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4-Fluorophenyl 2-Thienyl Ketone

    • Product Name 4-Fluorophenyl 2-Thienyl Ketone
    • Alias 4F-2TK
    • Einecs 252-005-0
    • 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

    516207

    Chemical Name 4-Fluorophenyl 2-Thienyl Ketone
    Cas Number 1014-70-4
    Molecular Formula C11H7FOS
    Molecular Weight 206.24
    Appearance White to off-white solid
    Melting Point 68-71°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles FC1=CC=C(C=C1)C(=O)C2=CC=CS2

    As an accredited 4-Fluorophenyl 2-Thienyl Ketone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, sealed with a screw cap, tamper-evident ring, labeled with hazard symbols and product details.
    Shipping 4-Fluorophenyl 2-Thienyl Ketone is shipped in tightly sealed, chemical-resistant containers to prevent contamination and ensure safety. Packages are clearly labeled according to regulatory guidelines and shipped via certified couriers. Handling and transport occur under controlled temperature conditions, complying with all relevant safety and hazardous material regulations.
    Storage 4-Fluorophenyl 2-Thienyl Ketone should be stored in a tightly sealed container, protected from light and moisture, in a cool, well-ventilated area. Keep away from sources of ignition and incompatible materials such as strong oxidizers. Recommended storage temperature is at or below room temperature (20–25°C). Ensure proper labeling and restrict access to authorized personnel only.
    Application of 4-Fluorophenyl 2-Thienyl Ketone

    Applications of 4-Fluorophenyl 2-Thienyl Ketone in Industrial Manufacturing

    4-Fluorophenyl 2-Thienyl Ketone is a specialty intermediate frequently used in advanced organic synthesis and fine chemical production. As an original manufacturer, we ensure supply chain transparency and compliance across each vertical. Below, we detail specific industrial applications, regulatory frameworks, integration stages, and final product pathways relevant to actual downstream industries.

    1. Pharmaceutical Intermediate Synthesis

    In pharmaceutical manufacturing, this compound serves as a critical intermediate for the synthesis of small-molecule APIs, especially those involving fluorinated motifs for superior pharmacokinetic profiles. Formulators integrate it during stepwise building-block assembly, where regioselectivity and purity directly influence yield. Processing conditions must address side-chain reactivity and maintain stringent traceability to support regulated drug registration filings.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia monographs (where intermediate registration is required)
    • FDA 21 CFR Part 211 (current Good Manufacturing Practice)
    • ISO 9001:2015 for quality management systems in pharmaceutical supply

    Typical usage ratio

    • 5–25% by mole in multi-step API synthesis; ratio determined by target molecule and reaction route optimization

    Downstream process integration

    • Enters amidation or reductive coupling stages during synthetic route construction
    • Purification through column chromatography or recrystallization prior to further derivatization
    • In-process controls monitor intermediate integrity prior to final condensation or ring-closure essays
    • Batched with nitrogen blanketing to prevent decomposition under scale-up

    Final product types

    • Targeted fluorinated drug substances (oncology, CNS candidates)
    • Building block for heterocyclic core drugs
    • Lead compounds under IND and NDA application
    • In-market generic and originator pharmaceuticals containing thienyl scaffolds

    2. Agrochemical Active Ingredient Development

    This ketone is directly utilized in the synthesis chain of certain novel herbicidal and fungicidal agents, where the 4-fluorophenyl group supports active-site binding enhancement. Research and scale trials typically integrate it at the heterocyclization phase, with additional consideration for crop protection residue limits. Production plants must document traceability and formal compliance to agrochemical formulation standards.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 17025 for agrochemical laboratory testing
    • REACH Annexes for registration and safe handling of precursors
    • Good Laboratory Practice (GLP, OECD 1-17) for toxicological documentation

    Typical usage ratio

    • 2–12% by mass depending on final molecule and crop-specific formulation standards; exact dose adjusted for residue studies and desired efficacy

    Downstream process integration

    • Charged during heterocycle assembly reactions for new fungicide chemistries
    • Solvent-based extraction for high-purity isolation prior to downstream formulation
    • Monitoring in-process for organosulfur retention and trace-level impurities
    • Post-reaction treated in granular or emulsifiable concentrate production lines

    Final product types

    • Active ingredient concentrates (herbicides, fungicides)
    • Ready-to-use plant protection spray formulations
    • Chemical seed coatings
    • Biocidal blends for regulated export

    3. OLED and Specialty Electronic Material Manufacturing

    In electronics and advanced materials sectors, this compound acts as an intermediate for synthesizing organic semiconducting molecules, such as specific electron-transporting and light-emitting components in OLEDs. Manufacturing involves precise stoichiometric control, particularly for thin-film deposition material purity and process stability in display or lighting device production.

    Industry compliance standards

    • RoHS 2.0 Directive (Restriction of Hazardous Substances in electrical equipment)
    • IEC 61249 for organic electronic material quality
    • IPC-4101 for base materials qualification
    • ISO/TS 16949 for automotive electronic applications

    Typical usage ratio

    • 0.5–8% by weight in bulk intermediate synthesis, adjusted based on target device architecture and functional group needs

    Downstream process integration

    • Input in Suzuki-Miyaura or Buchwald coupling reactions to generate OLED emitter or host molecules
    • Intermediate purified and analyzed for residual halides and sulfur content prior to device-grade formulation
    • Direct feeding into batch reactors for scale-up to kilogram-tonnage batches
    • Material transferred to downstream device coating and encapsulation stages

    Final product types

    • Blue and green electroluminescent emitters
    • Electron transport layer molecules for OLED panels
    • Voltage adjustment additives for display thin films
    • Specialty polymers for flexible electronic circuits

    4. Advanced Fine Chemical Synthesis

    R&D laboratories and fine chemical manufacturers use this molecule to develop specialty thienyl-phenyl derivatives for custom applications in dyes, analytical reagents, or sensor molecules. Controlled environments focus on single-batch precision, enabling advanced structure-activity investigations for demanding industrial customers. Analytical QC and technical documentation are crucial during pilot and commercial scale-up phases.

    Industry compliance standards

    • ISO 9001:2015 for fine chemical quality systems
    • Classification, Labelling and Packaging (CLP, EU Regulation 1272/2008)
    • REACH registration codes for specialty chemicals
    • OECD Good Laboratory Practices for analytical method validation

    Typical usage ratio

    • 1–10% by mole as a core building block; proportion varies by desired functional derivative and purification recovery yield

    Downstream process integration

    • Incorporated in as the aryl-ketone backbone within multi-step functionalization
    • Exhibits reactivity under organometallic and electrophilic aromatic substitution conditions during derivative synthesis
    • QC ensures homogeneity and trace impurity disclosure for advanced applications
    • Packaged in certified drums or containers for subsequent specialty use

    Final product types

    • Chromogenic agents for analytical instruments
    • Custom pharmaceutical reference standards
    • Specialty dyes for research and textile coloration
    • Sensors and probe molecules for industrial QC labs
    Free Quote

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