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2-Fluoro-5-Iodotoluene

    • Product Name 2-Fluoro-5-Iodotoluene
    • Alias 2-Fluoro-5-methyliodobenzene
    • Einecs (EINECS) 420-120-3
    • 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

    573237

    Chemical Name 2-Fluoro-5-Iodotoluene
    Cas Number 163055-74-3
    Molecular Formula C7H6FI
    Molecular Weight 236.03 g/mol
    Appearance Colorless to pale yellow liquid
    Density 1.808 g/cm3
    Boiling Point 216-218 °C
    Purity Typically ≥98%
    Smiles CC1=CC(=C(C=C1)I)F
    Inchi InChI=1S/C7H6FI/c1-5-2-3-6(8)4-7(5)9/h2-4H,1H3
    Refractive Index 1.585 (approximate)
    Storage Conditions Store at 2-8°C, in a tightly sealed container
    Solubility Insoluble in water; soluble in organic solvents
    Synonyms 2-Fluoro-5-iodo-1-methylbenzene

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2-Fluoro-5-Iodotoluene, sealed with a screw cap and labeled with safety information.
    Shipping 2-Fluoro-5-Iodotoluene is typically shipped in tightly sealed containers to prevent leaks and contamination. It should be transported in compliance with chemical safety regulations, protected from light, heat, and moisture. Proper labeling, documentation, and the use of hazard communication measures are required to ensure safe handling during transit.
    Storage 2-Fluoro-5-Iodotoluene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and moisture. Keep it away from sources of ignition, strong oxidizing agents, and incompatible materials. Store at ambient temperature and handle in accordance with standard chemical safety procedures, using personal protective equipment as required.
    Application of 2-Fluoro-5-Iodotoluene

    Applications of 2-Fluoro-5-Iodotoluene in Industrial Manufacturing

    Our 2-Fluoro-5-Iodotoluene supports a limited yet highly specialized set of downstream sectors. The following industrial workflows illustrate the direct incorporation of this API-grade chemical intermediate in real production environments, adhering to all relevant regulatory and processing controls. Each application below reflects genuine usage within global supply chains that leverage fluoro- and iodo-aromatic building blocks.

    1. Pharmaceutical Intermediate Synthesis for Active Pharmaceutical Ingredients (APIs)

    This halogenated toluene acts as a directed precursor in selective cross-coupling and functional group introduction during heterocyclic drug core assembly—particularly where both fluorine and iodine substituents enable regioselective transformation. Its utilization remains centered in manufacturing targeted therapies such as oncology and CNS actives, where precise substitution patterns are mandated by therapeutic pathways.

    Industry compliance standards

    • International Council for Harmonisation (ICH Q7) for GMP of Active Pharmaceutical Ingredients
    • U.S. FDA 21 CFR Part 210/211 for Finished Pharmaceuticals
    • European Pharmacopoeia (Ph. Eur.) Precursor Specification Protocols
    • Chinese Pharmacopoeia (ChP) API Grade Requirements

    Typical usage ratio

    • Usage is calibrated between 0.7–6 mol% of total reaction charge, depending on the stoichiometric route for Suzuki, Sonogashira, or Buchwald–Hartwig coupling steps. Final ratios depend on molar conversion efficiency and impurity profile control in pilot and scale-up settings.

    Downstream process integration

    • The material enters as a core building block in protected ring closure or direct halide exchange, generally after halogen-metal exchange activation or as the aryl halide component in coupling reactors under inert and moisture-controlled conditions, prior to further purification and API crystallization.

    Final product types

    • Targeted pharmaceutical actives (e.g., kinase inhibitors, fluorinated benzylamine derivatives, heterocyclic drugs for oncology and CNS applications)
    • Generic and branded small-molecule actives for regulated markets

    2. Advanced Agrochemical Synthesis (Herbicides & Fungicides)

    Aromatic fluoro-iodo toluenes enable agrochemical companies to introduce highly specific halogen patterns in the design of active moieties, impacting selectivity and environmental half-life. Downstream use focuses on the streamlined synthesis of triazole or pyridine derivatives as essential components in herbicidal and fungicidal formulations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 for Agrochemical Manufacturing
    • EU Regulation (EC) No 1107/2009 for Pesticide Active Substances
    • China GB 2763 for Maximum Residue Limits in Food Crops

    Typical usage ratio

    • Custom synthesis routes typically introduce it at 1–4% of total reaction mass, calculated as a limiting reagent in the aryl coupling stages, with ratios adjusted depending on required product purity and downstream functionalization steps.

    Downstream process integration

    • Used as the primary halogenated aromatic substrate in the arylation or halogen-metal exchange step of active ingredient synthesis, prior to condensation, heterocycle formation, or final salt formation, and followed by formulation into technical concentrates.

    Final product types

    • Fluorinated and iodinated pyridine/triazole-based herbicides
    • Triazole fungicidal actives used in broad-acre crop applications
    • Custom intermediate stocks for proprietary agrochemicals

    3. Custom Electronic Materials (OLED and Display Industry)

    In the field of organic electronics, halogen-substituted toluenes play a key role as intermediates for the controlled growth of conjugated aromatic layers. Our material's dual halogenation profile is frequently specified in the production of molecular precursors for electroluminescent polymer and small molecule emitters used in high-contrast panels and flexible OLED devices.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for Electronic Components
    • ISO/TS 80004-4:2011 Nanotechnology—Electric and Electronic Application Terms
    • IECQ QC 080000 Hazardous Substance Process Management
    • IEC 61249-2-21 for Halogen Content in Laminate Materials

    Typical usage ratio

    • Application-specific precursor synthesis requires 0.3–2.5 mol% of total monomer charge depending on target chain length and aryl distribution in the polymer or oligomer backbone.

    Downstream process integration

    • Introduced at the start of the organic synthesis route as the aryl halide donor for cross-coupling onto the core OLED emitter or conduction structure, prior to vacuum deposition or solution processing in cleanroom environments.

    Final product types

    • OLED emitter and host molecules (fluorinated carbazoles, arylamines)
    • Display-grade small-molecule fluorinated intermediates
    • Advanced photonic materials with tailored electroluminescent properties

    4. Fine Chemical Intermediates for Specialty Dyes and Pigments

    Dye and pigment manufacturers select fluoro-iodo aromatics as key intermediates for introducing unique substitution motifs in high-performance colorants. Utilization emphasizes reactivity in electrophilic and nucleophilic aromatic substitution, delivering chromophores with robust light stability and solubility profiles required for fiber, film, and ink applications.

    Industry compliance standards

    • REACH (EC 1907/2006) Registration for Chemicals
    • Oeko-Tex Standard 100 for Textile Chemicals
    • ISO 9001:2015 for Fine Chemical Manufacturing
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Code of Practice

    Typical usage ratio

    • Most pigment and dye syntheses require 0.5–3 wt% of total formulation input, with adjustment based on target color intensity and degree of fluorination in the final aromatic structure.

    Downstream process integration

    • Serves as a precursor in direct halogen exchange or as a coupling partner for extension of arylamine or azo chromophore scaffolds, entering batch reactors prior to isolation, milling, and dispersion processes.

    Final product types

    • High-performance textile dyes (e.g., arylazo and fluorobenzene pigments)
    • Specialty printing inks with enhanced fade resistance
    • Functional colorants for plastics, films, and coatings
    Free Quote

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