Description

Tilsuprost is a synthetic prostaglandin analog with specific biological activity. This compound is valued for its role as a key intermediate in advanced pharmaceutical research and development. It is primarily utilized by research institutions and pharmaceutical companies engaged in the synthesis of novel therapeutic agents. The product is supplied as Tilsuprost CAS NO 80225-28-1, ensuring precise identification for procurement and regulatory documentation.

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of prostaglandin-based active pharmaceutical ingredients (APIs).
• Biochemical Research: Used in laboratory studies to investigate prostaglandin receptor activity and related metabolic pathways.
• Drug Discovery: Employed in medicinal chemistry programs for the development of new ophthalmic or cardiovascular therapeutics.
• Reference Standard: Functions as an analytical standard for quality control and method validation in pharmaceutical manufacturing.

Basic Information

Product Name	Tilsuprost
CAS No.	80225-28-1
Molecular Formula	C23H29NO5
Molecular Weight	399.48 g/mol
Synonyms	9-Deoxy-9,10-didehydro-12-epi-PGF2α; 9,10-Didehydro-12-epi-prostaglandin F2α; UNII-5J0Q6S7124; 5-Heptenoic acid, 7-[(1R,2R,3R,5S)-2-[(1E,3R)-3-hydroxy-4-(3-hydroxy-1-octen-1-yl)-1-cyclopenten-1-yl]-3,5-dihydroxycyclopentyl]-, (5Z)-; Alfaprostol; Tilsuprostum
EINECS	Contact for details

Quality Control

Our Tilsuprost is produced under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identity confirmation by spectroscopic methods and purity determination by HPLC. A Certificate of Analysis (COA) detailing batch-specific results is provided to ensure traceability and compliance with your research or development protocols.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature (15-25°C) in a dry environment. For long-term storage, consider keeping the material under inert atmosphere to maintain stability.

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
Water Content (KF)	≤ 0.5%

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