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4,5-Dichlorophthalic Acid

    • Product Name 4,5-Dichlorophthalic Acid
    • Alias 4,5-Dichlorophthalic acid
    • Einecs 221-787-8
    • 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

    673439

    Chemical Name 4,5-Dichlorophthalic Acid
    Cas Number 6315-42-4
    Molecular Formula C8H4Cl2O4
    Molar Mass 235.02 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 265-270 °C
    Solubility In Water Slightly soluble
    Density 1.7 g/cm³ (approximate)
    Boiling Point Decomposes before boiling
    Purity Typically >98%
    Pka 2.5, 3.7 (approximate, carboxylic acids)
    Synonyms 4,5-Dichloro-1,2-benzenedicarboxylic acid

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

    Packing & Storage
    Packing 250g of 4,5-Dichlorophthalic Acid is packaged in a sealed, amber glass bottle with a tamper-evident screw cap and hazard label.
    Shipping 4,5-Dichlorophthalic Acid should be shipped in tightly sealed containers, clearly labeled, and protected from moisture. Transport in compliance with relevant chemical regulations, avoiding extremes of temperature and incompatible substances. Ensure packaging prevents leaks and damage. Suitable hazard labeling and documentation must accompany all shipments according to local, national, and international transport guidelines.
    Storage 4,5-Dichlorophthalic acid should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizing agents. Keep in a cool, dry, and well-ventilated area, protected from direct sunlight. Store at room temperature and avoid elevated heat. Ensure proper labelling and keep out of reach of untrained personnel. Follow local regulations for chemical storage.
    Application of 4,5-Dichlorophthalic Acid

    Applications of 4,5-Dichlorophthalic Acid in Industrial Manufacturing

    We manufacture 4,5-Dichlorophthalic Acid specifically for critical process applications where its unique chemical profile supports demanding downstream synthesis routes. Below are scenario-specific use cases reflecting current, compliant, and technically differentiated functions this material provides to global manufacturing partners.

    1. High-Performance Polyimide Resin Synthesis

    Leading electronic and aerospace firms use 4,5-Dichlorophthalic Acid as a key dianhydride precursor when synthesizing high thermo-oxidative stable polyimide resins for films, coatings, and insulating materials. The product's controlled halogenation improves resistance to aggressive environments, and strict raw material traceability aligns resin batches with advanced qualification standards.

    Industry compliance standards

    • IPC-4101 for flexible and rigid printed wiring board materials
    • UL 94 flammability for insulation films
    • RoHS Directive 2011/65/EU and its amendments on hazardous substances
    • AS9100 for aerospace material supply chain quality

    Typical usage ratio

    • Imide precursor matrices: 15–25% by weight relative to total dianhydride input, adjustable based on end-use thermal stability demands

    Downstream process integration

    • Reacts with diamines or diisocyanates in polyimide resin condensation, typically charged in nitrile or aprotic polar solvents during main batch compounding

    Final product types

    • Flexible polyimide films for flexible printed circuits
    • Molded polyimide insulators and connectors (electrical/electronics)
    • High-temperature-resistant polyimide adhesives
    • Aerospace wire and cable wraps

    2. Intermediate for Specialty Agrochemical Synthesis

    Producers of selective herbicides and fungicides use this acid as a chlorinated aromatic core in synthesizing specific phthalimide-based actives with targeted environmental dissipation rates. The compound’s reactivity enables manufacturers to build downstream molecular frameworks under controlled conditions, thereby streamlining registration compliance for active ingredients.

    Industry compliance standards

    • FAO/WHO JMPR specifications for pesticide purity
    • REACH Annex II (EU) for chemical intermediates
    • ISO 9001-controlled synthesis for agrochemical intermediates
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • 5–15% of total batch input in synthesis of final active, composition adjusted per target molecule structure and patent restrictions

    Downstream process integration

    • Charged during early condensation or cyclization step in active ingredient synthesis, often after in situ conversion to anhydride or phthalimide forms

    Final product types

    • Phthalimide-class herbicide technical concentrates
    • Systemic fungicide active ingredients for crops
    • Registration-grade agrochemical intermediates
    • Precursors for agrochemical formulation blends

    3. Monomer and Intermediate in Liquid Crystal Polymer (LCP) Manufacturing

    LCP manufacturers choose 4,5-Dichlorophthalic Acid to introduce halogenated aromatic segments, creating resins with higher flame retardancy and dimensional stability for telecom, automotive, and E&E connector applications. Careful documentation of the raw material entry enables customers to validate flame resistance and low warpage levels critical for precision components.

    Industry compliance standards

    • IEC 61249-2 for materials used in liquid crystal polymers
    • UL 94 V-0/V-1 for flame retardant ratings
    • ISO 1874-1 for LCP grades
    • EN 50581 for E&E restriction of hazardous substances

    Typical usage ratio

    • 10–18% as a co-monomer, dependent on desired glass transition temperature and halogen load for flame resistance

    Downstream process integration

    • Co-polymerizes with other aromatic acids and glycols in transesterification polycondensation reactors; charged as a crystalline solid during controlled feed steps

    Final product types

    • Precision LCP connectors for mobile devices
    • Surface mount E&E components
    • Heat-resistant telecommunication device housings
    • Automotive electrical module casings

    4. Precursor for Dyes and Pigments Based on Halogenated Phthalic Structures

    Leading colorant producers integrate 4,5-dichlorinated phthalic backbones when manufacturing high-performance dyes and pigments for plastics, coatings, and inks, taking advantage of the atypical di-halogen substitution to tailor chroma, fastness, and dispersion. The well-defined impurity profile ensures customers gain reproducible color strength batch-to-batch for demanding industrial applications.

    Industry compliance standards

    • EU Regulation (EC) No. 1272/2008 (CLP) for classification and labelling
    • EN 71-3 for colorant migration in toys
    • ISO 787 for general methods in pigment testing
    • AP89/1 requirements for organic colorants in food packaging applications

    Typical usage ratio

    • Varies 3–20% in colorant precursor formulas; refined based on targeted C.I. numbers and downstream dispersion needs

    Downstream process integration

    • Derivatized in halogenated phthalic pigment synthesis, often starting as an acid or converted to a phthalimide before coupling with chromophores

    Final product types

    • High-fastness organic pigments for engineering plastics
    • Solvent-based and water-based colorants for coatings
    • Specialty dyes for industrial printing inks
    • Non-migratory color concentrates for polyolefins

    5. Curing Agent Component for Epoxy Resin Formulations

    Composite and advanced materials manufacturers incorporate 4,5-Dichlorophthalic Acid as a modifier in epoxy curing agents, leveraging its dichloro functionality to produce thermosets with tailored chemical and hydrolytic resistance. The material’s performance consistency supports strict batch release and ensures reliable mechanical properties post cure.

    Industry compliance standards

    • EN 13986 for engineered wood panel adhesives
    • ASTM D3967 for resin flexural properties
    • GB/T 20172-2006 for chemical-resistant coatings
    • ISO 9001:2015 process traceability standards

    Typical usage ratio

    • 1–10% as a reactive diluent or hardener component, optimized in pilot-scale tests for target crosslink density and pot life

    Downstream process integration

    • Blended into epoxy resin base or curing agent during compounding prior to final application, typically under controlled temperature and mixing profiles

    Final product types

    • Chemical-resistant epoxy coatings for tanks and process equipment
    • Epoxy-based structural adhesives
    • Composite matrix materials for construction and automotive
    • Waterproofing formulations for civil engineering
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