Description

Beraprost is a synthetic, stable prostacyclin analog with potent vasodilatory and antiplatelet aggregation properties. This compound is a critical active pharmaceutical ingredient (API) for the development of treatments targeting vascular and circulatory disorders. It is essential for pharmaceutical manufacturers and research institutions focused on cardiovascular, pulmonary, and renal therapeutics.

Application

• Pharmaceutical API: Primary active ingredient in medications for pulmonary arterial hypertension (PAH).
• Cardiovascular Research: Used in preclinical and clinical studies investigating vasodilation, platelet inhibition, and ischemia-reperfusion injury.
• Chronic Kidney Disease (CKD) Therapy: Investigated for its potential to slow the progression of renal dysfunction.
• Peripheral Vascular Disease: Research into treatments for conditions like Buerger's disease and critical limb ischemia.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method development in pharmaceutical labs.
• Formulation Development: Used in the R&D of oral, intravenous, and inhalable drug delivery systems.

Basic Information

Product Name	Beraprost
CAS No.	88430-50-6
Molecular Formula	C24H30O4
Molecular Weight	382.50 g/mol
Synonyms	Beraprost Sodium; TRK-100; Procylin; 2,3,3a,8b-Tetrahydro-2-hydroxy-1-(3-hydroxy-4-methyl-1-octen-6-ynyl)-1H-cyclopenta[b]benzofuran-5-butanoic acid; BPS; DL-Beraprost; UNII-3N91C2L98I
EINECS	Contact for details

Quality Control

Our Beraprost is manufactured under strict quality management systems, targeting high purity grades suitable for pharmaceutical applications. Each batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We ensure compliance with relevant ICH guidelines and can support documentation for regulatory submissions.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0% Any single unknown impurity ≤0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Water Content (KF)	≤1.0%
Heavy Metals	≤20 ppm

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