Description

Urefibrate is a high-purity organic compound, specifically a fibrate derivative, used as a key pharmaceutical intermediate and research chemical. Its primary value lies in its role in the synthesis of advanced lipid-regulating agents and other active pharmaceutical ingredients (APIs). This product is essential for manufacturers and research institutions in the pharmaceutical, biotechnology, and fine chemical sectors requiring reliable, high-quality building blocks for drug development and production.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of fibrate-class lipid-modulating agents and other therapeutic compounds.
• Research & Development: Used in biochemical and pharmacological research to study metabolic pathways and develop new therapeutic entities.
• Fine Chemical Synthesis: Serves as a versatile precursor for the preparation of more complex, high-value specialty chemicals.
• Reference Standard: Employed as an analytical standard in quality control laboratories for method development and validation.

Basic Information

Product Name	Urefibrate
CAS No.	38647-79-9
Molecular Formula	C13H18ClNO3
Molecular Weight	271.74 g/mol
Synonyms	Urefibrate; 2-(4-Chlorophenoxy)-2-methylpropanoic acid isobutylcarbamoyl ester; Isobutyl 2-(p-chlorophenoxy)-2-methylpropionylcarbamate; CL 90250; NSC 329860; Chlofibrate derivative; Urefibrate (USAN)
EINECS	Contact for details

Quality Control

Our Urefibrate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical intermediate applications. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming identity, purity, and impurity profiles.

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 incompatible materials.

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.