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4'-Chloro-2'-Fluoroacetanilide

    • Product Name 4'-Chloro-2'-Fluoroacetanilide
    • Alias 4'-Chloro-2'-fluoroacetanilide
    • Einecs 629-736-3
    • 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

    653323

    Product Name 4'-Chloro-2'-Fluoroacetanilide
    Molecular Formula C8H7ClFNO
    Cas Number 86404-64-8
    Appearance White to off-white solid
    Melting Point 108-112°C
    Purity Typically >98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles CC(=O)NC1=CC(=C(C=C1)Cl)F
    Storage Conditions Store at 2-8°C, keep container tightly closed
    Synonyms N-(4-chloro-2-fluorophenyl)acetamide
    Hazard Statements Irritant to skin, eyes, and respiratory system

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

    Packing & Storage
    Packing A sealed amber glass bottle containing 100 grams of 4'-Chloro-2'-Fluoroacetanilide, labeled with chemical details and safety information.
    Shipping The shipping of 4'-Chloro-2'-Fluoroacetanilide complies with standard chemical transport regulations. The substance is securely packaged in sealed containers, clearly labeled, and protected from moisture, heat, and direct sunlight. Appropriate documentation and safety data sheets accompany the shipment to ensure safe handling and regulatory compliance during transit.
    Storage 4'-Chloro-2'-Fluoroacetanilide should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the chemical away from incompatible substances such as strong oxidizing agents. Ensure proper labeling, and avoid exposure to moisture. Use secondary containment and restrict access to trained personnel only.
    Application of 4'-Chloro-2'-Fluoroacetanilide

    Applications of 4'-Chloro-2'-Fluoroacetanilide in Industrial Manufacturing

    As an industrial chemical producer with years of experience in aromatic intermediates, we supply 4'-Chloro-2'-Fluoroacetanilide to specialized sectors strictly based on verified downstream applications. Its selectivity, halogen substitution, and chemical stability allow integration into several advanced synthesis routes. Below are the principal industrial manufacturing scenarios where this compound demonstrates clear performance and regulatory fit.

    1. Synthesis of Agrochemical Active Ingredients

    Key agrochemical formulators incorporate 4'-Chloro-2'-Fluoroacetanilide as an intermediate in the production of specific phenoxyalkanoic acid herbicides and substituted aniline-based crop protection agents. Its precise halogen pattern enables controlled aromatic substitution, supporting the synthesis of molecules for high-selectivity weed management. Production plants employ this compound during the pre-coupling or amidation stages to yield actives with integrity and compliance for agricultural standards.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • U.S. EPA Pesticide Registration Requirements (40 CFR Part 158)
    • REACH Regulation (EC) No 1907/2006
    • China GB 2763 Maximum Residue Limit Standards

    Typical usage ratio

    • Intermediate charge typically 0.14–0.23 molar equivalents per target molecule; actual feed rate optimized to minimize byproducts based on reaction scale, temperature, and conversion yield.

    Downstream process integration

    • Batch-fed in aromatic amination or amidation reactors after base activation.
    • Followed by workup and purification prior to coupling with chlorinated acid components in main active synthesis.

    Final product types

    • Selective herbicide actives (e.g., fluorinated anilide derivatives)
    • Plant growth regulator intermediates
    • Synthons for fungicidal substances

    2. Pharmaceutical Intermediate for Antipyretic and Analgesic Agents

    In API manufacturing, pharmaceutical companies utilize 4'-Chloro-2'-Fluoroacetanilide as a key stage intermediate in the preparation of next-generation N-acylarylamine analgesics. Its structure enables targeted substitution to build up paracetamol-like molecules with improved halogen-modified pharmacological profiles. Manufacturers value its reproducible reactivity and high purity output critical for successive acetylation and dehalogenation steps under GMP-controlled environments.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for API)
    • USP/EP/BP Monograph Specifications
    • Chinese Pharmacopoeia ChP (2020 Edition)
    • U.S. FDA DMF Requirements

    Typical usage ratio

    • 1.00 equivalent relative to coupling partner for intermediate formation; practical batch sizes vary from 50 g/L to 120 g/L depending on solvent and scale-up batch optimization.

    Downstream process integration

    • Introduced in acylation or condensation reactors following solvent exchange and base treatment steps.
    • Subsequent purification through crystallization and controlled filtration.

    Final product types

    • Halogen-modified acetaminophen intermediates
    • Advanced aniline-derived antipyretic agents
    • Pharmaceutical-grade starting materials for over-the-counter medications

    3. Dye Intermediate for Specialty Pigments

    The specialty dye sector employs 4'-Chloro-2'-Fluoroacetanilide as a diazo or coupling partner during the synthesis of functionalized monoazo and anthraquinone pigments. Its dual halogenation supports specific chromophore tuning and fastness performance demanded in automotive coatings, industrial plastics coloration, and high-performance printing inks. Downstream pigment manufacturers optimize its use for batch-to-batch chromatic control and improved dispersibility profiles.

    Industry compliance standards

    • EN 71-3 (Safety of Toys – Migration of Certain Elements)
    • ISO 9001:2015 (Quality Management Systems for Pigments)
    • OEKO-TEX Standard 100 for Colorants
    • China GB 9685—Standard for the Use of Additives in Food Contact Materials

    Typical usage ratio

    • Used at 0.10–0.16 mole per mole of coupling partner for monoazo pigment reactions, depending on desired hue intensity, pigment particle design, and end-use requirements.

    Downstream process integration

    • Charged to diazotization reaction vessel after buffered acidification.
    • Processed via slurry workup, filtration, and controlled drying to achieve optimal dispersity.

    Final product types

    • Disperse and solvent-stable pigments for coatings and plastics
    • High-performance printing dyes (e.g. for textiles and packaging)
    • Synthetic colorants for industrial inkjet applications

    4. Intermediate for Fluorinated Fine Chemicals

    Chemical manufacturers leverage 4'-Chloro-2'-Fluoroacetanilide as a precursor for synthesizing fluorine-containing aromatic building blocks. Owing to the robust halogen placement, it aids in the stepwise generation of advanced intermediates tailored for electronic, polymer, and material science applications. Process teams implement it for nucleophilic aromatic substitution and controlled hydrolysis, facilitating the construction of custom molecules for modern functional materials sectors.

    Industry compliance standards

    • ISO 14001:2015 (Environmental Management in Chemical Synthesis)
    • EU REACH Registration for Industrial Intermediates
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • TSCA Inventory Listing (U.S. EPA)

    Typical usage ratio

    • Reacts at 0.98–1.15 equivalents versus nucleophilic aromatic reactant; charge factors refined for maximum recovery yield and downstream purity in small to large reactors.

    Downstream process integration

    • Introduced during halogen-exchange or amide hydrolysis stages.
    • Subsequently processed by controlled crystallization, solvent washing, and drying.

    Final product types

    • Fluorinated aromatic monomers for specialty polymers
    • Electronic-grade intermediates for display and sensor applications
    • Reaction blocks for advanced material R&D
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