Description

Travoprost is a synthetic prostaglandin F2α analog and a potent, selective FP prostanoid receptor agonist. This high-purity active pharmaceutical ingredient (API) is critical for the development and manufacturing of advanced ophthalmic solutions. It is primarily required by pharmaceutical companies and research institutions focused on ocular therapeutics, specifically for the reduction of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension.

Application

• Primary Active Pharmaceutical Ingredient (API) in prescription ophthalmic solutions for glaucoma treatment.
• Research and Development of novel drug delivery systems for ocular applications.
• Formulation Studies for optimizing stability and bioavailability in topical eye drops.
• Reference Standard in analytical laboratories for quality control and method validation.
• Process Development for the synthesis of related prostaglandin analogs.

Basic Information

Product Name	Travoprost
CAS No.	157283-68-6
Molecular Formula	C₂₆H₃₅F₃O₆
Molecular Weight	500.55 g/mol
Synonyms	AL-6221; Travatan; PF-04475270; (Z)-7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-[(1E,3R)-3-hydroxy-4-[3-(trifluoromethyl)phenoxy]-1-buten-1-yl]cyclopentyl]-5-heptenoic acid isopropyl ester; Prostaglandin F2α analog; Fluprostenol isopropyl ester (related)
EINECS	Contact for details

Quality Control

Our Travoprost is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent specifications for identity, purity, and potency, suitable for pharmaceutical use. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming compliance with relevant in-house and international 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 nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.5% Any single impurity ≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Water Content (KF)	≤ 1.0%
Specific Rotation	Contact for details

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