Description

Ximoprofen CAS NO 56187-89-4 is a high-purity non-steroidal anti-inflammatory drug (NSAID) compound. It serves as a critical active pharmaceutical ingredient (API) and a key intermediate in advanced pharmaceutical synthesis. This compound is essential for manufacturers and research institutions focused on developing and producing anti-inflammatory and analgesic medications. Its consistent quality and reliable supply are paramount for ensuring the efficacy and safety of final pharmaceutical products.

Application

• Primary Active Pharmaceutical Ingredient (API) in anti-inflammatory and analgesic drug formulations.
• Key chemical intermediate in the synthesis of advanced NSAID derivatives and prodrugs.
• Reference standard for quality control and analytical method development in pharmaceutical laboratories.
• Research and development of novel therapeutic agents targeting cyclooxygenase (COX) enzymes.
• Pre-clinical and clinical studies investigating pharmacokinetics and pharmacodynamics of NSAIDs.

Basic Information

Product Name	Ximoprofen
CAS No.	56187-89-4
Molecular Formula	C16H14O3
Molecular Weight	254.28 g/mol
Synonyms	2-[4-(2-Oxocyclopentylmethyl)phenyl]propanoic Acid; KM-100; Ximoprofenum; UNII-7J8Q5F2Y0I; (±)-Ximoprofen; rac-Ximoprofen; Cyclopentylmethyl Phenyl Propanoic Acid Derivative
EINECS	Contact for details

Quality Control

Our Ximoprofen is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. We provide Certificates of Analysis (COA) with detailed results for parameters including assay, related substances, and residual solvents, supporting compliance with cGMP and ICH 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 the container tightly sealed to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.0% Any single impurity ≤ 0.5%
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.