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3-Fluorophenylacetylene

    • Product Name 3-Fluorophenylacetylene
    • Alias 3-fluoro-phenylacetylene
    • Einecs 703-196-6
    • 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

    689744

    Chemical Name 3-Fluorophenylacetylene
    Cas Number 403-71-8
    Molecular Formula C8H5F
    Molecular Weight 120.12
    Appearance Colorless to pale yellow liquid
    Boiling Point 165-167°C
    Density 1.08 g/cm3
    Refractive Index 1.555
    Smiles C#CC1=CC(=CC=C1)F
    Melting Point -21°C
    Flash Point 49°C
    Synonyms m-Fluorophenylacetylene
    Purity ≥98%
    Solubility Insoluble in water
    Storage Store at 2-8°C

    As an accredited 3-Fluorophenylacetylene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 5-gram amber glass bottle with a white screw cap, labeled "3-Fluorophenylacetylene, ≥98%," featuring hazard and safety information.
    Shipping 3-Fluorophenylacetylene is shipped in tightly sealed containers to prevent leaks and moisture ingress. It is transported as a hazardous material according to applicable regulations, typically by ground or air freight. The package is clearly labeled with chemical hazard information, and the shipment includes all necessary safety documentation and handling instructions.
    Storage 3-Fluorophenylacetylene should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent oxidation. Keep it in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible materials like strong oxidizers. Protect from light and moisture. Store in accordance with local regulations for hazardous chemicals.
    Application of 3-Fluorophenylacetylene

    Applications of 3-Fluorophenylacetylene in Industrial Manufacturing

    3-Fluorophenylacetylene serves as a key intermediate for several downstream manufacturing sectors. The following application scenarios reflect where our material directly supports critical synthesis steps in established processes, with precise formulation and compliance requirements defined by each segment.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers use 3-Fluorophenylacetylene as a building block in multi-step syntheses for targeted active pharmaceutical ingredients, especially in the production of fluorinated aromatic compounds with antineoplastic or central nervous system activity. The compound’s electron-rich acetylene moiety allows for regioselective coupling in Sonogashira and related cross-coupling transformations. Operators select dosage and process parameters based on route efficiency, impurity profiles, and regulatory needs imposed by the end API registration.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Parts 210 & 211 (US FDA)
    • European Pharmacopoeia and USP standards for process impurities and residual solvents
    • GMP inspection requirements from China NMPA, EMA, or country-specific authorities

    Typical usage ratio

    • 0.1–0.6 molar equivalents in targeted coupling or cyclization steps, determined by reaction stoichiometry and yield optimization during process development

    Downstream process integration

    • Charged as a coupling partner in Pd-catalyzed Sonogashira reaction vessels after in situ catalyst activation; typically added post-drying and base adjustment to ensure full conversion and minimize side-reactions

    Final product types

    • Anticancer intermediates: e.g., fluorinated phenylpyridines
    • CNS drug intermediates: e.g., substituted fluoroarene scaffolds
    • Fluorinated heterocyclic APIs

    2. Specialty Agrochemical Synthesis

    In the agrochemical sector, R&D and commercial plants integrate 3-Fluorophenylacetylene as a structural fragment during the synthesis of selective herbicide and insecticide actives containing fluorinated aryl acetylene motifs. Strict regulatory review requires both raw material traceability and batch-specific impurity controls. Process chemists determine the optimal charge relative to in situ halide intermediates, closely monitoring the stepwise addition to maintain crop safety criteria and active ingredient purity.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice
    • FAO/WHO pesticide specification guidelines
    • ISO 9001:2015 Quality Management System for agrochemical production
    • China ICAMA, US EPA, and EU Plant Protection Product (PPP) regulations

    Typical usage ratio

    • 0.2–0.8 mole per mole of key halide or boronic acid substrate, varying by target molecule and selectivity needs; adjusted for pilot or full-scale batch size

    Downstream process integration

    • Loaded during late-stage assembly in Suzuki, Sonogashira, or click-chemistry type couplings, after in-process control sample clearance

    Final product types

    • Selective herbicide actives: e.g., fluorinated arylpropiolates
    • Phenylacetylene-derived insecticides

    3. OLED and Organic Electronics Materials Manufacturing

    Producers of organic semiconductors use 3-Fluorophenylacetylene in the fabrication of advanced conjugated materials for organic light-emitting diodes, field-effect transistors, and solar cells. The presence of the fluorine substituent increases the electronic communication within π-conjugated systems, which is critical for device efficiency and color tuning. Formulation scientists integrate the compound into polydiacetylene or substituted polyacetylene matrices through controlled coupling polymerizations, with batch records closely referencing electronic-grade process standards to satisfy OLED panel manufacturers’ QC requirements.

    Industry compliance standards

    • IPC-4101B specification for base materials—general requirements for organic electronic components
    • IEC 60747-16 for semiconductor devices—OLED test methods
    • REACH Regulation (EC) No 1907/2006 for imported chemical substances in electronics manufacturing
    • RoHS 2015/863/EU Directive for hazardous materials restrictions

    Typical usage ratio

    • 1.5–10% by mole ratio relative to total monomer feedstock in proprietary precursor blends; ratio determined by desired emission wavelength and film morphology

    Downstream process integration

    • Introduced as a monomeric precursor in batch or continuous polymerization reactors for small molecule OLED materials or as a side-group modifier during prepolymer feed for cross-coupling polycondensation

    Final product types

    • Fluoroarene-containing OLED host emitters
    • Semiconducting polymer thin films for flexible display substrates
    • Electron transport/electron injection organic layers

    4. Advanced Coatings & Functional Polymers

    Manufacturers of high-performance surface coatings and specialty polymers use 3-Fluorophenylacetylene in the synthesis of functionalized resins, where its unique combination of fluorinated aromatic and unsaturated acetylene units imparts solvent resistance and tailored dielectric properties, particularly for industrial electronics encapsulation and high-frequency PCB coatings. Engineers optimize input level based on resin chain architecture, balancing cost with thermal/chemical requirements specified by end-user certifications.

    Industry compliance standards

    • ASTM D7803 for fluoropolymer-based coatings
    • IPC-4103B/WAM1 for base materials for high-speed/high-frequency printed boards
    • ISO 12944 for corrosion protection of steel structures by protective coatings, relevant when used on metallic substrates
    • UL 94 for flammability of polymeric materials (as relevant for electronics and aerospace applications)

    Typical usage ratio

    • 0.5–5% by weight in prepolymer formulations, adjustable according to the molecular weight and functional group density required for target resin performance

    Downstream process integration

    • Fed into the backbone functionalization stage of specialty polyurethane or epoxy resin synthesis, optionally via catalyzed addition to reactive backbone monomers prior to dispersion or film casting

    Final product types

    • High dielectric constant conformal coatings for printed circuit assemblies
    • Resistant fluorinated epoxy resins for industrial electronics
    • Low-friction fluoropolymeric thin films
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