Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

4-(Trifluoromethylthio)Phenol

    • Product Name 4-(Trifluoromethylthio)Phenol
    • Alias 4-(Trifluoromethylthio)Phenol; p-(Trifluoromethylthio)phenol
    • Einecs 252-527-4
    • 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
    VTB
    Specifications

    HS Code

    987441

    Chemical Name 4-(Trifluoromethylthio)Phenol
    Cas Number 827-98-5
    Molecular Formula C7H5F3OS
    Molecular Weight 194.18
    Appearance White to pale yellow crystalline powder
    Melting Point 55-59°C
    Boiling Point 109-111°C at 15 mmHg
    Density 1.49 g/cm3
    Refractive Index n20/D 1.522
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC(=CC=C1O)SC(F)(F)F
    Inchi InChI=1S/C7H5F3OS/c8-7(9,10)12-6-3-1-5(11)2-4-6/h1-4,11H

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

    Packing & Storage
    Packing Brown glass bottle, 25 grams, sealed with a secure cap; labeled with chemical name, hazard warnings, manufacturer's information, and batch number.
    Shipping 4-(Trifluoromethylthio)phenol is shipped in tightly sealed containers under cool, dry conditions, and protected from light and moisture. Classified as a hazardous material, it requires careful labeling and documentation. Appropriate personal protective equipment (PPE) and adherence to chemical transport regulations ensure safe handling during transit.
    Storage 4-(Trifluoromethylthio)phenol should be stored in a tightly sealed container, protected from light and moisture, and kept in a cool, well-ventilated area. Store away from incompatible substances such as strong oxidizers and bases. Ensure appropriate labeling, and follow all regulations for hazardous chemical storage. Use secondary containment to prevent spills and always wear suitable protective equipment when handling.
    Application of 4-(Trifluoromethylthio)Phenol

    Applications of 4-(Trifluoromethylthio)Phenol in Industrial Manufacturing

    4-(Trifluoromethylthio)Phenol serves specialized functions in several high-performance industrial production environments, where its unique physicochemical characteristics provide needed modifications in molecular structure. Our ongoing involvement with leading downstream manufacturers ensures stable product quality and regulatory compliance tailored to specific application demands. Below, we summarize the authentic industrial uses for this material, focusing on precise integration details relevant to process chemists, formulators, and production managers.

    1. Advanced Agrochemical Synthesis

    Downstream agrochemical producers introduce 4-(Trifluoromethylthio)Phenol as a key intermediate in the manufacture of sulfur-containing phenoxy-based herbicides and fungicides. The electron-withdrawing trifluoromethylthio group increases target molecule stability and bioactivity, especially in actives formulated for resistance management. Production lines carefully meter the material to match reaction stoichiometry and control impurity profiles.

    Industry compliance standards

    • GB 4839-2016 (Pesticide - Technical Requirements for Active Ingredients)
    • FAO/WHO Specifications for Plant Protection Products
    • REACH (EC 1907/2006) registration and dossier requirements for supplied intermediates
    • ISO 9001:2015 Certified Quality Management for agrochemical production

    Typical usage ratio

    • 5–12% w/w relative to total mass of stepwise synthesis batch, depending on targeted crop-protection molecule and desired substitution level

    Downstream process integration

    • Added during the nucleophilic aromatic substitution stage under controlled temperature and basic conditions, preceding final cyclization or esterification
    • QC technicians monitor residual content in final actives to confirm full conversion

    Final product types

    • Post-emergence herbicide technicals for cereal crops
    • Broad-spectrum fungicidal concentrates
    • Registered plant protection agents for regional distribution

    2. Pharmaceutical Intermediate Production

    Pharmaceutical API manufacturers use 4-(Trifluoromethylthio)Phenol as a building block in the synthesis of antithrombotic, anti-inflammatory, and central nervous system drug candidates involving fluorinated aromatic scaffolds. The compound's high reactivity and selective substitution facilitate late-stage functionalization in multi-step synthetic sequences. Accurate metering minimizes undesirable by-product formation compliant with current regulatory requirements for genotoxic impurities.

    Industry compliance standards

    • US Pharmacopeia (USP) General Chapter <823> for intermediates
    • ICH Q7 Good Manufacturing Practices for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) for process intermediates
    • FDA cGMP (21 CFR Parts 210 & 211) for contract manufacturing

    Typical usage ratio

    • 0.5–3 molar equivalents per synthetic step, precisely calculated based on targeted molecular transformations and impurity control needs

    Downstream process integration

    • Charged into vessel during regioselective aromatic substitution or as a capping reagent after core skeleton assembly
    • Process chemists sample and validate conversion prior to purification or scale-up

    Final product types

    • Sulfur and fluorine-substituted API intermediates
    • Research batches for NCE (New Chemical Entity) evaluation
    • Pilot-scale API process batches for clinical studies

    3. High-Performance Polymer Modification

    Polymers and specialty resin producers incorporate 4-(Trifluoromethylthio)Phenol to adjust hydrophobicity, chemical resistance, and electrical properties for performance materials used in electronics and coatings. The trifluoromethylthio functionality delivers targeted surface energy control and modifies cure kinetics during thermoset cross-linking. Adjustments to load level and process conditions enable manufacturers to balance final mechanical strength and insulation requirements.

    Industry compliance standards

    • IEC 61249-2-21 for halogen-free base materials
    • RoHS Directive (2011/65/EU, Annex II) on restricted substances in electronics
    • ASTM D3418 for Differential Scanning Calorimetry (DSC) in polymer systems
    • EN ISO 9001:2015 for polymer compounding process management

    Typical usage ratio

    • 0.1–4 phr (parts per hundred resin) depending on matrix compatibility and targeted dielectric loss factor

    Downstream process integration

    • Introduced to the resin blend before extrusion or in-situ polymerization under inert atmosphere to prevent side reactions
    • Post-addition blending under monitored shear to ensure full dispersion

    Final product types

    • High-durability circuit board laminates
    • Specialty wire coatings for industrial cables
    • Engineered thermoset and thermoplastic parts for electronics housings

    4. Custom Dye and Pigment Manufacture

    Specialty dye and pigment producers deploy 4-(Trifluoromethylthio)Phenol in fine-tuned aromatic substitution and coupling reactions that enhance color depth, fastness, and solvent resistance in fluorinated pigment systems. The compound's high nucleophilicity enables efficient coupling to diazonium salts or during oxidative azo synthesis. Color chemists adjust usage based on target shade intensity and stability factors for high-value textile and plastics applications.

    Industry compliance standards

    • OEKO-TEX Standard 100 for hazardous chemical exclusion in textiles
    • EN 71-3 Safety of Toys – migration of certain elements for pigment use
    • REACH Annex XVII for restricted aromatic amines (monitor reaction purity)
    • SQAS (Safety & Quality Assessment for Sustainability) for pigment logistics

    Typical usage ratio

    • 0.2–1.8 molar equivalents based on coupling partner and anticipated hue performance

    Downstream process integration

    • Added during controlled temperature aromatic coupling in aqueous or organic phase, with real-time UV-Vis monitoring of chromophore development
    • Intermediates subsequently purified and milled for optimal pigment particle size

    Final product types

    • Fluorinated azo dyes for synthetic textiles
    • High-resistance pigments for automotive and plastic coatings
    • Color lakes for industrial printing inks
    Free Quote

    Competitive 4-(Trifluoromethylthio)Phenol prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance