenyl)propanehydroxamic acid; α-Methyl-4-(2-methylpropyl)benzeneacetic acid hydroxamide
EINECS	Contact for details

Quality Control

Our Ibuproxam is produced and tested under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure identity, purity, and consistency. A comprehensive Certificate of Analysis (COA) detailing specifications such as assay, related substances, and residual solvents is provided with every shipment to support your quality assurance protocols.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (typically 15-25°C). Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Loss on Drying	≤0.5%
Residue on Ignition	≤0.1%

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