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HS Code |
976541 |
| Iupac Name | 2,6-Dimethoxy-1,4-benzoquinone |
| Molecular Formula | C8H8O4 |
| Molecular Weight | 168.15 g/mol |
| Cas Number | 530-61-6 |
| Appearance | Yellow crystalline solid |
| Melting Point | 168-170 °C |
| Boiling Point | 391.3 °C at 760 mmHg |
| Solubility In Water | Slightly soluble |
| Density | 1.328 g/cm³ |
| Smiles | COC1=CC(=O)C(=C(OC)C1=O) |
| Pubchem Cid | 10345 |
As an accredited 2,6-Dimethoxy-1,4-Benzoquinone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2,6-Dimethoxy-1,4-Benzoquinone; features tamper-evident cap and chemical hazard labeling. |
| Shipping | 2,6-Dimethoxy-1,4-Benzoquinone is shipped in tightly sealed containers, under cool, dry conditions to prevent moisture absorption and degradation. It should be labeled according to chemical hazard regulations, and handled with care during transport to avoid exposure. Ensure compliance with local, national, and international shipping guidelines for hazardous substances. |
| Storage | 2,6-Dimethoxy-1,4-Benzoquinone should be stored in a tightly closed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Ensure it is kept away from incompatible substances such as strong oxidizers and bases. Properly label the storage container and handle the chemical using appropriate personal protective equipment to prevent exposure. |
Applications of 2,6-Dimethoxy-1,4-Benzoquinone in Industrial ManufacturingAs a direct manufacturer of 2,6-Dimethoxy-1,4-Benzoquinone, we have supported clients in multiple specialized industries with consistent material quality and transparent application guidance. Below, we present key industrial application scenarios where this compound delivers function-critical performance and meets rigorous compliance and process standards. 1. Electron Transfer Mediators in Enzymatic Glucose SensorsIndustrial-scale glucose biosensor manufacturing utilizes 2,6-Dimethoxy-1,4-Benzoquinone as an essential electron transfer mediator due to its redox properties and chemical stability. The compound gets directly integrated within the enzyme matrix layer during screen printing or electrodeposition steps, supporting consistent electron shuttling between glucose oxidase and the electrode. Manufacturers must calibrate content based on electrode surface area and enzymatic activity, closely matching international sensor reliability and biocompatibility standards. The resulting biosensors target clinical diagnostics, food processing, and fermentation monitoring tools. Industry compliance standards
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2. Photoinitiators and Quenchers for Photoresist ProcessingAdvanced photoresist formulations in semiconductor and printed circuit board (PCB) industries employ 2,6-Dimethoxy-1,4-Benzoquinone as a photoactive additive. The compound functions as an effective photoinitiator or as a quencher to modulate radical polymerization rates in negative working resists. It enters the blending stage alongside primary photoinitiators and sensitizers, allowing precise control of cross-linking depth and profile under UV exposure. Strict adherence to electronic-grade purity and process contamination limits is essential for downstream lithography and etching success. Industry compliance standards
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3. Redox Catalysis for Fine Chemicals SynthesisProducers of specialty organics and pharmaceutical intermediates utilize this benzoquinone derivative as a stoichiometric or catalytic oxidizing agent in highly controlled batch or flow processes. Its stable redox cycling and minimal byproduct formation are vital for yield optimization and purification efficiency. It typically enters the reaction vessel during charge make-up, either as a slurry or dissolved in compatible solvents, timed with substrate feed. Adherence to cGMP principles for batch traceability is standard in pharma applications, with comprehensive HPLC-based QC procedures mandated downstream. Industry compliance standards
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4. Electrochemical Research ReagentsAcademic and industrial R&D facilities frequently require 2,6-Dimethoxy-1,4-Benzoquinone as a model compound for studying electron transfer, charge transport, and redox cycling within electrochemical cell construction. Laboratories use it in electrolyte and electrode formulations to test device stability and degradation diagnostics. Material is introduced during electrolyte blending, coin cell assembly, or ink formulation, with documentation of dosage and purity levels per lab safety and analytical protocols. Industry compliance standards
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5. Oxidative Polymerization Initiators for Conductive PolymersManufacturers of conductive polymer coatings and films—such as those based on polyaniline or polypyrrole—may leverage this benzoquinone as an initiator or co-initiator in oxidative polymerization systems, supporting efficient polymer chain growth with few side reactions. The chemical is introduced at the monomer blending stage or added incrementally during the polymerization run under rigorous process control. The resulting materials are specified for advanced electronic applications and anti-corrosive coatings. Industry compliance standards
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Meeting the needs of our customers means understanding the real-world impact of a product, not just its molecular formula. In our production halls, 2,6-Dimethoxy-1,4-Benzoquinone, known to those in the chemistry sector for its distinctive quinone core structure, has proven its value far beyond its appearance on a technical data sheet. Our team knows that every shipment leaving our plant carries not just chemical powder but the effort, precision, and trust built into every batch. Years in chemical manufacturing have made clear: consistency in purity, crystal formation, and the absence of unwanted isomeric by-products mean less waste, more predictable reactions, and stronger end products.
We have worked with this compound long enough to appreciate the subtleties in its behavior. Its pale yellow hue hints at the reactivity that synthetic chemists pursue. Our facility assures customers that each batch matches the rigorous expectation tied to years of hands-on trial and process optimization. Early on, we learned that keeping metal-ion contamination low preserves its reactivity as an electron acceptor, especially when used in organic synthesis or as an intermediate.
Engineers and researchers look for more than just a CAS number. A pure sample of 2,6-Dimethoxy-1,4-Benzoquinone arrives as fine crystals, free-flowing and stable under dry, cool conditions. At our site, every lot is checked for melting range, purity by HPLC, and residue on ignition. Our preferred recovery method minimizes degradation and oxidation at each stage. Keeping the moisture content minimal extends the shelf life and simplifies dissolution in common organic solvents, which many customers appreciate when scaling up reactions or preparing analytical standards.
Supplying this molecule across electronics, pharmaceuticals, and specialty chemistry has shown us the value of lot-to-lot reliability. This attention to process stability reflects in the final product, especially when high yield and low impurity levels are essential. Customers have told us that their most sensitive work—especially those relying on redox mediation or electron transfer—depends heavily on knowing the starting material’s purity is not just a number but a guarantee rooted in continuous process improvement.
We have seen 2,6-Dimethoxy-1,4-Benzoquinone prove itself as an antioxidant and redox mediator across various settings. In our experience, the way it stabilizes free radicals gives it an edge over more common benzoquinones, thanks in large part to the electron-donating methoxy groups at the 2 and 6 positions. This structure also enhances solubility in organic solvents, which researchers in pharmaceuticals and polymer science value.
In lab-scale synthesis, this molecule serves as an essential intermediate, especially when synthesizing complex heterocycles or modifying biologically active scaffolds. It shows a tendency to offer selectivity in oxidative coupling reactions, which has caught the attention of several clients aiming to scale up production of key building blocks. We have supplied kilogram quantities for research into polymerization catalysts, where its controlled redox activity minimizes side reactions compared to the simpler 1,4-benzoquinone or its 2,5-dimethoxy isomer.
Some of our long-term partners in the electronics sector rely on its electron-accepting abilities for developing organic semiconductors. Here, the distinction between high-purity and off-color sample material can translate into significant differences in device performance, as trace contaminants or moisture can undermine sensitive organic electronic devices. In these applications, our control over residual metal and solvent levels sets us apart—reviewed with methods such as ICP-MS and Karl Fischer titration, developed over years of direct feedback from users pushing the boundaries of thin-film electronics or photochemical devices.
In the field of natural product synthesis, chemists often choose this molecule to test new catalytic cycles or explore oxidative transformations with milder conditions. As the manufacturer, we pay close attention to feedback about solubility, dusting characteristics, and packaging integrity, which can shave hours off prep times in high-throughput labs.
Our teams have spent years comparing 2,6-Dimethoxy-1,4-Benzoquinone with more common quinones such as 1,4-benzoquinone or the 2,5-dimethoxy variant. In practice, the methoxy group placement changes both the electron distribution and the solubility profile, which directly affects how the compound performs in a given reaction.
For researchers who run iterative syntheses or screening campaigns, the difference can be glaring. The 2,6-disubstituted material offers higher solubility in polar aprotic solvents, and a marked increase in reactivity under mild conditions. This allows for lower loadings and fewer by-products, reducing purification time and waste disposal cost. The unique arrangement of methoxy groups blocks certain side-reactions that plague unsubstituted benzoquinones, especially in catalytic and photochemical applications where over-oxidation and polymerization are prevalent risks.
The 2,5-dimethoxy alternative, often considered for its own chemical niche, displays a different electronic environment. We have run side-by-side tests and fielded feedback from process chemists who say that the 2,6 variant they receive from us grants more reproducible control over redox potential, which is vital for fine-tuning catalytic cycles or designing novel organic electronic components. These differences, tangible inside our plant and at our customers’ benches, shape the choice between one product and another.
Our production records reveal fewer complaints and more reorders where 2,6-dimethoxy material replaces the 2,5- isomer, especially for research projects focused on fine chemicals, pharmaceuticals, or material science. Clients frequently mention how the consistency of our 2,6- product simplifies switching protocols. For us, these outcomes point to the clear chemical distinction—and practical benefits—of staying true to this specific substitution pattern.
From sourcing starting materials to final packaging, overseeing the process as a manufacturer leaves little room for shortcuts. We have invested in reaction vessels that resist corrosion and cross-contamination, and each solvent batch is tracked with a full certificate of analysis. This level of scrutiny isn’t just about compliance; it’s rooted in the moments when a small trace of impurity caused a customer to lose weeks of work. Our staff has tracked down every possible route for contamination, from glassware rinses to the seals on our drum closures. Anyone running a pilot plant or a kilo-lab knows the value of this vigilance.
Years ago, an off-color batch taught us a valuable lesson: not all crystallization techniques deliver the same particle morphology or purity. Since then, we’ve refined our filtration and recrystallization steps, using methods developed in our own analytical department. We calibrate our detection instruments regularly, and rotate stock to avoid aging issues—particularly discoloration or changes in flow that can indicate degradation.
Every batch comes with a printout of its chromatographic trace, and our team keeps open lines with researchers who try new formulations or push for ultra-high-purity lots for regulatory submissions. Direct feedback has shaped our workflows: customers who needed reliable results for scale-up or process validation helped us set stricter batch-release criteria, often higher than industry minimums.
We have spent time with formulators, bench chemists, and production supervisors to redesign our packaging. Our containers feature tamper-proof seals and resealable liners, made from chemically compatible plastics that resist static and moisture ingress. Our logistics crew minimize cycling through different temperature environments to limit any risk of caking or degradation before the product reaches your bench. This attention to detail matters most on days when tight timelines hinge on reliable supply.
Our labels provide clear information, lot numbers, and QR codes for instant access to batch documentation—a request that came from a process manager looking to cut down on paperwork during audits. Each change in packaging design comes from a real challenge faced in the field, not a marketing pitch.
Having built up a customer base that stretches from university research labs to multinational pharmaceutical R&D teams, we have learned to see the world from both the tiny microgram scale and the scale-up stages that fill drums. Whether for an innovation in organic electronics or a pilot batch of a new active ingredient, each group expects more than just quick delivery. They want knowledge—gleaned from daily experience.
We document every out-of-spec incident, trace its source, and log corrections in a system we review each quarter. A few years ago, our product manager noticed that researchers working in photochemistry labs raised concerns about product discoloration. Investigations led to upgrades in our packaging and inert gas purging routines, which have since become standard. Customer questions about application-specific requirements often result in custom batch preparations, finished with different drying, milling, or sieving protocols.
Rapid iterations and honest technical support have become our hallmark. This flow of information, from bench to production to support, closes the loop, leading our team to detect issues earlier and roll out improvements that stick. We have adopted process analytical technology to follow reactions in real-time, reducing impurity formation at source rather than relying on end-of-line clean-up.
Supplying a compound used in regulated sectors means more than keeping assays high. We coordinate with compliance consultants and maintain a documentation chain that covers batch traceability, controlled substance declarations, and up-to-date safety and environmental data. We have walked auditors through our plant and responded to their recommendations, streamlining areas such as material transport and waste minimization.
Our safety officers have developed batch documentation tailored to customer needs, answering questions from downstream users who depend on transparency and clear origin data for regulatory filings. As more industries adopt stricter quality norms, our aim is to anticipate new compliance standards rather than just react.
Environmental responsibility shapes our solvent recycling practices and emission controls. Every kilogram of 2,6-Dimethoxy-1,4-Benzoquinone passes through quality gates with environmental criteria as critical as yield or color. We review supplier certifications regularly, working with partners who share the same focus on verified, sustainable sourcing.
After years as a chemical manufacturer, we recognize no two batches are identical. Small variances in temperature control, raw material lot, or minor impurities in process water once led to unexpected outcomes in demanding syntheses. Our production experts now chart every run, noting subtle changes in crystal size, color development, or filtration rate, which feed back into improved process control.
Customers pushing the boundaries in their industries often come back to us with new requirements. They may seek a different particle size for flow reactors or higher lots for evaluation of new synthetic pathways. We respond with pilot campaigns using the same analytical rigor as our standard offerings. This real-world data gets incorporated into future batch runs, making our process not static but continuously responsive to practical feedback.
Lessons gained from handling spills, refining storage protocols, or troubleshooting material inconsistency translate into a shared body of experience that shapes our next batch. For new users or those facing specific technical hurdles, our technical staff can walk through these scenarios, help troubleshoot and suggest adjustments learned over hundreds of production runs.
Chemists and engineers evaluating this product ask targeted questions about purity, stability, and performance in their specific processes. With our position as a direct manufacturer, we can answer these inquiries with actual run data, root cause analyses, and documented process changes. Our bulk customers ask for long-term supply contracts, and our team coordinates production schedules and raw material procurement well in advance to avoid shortages or abrupt changes in quality.
Those moving from benchtop scale to pilot production frequently need stepwise increases in quantity. We accommodate these with staged batch releases, each matched to detailed quality reports. Our delivery records and customer follow-up show that this staged approach minimizes project delays and allows researchers to catch and resolve formulation or process issues before large-scale commitment. For start-ups or established firms, this means managing risk more effectively.
Over time, many customers mention that their own internal audits or quality initiatives benefit from direct communication with the production floor. We encourage site visits, provide analytical support, and test returned samples to close the feedback cycle. This keeps us accountable and drives home the notion that no product sits in a vacuum—it always fills a need shaped by real projects and the lessons learned under pressure.
We often see our 2,6-Dimethoxy-1,4-Benzoquinone take on unexpected roles. Whether catalyzing novel cross-coupling reactions or stabilizing delicate functional groups in new drug scaffolds, the range of applications widens as our partners push into new territories. Some bring us details about niche processes, such as electrochemical sensors or tunable organic photovoltaic devices, that require enhanced oxidation stability or tighter particle size distribution.
In conversations with innovators, we collaborate to redesign synthesis pathways or trial alternate purification methods, often resulting in custom product grades. Shared technical sessions help explain anomalies or find routes around bottlenecks. This spirit of collaboration, rooted in technical transparency and pragmatism, gives rise to improvements that ripple back into our catalog offerings.
Customers with a need for ultra-low contaminant levels suggest ideas for extra purification steps or special packaging to meet sensitive detection limits. In response, we prototype smaller scale crystallizations, run extra analytical checks, and document each step so others benefit from the process.
Having made, handled, and shipped tons of 2,6-Dimethoxy-1,4-Benzoquinone over years, our facility stands as a testament to the value of deep institutional knowledge. Continuous investment in our people—training in analytical techniques, understanding failure modes, sharing best practices—ensures our product keeps pace with rising expectations.
Users needing higher batch consistency, stricter control over trace metals, or finer crystal fractions have shaped not just our process but our company. We see ourselves as custodians of proven methodology, open to change through shared learning, with every drum that leaves our site carrying our hard-earned reputation.
In an industry where reputation rests on the smallest detail, and where unchecked assumptions can result in lost opportunities or compromised research, we believe in the value of open dialogue and thorough documentation. Each lot represents hundreds of decisions, from raw material selection to drying conditions, all of which stem from the lessons and relationships built over decades of direct manufacture.