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3'-Trifluoromethylisobutyranilide

    • Product Name 3'-Trifluoromethylisobutyranilide
    • Alias TFMPIA
    • Einecs 223-335-2
    • 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

    877616

    Cas Number 116639-57-1
    Molecular Formula C11H12F3NO
    Molecular Weight 231.22 g/mol
    Iupac Name 2-methyl-2-(3-(trifluoromethyl)phenyl)propanamide
    Appearance White to off-white solid
    Boiling Point Unknown
    Melting Point 45-48 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density Unknown
    Smiles CC(C)(C(=O)N)C1=CC(=CC=C1)C(F)(F)F
    Inchi InChI=1S/C11H12F3NO/c1-11(2,10(15)16)8-5-4-6-9(7-8)12-3/h4-7H,1-3H3,(H2,15,16)
    Purity Typically >98%
    Storage Temperature Store at 2-8°C
    Refractive Index Unknown

    As an accredited 3'-Trifluoromethylisobutyranilide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 10g bottle of 3'-Trifluoromethylisobutyranilide is securely sealed in amber glass, labeled with hazard symbols and product information.
    Shipping 3'-Trifluoromethylisobutyranilide is shipped in securely sealed containers to prevent leaks or contamination. It is packed in accordance with chemical safety regulations, often placed within cushioned, sturdy packaging. The shipment includes safety documentation and is labeled as a potentially hazardous material, requiring careful handling and compliance with all relevant transport guidelines.
    Storage 3'-Trifluoromethylisobutyranilide 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. Keep the container protected from direct sunlight and moisture. Ensure the storage area is clearly labeled and access is restricted to trained personnel. Follow all relevant regulations and safety guidelines.
    Application of 3'-Trifluoromethylisobutyranilide

    Applications of 3'-Trifluoromethylisobutyranilide in Industrial Manufacturing

    3'-Trifluoromethylisobutyranilide is a high-value specialty intermediate recognized for its performance in select industrial synthesis chains. As the direct manufacturer, we produce this compound to stringent quality and traceability standards to enable reliable downstream conversion across regulated sectors. Below, we detail application-specific integration practices across four validated endpoints.

    1. Synthesis of Agrochemical Actives

    Major manufacturers in the crop protection sector leverage 3'-Trifluoromethylisobutyranilide as an aromatic core in the synthesis of certain fluorinated anilide-based herbicides and fungicides. Production lines incorporate this intermediate during advanced-stage coupling and amidation reactions, as it provides chemical stability and enhances target binding affinity in specific agroactive molecules. Our QC protocols ensure batch-to-batch consistency for ease of scale-up at downstream technical plants.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)
    • ISO 9001 Quality Management (raw material traceability)
    • REACH Registration (Europe: verification of use in active synthesis)

    Typical usage ratio

    • Between 8–15% w/w in targeted synthesis steps; final concentration depends on desired active structure and yield optimization parameters.

    Downstream process integration

    • Charged into alkylation or acylation reactors post-initial heterocycle formation; undergoes direct amide/ester linkage to build complex agroactive frameworks.

    Final product types

    • Selective herbicide actives (e.g., substituted anilide derivatives)
    • Fungicidal active agents for seed treatments
    • Active ingredient concentrates (technical-grade agrochemicals)

    2. Pharmaceutical Intermediate for Trifluoromethylated APIs

    Producers of advanced pharmaceutical ingredients utilize this raw material in the synthesis of fluorinated drug intermediates, especially within the anti-inflammatory and CNS agent categories. Process chemists value its electron-withdrawing group for modulating biological activity and metabolic stability. Integration typically occurs at intermediate stages during amide formation, where rigorous traceability and contaminant controls are mandatory for regulatory audit-readiness.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF / EP Monographs on fluorinated anilides where applicable
    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals)
    • DMF (Drug Master File) supporting documentation

    Typical usage ratio

    • Utilized at intermediate molar equivalents, with 5–12% w/w based on specific reaction stoichiometry and stepwise yield requirements; adjusted per target API and scale.

    Downstream process integration

    • Fed into key coupling reactions on API synthesis trains, commonly after completion of core scaffold construction and prior to molecular functionalization or purification steps.

    Final product types

    • Trifluoromethylated anti-inflammatory API intermediates
    • Neuropsychiatric small-molecule drug substances
    • Finished APIs after additional transformations

    3. Intermediate in Fluorinated Polymer Precursors

    Producers specializing in engineered functional polymers incorporate this compound as a chain modifier or co-monomer precursor to endow specialty fluorinated polymer resins with improved dielectric and chemical resistance properties. Entry points for the intermediate occur in custom polymerization processes, especially for use in high-value electronic encapsulation and membrane production. Strict product qualification is required at this stage due to demands for ultra-low impurity profiles.

    Industry compliance standards

    • RoHS Directive (for electronic components and resin applications)
    • ISO 9001:2015 (QMS for advanced materials production)
    • UL 94 Flame Class (for polymer safety if used in finished resin systems)
    • Company-specific protocols for incoming raw material qualification

    Typical usage ratio

    • Incorporated at 4–9% w/w in copolymer blend formulations; selected according to targeted end-use dielectric or chemical barrier performance.

    Downstream process integration

    • Charged during solution or emulsion polymerization in stage-wise addition, prior to crosslinking and final polymer fractionation.

    Final product types

    • Fluorinated polyurethane resins
    • Dielectric coatings and encapsulant films
    • Specialty engineering plastics for electronics

    4. Intermediate for Specialty Dye and Pigment Synthesis

    Manufacturers of advanced fluorinated dyes and pigment molecules integrate this intermediate in synthesis chains targeting high-stability colorants for inks, plastics, and optoelectronic coatings. Its trifluoromethyl substituent enables desirable lightfastness and chemical inertness when introduced into chromophoric cores. The compound is most often deployed after preliminary condensation reactions to facilitate ring-substituted dye structures.

    Industry compliance standards

    • EN 71-3 (Safety of toy colorants — if used in colorant systems intended for toys)
    • REACH Regulation Annex XVII (restrictions on hazardous substances in pigments/dyes for EU markets)
    • ISO 787 (General methods of test for pigments and extenders)
    • Company-level QC protocols for pigment manufacturers

    Typical usage ratio

    • Typically introduced at 7–14% w/w relative to precursor mass; level determined based on color intensity and fastness specifications in end-use formulation.

    Downstream process integration

    • Added post-initial aromatic condensation during amide or azo coupling reactions, then followed by purification and milling to target particle size distributions.

    Final product types

    • High-durability printing ink colorants
    • Fluorinated organic pigments for plastics compounding
    • Lightfast dyes used in optoelectronic coatings
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