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Flugestone

    • Product Name Flugestone
    • Alias Flurogestone
    • Einecs 206-642-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    124738

    Name Flugestone
    Chemical Formula C21H29FO4
    Molecular Weight 364.45 g/mol
    Iupac Name 17a-hydroxy-9α-fluoro-11β,17-dimethylprogesterone
    Cas Number 2529-45-5
    Drug Class Progestin
    Appearance White to off-white crystalline powder
    Solubility Practically insoluble in water
    Route Of Administration Mainly veterinary, often via intravaginal or subcutaneous
    Primary Use Regulation of estrus in animals
    Synonyms Fluorogestone, Flugestone acetate
    Storage Conditions Store at controlled room temperature, away from light and moisture

    As an accredited Flugestone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Flugestone is packaged in a sealed amber glass vial, 10 grams, labeled with chemical name, batch number, and safety instructions.
    Shipping Flugestone should be shipped in secure, tightly sealed containers, protected from light and moisture. It must be kept at controlled room temperature and clearly labeled. Shipping must comply with regulatory guidelines for pharmaceutical chemicals, including proper documentation and hazard labeling if applicable. Handle with care to avoid contamination or spillage during transit.
    Storage Flugestone should be stored in a tightly closed container, protected from light, moisture, and heat. It should be kept at room temperature, ideally between 15°C and 30°C (59°F–86°F). Store in a well-ventilated, secure place away from incompatible substances, such as strong oxidizing agents. Ensure only authorized personnel have access, and always follow local regulations and guidelines for storage of pharmaceuticals.
    Application of Flugestone

    Applications of Flugestone in Industrial Manufacturing

    As an established manufacturer, we supply flugestone for specialized industrial sectors where its precise hormonal activity is critical to finished product performance. Below we outline the core industrial application scenarios where flugestone serves as a key active component in production, with details on compliance frameworks, formulation norms, integration methods, and downstream product formats.

    1. Livestock Reproductive Hormone Preparations

    Flugestone acetate operates as a progestagen source in the formulation of veterinary drugs used to synchronize estrus in farm animals, including cattle, sheep, and goats. Pharmaceutical manufacturers formulate injectable suspensions, oral solutions, and intravaginal delivery systems by incorporating the material at controlled concentrations for regulation of breeding programs. Process engineers accurately meter flugestone during the compounding and blending phase, ensuring batch uniformity and compliance with national and international veterinary guidelines. Production relies on validated mixing, sterile filtration, and aseptic packaging technology to maintain consistent release characteristics suitable for use in herd management protocols, with the finished goods released following strict adherence to residue and withdrawal period regulations.

    Industry compliance standards

    • European Pharmacopoeia (Ph. Eur.) monographs for veterinary hormones
    • US FDA Center for Veterinary Medicine (CVM) regulations
    • China Ministry of Agriculture veterinary drug GMP
    • EU Regulation (EC) No 470/2009 for veterinary MRLs (Maximum Residue Limits)

    Typical usage ratio

    • 0.2%–0.5% by weight in intravaginal devices (e.g., CIDR); 0.5–1.0 mg per dose in oral solutions; precise level varies by target animal, device structure, and release curve required

    Downstream process integration

    • Metered addition during bulk formulation, followed by high-shear mixing
    • Uniform dispersion in polymer matrices for controlled release devices
    • Sterile filling and sealing under GMP conditions

    Final product types

    • Intravaginal progesterone-releasing devices for cattle, sheep, goats
    • Oral or injectable veterinary hormone suspensions
    • Synchronized estrus drug kits for commercial livestock herds

    2. Companion Animal Hormonal Therapy Production

    Animal pharmaceutical manufacturers utilize flugestone in compounding hormonal therapeutics that address reproductive disorders and cycle management in canines and felines. Formulators incorporate the active during wet-phase blending and emulsification stages for oral suspensions and pills, controlling the release profile for moderate hormone delivery in small doses. Downstream QC includes batch-release hormone analysis to assure dosing uniformity. End use requires that each batch meets all local pharmacopoeial and pet-specific veterinary drug compliance requirements, with disposal and environmental persistence considerations managed under regulatory frameworks.

    Industry compliance standards

    • British Pharmacopoeia Veterinary (BPVET) requirements
    • US FDA animal drug approval (NADA/ANADA process)
    • Global GMP (Good Manufacturing Practice) for veterinary pharmaceuticals
    • Local animal treatment guidelines and withdrawal management

    Typical usage ratio

    • 0.05%–0.15% by weight in oral tablets or suspensions; adjusted according to animal body weight recommendations and prescription dosing

    Downstream process integration

    • Accurate active blending in wet powder or microcrystalline matrix stage
    • Tabletting or bottle-filling of measured doses under environmental controls
    • End-of-line in-process QC verification of hormone consistency

    Final product types

    • Prescription tablets for estrus suppression in dogs and cats
    • Oral suspensions for reproductive cycle regulation
    • Veterinary specialty compounded hormone solutions for clinical dispensing

    3. Industrial-Scale Controlled Release Devices for Breeding Management

    Flugestone serves as a hormonal loading ingredient for manufacturers of industrial-scale controlled release delivery systems, primarily for large-scale herd breeding synchronization programs in the livestock industry. Downstream processors employ melt extrusion, polymer casting, and cross-linking polymerization techniques to encase precise hormone quantities within biocompatible carriers. Rigorous pre-shipment lot sampling and accelerated stability trials ensure that each device delivers the required hormone over an extended period, aligning with outcomes measured by field reproductive specialists.

    Industry compliance standards

    • European Medicines Agency (EMA) Guidelines on Veterinary Drug Quality
    • ISO 9001 Quality Management for medical devices (where applicable)
    • WHO Good Manufacturing Practices for pharmaceutical products
    • FAO and OIE animal health hormone administration protocols

    Typical usage ratio

    • 5–30 mg active per device, calibrated to cattle, sheep, or goat weight and holding period (typically 7–14 days); ratio computed via device loading studies

    Downstream process integration

    • Precision hormone metering and blending into hot-melt polymer base
    • Device molding with controlled setting and curing conditions
    • Batch sampling for in vitro release curve validation

    Final product types

    • Sustained-release intravaginal implants
    • Timed multiple-dose breeding management tools
    • Veterinary prescription-only breeding aids for intensive livestock

    4. Research-Grade Hormone Preparations for Animal Science Studies

    Specialty chemical suppliers and laboratory formulation units rely on flugestone within the development of research-grade hormone solutions for animal reproductive physiology experiments, toxicology studies, and field trial projects. Laboratory managers handle small-batch solution preparations, dissolve the active in ethanol or aqueous vehicle at protocol-defined strengths, and filter sterilize aliquots for controlled animal dosing. These segments require traceable batch origin, comprehensive purity documentation, and rapid lot turnaround for project timelines, with end use governed by institutional review boards and laboratory best practice codes.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) guidelines
    • Institutional Animal Care and Use Committee (IACUC) protocols
    • ISO 17025 certification for testing laboratories
    • National Research Council guide for laboratory animal care

    Typical usage ratio

    • 0.01%–0.1% (w/v) in solution, dependent on research protocol, animal model, and hormone exposure scenario

    Downstream process integration

    • Measured dissolution in ethanol or buffered solution
    • Aliquot sterile filtration and QC assay validation
    • Dispensing into single-use ampoules or bulk containers for research

    Final product types

    • Reference standard solutions for animal endocrine studies
    • Experimental veterinary drug preparations for preclinical trials
    • Positive control materials for laboratory assay validation
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