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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 | 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. |
Applications of 2,5-Dihydroxy-1,4-Benzoquinone in Industrial Manufacturing2,5-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 ManufacturingBattery 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
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2. Organic Semiconductor and Conductive Polymer SynthesisOrganic 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
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3. Advanced Dye and Pigment Intermediates for Specialty TextilesTextile 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
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4. Redox Mediators for Industrial Electrochemical ProcessesElectrochemical 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
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5. Analytical Reagent Preparation for Laboratory and Diagnostic KitsDiagnostic 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
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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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.