Description

Ponfibrate CAS NO 53341-49-4 is a high-purity pharmaceutical intermediate and active pharmaceutical ingredient (API) belonging to the fibrate class of compounds. It is a critical building block in the synthesis of advanced lipid-regulating agents used to manage cholesterol and triglyceride levels. This compound is essential for pharmaceutical manufacturers and research institutions focused on developing and producing cardiovascular therapeutics. Our supply is characterized by stringent quality control, ensuring reliability for sensitive formulation processes.

Application

• Pharmaceutical API Synthesis: Primary use as an active pharmaceutical ingredient in the manufacture of lipid-lowering medications.
• Cardiovascular Drug Development: Key intermediate in research and development of new fibrate-based therapies for hyperlipidemia.
• Biochemical Research: Used as a reference standard and tool compound in metabolic and pharmacological studies.
• Generic Drug Production: Essential for the cost-effective production of generic versions of established fibrate drugs.
• Precision Medicine Formulations: Serves as a base for developing targeted drug delivery systems and combination therapies.
• Contract Manufacturing (CMO): Supplied to contract manufacturing organizations for large-scale, GMP-compliant production runs.

Basic Information

Product Name	Ponfibrate
CAS No.	53341-49-4
Molecular Formula	C23H28O5
Molecular Weight	384.47 g/mol
Synonyms	Ponfibrate; 2-[4-(4-Chlorobenzoyl)phenoxy]-2-methylpropanoic Acid Isopropyl Ester; Isopropyl 2-[p-(p-Chlorobenzoyl)phenoxy]-2-methylpropionate; CL-102,603; Procetofen; Procetofene; Lipanthyl (related to final drug form); Fenofibrate (related compound, verify specific isomer).
EINECS	Contact for details

Quality Control

Our Ponfibrate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, assay, and impurity profiling via HPLC, to ensure it meets high-purity standards suitable for pharmaceutical use. We provide full traceability and Certificates of Analysis (COA) are available for every shipment. Our processes are designed to align with ICH guidelines and GMP principles where applicable.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). Keep away from incompatible materials such as strong oxidizing agents. The container should be kept 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 matches reference standard
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.0% Any single unknown impurity ≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%
Heavy Metals	≤ 20 ppm

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