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2,4-Dichloro-5-Fluorobenzoic Acid

    • Product Name 2,4-Dichloro-5-Fluorobenzoic Acid
    • Alias 2,4-DCFA
    • Einecs 'EINECS 260-951-7'
    • 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

    379307

    Chemical Name 2,4-Dichloro-5-Fluorobenzoic Acid
    Molecular Formula C7H3Cl2FO2
    Molecular Weight 225.01 g/mol
    Cas Number 393-53-1
    Appearance White to off-white solid
    Melting Point 182-184°C
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Storage Temperature Room temperature, dry conditions
    Smiles C1=C(C(=CC(=C1Cl)F)Cl)C(=O)O
    Inchi InChI=1S/C7H3Cl2FO2/c8-4-1-3(7(11)12)2-5(9)6(4)10/h1-2H,(H,11,12)
    Synonyms 2,4-Dichloro-5-fluorobenzoic acid

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

    Packing & Storage
    Packing White, tightly sealed HDPE bottle containing 100 grams of 2,4-Dichloro-5-Fluorobenzoic Acid, labeled with hazard symbols and lot details.
    Shipping **Shipping Description:** 2,4-Dichloro-5-Fluorobenzoic Acid is shipped in sealed, chemically resistant containers to prevent contamination and moisture exposure. Packages comply with relevant regulations for transport of chemical substances. The chemical is clearly labeled, with safety data sheets provided. Store and ship at ambient temperature, away from incompatible materials and direct sunlight.
    Storage 2,4-Dichloro-5-Fluorobenzoic Acid should be stored in a tightly closed container, in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and bases. Protect from moisture and direct sunlight. Properly label the container and keep it out of reach of unauthorized personnel. Use secondary containment to prevent accidental spills.
    Application of 2,4-Dichloro-5-Fluorobenzoic Acid

    Applications of 2,4-Dichloro-5-Fluorobenzoic Acid in Industrial Manufacturing

    We specialize in producing 2,4-Dichloro-5-Fluorobenzoic Acid for integration in advanced industrial sectors. Our product supports key manufacturing operations where specific molecular frameworks and reliable chemical consistency are essential for high-performance downstream synthesis.

    1. Agrochemical Intermediate for Herbicide Synthesis

    This material serves as a specialized intermediate in the multi-step synthesis of selective herbicide actives such as fluoro-chlorinated phenoxy compounds. Its high purity and reliable halogen position enable efficient downstream coupling reactions in plant protection formulation plants. Companies incorporate it during the main condensation step, maintaining precise temperature and solvent control to yield target actives while reducing unwanted byproducts. Manufacturers appreciate consistent lot quality, as deviations influence conversion rates and downstream isolation efficiency.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for chemical processing
    • GB 2069-2008 Agricultural Chemical Manufacturing Standards (China)
    • REACH (EC No 1907/2006) for raw materials entering the EU herbicide market
    • EU Directive 91/414/EEC regarding active plant protection substances

    Typical usage ratio

    • 10–25% of total weight in active ingredient core synthesis; varies with molecular design and crop selectivity targets

    Downstream process integration

    • Entry point: Direct coupling after halogen exchange or esterification step
    • Pre-purified to avoid impurity transfer into downstream hydrogenation operations
    • Soluble in polar aprotic solvents used during oxidative coupling
    • Waste and mother liquor recycled for solvent recovery

    Final product types

    • Selective post-emergence herbicides for cereal and maize fields
    • Sulfonylurea derivatives for grass weed control
    • Fluorinated benzoate-based herbicide actives
    • Bulk technical herbicidal actives for formulation

    2. Pharmaceutical Intermediate for Fluorinated API Synthesis

    Pharmaceutical producers deploy this compound as a core intermediate in the synthesis route leading to specialty fluorinated drug substances. Its fluorine and halide pattern supports efficient building-block construction for anti-inflammatory and anti-infective actives. The material enables direct amidation or halogen-metal exchange reactions, which are tightly controlled in GMP-compliant facilities. Our strict in-process QC assures medical-grade consistency, minimizing risk of batch failure in high-value API production lines.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211: US FDA cGMP for finished pharmaceuticals
    • EU-GMP Part II for API intermediate supply
    • USP/NF monograph alignment for intermediate purity

    Typical usage ratio

    • Ranges from 5–15% in major API synthesis processes; determined via route optimization and target dosage form

    Downstream process integration

    • Added post-halogenation for active moiety assembly
    • Dried and micronized for efficient scale-up in automated lines
    • QC testing batchwise before moving to catalytic coupling or amidation step
    • Integrated digital traceability from incoming QA sampling to release of finished API

    Final product types

    • Fluorinated anti-inflammatory oral drug substances
    • Halogenated benzamide-based antibiotics
    • Key intermediates in anti-infective and anti-cancer APIs
    • Contrast agent intermediates for diagnostic imaging

    3. Advanced Dye and Pigment Precursor

    Major dye and pigment manufacturing utilizes the compound as a high-purity source of halogenated benzoic acid for specialty pigment molecule assembly. Its chemical structure supports selective introduction of fluorine and chlorine functionalities necessary for performance textile dyes. Producers demand accurate control of substitution patterns, which directly affect lightfastness and hue stabilization. This raw material is integrated in the diazotization and coupling phase, helping dye manufacturers meet increasingly demanding performance and regulatory targets in textile and plastics markets.

    Industry compliance standards

    • OEKO-TEX STANDARD 100 for textile safety
    • EN 71-3:2019 (Toy Safety, migration of certain elements – applicable to colored plastic parts)
    • ISO 18451-1:2019 for pigment classification and definitions
    • REACH Annex XVII for restriction of hazardous substances in dyes

    Typical usage ratio

    • 8–22% as a core aromatic base in pigment and specialty dye synthesis; dosage determined by chromophore design and fastness requirements

    Downstream process integration

    • Enters the diazo coupling stage after halogen introduction
    • Dissolved in organic solvents alongside auxiliary acids for enhanced molecular dispersion
    • Purification via recrystallization to secure consistent color grade
    • Effluent managed according to EU/PRC environmental discharge requirements

    Final product types

    • Fluorochloro textile reactive dyes
    • Specialty pigments for automotive coatings
    • High-performance colorants for polymer compounding
    • Water-based ink dispersions for digital textile printing

    4. Electronic Chemicals: Liquid Crystal Intermediates

    Producers of advanced liquid crystal compounds for display technologies use this material as a critical halogenated benzoic acid derivative. Its precise substitution supports assembly of fluorinated biphenyl and phenylbenzoate intermediates—required in TFT-LCD and OLED panel production. Manufacturers integrate this fine chemical in controlled environments, ensuring batch traceability and ultra-low metal contamination. This step greatly influences the electro-optical properties of the final display via the purity and composition of the precursor input.

    Industry compliance standards

    • IEC 61249-2-21: 2003 for halogen-free requirements in electronics
    • JEITA ET-7304 (for purity and contamination limits in display precursor chemicals)
    • ISO 9001 for electronic chemical production
    • RoHS 2011/65/EU for restricted hazardous substances in electronics

    Typical usage ratio

    • 1.5–7% relative to total precursor batch mass, with adjustment according to target liquid crystal phase and dielectric constants

    Downstream process integration

    • Added post-purification in ultra-clean reactors for intermediate phenyl assembly
    • Filtered below 1 ppm metal content before condensation coupling
    • Consistency in melting point and Halide content monitored at each batch stage
    • Direct transfer to LC assembly zone after in-house QC pass/fail testing

    Final product types

    • Biphenyl-based liquid crystal intermediates
    • Phenylbenzoate derivatives for high-k dielectric LCD panels
    • OLED precursor blends
    • Electronic grade intermediates for display module manufacturers

    5. Specialty Polymer Additive Precursor

    Processors in specialty polymer sector employ this halogenated compound as a stable aromatic acid precursor for constructing flame-retardant or high-performance engineering plastics. Its precise incorporation during the monomer or co-reactant blending directly contributes to controlled fluorine and chlorine content within the final polymer matrix. Reliable material delivery and consistent melting profile improve scale-up and lot-to-lot reproducibility in bulk extrusion or copolymerization lines.

    Industry compliance standards

    • UL 94 (Standard for safety of flammability of plastic materials)
    • EN ISO 1043 (Polymer identification and marking standards)
    • GB 4806.6-2016 (package material requirements in China—for food contact plastics where applicable)
    • EU Regulation (EC) No 10/2011 (food-contact plastic additive migration limits—when used in relevant polymers)

    Typical usage ratio

    • 0.3–3% based on polymer batch weight; dosage adjusted for target flammability, flexibility, or color stability properties

    Downstream process integration

    • Introduced at the resin pre-blending stage for copolymer or polymer additive batching
    • Fully dissolved in plasticizer or solvent matrix before entering reactor
    • Monitored for absorption rate and reactivity via inline FT-NIR or GC analysis
    • Co-extruded with base resin to achieve desired dispersion and functionality

    Final product types

    • Flame-retardant engineering plastics
    • Polyolefin or PVC specialty compounds
    • High-temperature stable polymer films
    • Functional food packaging materials (where authorized)
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