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, which makes it a critical intermediate for advanced pharmaceutical research and development. This compound is essential for researchers and manufacturers in the ophthalmology and pharmaceutical sectors, particularly for developing treatments targeting intraocular pressure.

Application

• Pharmaceutical Intermediate: Serves as a key building block in the synthesis of advanced ophthalmic medications.
• Ophthalmic Research: Used in preclinical and clinical research for developing novel glaucoma and ocular hypertension treatments.
• API Development: A critical starting material for the production of prostaglandin-based active pharmaceutical ingredients.
• Biochemical Studies: Employed in pharmacological studies to investigate prostaglandin receptor activity and signaling pathways.
• Reference Standard: Utilized as an analytical reference standard in quality control laboratories for method development and validation.

Basic Information

Product Name	Tiaprost
CAS No.	71116-82-0
Molecular Formula	C₂₃H₂₉FO₅
Molecular Weight	404.47 g/mol
Synonyms	9,11,15-Trihydroxy-17-phenyl-18,19,20-trinorprosta-5,13-dien-1-oic acid; Travoprost Impurity C; 15(R)-Travoprost; AL-6221; 17-Phenyl-18,19,20-trinorprostaglandin F2α; U-101,603; Prostaglandin F2α analog; Travoprost related compound C
EINECS	Contact for details

Quality Control

Our Tiaprost is manufactured under strict quality management systems to ensure the highest standards of purity and consistency. Each batch undergoes comprehensive analytical testing, including HPLC for assay and impurity profiling, to meet stringent specifications for pharmaceutical intermediates. Certificates of Analysis (COA) documenting full compliance are available upon request.

Storage

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

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches 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
Heavy Metals	≤ 20 ppm

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