Description

Tiaprost is a synthetic prostaglandin analog, a high-purity active pharmaceutical ingredient (API) with significant therapeutic potential. Its primary value lies in its potent biological activity, making it a critical intermediate for advanced pharmaceutical research and development. This compound is essential for manufacturers and research institutions in the ophthalmic and pharmaceutical sectors, particularly for developing treatments targeting intraocular pressure and other prostaglandin-mediated pathways.

Application

• Ophthalmic Drug Development: Primary application as a key intermediate in the synthesis of prostaglandin-based medications for glaucoma and ocular hypertension.
• Pharmaceutical Research: Used as a reference standard and building block in medicinal chemistry for developing new therapeutic agents.
• API Manufacturing: Serves as a critical raw material for the commercial-scale production of finished dosage forms.
• Biochemical Studies: Employed in preclinical and clinical research to study prostaglandin receptor activity and related biological mechanisms.

Basic Information

Product Name	Tiaprost
CAS No.	62251-61-0
Molecular Formula	C₂₃H₃₃FO₅
Molecular Weight	408.51 g/mol
Synonyms	9,11,15-Trihydroxy-17-phenyl-18,19,20-trinor-16-(3-trifluoromethylphenoxy)-prosta-5,13-dien-1-oic acid; Travoprost Impurity C; Travoprost Related Compound C; AL-6221; U-62211; AL 6221; U 62211; Fluprostenol Isopropyl Ester Analog
EINECS	Contact for details

Quality Control

Our Tiaprost is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent purity and identity criteria, suitable for pharmaceutical applications. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming compliance with in-house specifications. We support development with regulatory-grade materials, and custom purity grades are available upon request.

Storage

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

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%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Heavy Metals	≤ 20 ppm
Loss on Drying	≤ 1.0%

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