Description

17- Phenyl Trinor Prostaglandin F2α Methyl Amide is a high-purity synthetic prostaglandin analog, a key intermediate in advanced pharmaceutical research and development. This compound is valued for its specific biological activity and structural role in creating novel therapeutic agents. It is primarily utilized by pharmaceutical R&D laboratories and fine chemical manufacturers focused on developing treatments for ophthalmic and cardiovascular conditions.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of advanced prostaglandin-based active pharmaceutical ingredients (APIs).
• Ophthalmic Drug Research: Used in the development of next-generation glaucoma and ocular hypertension medications, such as prostaglandin analogs.
• Cardiovascular Research: Serves as a precursor in studies targeting vascular tone and platelet aggregation.
• Biochemical Standard: Acts as a reference standard for analytical method development and quality control in pharmaceutical manufacturing.
• Contract Synthesis: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects.
• Academic & Institutional Research: Used in university and institutional labs for pharmacological studies and signal transduction pathway analysis.

Basic Information

Product Name	17- Phenyl Trinor Prostaglandin F2α Methyl Amide
CAS No.	155206-01-2
Molecular Formula	C25H35NO4
Molecular Weight	413.55 g/mol
Synonyms	17-Phenyl-18,19,20-trinor-PGF2α methyl amide; Travoprost Impurity; Travoprost Related Compound; 9,11,15-Trihydroxy-17-phenyl-18,19,20-trinor-prost-5-en-1-oic acid, methyl amide; AL-6221; AL6221; Prostaglandin F2α analog; Phenyl trinor prostaglandin methyl amide
EINECS	Contact for details

Quality Control

Our 17- Phenyl Trinor Prostaglandin F2α Methyl Amide is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation, to ensure it meets the stringent requirements for pharmaceutical intermediate use. A Certificate of Analysis (COA) detailing all specifications and test results is provided with every shipment to guarantee traceability and batch-to-batch consistency.

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 (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment. For long-term storage, consider using desiccants.

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%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%

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