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3-Chloro-4-Hydroxybenzotrifluoride

    • Product Name 3-Chloro-4-Hydroxybenzotrifluoride
    • Alias 3-Chloro-4-(trifluoromethyl)phenol
    • Einecs 408-040-2
    • 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

    114404

    Chemical Name 3-Chloro-4-Hydroxybenzotrifluoride
    Cas Number 878-58-4
    Molecular Formula C7H4ClF3O
    Molecular Weight 196.55 g/mol
    Appearance White to off-white solid
    Melting Point 57-60°C
    Boiling Point 234°C
    Solubility In Water Slightly soluble
    Density 1.47 g/cm³
    Refractive Index 1.545
    Flash Point 109°C
    Purity Typically ≥98%
    Smiles C1=CC(=C(C=C1F)O)Cl

    As an accredited 3-Chloro-4-Hydroxybenzotrifluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g of 3-Chloro-4-Hydroxybenzotrifluoride is supplied in a sealed amber glass bottle with hazard labeling and safety cap.
    Shipping 3-Chloro-4-Hydroxybenzotrifluoride should be shipped in tightly sealed containers, protected from light and moisture. Transport according to local, national, and international regulations for hazardous chemicals. Ensure the package is clearly labeled, and safety data sheets accompany the shipment. Handle with care to prevent spillage and exposure during transit.
    Storage 3-Chloro-4-Hydroxybenzotrifluoride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances, such as strong oxidizing agents and bases. Protect from moisture, heat, and direct sunlight. Ensure proper labeling and keep away from food and drink. Use secondary containment to prevent spills and ensure storage area is equipped for chemical emergencies.
    Application of 3-Chloro-4-Hydroxybenzotrifluoride

    Applications of 3-Chloro-4-Hydroxybenzotrifluoride in Industrial Manufacturing

    3-Chloro-4-Hydroxybenzotrifluoride serves as a key intermediate in specialized industrial sectors where chemical purity and precise formulation control are essential. Below, we detail the most significant downstream applications, focusing on real manufacturing environments and processes based on current industry practices and regulatory frameworks.

    1. Agrochemical Synthesis (Herbicide and Fungicide Intermediates)

    This compound is widely used in the synthesis of phenoxy acids and other selective herbicide intermediates. Manufacturers incorporate it during the chlorination or trifluoromethylation stages to achieve target molecule specificity and enhanced active ingredient stability. Strict attention is paid to transition purity during the stage where 3-Chloro-4-Hydroxybenzotrifluoride is introduced, ensuring compliance and minimizing impurity carryover. End products are formulated to meet high active ingredient content with minimal contaminant levels, driven by crop protection requirements and environmental legislation.

    Industry compliance standards

    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)
    • US EPA FIFRA standards for pesticide manufacturing
    • China GB 2763 Maximum Residue Limits for Pesticides
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • 5–25% by weight in herbicide intermediate synthesis, adjusted according to desired activity and downstream reaction sequence

    Downstream process integration

    • Introduced during initial condensation or coupling reactions to generate desired substituted aromatic building blocks

    Final product types

    • Selective herbicides (e.g., phenoxyacetic acid derivatives)
    • Systemic fungicides with high environmental resistance

    2. Pharmaceutical Intermediate Manufacturing

    Producers of specialty APIs utilize this compound as a key precursor for non-steroidal anti-inflammatory drugs and certain antibacterial agents. The material enters the synthetic pathway during step-growth or nucleophilic aromatic substitution stages to build advanced scaffolds. Precise control over reactant ratios and side-product formation enables compliance with international pharmacopeial standards and GMP batch release protocols. Downstream QC testing ensures batch-to-batch consistency and target impurity profiles.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF (United States Pharmacopeia/National Formulary)
    • European Pharmacopoeia (Ph. Eur.) monographs
    • China Pharmacopoeia (ChP) requirements for drug substances

    Typical usage ratio

    • 10–30% by weight depending on molecular complexity and efficiency of the key coupling or substitution steps

    Downstream process integration

    • Added at the controlled aromatic substitution stage or ester/amide formation during pharmaceutical intermediate build-up

    Final product types

    • API intermediates for NSAIDs and antipyretic-analgesic drugs
    • Intermediates for antibacterial agents targeting Gram-negative bacteria

    3. High-Performance Coating Resin Production

    Chemical resin manufacturers rely on this raw material for introducing trifluoromethyl and chlorinated groups into specialty polyester and epoxy resin backbones. This results in end products with increased thermal stability, chemical resistance, and reduced surface energy. The controlled addition during polymer modification or functional monomer synthesis provides precision in performance parameters and ensures adherence to migratory chemical limits in end-use regulations for coatings.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for registration and downstream user requirements
    • Directive 2004/42/EC (VOC limits in paints and varnishes)
    • ASTM D5402 (Solvent Resistance of Organic Coatings)
    • China GB/T 22374-2018 (Coating Product Technical Requirement)

    Typical usage ratio

    • 2–10% by weight in resin backbone modification, varied for specific resistance and durability targets

    Downstream process integration

    • Added during controlled copolymerization or prepolymer modification prior to cross-linker addition or final resin formation

    Final product types

    • Weather-resistant industrial coatings
    • Anti-corrosive paints for infrastructure
    • Specialty fluorinated powder coatings

    4. Electronic Specialty Chemical Manufacturing

    Producers of advanced electronic materials use this compound in the synthesis of fluorinated aromatic intermediates for liquid crystal display (LCD) monomers and semiconductor wet chemicals. The controlled insertion provides dielectric property enhancement and chemical purity, crucial for minimizing performance drift in electronic substrates and display panels. Rigorous analytical process monitoring ensures absence of ionic and particulate contaminants.

    Industry compliance standards

    • JEITA ET-7304 (Electronic Components Material Quality)
    • SEMI C3 (Specifications for Electronic Grade Chemicals)
    • IPC-4552 (Quality Standards for Electronic Coatings)
    • China GB/T 26572-2011 (Electronic Information Products Limits of Toxic Substances)

    Typical usage ratio

    • 1–8% by weight in key aromatic intermediate synthesis, tightly adjusted by analytical monitoring based on target purity

    Downstream process integration

    • Integrated at fluorinated aryl synthesis or during halide exchange/condensation steps supplying LCD or semiconductor lines

    Final product types

    • Fluorinated monomers for LCDs
    • Specialty etchants and cleans for microelectronics
    • Precursor resins for advanced printed circuit boards

    5. Dye and Pigment Intermediate Processing

    Manufacturers use this material in colorant intermediate synthesis, providing robust resistance to bleaching and chemical degradation. The product is introduced at the substitution or condensation step to influence hue and fastness properties. Contaminant profiling and colorimetric adjustment during final purification ensure the dyes meet both performance and safety requirements, particularly for industrial and textile use.

    Industry compliance standards

    • OEKO-TEX Standard 100 (Textile Safety)
    • REACH Annex XVII (Restrictions on dyes and pigments)
    • China GB 20412 Textile Dye Industry Standard
    • EN ISO 105 (Textile Tests for Color Fastness)

    Typical usage ratio

    • 3–15% by weight, adjusted for desired dye shade and stability requirements in targeted applications

    Downstream process integration

    • Added at the azo coupling or condensation stage to tailor molecular structure of final dye/pigment intermediates

    Final product types

    • Reactive dyes for cotton and synthetic fibers
    • High-purity organic pigments with chemical resistance

    6. Fine Chemical Synthesis for Advanced Materials

    Developers of high-value specialty chemicals include this raw material when constructing advanced functionalized aromatics needed for niche applications such as liquid crystals or precision optical compounds. Close monitoring of addition timing and temperature control ensures desired substituent incorporation and minimal formation of by-products, supporting traceable lot histories and material certification for critical-application manufacturers.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for fine chemical synthesis
    • Chemical Manufacturer’s Association Responsible Care Management System
    • China GB/T 3723-2017 (Sampling Methods for Chemical Products)
    • RoHS Directive 2011/65/EU (for final device use)

    Typical usage ratio

    • 1–12% by weight, set according to required functionality and end-use device specification

    Downstream process integration

    • Incorporated at high-selectivity functionalization or cyclization steps during advanced material build-up

    Final product types

    • Customized semifinished aromatics for research and development
    • Optically active compounds for device integration
    • Niche advanced materials for display or sensor applications
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