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2,5-Bis(Trifluoromethyl)Aniline

    • Product Name 2,5-Bis(Trifluoromethyl)Aniline
    • Alias 2,5-Bis(trifluoromethyl)benzenamine
    • Einecs 'EINECS 222-204-6'
    • 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

    518891

    Chemical Name 2,5-Bis(Trifluoromethyl)Aniline
    Molecular Formula C8H5F6N
    Molecular Weight 229.12 g/mol
    Cas Number 328-84-7
    Appearance White to off-white solid
    Boiling Point 198-200°C
    Melting Point 45-49°C
    Density 1.49 g/cm³
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents such as dichloromethane, ethanol
    Smiles C1=CC(=C(C=C1N)C(F)(F)F)C(F)(F)F
    Inchi InChI=1S/C8H5F6N/c9-7(10,11)5-1-2-6(15)4(3-5)8(12,13)14
    Refractive Index 1.480 (predicted)
    Storage Temperature Store at 2-8°C
    Flash Point 106°C

    As an accredited 2,5-Bis(Trifluoromethyl)Aniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle, tightly sealed with a white screw cap, labeled with hazard symbols and `2,5-Bis(Trifluoromethyl)Aniline` details.
    Shipping **Shipping Description for 2,5-Bis(Trifluoromethyl)Aniline:** This chemical should be shipped in tightly sealed containers, protected from light and moisture. Store in a cool, well-ventilated area, away from incompatible substances. Label all packaging according to relevant safety regulations. Consult the MSDS for transport classifications and specific hazard precautions prior to shipping.
    Storage 2,5-Bis(Trifluoromethyl)Aniline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as oxidizers and acids. Protect from light and moisture. Ensure proper labeling and keep away from direct sunlight. Use appropriate chemical storage cabinets for hazardous organics and limit access to trained personnel.
    Application of 2,5-Bis(Trifluoromethyl)Aniline

    Applications of 2,5-Bis(Trifluoromethyl)Aniline in Industrial Manufacturing

    Our production of 2,5-Bis(Trifluoromethyl)Aniline serves as a critical intermediate across several high-value industrial sectors. As a direct manufacturer, we support downstream companies implementing this fluorinated compound in advanced synthesis, specialty coatings, pharmaceutical research, and agrochemical development.

    1. Advanced Pharmaceutical Intermediates

    Pharmaceutical manufacturers employ 2,5-Bis(Trifluoromethyl)Aniline when designing and scaling up small-molecule drug candidates requiring enhanced metabolic stability and fluorine incorporation at specific ring positions. It is mainly used in the synthesis of next-generation kinase inhibitors, CNS drug scaffolds, and API fluorination, where the electron-withdrawing effect of trifluoromethyl improves pharmacokinetic profiles and target selectivity. Integration into multi-step organic synthesis typically takes place during amidation, urea coupling, or as a nucleophilic aromatic substitution partner.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Ph. Eur. (European Pharmacopoeia) requirements for fluorinated intermediates
    • USP guidelines on impurity profiles for registered starting materials
    • 21 CFR Part 211: US FDA Current Good Manufacturing Practice (cGMP)

    Typical usage ratio

    • Ranges from 0.1 to 0.5 molar equivalents per target intermediate in step-growth synthesis
    • Adjusted based on target molecule yield and fluorine incorporation efficiency

    Downstream process integration

    • Introduced during aromatic amination or coupling when building core structures
    • Precursor in amide or urea bond formation steps relevant to lead optimization
    • Intermediate in regulated GMP-compliant production suites

    Final product types

    • Active pharmaceutical ingredients for oncology and CNS therapies
    • Fluorinated advanced intermediates for generic drug manufacturing
    • Synthetic building blocks for patent-protected research molecules

    2. Synthesis of Agrochemical Active Compounds

    Leading agrochemical producers use this aniline derivative as a fluorine source in the synthesis of novel herbicides, insecticides, and fungicides. Its trifluoromethyl groups enhance the bioactivity and environmental stability of pyridine and quinoline rings, commonly found in crop protection agents. The compound features in key steps such as selective amination and ring closure reactions, supporting the design of active molecules with improved resistance to degradation, allowing better crop safety and regulatory compliance.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC) No 1907/2006, Annex XVII (EU)
    • OECD Guidelines for the Testing of Chemicals
    • ISO 9001:2015 Quality Management for chemical synthesis

    Typical usage ratio

    • 0.1–0.4 molar equivalents per agrochemical active core structure
    • Ratio may adjust depending on final product’s required fluorine content

    Downstream process integration

    • Feeds into aromatic amination and cyclization stages of active ingredient synthesis
    • Used in pilot and full-scale production lines for new chemical entities (NCEs) under regulatory scrutiny

    Final product types

    • Selective fungicides and insecticides with improved field stability
    • Precursor molecules for broad-spectrum herbicides
    • Plant protection products subjected to global residue reviews

    3. Fluorinated Polymer Synthesis

    Specialty polymer producers adopt this compound to design high-performance fluorinated aromatic polymers aimed at demanding electronic, aerospace, and membrane applications. The presence of two trifluoromethyl groups provides rigidity to the polymer backbone, increases thermal and chemical resistance, and improves dielectric properties. This material is introduced during the polycondensation or polyaddition reaction, mainly for forming high-grade polyimides, polyamides, and specialty fluoropolymers with controlled molecular weight distribution.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for polymer manufacturing
    • RoHS (EU Directive 2011/65/EU) for electronics and electrical polymers
    • ASTM D3418 for thermoplastic transition properties
    • UL 94 Flammability Standards for plastics

    Typical usage ratio

    • 5–20 wt% incorporation in copolymer backbones
    • Adjusted according to polymer chain length and desired final property profile

    Downstream process integration

    • Blended with dianhydrides or diacids at the monomer pre-polymerization stage
    • Used in continuous and batch polymerization reactors, with in-line fluorine content monitoring

    Final product types

    • High-temperature-resistant polyimide sheets for flexible circuits
    • Membrane materials for organic solvent nanofiltration
    • Specialty fluoropolymers for aerospace coatings

    4. Electronics Specialty Coatings

    The electronics sector leverages 2,5-Bis(Trifluoromethyl)Aniline in the formulation of specialty coatings where moisture barrier performance, dielectric strength, and chemical inertness are essential. Formulators use this raw material to synthesize advanced coating resins, such as fluorinated polyacrylate or polyimide varnishes, applied to semiconductors, high-voltage capacitors, and sensor units. The feedstock enters reaction sequences that require precise control of functional group distribution and batch purity to meet end-customer technical standards.

    Industry compliance standards

    • IPC-4101B: Base Materials for Rigid and Multilayer Printed Boards
    • IEC 60695-11-10: Fire Hazard Testing for Electronic Equipment
    • JIS C 5013: Electronic Coating Specifications (Japan)
    • RoHS (Restriction of Hazardous Substances) Compliance

    Typical usage ratio

    • Incorporation levels from 2% to 10% by weight in custom resin batches
    • Fine-tuned to achieve target dielectric loss and hydrophobicity depending on device class

    Downstream process integration

    • Introduced at resin pre-polymer formulation or as a post-functionalization fluorinating agent
    • Applied via dip coating, spray, or spin processes onto substrates under cleanroom management

    Final product types

    • Moisture-barrier coatings for PCBs and microelectronic assemblies
    • Insulating films used in high-frequency communication modules
    • Protective sensor coatings for industrial process automation

    5. Fine Chemical Synthesis & Custom Research Chemicals

    Contract research and fine chemical facilities procure 2,5-Bis(Trifluoromethyl)Aniline for the development of specialty intermediates, reference standards, and analytical markers required in life science, diagnostics, and material science applications. Due to its strong electron-withdrawing fluorinated groups, chemists select this compound for rapid screening of ring-substituted anilines during lead compound discovery, combinatorial chemistry, and in the generation of isotopically labeled standards for LC-MS quantification studies.

    Industry compliance standards

    • ISO 17034: General Requirements for the Competence of Reference Material Producers
    • GLP (Good Laboratory Practice) for custom synthesis
    • IUPAC guidelines for chemical identifier accuracy
    • REACH (EC) 1907/2006 for research and laboratory chemicals

    Typical usage ratio

    • Milligram to gram-scale for analytical method development or discovery chemistry
    • Larger scale (up to kilogram) for specialty catalog or test kit production

    Downstream process integration

    • Synthesized into target markers via controlled aromatic substitution
    • Serves as a late-stage custom intermediate or label during scale-up pilot projects

    Final product types

    • Certified reference materials for LC-MS and GC-MS laboratories
    • Isotopically labeled research standards
    • Specialty analytical probes for diagnostic reagent kits
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