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(Difluoromethoxy)Benzene

    • Product Name (Difluoromethoxy)Benzene
    • Alias 1,1-Difluoro-1-methoxybenzene
    • Einecs 407-270-1
    • 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

    452075

    Iupac Name 1-(Difluoromethoxy)benzene
    Molecular Formula C7H6F2O
    Molar Mass 144.12 g/mol
    Cas Number 366-99-8
    Appearance Colorless liquid
    Boiling Point 153-155 °C
    Density 1.188 g/cm3
    Refractive Index 1.473
    Melting Point -17 °C
    Flash Point 50 °C
    Smiles C1=CC=C(C=C1)OCF2
    Pubchem Cid 10861

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

    Packing & Storage
    Packing A 100 mL amber glass bottle, tightly sealed, labeled “(Difluoromethoxy)Benzene,” includes hazard symbols and handling instructions.
    Shipping (Difluoromethoxy)benzene is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It must be kept in a cool, well-ventilated area and handled according to standard chemical safety protocols. Packaging complies with relevant hazardous materials regulations to ensure safe transport and prevent leaks or accidental exposure.
    Storage (Difluoromethoxy)benzene should be stored in a tightly sealed container, away from direct sunlight, heat, and sources of ignition, in a cool, dry, and well-ventilated area. Keep it separate from incompatible materials such as strong oxidizers. Store at ambient temperature and ensure proper labeling. Use secondary containment to prevent spills and follow all relevant safety and regulatory guidelines.
    Application of (Difluoromethoxy)Benzene

    Applications of (Difluoromethoxy)Benzene in Industrial Manufacturing

    (Difluoromethoxy)Benzene serves as a key intermediate for specialty downstream applications in pharmaceuticals, crop protection, advanced materials, and specialty polymers. As the original manufacturer, we support clients with tailored product grades, process compatibility, and full regulatory transparency for each commercial scenario. Below we detail the specific roles, regulatory requirements, and process attributes across the primary value chains utilizing our material.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    In pharmaceutical manufacturing, (Difluoromethoxy)Benzene acts as a building block for synthesizing APIs, especially fluorinated aromatic compounds used in anti-inflammatory, anti-tumor, and central nervous system drugs. Customers introduce it via electrophilic aromatic substitution, forming advanced intermediates required for subsequent coupling or heterocyclic ring construction. Close collaboration with formulation chemists and adherence to validated QMS and traceability standards are mandatory throughout the production sequence. Our material is supplied in pharmaceutical grade, meeting specifications for impurity profile, residual solvents, and controlled batch consistency.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP; ICH Q7)
    • European Pharmacopoeia (Ph. Eur.) Monographs for Intermediates
    • US FDA 21 CFR Part 211 (Finished Pharmaceuticals)
    • ICH Q3A/B (Impurities Guideline)

    Typical usage ratio

    • 5–20 mol% relative to base aromatic substrate; the exact ratio depends on the specific target structure and desired substitution pattern within the final API intermediate.

    Downstream process integration

    • Introduced during the aromatic substitution or metal-catalyzed coupling steps, generally in solvent-controlled, anhydrous conditions prior to API crystallization and purification.

    Final product types

    • Fluorinated active pharmaceutical ingredients used in anti-infective, anti-cancer, or neurological therapies (e.g., difluorinated aryl compounds, advanced CNS drugs).

    2. Agrochemical Synthesis for Crop Protection Agents

    Clients in the crop protection sector incorporate (Difluoromethoxy)Benzene as a key intermediate for synthesizing selective herbicides and systemic fungicides. It facilitates the creation of difluorinated aromatic rings, improving environmental stability and bioactivity of registered actives. It typically enters amidation or condensation reactions during multi-step synthesis, where precise mol input and strict process monitoring are enforced to ensure downstream field efficacy and residue compliance.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management Systems for Pesticide Ingredients
    • OECD Good Laboratory Practices (GLP) for pesticide R&D
    • REACH Registration (EU Regulation (EC) No 1907/2006)

    Typical usage ratio

    • Variable between 3–12 wt% within the multi-step reaction matrix; the amount depends on the molecular structure of the desired active ingredient and the number of aromatic fluorination steps incorporated.

    Downstream process integration

    • Employed in the key condensation or acylation phase of the synthetic route, generally as a ring substrate or fluorine donor during scaffold assembly, immediately preceding chiral resolution or formulation stages.

    Final product types

    • Formulated herbicides and fungicides for cereals, fruits, and vegetable protection (e.g., difluoromethoxy-substituted triazole or pyridine compounds).

    3. Advanced Materials – Specialty Liquid Crystals for Display Technologies

    Manufacturers of high-performance liquid crystals employ (Difluoromethoxy)Benzene as an intermediate for producing difluoroaromatic mesogens used in LCD panels and organic electronic devices. The compound delivers unique polarizability and thermal stability, enhancing molecular alignment and contrast in modern displays. It is precisely dosed during multi-stage alkylation and subsequent esterification or etherification reaction sequences in electronics-grade material synthesis.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • IEC 62321 (Determination of Certain Substances in Electrotechnical Products)
    • ISO 9001:2015 for Electronic Chemical Manufacturing
    • IPC-4101/41 (Specification for Base Materials in Electronics)

    Typical usage ratio

    • Typically 2–8 wt% in alkoxyaryl core synthesis, adjusted for desired electro-optical properties and final nematic phase requirements.

    Downstream process integration

    • Functions as a raw material in the initial arylation or alkoxylation step for creating difluoro-substituted mesogenic cores, prior to purification and blending into LC mixtures.

    Final product types

    • Advanced nematic and smectic liquid crystal mixtures for LCD modules, display backplanes, and organic transistor components.

    4. Intermediate for Specialty Polymer Synthesis

    Polymer manufacturers utilize (Difluoromethoxy)Benzene in the production of specialty polyarylene ethers and aromatic fluoropolymers, targeting high chemical resistance and low dielectric properties. It participates in nucleophilic substitution or etherification with dihalogenated monomers, forming the backbone of high-performance plastics used in electronics, membranes, and chemical process equipment. Quality assurance teams apply material traceability and chain-of-custody standards throughout integration.

    Industry compliance standards

    • ISO 9001:2015 for Polymer Manufacturing
    • UL 94 (Flammability Standard for Plastics)
    • ASTM D543 (Resistance of Plastics to Chemical Reagents)
    • RoHS 2 (EU 2015/863) for Electronic Polymer Components

    Typical usage ratio

    • 2–10 mol% as a comonomer with halogenated aromatic units; the ratio is tuned for molecular weight, Tg, and chemical barrier properties in the final polymer matrix.

    Downstream process integration

    • Charged during the polymerization (nucleophilic aromatic substitution) step as one of the key bis-aryl monomers, just before polycondensation and post-polymer extrusion.

    Final product types

    • Specialty polyarylene ether films, fluorinated polymer membranes, and high-durability insulating materials for electronics and industrial applications.
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