Description

Ibuverine is a high-purity pharmaceutical intermediate and active ingredient, identified by CAS NO 31221-85-9. It is valued for its critical role in the synthesis of advanced therapeutic agents, ensuring high efficacy and process reliability. This compound is essential for manufacturers in the pharmaceutical and fine chemical industries seeking consistent quality for research, development, and production.

Application

• Pharmaceutical Synthesis: A key intermediate in the production of specific active pharmaceutical ingredients (APIs).
• Research & Development: Used in medicinal chemistry for the discovery and optimization of new drug candidates.
• Fine Chemical Production: Serves as a building block for complex organic molecules in specialty chemical manufacturing.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for cGMP production.
• Analytical Reference Standard: Utilized as a high-purity standard for quality control and method validation in analytical laboratories.

Basic Information

Product Name	Ibuverine
CAS No.	31221-85-9
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Ibuverine; 2-(4-Isobutylphenyl)propionic Acid 2-(Diethylamino)ethyl Ester; Ibuprofen Diethylaminoethyl Ester; Ibuprofen DEAE Ester; Ibuproxam; Fenoprofen Diethylaminoethyl Ester (related compound); NSC 113927; SQ 10,643
EINECS	Contact for details

Quality Control

Our Ibuverine is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. We provide comprehensive quality documentation, including detailed Certificates of Analysis (COA) that confirm identity, purity, and impurity profiles. The product is suitable for use in environments requiring adherence to cGMP and ISO standards.

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
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.