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2-Bromo-4-Fluoro-6-(Trifluoromethyl)Aniline

    • Product Name 2-Bromo-4-Fluoro-6-(Trifluoromethyl)Aniline
    • Alias 2-Bromo-4-fluoro-6-(trifluoromethyl)benzenamine
    • Einecs 816-669-6
    • 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

    517508

    Productname 2-Bromo-4-Fluoro-6-(Trifluoromethyl)Aniline
    Casnumber 915088-01-4
    Molecularformula C7H4BrF4N
    Molecularweight 259.01
    Appearance White to off-white solid
    Meltingpoint 50-54°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as DMSO and dichloromethane
    Smiles Nc1c(Br)cc(F)cc1C(F)(F)F
    Inchi InChI=1S/C7H4BrF4N/c8-5-3-4(9)1-2-6(5)7(10,11)12/h1-3H,9H2
    Synonyms 2-Bromo-4-fluoro-6-(trifluoromethyl)benzenamine
    Storagecondition Store at 2-8°C, protected from moisture and light

    As an accredited 2-Bromo-4-Fluoro-6-(Trifluoromethyl)Aniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25g, tightly sealed with screw cap, clearly labeled with chemical name, structure, and hazard warnings.
    Shipping 2-Bromo-4-Fluoro-6-(Trifluoromethyl)aniline is shipped in tightly sealed containers, protected from light and moisture. It is packed to prevent leaks and contamination, complying with all relevant chemical transport regulations. Appropriate hazard labeling and documentation are provided. Temperature control may be applied if required by the compound’s stability or safety guidelines.
    Storage Store **2-Bromo-4-fluoro-6-(trifluoromethyl)aniline** in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of moisture, heat, and ignition. Protect from direct sunlight, incompatible substances such as strong oxidizers and acids, and prevent contact with skin or eyes. Ensure proper labeling and comply with relevant chemical and safety regulations.
    Application of 2-Bromo-4-Fluoro-6-(Trifluoromethyl)Aniline

    Applications of 2-Bromo-4-Fluoro-6-(Trifluoromethyl)Aniline in Industrial Manufacturing

    As a specialized manufacturer, we supply 2-Bromo-4-Fluoro-6-(Trifluoromethyl)Aniline to innovation-driven sectors with demanding requirements for performance, compliance, and synthesis precision. Below, we outline its deployment in select downstream industries, reflecting real-world formulation practices, standardization demands, and production integration.

    1. Agrochemical Intermediate Synthesis

    Leading crop protection companies leverage this compound as a building block in the synthesis of advanced herbicide and fungicide actives featuring multiple halogen substitutions. Chemists incorporate it during the early active ingredient assembly stage, ensuring effective downstream substitution or coupling for structure-activity optimization.

    Industry compliance standards

    • ISO 9001:2015 for quality management in chemical synthesis
    • Globally Harmonized System (GHS) for hazard labeling and safety
    • OECD Guidelines for Testing of Chemicals (relevant to agrochemical registration dossiers)
    • REACH regulation (EC No 1907/2006) for European market registration

    Typical usage ratio

    • 10–18% molar ratio as a precursor in total reaction batch, optimized based on target active herbicidal or fungicidal structure

    Downstream process integration

    • Acts as the halogenated aniline source in nucleophilic aromatic substitution or palladium-catalyzed coupling, generally entering at the initial core construction step for high-value agrochemical actives

    Final product types

    • Novel triazole fungicides
    • Fluorinated phenoxy herbicides
    • Environmentally persistent crop protection intermediates

    2. Pharmaceutical API Intermediate Manufacturing

    Pharmaceutical chemical suppliers integrate this high-purity aniline derivative in the synthesis of non-steroidal anti-inflammatory drug (NSAID) scaffolds and select oncology small molecule intermediates, where its unique substitution pattern imparts defined pharmacokinetic properties.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Parts 210/211 (US FDA cGMP rules for pharma manufacturing)
    • European Pharmacopoeia monographs for intermediates and impurities
    • USP General Chapters <467> (Residual Solvents) and <231> (Elemental Impurities)

    Typical usage ratio

    • 8–12% moles of input in multistep synthesis, subject to structural route and target API yield factors

    Downstream process integration

    • Introduced in the heterocyclic ring formation or aryl amination step, preceding final API assembly and critical purification

    Final product types

    • High-purity NSAID intermediates
    • Trifluoromethylated kinase inhibitor precursors
    • Specialty oncology drug cores

    3. Advanced Electronic Chemical Synthesis

    Producers of organic electronic materials use this compound to construct rigid ligand frameworks and electron-acceptor units for semiconductors, OLEDs, and display materials, utilizing its electron-withdrawing substituents for device performance tuning.

    Industry compliance standards

    • IEC 62474: Material Declaration for Electronic Industry
    • RoHS (2011/65/EU): Restriction of Hazardous Substances Directive (for finished devices)
    • ISO 14001:2015 (Environmental management) in production
    • JEDEC JESD720C: Definitions for Green Electronic Components

    Typical usage ratio

    • 5–10% w/w relative to total electronic chemical batch, adjusted for conjugation density and polymer backbone length

    Downstream process integration

    • Serves as the meta-position functionalized aryl input during Suzuki or Buchwald-Hartwig coupling in advanced polymer and small-molecule electronics synthesis

    Final product types

    • High-performance OLED emitting layers
    • Organic thin-film transistor (OTFT) precursors
    • Flexible display functional coatings

    4. Specialty Dye and Pigment Synthesis

    Dye manufacturers incorporate this raw material as a diazotizable amine for producing halogenated and trifluoromethylated azo dyes, targeting high-stability colorants for demanding plastics, fibers, and high-performance coatings.

    Industry compliance standards

    • EN 71-3:2019 (Migration of certain elements for toy and textile colorants)
    • OEKO-TEX Standard 100 (for textile dye safety assessment)
    • ISO 18314-1:2015 (Analytical methods for colorants)
    • Global Automotive Declarable Substance List (GADSL) for pigment raw materials

    Typical usage ratio

    • 12–20% w/w of total amine charge for targeted diazotization reactions, varied per shade intensity and application durability design

    Downstream process integration

    • Employed as the primary amine in controlled diazotization-condensation for producing complex azo architectures, prior to granulation and dispersion into application-ready pigment forms

    Final product types

    • High-durability textile dyes
    • Automotive plastics pigments
    • Engineered specialty colorants for high-temperature industrial coatings

    5. High-Performance Polymer Modifier Synthesis

    Producers of specialty fluorinated polymers use this compound for the synthesis of aryl-functional monomers and chain-extender units, focusing on enhanced chemical resistance and thermal stability in end-use engineered plastics.

    Industry compliance standards

    • ISO 9001:2015 (Quality management in polymer production)
    • UL 94 (Flammability rating for plastics)
    • ASTM D543 (Chemical resistance of plastics)
    • FDA 21 CFR §177.1550 (Indirect food additives: Polymers, where applicable)

    Typical usage ratio

    • 2–6% w/w relative to base monomer feed in block copolymer synthesis, balanced for final product mechanical strength and chemical durability

    Downstream process integration

    • Integrated as a functional comonomer either via solution polymerization or melt-phase addition for creating high-Tg or chemical-resistant fluoropolymer grades

    Final product types

    • Fluorinated engineering plastics
    • High-stability coating resins
    • Polymer membranes for specialty filtration and electronics
    Free Quote

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