Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

9,10-Dichloroanthracene

    • Product Name 9,10-Dichloroanthracene
    • Alias anthracene, 9,10-dichloro-
    • Einecs 214-366-9
    • 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

    587250

    Name 9,10-Dichloroanthracene
    Cas Number 1498-98-0
    Molecular Formula C14H8Cl2
    Molar Mass 247.12 g/mol
    Appearance Yellow crystalline solid
    Melting Point 263-265°C
    Solubility In Water Insoluble
    Density 1.43 g/cm³ (estimated)
    Pubchem Cid 13308
    Smiles Clc1ccc2c(c1)ccc3c2ccc(c3)Cl
    Inchi InChI=1S/C14H8Cl2/c15-9-5-1-3-7-11(9)13-8-4-2-6-10(13)12(7)16/h1-8H
    Synonyms 9,10-Dichloro-9,10-dihydroanthracene

    As an accredited 9,10-Dichloroanthracene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 9,10-Dichloroanthracene, 25g: Supplied in an amber glass bottle with a secure screw cap, labeled with hazard symbols and product details.
    Shipping 9,10-Dichloroanthracene should be shipped in tightly sealed containers, protected from light, moisture, and physical damage. It is classified as a hazardous chemical, requiring proper labeling and documentation according to relevant regulations (such as DOT or IATA). Use appropriate secondary containment and ensure compliance with local, national, and international shipping requirements.
    Storage 9,10-Dichloroanthracene should be stored in a tightly sealed container, placed in a cool, dry, and well-ventilated area away from sources of ignition. Keep it away from incompatible substances such as strong oxidizing agents. Protect from direct sunlight and moisture. Properly label storage containers, and ensure access is limited to trained personnel equipped with appropriate protective gear.
    Application of 9,10-Dichloroanthracene

    Applications of 9,10-Dichloroanthracene in Industrial Manufacturing

    As a direct manufacturer of 9,10-Dichloroanthracene, we support specialized industrial customers across select downstream sectors. Our raw material plays a defined functional role in key synthesis, performance dye formulation, and specialty chemical production routes. The following sections outline precise industrial applications, with verified compliance and processing information.

    1. High-Performance Organic Semiconductor Production

    9,10-Dichloroanthracene serves as a tailored building block in the synthesis of organic semiconductors, often for devices such as organic field-effect transistors (OFETs) and photodetectors. Its electron-withdrawing characteristics promote desirable charge-transport properties. Customers incorporate the material at the monomer stage, where selective chlorination assists in modulating the bandgap of advanced polyaromatic frameworks. This direct integration occurs in controlled synthesis environments to ensure high molecular purity and reproducibility for downstream device fabrication.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • RoHS (2011/65/EU) for electronic component applications
    • REACH Regulation (EC) No 1907/2006 (European Registration)

    Typical usage ratio

    • 0.2–3% w/w relative to total monomer mass, adjusted per desired electronic property profile

    Downstream process integration

    • Direct addition during monomer condensation or polymerization step
    • Purification by recrystallization and column chromatography
    • Melting point verification and purity analysis via HPLC before device assembly

    Final product types

    • Thin-film OFET layers
    • Organic photodetector matrices
    • Sensor interface circuits

    2. Specialty Dye Intermediate for VAT Yellow Pigments

    Many producers use 9,10-Dichloroanthracene as a precursor for high-grade vat yellow dyes. The chlorinated anthracene skeleton allows for selective transformation into dye intermediates with improved photostability and wash fastness required in technical textiles and high-performance coatings. Chlorinated intermediates help optimize final pigment hues and enhance chemical resistance, making this raw material critical for advanced dye synthesis routes.

    Industry compliance standards

    • OEKO-TEX® Eco Passport (dye chemical safety)
    • ISO 105-B02 and ISO 105-C06 (color fastness testing)
    • ZDHC MRSL V3.0 (Restricted Substances List)

    Typical usage ratio

    • Up to 7% w/w depending on molecular pathway and target substructure
    • Ratios fine-tuned per pigment performance and depth requirements

    Downstream process integration

    • Introduced during early-stage oxidative coupling in dye intermediate manufacturing
    • Chlorine atoms retained or functionalized during final pigment derivatization
    • Post-reaction washing and drying phases to eliminate by-products

    Final product types

    • Vat Yellow 34 & related dyes
    • High-stability pigment dispersions
    • Technical fiber masterbatches

    3. Precursor for Fluorescent Probe Synthesis

    Chemicals and life science companies employ 9,10-Dichloroanthracene in the design of fluorescent probes and markers used in advanced analytical chemistry. Its rigid aromatic framework and halide functionalities support further substitution, providing a customizable foundation for target-specific fluorophores. Manufacturing processes require accurate dosing and high batch reproducibility, especially when integrating the molecule into larger conjugated dye systems intended for sensitive laboratory and clinical detection kits.

    Industry compliance standards

    • IUPAC Nomenclature and Purity Guidelines
    • ISO/IEC 17025 Testing Laboratory Accreditation
    • Good Laboratory Practice (GLP) compliance (OECD Series on Principles)

    Typical usage ratio

    • 0.05–0.8% by weight in probe synthesis, modified per emission intensity and linker requirements

    Downstream process integration

    • Reacted at early stage of multi-step fluorophore formation
    • Mono- or di-substitution for spectral tuning
    • Final purification by preparative chromatography

    Final product types

    • Blue-green fluorescent probes for biological imaging
    • Reference standards for lab analytics
    • Sensitive fluorescence-tagged conjugates

    4. Photooxidation Sensitizer Development for Chemical Processing

    Manufacturers leverage 9,10-Dichloroanthracene as a sensitizer in targeted photooxidation processes, including advanced organic transformations and environmental oxidation systems. The dual halogenated structure increases triplet yield and lifetime, essential for scalable, controlled light-driven reactions. Large-scale applications rely on this material to boost photochemical efficiency in the synthesis of oxidized aromatics, intermediates for pharmaceutical and agrochemical manufacturing, and specialty chemicals where precise oxidation is required.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Systems
    • Process Safety Management (OSHA 1910.119 for chemical facilities)
    • Specific customer HSE specifications depending on geographic site

    Typical usage ratio

    • 0.1–1.0 mol% based on substrate concentration, optimized for light source and solvent system

    Downstream process integration

    • Dosed into batch or continuous photoreactor streams
    • Light irradiation at defined wavelengths (e.g., 365–420 nm)
    • Post-reaction removal and recovery processes

    Final product types

    • Oxidized aromatic intermediates for fine chemicals
    • Advanced intermediates for plant regulators
    • Photooxidation process catalysts for reuse
    Free Quote

    Competitive 9,10-Dichloroanthracene 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.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    9,10-Dichloroanthracene: A Reliable Choice from the Source

    Bringing a molecule like 9,10-Dichloroanthracene from the lab bench to full-scale manufacturing presents a unique set of technical demands and quality challenges. Over years of working with polycyclic aromatic compounds, our experience in producing 9,10-Dichloroanthracene (also known as 9,10-DCA) has highlighted both its practical advantages and several crucial distinctions from other chlorinated anthracenes. This isn’t a commodity chemical pulled off a shelf – it’s a result of process discipline, hands-on troubleshooting, and refinements forged by real-world feedback from R&D and industrial customers alike.

    Behind Each Batch: Precision That Comes from Experience

    Our 9,10-Dichloroanthracene follows a synthesis route we have refined for over a decade. Using high-purity anthracene and carefully controlled chlorination, we ensure selective substitution of chlorine atoms at the 9 and 10 positions. These steps call not just for precise control of temperature and reactant ratios but also for a keen understanding of reaction kinetics and impurity profiles. We draw on years of data reviewing chromatograms and hands-on runs to limit isomer contamination and over-chlorinated byproducts.

    The resulting 9,10-Dichloroanthracene is a pale solid, often described visually as light greenish-yellow crystals, with a melting point comfortably above 200°C. Most requests call for a minimum purity above 98%, measured by HPLC or GC, since trace polyhalogenated impurities complicate functionalization and downstream coupling reactions. Reliable melting range and narrow impurity profiles matter to customers using our material as an intermediate in specialty dye production, materials chemistry, and some photochemical systems.

    Why Formulators, Researchers, and Material Scientists Keep Coming Back

    Industrial and university customers both often ask us how 9,10-DCA stands apart from plain anthracene or mono-chlorinated variants for their work. It’s more than just packing a couple of chlorine atoms onto the anthracene backbone. Replacing two hydrogens at those central positions introduces a strong electron-withdrawing effect, changing the molecule’s reactivity, color properties, and solubility. These modifications open new windows in optoelectronic research and light-emitting materials, especially as a building block for organic semiconductors. Where anthracene itself is too reactive toward oxidation or not quite stable enough under device-testing conditions, the dichloro version offers a longer life span and a different energy gap.

    We’ve also worked with photochemists testing singlet oxygen sensitizers, and our conversations often circle back to purity. Even a small misstep in washing or post-chlorination cleanup leaves traces of polychloroanthracenes, which kill yields or cause fluorescence quenching in downstream work. We triple-check columns not just to hit the numbers but to ensure the side-product profile matches what our lab partners report back through their NMR and UV-Vis analyses. Transparency in the real impurity content—not just a sales-sheet claim—sets expectations right for people synthesizing extended aromatic systems or doing sensor platform development.

    Real Manufacturing: More Than Just Tonnage

    Producing 9,10-Dichloroanthracene starts with reliable sourcing of high-purity anthracene. Early on, we learned that even minor polycyclic aromatic hydrocarbon contamination in the anthracene feedstock alters reaction selectivity, leading to a difficult chromatographic separation later. We take a batch records-based approach. Routine incoming inspections, melt-point checks, and trace heavy-metal analysis screen out inconsistent raw materials long before the chlorination step starts.

    During the synthesis stage, finely tuning the chlorine addition rate and agitation speed proved critical in minimizing polychlorination. Early trials with uncontrolled addition produced off-spec gunk requiring repeated reprocessing, which wastes solvents and increases hazardous waste overhead. Running small-scale pilots allowed us to map the reaction’s sensitivity to temperature swings and scale-up risks. Each time we take on a larger production lot, we gather new data to refine our process control charts.

    Differences That Matter: Comparing to Other Halogenated Anthracenes

    In the broader family of chlorinated anthracenes, each product finds a niche driven by its molecular structure. For example, 9-chloroanthracene or 2,6-dichloroanthracene see action in other corners of advanced materials, but the 9,10-substituted version offers a well-balanced mix of stability and functional reactivity. Compared to polychlorinated analogs like 1,5,8,9-tetrachloroanthracene, 9,10-DCA introduces fewer chlorine atoms, keeping it more reactive for subsequent coupling or substitution steps.

    This difference becomes clear in photophysics: the 9,10 positions directly influence the molecule’s electronic transitions, shifting absorption and emission bands more predictably than other substitution patterns. Formulators looking to tune light-emitting device colors or exploit energy transfer pathways often choose 9,10-DCA precisely for these predictable shifts. Moreover, its lower total chlorine content compared to higher analogs keeps it easier to handle from both a waste management and regulatory point of view. Customers focused on minimizing chlorinated waste in their own plants prefer the more focused substitution pattern.

    Supporting Specialty Applications: From Lab to Pilot Scale

    We’ve supplied custom orders for 9,10-DCA to research groups working in OLED development, chemiluminescent systems, and advanced sensor platforms. Larger customers in dye manufacturing and high-performance plastics value consistent melting range and particle size. Particle morphology might seem trivial, but our grinding and sieving routine is based on direct customer feedback; poor flow leads to losses and dusting during automated feeding. To keep things straightforward, we standardize crystal size within a range that balances ease of handling and fast dissolution in organic solvents most used by our partners.

    Intermediate manufacturers focusing on Suzuki or Stille couplings also value our minimal trace halogen content and tight melting-point specification, since catalytic cycles tend to be poisoned by unexpected byproducts. People working in pilot plants tell us they appreciate technical support that goes beyond box-shipping, including sharing our HPLC and NMR data packages when developing new processes. These technical exchanges build trust over time and sharpen our feedback loops, pointing out where trace organics or batch-to-batch differences could skew research results or pilot outcomes.

    Challenges in Production: What We’ve Learned

    Producing 9,10-Dichloroanthracene is not plug-and-play chemistry. Even small errors in temperature ramping or quenching steps introduce new isomers or degrade the product. Recovering clean product from mixed halogenated anthracene waste calls for careful crystallization and careful footwork with solvent choices. Unlike some aromatic halides, which easily partition from waste, 9,10-DCA can co-elute with close relatives unless columns are carefully optimized. We run TLC and HPLC checks at multiple stages rather than only at the end, which helps us catch process drift soon enough to salvage valuable intermediates.

    Waste handling presents challenges too. Chlorinated aromatic residues count as hazardous material, and we allocate resources for on-site solvent recycling and off-site disposal partners who can assure compliance and minimize total environmental impact. It’s not just about sending off drums for disposal. Drilling into production numbers, optimizing yields, and reducing waste production through lean batch design keep both our cost structure and regulatory reporting straightforward.

    Meeting Evolving Standards: Environment and Safety

    Environmental safety rules surrounding chlorinated aromatics have tightened in recent years. We stay current with new thresholds set by agencies such as REACH and the EPA, investing in containment and air handling upgrades in our production shops. Our in-house EHS team tracks every batch, ensuring traceability from raw material entry to final packaged product. We work to keep worker exposure minimal by semi-automating volatile handling steps and monitoring air quality regularly with third-party labs.

    Dust from chlorinated anthracene presents both safety and quality risks, so we handle grinding operations in enclosures with high-efficiency capture and custom venting. Lab coats and gloves help, but our layout is designed for flow that limits points of contact with open product streams. Each improvement in containment came after real-world incidents or close calls where small spills, if left unchecked, could have created bigger issues. Our process engineers and line workers routinely suggest—and implement—practical tweaks for safer workflows.

    Keeping Traceability and Quality Real

    Every drum or jar leaving our site comes from a batch with an unbroken record, detailing not only analytical results but also production lot history, QC data, and handling protocols. We don’t just print barcodes – we maintain full digital records going several years back, so that if a customer finds question during their analytical testing, we can trace not only the batch but the specific production timeline. Our technical staff supports customers by sharing details of analytical methods and not just COA numbers, fostering open discussions that help both sides dial in their product requirements.

    Sometimes a customer flags unknown signals in their GC or LC runs, and our chemists dive into previous batch histories to double-check if a new byproduct pattern has appeared. These cycles of investigation lead us to occasional tweaks—swapping out a reactant supplier, or adjusting post-chlorination purification methods. Our internal drive is to avoid surprises for our partners, who rely on reproducibility from small gram quantities to multi-kilogram lots.

    True Batch-to-Batch Consistency: Lessons from Scale-Up

    Scaling up 9,10-DCA production has meant grappling with thermal gradients, mixing efficiency, and solvent recovery rates. Moving from 1-liter glassware to reactor trains doesn’t always translate perfectly: slight temperature inconsistencies at scale triggered hot spots, which nudged impurity levels upwards. Surprises like localized over-chlorination cost us both yield and downstream purification effort. We learned to add more temperature probes and to use real-time in-process analytics, tightening our window for chlorination and shifting quenching targets accordingly.

    Process chemists on our team track every deviation and experiment with blend-back protocols for off-grade batches where feasible. Instead of hiding issues, internal reports drive process improvement meetings. For customers, this means greater predictability—an analyst in a device development group or a chemist in an academic lab can request previous batch data and get a full run history, ensuring their method development rests on solid ground. This open-door approach came from early missteps, when an off-grade batch slipped past our final checks. Today’s system splits the QA process into pre-pack samples, finished goods retests, and post-shipment follow-ups when necessary.

    Supporting Customer Success: Long-Term Partnerships

    We believe in building reliability not just into the molecule, but into our relationships. Researchers developing purified standards, electronic materials, or advanced dyes require openness from their suppliers. Projects often call for fast-turn customizations: a tighter specification one quarter, a different lot form the next cycle, or a special blend. We answer these requests with technical consultation, shipping options, and—sometimes—good old-fashioned bench work to run small feasibility trials. These trials test compatibility or performance in our customers’ specific applications, guiding our next round of process improvements or specification adjustments.

    While a lot of attention gets paid to packing specs, we take care to package 9,10-DCA in sealed vessels or custom drums to control moisture and light exposure. Some customers pass on feedback about slight color changes after long shipping routes. We adjust this by switching to more robust packaging, combined with desiccants where required. This journey of iterative learning helps our customers focus on their own chemistry rather than fighting packaging-related variability.

    Recommendations for End Users: Insights Gained Over Years

    Using 9,10-Dichloroanthracene efficiently means understanding its melting and solubility idiosyncrasies. Based on user feedback, dissolving in hot chlorinated solvents or aromatic hydrocarbons works best, and we advise gently warming the mixture to avoid excessive decomposition. Filtering out insoluble trace residues prior to key reactions, like halide couplings or Friedel-Crafts reactions, improves yields. Avoiding exposure to UV or excessive oxygen before use preserves its photophysical profile, especially for optoelectronic applications.

    Customers scaling from grams to kilograms sometimes experience variable performance due to subtle batch variances or storage conditions. We encourage storing material in tightly sealed, amber containers, and minimizing repeated exposure to air. Our technical support team frequently provides best-practice guides, based on customer-reported use-cases, to support those transitioning from bench chemistry to pilot or production scale.

    Looking Forward: Adapting Together in the Specialty Chemistry Landscape

    Demand for 9,10-Dichloroanthracene evolves with advances in materials science, organic electronics, and specialty dye chemistry. We watch trends in organic solid-state lighting and energy storage, keeping a pulse on what our academic and industry partners are pushing towards. We diversify production allotments to meet spikes from new research projects and phase in improvements driven by the feedback from real-world experiments—sometimes making batch tweaks even when only a single customer flags an inconsistency.

    Collaborating directly with customers and learning from their process challenges keeps us grounded. We pursue tangible improvements in quality, handling, and consistency, not just regulatory checkboxes. By combining hands-on manufacturing insight, analytical follow-through, and direct technical exchange, we keep 9,10-Dichloroanthracene reliable for demanding applications where purity, stability, and reactivity matter most.

    Experienced teams, robust process controls, and open collaboration set this product apart. Feedback from each lot sharpens our next batch, and each new application opens the door to better chemistry. Whether refining an old process or pioneering a new field, trust in the source creates lasting impact for researchers, formulators, and partners throughout the specialty chemical ecosystem.