Description

(+-)-Beraprost Sodium CAS NO 223556-34-1 is a stable, orally active prostacyclin (PGI2) analog and a potent vasodilator and platelet aggregation inhibitor. This compound is of significant interest for its potential therapeutic applications in treating vascular disorders. It is primarily utilized by pharmaceutical research and development organizations, as well as by manufacturers of active pharmaceutical ingredients (APIs) and fine chemicals.

Application

• Pharmaceutical Research & Development (R&D): Serves as a key intermediate or reference standard in the development of novel cardiovascular and pulmonary arterial hypertension (PAH) therapies.
• Active Pharmaceutical Ingredient (API) Synthesis: Used in the manufacturing process of pharmaceutical formulations targeting peripheral vascular diseases.
• Biochemical Research: Employed in in-vitro and in-vivo studies to investigate prostacyclin receptor (IP receptor) signaling pathways and vascular physiology.
• Reference Standard: Acts as a high-purity analytical standard for quality control and method validation in pharmaceutical analysis using techniques like HPLC.

Basic Information

Product Name	(+-)-Beraprost Sodium
CAS No.	223556-34-1
Molecular Formula	C24H29NaO6
Molecular Weight	436.48 g/mol
Synonyms	Beraprost Sodium (racemic); BPS; 2,3,3a,8b-Tetrahydro-2-hydroxy-1-(3-hydroxy-2-methyl-1-octen-6-ynyl)-1H-cyclopenta[b]benzofuran-5-butanoic acid sodium salt; Procylin; Dorner; TRK-100; (±)-Beraprost Sodium
EINECS	Contact for details

Quality Control

Our (+-)-Beraprost Sodium is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide full traceability and Certificates of Analysis (COA) are available for all shipments, detailing results from HPLC, NMR, and other relevant pharmacopeial methods.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept under dry, inert conditions to maintain stability and potency.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 2.0%
Residue on Ignition	≤ 0.5%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%

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