Description

16-Phenoxy Tetranor Prostaglandin F2Alpha CAS NO 51705-19-2 is a synthetic prostaglandin analog, a key intermediate in the development of advanced pharmaceutical compounds. This high-purity intermediate is critical for ensuring the efficacy and consistency of final active pharmaceutical ingredients (APIs) in therapeutic applications. It is primarily required by pharmaceutical R&D laboratories and manufacturers specializing in ophthalmic solutions, dermatological treatments, and other prostaglandin-based therapies.

Application

• Pharmaceutical Intermediate: A crucial building block in the synthesis of prostaglandin-based Active Pharmaceutical Ingredients (APIs).
• Ophthalmic Drug Development: Used in research and production of medications for glaucoma and ocular hypertension.
• Dermatological Research: Serves as a precursor in the development of treatments for hair growth disorders and skin conditions.
• Biochemical Research: A valuable tool for studying prostaglandin receptor activity and signaling pathways in vitro.
• Veterinary Medicine: Employed in the development of prostaglandin-based therapeutics for animal health.
• Reference Standard: Used as a high-purity analytical standard for quality control and method validation in pharmaceutical analysis.

Basic Information

Product Name	16-Phenoxy Tetranor Prostaglandin F2Alpha
CAS No.	51705-19-2
Molecular Formula	C₂₃H₃₄O₅
Molecular Weight	390.51 g/mol
Synonyms	16-Phenoxy Tetranor PGF2α; 16-Phenoxy Tetranor Prostaglandin F2α; 9α,11α,15-Trihydroxy-16-phenoxy-17,18,19,20-tetranorprosta-5,13-dien-1-oic acid; Travoprost Impurity; Travoprost Related Compound; Prostaglandin F2α Analog; 16-Phenoxy-17,18,19,20-tetranor-PGF2α; PGF2α Phenoxy Tetranor Analog
EINECS	Contact for details

Quality Control

Our 16-Phenoxy Tetranor Prostaglandin F2Alpha is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, identity confirmation by IR and NMR, and residual solvent analysis, to ensure it meets the stringent requirements for pharmaceutical intermediates. Certificates of Analysis (COA) are provided with every shipment, detailing all specifications and test results.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature (15-25°C) or as specified on the label or COA. This product is easily oxidized; for long-term storage, consider under an inert atmosphere (e.g., nitrogen or argon). Keep the container in a dry, well-ventilated place.

Specification

Item	Specification
Appearance	White to off-white powder
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 impurity ≤ 1.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Water Content (KF)	≤ 0.5%

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