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2,3,4,5,6-Pentafluorotoluene

    • Product Name 2,3,4,5,6-Pentafluorotoluene
    • Alias Pentafluoromethylbenzene
    • Einecs 206-030-5
    • 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

    128582

    Cas Number 771-62-8
    Molecular Formula C7H3F5
    Molecular Weight 182.09 g/mol
    Appearance Colorless liquid
    Boiling Point 104-106 °C (at 760 mmHg)
    Melting Point -7 °C
    Density 1.505 g/cm³ at 25 °C
    Flash Point 23 °C (closed cup)
    Refractive Index n20/D 1.44
    Solubility In Water Insoluble
    Smiles Cc1c(F)c(F)c(F)c(F)c1F
    Inchi InChI=1S/C7H3F5/c1-2-3(8)5(10)7(12)6(11)4(2)9/h1H3
    Synonyms Pentafluoromethylbenzene
    Vapor Pressure 19 mmHg at 25 °C
    Logp 3.7

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

    Packing & Storage
    Packing The 100 mL amber glass bottle is tightly sealed, labeled "2,3,4,5,6-Pentafluorotoluene," and includes hazard and handling information.
    Shipping 2,3,4,5,6-Pentafluorotoluene is typically shipped in sealed glass or HDPE containers to prevent leaks and contamination. It should be packed securely, protected from heat and ignition sources, and labeled according to relevant regulations. Ensure compliance with local, national, and international shipping guidelines for handling hazardous organic chemicals.
    Storage 2,3,4,5,6-Pentafluorotoluene should be stored in a tightly closed container in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible substances like strong oxidizers. Avoid exposure to direct sunlight. Ensure containers are properly labeled and kept in a chemical storage cabinet suitable for flammable liquids. Handle with appropriate personal protective equipment to prevent spills or leaks.
    Application of 2,3,4,5,6-Pentafluorotoluene

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

    As an original manufacturer, we supply 2,3,4,5,6-pentafluorotoluene to specialized chemical industries that require high-purity aromatic fluorocarbons for advanced synthesis. This material serves as a precision-building block in a range of narrowly-defined, high-value downstream applications. Below, we outline the principal industrial uses where our product delivers distinct process and performance benefits.

    1. Agrochemical Intermediate Synthesis

    Downstream producers in the agrochemical sector rely on this pentafluorinated aromatic for the targeted synthesis of fluoroaryl pesticide actives and their precursors. Customers utilize its electron-deficient ring structure in nucleophilic aromatic substitution, streamlining the formation of custom herbicide scaffolds requiring increased metabolic stability. Our product integrates at a predictable point within their multi-step batch syntheses, supporting both pilot and full-scale technical grade production.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Active Ingredients
    • ISO 9001:2015 Quality Management Systems
    • OECD Principles of Good Laboratory Practice (GLP) during development
    • EU Regulation (EC) No. 1107/2009 for plant protection products

    Typical usage ratio

    • 5-30% by molar proportion in active ingredient synthesis, adjusted by desired substitution pattern and reaction pathway

    Downstream process integration

    • Added to aromatic fluorination or cross-coupling stage; forms a key structural motif during nucleophilic aromatic substitution

    Final product types

    • Herbicide actives (e.g., fluorinated nicotinoids, triazoles)
    • Insecticide intermediates
    • Fungicide precursors for patented molecules

    2. Pharmaceutical Intermediate Manufacture

    API manufacturers employ this specialty aromatic as an efficient fluorine donor for heterocyclic coupling, especially in the synthesis of next-generation CNS and oncology drugs, where metabolic and chemical stability is critical. It enables regioselective substitutions on electron-poor aromatic rings, providing a reproducible building block for route scouting and late-stage functionalization under cGMP environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Directive 2017/1572 for medicinal products
    • Pharmacopoeia monograph compliance (USP, EP, JP, as required)
    • REACH (EC 1907/2006) Registration for intermediates

    Typical usage ratio

    • 10-40% by weight relative to key starting material in target structure synthesis; varies with position-specific substitution

    Downstream process integration

    • Employed in nucleophilic aromatic substitution or cross-coupling with heteroaryl partners; integrated at intermediate step before final API crystallization

    Final product types

    • Intermediates for CNS active drugs (e.g., fluorinated arylpiperazines)
    • Fluorinated oncology API scaffolds
    • Advanced intermediates for antiviral agents

    3. Electronic Chemicals for LCD Liquid Crystal Precursors

    Specialty electronic chemical producers utilize pentafluorotoluene as a raw material for the synthesis of mesogenic units and spacers essential to high-performance LCD liquid crystal blends. Its controlled reactivity and high fluorine content influence dielectric anisotropy and viscosity behavior, directly shaping downstream liquid crystal mixture design for advanced flat-panel displays.

    Industry compliance standards

    • SEMI MS Standards for Materials Used in LCD Manufacturing
    • IEC 60747-5-5 for semiconductor device safety
    • RoHS 2011/65/EU for electronic device components
    • ISO 14001:2015 Environmental Management for production facilities

    Typical usage ratio

    • 3-15% in oligomerization reactions; percentage determined by target mesogen structure and final dipole adjustment requirements

    Downstream process integration

    • Introduced during custom mesogen synthesis via Friedel–Crafts or Suzuki coupling steps; fluorocarbon segment controls product morphology

    Final product types

    • Custom designed LC molecules for use in TFT-LCD production
    • Intermediate spacers for OLED and AMOLED applications
    • Synthetic modules for advanced display fluid mixtures

    4. Polymer Additives and Functional Monomer Production

    Producers in specialty polymers incorporate this perfluorotoluene derivative to synthesize highly fluorinated comonomers and tailor-make surface-active polymer backbones. Its electron-withdrawing strength assists in crafting specialty resins and coatings with unique oil/water repellency or electrical insulation. Process integration focuses on batch or continuous solution polymerization environments, predominantly in performance films and engineered surface treatments.

    Industry compliance standards

    • ASTM D758-15 Standard Test Methods for Fluoropolymer Materials
    • UL 94 Flammability test for polymer applications
    • ISO 10993-5 for medical-contact polymers
    • REACH SVHC requirements for downstream chemical safety

    Typical usage ratio

    • 1-12% incorporation in fluorinated monomer streams, with exact ratio tailored for desired final functional group density and performance attributes

    Downstream process integration

    • Directly entered in pre-polymerization or comonomer feed; participates as a chain modifier or end-group introducer during solution, emulsion or bulk polymerization

    Final product types

    • Hydrophobic and oleophobic coatings for industrial films
    • Specialty electrical insulation components
    • Protective surface treatment polymers for electronics and automotive markets

    5. Advanced Fluorochemicals for Specialty Solvents and Analytical Reagents

    Specialty chemical formulators employ this pentafluoroarene in the synthesis of selective fluorochemical solvents and derivatizing agents for chromatography and analytical chemistry. Its consistent purity level and reactivity support production processes that require minimal residue and precise molecular functionalization, facilitating strict performance in extraction, separation or analytical sample prep.

    Industry compliance standards

    • ACS Reagent Chemicals specifications for analytical reagents
    • ISO/IEC 17025:2017 for chemical testing laboratories
    • 21 CFR Part 211 for solvent use in QC of pharmaceuticals
    • Relevant National Standard Methods (EPA, ASTM D4307-03)

    Typical usage ratio

    • Varies based on target derivative or solvent product: typically 2-10% in reagent synthesis recipes

    Downstream process integration

    • Incorporated at the initial transformation step as a reactant for fluorinated solvent manufacturing or at final derivatization for analytical reagent creation

    Final product types

    • Specialty GC and HPLC derivatization agents
    • High-purity fluorinated solvents for trace analysis
    • Reference standards for method validation in chemical testing
    Free Quote

    Competitive 2,3,4,5,6-Pentafluorotoluene 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.

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    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

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