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Anthracene-1,4,9,10-Tetraol

    • Product Name Anthracene-1,4,9,10-Tetraol
    • Alias 1,4,9,10-Tetrahydroxyanthracene
    • Einecs 207-563-8
    • 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

    273400

    Cas Number 481-18-5
    Molecular Formula C14H10O4
    Molecular Weight 242.23
    Iupac Name Anthracene-1,4,9,10-tetraol
    Appearance Yellow to brown solid
    Melting Point 262-264°C
    Solubility In Water Slightly soluble
    Density 1.643 g/cm³
    Boiling Point Decomposes before boiling
    Pubchem Cid 128159
    Smiles C1=CC2=C(C=C1O)C3=CC(=O)C=C(C3=C2O)O
    Inchikey OZFLPIIZPJKUCH-UHFFFAOYSA-N

    As an accredited Anthracene-1,4,9,10-Tetraol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g Anthracene-1,4,9,10-Tetraol comes in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping Anthracene-1,4,9,10-tetraol should be shipped in tightly sealed containers, protected from light and moisture. Ensure proper labeling and follow all local and international regulations for hazardous materials. Use secondary containment to prevent spillage, and handle with gloves and protective equipment during packaging and transport. Store in a cool, dry environment.
    Storage Anthracene-1,4,9,10-tetraol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and light to prevent degradation. Proper labelling is essential, and access should be limited to trained personnel. Always follow institutional and safety guidelines for chemical storage.
    Application of Anthracene-1,4,9,10-Tetraol

    Applications of Anthracene-1,4,9,10-Tetraol in Industrial Manufacturing

    As a dedicated chemical raw material manufacturer, we supply Anthracene-1,4,9,10-Tetraol directly to industrial clients with strict quality and performance requirements. This compound serves distinct roles in specialized downstream manufacturing sectors. Below, we detail verified applications, highlighting process-critical details and compliance factors for each use case.

    1. Organic Semiconductors for Electronic Devices

    Manufacturers use our Anthracene-1,4,9,10-Tetraol as a precursor in the synthesis of polycyclic aromatic hydrocarbon-based organic semiconductors. Its hydroxyl groups enable targeted functionalization, improving charge mobility and film-forming characteristics required in thin-film transistors and OLEDs. The compound enters the process after initial purification and undergoes coupling or substitution reactions to produce custom conductive materials used in electronic display panels, flexible circuits, and photodetectors. Handling requires strict control of impurities and moisture to preserve electrical performance standards.

    Industry compliance standards

    • IEC 62679-2 for electronic display materials
    • RoHS 2011/65/EU substance restrictions
    • REACH (EC) No.1907/2006 substance registration
    • ISO 9001:2015 certified quality management systems

    Typical usage ratio

    • 2–8% by mass in active layer formulations, adjusted for polymer matrix and targeted substrate conductivity

    Downstream process integration

    • Entered at the conjugated monomer synthesis stage and during solution casting or vacuum deposition of semiconductor films

    Final product types

    • OLED display films
    • Organic photodetectors
    • Flexible electronic circuits
    • Thin-film transistors

    2. Colorant Precursors for Technical Dyes

    Leading dye and pigment producers use Anthracene-1,4,9,10-Tetraol as a high-purity starting material for vat dye and anthraquinone dye synthesis. Its structure permits precise oxidative conversion and sulfonation, forming colorants with tailored lightfastness and solubility. Careful batching and quality checks ensure consistent color yield and compatibility with downstream textile or plastics processing. The raw material feeds into oxidative coupling reactors, producing saturated colors for technical fiber dyeing and industrial coatings.

    Industry compliance standards

    • OEKO-TEX Standard 100 banned substance guidance
    • GHS compliant labeling (CLP Regulation (EC) No 1272/2008)
    • ISO 105 for textile colorfastness testing
    • EN 71-3 for toy coatings if applicable

    Typical usage ratio

    • 5–20% in dye intermediates, optimized by oxidation conditions and final dye structure requirements

    Downstream process integration

    • Charged to oxidation reactors following pre-mixing and solvent exchange for anthraquinone dye production

    Final product types

    • Textile vat dyes
    • Technical pigments for plastics
    • Industrial coating colorants
    • Heat-resistant specialty dyes

    3. Redox Mediators in Electrochemical Energy Storage

    Specialty battery and supercapacitor companies employ this tetrahydroxy-anthracene derivative as a redox mediator in advanced electrochemical storage systems. Its multi-electron transfer capability enhances both energy density and charge retention in flow battery formulations. The compound integrates at electrolyte compounding and purification stages, where it undergoes controlled dissolution and filtration to remove metallic ion contaminants. Accurate dosage and regular quality monitoring are necessary to sustain system cycling stability and avoid electrode fouling during battery assembly and operation.

    Industry compliance standards

    • IEC 62619 for secondary battery safety
    • UN 38.3 for transport safety of energy storage products
    • ISO 14001:2015 environmental management systems
    • REACH SVHC monitoring for secondary raw materials

    Typical usage ratio

    • 0.3–2 mol/L in redox-active electrolyte solutions, adjusted according to system energy density targets and cell design

    Downstream process integration

    • Dissolved into aqueous or non-aqueous electrolyte formulations prior to cell stack filling or flow battery system commissioning

    Final product types

    • Organic redox flow batteries
    • Hybrid supercapacitor systems
    • Grid-scale energy storage cells
    • Auxiliary power modules for backup systems

    4. Photoinitiator Systems in Specialty Coatings

    Manufacturers in the specialty coatings sector use the compound to prepare custom photoinitiator systems for UV-curable coatings and inks. Its aromatic core and hydroxyl functionality enable synergistic effects with benzoin ethers or thioxanthone derivatives, increasing curing speed and depth on challenging substrates. The raw material is introduced at the photoinitiator batch blend stage and must pass spectral purity controls to guarantee reproducible curing profiles and minimal residue in end coatings. Operational protocols specify dust control and exclusion of incompatible additives to prevent side reactions during downstream compounding.

    Industry compliance standards

    • ISO 17025 laboratory testing for photoinitiators
    • EN 71-3 migration limits for coatings used on children’s items
    • European Printing Ink Association (EuPIA) guidance for food packaging inks
    • Directive 2004/42/EC VOC content restrictions

    Typical usage ratio

    • 0.5–4% by weight in UV-curable raw coating blends, fine-tuned for substrate transparency and required curing rate

    Downstream process integration

    • Added to the master photoinitiator blend before let-down with prepolymer resins and reactive diluents

    Final product types

    • UV-cured industrial finishes
    • LED-cured printing inks
    • Protective varnishes for electronic components
    • Optical fiber coatings

    5. Pharmaceutical Intermediates for Antitumor Agents

    Producers of active pharmaceutical ingredients source our material for multi-step syntheses of certain antitumor agent scaffolds belonging to the anthracycline class. Its tetrahydroxy configuration allows site-selective glycosylation and ring functionalization under controlled GMP conditions. The material enters after initial deprotection during the building of aglycon fragments and requires full traceability, with batch records maintained through every synthetic stage in line with regulatory filings. Handling is supported by validated cleaning protocols, cross-contamination prevention, and impurity profiling according to pharmacopeial monographs and ICH guidelines.

    Industry compliance standards

    • US Pharmacopeia (USP) and European Pharmacopoeia (Ph. Eur.) specifications for intermediates
    • ICH Q7 Good Manufacturing Practice for API manufacturing
    • FDA 21 CFR Part 210/211 for pharmaceutical process controls
    • GMP traceability and batch record requirements

    Typical usage ratio

    • Batch-specific, ranging 1–10 mmol scale per intermediate stage depending on process route and final yield optimization

    Downstream process integration

    • Incorporated during aglycon fragment synthesis prior to glycosylation and further purification steps

    Final product types

    • Raw materials for APIs in anthracycline antitumor drugs
    • Pharmaceutical intermediates for oncology products
    • Specialty glycosylated aromatic compounds for clinical candidates
    • Fine chemical intermediates for R&D in cancer therapeutics
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    Certification & Compliance
    More Introduction

    Anthracene-1,4,9,10-Tetraol: Manufacturer’s Perspective

    Deep Roots in Polyhydroxy Aromatics

    Producing anthracene-1,4,9,10-tetraol in our facility pushes the boundaries of fine chemical synthesis every day. This molecule—sometimes called 1,4,9,10-tetrahydroxyanthracene—challenges even accomplished chemists because it packs four hydroxyl groups tightly into the anthracene frame. Each batch brings a sense of accomplishment, not only from consistent purity but from being able to ship out a compound trusted for demanding applications. Nobody starts manufacturing tetrahydroxyanthracene lightly; it requires commitment across quality control, process engineering, and environmental responsibility.

    Our flagship product, offered under model ATH-1410, reflects years of design and optimization. We target high-purity grades typically above 98%, as tiny contaminants can throw off downstream reactions. Particle size depends on customer request, but most partners ask for fine, free-flowing powder that stays stable in dry air and handles well both in labs and pilot plant setups. Moisture content sits low, crucial for users who need exact dosing or who run moisture-sensitive chemistry. Every lot undergoes identity confirmation with HPLC and NMR spectral analysis, so researchers get a transparent trace from raw material to final vial.

    Chemistry and Value

    Chemically, anthracene-1,4,9,10-tetraol stands apart from lower polyhydroxy anthracenes. The four hydroxyls drive solubility in polar solvents and unlock a swath of reactivity unavailable to less functionalized analogues. In real-world use, the high hydroxyl content supports roles far outside simple dye manufacture or intermediate formation. Our customers range from university labs unraveling biochemical mimics, to advanced material developers searching for new photoconductors, to manufacturers building polycyclic aromatic derivatives with tailored electronic properties.

    Handling multi-hydroxyl anthracenes brings unique hazards and opportunities. In our facility, the reactivity of ATH-1410 demands extra safeguards to avoid over-oxidation or unwanted condensation during synthesis and storage. We coat process vessels with select polymers and use nitrogen blanketing during particularly moisture-sensitive steps. Not every chemical company can support such careful handling, but each of these efforts pays off in product consistency and traceability. Regular out-of-specification logs show fewer deviations year to year because our technicians track every change, test every solvent batch, and invest time in keeping all production equipment calibrated—to the point where the staff jokes that our tetraol sometimes gets better care than people do.

    Application Domains Fuel Our Progress

    One driver for our ongoing process upgrades comes directly from user feedback. Anthracene-1,4,9,10-tetraol first attracted attention in biomimetic oxidative enzyme research, where it models natural polyphenol functionality. Sulfation, glycosylation, and coupling reactions each highlight the distinctive chemistry of tetrahydroxy anthracenes, providing an essential control substance for synthetic studies. Graduate students and principal investigators across the world have shared methods for modifying our tetraol for use in sensors and organic electronics. The aromatic backbone coupled with four phenolic groups means this molecule rarely sits on a shelf for long—it quickly becomes a tool for exploring radical scavenging, ligand frameworks, or as a building block in advanced dyes.

    On the industrial side, anthracene-1,4,9,10-tetraol’s potential for facilitating redox catalysis has caught the eye of more process-focused outfits. One client cites that large-scale testing with our ATH-1410 cut down their step count during the synthesis of certain high-performance pigments, crediting its superior reactivity for the breakthrough. Another team working in the renewable energy sector requested a custom particle size for use in novel electrode coatings aimed at boosting cycle life. These collaborations feed back into our R&D cycle, where each new customer demand pushes us to further refine crystal morphology, improve handling, and ensure tighter purity specs.

    Few people realize that the jump from one, to two, to four hydroxyl groups on the anthracene core doesn’t just present a difference in reactivity; it actually alters how the molecule fits into supramolecular assemblies and influences stacking interactions in solid-state devices. That means our tetraol goes places where the mono- or dihydroxy versions never could—both literally and figuratively. Down in the production unit, you hear regular debates between analysts about whether a small tweak in synthesis or purification might bump up shelf-life or bring new features to the customers at the cutting edge of organic semiconductor research.

    Why Users Need More Than Just Product Specs

    Clients count on specific batch data, but many return again and again because we supply more than a certificate of analysis or a matching HPLC trace. People ask about solubility in water, DMF, ether mixtures. We run those bench tests, since no technical data resource can substitute for trying to dissolve this stubborn powder in a real-world flask. Preparing a kilogram package for export means working closely with the shipping team to keep it airtight and light-protected, since those hydroxyls want to oxidize if left even a day too long under humid warehouse air. By keeping our focus on the practical—a commitment that never gets lost among graphs and tables—production managers and chemists see us as problem solvers, not just suppliers.

    Every manufacturing run teaches us something new, especially as research customers push the limits. Sometimes it’s about how subtle variations in temperature during recrystallization influence the final solid’s filterability, or how trace iron content can poison downstream catalysts unless we scrub it to parts per billion. We keep a close eye on the things only real frequent producers learn: how to avoid accidental degradation, which containers reduce risk of contamination, and how to spot a batch with potential problems before it ever leaves the floor. Every lot of ATH-1410 has its history, written in the day-to-day logs by technicians who catch shifts in color, weight, or finish that outpace any automated alert system.

    Comparison with Other Anthracene Derivatives

    Anthracene-1,4,9,10-tetraol doesn’t fit the easy mold of just being a “higher order” version of 9,10-anthraquinone or 1,4-dihydroxyanthracene. Chemically, the four hydroxyls challenge the electron distribution—making it more prone to participate in certain redox cycles, but also more resistant to premature polymerization during synthetic handling. That subtlety matters. The 1,4,9,10 tetraol form unlocks specific hydrogen-bonding patterns that let it work in supramolecular chemistry, where other analogues simply can’t assemble into the right structures.

    We regularly get requests from researchers who have tried commercial 9,10-dihydroxyanthracene or 1,4-dihydroxyanthracene and then seek our tetraol because their own protocols call for something less prone to re-oxidation yet more reactive toward cross-coupling agents. Shipping out higher functionality means we handle a critical transition in benzenoid aromatic chemistry; nothing else substitutes if the research hinges on the exact pattern of available hydroxyl groups. Where single or double hydroxyl anthracenes give moderate solubility, our tetraol moves into high-polarity solvent territory—opening doors in aqueous or semi-aqueous reactions.

    Some customers use the higher site availability to construct dendritic scaffolds with targeted functionalization, where the lesser hydroxylated anthracenes can’t reach the necessary branching points. ATH-1410’s fine control over both purity and particle surface also enables more reproducible conjugation for applications in catalysis, particularly in bioinspired catalytic cycles where full site occupancy impacts turnover number.

    Tackling Technical Challenges in Synthesis

    Making anthracene-1,4,9,10-tetraol isn’t as simple as stringing together hydroxylation steps. Sourcing starting anthracene with trace metal control takes priority, as impurities can spark off-color byproducts. Scale-up requires precise stoichiometry of oxidants so each aromatic ring gets hydroxylated and not overburned into quinones or ring-opened fragments. We install redundant pH monitoring and stick to slow temperature ramps to get clean, repeatable conversion with high yield. Every operator running the ATH-1410 production line brings hands-on experience with multi-step extractions, since product loses purity fast if you shortcut any phase separation or improper neutralization.

    Monitoring end-point is another learned skill. Too late, and side reactions start creeping in. Too soon, and the product has more mono- or dihydroxy impurities. Walking the line takes both training and deep respect for the fine chemistry at play. Cleaning every vessel counts for more than most realize: even a few milligrams of residual peroxides or spent acid slow the next batch and can carry through to contaminate the end user’s chromatographic analyses.

    We spend on robust ventilation, given the aromatic odor that develops from even trace exposure to air during handling, and run all packaging under controlled humidity. Our staff can recall weeks lost to learning the best bottle liners or finding out that a slightly different PTFE cap makes the difference between a six-month stable product and one that clumps or yellows before use.

    Every kilogram produced has a series of sign-offs, from raw material inspection to packed shipment, with traceability on all solvents, reagents, and analytical test points. Regulatory compliance with environmental and workplace safety rules guides each process step—not from an abstract sense of obligation, but a real concern for both user safety and long-term company sustainability. The knowledge from each production campaign doesn’t vanish; it’s stored in manuals, discussed in meetings, and passes to new team members through hands-on learning.

    Supporting Innovation on the Customer Side

    Our direct relationships with research partners and development labs reveal a recurring theme: project success often depends as much on supplier expertise as on the molecule itself. We’ve recounted times where a new reaction failed repeatedly until we tweaked drying or packaging protocols. People email our technical line for troubleshooting unexpected results, not just to reorder product. This day-to-day problem solving grows our reputation and encourages the next wave of innovation.

    Examples from real customers highlight product flexibility. One client developed new conductive polymer films using our tetraol as a monomer component, reporting improved self-assembly—likely due to the way the four hydroxyls promote intermolecular hydrogen bonding. Another team developed new chelating ligands that fasten to rare earth metals more tightly when built from our material. Each use case runs on complex chemistry, but the common denominator remains reliable supply and consistent product performance.

    Anthracene-1,4,9,10-tetraol’s track record as a building block for high-value transformations spurs us to keep innovating. Researchers can’t afford setbacks from irregular batches; they rely on lot-to-lot consistency and transparent batch histories. As research in organic electronics and biochemistry advances, our ability to meet stringent quality targets translates directly into faster progress and more credible publications for our users.

    Continuous Improvement Drives Success

    In this business, nothing stands still. We invest in continuous training, both for chemists and technicians, so lessons learned on one process extend to improvements everywhere. Equipment upgrades, from new filtration systems to better packing lines, are less about show and more about reducing chipping, caking, or cross-contamination. Batch records grow thicker with each optimization — not to fulfill a formality, but to create a living memory of what works and what we still need to tackle.

    Challenges keep coming. From specific requests for new particle morphologies, to demands for kilogram-scale custom synthesis, to tighter impurity tolerances and bespoke solvent recommendations, we adjust and learn. Enduring relationships with equipment vendors and research institutions help us access new monitoring technologies. Even routine raw material contracts get renegotiated for higher upstream documentation, so we keep unexplained impurities from entering production.

    We put resources behind workplace safety for our own teams, because a clean and organized shop floor with monitored air quality sets the tone for everything that follows. Team meetings run longer than outsiders might expect, because every near miss or minor deviation in process gets discussed—not swept under the rug. These shared lessons go back into practice, driving the next cycle of improvement.

    Real-World Impact Connects Us to Industry Progress

    Manufacturing a molecule like anthracene-1,4,9,10-tetraol gives a seat at the table for the advancement of organic materials science. Year by year, we hear from professionals using our tetraol in broader and more unpredictable ways—fuel-cell component synthesis, new water purification membranes, or unusual photochromic dyes. Some of these applications demand such tight control over byproducts that they shape entire new product lines for us to investigate.

    Being a first-line producer gives us insight into where market trends pull the next batch of research. For example, as demand grows for chemical feedstocks that balance both performance and environmental acceptability, ingredients like anthracene-1,4,9,10-tetraol face ever-closer scrutiny for toxicity, residue, and reproducibility. Our data shows that proper handling and documentation at the source makes downstream compliance much easier for clients working in regulated industries. We run extensive documentation of all hazardous steps, implement operator training on every new piece of equipment, and maintain transparent logs so audits run smoothly.

    Supporting scientific discovery takes more than a catalog and a shipping label. It requires empathy for researchers’ challenges, and a willingness to iterate on the details—from solvent choices to storage containers—so partners can focus on their science without product-forced troubleshooting. Even as manufacturing scales up or pivots to meet new demand, we keep attention fixed on operational discipline, transparent process control, and rapid response to technical queries.

    Looking Ahead

    With more industries moving towards advanced organic molecules, demand for high-quality anthracene-1,4,9,10-tetraol continues to rise. The feedback loop with innovative users keeps us motivated to push both synthetic routes and analytical rigor to new heights. Each kilo shipped out brings us closer to understanding where chemistry and technology intersect, and how a single finely tailored polyhydroxy aromatic can enable technology leaps in dozens of unique fields.

    While other anthracene derivatives serve broad and sometimes interchangeable roles, the specific features of anthracene-1,4,9,10-tetraol—its reactivity, solubility, and handling needs—ensure it remains a specialty chemical best delivered by manufacturers who invest in careful, open production. We welcome ongoing collaboration and continue to treat every order, large or small, as an opportunity to deepen our know-how and contribute to both the science and industry of advanced aromatic compounds.