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4-Trifluoromethylphenol

    • Product Name 4-Trifluoromethylphenol
    • Alias p-(Trifluoromethyl)phenol
    • Einecs 228-587-0
    • 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

    438959

    Chemical Name 4-Trifluoromethylphenol
    Cas Number 402-45-9
    Molecular Formula C7H5F3O
    Molecular Weight 162.11
    Appearance White to off-white solid
    Melting Point 61-64°C
    Boiling Point 191-193°C
    Density 1.32 g/cm3
    Solubility In Water Slightly soluble
    Smiles CC1=CC=C(C=C1)O
    Inchi InChI=1S/C7H5F3O/c8-7(9,10)5-1-3-6(11)4-2-5/h1-4,11H
    Refractive Index 1.475
    Synonyms 4-(Trifluoromethyl)phenol

    As an accredited 4-Trifluoromethylphenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 4-Trifluoromethylphenol, 25g, is supplied in a sealed amber glass bottle with tamper-evident cap and detailed hazard labeling.
    Shipping 4-Trifluoromethylphenol is shipped in tightly sealed containers under ambient conditions. It should be protected from moisture and direct sunlight. Packaging complies with relevant safety and transport regulations (such as DOT or IATA). Ensure labeling indicating chemical hazards. Handle with appropriate personal protective equipment during receipt and unpacking to prevent exposure.
    Storage 4-Trifluoromethylphenol should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents and bases. The storage area should be protected from direct sunlight and sources of ignition. Proper labeling and secondary containment are advised to prevent leaks, spills, or accidental exposure.
    Application of 4-Trifluoromethylphenol

    Applications of 4-Trifluoromethylphenol in Industrial Manufacturing

    4-Trifluoromethylphenol serves key roles in high-value synthetic processes for fine chemicals, pharmaceuticals, agrochemicals, monomers, and advanced materials. Our in-house production enables strict quality control and reliable supply for diverse integration into industry-leading sectors. Each downstream application adheres to distinguished standards and employs tailored use protocols for consistent, safe, and scalable operations.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers use 4-Trifluoromethylphenol as a masked phenol or nucleophilic aromatic precursor in building blocks for small-molecule APIs, especially where metabolic stability and electron-withdrawing substitution are critical. It enters early or mid-stage synthetic routes to introduce the trifluoromethylphenyl motif. QC laboratories conduct close analytical monitoring to meet the narrow impurity profiles required for regulated drug substances.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs
    • US FDA cGMP for APIs (21 CFR Part 211 & 210)

    Typical usage ratio

    • Ranges from 1–15% molar equivalent relative to target API backbone, depending on stage and structure requirements in process route. Adjustment made according to step yield and waste minimization.

    Downstream process integration

    • Coupling or substitution reactions under mild to moderate conditions; mainly in heterocycle formation, etherifications, or Suzuki-Miyaura and Buchwald-Hartwig couplings within GMP synthesis operations.

    Final product types

    • Small molecule APIs featuring trifluoromethylphenyl rings (e.g., CNS agents, antineoplastics, antivirals)
    • Key regulated pharmaceutical intermediates supplied to licensed drug producers

    2. Agrochemical Active Ingredient Manufacturing

    The compound is regularly incorporated in the synthesis of selective herbicides and modern insecticides. It introduces fluorinated aromatics, which are essential for increasing compound bioactivity and stability against degradation in agrochemical actives. Large-scale manufacturers integrate it at defined process steps to boost overall product performance within international regulatory limits.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • REACH registration and compliance for substances and intermediates
    • ISO 9001:2015 quality management for pesticide manufacturers

    Typical usage ratio

    • Generally 2–8% weight by weight in targeted aromatic substitution steps; ratio depends on active ingredient formulation and activity profile demanded by pesticide product registrations.

    Downstream process integration

    • Introduced during aromatic functionalization, mainly etherification or amination reactions, before formulation blending and packaging in centralized agrochemical plants.

    Final product types

    • Formulated herbicides for cereal and broadleaf crops
    • Next-generation insecticides with improved synthetic stability

    3. Specialty Polymer Monomer & Additive Synthesis

    In the advanced polymer industry, 4-Trifluoromethylphenol acts as a reactive monomer or chain modifier. It is incorporated into copolymerization or as a capping agent in production of high-performance materials with enhanced chemical resistance, dielectric properties, and low surface energy. The compound is handled under inert atmosphere in controlled batch reactors to prevent side reactions and optimize molecular structure during upscaling.

    Industry compliance standards

    • ISO 14001 Environmental Management System for chemical processing
    • RoHS restriction compliance for electronic-grade polymers
    • ASTM D638-14 standard for tensile properties of plastics

    Typical usage ratio

    • Usually 0.5–5% by weight depending on polymer architecture and property targets; higher fractions possible for desired surface or dielectric attributes.

    Downstream process integration

    • Enters during prepolymerization mixing; activated by initiators or catalysts; followed by thermal curing or extrusion, with off-gas monitoring for safe handling of fluorinated intermediates.

    Final product types

    • Fluorinated polyaryletherketones and related specialty resins
    • Electronic encapsulants and high-frequency insulators
    • Coating resins for corrosion-resistant components

    4. Chemical Vapor Deposition Precursors in Electronics

    Electronics manufacturers employ 4-Trifluoromethylphenol as a specialized organic precursor in chemical vapor deposition (CVD) processes for microelectronics and flat panel displays. Its volatility and thermal decomposition properties enable selective deposition of fluorinated carbon or polyaryl thin films under low-oxygen conditions. Process engineering controls exposure and monitors exhaust to meet repeatability and emission benchmarks.

    Industry compliance standards

    • SEMATECH process protocols for microelectronics fabrication
    • IEC 62474 material declaration for electronic industry
    • ISO/TS 16949 for quality management in electronics supply

    Typical usage ratio

    • Loaded at 3–10% in gas phase relative to carrier flows; precise dosage set by target film thickness and uniformity across large substrates.

    Downstream process integration

    • Vaporized and introduced in CVD chambers with staged temperature ramps and vacuum control; effluent monitoring ensures residual monomer minimization prior to wafer unloading.

    Final product types

    • Thin film transistors (TFTs) for LCD and OLED displays
    • Dielectric coatings for integrated circuit (IC) packaging
    • Printed flexible electronics components

    5. Advanced Organic Synthesis for Fine Chemicals

    Chemical synthesis networks for fine aromatic compounds and specialty intermediates make use of 4-Trifluoromethylphenol as a functional handle for preparing fluorinated building blocks. Manufacturers appreciate its reactivity in nucleophilic substitution, aryl halide coupling, and protective group strategies. This enables efficient scale-up of value-added organofluorine compounds for diverse end-users, applying analytical controls for traceability and batch-to-batch consistency.

    Industry compliance standards

    • ISO 9001:2015 for quality assurance in fine chemicals manufacture
    • REACH registration for specialty intermediates within the EU
    • Responsible Care management system for environmental and process safety

    Typical usage ratio

    • Formulation rates typically at 1–10% by weight in coupling and substitution reactions; variations based on desired yield and side product minimization.

    Downstream process integration

    • Feeds directly into batch reactors for Grignard, Friedel-Crafts, or transition metal-catalyzed processes; followed by distillation and purification to isolate high-purity fluorinated intermediates.

    Final product types

    • Trifluoromethoxybenzene derivatives
    • Functionalized aromatic acids and esters
    • Key intermediates for manufacturers of pigments, flavors, and other specialties
    Free Quote

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