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Alpha,Alpha'-Dichloro-P-Xylene

    • Product Name Alpha,Alpha'-Dichloro-P-Xylene
    • Alias DCDPX
    • Einecs 204-337-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    927699

    Chemicalname Alpha,Alpha'-Dichloro-P-Xylene
    Casnumber 623-23-8
    Molecularformula C8H8Cl2
    Molecularweight 175.06 g/mol
    Appearance White to off-white crystalline solid
    Meltingpoint 92-95 °C
    Boilingpoint 265 °C
    Density 1.27 g/cm3
    Solubilityinwater Insoluble
    Flashpoint 120 °C
    Refractiveindex 1.577
    Synonyms 1,4-Bis(chloromethyl)benzene

    As an accredited Alpha,Alpha'-Dichloro-P-Xylene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Alpha,Alpha'-Dichloro-P-Xylene is packaged in a 100g amber glass bottle with a tightly sealed cap and hazard labeling.
    Shipping Alpha,Alpha'-Dichloro-P-Xylene should be shipped in tightly sealed containers, properly labeled as hazardous material. It must be protected from heat, moisture, and incompatible substances. Shipping should comply with local, national, and international regulations for hazardous chemicals, including appropriate UN number, packing group, and safety documentation for transport by road, air, or sea.
    Storage Alpha,Alpha'-Dichloro-P-Xylene should be stored in a tightly closed container in a cool, dry, well-ventilated area away from heat, sparks, and open flames. Keep it away from incompatible substances such as oxidizing agents. Store it in a designated chemical storage cabinet and avoid direct sunlight. Ensure appropriate labeling and restrict access to authorized personnel only.
    Application of Alpha,Alpha'-Dichloro-P-Xylene

    Applications of Alpha,Alpha'-Dichloro-P-Xylene in Industrial Manufacturing

    Alpha,Alpha'-Dichloro-P-Xylene serves as a critical intermediate across several tightly defined chemical manufacturing sectors. Our direct production experience ensures consistent quality and supply to manufacturers who demand precise, compliant integration into downstream processes. Below, we outline the primary real-world application fields, highlighting compliance requirements, dosage guidelines, points of addition within the process, and the range of downstream products produced.

    1. Intermediate for Agrochemical Active Ingredient Synthesis

    Many leading agrochemical producers use this compound to synthesize key intermediates in herbicide and fungicide manufacturing. It enters multi-stage chlorination and coupling reactions, supporting the development of substituted aromatic cores found in modern crop protection actives. Manufacturers closely audit the traceability and purity of all intermediates to satisfy sector compliance and registration with regulatory authorities.

    Industry compliance standards

    • Regulation (EC) No 1907/2006 (REACH) – substance registration and safety data requirements
    • ISO 9001:2015 Quality Management Systems (for chemical production)
    • European Plant Protection Product Regulation (EU) 1107/2009
    • US EPA Pesticide Registration Requirements (40 CFR Parts 150–189)

    Typical usage ratio

    • 10–25% by mass as an aromatic halide precursor in targeted synthesis pathways, adjusted based on target molecule and downstream process yield studies

    Downstream process integration

    • Charged directly into halogenation or nucleophilic substitution reactors following upstream aromatic methylation stages; monitored for residual chloride and byproduct content before further coupling reactions

    Final product types

    • Precursor compounds for triazole and pyridine-based herbicides
    • Intermediate building blocks for strobilurin and azole fungicides
    • Raw material for new-generation selective weed control products

    2. Monomer Precursor in High-Performance Polymer Production

    The compound’s di-chlorinated aromatic structure is essential in the synthesis of specialty monomers for engineering plastics designed for electrical insulation and flame retardancy. It enters polycondensation reactions where its chemical reactivity determines final polymer chain architecture and performance in demanding industrial settings such as electronics and automotive.

    Industry compliance standards

    • UL 94 Flammability Standard for Plastic Materials
    • IEC 60695 Fire Hazard Testing in Electronics and Electrical Devices
    • ISO 14001:2015 Environmental Management for polymer manufacturing
    • RoHS Directive 2011/65/EU (for electronics applications)

    Typical usage ratio

    • 5–18% by mass as a monomer or comonomer component, selected based on the desired degree of halogenation and molecular weight control during the polycondensation process

    Downstream process integration

    • Added into polycondensation reactors with other di-acid chlorides or diamines; purity and controlled dosing are crucial for achieving target molecular mass control and minimizing oligomer formation

    Final product types

    • Polyarylate and polyester resins used in circuit board laminates
    • Thermoplastic components for industrial connectors and insulation tapes
    • Injection-molded flame-retardant housings for electrical equipment

    3. API Intermediate for Pharmaceutical Synthesis

    In pharmaceutical manufacturing, producers employ this chemical primarily as a synthetic intermediate for producing select active pharmaceutical ingredients through aromatic substitution processes. Stringent regulatory oversight applies throughout both synthesis and purification stages to guarantee end-product safety and performance in regulated markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP)
    • European Pharmacopoeia (EP)
    • WHO Good Manufacturing Practices for Pharmaceutical Products

    Typical usage ratio

    • 3–9% by mass in early stage API intermediate synthesis, adjusted according to substitution reaction pathway and purification efficiency requirements

    Downstream process integration

    • Introduced in aromatic nucleophilic substitution steps; handled in closed system reactors to control solvent exposure and limit cross-contamination, followed by fractional crystallization or chromatographic purification

    Final product types

    • Nitro-substituted pharmaceutical intermediates
    • Intermediates for nervous system APIs
    • Synthons for advanced antimicrobial and cardiovascular drug substances

    4. Manufacturing of Liquid Crystal Display (LCD) Materials

    Manufacturers of specialty chemicals for the electronics sector utilize this compound in the synthesis of core aromatic mesogens for LCD industry applications. Material traceability, batch reproducibility, and the ability to meet electronics-grade impurity specifications represent key process elements in this sector.

    Industry compliance standards

    • IEC 61249-2-21: Halogenated flame retardants for base material in printed wiring boards
    • JIS C 5018 Standards for Liquid Crystal Quality
    • ISO 14644-1 Cleanroom Standards for electronics processing
    • IPC-4101C Standards for Laminates and Prepregs

    Typical usage ratio

    • 7–14% by mass, dependent on process scaling and the number of mesogenic units incorporated per molecule for desired optical properties

    Downstream process integration

    • Fed into etherification or esterification reactions within lined batch reactors; post-reaction purification via distillation and recrystallization under cleanroom conditions ensures minimization of metal and halogen contaminant carryover

    Final product types

    • Liquid crystal mesogen compounds for LCD panels
    • Precursors for high-contrast TFT display materials
    • Specialty alignment layers for flexible electronic screens

    5. Synthesis of Specialty Dyes and Pigments

    Producers in the dye and pigment industry employ this raw material to obtain halogenated aromatic structures that provide desirable fastness properties and coloration effects for industrial textile and plastics coloration. A key attribute is the ability of the chlorinated moieties to enhance product light stability, color purity, and wash resistance, essential for high-demand end-uses.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile additives
    • EN 71-3 Safety of Toys (Migration of Certain Elements)
    • ISO 9001:2015 Quality certification for dye and pigment production
    • REACH Annex XVII for restrictions on hazardous substances in colored products

    Typical usage ratio

    • 6–15% by mass as an aromatic halogenated precursor, controlled depending on the targeted chromophore structure and application substrate

    Downstream process integration

    • Incoporated in aromatic condensation or coupling reactions; loaded via separate feed to minimize cross-reactivity and maintain high selectivity for mono- or di-substituted pigment frameworks

    Final product types

    • Textile dyes with improved chlorine fastness
    • Industrial and automotive pigment dispersions
    • Color concentrates for high-density polyethylene and PVC
    Free Quote

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