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1,8,9-Trihydroxyanthracene

    • Product Name 1,8,9-Trihydroxyanthracene
    • Alias Anthralin
    • Einecs 220-626-2
    • 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

    227021

    Iupac Name 1,8,9-Trihydroxyanthracene
    Molecular Formula C14H10O3
    Cas Number 610-29-1
    Appearance Yellow to brown solid
    Melting Point 242-244°C
    Solubility In Water Poorly soluble
    Boiling Point Decomposes before boiling
    Density 1.47 g/cm³ (estimated)
    Structural Formula C6H4(CO)2C6H3(OH)3
    Pubchem Cid 10845
    Smiles C1=CC2=C(C(=C1)O)C(=CC3=CC=CC=C3C2=O)O
    Inchi InChI=1S/C14H10O3/c15-10-5-6-11-13(7-10)14(17)12(16)4-2-1-3-8-12/h1-8,15-17H

    As an accredited 1,8,9-Trihydroxyanthracene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with a secure screw cap, labeled "1,8,9-Trihydroxyanthracene," includes hazard and storage instructions.
    Shipping **Shipping Description for 1,8,9-Trihydroxyanthracene:** 1,8,9-Trihydroxyanthracene should be shipped in tightly sealed containers, protected from light and moisture. Store at room temperature, away from incompatible substances. Follow all local, national, and international regulations for shipping chemicals. Ensure containers are properly labeled and cushioned to prevent breakage during transport. Handle with appropriate personal protective equipment.
    Storage 1,8,9-Trihydroxyanthracene should be stored in a tightly sealed container, away from light, heat, and moisture. Store it in a cool, well-ventilated area, separate from incompatible substances such as strong oxidizing agents. Ensure appropriate chemical labeling and secondary containment to prevent spills. Use personal protective equipment when handling and follow all relevant safety guidelines and regulations for hazardous chemicals.
    Application of 1,8,9-Trihydroxyanthracene

    Applications of 1,8,9-Trihydroxyanthracene in Industrial Manufacturing

    As an established producer of 1,8,9-Trihydroxyanthracene, we supply this advanced anthracene derivative to specialty downstream sectors with precise requirements. The following sections detail its integration within authentically segmented industrial tracks, covering compliance, usage ratios, workflow positions, and delivered product formats.

    1. Pharmaceutical Intermediates for Anticancer Agent Synthesis

    1,8,9-Trihydroxyanthracene serves as a critical intermediate for synthesizing select anticancer compounds, especially anthracycline-based actives. Research-grade manufacturers employ it during multi-step organic synthesis, particularly for functionalizing core ring systems to yield high-purity drug intermediates. It supports fine control over substitution patterns required by active pharmaceutical ingredient (API) specifications, with stringent trace control for finished oncology products.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia monographs for intermediates
    • 21 CFR Part 211 US FDA cGMP for Drugs
    • USP <795> and <797> Compounding Standards

    Typical usage ratio

    • Between 0.5% and 2.5% w/w within total reactant mass, adjusted based on desired intermediate yield and reaction path selectivity.

    Downstream process integration

    • Enters during ring oxidation or hydroxylation step prior to subsequent functionalization and purification phases.
    • Followed by isolation and chromatographic purification to ensure batch uniformity.

    Final product types

    • Anthracycline API intermediates (e.g., daunorubicin, doxorubicin precursors)
    • Chemically defined lead compounds for oncology R&D pipelines
    • Reference substances for quality control laboratories
    • Custom pharmaceutical building blocks

    2. Synthesis of Organic Semiconductor Dyes for Optoelectronics

    Downstream specialty chemical manufacturers utilize 1,8,9-Trihydroxyanthracene as a functional precursor in the fabrication of anthracene-based dyes for organic semiconductors. Its three positioned hydroxyl groups permit controlled derivatization, vital for producing conjugated dye cores with precise electronic absorption and emission profiles. Consistent material grade and minimal trace metal content are vital for reliable semiconductor device characteristics.

    Industry compliance standards

    • ISO 9001 certified quality management for specialty chemical production
    • IEC 61249-2-21 for halogen-free electronics materials
    • RoHS Directive (2011/65/EU) for electronic component purity
    • REACH chemical registration and documentation

    Typical usage ratio

    • Utilized at levels from 1% to 5% w/w in dye precursor solutions, with concentration depending on molecular weight targets and substrate compatibility.

    Downstream process integration

    • Introduced during dye core formation prior to electrophilic substitution or complexation.
    • Subsequent processing includes purification, drying, and application onto substrates via solution casting or vapor deposition.

    Final product types

    • Organic emitting diodes (OLED) dye blends
    • Photoactive inkjet printing materials
    • Sensing and imaging pixels
    • Organic thin-film transistors (OTFTs)

    3. Colorant Precursor for High-Performance Polymeric Pigments

    The material acts as a key building block within the polymer colorant sector, enabling the production of heat-resistant, high-stability anthracene pigments. Its hydroxylated structure binds with copolymerizable monomers, supporting permanent color addition to engineering plastics, coatings, and fibers. Only high-purity, low-impurity batches can fulfill pigment industry demands for batch-to-batch color consistency and regulatory approval for specialty applications.

    Industry compliance standards

    • EN 71-3 Safety of Toys (for pigments used in toys/coatings)
    • FDA 21 CFR 177.2600 (elastomers)
    • ISO 18451-1 Pigments and Extenders: Terminology
    • REACH Annex XVII restrictions for aromatic amines

    Typical usage ratio

    • Added at 0.2% to 1% as a pigment precursor in the total polymer blend, adjusted for targeted color saturation and substrate compatibility.

    Downstream process integration

    • Reacted in situ during polymerization or added at melt blending stage with other colorants and stabilizers.
    • Subsequent compounding and extrusion yield pelleted or powdered masterbatch formats.

    Final product types

    • High-performance color masterbatches for engineering resins
    • Colored specialty fibers
    • UV-stabilized automotive plastics
    • Long-life powder coatings

    4. Analytical Reference Standard for Environmental and Forensic Labs

    Certified labs specializing in environmental analysis and forensic chemistry require 1,8,9-Trihydroxyanthracene as a traceable standard for quantifying polycyclic aromatic compounds. Its use ensures calibration integrity in high-performance liquid chromatography (HPLC) and mass spectrometry (MS) when monitoring anthropogenic and natural PAHs. Supply in analytical grade quality with full characterization meets method validation demands.

    Industry compliance standards

    • ISO/IEC 17025 Accreditation for Testing Laboratories
    • EPA SW-846 Method 8270D (for semi-volatile organics)
    • Standard Methods for the Examination of Water and Wastewater (SM 6440)
    • USP Reference Standards—General Chapter <11>

    Typical usage ratio

    • Dosed as calibration standard at 0.01–1 mg/L for trace quantitation, adjustable depending on sensitivity requirements and matrix complexity.

    Downstream process integration

    • Dissolved in analytical solvent for direct injection or column calibration.
    • Used in preparing matrix-matched standards and method blanks for regulatory reporting.

    Final product types

    • Certified reference materials (CRM) for environmental laboratories
    • Analytical working standards for soil, water, and air testing
    • Forensic calibration kits
    • Spiked test samples for instrument validation
    Free Quote

    Competitive 1,8,9-Trihydroxyanthracene prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 1,8,9-Trihydroxyanthracene: Expert Insights from the Manufacturer

    Our Perspective on Quality and Purpose

    Every batch of 1,8,9-Trihydroxyanthracene we produce reflects years of experience in anthracene derivative synthesis. As a manufacturer, we see more than a chemical identifier or a point on a specification sheet—this is a compound with real substance and real uses, designed to meet the ongoing challenges in both research and industrial application. Our facility relies on robust quality control during synthesis and post-processing, ensuring consistency in color, purity, and crystalline form. That foundation has attracted a range of partners, especially those who care about downstream stability and reactivity.

    Understanding the Identity of 1,8,9-Trihydroxyanthracene

    The defining feature of 1,8,9-Trihydroxyanthracene is the presence of three phenolic hydroxyl groups positioned at the 1, 8, and 9 carbons on the anthracene skeleton. This structure gives the molecule a unique reactivity profile. We typically deliver the product in powder form, fine and free-flowing, making it easy to handle in both academic and industrial settings. No two batches leave our line until confirmed by HPLC and NMR analysis, minimizing the variability that can disrupt downstream reactions.

    Meeting Consistent Laboratory and Industrial Needs

    Every user approaches our product from a specific angle, but a common thread runs through requests for high assay and minimal impurities. In our experience, synthetic routes starting from pure anthracene under controlled oxidation consistently generate the triol with minimal byproducts, which is critical in research where yield and selectivity matter. Experienced chemists gravitate toward our product for cross-coupling, dye manufacture, and redox studies. The trihydroxy configuration opens unique opportunities in ligand design and as a precursor for advanced dye stuff.

    Why Trihydroxyanthracene Matters in Dye Chemistry

    Applying the compound in dye synthesis requires a nuanced understanding of its structure-reactivity relationship. The three hydroxyl groups activate the aromatic core toward electrophilic substitution and facilitate both chelation and hydrogen bonding. Several dye manufacturers prefer this molecule as a starting point for new classes of colorants, especially those looking to maximize resistance to photodegradation or tailor spectral absorption properties. Our technical team works directly with these users to adjust crystallinity or moisture profile on request, accommodating the nuanced needs of specific reaction pathways.

    Direct Experience: Sourcing and Processing Challenges

    A lot goes on behind the scenes before a gram of 1,8,9-Trihydroxyanthracene reaches a laboratory shelf. Sourcing anthracene of sufficient quality is not trivial. Crude anthracene often carries polycyclic impurities from initial coal tar processing or other hydrocarbon feedstocks. These impurities translate into lower oxidative selectivity and more difficult purification during trihydroxy conversion. We have responded to these challenges by investing in improved chromatographic setup and better high vacuum handling during purification. Feedback from partners highlights the low level of aromatic impurities remaining after our process, which supports cleaner reactions—something you notice immediately when scaling up.

    Advanced Applications: Expanding Reach Beyond the Bench

    Industrial clients share stories of new resin systems and sensor materials built around the core of our trihydroxyanthracene. The molecule serves as a strong electron donor in redox polymer matrices, which bolsters conductivity in sensor coatings. The breadth of use cases spans from analytical chemistry to electroactive polymers. Some clients use the trihydroxyanthracene to prepare intermediates for pharmaceuticals, leveraging its arrangement of hydroxyls to build larger, more functional molecules. In each setting, consistency remains paramount, especially where FDA or REACH compliance depends on tight lot-to-lot purity.

    How 1,8,9-Trihydroxyanthracene Stands Apart from Related Anthracene Derivatives

    Manufacturing experience has shown us the clear distinctions among anthracene derivatives. 1,8,9-Trihydroxyanthracene differs markedly from 1,5-dihydroxy or 1,2,3,4-tetrahydroxy variants in both handling and reactivity. Batch yields differ due to the enhanced solubility in polar solvents—an attribute that can help or hinder reactions, depending on application. While the dihydroxy forms excel in specific oxidations or as limited hydrogen donors, the 1,8,9 configuration is prized for its triple hydroxyl versatility and the resulting enhanced chelating ability.

    Some researchers rely on 9,10-anthraquinone as a popular substrate, but our experience has shown that the trihydroxyanthracene’s trio of hydroxyls brings unmatched reactivity for certain esterification and coupling reactions. Process engineers trust our triol when designing layered materials, as the unique positioning of functional groups confers both planarity and hydrogen bonding network control. Our clients often remark on how switching from a dihydroxy to this triol allows them to fine-tune binding constants, stabilities, or electron donation potential in their research.

    Overcoming Reproducibility Problems in Research and Manufacturing

    Over the years, researchers have reported inconsistent yields and product behavior when relying on poor-grade or variably synthesized trihydroxyanthracene. Small impurity profiles—trace metals, oxidized byproducts, incomplete dehydration—translate into failed reactions downstream. We address this by combining careful feedstock selection, consistent oxygen source quality, and staged purification. Routinely recording melt points and color reaction results against authenticated controls allows us to verify batch-to-batch integrity. Academic and industrial partners often mention the peace of mind that comes from using material with comprehensive traceability, supported by replicable analytical verification.

    Solutions for Handling and Storage

    Handling the fine powder demands respect for both moisture and ambient oxygen. The best results come from storing in well-sealed, inert-atmosphere containers, which we supply directly from our line. Some clients worry about slow discoloration over months, but our protocol—unopened, desiccated, and away from UV—keeps the color and purity for extended periods. The powder’s tendency to aggregate under humid conditions led us to improve our drying room environment, preventing caking and sticking that complicates weighing. Experience tells us these small procedural shifts protect product value down the line.

    Supporting Sustainable Chemistry

    We hear a growing call for greener approaches and we have been evolving our process accordingly. Shifting from traditional oxidants toward more benign choices has cut the environmental impact of each kilogram produced. Water-washing regimes have given way to closed-loop solvent recovery and more efficient waste removal. Clients in research and manufacturing appreciate the detailed breakdown we provide of the process, including solvent, reagent, and energy use. Where clients need high-purity trihydroxyanthracene for use in pharmaceuticals or regulated products, this granular transparency supports safer, more documentable chains of custody.

    Collaborative Troubleshooting and Innovation

    Direct dialogue with users keeps our process rooted in real-world demands. Sometimes an academic team seeks a batch with lower residual solvent for sensitive spectroscopy; at other times, an industrial chemist needs tighter control of particle size for blending into viscous formulations. Our setup allows us to pivot and adapt to these requirements, often suggesting solutions born from troubleshooting our own production hiccups—like fine-tuning the final crystallization step or switching filtration media to reduce trace metal carry-over. Clients benefit from process notes and hands-on advice, cultivated through years of trial, feedback, and real-world use.

    Product Consistency and Batch Scale-Up Insights

    Scaling from gram to kilo quantities reveals a lot about the subtleties of this compound. Small-scale syntheses sometimes mask side-reactions or physical quirks that only show up at larger volumes. To maintain product consistency, technicians carefully monitor temperature gradients in reactors, oxygen flow rates, and purification timing. Any small deviation at scale can throw off batch quality, and even a visually subtle shift in crystal form can impact downstream efficacy. Support from routine QC feedback loops has allowed us to spot these drifts early and adjust protocols quickly—not based on a generic chart, but on the data collected in our facility, with our people, making this very product.

    Lowering the Risk of Cross-Reactivity in Production Lines

    Running multiple anthracene derivatives on the same facility line can cause cross-reactivity or contamination, if not properly segregated. Dedicated glassware, solvent streams, and documentation routines prevent accidental introduction of other hydroxyanthracenes or unwanted oxidative byproducts. It’s tempting to use a single line for efficiency, but our experience says clear separation delivers more reliable and purer trihydroxyanthracene. We encourage partners to visit or audit our process firsthand—transparency breeds trust and signals a realistic approach to dependable manufacturing in sensitive sectors.

    Responding to Regulatory and Analytical Accountability

    Trends in regulation push for detailed traceability and full batch histories, especially as trihydroxyanthracene finds more routes into regulated fields. Our records go beyond lot numbers, tracking solvents, temperature ramps, and even operator signatures on each stage. Clients heading toward regulatory submissions value being able to match our batch sheets exactly to their internal records. Years of regulatory feedback have informed even minor tweaks—such as refining the sequence of drying steps as audit responses.

    Clients rely on clear, honest answers about what we test, what we detect, and how we ensure purity. Instead of relying only on off-the-shelf test kits, we run our own analyses, cross-referencing supplier COAs with our own spectra. This extra layer of internal validation prevents surprises and reassures our industrial users who have zero tolerance for unexpected physical or chemical drift.

    Developing New Applications and Enabling Research

    As researchers uncover new reactivity or envision untested applications for trihydroxyanthracene, our plant serves as a proving ground for feasibility. Sometimes that means preparing special small batches with increased dryness or broader particle size, or collaborating on custom blends with other aromatic building blocks. Industrial innovators looking to graft functional groups or expand molecular frameworks rely on our ability to tune input variables based on open, data-driven conversations. Our in-house expertise, built from running this synthesis over many years, allows for realistic advice, not just theoretical possibilities.

    Supporting Customers With Authentic Manufacturing Experience

    Chemistry never stays static—the needs of technical teams change over time as new challenges or specifications arise. Having direct experience with the quirks of sourcing, reacting, and purifying trihydroxyanthracene means advice carries practical weight. The trust partners show by returning for repeat lots, or by asking us to troubleshoot their own syntheses, comes from sharing clear, honest information. We’ve learned to never overstate the product’s simplicity or understate the potential for problem-solving; chemicals like this demand respect and experience in every step, from raw material to final packaging.

    The Everyday Commitment to Purity and Usability

    Quality always finds its roots in daily routines: clean glassware, solid timing, careful testing, and real accountability. Whether the end use calls for a visible dye, an electronic interface, or a building block for a new pharmaceutical, trihydroxyanthracene only delivers on its potential if every gram is built on reliable chemistry. The connection between the process inside the reactor and tangible performance at the customer’s bench is what keeps us focused—not just reaching a number or hitting a COA target, but raising the standard for what anthracene derivatives can achieve in applied science and technology.

    By delivering this consistency and supporting customers with our hands-on, real-world expertise, we help drive innovation and trust. The feedback we receive continually steers our process, ensuring we address challenges before they become problems. Our commitment to transparency, responsive technical support, and constant process improvement aims to make 1,8,9-Trihydroxyanthracene a foundation for progress, not just another product on the shelf.