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Bis(2,2,2-Trifluoroethyl)Amine

    • Product Name Bis(2,2,2-Trifluoroethyl)Amine
    • Alias Bis(trifluoroethyl)amine
    • Einecs 252-091-3
    • 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

    181351

    Productname Bis(2,2,2-Trifluoroethyl)Amine
    Casnumber 429-60-7
    Molecularformula C4H5F6N
    Molecularweight 183.08
    Appearance Colorless liquid
    Boilingpoint 95-96°C
    Density 1.376 g/cm³ at 25°C
    Refractiveindex 1.326
    Meltingpoint -45°C
    Flashpoint 24°C
    Solubility Soluble in most organic solvents
    Chemicalstructure CF3CH2NHCH2CF3

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

    Packing & Storage
    Packing The 100-gram Bis(2,2,2-Trifluoroethyl)Amine is supplied in a tightly sealed amber glass bottle with a secure screw cap.
    Shipping Bis(2,2,2-Trifluoroethyl)Amine should be shipped in tightly sealed, chemical-resistant containers under cool, dry conditions. It must be labeled according to relevant hazardous material shipping regulations and protected from physical damage, sources of ignition, and incompatible substances. Ensure appropriate documentation and safety data accompany the shipment for safe transport and handling.
    Storage Bis(2,2,2-Trifluoroethyl)Amine 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 and acids. Protect the chemical from moisture and direct sunlight. Ensure proper chemical labeling and secondary containment in accordance with local regulations and safety data sheet recommendations.
    Application of Bis(2,2,2-Trifluoroethyl)Amine

    Applications of Bis(2,2,2-Trifluoroethyl)Amine in Industrial Manufacturing

    Bis(2,2,2-Trifluoroethyl)Amine finds specialized use in industrial manufacturing due to its unique nucleophilicity, fluorine content, and volatility profile. We serve leading producers in pharmaceuticals, agrochemicals, fluorinated polymer intermediates, specialty coatings, and electronics. The following illustrates real downstream fields where manufacturers utilize this compound as a raw material and process intermediate.

    1. Pharmaceutical API Intermediate Synthesis

    Manufacturers in the pharmaceutical industry rely on Bis(2,2,2-Trifluoroethyl)Amine as a critical building block in the synthesis of certain nitrogen-containing, fluorinated active pharmaceutical ingredients. This raw material participates directly in alkylation or amidation reactions, imparting metabolic stability and increased bioavailability in target molecules. Operations typically introduce the amine in controlled batch reactions with strict process monitoring, as trace impurities can affect yield and product purification workflow. Selection of this amine supports development of APIs formulated for central nervous system and oncological therapeutic classes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapter <825> and Section <1079.2>
    • European Pharmacopoeia monographs, quality guidelines (Ph. Eur.)
    • FDA cGMP Title 21 CFR Part 210/211

    Typical usage ratio

    • 5%–18% molar basis in coupling or alkylation steps, adjusted based on API target yield and solvent polarity
    • Excess up to 1.2 equivalents used where complete conversion is required

    Downstream process integration

    • Added post-protection, pre-coupling in amide or urea forming synthetic schemes
    • Entry point: 2nd or 3rd intermediate stage in multi-step pharmaceutical API process
    • Removed by extraction or aqueous wash post-reaction before downstream purification

    Final product types

    • Fluorinated small molecule APIs for CNS disorders
    • Oncological drug compounds with trifluoroethyl side chains
    • Precursor molecules for antiviral research submitted for regulatory approval

    2. Agrochemical Intermediate and Herbicide Manufacturing

    Bis(2,2,2-Trifluoroethyl)Amine is integral to the synthesis of certain fluorinated herbicides and insecticides. Agrochemical formulators exploit the amine’s electron-withdrawing fluorine for tuning alkyl amine-based structures, contributing to increased pesticidal activity and improved plant selectivity. Downstream users often use this amine in the formation of sulfonamide or carbamate functionalities during large-scale continuous or fed-batch production, where maintaining precise ratio control is critical to minimize toxic by-product formation.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Guidelines for the Testing of Chemicals (Section 1 and 3)
    • ECHA REACH registration and CLP Regulation (EC) No 1272/2008
    • ISO 9001:2015 for Agrochemical Manufacturing Facilities

    Typical usage ratio

    • 3%–12% (by mass) amine to initial chlorinated precursor during sulfonamide/carbamate synthesis
    • Usage modulated according to degree of fluorination and electronic effects in parent structure

    Downstream process integration

    • Direct amination step after halogenation or activation of aromatic substrate
    • Inline addition to stirred-tank reactors during continuous herbicide intermediate production
    • Final incorporation within co-solvent system prior to crystallization and formulation

    Final product types

    • Fluorinated sulfonylurea and carbamate herbicides
    • Systemic insecticides with alkylated amine side chains
    • Pre-blends for broadleaf weed control

    3. Fluorinated Polymer and Monomer Intermediate Production

    Polymer manufacturers use Bis(2,2,2-Trifluoroethyl)Amine for synthesizing fluorine-modified monomers offering low surface energy, chemical resistance, and dielectric performance. The amine acts both as a nucleophilic initiator and as an end-capping reagent in the preparation of specialty polyamides, polyurethanes, and copolymers for high-end applications. Its controlled addition minimizes crosslinking and facilitates targeted end-group functionality, which is essential for producing specialty films and coatings.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Systems for Chemical Manufacturing
    • ASTM D3159 Standard for Fluoropolymer Materials
    • RoHS Directive 2011/65/EU (where used in electronics applications)
    • UL 94 Flammability Standards for Polymeric Materials

    Typical usage ratio

    • 0.5%–3.5% by weight in specialty monomer or prepolymer recipe
    • Maintained at low levels to control degree of fluorination and physical properties

    Downstream process integration

    • Introduced at initial oligomer synthesis or chain termination stage
    • Utilized as end-capper in step-growth polymerization to impart tailored hydrophobicity
    • Participates in copolymerization with other fluorinated or aromatic units

    Final product types

    • Fluorinated polyamide and polyurethane films
    • Wire and cable insulation with high dielectric resistance
    • Nonstick and anti-graffiti industrial coating resins

    4. Electronics Chemicals – Etching and Interlayer Dielectric Formulations

    In advanced electronics, Bis(2,2,2-Trifluoroethyl)Amine enters use as a building block for high-purity etchants and as a modifier in interlayer dielectric production. Its molecular structure provides etch selectivity and stability during deep silicon or compound semiconductor etching. Manufacturers blend the amine to achieve controlled volatility and minimal ionic contamination, especially for applications in semiconductor fabrication cleanrooms meeting strict trace metal specifications.

    Industry compliance standards

    • SEMI S2 and SEMI C93 standards for Electronic Materials
    • IEC 60747-1:2010 (Semiconductor Devices – General Rules)
    • JIS K 5600 for Electrical Insulation Materials
    • ISO 14644-1 Cleanroom Classification

    Typical usage ratio

    • 0.1%–2% wt. in etchant or dielectric modifier solutions, tuned based on substrate selectivity and etch depth control
    • Lower limit adopted for high-density, fine-pitch ICs

    Downstream process integration

    • Dispensed directly into micro-etch baths or spin-on interlayer formulations
    • Employed in step between wafer cleaning and deposition
    • Strict monitoring using inline purity analytics to control ionic content

    Final product types

    • Finely patterned semiconductor wafers
    • High-speed, low-dielectric constant interlayer films
    • Specialty etchant blends for MEMS manufacturing

    5. Specialty Coatings for Corrosion and Weather Resistance

    In the coatings sector, downstream users blend Bis(2,2,2-Trifluoroethyl)Amine as a reactive component for creating high-performance, fluorinated resin systems. The resulting coatings feature superior UV stability, moisture barrier properties, and resistance to aggressive chemicals, required by the aerospace, marine, and industrial asset protection markets. Formulators accurately meter this amine to promote covalent bonding within the resin matrix, while controlling final viscosity and VOC compliance.

    Industry compliance standards

    • ASTM D6900 and D6578 for Fluoropolymer Coating Performance
    • U.S. EPA National Emission Standards for Hazardous Air Pollutants (NESHAP)
    • REACH Annex XVII Restrictions for Coating Components
    • ISO 12944-6 for Paints and Varnishes — Corrosion Protection

    Typical usage ratio

    • 2%–8% by weight in fluorinated resin matrices, balanced against base polymer and required performance criteria
    • Higher ratios provide increased water resistance, reduced with higher MW base resins

    Downstream process integration

    • Added during resin synthesis as a key intermediate
    • Incorporated at pre-polymer or adduct formation stage
    • Post-addition possible for certain crosslinking formulations

    Final product types

    • Marine coatings with enhanced salt spray resistance
    • Aerospace exterior finishes
    • Protective paints for offshore and chemical plant infrastructure
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