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2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene

    • Product Name 2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene
    • Alias TFABO
    • Einecs 605-155-5
    • 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

    190603

    Chemicalname 2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene
    Molecularformula C8H4F4N2O2
    Molecularweight 236.12 g/mol
    Casnumber 342879-86-3
    Appearance White to off-white solid
    Solubility Soluble in common organic solvents
    Purity Typically ≥ 97%
    Smiles Nc1cc2oc(cc2oc1F)F
    Inchi InChI=1S/C8H4F4N2O2/c9-8(10)5-3-13-6-2-1-4(12)7(14-6)11-5/h1-3H,12H2
    Storagetemperature Store at 2-8°C

    As an accredited 2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 mg of 2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene, sealed in an amber glass vial with tamper-evident cap, labeled.
    Shipping 2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene should be shipped in tightly sealed containers under dry, cool conditions. Handle and transport as a hazardous chemical, following all relevant regulations for toxic and potentially environmentally harmful substances. Avoid physical damage, excessive heat, and direct sunlight. Proper labeling and documentation must accompany the shipment.
    Storage 2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Protect from moisture and direct sunlight. Use chemical-resistant containers, and label clearly. Access should be restricted to trained personnel, with proper personal protective equipment available nearby.
    Application of 2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene

    Applications of 2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene in Industrial Manufacturing

    We supply 2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene, which has enabled new advances in specialty organofluorine chemistry. Below, we detail downstream applications where this intermediate forms an essential and differentiated role. Each scenario below draws from commercially validated production models, with focused discussion of industry compliance, formulation, process flow, and product output.

    1. Advanced Pharmaceutical Intermediate Synthesis

    Major pharmaceutical companies use this fluorinated benzodioxene as a key amine-containing building block when synthesizing heterocyclic scaffolds for selective kinase inhibitors and antiviral drugs. Its electron-withdrawing and sterically hindered properties help improve drug candidate stability during complex multi-step syntheses. Downstream integration mainly appears in the late intermediate coupling stages during small molecule API (active pharmaceutical ingredient) manufacturing for advanced therapeutic candidates.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA cGMP regulations)
    • EU GMP Part II (EMA)
    • USP <467> (organic volatile impurities control in APIs)

    Typical usage ratio

    • 0.5–5% molar equivalent in reactive coupling stages; adjusted based on targeted heterocyclic core and impurity risk profile

    Downstream process integration

    • Added at the amidation or Suzuki coupling stage, generally after halogenation and before protective group removal operations

    Final product types

    • Fluorinated kinase inhibitor APIs
    • Next-generation antiviral actives
    • Late-stage intermediates for CNS therapeutic agents

    2. Fluorinated Specialty Polymer Synthesis

    Leading electronics and membrane manufacturers use this compound as a highly effective polycondensation monomer for synthesizing high-performance polymers with strong thermal and solvent resistance. It delivers improved dielectric properties and chemical inertness, which are critical for advanced filtration membranes and thin-film applications. The raw material gets incorporated during the polycondensation reaction, predominantly forming part of the backbone in aromatic copolymers.

    Industry compliance standards

    • ISO 9001:2015 (Quality management system for polymer processing)
    • IEC 61249-2-21 (requirements for halogen-free insulating materials in electronics)
    • RoHS Directive 2011/65/EU (for electronic components)
    • REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • 3–15% weight basis in polycondensation with other aromatic diols and diacids; the ratio is defined by the required fluorine content and foil thickness

    Downstream process integration

    • Dosed together with other monomers in the melt-phase or solution-phase polycondensation reactor to directly affect backbone structure

    Final product types

    • Microporous filtration membranes for fuel cells
    • Etch-resistant electronic films
    • High-frequency PCB dielectric layers

    3. Agrochemical Active Ingredient Intermediate

    Agrochemical R&D and production teams introduce this aminated, heavily fluorinated intermediate when constructing new classes of crop protection actives, specifically for developing fungicides with strong field persistence and reduced mammalian toxicity. The material is integrated in the early to mid-stage pathway for assembling fused heterocyclic structures common to next-generation systemic fungicides. Quality documentation and exposure controls require full traceability throughout the downstream synthesis workflow.

    Industry compliance standards

    • FAO/WHO JMPR (Joint FAO/WHO Meeting on Pesticide Residues) guidance
    • OECD Guidelines for the Testing of Chemicals (Mono- and Multi-Constituent Substances)
    • ISO 17025 laboratory control for process testing
    • China ICAMA registration standards for new agrochemical active development

    Typical usage ratio

    • 10–30% mole fraction when directly building the fluoroaromatic backbone structure; actual fraction adapted for ring closure efficiency

    Downstream process integration

    • Introduced prior to cyclization or N-arylation steps, immediately following the initial fluorinated arene construction

    Final product types

    • Systemic fungicide technical concentrates
    • Advanced triazole-based field crop protectants
    • High-selectivity pre-emergent herbicide intermediates

    4. OLED Material Intermediate

    Display panel manufacturers and materials formulators apply this specialty compound as a precursor for creating blue- and green-emitter fluorinated organic semiconductor materials. The amine functionality, combined with the tetrafluoro substitution, tailors emission wavelength and enhances oxidative stability needed in high luminance OLED construction. Use is focused on fine chemical synthesis for constructing emitter cores or electron transport layers, with purity and heavy metal trace limits stringently monitored for panel reliability.

    Industry compliance standards

    • IEC 62341 (OLED panels for general lighting and displays)
    • RoHS Directive 2011/65/EU (for eliminating hazardous substances in electronic components)
    • ISO 14644-1/2 (clean manufacturing conditions)
    • QMS ISO 9001:2015 for specialty electronic material manufacturing

    Typical usage ratio

    • 2–8% w/w basis in emitter/electron transporter synthetic routes; percentage adjusted according to desired wavelength shift and carrier mobility

    Downstream process integration

    • Added as the primary amine-fluorinated coupling agent in the condensation or Buchwald–Hartwig amination stages when assembling the core electroluminescent architecture

    Final product types

    • Blue and green emitter dopants for OLED displays
    • Electron transport layer intermediates for AMOLED screens
    • Organo-fluorine fine chemicals for display ink formulation

    5. Performance Coating Resin Modification

    Coatings manufacturers incorporate this benzodioxene derivative as a resin modifier to introduce fluorine content, substantially increasing chemical and UV resistance in functional coatings. Its reactive amino group facilitates copolymerization or crosslinking with epoxy or acrylic resins, while the tetrafluoro groups help minimize surface energy and migration of aggressive chemicals. The compound typically enters at the oligomer building or curing stage to impart end-use durability for specialty industrial surfaces.

    Industry compliance standards

    • ISO 12944-6 (Corrosion protection by protective paint systems)
    • ASTM D3023 (Resistance of organic coatings to chemicals)
    • REACH Regulation (EC) No 1907/2006
    • IEC 60068-2-5 (UV exposure resistance of coating materials)

    Typical usage ratio

    • 1–10% by mass, blended according to the required balance of chemical resistance and batch viscosity control

    Downstream process integration

    • Charged during the prepolymerization phase or at the resin final adaptation stage, often directly into the cross-linking reactor vessel

    Final product types

    • Fluorinated protective coatings for industrial piping
    • Anti-soiling surface treatment resins for solar panels
    • Corrosion-resistant powder coating resins
    Free Quote

    Competitive 2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene prices that fit your budget—flexible terms and customized quotes for every order.

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