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2,5-Dihydroxy-1,4-Benzoquinone

    • Product Name 2,5-Dihydroxy-1,4-Benzoquinone
    • Einecs 204-617-8
    • 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

    882336

    Cas Number 615-94-1
    Molecular Formula C6H4O4
    Molecular Weight 140.09
    Iupac Name 2,5-Dihydroxy-1,4-benzoquinone
    Appearance Yellow to orange crystals
    Melting Point 287-290°C (decomposes)
    Boiling Point N/A (decomposes before boiling)
    Density 1.721 g/cm³
    Solubility In Water Soluble
    Pubchem Cid 11861
    Smiles C1=C(C(=O)C(=O)C=C1O)O
    Inchi InChI=1S/C6H4O4/c7-3-1-2-4(8)6(10)5(3)9/h1-2,9-10H

    As an accredited 2,5-Dihydroxy-1,4-Benzoquinone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100g amber glass bottle, tightly sealed, labeled "2,5-Dihydroxy-1,4-Benzoquinone," featuring hazard symbols and storage instructions.
    Shipping 2,5-Dihydroxy-1,4-Benzoquinone is shipped in sealed, chemical-resistant containers to prevent moisture absorption and contamination. The containers are labeled with hazard information and handled according to safety regulations. Transport complies with local and international guidelines for chemicals, ensuring secure packaging, limited exposure, and appropriate documentation throughout shipping.
    Storage 2,5-Dihydroxy-1,4-Benzoquinone should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizing agents. Store at room temperature in a cool, dry, and well-ventilated area. Ensure the container is clearly labeled, and avoid excessive heat or direct sunlight to preserve stability and prevent decomposition of the compound.
    Application of 2,5-Dihydroxy-1,4-Benzoquinone

    Applications of 2,5-Dihydroxy-1,4-Benzoquinone in Industrial Manufacturing

    2,5-Dihydroxy-1,4-Benzoquinone is a specialized quinone derivative used in several advanced chemical manufacturing sectors. Our material supports demanding downstream processes that require stringent compliance, reliable batch consistency, and high-performance oxidation or redox properties. Below we detail practical application scenarios where our customers incorporate this raw material, highlighting its integration into distinctive production environments.

    1. High-Performance Lithium-Ion Battery Electrode Manufacturing

    Battery manufacturers employ 2,5-Dihydroxy-1,4-Benzoquinone as an organic cathode component due to its reversible redox chemistry and stable cycling characteristics. It is integrated into next-generation lithium-ion and sodium-ion battery platforms focused on sustainability and high energy density. The compound’s unique electron-accepting profile addresses requirements for eco-friendly, cobalt-free battery technologies within the rechargeable cell industry.

    Industry compliance standards

    • IEC 62660-2 (Secondary lithium-ion cells for automotive applications – Safety requirements)
    • RoHS Directive (2011/65/EU) for heavy metal and substance restrictions
    • GB/T 31484-2015 (Chinese standard for lithium-ion batteries cyclic performance)
    • ISO 9001:2015 certified production/QC systems

    Typical usage ratio

    • 2–12% by total cathode blend weight; adjusted for cell design, target capacity, and cycling profile

    Downstream process integration

    • Mixing into cathode slurry during wet preparation prior to electrode coating; follows substrate drying, calendaring, and cell stacking

    Final product types

    • Rechargeable Li-ion battery cells (pouch, cylindrical, prismatic)
    • Stationary energy storage batteries
    • Electric vehicle and e-bike battery modules

    2. Organic Semiconductor and Conductive Polymer Synthesis

    Organic electronics producers adopt 2,5-Dihydroxy-1,4-Benzoquinone as a key building block in the controlled polymerization of n-type semiconducting materials. It serves both as a redox-active monomer and a dopant precursor, enabling fine-tuning of charge transport and stability in organic field-effect transistors, flexible displays, and printed circuitry. The compound’s electronic structure underpins reproducible batch polymerization in commercial-scale synthesis lines.

    Industry compliance standards

    • Directive 2011/65/EU (RoHS)
    • REACH Regulation (EC) No 1907/2006 (SVHC screenings for electronic-grade materials)
    • IEC 62341-5-1 (OLED display materials reliability testing)

    Typical usage ratio

    • 0.5–4 mol% relative to primary polymer monomer; varied to maintain conductivity and film thickness per device design

    Downstream process integration

    • Incorporation during monomer solution blending; used in step-growth polymerization or in-situ doping stages prior to thin film deposition

    Final product types

    • Flexible polymer-based semiconductors
    • Organic TFT displays
    • Printed logic circuits

    3. Advanced Dye and Pigment Intermediates for Specialty Textiles

    Textile and pigment manufacturers use 2,5-Dihydroxy-1,4-Benzoquinone in targeted synthesis of complex azo and anthraquinone dye precursors. It acts as a controlled oxidation agent and chromophore modifier, enabling reproducible hue development, especially in the production of high-fastness dyes for technical fibers and performance apparel. Its reactivity supports continuous flow synthesis and batch dye manufacturing lines geared for industrial textiles.

    Industry compliance standards

    • OEKO-TEX Standard 100 Class I-IV limits for textile chemicals
    • ZDHC MRSL (Level 3) compliance for auxiliary dye substances
    • EN 71-3 (Migration of certain elements in toys and children’s textiles)
    • ISO 14001 for environmental management systems

    Typical usage ratio

    • 0.2–1.5% of total dye batch weight, customized based on fiber substrate and shade intensity

    Downstream process integration

    • Initiated during dye precursor formation; enters at the oxidation step before coupling, followed by purification, blending, and granulation or standardization

    Final product types

    • Reactive and disperse textile dyes
    • Anthraquinone pigment intermediates
    • Colorants for flame-retardant synthetic fibers

    4. Redox Mediators for Industrial Electrochemical Processes

    Electrochemical manufacturers deploy 2,5-Dihydroxy-1,4-Benzoquinone as a water-soluble redox mediator to accelerate selective oxidation reactions and electron transfer in metal-recovery electrolytic cells. Its high redox potential and stability in aqueous and non-aqueous media support efficient, cost-effective turnover across recovery, refining, and organic electrosynthesis platforms. This compound streamlines yields and process selectivity in chemical plants piloting green electrochemical methodologies.

    Industry compliance standards

    • ISO 18314-2 (General tests of chemical analysis in electrolytic processes)
    • OSHA 29 CFR 1910.119 (Process safety management for chemical production)
    • Directive 2012/18/EU (Seveso III for hazardous substances handling in the EU)

    Typical usage ratio

    • 50–200 mg/L in process electrolyte solution; levels optimized for target substrate and current density

    Downstream process integration

    • Dosed into recirculating electrolyte just before electrolysis; maintained via automated dosing systems during operation

    Final product types

    • Refined electronic-grade metal salts
    • Electrochemically produced specialty organics
    • Waste minimization secondary raw materials

    5. Analytical Reagent Preparation for Laboratory and Diagnostic Kits

    Diagnostic kit and research reagent producers value 2,5-Dihydroxy-1,4-Benzoquinone as a redox indicator and substrate in colorimetric and electrochemical assays. Its defined redox potential and pure spectral signature achieve high sensitivity and reproducibility, supporting enzyme kinetics studies, food safety testing, and biochemistry kits. Stringent source traceability and low metal contaminant profiles ensure laboratory reliability for regulated analytical supply chains.

    Industry compliance standards

    • ISO 13485:2016 for In Vitro Diagnostic (IVD) reagent manufacturing
    • EP/USP analytical reagent monographs
    • CFR 21 Part 820 (FDA Quality System Regulation, laboratory diagnostics)

    Typical usage ratio

    • 10–200 μM concentration in assay buffer or preparation, specified per method protocol

    Downstream process integration

    • Introduced during reagent blending; aliquoted or lyophilized in final test kit packaging for end-user dilution

    Final product types

    • Clinical diagnostic colorimetric kits
    • Enzyme assay substrates
    • Ready-to-use laboratory reagent vials
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    Certification & Compliance
    More Introduction

    2,5-Dihydroxy-1,4-Benzoquinone — A Behind-the-Scenes Look at a Versatile Chemical

    What 2,5-Dihydroxy-1,4-Benzoquinone Brings to the Table

    Producing 2,5-Dihydroxy-1,4-Benzoquinone, often called DHBQ, has shaped our understanding of how subtle chemistry can make an outsized difference across a wide range of industries. This substance has held onto a reputation for reliability and unique function, earned by years spent in labs, plants, and workshops all over the world. Anyone who spends enough time around organic chemistry recognizes how DHBQ manages to anchor itself in niche applications while also opening up paths for innovation.

    We manufacture DHBQ in batches controlled with attention to detail every step of the way. Getting to a point where the product meets strict standards—solid, reddish crystals, melting in the 200–205°C range—requires patience and an appreciation for small process variables. The dedication stems from knowing that even minute impurities or shifts in handling create ripple effects for customers downstream, especially those in specialty materials, electrochemical research, and advanced coatings work.

    DHBQ vs. Other Benzoquinones

    Among benzoquinones, DHBQ carves out a technical and practical territory of its own. Compared to the more ubiquitous 1,4-benzoquinone (para-benzoquinone), DHBQ stands apart because of its paired hydroxy groups. This symmetrical addition of hydroxyls at the 2 and 5 positions transforms reactivity, solubility, and hydrogen-bonding traits. The core looks familiar, but the chemistry shifts dramatically. These hydroxyls enable varied coordination patterns and redox activity that lead to applications not available with other benzoquinones.

    For researchers and engineers, the choice between classical 1,4-benzoquinone and DHBQ hinges on the target transformation or the properties sought in a final product. DHBQ’s dual hydroxy groups encourage complex molecular assemblies and metal-ion binding that set the stage for new families of conductive polymers, charge-transfer complexes, and hybrid materials. Start exploring organic electronics or energy storage, and it soon becomes clear why DHBQ often takes priority over its relatives.

    Applications That Rely on Consistency and Quality

    Labs and manufacturers come back to DHBQ because of its reproducible performance. For years, we’ve watched research groups push the envelope for organic battery and supercapacitor technologies, using DHBQ as a redox-active core. Energy storage devices that combine reasonable potential, reversibility, and environmental compatibility call for raw materials free of unwanted side reactions. Our experience tells us that stable sourcing—from precise starting materials to careful recrystallization—pays off downstream, especially at scale.

    The realm of organic semiconductors and conductive polymers also builds on DHBQ. People expect more than simple performance metrics. They want control over electrical properties, with the option to tune redox potentials or film formation. DHBQ’s structure, with its hydrogen-bond donors and acceptors, offers a platform for exploring supramolecular systems and crosslinked networks.

    For us, ensuring each lot of DHBQ displays reproducible color, melting behavior, and crystalline structure stands as a point of pride. Customers in pigment formulation and dye research tell us how much they depend on those attributes, especially when developing materials for printing, inkjet, or textile applications. The strong chromophore and its consistency allow researchers to screen colorfastness, photostability, and interaction with mordants—without having to re-profile for every batch.

    Handling, Stability, and Scale-Up—A Manufacturer’s Perspective

    Producing and handling DHBQ on a manufacturing scale brings daily exposure to challenges different from those in a small research environment. Over the years, we have wrestled with purity targets, product stability, and the practicalities of scale-up. Hydroxyquinones tend to oxidize further or undergo side reactions if exposed to certain contaminants. Routine batch monitoring picks up on the subtle color changes or shifts in melting point, signaling the need for tighter controls or, sometimes, a return to the foundational synthesis steps.

    Scale-up is not just a matter of multiplying quantities. The reality involves recalculating solvent loads, heat transfer, crystallization rates, and mechanical handling. For instance, the tendency of DHBQ to sublimate or discolor below its melting point becomes a genuine process hazard unless humidity and temperature are tightly regulated. Tanks, reactors, lines, and storage bins see regular inspection because any contamination—especially from reductants or transition metals—has the potential to change final product specs. People may not see these day-to-day process details, but the final bags of DHBQ reaching the client are the outcome of this attention.

    Improving Supply Chain Reliability for Research and Industry

    Long-term partnerships grow from reliable supply, predictable quality, and responsiveness during bottlenecks. Over time, we’ve adapted internal logistics around these lessons. DHBQ cannot always move in the same channels as simpler aromatic compounds. Packaging must defend against light, air, and moisture, so drums are lined, shipments use desiccants, and lot traceability stays up-to-date. On-site quality labs cross-check each new run, which lets downstream users order with confidence that physical and chemical properties will match historic shipments.

    The shift to greener chemistry has increased demand for high-purity DHBQ from the battery and electronics world. Researchers seek to avoid trace metal catalysts and halogenated solvents both in their own labs and in the chemicals they procure. We focus on routes that avoid hazardous raw materials and promote recovery of spent process streams. These changes don’t just improve product safety—they keep waste down, streamline regulatory filings, and enhance product acceptance for environmental labeling.

    Supporting Innovation in Materials Science

    Chemists, engineers, and R&D teams build new technology on dependable building blocks. In organic frameworks, redox-active molecules serve as fundamental scaffolds. DHBQ holds a central position in the design of hydrogen-bonded organic frameworks, charge-transfer salts, and new coordination polymers. These systems open up possibilities for sensing, exchange membranes, or selective catalysis—sometimes in unanticipated directions.

    Working with research consortia, we’ve noticed firsthand how the nuanced reactivity of DHBQ supports the construction of supramolecular assemblies or electroactive frameworks. The ability to form dense hydrogen-bonded chains, support reversible electron transfer, or chelate specialty metals pushes development into new territories. Each time a customer launches a new line of sustainable energy devices or pushes the limits of polymer conductivity, we see our own process improvements reflected in their results.

    Understanding Market Shifts and Regulatory Realities

    DHBQ’s appeal is broadening, along with the pressure for clear regulatory compliance and sustainability benchmarks. Compliance audits, documentation, and real traceability now matter in nearly every region we supply. Tracking material provenance and process chemistry earns us trust from partners in pharmaceutical research, electrochemical device manufacturing, and functional dye production. Our site checks trade compliance, follows green chemistry guidelines, and stands open to customer audits whenever necessary.

    Regulatory changes sometimes arrive faster than anticipated. For example, the tightening of limits for certain organic impurities or solvent residues has forced redesigns in multiple steps of the DHBQ process. Chronic vigilance, combined with flexibility at the plant floor, becomes essential. Real-world examples have shown that advance warning—tracking changes in allowable impurity profiles or documenting improvements in environmental health and safety—translates into smoother transitions for customers and more sustainable supply.

    The Real-World Impact: Customers and Outcomes

    Customer stories often teach us more than technical treatises. Electrochemistry startup teams share how trace-level consistency in DHBQ purity let them push battery prototypes closer to commercial launch. Color chemistry labs report testing multiple sources before settling on batches with the most reliable photostability. Among specialty chemical producers, headaches disappear when every shipment matches up—granule size and color, melting point and IR spectrum, all in the expected range.

    Balancing technical progress with practical realities calls for a manufacturer willing to take responsibility for the product through its entire journey. From site-specific packaging for sensitive users to troubleshooting shipment delays, supporting customers doesn’t stop at the warehouse door. Responding to questions—about handling, application, regulatory status, or competitive comparison—forms a daily part of the manufacturing routine. This feedback loop closes the gap between research ambitions and real, workable results.

    Technical Nuances: Synthesis, Purification, and Verification

    Producing DHBQ starts with a grasp of oxidative chemistry and precision machinery. Bulk starting materials, typically hydroquinone derivatives or related phenols, demand precise reactivity control under defined temperature and pressure. The details—the rate of oxidant feed, the solvent choice, the timing on filtration—make all the difference. Minor lapses can result in excessive side products, poor yield, or product instability. Distilling practical wisdom from repeated batch runs, our team adjusts each step based on direct observation of product behavior.

    Purification means more than just a final recrystallization. Protective atmospheres, temperature staging, and multi-solvent washing contribute to the color and shelf stability customers expect. Downstream, drying systems must avoid overheating or atmospheric exposure that could prompt decomposition. Each technician tasked with sampling and analysis learns that visual inspection still ranks alongside HPLC and NMR; off-color fractions are removed before final lot assembly.

    Verification layers analytical tools so every batch can be compared to historical records: melting point, NMR, FTIR, UV-vis absorbance spectra, even particle size distribution for certain end uses. Meeting both established pharmacopeia standards and the creative needs of advanced materials developers makes the entire operation more responsive to evolving targets.

    Facing the Next Generation: Evolving Uses for DHBQ

    The push for renewable energy and biodegradable materials accelerates demand for organic, metal-free, and sustainable functional molecules. DHBQ’s clean redox profile and compatibility with solvent-free fabrication methods slot comfortably into this agenda. Battery designers look for molecules with tunable redox states, predictable degradation products, and compatibility with greener electrolytes. Textile innovators rely on stable, photoreactive cores that don’t fade or degrade under modern processing conditions.

    Every time we walk the manufacturing floor or review new research partnerships, the quiet reliability of DHBQ comes back into focus. Unlike more hazardous or volatile relatives, DHBQ strikes a balance between reactivity and storage. It lets manufacturers work without excessive special handling, and it supports broad exploration of function—whether in a dye, a film, or a hybrid composite.

    A Manufacture’s Takeaway — Value, Trust, and Ongoing Progress

    Manufacturing DHBQ demands a level of personal investment. Years spent refining batch protocols, walking through analytical results, and digging through customer feedback build up the institutional expertise that customers come to expect. Price and availability matter, but so does working with a supplier who understands the variable demands and nuanced requirements of complex chemical industries.

    Looking to the future, continued improvements in process sustainability and product traceability will shape both our operation and the downstream sectors reliant on DHBQ. Pushing for even tighter impurity profiles, introducing real-time analytics, and integrating renewable sourcing options have already shown promise in pilot runs. The willingness to change, grounded in a foundation of experience with what works and what doesn’t, marks the difference between a commodity vendor and a committed partner.

    We welcome engineers, researchers, and formulators to share feedback and ideas about new uses, needed specifications, or support through the regulatory landscape. Sharing knowledge about how DHBQ performs in practice keeps our process grounded and reinforces the ties between tried-and-true production and innovation. This ongoing exchange ensures DHBQ will continue shaping science and manufacturing, offering reliability where it matters and versatility where opportunity arises.