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2,4-Bis(Trifluoromethyl)Benzoyl Chloride

    • Product Name 2,4-Bis(Trifluoromethyl)Benzoyl Chloride
    • Alias BTBC
    • Einecs 246-259-4
    • 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

    289706

    Product Name 2,4-Bis(Trifluoromethyl)Benzoyl Chloride
    Cas Number 328-36-7
    Molecular Formula C9H3ClF6O
    Molecular Weight 278.57
    Appearance Colorless to pale yellow liquid
    Boiling Point 100-102°C at 13 mmHg
    Density 1.536 g/cm3
    Purity Typically ≥98%
    Refractive Index n20/D 1.464
    Solubility Reacts with water, soluble in organic solvents
    Synonyms 2,4-Bis(trifluoromethyl)benzoyl chloride

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

    Packing & Storage
    Packing Amber glass bottle, 50 grams, tightly sealed with a PTFE-lined cap, labeled with hazard warnings and chemical identification, inside protective outer box.
    Shipping 2,4-Bis(Trifluoromethyl)Benzoyl Chloride is shipped as a hazardous chemical, typically packed in sealed, inert containers to prevent moisture and air exposure. It is transported under strict regulations, with appropriate labeling, safety documentation, and temperature controls as required to ensure safe handling and compliance with international and domestic shipping standards.
    Storage 2,4-Bis(Trifluoromethyl)Benzoyl Chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture, heat, and incompatible substances (such as bases and strong oxidizers). Store under inert gas, such as nitrogen, if possible. Avoid exposure to light and sources of ignition. Use secondary containment to prevent spills and follow all safety regulations.
    Application of 2,4-Bis(Trifluoromethyl)Benzoyl Chloride

    Applications of 2,4-Bis(Trifluoromethyl)Benzoyl Chloride in Industrial Manufacturing

    2,4-Bis(Trifluoromethyl)Benzoyl Chloride serves as a high-value intermediate for demanding applications in fluorinated chemistry, polymer modification, advanced pharmaceuticals, and high-performance coating materials. As a manufacturer, we ensure strict batch control and traceability to meet the expectations of global industrial clients.

    1. Pharmaceutical API Fluorination for Small Molecule Drugs

    Our material is recognized for introducing bis(trifluoromethyl) groups in selective acylation steps during the synthesis of fluorinated pharmaceutical intermediates. Large-scale pharmaceutical plants use this specialty acyl chloride in process routes for drug candidates requiring improved metabolic stability or targeted fluorine incorporation. The product finds particular relevance in late-stage functionalization under tightly controlled environments, where reactivity, purity, and reproducibility drive process value. Diligent monitoring of residual chloride and organofluorine byproducts is standard during downstream synthesis.

    Industry compliance standards

    • ICH Q7 GMP Guidelines
    • US FDA 21 CFR Part 211
    • EU GMP Vol 4 Part II
    • Chinese Pharmacopoeia API synthesis requirements

    Typical usage ratio

    • Used at 0.95–1.10 mol equivalent relative to aminated or alcohol-containing intermediates, with precise adjustment by process scale and impurity control requirements.

    Downstream process integration

    • Added during the acylation step of pharmaceutical intermediate synthesis, typically in polar aprotic solvents, followed by controlled quenching and neutralization.

    Final product types

    • Advanced fluorinated pharmaceutical intermediates
    • Specialty APIs for central nervous system therapeutics
    • Fluorinated kinase inhibitors
    • Intermediates for oncology drug development

    2. Synthesis of Fluorinated Aromatic Polyimides for High-Temperature Polymers

    In high-performance plastics manufacturing, this acyl chloride is utilized to modify polymer backbone structures, particularly in the production of fluorinated polyimides. The introduction of bis(trifluoromethyl) moieties improves polymer thermal resistance, dielectric stability, and chemical durability. Polymerization engineers dose the material under anhydrous and controlled-temperature conditions for polycondensation with aromatic diamines, targeting repeat unit incorporation while limiting gel formation. Downstream quality control includes FTIR and NMR validation for fluorine placement and residual monomer analysis.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • ASTM D5207-07 for polyimide film properties
    • RoHS (Restriction of Hazardous Substances - for electronics applications)
    • UL 94 V-0 (flammability for polyimide components)

    Typical usage ratio

    • 0.80–1.20 mol per mol aromatic diamine, determined by desired fluorine loading and target polymer chain length.

    Downstream process integration

    • Employed in the dianhydride-acyl chloride route during prepolymer formation, then followed by thermal imidization to achieve the final polymer structure.

    Final product types

    • Flexible printed circuit substrates
    • Gas separation membranes
    • High-temperature wire enamels
    • Insulating films for aerospace electronics

    3. UV-Curable Resin Formulation for Specialty Coatings

    Manufacturers of UV-curable coatings use our product to synthesize photoinitiators and specialty resins that demand electron-withdrawing substituents for improved cure rates and stability. The bis(trifluoromethyl)benzoyl group enhances both photoinitiation efficiency and weather resistance, especially when incorporated into benzoin or benzil-type derivatives. Formulators control addition during controlled condensation or Friedel–Crafts processes, and production lines employ in-house characterization to confirm functional group integrity.

    Industry compliance standards

    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) compliance
    • ISO 14001:2015 Environmental Management Systems
    • EU Directive 2011/65/EU (RoHS for coated electronics)
    • China HJ 2547-2016 (Limit standards for hazardous substance in coatings)

    Typical usage ratio

    • 0.2–1.5% by weight of total resin mass, with higher loads for thicker films or enhanced UV-blocking properties.

    Downstream process integration

    • Utilized at early-stage monomer functionalization, later formulated into the final UV-curable resin prepolymer or photoinitiator mix, and subjected to in-line curing QC.

    Final product types

    • UV-cured optoelectronic coatings
    • Hard coats for automotive displays
    • Scratch-resistant varnishes for plastics
    • Protective overcoats on printed circuit boards

    4. Agrochemical Intermediate for Advanced Herbicide Synthesis

    Large-scale agrochemical plants deploy 2,4-Bis(Trifluoromethyl)Benzoyl Chloride as an acylating building block for selective fluorinated herbicides. The compound enables ring modifications that enhance bioactivity and stability against photolysis, especially for pre-emergence and post-emergence weed control agents. Agrochemical formulators incorporate the product in multi-step synthesis, followed by extensive downstream purification and residue analysis to comply with strict residue standards.

    Industry compliance standards

    • FAO/WHO Specification for Plant Protection Products
    • ISO 17025 for analytical laboratory practices
    • US EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act)
    • China GB 2763 Maximum Residue Limits (MRLs) for Pesticides

    Typical usage ratio

    • Employed at stoichiometric ratios ranging from 0.85–1.15 mol per mol of nucleophilic substrate, optimized per batch for conversion efficiency and impurity minimization.

    Downstream process integration

    • Integrated into the controlled acylation of heterocyclic or phenolic scaffolds during active substance synthesis, prior to formulation and microencapsulation steps.

    Final product types

    • Fluorinated herbicide actives
    • Selective broadleaf and grass weed management agents
    • Intermediate compounds for crop protection R&D
    • Advanced pre- and post-emergence weed control products
    Free Quote

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