Description

Ibuproxam is a non-steroidal anti-inflammatory drug (NSAID) intermediate and a derivative of ibuprofen. This compound is of significant commercial interest for its role in the synthesis of active pharmaceutical ingredients (APIs) and for research into novel therapeutic agents. It is primarily utilized by pharmaceutical manufacturers and research institutions engaged in the development of analgesic and anti-inflammatory medications.

Application

• Pharmaceutical Intermediate: Key starting material or intermediate in the synthesis of ibuprofen and related NSAID APIs.
• Analgesic Research: Used in preclinical and clinical research to study the mechanisms and efficacy of pain relief medications.
• Anti-inflammatory Drug Development: Serves as a core structure for developing new compounds with improved anti-inflammatory properties and reduced side effects.
• Reference Standard: Employed as an analytical standard in quality control laboratories for method development and impurity profiling.
• Chemical Synthesis: Utilized in organic synthesis for preparing more complex molecules and prodrugs.

Basic Information

Product Name	Ibuproxam
CAS No.	53648-05-8
Molecular Formula	C13H18O2
Molecular Weight	206.28 g/mol
Synonyms	2-(4-Isobutylphenyl)propionohydroxamic Acid; Ibuprofen Hydroxamic Acid; Ibuproxamum; NSC 329680; p-Isobutylhydratropic Acid Hydroxamate; (±)-Ibuproxam; (RS)-Ibuproxam
EINECS	Contact for details

Quality Control

Our Ibuproxam is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide full traceability and Certificates of Analysis (COA) are available for all shipments, detailing key parameters such as assay and impurity profiles. Our quality commitment supports compliance with cGMP and other relevant pharmaceutical guidelines.

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 heat, open flames, and incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥98.0%
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%

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