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4'-Fluoro-2'-Nitroacetanilide

    • Product Name 4'-Fluoro-2'-Nitroacetanilide
    • Alias 4'-Fluoro-2'-Nitroacetanilide
    • Einecs 625-280-5
    • 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

    770703

    Productname 4'-Fluoro-2'-Nitroacetanilide
    Molecularformula C8H7FN2O3
    Casnumber 211504-71-5
    Appearance Yellow to brown solid
    Meltingpoint 146-150°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles CC(=O)NC1=CC=C(F)C(=C1)[N+](=O)[O-]
    Inchi InChI=1S/C8H7FN2O3/c1-5(12)11-7-3-2-6(9)8(4-7)10(13)14/h2-4H,1H3,(H,11,12)
    Storagetemperature Store at 2-8°C
    Hazardclass Irritant

    As an accredited 4'-Fluoro-2'-Nitroacetanilide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 grams of 4'-Fluoro-2'-Nitroacetanilide, securely sealed in a white HDPE bottle with clear labeling and hazard warnings.
    Shipping 4'-Fluoro-2'-Nitroacetanilide is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It is classified as a laboratory chemical and must be handled by qualified personnel. Ensure compliance with all local, national, and international regulations. Appropriate labeling and documentation accompany the shipment to guarantee safe transport and handling.
    Storage 4'-Fluoro-2'-Nitroacetanilide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sunlight and sources of ignition. Keep the chemical away from incompatible materials like strong oxidizing agents. Store at room temperature and avoid moisture. Label the container clearly, and follow all relevant chemical storage safety regulations and guidelines.
    Application of 4'-Fluoro-2'-Nitroacetanilide

    Applications of 4'-Fluoro-2'-Nitroacetanilide in Industrial Manufacturing

    4'-Fluoro-2'-Nitroacetanilide provides essential functional groups for advanced chemical synthesis in several industrial verticals. As an established manufacturer, we support global partners with consistent product quality for demanding applications in pharmaceutical intermediates, agrochemical synthesis, dye precursors, and specialty fine chemicals. Below we outline key downstream integrations, compliance protocols, recommended ratios, and main finished product examples for professional industrial users.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical process teams use this material as a building block for the synthesis of selective active pharmaceutical ingredient (API) intermediates, particularly within nitroaniline-based drug frameworks. The compound’s fluorinated aromatic structure enables precision in sequential nitration and reduction reactions under controlled hydrogenation. Downstream users deploy it primarily in the preparation of substituted acetanilides, which serve as core intermediates for anti-inflammatory and central nervous system drug development. Quality assurance mandates tracking impurities and residual solvents in every batch during cGMP-compliant production.

    Industry compliance standards

    • ICH Q7A GMP Guidelines
    • EU Regulation (EC) No. 1907/2006 (REACH)
    • US FDA 21 CFR Part 211
    • European Pharmacopoeia monograph alignment for relevant APIs

    Typical usage ratio

    • 10–30% of total reaction mass in multi-step synthesis routes, with specific ratio adjusted based on target yield and downstream conversion efficiency

    Downstream process integration

    • Charged into nitration or acylation reactors during initial or early-stage synthesis; followed by reduction, purification, filtration, and solvent removal steps under quality-controlled conditions

    Final product types

    • Intermediate compounds for NSAIDs (e.g., selective COX inhibitors)
    • Precursors to anti-psychotic or anti-inflammatory drugs
    • Key intermediates for fluorinated pharmaceutical products
    • Building blocks for niche specialty APIs

    2. Agrochemical Synthesis (Herbicide and Fungicide Intermediates)

    The agrochemical industry employs this compound in the synthesis of modern herbicide and fungicide intermediates, benefiting from its dual nitro and fluoro substitutions which enhance target specificity. Process chemists integrate the material into selective coupling and cyclization reactions for the formation of active halogenated anilide scaffolds, which downstream partners further convert to crop protection agents. Strict batch traceability and purity monitoring are required to meet international agrochemical regulatory submissions.

    Industry compliance standards

    • Food and Agriculture Organization (FAO) Specification Requirements
    • OECD Good Laboratory Practice (GLP)
    • China GB 2763-2021 for pesticide residue standards
    • Regulation EC No. 1107/2009 concerning the placing of plant protection products on the market

    Typical usage ratio

    • 5–20% w/w in intermediate coupling reactions; adjusted to minimize by-product formation and meet downstream conversion targets

    Downstream process integration

    • Added during condensation or halogenation stages, followed by isolation and advanced purification steps forming agrochemical pre-active ingredients

    Final product types

    • Intermediates for fluorinated herbicides
    • Fungicide anilide derivatives
    • Crop protection active ingredient scaffolds
    • Key residues for registration dossiers

    3. Dye and Pigment Intermediate Manufacturing

    Advanced pigment manufacturers utilize this compound in the precision synthesis of azo and disperse dyes. The nitro and fluoro substitutions impart brightness and specific fastness properties ideal for high-performance textile applications. Synthesizers use this material in diazotization reactions, where meticulous temperature and pH control are vital to achieve target chromophore strength and shade purity. Batch consistency and spectral uniformity depend on accurate input ratios of this key raw material in the dye backbone assembly.

    Industry compliance standards

    • Oeko-Tex Standard 100 (textile chemical safety)
    • REACH Annex XVII (restricted azo dyes)
    • ZDHC Manufacturing Restricted Substances List
    • ISO 9001:2015 (process quality management)

    Typical usage ratio

    • 12–25% relative to total aromatic amine input; engineers adjust for desired color depth and light fastness

    Downstream process integration

    • Supplied to diazotization reactors, followed by coupling to activated aromatic systems, crystallization, and spray-drying for dispersal pigments or powder dyes

    Final product types

    • Disperse dyes for polyester textiles
    • Azo pigment intermediates
    • High-fastness textile dyes
    • Custom colorants for industrial coatings

    4. Development of Specialty Fine Chemicals (Electronic and Imaging Applications)

    Specialty fine chemical companies use this raw material to produce intermediates for electronic chemical formulations, such as light-sensitive compounds in photoresist materials for semiconductor manufacturing and advanced imaging agents. Its electron-withdrawing nitro and fluoro groups enable unique reactivity profiles required for the synthesis of high-purity materials, including functionalized anilides and nitroarene derivatives. Process engineers manage controlled anhydrous conditions and trace metal analysis to ensure batch consistency aligned with stringent electronic and imaging sector needs.

    Industry compliance standards

    • SEMI Standards for electronic materials
    • ISO 14644 (Cleanrooms and associated controlled environments)
    • JEITA Guideline for raw materials in electronic components
    • Internal customer-specific purity and traceability specifications

    Typical usage ratio

    • 5–18% input mass in functional group modifications; ratio set based on reactivity profile, target impurity levels, and downstream integration

    Downstream process integration

    • Introduced at key condensation or substitution process steps in photochemical material production; includes precision distillation and finishing for high-purity output

    Final product types

    • Photosensitive intermediates for etching resists
    • Electronic grade nitroarene derivatives
    • Specialty imaging agents
    • Halogenated intermediates for LCD color filters
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