Description

Flugestone 17-Acetate is a synthetic progestogen steroid derivative, widely recognized for its potent hormonal activity. This compound is a critical intermediate in the synthesis of advanced pharmaceutical agents, particularly in the field of veterinary and human reproductive medicine. It is essential for manufacturers and research institutions developing hormone-based therapeutics, fertility treatments, and specialized veterinary products.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of advanced progestogen and corticosteroid APIs.
• Veterinary Medicine: Used in the formulation of estrus synchronization and fertility control agents for livestock.
• Reproductive Health Research: Serves as a reference standard and active component in studies related to progesterone receptor activity.
• Hormone Therapy Development: Employed in R&D for creating treatments targeting hormonal imbalances and related disorders.
• Reference Standard: Utilized in analytical laboratories for method development, validation, and quality control testing of steroid-based products.

Basic Information

Product Name	Flugestone 17-Acetate
CAS No.	2529-45-5
Molecular Formula	C23H31FO5
Molecular Weight	406.49 g/mol
Synonyms	Flurogestone Acetate; 6α-Fluoro-17α-acetoxyprogesterone; 6α-Fluoro-17α-hydroxypregn-4-ene-3,20-dione 17-acetate; 17α-Acetoxy-6α-fluoroprogosterone; Cronolone; SC-9880; Flugestonum; Flugeston
EINECS	219-775-4

Quality Control

Our Flugestone 17-Acetate 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 stringent specifications for pharmaceutical use. A Certificate of Analysis (COA) documenting all test results is provided with every shipment.

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 low-humidity 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)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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