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1,4-Difluoro-2,5-Dimethoxybenzene

    • Product Name 1,4-Difluoro-2,5-Dimethoxybenzene
    • Alias 1,4-Difluoro-2,5-dimethoxybenzene
    • Einecs 216-469-4
    • 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

    243358

    Cas Number 2296-83-7
    Molecular Formula C8H8F2O2
    Molecular Weight 174.15 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 94-96°C at 15 mmHg
    Density 1.204 g/cm³
    Refractive Index 1.513 (at 20°C)
    Solubility In Water Insoluble
    Flash Point 110°C
    Smiles COC1=CC(F)=C(F)C=C1OC
    Inchi InChI=1S/C8H8F2O2/c1-11-7-3-6(9)4-8(10)5-7-12-2/h3-5H,1-2H3

    As an accredited 1,4-Difluoro-2,5-Dimethoxybenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, sealed with a PTFE-lined cap, white printed hazard label, and CAS number for identification.
    Shipping **Shipping Description:** 1,4-Difluoro-2,5-Dimethoxybenzene should be shipped in tightly sealed chemical containers, protected from moisture, heat, and direct sunlight. The package must be clearly labeled, handled as a laboratory chemical, and transported according to relevant national and international regulations for hazardous materials. Ensure appropriate documentation accompanies the shipment.
    Storage **Storage for 1,4-Difluoro-2,5-Dimethoxybenzene:** Store in a tightly closed container, in a cool, dry, well-ventilated area away from direct sunlight, heat, and incompatible substances such as strong oxidizers. Keep away from sources of ignition. Avoid moisture exposure. Label the container clearly and ensure appropriate safety measures (gloves, goggles) are available for handling. Store under recommended chemical storage protocols.
    Application of 1,4-Difluoro-2,5-Dimethoxybenzene

    Applications of 1,4-Difluoro-2,5-Dimethoxybenzene in Industrial Manufacturing

    1,4-Difluoro-2,5-Dimethoxybenzene serves as a key intermediate in several specialized chemical manufacturing processes. Our experience as an integrated production site ensures precise quality management and full traceability from upstream synthesis to shipment. Below, we detail real downstream industrial applications, including sector-specific standards, practical formulation ranges, relevant process stages, and typical end products.

    1. Advanced Lithium-Ion Battery Electrolyte Additives

    Producers of high-performance lithium-ion batteries utilize this compound to modify electrolyte compositions for enhanced cycle life, stability, and safety. Using controlled dosing, formulation chemists integrate it during the wet mixing phase, optimizing electrochemical properties in both consumer electronics and automotive-grade batteries. This compound’s stability under electrochemical stress meets the requirements of next-generation battery cells.

    Industry compliance standards

    • IEC 62660-2 for lithium-ion cells automotive use
    • UN Manual of Tests and Criteria for battery transport (UN 38.3)
    • Quality Management System: IATF 16949 for automotive battery supply chains
    • RoHS 3 (Directive 2015/863/EU) restricts hazardous substances

    Typical usage ratio

    • 0.2–1.0% by weight in liquid electrolyte mixture, adjusted according to targeted charge-discharge performance and temperature endurance
    • Fine-tuned using electrochemical impedance and cycle testing data

    Downstream process integration

    • Introduced during electrolyte formulation alongside solvents (EC, DMC, DEC)
    • Pre-mixed before cell filling and vacuum degassing
    • Retention monitored via GC-MS prior to assembly

    Final product types

    • Electric vehicle lithium-ion battery packs
    • Consumer electronics power cells
    • Grid-scale energy storage modules
    • High-rate power tool batteries

    2. Pharmaceutical Intermediate for Active Compound Synthesis

    The molecule functions as a critical intermediate in synthesizing certain fluorinated API precursors and research drugs, especially in the neuropharmaceutical and oncology fields. Process chemists introduce it during multi-step organic synthesis, controlling reaction kinetics and purity through established GMP protocols. The structural motif contributes to specific receptor affinities and metabolic profiles in the final active compounds.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Annex 8 for starting material traceability
    • USP-NF and Ph. Eur. monographs (for relevant APIs)
    • ISO 13485 for pharmaceutical raw material supply chains

    Typical usage ratio

    • Stoichiometric addition from 0.8 to 1.2 equivalents based on targeted step yield
    • Ratio modified according to specific catalyst or coupling partners in process segment

    Downstream process integration

    • Added during early-stage Suzuki-Miyaura, Buchwald-Hartwig, or nucleophilic aromatic substitution steps
    • Monitored for residual solvent and trace metals post-reaction
    • Purified using column chromatography or crystallization before downstream transformations

    Final product types

    • Fluorinated anti-cancer research agents
    • CNS-active drug candidates
    • Advanced building blocks for peptide conjugate APIs
    • Preclinical small-molecule probes

    3. Organic Electronic Material Synthesis (OLED & OPV)

    Researchers and manufacturing chemists in organic electronics use this benzene derivative as a core fragment for constructing electron-transport layers and host materials in OLED (organic light-emitting diode) and OPV (organic photovoltaic) devices. It is introduced at specific condensation or polymerization steps to modulate bandgap and film-forming characteristics, enhancing charge-carrier mobility and device longevity in display and solar panel applications.

    Industry compliance standards

    • IEC 62341 standards for OLED panels
    • REACH Regulation (EC) No 1907/2006 for chemical substances
    • RoHS 3 Directive for finished consumer devices
    • UL 94 for flammability of plastic materials

    Typical usage ratio

    • 5–20 mol% as functional monomer or co-monomer in polymeric or small-molecule emitters
    • Adjusted according to emission spectrum and film thickness targeting device efficiency

    Downstream process integration

    • Engaged during monomer synthesis or copolymerization (Suzuki coupling, Wittig, or Stille reactions)
    • Film casting or spin coating onto pre-patterned ITO substrates
    • Quality verified via UV-Vis and photoluminescence spectroscopy

    Final product types

    • OLED display panels for mobile devices
    • OPV active layer inks and printable films
    • Encapsulated lighting modules
    • Flexible wearable electronic components

    4. Agrochemical Intermediate for Advanced Fungicides

    Agrochemical formulators utilize this aromatic compound as a core intermediate to construct complex active ingredients for systemic fungicides. Its difluoro and methoxy substitution enable precision incorporation into target molecules, improving bioactivity and photostability. Integration occurs during key cross-coupling and chlorination steps under validated process controls to ensure compliance with pesticide regulations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • US EPA 40 CFR Part 180: Tolerances and Exemptions for pesticide chemicals in food
    • EU Regulation (EC) No 1107/2009 for agrochemical production
    • ISO 9001:2015 for agrochemical intermediates

    Typical usage ratio

    • 0.3 to 0.7 molar equivalents per active per synthesis batch, adjusted to target impurity limits and reaction conversion
    • Final ratio determined by pilot scale-up trials

    Downstream process integration

    • Employed at early aromatic substitution or C–C coupling stages
    • Isolated, then transferred to chlorination or methylation steps
    • QC teams monitor residual intermediates and byproducts per batch

    Final product types

    • Modern fungicide active substances (e.g., triazole-based)
    • High-purity technical concentrates for crop protection
    • Pre-formulated granules and EC formulations
    • Seed treatment pesticide products
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