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2-Chloro-3,4-Difluoronitrobenzene

    • Product Name 2-Chloro-3,4-Difluoronitrobenzene
    • Alias 2-Chloro-3,4-difluoro-1-nitrobenzene
    • Einecs 700-967-1
    • 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
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    Specifications

    HS Code

    603903

    Product Name 2-Chloro-3,4-Difluoronitrobenzene
    Cas Number 64248-56-6
    Molecular Formula C6H2ClF2NO2
    Molecular Weight 193.54 g/mol
    Appearance Yellow to brown crystalline solid
    Melting Point 40-44 °C
    Boiling Point 230-235 °C
    Density 1.6 g/cm3 (approximate)
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles O=[N+](O-)C1=CC(F)=C(F)C(Cl)=C1
    Inchi InChI=1S/C6H2ClF2NO2/c7-5-3(8)1-2-4(6(5)9)10(11)12/h1-2H
    Storage Conditions Store in a cool, dry, well-ventilated place

    As an accredited 2-Chloro-3,4-Difluoronitrobenzene 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 100 grams; features a white screw cap, hazard labeling, and clear identification of 2-Chloro-3,4-Difluoronitrobenzene.
    Shipping 2-Chloro-3,4-difluoronitrobenzene is typically shipped in sealed, chemical-resistant containers, labeled according to hazardous material regulations. It should be transported under cool, dry conditions, away from incompatible substances. Proper documentation, including safety data sheets (SDS), is required to ensure compliance with local and international shipping regulations for hazardous chemicals.
    Storage Store 2-Chloro-3,4-difluoronitrobenzene in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong bases and oxidizers. Protect from moisture and direct sunlight. Label the storage area and container clearly, complying with all relevant safety regulations. Use secondary containment to prevent accidental release or spills.
    Application of 2-Chloro-3,4-Difluoronitrobenzene

    Applications of 2-Chloro-3,4-Difluoronitrobenzene in Industrial Manufacturing

    2-Chloro-3,4-Difluoronitrobenzene serves as a specialized intermediate in multiple advanced chemical production pathways. As the original manufacturer, we supply this raw material directly to leading formulators and downstream operators engaged in complex synthesis for pharmaceutical active ingredients, crop protection molecules, advanced pigments, and liquid crystal materials. Below, we detail the principal application segments based on verifiable industrial practice.

    1. Pharmaceutical Intermediate Synthesis

    Major pharmaceutical companies incorporate 2-Chloro-3,4-Difluoronitrobenzene in the multi-step synthesis of select active pharmaceutical ingredients (APIs), especially in the development of heterocyclic core structures for anti-infective and oncological drugs. This compound reacts at specific nitration and halogenation steps to introduce critical fluoro and chloro substituents into the molecular backbone, supporting defined structure-activity relationships as required by regulatory submissions and clinical protocols.

    Industry compliance standards

    • Good Manufacturing Practice (GMP, ICH Q7)
    • United States Pharmacopeia (USP) where API synthesis applies
    • European Pharmacopoeia (Ph. Eur.) compliance in API synthesis trails
    • REACH Annex XIV registration (ECHA, EU)

    Typical usage ratio

    • 0.7–1.8 molar equivalents in advanced intermediate coupling; adjusted per API yield and process optimization studies

    Downstream process integration

    • Addition in Step 2–4 during aromatic substitution or nucleophilic aromatic substitution stages
    • Integrated reaction with amines or organometallic reagents in closed reactor systems
    • Subsequent hydrogenation or cyclization for final core assembly

    Final product types

    • Pharmaceutical intermediates (custom-monitored batches)
    • Small-molecule APIs for anti-cancer and anti-infective drugs
    • Building-blocks for contract manufacturing organizations (CMOs)

    2. Agrochemical Synthesis (Herbicide and Insecticide Intermediates)

    Producers of innovative crop protection solutions utilize this material as a key intermediate in synthesizing difluorinated benzene frameworks for next-generation herbicides and insecticides. Through controlled displacement reactions, it supports the introduction of stability-enhancing fluoro groups integral to improved bioactivity and selective binding in modern agrochemical formulations. Constant attention to downstream recovery and by-product control ensures production meets strict agricultural regulatory criteria worldwide.

    Industry compliance standards

    • FAO/WHO specifications for active ingredients
    • ISO 9001:2015 for agrochemical manufacturing facilities
    • REACH compliance (substance and intermediate regulations, ECHA)
    • Globally Harmonized System (GHS) label and documentation for export

    Typical usage ratio

    • 2%–12% by weight within multi-step route to target active ingredient; range set by crop protection agent selectivity and required fluorination degree

    Downstream process integration

    • Initial halogen exchange or nitro-reduction prior to coupling with amines or heterocycles
    • Continuous-flow or batch reactors with real-time monitoring for yield and purity
    • Incorporation into final active or advanced intermediate before granulation or suspension concentrate formulation

    Final product types

    • Difluoro-substituted herbicide actives
    • Insecticidal key intermediates
    • Technical grade agrochemical actives pre-formulation

    3. High-Performance Pigment Manufacturing

    Manufacturers of specialty pigments deploy this compound as a base substrate for constructing complex azo and phthalocyanine colorants with high thermal and chemical resistance. Its twin fluoro substituents enhance final pigment brilliance and durability through participation in nucleophilic aromatic substitution, yielding specialty hues for plastics, coatings, and printing inks intended for stringent performance environments such as automotive and electronic markets.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances Directive, EU) in pigment application
    • EN 71-3 (Toy Safety – migration of certain elements) for pigments used in toys
    • ISO 9001:2015 for pigment quality management
    • Color Index (C.I.) registration for international pigment trading

    Typical usage ratio

    • 0.5–5.0% by mass in pigment synthesis batch, calibrated by desired chromaticity and heat resistance levels

    Downstream process integration

    • Coupling reaction with diazonium salts or phthalic anhydride under controlled temperature
    • Stage-specific treatment in glass-lined reactors to promote uniform fluorine incorporation
    • Purification through filtration, washing, and drying before pigment isolation

    Final product types

    • High-stability organic pigments for automotive coatings
    • Heat- and light-fast colorants for technical plastics
    • Specialty inks for industrial and security printing

    4. Liquid Crystal Material Precursor

    Producers of advanced display materials source this raw material to engineer fluorinated aromatic compounds, which impart controlled birefringence and improved voltage response in TFT-LCD and OLED substrates. In liquid crystal chemistry, tightly regulated introduction of chloro and fluoro substituents establishes the dielectric and alignment properties required for high-resolution, energy-efficient screens, driving demands for strict batch-to-batch consistency and trace impurity control during production scale-up.

    Industry compliance standards

    • JCIA Responsible Care Program (Japan)
    • IEC 61249 (Material standards for electronic components and circuitry)
    • ISO 14001 (Environmental Management System) for electronics chemicals
    • RoHS directive for electronic material compliance

    Typical usage ratio

    • 1.5–6.0 mol% within the precursor formulation, precisely calculated per required dielectric anisotropy and viscosity in final liquid crystal composition

    Downstream process integration

    • Condensation with difluorophenyl or biphenyl derivatives via nucleophilic substitution
    • Solvent-based synthesis under strict inert conditions to prevent trace contamination
    • Final purification through column chromatography before blend preparation

    Final product types

    • Liquid crystal monomers for TFT-LCD displays
    • Specialty intermediates for OLED material development
    • High-purity electronic solvents and alignment agents
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