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3-(1,1,2,2-Tetrafluoroethoxy)Aniline

    • Product Name 3-(1,1,2,2-Tetrafluoroethoxy)Aniline
    • Alias 3-(1,1,2,2-Tetrafluoroethoxy)phenylamine
    • Einecs 701-302-8
    • 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
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    Specifications

    HS Code

    108133

    Iupac Name 3-(1,1,2,2-Tetrafluoroethoxy)aniline
    Cas Number 886762-18-1
    Molecular Formula C8H7F4NO
    Molecular Weight 209.14
    Appearance Colorless to pale yellow liquid
    Boiling Point 94-96°C at 13 mmHg
    Density 1.362 g/cm³
    Solubility Slightly soluble in water, soluble in common organic solvents
    Smiles C1=CC(=CC(=C1)N)OCC(F)(F)C(F)F
    Refractive Index 1.498
    Purity Typically ≥ 97%

    As an accredited 3-(1,1,2,2-Tetrafluoroethoxy)Aniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The bottle contains 25 grams of 3-(1,1,2,2-Tetrafluoroethoxy)aniline, sealed in an amber glass vial with tamper-evident cap.
    Shipping 3-(1,1,2,2-Tetrafluoroethoxy)aniline is shipped in tightly sealed containers, protected from moisture and direct sunlight. It should be packed according to chemical transport regulations, with clear labeling and safety documentation included. The package must ensure minimal exposure to environmental factors, and carriers should comply with regulations for hazardous or specialty chemicals.
    Storage Store 3-(1,1,2,2-tetrafluoroethoxy)aniline in a tightly sealed container under a dry, inert atmosphere, such as nitrogen or argon. Keep in a cool, well-ventilated area away from direct sunlight, sources of ignition, moisture, and incompatible substances like strong oxidizers or acids. Label the container clearly and use secondary containment to prevent leaks or spills.
    Application of 3-(1,1,2,2-Tetrafluoroethoxy)Aniline

    Applications of 3-(1,1,2,2-Tetrafluoroethoxy)Aniline in Industrial Manufacturing

    As a direct manufacturer specializing in advanced fluorinated aromatic intermediates, we supply 3-(1,1,2,2-Tetrafluoroethoxy)Aniline with consistent high purity for integration into key downstream industries. Below we outline principal application scenarios based on current market adoption, typical formulation practices, and real-world process requirements for this raw material.

    1. High-Performance Polyimide Synthesis for Electronics Substrates

    Leading producers of flexible printed circuits and high-frequency insulation films incorporate this specialty aniline derivative during diamine preparation steps to enhance polymer dielectric properties. Its fluorinated structure reduces permittivity and increases thermal stability, supporting miniaturized PCB design and reliability in advanced electronic devices. Manufacturers factor in the regulatory and performance requirements imposed by end-market electronics and substrates sectors.

    Industry compliance standards

    • IPC-4101B (laminate and prepreg standards)
    • RoHS Directive (2011/65/EU) – restriction of hazardous substances
    • IEC 61249-2-7 (halogen-free material requirements)
    • UL 94 V-0 (flammability classification for plastics)

    Typical usage ratio

    • 5–15% by mol of total diamine input, adjusted based on target dielectric constant and heat resistance

    Downstream process integration

    • Direct amine monomer blending during the polycondensation step; reacts with dianhydrides under controlled solvent and temperature conditions before film casting or fiber spinning

    Final product types

    • Flexible copper-clad laminates (FCCL) for HDI PCB
    • High-speed connector insulation films
    • Interposer and flexible display substrates
    • Thermal management circuit films

    2. Synthesis of Fluorinated Benzoxazole Polymers for Gas Separation Membranes

    Membrane manufacturers use this advanced aniline as a key aromatic amine for synthesizing polybenzoxazoles (PBO) with tailored gas selectivity and mechanical strength, ideal for hydrogen and carbon dioxide separation. Its fluorine side groups disrupt chain packing, delivering increased permeability essential for next-generation industrial gas processing facilities. This application addresses both purity and regulatory concerns unique to the gas membrane industry.

    Industry compliance standards

    • ISO 15848-1: High-integrity gas separation materials testing
    • REACH Regulation (EC 1907/2006) – substance pre-registration and use in polymers
    • ASME B31.3 (chemical plant and refinery piping standards for polymer equipment)

    Typical usage ratio

    • 8–18 mol% relative to the total diamine structure, adjusted to permeability/selectivity targets and membrane thickness requirements

    Downstream process integration

    • Amination input in PBO polymerization, then casting into solution films using NMP or DMAc solvents before controlled imidization/thermal treatment

    Final product types

    • Hydrogen purification membranes
    • CO2 and natural gas dehydration modules
    • Permeation elements for biogas upgrading

    3. Intermediate for Agrochemical Active Ingredient Synthesis

    Chemical companies engaged in the production of herbicide and fungicide actives integrate this fluorinated aniline in multi-step syntheses targeting molecules with both high field efficacy and environmental persistence. Its electron-withdrawing ether-fluorine group enhances metabolic stability, making it essential in formulating next-generation crop protection agents subjected to strict residue and ecotoxicological controls worldwide.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals (Section 1 & 2, substance characterization and toxicity studies)
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • GLP (Good Laboratory Practice, OECD Principles)
    • EPA 40 CFR Part 180 (tolerance for pesticide residues in food)

    Typical usage ratio

    • 15–25% molar ratio as a ring-building block in active ingredient core; final percentage depends on the desired balance between potency and biodegradation profile

    Downstream process integration

    • Utilized in early-phase aromatic coupling or as a nucleophile for subsequent halogen substitution; followed by purification, salt formation, and formulation into technical concentrates

    Final product types

    • New-generation systemic herbicides
    • Protective fungicidal agents
    • Seed treatment micro-encapsulates

    4. Precise Functionalization in Fluorinated Liquid Crystal Monomer Synthesis

    LC display chemical suppliers employ this compound as a functional handle to introduce targeted polar and fluorinated properties in the design of LC monomers for advanced display panels. Modifying the aromatic amine content fine-tunes viscosity, birefringence, and nematic range for smartphone, automotive, and large-scale TV panel manufacturing lines. Strict purity controls and liquid crystal application standards govern its use.

    Industry compliance standards

    • JEITA EM-3509 (Evaluation methods for electronic displays)
    • ROHS compliance (Hazardous Substances in Electronics)
    • ISO 9001:2015 (Production quality management for specialty chemicals)

    Typical usage ratio

    • 1–5% by weight in monomer synthesis batches, ratio adjusted based on targeted refractive indices and electro-optical response

    Downstream process integration

    • Undergoes condensation or coupling reactions as a nucleophile to build liquid crystalline aromatic monomers, followed by purification prior to final LC mixing

    Final product types

    • TFT-LCD and IPS LCD panel liquid crystal blends
    • Nematic and chiral LC monomer masterbatches
    • Specialty LC mixtures for OLED encapsulation layers

    5. Precursor in Engineered Fluorinated Polyurethane Coatings

    Leading OEM and industrial coating manufacturers integrate this material as a chain-extending aromatic amine to impart high hydrophobicity and chemical resistance to polyurethane resin systems. Formulators rely on its structural effect for applications where coatings require long-term durability in aggressive chemical, solvent-rich, or outdoor environments—especially for aerospace, rail, and specialist anti-corrosion needs.

    Industry compliance standards

    • ASTM D522 (flexibility of coatings)
    • ISO 12944-6 (Corrosion protection of steel structures by protective paint systems)
    • REACH Annex XVII (restriction of certain isocyanates and aromatic amines in coatings)

    Typical usage ratio

    • 2–7% as active amine equivalent in isocyanate-to-amine curing ratio, adjusted to substrate adhesion and resistance property targets

    Downstream process integration

    • Added during pre-polymer mixing and curing stages to form segmented polyurethanes; subsequent dispersion, pigmenting, and application by spray or dip

    Final product types

    • High-resilience anti-graffiti coatings
    • Chemical-resistant industrial floor finishes
    • Aerospace and rail exterior protective layers
    • Heavy-duty marine repair coatings
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