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3,5-Dichloro-2,4,6-Trifluorobenzotrifluoride

    • Product Name 3,5-Dichloro-2,4,6-Trifluorobenzotrifluoride
    • Alias BTF
    • Einecs 408-350-8
    • 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

    128540

    Productname 3,5-Dichloro-2,4,6-Trifluorobenzotrifluoride
    Casnumber 141335-45-5
    Molecularformula C7Cl2F5
    Molecularweight 254.97
    Appearance Colorless to pale yellow liquid
    Boilingpoint 142-144°C
    Meltingpoint -14°C
    Density 1.68 g/cm³
    Refractiveindex 1.430
    Flashpoint 56°C
    Solubility Insoluble in water
    Purity Typically ≥98%
    Synonyms Benzotrifluoride, 3,5-dichloro-2,4,6-trifluoro-

    As an accredited 3,5-Dichloro-2,4,6-Trifluorobenzotrifluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1 kg HDPE bottle labeled "3,5-Dichloro-2,4,6-Trifluorobenzotrifluoride," hazard symbols, lot number, manufacturer, and handling instructions.
    Shipping 3,5-Dichloro-2,4,6-Trifluorobenzotrifluoride should be shipped in tightly sealed containers, clearly labeled, and protected from physical damage. It requires storage in a cool, dry, well-ventilated area away from incompatible substances. Compliant with local, national, and international hazardous material regulations. Ensure SDS documentation accompanies shipments, and trained personnel handle transportation.
    Storage **3,5-Dichloro-2,4,6-trifluorobenzotrifluoride** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat, sparks, and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature and ensure proper chemical labeling. Use secondary containment to prevent leaks or spills and follow all relevant safety regulations.
    Application of 3,5-Dichloro-2,4,6-Trifluorobenzotrifluoride

    Applications of 3,5-Dichloro-2,4,6-Trifluorobenzotrifluoride in Industrial Manufacturing

    As the direct manufacturer of 3,5-Dichloro-2,4,6-trifluorobenzotrifluoride, we supply material with the analytical and containment integrity required for consistently demanding downstream processing. The following sectors represent the current primary end-uses in which this specialty intermediate has established track records within integrated industrial supply chains. Each application scenario includes relevance to regulatory standards, dosage parameters in industrial practice, its technical entry point in production lines, and typical finished goods obtained by our global clients.

    1. Synthesis of Agrochemical Active Ingredients

    Crop protection formulators in major markets leverage our intermediate in the multi-step synthesis of several fluorinated and chlorinated herbicide and fungicide actives. Its role as an aromatic source in nucleophilic aromatic substitution and halogen-exchange routes allows precise introduction of functional groups, key for selectivity and environmental profile tuning of modern agrochemicals.

    Industry compliance standards

    • REACH (EU Regulation EC 1907/2006) pre-registration and registration status for intermediates
    • FIFRA (US EPA Federal Insecticide, Fungicide, and Rodenticide Act) technical guidelines
    • China National Standard GB 2763 residue guidelines for plant protection compounds
    • ISO 9001:2015 Quality Management System for traceability and batch control in precursor supply

    Typical usage ratio

    • 0.5–5% w/w as part of step-growth or substitution batch reactions, depending on target active molecule’s structure and efficiency of downstream substitutions; exact ratio determined through process optimization for yield versus unreacted aromatic intermediate

    Downstream process integration

    • Charged at early-stage synthesis for introduction of fluoro-chloro aromatic core; typically involved before nitration, alkoxylation, or alkylation reaction stages in multi-step technical synthesis

    Final product types

    • Fluorinated herbicides (e.g., for cereal or soybean applications)
    • Chlorinated fungicide actives used in high-value fruit or vegetable protection
    • Synthons for seed treatment formulants

    2. API Building Block in Advanced Pharmaceutical Synthesis

    Pharmaceutical manufacturers use our material primarily as a halogenated aromatic starting block in the custom synthesis of advanced pharmaceutical intermediates (APIs), taking advantage of its high purity and analytical batch documentation to support regulatory submissions. Key uses involve the preparation of heterocyclic scaffolds or selective fluorination in investigational drug candidates.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients (EU, US, JP)
    • USP (United States Pharmacopeia) and Ph. Eur. (European Pharmacopoeia) references for related substances when applicable
    • Drug Master File (DMF) supportive documentation
    • Regular internal and third-party audits under cGMP requirements when used for clinical synthesis

    Typical usage ratio

    • 0.2–1.5 molar equivalents relative to the main nitrogen or oxygen nucleophile during halogen-exchange or aromatic substitution steps; precise usage set according to stoichiometry and byproduct minimization protocols

    Downstream process integration

    • Fed into parallel or single-pot synthesis routes for heterocycle assembly, or used as a late-stage functionalization agent for fluorinated pharmaceutical intermediates; custom unit operations may include Grignard, Suzuki, or SNAr coupling reactions

    Final product types

    • Intermediates for CNS and oncology drugs in late-phase R&D or semi-commercial production
    • Registered starting materials for anti-infective and specialty pharmaceutical actives
    • Non-sterile advanced intermediates supplied to custom synthesis partners

    3. Electronics-Grade Surface Treatment and Etching Chemicals

    Producers specializing in semiconductor and advanced electronic substrates employ our compound as a functional additive for fluorinated etchants and cleaners, supporting precision patterning and dielectrics modification. Strict control of trace metals and ionic content is critical for these applications to avoid micro-level contamination in production lines.

    Industry compliance standards

    • SEMI Standards (Semiconductor Equipment and Materials International), appraising chemical purity and trace element levels
    • TEL-QA (Tokyo Electron Ltd. Quality Assurance) program for electronics chemical suppliers
    • Analytical controls under IEC 60747-1 for purity
    • Custom OEM audits for contamination risk assessment

    Typical usage ratio

    • 0.1–2.5% v/v, adjusted based on the required etching profile, substrate thickness, and compatibility with other fluorinated or chlorinated process chemicals; loading determined by pilot-scale mock runs and cleanroom approval benchmarks

    Downstream process integration

    • Dosed into aqueous or semi-aqueous micro-etching baths used for patterned wafer treatment or as a trace additive in plasma-resistant cleaning fluids for photoresist residue removal in lithography steps

    Final product types

    • Cleaned and prepared semiconductor wafers (silicon, III-V compounds, advanced logic devices)
    • Dielectric films with engineered surface energy and low defect rate
    • LCD thin film transistor (TFT) glass panels

    4. High-Performance Polymer Synthesis (Fluoropolymers Specialty Segment)

    Our customers in polymer production integrate this compound as a co-monomer or functional chain terminator in the development of specialist fluoropolymers. Incorporation imparts unique properties for high chemical and thermal resistance, largely for coatings and membrane materials used under harsh processing conditions or where low dielectric loss is essential.

    Industry compliance standards

    • ASTM D543 standards on chemical resistance for polymer materials
    • FDA 21 CFR 177.1550 for fluoropolymer food contact materials (where applicable to end-use)
    • UL 94 for flame retardancy of polymer finished goods
    • ISO 14001 for environmental safety during polymerization

    Typical usage ratio

    • 0.3–2% w/w fed as a specialty monomer component or chain ender; adjusted based on targeted molecular weight, degree of substitution, and specific mechanical/thermal performance criteria

    Downstream process integration

    • Metered at defined stage of copolymerization reactor process (solution, emulsion, or suspension techniques), often with continuous monitoring for trace unreacted aromatic residues by in-line QC systems

    Final product types

    • Engineered fluoropolymer coatings for electronics and chemical plant hardware
    • Low-permeability and solvent-resistant membranes
    • High-frequency electrical insulation films

    5. Fine Chemical Intermediate for Specialty Dyes and Pigments

    Manufacturers serving the specialty textile and plastics coloration sectors use this intermediate for synthesizing certain high-performance, lightfast additives. The aromatic halogen–fluorine arrangement enables creation of pigments with improved UV and chemical resistance, suitable for applications in demanding outdoor or high-stress environments.

    Industry compliance standards

    • EN 71-3 safety of toys—migration of certain elements, where relevant for colorants
    • Oeko-Tex Standard 100 for harmful substance control in textiles
    • ROHS (Restriction of Hazardous Substances Directive) for electronics-related pigmented plastics
    • ASTM D4303 lightfastness ratings for artist and industrial dyes

    Typical usage ratio

    • Typically 0.05–1% molar ratio in pigment or dye synthesis, depending on reactivity with specific coupling partners and final color stability requirements; process engineers select optimal levels based on product stability and color strength assays

    Downstream process integration

    • Added at the coupling or condensation stage of dye or pigment synthesis, allowing halogen substitution or extension of conjugated aromatic systems for desired chromatic and fastness properties

    Final product types

    • High-durability fluorinated dyes for technical textiles
    • Outdoor-grade solvent-based pigments for plastics and coatings
    • Specialty inkjet and toner colorants for imaging applications
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