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Alpha,Alpha,Alpha,Alpha',Alpha'-Pentachloro-2-Xylene

    • Product Name Alpha,Alpha,Alpha,Alpha',Alpha'-Pentachloro-2-Xylene
    • Alias Pentasol
    • Einecs 215-742-3
    • 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
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    Specifications

    HS Code

    676498

    Chemicalname Alpha,Alpha,Alpha,Alpha',Alpha'-Pentachloro-2-Xylene
    Molecularformula C8H3Cl5
    Molecularweight 296.32 g/mol
    Casnumber 2234-13-1
    Appearance White to pale yellow solid
    Meltingpoint 142-144 °C
    Density 1.7 g/cm3 (approximate)
    Solubilityinwater Insoluble
    Chemicalstructure Benzene ring with two methyl groups each substituted with five chlorines
    Synonyms 2-Xylene pentachloro derivative
    Pubchemcid 22384
    Stability Stable under recommended storage conditions

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

    Packing & Storage
    Packing The packaging consists of a 100g amber glass bottle with a secure screw cap, featuring hazard labels and clear chemical identification.
    Shipping Alpha,Alpha,Alpha,Alpha',Alpha'-Pentachloro-2-Xylene should be shipped in accordance with hazardous materials regulations. Use sealed, chemically resistant containers placed in robust, cushioned packaging. Clearly label the package with appropriate hazard and handling symbols. Transport via certified carriers, ensuring compliance with local, national, and international dangerous goods transport standards (such as DOT and IATA).
    Storage **Storage Description for Alpha,Alpha,Alpha,Alpha',Alpha'-Pentachloro-2-Xylene:** Store in a tightly closed container in a cool, dry, well-ventilated area, away from incompatible substances such as oxidizing agents. Protect from direct sunlight, moisture, and sources of ignition. Use secondary containment to prevent leaks. Label containers appropriately and keep them away from heat or flame. Ensure access to safety equipment like eye wash stations and showers nearby.
    Application of Alpha,Alpha,Alpha,Alpha',Alpha'-Pentachloro-2-Xylene

    Applications of Alpha,Alpha,Alpha,Alpha',Alpha'-Pentachloro-2-Xylene in Industrial Manufacturing

    As a specialized producer, we deliver Alpha,Alpha,Alpha,Alpha',Alpha'-Pentachloro-2-Xylene with batch consistency and precise technical parameters to support critical downstream chemical syntheses. The following sections outline distinct industrial segments where this chlorinated xylene derivative finds confirmed application, detailing the exacting requirements, formulation ratios, integration stages, and characteristic end uses demanded by each sector.

    1. Intermediate for Pharmaceutical Agrochemical Synthesis

    Industry formulators rely on this pentachloro-2-xylene as a halogenated aromatic intermediate to build complex molecules, particularly for select agrochemical and pharmaceutical actives. The compound's multiple chlorine atoms facilitate efficient nucleophilic aromatic substitution and metalation steps, giving reproducible yields in multi-stage synthesis under controlled conditions. Our material delivers lot-to-lot traceability for process validation, critical to API and crop protection actives manufacturing.

    Industry compliance standards

    • GMP (Good Manufacturing Practice) for pharmaceutical intermediates (ICH Q7/WHO GMP)
    • EPA TSCA (Toxic Substances Control Act) for chemical intermediates in the US
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) compliance in the EU
    • Chemical Synthesis Quality Systems (ISO 9001:2015)

    Typical usage ratio

    • Range: 0.5–2.5 molar equivalents per batch, adjusted according to downstream substitution targets and yield optimization
    • Mole ratio determined by target molecule structure and process stoichiometry

    Downstream process integration

    • Material charged to halogen-metal exchange or SNAr (nucleophilic aromatic substitution) reactors as core aromatic substrate
    • Added in inert atmosphere to minimize side reactions before sequential condensation or further transformation

    Final product types

    • Herbicide and fungicide technical-grade active ingredients
    • Building-block intermediates for nonsteroidal anti-inflammatory drugs (NSAIDs)
    • Other specialty halogenated pharmaceuticals

    2. Dye and Pigment Precursor Manufacturing

    Dye and pigment plants employ this pentachlorinated compound as a precursor for specific chlorinated xylene dyes and vat colorants. Its poly-chlorine structure supports targeted nitration and sulfonation, yielding intensely colored materials with improved weather and chemical resistance. Standardized feedstock traceability and impurity profile are essential to avoid color defects and meet sectoral finished colorant purity levels.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile and dye applications
    • EN 71-3 for pigments used in toys and textiles (European safety standard)
    • Tested to ISO 787/1 for pigment chemical requirements
    • RoHS restrictions for heavy metals and regulated substances

    Typical usage ratio

    • 0.8–1.4 moles per colorant batch, modulated to deliver target chromophore reactant excess and optimize reaction conversions
    • Ratio varies with desired color depth and chlorination level required in the final dye molecule

    Downstream process integration

    • Fed to dye reactors as the principal aromatic substrate before nitration or sulfonation reactions
    • Processed under strict temperature control to preserve isomeric purity

    Final product types

    • Chlorinated vat dyes for synthetic fibers
    • Technical colorants for printing inks
    • Pigments used in plastics and automotive finishes

    3. Flame Retardant Additive Synthesis

    Technical composite manufacturers use this chlorinated xylene as a feedstock in closed-system synthesis of organic flame retardants. The compound's high chlorine content ensures the resulting flame retardant intermediates meet stringent thermal stability and migration-resistance thresholds demanded by polymer and circuit board industries. Its consistent composition ensures that subsequent bromination or phosphination chemistries achieve predictable functional group placement.

    Industry compliance standards

    • UL 94 (Underwriters Laboratories) for flame retardancy in plastics and foams
    • IEC 60695 for electrical insulation materials
    • EN 14582 for halogenated compound analysis in flame retardant feedstocks
    • ISO 178 for flexural properties of plastics (finished product characterization)

    Typical usage ratio

    • Applied at 1.2–3.0 wt% in bulk synthesis, with adjustments depending on target halogen content of downstream flame retardant intermediate
    • Optimized in pilot formulation studies for maximum fire-suppression effectiveness

    Downstream process integration

    • Introduced to high-temperature synthesis stage for halogenated flame retardant production
    • Blended with other aromatic halides in multiphasic reactors to build polyhalogenated structures

    Final product types

    • Aromatic brominated and phosphinated flame retardant intermediates
    • Finished halogenated flame retardant additives for polymer compounding
    • Masterbatch concentrates for electrical insulation and circuit board lamination

    4. Specialty Resin and Polymer Modifier Production

    Engineered resin producers incorporate this pentachlorinated aromatic in the synthesis of specialty thermoset and thermoplastic modifiers, where increased fire resistance and dimensional stability are required. By introducing controlled quantities during oligomer synthesis, manufacturers adjust polymer backbone chlorination and achieve regulatory compliant flame rating and mechanical properties, especially for automotive and electronic housings.

    Industry compliance standards

    • ASTM D2863 for oxygen index in plastics
    • UL 746C for polymeric materials used in electrical equipment
    • ISO 11357 for differential scanning calorimetry of polymers
    • RoHS Directive (chemicals in consumer electronics)

    Typical usage ratio

    • 0.2–0.8 wt% in resin modifier syntheses, with content tailored to targeted V-0 or V-1 flammability rating
    • Ratio chosen based on resin matrix and performance profile needed

    Downstream process integration

    • Loaded to prepolymer reactors as a reactive halogenated monomer during resin backbone formation
    • Integrated in continuous or semi-batch process lines

    Final product types

    • Halogenated polyester and vinyl ester resin additives
    • Modified engineering plastics for electrical housings
    • Specialty adhesive polymers with enhanced fire resistance

    5. Chemical Reference Standards and Quality Control

    Accredited analytical laboratories and reference material producers acquire pentachlorinated xylene to serve as a calibration and spiking standard for environmental monitoring, residue analysis, and industrial hygiene programs. Its well-characterized purity, high chemical stability, and unique chromatographic profile provide critical benchmarks for validating halogenated aromatic detection methods in complex environmental matrices.

    Industry compliance standards

    • ISO 17034 for reference material production
    • ISO/IEC 17025 for chemical testing and calibration laboratories
    • EPA Method 8270 GC/MS for semi-volatile organics
    • EN 12673 for chemical concentration measurement standards

    Typical usage ratio

    • 100–500 μg/L spike levels for chromatographic method validation and calibration
    • Adjusted for matrix concentration and detection sensitivity of the assay

    Downstream process integration

    • Diluted and aliquoted into standard reference solutions used during environmental and occupational exposure testing
    • Utilized as an internal standard or matrix spike in GC/MS and HPLC protocols

    Final product types

    • Chemical reference standard solutions
    • Quality control spiking materials for environmental laboratories
    • Certified analytical reference materials for industrial hygiene
    Free Quote

    Competitive Alpha,Alpha,Alpha,Alpha',Alpha'-Pentachloro-2-Xylene prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    Alpha,Alpha,Alpha,Alpha',Alpha'-Pentachloro-2-Xylene: A Chemist’s Take on a Specialized Aromatic Compound

    Introduction: Experience Behind the Molecule

    Chemical manufacturing calls for responsibility, focus, and a clear understanding of the necessary compounds behind modern industry. Alpha,Alpha,Alpha,Alpha',Alpha'-Pentachloro-2-Xylene stands out in our synthesis portfolio as an example of persistent innovation. In our years of working with chlorinated aromatics, very few molecules reveal the unusual utility found here. Preparing this xylene derivative pushes our processes beyond basic halogenation. We see demand for this molecule from sectors that view it not merely as a raw input but as a solution to real-world formulation hurdles.

    Structuring and Purity: Looking Beyond the Standard Xylenes

    A quick look at the molecule’s structure explains its unique character: five chlorine atoms occupy the methyl positions of a xylene core. This gives pentachloro-2-xylene properties rarely seen with simpler aromatic hydrocarbons. Standard ortho-, meta-, and para-xylenes display clear, well-studied reactivity profiles, but none hold the same electron-withdrawing power and density. With chlorines locked onto adjacent carbons and methyl groups, steric hindrance and the compound’s toughness against oxidation increase substantially.

    In our facility, controlling chlorination degree is not left to chance. Sourcing pure feedstock and strict attention to process temperature, feed rate, and catalyst life all matter. We rely on high-performance glass-lined reactors to keep contamination down, since even traces of polyvalent ions or unreacted byproducts will foul downstream yields. Analytical chemists in our team don't just run GC and HPLC as routine—they review chromatograms, verify that no unintended isomers sneak in, and look for unexpected impurity peaks. A batch isn’t accepted for release until these standards are met.

    How Pentachloro-2-Xylene Finds Its Use

    Customers interested in this specialty chemical come from several disciplines. We most often see requests from those involved in synthesizing advanced crop protection agents and related agrochemical intermediates. Its structure accommodates multiple insertion and substitution reactions, enabling design work where stability and functionalization flexibility matter. Because of the molecule’s electron-withdrawing character, attaching functional groups to this ring behaves differently than on lighter xylenes or mono-chlorinated variants. Several notable synthetic routes for herbicide or fungicide actives use pentachloro-2-xylene as a building block.

    Our materials scientists have also supported customers leveraging its thermal stability and chemical resistivity in research. In some polymer or high-end material applications, introducing ring-chlorinated aromatic units improves fire resistance and decreases flammability. Reports from polymer consulting labs have shown surprisingly strong retention of mechanical integrity under elevated temperatures after integrating pentachloro-2-xylene units. Specialty adhesives, certain protective coatings, and sealant formulations—typically those needing long-term durability under harsh chemical exposures—see enhanced stability from this compound’s inclusion, compared to formulations using mono- or trichlorinated xylenes.

    Environmental engineering teams have approached us to discuss the unique sorption and partitioning behavior these hydrocarbons can bring to phase-transfer systems. These applications stem from the molecule’s altered hydrophobic-lipophilic balance, allowing it to modify the interaction of phases in extraction, separation or cleanup scenarios. It doesn’t qualify as a commodity “solvent,” but its selective affinity can create very different outcomes when used in place of simpler aromatics.

    Application Distinctions: Pentachloro Versus Other Xylenes

    Finding out how this pentachloro derivative differs from the commodity xylenes means spending time in both production and application labs. Standard xylenes are industrial workhorses—used in coatings, printing inks, and fuel blending—but exhibit higher volatility and relatively limited reactivity range for modern synthesis needs. Pentachloro-2-xylene offers greater resistance to photo-oxidation and a much lower rate of electrophilic substitution due to the chlorine substitution pattern, which preserves the aromatic ring’s integrity through harsher synthetic and processing steps.

    Trichlorinated or tetrachlorinated xylenes, sometimes favored for less critical uses, afford different balances of cost and chemical durability. In our manufacturing, we have found pentachloro-2-xylene’s five chlorines decisively extend both physical resistance and shelf life. Chemists lean toward this molecule when planning multi-stage reactions where decomposing side products can devastate purity or end-use quality. Also, our observations confirm that the higher substitution discourages biotransformation and breakdown, which some customers prize when seeking long-lived intermediates or actives in agricultural applications.

    Manufacturing Experience: Reliability Comes from Practice

    Continuous manufacturing experience has taught us how even subtle process variations impact end results. The number of ways halogenation can go wrong still catches inexperienced producers by surprise. In our early years, learning the importance of precise chlorine flow control and temperature gradients led to several costly batches that missed the target specification, either through overchlorination or by introducing unwanted isomeric impurities. Over time, our engineering teams developed real-time monitoring with inline Raman spectroscopy and automated dosing, moving away from batch-only controls.

    Pentachloro-2-xylene requires storage solutions tailored to its density and handling characteristics. Unlike more volatile aromatics, this material behaves with a heavier, more syrup-like viscosity, especially in cooler environments. We invested in jacketed storage systems and dedicated pump lines, avoiding the lingering residue issues that can foul shared lines of lighter hydrocarbons. Our maintenance team custom-fit gaskets, and after early trials with commercial pump seals let trace air ingress lead to discolored product, switched over to more robust fluoropolymer linings.

    We learned the importance of safe handling firsthand. Chlorinated aromatics in high concentration exact stricter infrastructure demands. Double-sealed loading bays and fume extraction tracks, along with years of safety reviews, define our site standards—not simply compliance but a refusal to accept avoidable risk. These measures stem from the hard lessons early on, when mishandled drum transfers and poor weatherproofing resulted in unwanted emissions and some expensive cleanup.

    Testing and Quality: Small Differences, Big Outcomes

    Every lot heading out of our facility tells the story of its origin. Testing doesn’t end at meeting catalog values; repeatable outcomes matter for our partners developing registrations or process validations. Feedstock chloride analysis, batch-to-batch refractive index, and careful water assay all matter in producing a grade that lets downstream chemists work confidently. We keep reference samples of every batch for years, providing the foundation for regulatory submissions and long-term application studies. Feedback from our larger customers prompted us to extend detection limits for trace heavy metals, as these impurities—even at sub-ppm levels—affect catalysis and product color.

    We also factor in logistics and transit stability. Alpha,Alpha,Alpha,Alpha',Alpha'-Pentachloro-2-Xylene doesn’t always travel in standardized drums; some customers prefer lined IBCs or even shipped-in-plant containers. Overland transit exposes material to temperature swings, so vapor recovery and pressure monitoring play a key role in ensuring the chemical reaches its destination in the same condition it left our plant. These behind-the-scenes details, learned over time, build trust in every delivery.

    Environmental Considerations and the Path Forward

    Production and use of highly chlorinated aromatics raise justified concern in regulatory circles. Decades ago, the industry often focused only on throughput; today, we think about lifecycle impacts and byproduct management at every stage. All vented or liquid residues pass through multi-stage treatment, and we rigorously monitor outflows for organochlorine content. Our sustainability initiative doesn’t end at compliance. In our pursuit of lower-impact production, we continually test new catalyst systems and scrubber media that clamp down on fugitive emissions.

    We pay close attention to disposal requirements in countries where pentachloro-2-xylene is employed. Our experience working with customers in Europe and North America highlighted the value of clear, standardized waste handling procedures. These lessons, shared with all buyers, save them time and prevent regulatory headaches. Over the years, our plant audits from both local and international agencies proved beneficial—external scrutiny keeps our practices sharp and brings focus where voluntary improvements are possible. Future improvements in closed-loop recycling for spent solvents and unreacted feedstock remain on our development roadmap.

    Research Focus: Answering Application-Specific Demands

    Customer requests rarely stand still. We continue to work with formulating teams who need variants with tighter color, water, or residue specs. One major research project in our pipeline explores potential for selective mono-functionalization of the pentachloro ring, an ambitious approach that could unlock new reaction pathways for agrochemical and polymer clients. Laboratory-scale runs already hint at the promise of more targeted synthesis—a world away from brute-force halogenation techniques.

    Success in these specialties depends on a close dialogue between plant engineering, analytical support, and end-user feedback. Lessons from trial applications guide our improvements. For example, a collaborative study with a partner specializing in epoxy coatings revealed that the presence of trace polyaromatic impurities increased haze formation during curing. By adjusting our fractional distillation techniques, we could curb these minor but impactful side-products. The learning never truly stops, and real application data guide our progress more than theoretical spec lists ever can.

    Summary: Why Practical Know-How Matters

    Alpha,Alpha,Alpha,Alpha',Alpha'-Pentachloro-2-Xylene stays relevant through its proven performance, not just its complex name or formula. Over decades, the chemists and production teams in our plant learned that producing this compound is more than halogenating xylene. From controlling process parameters to storing and dispatching the dense product, every step shapes its final value for our customers. Partnering with sectors that push past the limits of commodity aromatics, we embrace both the technical and regulatory challenges this molecule presents.

    Our journey with this specialty chemical reflects both the evolution of our industry and attention to detail that comes from ground-level manufacturing experience. Every improvement, every new application, every lesson learned in the plant or the lab, finds its way into the next batch. In this way, we support scientific progress and safer, more effective industry outcomes, not just by making molecules but by understanding the story behind each one.