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Tetrafluoroterephthalonitrile

    • Product Name Tetrafluoroterephthalonitrile
    • Alias TFTPN
    • Einecs 206-201-1
    • 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

    957465

    Name Tetrafluoroterephthalonitrile
    Cas Number 1684-14-2
    Molecular Formula C8F4N2
    Molecular Weight 200.09 g/mol
    Appearance White to off-white solid
    Melting Point 139-142 °C
    Solubility Slightly soluble in organic solvents
    Density 1.65 g/cm³ (estimated)
    Purity Typically >98%
    Synonyms 2,3,5,6-Tetrafluoroterephthalonitrile
    Inchi InChI=1S/C8F4N2/c9-5-3(1-13)7(11)8(12)4(6(5)10)2-14
    Smiles C1(=C(C(=C(C(=C1F)F)C#N)F)C#N)F
    Storage Temperature Store at room temperature

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

    Packing & Storage
    Packing Tetrafluoroterephthalonitrile, 25g, is packaged in a sealed amber glass bottle with secure screw cap and warning hazard labels.
    Shipping Tetrafluoroterephthalonitrile should be shipped in tightly sealed, chemical-resistant containers, clearly labeled according to hazard regulations. Transport in compliance with local, national, and international chemical shipping guidelines. Store away from moisture, heat, and incompatible materials, within a cool, ventilated area. Ensure appropriate documentation, including safety data sheets, accompanies all shipments.
    Storage Tetrafluoroterephthalonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture and incompatible substances such as strong oxidizers. Store it at room temperature and protect it from light. Clearly label the container and ensure access is restricted to trained personnel. Use appropriate secondary containment to avoid accidental spills.
    Application of Tetrafluoroterephthalonitrile

    Applications of Tetrafluoroterephthalonitrile in Industrial Manufacturing

    Tetrafluoroterephthalonitrile delivers highly specialized reactivity in advanced materials manufacturing, supporting diverse formulations in plastics, electronics, and polymer processing. As an experienced manufacturer, we have summarized the following downstream application scenarios based on genuine end user practice and industry insight.

    1. High-Performance Polyaryletherketone (PAEK) Synthesis

    Many engineering plastics producers incorporate this intermediate during the polycondensation stage, where it introduces fluorinated aromatic structures that enhance thermal and chemical resistance. Integrating it into the formulation allows for precise adjustment of polymer architecture, supporting the production of transparent and flame-retardant PAEK grades for demanding sectors.

    Industry compliance standards

    • ISO 1043-1:2011 (Plastics — Symbols and abbreviated terms for high-performance polymers)
    • ASTM D6262-12 (Standard for PAEK resins)
    • UL 94 (Flammability of plastic materials for parts in devices and appliances)
    • REACH Registration (EU Regulation EC 1907/2006)

    Typical usage ratio

    • 0.5–5.0 mol% of aromatic dinitrile units per total diacid/diol monomer feed; formulation adjusted for target molecular weight and property profile.

    Downstream process integration

    • Direct addition into polycondensation reactors, introduced as a functional comonomer alongside aromatic dihydroxy or diacid chlorides. Monomer feed ratio controlled continuously.

    Final product types

    • Fluorinated PAEK pellets for injection molding compounds
    • High transparency extruded sheets
    • Flame-retardant PAEK resin grades supplied to aerospace and transportation sectors

    2. Proton Exchange Membrane (PEM) Material Fabrication

    Leading membrane manufacturers utilize this compound to boost oxidative and hydrolytic durability in proton exchange membranes, critical in fuel cell assemblies. Its highly fluorinated structure supports sulfonation sites' incorporation, delivering improved proton conductivity without compromising chemical stability.

    Industry compliance standards

    • IEC 62282-2 (Fuel cell technologies – Fuel cell modules)
    • ISO 14687-2:2019 (Proton exchange membrane performance requirements)
    • RoHS Directive (EU 2011/65/EU restriction of hazardous substances)
    • ISO 14001:2015 (Environmental management systems)

    Typical usage ratio

    • Typically 2–8 wt% in aromatic copolymer backbone, optimized to balance membrane chemical durability with ion exchange capacity, based on type of sulfonating agent and molecular weight targets.

    Downstream process integration

    • Copolymerization with other aromatic monomers, followed by solution casting or extrusion to form membranes; monomer blend optimized to deliver specific ion-conductivity and mechanical requirements.

    Final product types

    • PEM rolls and sheets for automotive fuel cells
    • Membrane-electrode assemblies (MEAs)
    • Stationary fuel cell PEM modules for backup power solutions

    3. Liquid Crystal Polymer (LCP) Synthesis

    Producers of high-frequency electronic components select this intermediate as a reactive monomer to support rod-like mesogenic structure formation in LCPs. Its presence ensures enhanced dielectric stability and maintains low moisture absorption—vital for miniaturized connectors and thin-film circuits that demand exacting dimensional and thermal stability over time.

    Industry compliance standards

    • IPC-4101C (Specifications for base materials for printed boards)
    • IEC 61249-2-37:2017 (Materials for printed boards and other interconnecting structures)
    • UL 94 V-0 (Flammability standards for electronic component plastics)
    • JIS C 5011-1 (Japanese industrial standard for LCPs in electronics)

    Typical usage ratio

    • 1–4 mol% of difunctionalized dinitrile units in polycondensation batch; precise ratio determined by desired melting point and mechanical property targets.

    Downstream process integration

    • Incorporation during melt or solution polycondensation with diols/diacids to achieve target mesogenic segment length; post-polymerization blending and compounding possible depending on downstream molding or extrusion steps.

    Final product types

    • LCP-based granules for high-frequency PCB connectors
    • High-gloss, thin-walled LCP films for FPC antennas
    • Precision-molded LCP housing for microelectronic devices

    4. Pesticide Active Ingredient Intermediate

    Agrochemical manufacturers employ this fluorinated aromatic compound as a scaffold in the multi-step synthesis of specialty insecticides and fungicides. Its stable core enables the introduction of further functional groups, tailoring bioactivity to meet regulatory residue limits while improving crop protection profiles, especially in broad-acre cereals and fruits.

    Industry compliance standards

    • EU Regulation (EC) No 1107/2009 (Plant protection products)
    • FAO/WHO JMPR Guidelines (Pesticide residue limits)
    • US EPA Pesticide Registration (40 CFR Part 152)
    • ISO 9001:2015 (Quality management systems for agrochemicals)

    Typical usage ratio

    • Used as 1 of 2–3 main aromatic cores in synthesis, often 0.4–1.2 eq per multi-step batch; final ratio depends on targeted active ingredient yield and derivatization efficiency.

    Downstream process integration

    • Subjected to nucleophilic substitution and further fluorination or amination steps in agrosynthesis reactors prior to formulation with carriers, dispersants, and protective adjuvants.

    Final product types

    • Specialty insecticide technical grade for grain protection
    • Fungicidal actives for fruit and vegetable sprays
    • Precursor ingredients for registered crop protection formulas

    5. Electronic-Grade Polyimide Monomer Production

    Manufacturers specializing in flexible printed circuit boards use this dinitrile in the preparation of fluorinated aromatic diamines, which serve as core monomers for high-performance polyimide films. Its incorporation imparts lower water uptake, enhanced dielectric breakdown strength, and thermal stability, all necessary for modern compact, multilayer electronic assemblies.

    Industry compliance standards

    • IPC-4101E (Base materials for printed boards)
    • RoHS (Restriction of Hazardous Substances Directive EU 2011/65/EU)
    • UL 746B (Polymeric Materials Use in Electrical Equipment Evaluations)
    • JEITA ET-7302 (Standards for flexible polyimide substrates)

    Typical usage ratio

    • 0.8–2.5 mol% relative to total aromatic diamine input; blend ratios chosen by downstream formulators to meet dielectric and flexibility targets for specific device substrates.

    Downstream process integration

    • Conversion via catalytic hydrogenation to tetrafluoro-substituted diamines, directly fed to polyamic acid polymerization lines prior to thermal or chemical imidization. Careful stoichiometry control ensures uniformity in final molecular weight distribution.

    Final product types

    • Flexible polyimide films for mobile displays
    • Multi-layer flexible printed circuits
    • Thin gauge insulating coatings for semiconductor components

    6. Gas Separation Membrane Material Manufacturing

    Producers of specialty gas separation modules introduce this compound into the backbone of aromatic polymers to reduce gas diffusion coefficients while maintaining mechanical robustness. Its unique fluorination pattern substantially increases selectivity, making it central to membranes for demanding oxygen, nitrogen, and hydrogen separation in industrial gas supply systems.

    Industry compliance standards

    • ISO 9001:2015 (Membrane production quality systems)
    • EN 14170 (Membranes for gas separation and module test methods)
    • ASME B31.3 (Process Piping for gas module housing compatibility)
    • REACH (EC 1907/2006) compliance for fluorinated materials

    Typical usage ratio

    • Varies from 6–12 wt% as comonomer in aromatic copolymer formulation; higher ratios boost selectivity for specific gas pairs but can affect throughput, so adaptation occurs by membrane grade and specification.

    Downstream process integration

    • Feedstock for solution or interfacial polymerization during membrane casting or hollow fiber spinning. Monomer batch adjustments based on permeance and selectivity QC tests.

    Final product types

    • Hollow fiber membranes for oxygen enrichment
    • Flat sheet membranes for nitrogen production
    • Hydrogen purification membranes for industrial gas plants
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