Description

Beraprost is a synthetic, stable prostacyclin analog known for its potent vasodilatory and antiplatelet properties. This compound is critical for research and development in the pharmaceutical sector, particularly for investigating treatments for pulmonary arterial hypertension and peripheral vascular diseases. It is essential for pharmaceutical manufacturers, R&D laboratories, and academic institutions focused on cardiovascular therapeutics and prostaglandin research.

Application

• Pharmaceutical Active Ingredient (API): Primary use in the development and manufacturing of medications for pulmonary arterial hypertension (PAH).
• Cardiovascular Research: A key tool for studying vasodilation, platelet aggregation inhibition, and vascular remodeling in preclinical models.
• Cell Signaling Studies: Used to investigate the role of the IP receptor and prostacyclin pathways in various physiological and pathological processes.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method development in pharmaceutical analysis.

Basic Information

Product Name	Beraprost
CAS No.	223556-33-0
Molecular Formula	C24H30O4
Molecular Weight	382.50 g/mol
Synonyms	Beraprost Sodium; BPS; 2,3,3a,8b-Tetrahydro-2-hydroxy-1-(3-hydroxy-4-methyl-1-octen-6-ynyl)-1H-cyclopenta[b]benzofuran-5-butyric Acid; DL-Beraprost; TRK-100; Procylin
EINECS	Contact for details

Quality Control

Our Beraprost is manufactured under strict quality management systems to ensure high purity and batch-to-batch consistency, suitable for pharmaceutical research and development. Each batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We adhere to relevant ICH guidelines and can support development aligned with cGMP standards.

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 (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment to prevent degradation.

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%
Water Content (KF)	≤1.0%
Residue on Ignition	≤0.1%

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