Description

Prostaglandin F2α Serinol Amide is a chemically modified analog of Prostaglandin F2α, designed to enhance stability and bioavailability for advanced research and development applications. This compound is critical for scientists exploring novel pathways in cellular signaling and receptor interaction studies. It is primarily utilized by pharmaceutical R&D teams and biotechnology companies focused on developing new therapeutic agents, particularly in the fields of ophthalmology, reproductive health, and inflammation.

Application

• Pharmaceutical Research & Development: Serves as a key intermediate or active pharmaceutical ingredient (API) in the development of novel prostaglandin-based therapeutics.
• Ophthalmic Drug Development: Investigated for potential use in glaucoma treatments and other intraocular pressure management solutions due to its prostaglandin activity.
• Biochemical Research: Used as a high-purity reference standard and probe in studying FP receptor signaling pathways and related biological mechanisms.
• Reproductive Health Studies: Applied in research concerning luteolysis and the regulation of reproductive cycles.
• Cosmeceutical R&D: Explored for potential applications in eyelash growth serums and other dermatological formulations.
• Academic Research: Utilized in university and institutional labs for fundamental studies on lipid mediators and their physiological roles.

Basic Information

Product Name	Prostaglandin F2α Serinol Amide
CAS No.	1135226-99-1
Molecular Formula	C23H39NO6
Molecular Weight	425.56 g/mol
Synonyms	PGF2α Serinol Amide; 9α,11α,15S-Trihydroxy-17S,18,19,20-tetranor-5-cis-13-trans-prostadienoic Acid Serinol Amide; (Z)-7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-[(E,3S)-3-hydroxyoct-1-en-1-yl]cyclopentyl]hept-5-enamide of 2-Amino-1,3-propanediol; Prostaglandin F2α-1,3-Dihydroxy-2-propylamide; Travoprost Related Compound; PGF2α-SA; FP Prostaglandin Agonist Intermediate.
EINECS	Contact for details

Quality Control

Our Prostaglandin F2α Serinol Amide is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, NMR and MS for structural confirmation, and stringent controls for residual solvents and impurities. We provide Certificates of Analysis (COA) with each shipment, detailing all specifications and test results to ensure compliance with your research or cGMP-grade requirements.

Storage

Preserve in a tightly closed container, protected from light. Store at -20°C or below under an inert atmosphere (e.g., argon or nitrogen) to prevent oxidation. The product is hygroscopic and must be kept in a dry environment. Allow the sealed vial to equilibrate to room temperature before opening to minimize moisture condensation.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (HPLC)	Conforms to reference standard
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Single Unknown Impurity (HPLC)	≤ 0.5%
Total Impurities (HPLC)	≤ 2.0%
Water Content (KF)	≤ 1.0%
Residual Solvents (GC)	Meets ICH guidelines

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