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HS Code |
926340 |
| Chemical Name | 2,3-Dimethoxy-1,4-Benzoquinone |
| Molecular Formula | C8H8O4 |
| Molecular Weight | 168.15 g/mol |
| Cas Number | 2091-50-3 |
| Appearance | Yellow to orange crystalline solid |
| Melting Point | 162-165°C |
| Solubility In Water | Slightly soluble |
| Density | 1.35 g/cm³ (approximate) |
| Smiles | COC1=C(C(=O)C=C(C1=O)OC) |
| Inchi | InChI=1S/C8H8O4/c1-11-5-3-6(9)8(12-2)7(10)4-5/h3-4H,1-2H3 |
| Synonyms | 2,3-Dimethoxy-p-benzoquinone |
As an accredited 2,3-Dimethoxy-1,4-Benzoquinone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging contains 10 grams of 2,3-Dimethoxy-1,4-Benzoquinone, sealed in an amber glass bottle with tamper-evident cap. |
| Shipping | 2,3-Dimethoxy-1,4-Benzoquinone is shipped in tightly sealed containers, protected from moisture, light, and incompatible substances. It should be handled with appropriate safety precautions, including labeling as a harmful or irritant substance. Shipping complies with relevant regulations for chemicals, typically via ground or air, ensuring safe and secure transport to prevent leaks or spills. |
| Storage | 2,3-Dimethoxy-1,4-Benzoquinone should be stored in a tightly sealed container, protected from light, moisture, and heat. Keep it in a cool, dry, and well-ventilated area away from incompatible substances such as strong reducing agents or acids. Store under an inert atmosphere if possible to prevent oxidation and degradation. Clearly label the container and ensure safe handling procedures. |
Applications of 2,3-Dimethoxy-1,4-Benzoquinone in Industrial Manufacturing2,3-Dimethoxy-1,4-Benzoquinone supports key production processes across specialty chemical manufacturing. The following scenarios reflect established industrial integrations, highlighting technical requirements and regulatory alignment from a direct producer’s experience. 1. Enzymatic Co-Substrate in Biocatalytic GlycosylationEnzyme manufacturers regularly incorporate 2,3-Dimethoxy-1,4-Benzoquinone as a redox-active co-substrate for laccase-mediator systems during the enzymatic conversion of phenolic compounds. Its defined electron transfer properties enhance glycosylation reactions, increasing product conversion rates and selectivity where downstream purification and reproducibility are essential for specialty intermediates. Industry compliance standards
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2. Intermediate for Agrochemical SynthesisAgrochemical formulators integrate this material as a redox intermediate in the multi-step synthesis of selective pesticides and herbicides. The compound’s specific oxidation-reduction behavior enables controlled transformation of aromatic starters, supporting reproducible synthesis routes for active agro ingredients that undergo further purification and formulation prior to field applications. Industry compliance standards
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3. Electron Mediator in Electrochemical Sensor ManufacturingProducers of electrochemical biosensors apply 2,3-Dimethoxy-1,4-Benzoquinone as an electron mediator in sensor electrode modification. It enables the mediation of electron transfer between biological recognition elements and conductive substrates, resulting in improved detection limits and signal reproducibility for glucose and other analyte sensors manufactured at scale for biomedical and food analysis markets. Industry compliance standards
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4. Photoinitiator Carrier in Specialty Inkjet Ink FormulationsDigital ink manufacturers incorporate this compound as a photoinitiator carrier for cationic UV-curable inkjet inks. Its predictable release of radical species under controlled UV exposure enables consistent curing rates for specialty graphic and electronic printing. Manufacturers rely on its stability and reproducibility during large batch dispersion and inklet assembly. Industry compliance standards
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In our plant, we produce a wide spectrum of fine chemicals, but 2,3-Dimethoxy-1,4-Benzoquinone holds a special place on the line. This compound, known for the model name DMBQ, comes in as a bright yellow crystalline powder. Chemists and manufacturers know its structure well—two methoxy groups on the benzoquinone backbone change how it reacts, stores, and functions. Over the years, we have fine-tuned its synthesis to focus on reliability, purity, and process efficiency. Consistency takes real-world effort: maintaining stable reaction conditions, guarding against contamination, and mastering post-synthesis purification. We see our buyers notice the difference when these factors get attention in the production stage.
Here at our facility, DMBQ exits the reactor with purity levels commonly above 98%, often even tighter through recrystallization and filtration. Particle size isn’t just an afterthought—grinding and sieving during final processing help with downstream usage, whether it’s destined for research or production-scale purposes. Melting point for DMBQ sits around 195–198°C, an aspect we consistently verify to anchor identity and purity checks. In moisture-sensitive work, our processes ensure water content stays below 0.2%, which prevents unwanted reactivity on customer end. Each lot undergoes full spectral analysis—NMR, IR, trace analysis—so researchers and technicians trust that each shipment means what it says on the label.
Those working in organic synthesis know DMBQ as an oxidant and electron transfer agent. We notice recurring orders from labs focusing on bioorganic conversion, radical cyclization, and redox regulation. Medicinal chemists turn to this molecule in synthesis cycles for developing active pharmaceutical ingredients and exploring natural product analogs. DMBQ catalyzes transformations that demand mild conditions, so it often finds use in pharmaceutical screening or research on enzyme-mimics. On the industrial side, we supply specialty polymer and dye manufacturers needing redox reagents that do not introduce metal ion impurities. Small but distinct differences in purity—or in isomeric byproducts from careless production—change performance in such applications, so our quality control pays dividends far beyond the plant gate.
Choosing between different benzoquinones isn’t just a matter of price or purity. The substitution at the 2,3-positions with methoxy groups extends the compound’s electron-withdrawing and donating behavior. Our customers in electrochemistry and biosensor research report DMBQ’s redox potential fits projects that require sharper selectivity compared to standard 1,4-benzoquinone or even 2,6-dimethoxy-1,4-benzoquinone. Different positions for methoxy groups tweak the aromatic core’s reactivity. DMBQ shows improved solubility in polar organics and less basic hydrolysis compared to unsubstituted quinone, which can sometimes mean longer shelf-life and more predictable handling.
Comparing DMBQ to its isomer, 2,5-dimethoxy-1,4-benzoquinone, we find 2,3 is more sensitive to proton-coupled electron transfer—beneficial or detrimental, depending on setup. Some manufacturers cut corners by blending isomers to reduce costs, but we keep our material strictly 2,3-substituted, knowing customers notice failure points in their own processes if material doesn’t match spec. Downstream biotech projects can stall from trace impurities or misidentified byproducts, especially during scaleup for pilot batches. Our lab teams historically deal with customer troubleshooting, and we have seen how such contamination affects results and reputations.
Making DMBQ on a scalable, reliable basis isn’t a walk in the park. Typical synthetic routes start from 2,3-dimethoxyaniline or related derivatives, followed by precise oxidation steps. Securing upstream raw materials—especially at high grades—requires active supplier management. Over the years, we noticed fluctuations in precursor purity have the biggest impact on final DMBQ quality. Stringent inspection of each drum, combined with post-synthetic purification, anchors routine consistency. For solvent choices, we’ve shifted away from outdated chlorinated solvents to reduce hazards and environmental load.
Factory teams handle temperature and time profiles tightly, since over-oxidation produces unwanted tars or isomerizes the product. Post-reaction, we adopted multi-stage filtration to separate any colloidal byproducts, followed by vacuum-drying to achieve the crystalline final state. Our experience tells us the work isn’t over until analytical checks prove that purity and isomer ratio stay within narrow targets. Even packing and storing the powder needs care, since exposure to light or high humidity can slowly degrade the product.
Putting broad labels on chemical usage never tells the full story. Our shipping records and customer feedback paint a clearer picture of where DMBQ proves its worth. In recent years, interest has risen from biosensor innovators. Their projects, often in academic or startup environments, rely on the reliable redox cycling properties of DMBQ to convert subtle biological signals into readable outputs. They require not only consistent quality but deep documentation: batch-to-batch traceability, impurity profiles, and stability data.
On the medicinal chemistry side, DMBQ’s profile as a mild oxidant enables stepwise syntheses in lead optimization workflows. We often support ongoing collaborations with contract research organizations, who value quick turnarounds and clear data on each batch. Sometimes, we see requests for nonstandard particle sizes or custom packouts. Experience taught us that direct communication with scientists at the bench speeds up process troubleshooting and ensures the right fit for project goals.
For polymer and dye manufacturers, trace metal analysis matters—any extraneous cations or unreacted starting material degrade end-product quality. In some downstream coatings and specialty oligomers, DMBQ activates controlled polymerization processes. These partners rely on steady supply, with sampling and retention policies to allow for backtracking in case unexpected results arise. Several years ago, a customer traced a polymer performance drop back to a minor byproduct from an upstream supplier. That drove us to increase our internal random sampling and invest in more inline analytics, so each lot reflects not just technical compliance, but earned trust.
Our experience working alongside R&D teams brought home the importance of technical exchange. Standard chemical specs often fail to capture the operational nuance. Research groups will reach out when a quinone fails to dissolve as expected or when subtle byproducts sneak into their analysis. With DMBQ, even minor variation in the 2,3 substitution—such as O-methylprotection during synthesis—alters reactivity in downstream procedures. We routinely share analytical data down to isomer ratios or trace aromatic contaminants to prevent trial-and-error headaches for researchers.
Open feedback cycles between users and producers reveal where process upgrades give dividends. In one long-standing relationship with a process development group, we isolated that certain flash chromatography residues from their isolation steps came from a single uncontrolled variable in the methoxylation phase. By modifying our quenching protocol and adding a dual-filtration step, end customers reported a 30% reduction in side reactions. These sorts of incremental improvements often follow phone calls and joint troubleshooting, which simply can't be simulated through paperwork and spec sheets alone.
A factory-centered viewpoint on DMBQ means knowing firsthand which parameters drive performance and which just clutter the certificate of analysis. In actual applications, moisture content remains one of the most important but underappreciated specs. Our quality engineers run additional Karl Fischer tests to offer actionable water content numbers, especially for groups using DMBQ in moisture-critical redox cycles. Over the last decade, advances in online monitoring and analytic chromatography helped us catch outlier batches early, keeping downstream projects running without delay.
Sustainability considerations factor more in decision-making now, both at the buyer and producer sides. We update solvents and cooling methods every few years, always looking to reduce energy load and any regulated waste. Years ago, heavy reliance on chlorinated solvents marked benzoquinone production. Our plant switched to greener alternatives, which involved savings not just in handling costs but also in overall worker exposure risks. In practice, these steps improve both compliance and day-to-day reliability, since better-controlled environments yield more consistent product.
We’ve tracked demand for DMBQ across dozens of sectors. The push for high-throughput synthesis and automated screening drives a need for higher quality controls on core reagents. As market requirements for documentation and compliance get more stringent, our data management and lot-tracing services become more central to day-to-day operations. It’s become necessary to not just provide analytical purity numbers but to issue full impurity profiles, storage guidance, and even retrospective batch reports. More customers now request historic batch data and usage case summaries, so we built our systems for document retrieval and technical support, cutting down delays caused by missing paperwork or unclear chain-of-custody issues.
In the past few years, biosensor innovation and green chemistry initiatives led to higher interest in DMBQ with well-documented supply chains. We see a move from speculative buying to partnership-driven procurement—customers expect their questions about sourcing and storage to be answered by real people familiar with the factory process, not just a sales pipeline. Those building new pharmaceutical or agrichemical projects value access to in-house chemists as much as to the material itself; technical dialogue up front saves time in the long run and supports real-world product launches.
Even in a controlled manufacturing environment, DMBQ presents its share of hurdles. Its sensitivity to strong base and strong acid means process engineers can't shortcut dissolution or heating steps—improper pH or temperature quickly leads to degradation or color change. We operate with closed-transfer systems to reduce air and moisture contact while loading, a step that reduced rejected batches by over 15%. For orders requiring specific particle sizes, our team upgraded mechanical sieving with air classifiers to eliminate fines and dust, allowing smooth transfer downstream.
One overlooked factor is proper light shielding during storage and transport. We package DMBQ in opaque, airtight liners to deter slow photolytic breakdown. Based on direct customer input, labeling changes describing best-storage practices helped curb confusion in multi-user labs handling the compound. Those hoping to use DMBQ in combinatorial screening or microvolume systems often seek guidance to avoid false positives from trace redox-active contaminants. Our experience shows that batch-level trace analysis not only creates transparency but saves valuable research time.
Our relationship with research partners goes beyond supplying a bottle. Discussions with research group leaders highlighted what matters in practice—thorough documentation, quick turnaround on technical questions, and openness in reporting anomalies. DMBQ often finds itself at the center of exploratory work, where unanticipated reactivity can result from interactions with less-characterized reaction partners. Providing spectral data and impurity profiles saves time for customers and avoids costly missteps, especially in new application areas such as enzyme-mimetic catalysis or energy storage trials.
We host annual open-house visits for institutional buyers and academic partners. They see the lines and talk through synthesis and analytical approaches with our process and QC teams in person. Such contact builds the kind of confidence no certificate alone can offer, especially for those transferring methods from bench to kilo scale. Teams designing new devices or setting up pilot manufacture appreciate access not just to material, but to in-plant experience. This bridge between theory and practice sets factory-made DMBQ apart from generic, third-party offerings.
Buyers sometimes ask why sourcing directly from a manufacturer affects the product in their own labs or plants. From our side, we see the effects in every step—from raw material choice and process tuning to quality checks and technical support. In house, we never blend lots or isomers to fill orders; consistency starts with disciplined sourcing and process repetition. Our teams take pride in batch traceability, making sure customer feedback feeds process adjustments instead of being filed away. Years of historical data and lab logs provide a resource for tracking subtle trends in product behavior—a resource too easily lost when supply chains fragment.
Over decades, we’ve watched research and industrial needs evolve. DMBQ has grown from a niche specialty product to a widely requested chemical in life sciences, advanced materials, and electrochemistry. Fast feedback, clear batch documentation, and a willingness to troubleshoot alongside customers become the differentiators in crowded markets. Manufacturing direct has taught our team that performance in end-use is not an accident—it’s the sum total of process discipline, raw material quality, and honest dialogue along the way.
While third-party resellers come and go, our approach to DMBQ remains built on the same groundwork: precision, consistency, and accountability for every lot that leaves the plant. Each kilogram accompanied by real data and expert support adds more to the value chain than any label alone ever could. Through years of production, testing, and collaborating with users at all stages of the chemical value chain, our view of DMBQ deepened. It's not just a reagent; it's a product shaped as much by factory expertise and open communication as by chemical bonds and batch analytics.