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Allylpentafluorobenzene

    • Product Name Allylpentafluorobenzene
    • Alias 1-allyl-2,3,4,5,6-pentafluorobenzene
    • Einecs 242-044-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    322460

    Chemical Name Allylpentafluorobenzene
    Molecular Formula C9H5F5
    Molar Mass 208.13 g/mol
    Cas Number 4028-63-1
    Appearance Colorless liquid
    Boiling Point 154-156°C
    Density 1.273 g/cm³
    Flash Point 51°C
    Refractive Index 1.456
    Smiles C=CCc1c(F)c(F)c(F)c(F)c1F

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

    Packing & Storage
    Packing Allylpentafluorobenzene is supplied in a 25 g amber glass bottle with a screw cap, labeled with hazard and product information.
    Shipping Allylpentafluorobenzene should be shipped in tightly sealed, chemical-resistant containers under cool, dry conditions. It must comply with all local, national, and international transportation regulations for hazardous materials. Clearly label packages with hazard warnings, and handle with care to avoid leaks or spills. Compatible absorbent material should be included in case of accidental release.
    Storage Allylpentafluorobenzene should be stored in a tightly sealed container, away from sources of ignition, heat, and incompatible materials such as strong oxidizers. Store in a cool, dry, and well-ventilated area, preferably in a dedicated chemical storage cabinet. Protect from direct sunlight and moisture. Proper labeling and secondary containment are recommended to prevent spills and leaks.
    Application of Allylpentafluorobenzene

    Applications of Allylpentafluorobenzene in Industrial Manufacturing

    Allylpentafluorobenzene is a specialized fluorinated aromatic compound with distinct reactivity and stability, making it a preferred building block in advanced materials synthesis. As the original manufacturer, we support downstream partners in pharmaceuticals, specialty agrochemicals, advanced polymer engineering, and electronics materials with consistent quality and technical onboarding.

    1. Pharmaceutical Intermediate Synthesis

    Many pharmaceutical R&D and manufacturing teams utilize this unique aryl reagent in developing targeted fluorinated drug scaffolds where precise substitution patterns can enhance metabolic stability and bioavailability. Consistent purification and defined reactivity under selective cross-coupling conditions allow direct involvement in multi-step API synthesis, particularly for next-generation oncology and CNS candidates. Downstream formulations often require process optimization to ensure minimal by-product formation in late-stage intermediate coupling.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP General Chapter <1078> Good Storage and Distribution Practices for Drug Products
    • European Pharmacopoeia, Fluorinated Compound Specifications
    • FDA 21 CFR Part 211 — Current Good Manufacturing Practice for Finished Pharmaceuticals

    Typical usage ratio

    • Appears in fluorination or cross-coupling reaction streams at loadings of 0.5–5 mol%, adjusted per stoichiometric requirements of downstream arylation or functionalization steps

    Downstream process integration

    • Charged during palladium-catalyzed Suzuki-Miyaura or Heck reactions as either substrate or coupling partner, with on-site purification for immediate conversion
    • Also added in continuous flow synthesis set-ups for improved scale-up and process analytics

    Final product types

    • Pharmaceutical actives and intermediates with fluorinated aromatic motifs (oncology agents, anti-inflammatories, CNS drug leads)
    • Reference compounds and ligand scaffolds for medicinal chemistry libraries

    2. Agrochemical Intermediate Production

    Leading agrochemical formulators and synthesis companies employ this compound as a core reactant for constructing highly selective, persistent active ingredients in herbicide and fungicide development. The pentafluorophenyl ring enables differentiated biological interactions and target specificity, improving environmental fate and residual performance. Downstream use centers on custom fine chemical synthesis and formulation of crop protection compositions in continuous reactors under strict regulatory oversight.

    Industry compliance standards

    • ISO 9001:2015 for Quality Management Systems in Chemical Manufacturing
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EU)
    • OECD Principles on Good Laboratory Practice (GLP) for Agrochemical Development
    • FAO/WHO Specification Standards for Pesticide Ingredients

    Typical usage ratio

    • Used in intermediate-building blocks at 1–10 wt%, depending on desired active loading and the complexity of downstream product structure

    Downstream process integration

    • Introduced during palladium-catalyzed arylation or nucleophilic substitution for the assembly of fluorinated heterocycles
    • Incorporated in final crystallization and formulation steps for active ingredient isolation

    Final product types

    • Herbicidal and fungicidal compounds with high photostability
    • Chemical intermediates for seed treatment agents and crop protection blends

    3. High-Performance Polymer and Resin Modification

    Advanced material engineers specify this aryl compound for the controlled modification of specialty polymers, leveraging the pentafluorophenyl moiety’s effects on chemical resistance and dielectric properties. Copolymerization or end-group functionalization achieves finely tuned surface energy and thermal performance, essential for aerospace, filtration, and chemical processing applications. Strict protocol oversight governs the integration and handling of fluorinated monomeric components.

    Industry compliance standards

    • ASTM D4762 — Standard Guide for Testing Polymer Matrix Composite Materials
    • ISO 9001:2015 Quality Assurance
    • RoHS Directive 2011/65/EU for Electrical/Electronic Equipment
    • UL 94 Flammability Standards (related to finished polymer parts)

    Typical usage ratio

    • Typically introduced at 0.2–2 mol% as a functional comonomer or chain modifier; precise ratios depend on targeted mechanical/dielectric property adjustments

    Downstream process integration

    • Blended in pre-polymer mix before curing or copolymerization in solvent-resistant reactor vessels
    • Used in functional group end-capping post-polymerization with in-process analytical monitoring

    Final product types

    • Membranes for aggressive chemical filtration
    • Dielectric films for microelectronics and flexible circuitry
    • Corrosion-resistant linings and coatings

    4. Electronics and Semiconductor Surface Treatments

    Semiconductor and electronics manufacturers employ this highly fluorinated aromatic in niche etching mask development, as well as surface functionalization agents for passivation and adhesion modification in microfabrication steps. The unique electronic structure enables controlled reactivity and etch resistance across demanding plasma or wet-processing environments, complying with stringent purity standards and trace residue control.

    Industry compliance standards

    • SEMI C93 — Specification for Electronic Grade Organic Chemicals
    • IPC-4101E for Base Materials for High-Performance Printed Boards
    • ISO/TS 16949 for Automotive-Related Electronics Manufacturing Quality
    • JEDEC JESD46-D for Moisture/Reflow Sensitivity in Finished Components

    Typical usage ratio

    • Applied in surface coatings or developer baths at 0.1–1.5 wt%, inverted or increased based on wafer type and feature density in advanced nodes

    Downstream process integration

    • Dosed into etch mask resin formulations just prior to spin-coating during photolithography
    • Utilized as a terminal modification reagent in post-deposition surface treatments of thin films and microelectronic devices

    Final product types

    • Photoresist masks for advanced node semiconductor wafers
    • Electronic substrates with modified adhesion and wetting profiles
    • Surface-modified microelectronic assemblies for high-performance circuit integration
    Free Quote

    Competitive Allylpentafluorobenzene prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@sinochem-nanjing.com.

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    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

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