Description

Viprostol is a synthetic prostaglandin analog with specific biological activity. This compound is valued in advanced pharmaceutical research and development for its targeted pharmacological properties. It serves as a critical intermediate or active pharmaceutical ingredient (API) for researchers and manufacturers in the life sciences sector, particularly those developing specialized therapeutic agents.

Application

• Pharmaceutical Intermediate: Serves as a key building block in the synthesis of more complex prostaglandin-based drug candidates.
• Biomedical Research: Used as a reference standard or experimental compound in pharmacological studies investigating prostaglandin pathways.
• API Development: Acts as an Active Pharmaceutical Ingredient in the formulation of developmental drugs targeting specific receptor-mediated processes.
• Chemical Synthesis: Employed in organic synthesis for the preparation of novel analogs with modified biological activity.

Basic Information

Product Name	Viprostol
CAS No.	73647-73-1
Molecular Formula	C₂₃H₃₈O₅
Molecular Weight	394.55 g/mol
Synonyms	Viprostol; 9-Deoxo-9a-methyl-9a-homo-9-oxoprostaglandin F1α; 9a-Methyl-9a-homo-9-oxoprostaglandin F1α; CL 115,347; (5Z,9a,13E,15S)-9,15-Dihydroxy-11-oxo-16-phenoxy-17,18,19,20-tetranorprosta-5,13-dienoic acid methyl ester; Prostaglandin F1α analog
EINECS	Contact for details

Quality Control

Our Viprostol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via spectroscopic methods, to ensure it meets the high standards required for research and development. A Certificate of Analysis (COA) detailing all specifications is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store under an inert atmosphere (e.g., nitrogen or argon) at controlled room temperature (15-25°C) to minimize oxidation. The container should be kept in a cool, dry, and well-ventilated area.

Specification

Item	Specification
Appearance	White to off-white solid
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 guidelines

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