|
HS Code |
325418 |
| Iupac Name | 2,3-dimethylbenzene-1,4-diol |
| Cas Number | 608-45-7 |
| Molecular Formula | C8H10O2 |
| Molar Mass | 138.17 g/mol |
| Appearance | White to off-white crystalline solid |
| Melting Point | 142-146 °C |
| Solubility In Water | Moderately soluble |
| Density | 1.16 g/cm³ |
| Pubchem Cid | 12039 |
| Smiles | CC1=CC(=C(C=C1O)C)O |
| Inchi | InChI=1S/C8H10O2/c1-5-3-6(2)8(10)4-7(5)9/h3-4,9-10H,1-2H3 |
As an accredited 2,3-Dimethylhydroquinone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2,3-Dimethylhydroquinone, sealed in an amber glass bottle with a secure screw cap, labeled with hazard warnings. |
| Shipping | **Shipping Description for 2,3-Dimethylhydroquinone:** 2,3-Dimethylhydroquinone should be shipped in well-sealed containers, protected from light, moisture, and heat. Ensure the packaging complies with local, national, and international regulations for chemical transport. Clearly label containers and include Material Safety Data Sheets. Handle with care, avoiding any exposure or spillage during transit. |
| Storage | 2,3-Dimethylhydroquinone should be stored in a tightly sealed container, protected from light and moisture. Store it in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Label the container clearly and keep away from direct sunlight and heat to prevent degradation. Ensure appropriate safety protocols are followed during handling. |
Competitive 2,3-Dimethylhydroquinone prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615380400285 or mail to sales2@liwei-chem.com.
We will respond to you as soon as possible.
Tel: +8615380400285
Email: sales2@liwei-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Years of hands-on production have taught us that 2,3-Dimethylhydroquinone offers something distinct in the world of substituted hydroquinones. In our manufacturing facility, we’ve run countless batches, each time refining the quality and consistency to suit chemists working across electronics, pharmaceuticals, dyes, and specialty polymers. The difference this compound makes, whether as an intermediate or a reductant, comes down to the benefits its molecular structure delivers. Our process keeps the product clear, granular, and highly pure to avoid headaches on the customer’s end. Every lot starts with carefully controlled reactions, using select methylating agents and stringent filtration, to keep impurities out. We run thorough HPLC checks to maintain R&D-grade purity, and our specification sheets rarely see deviations larger than a decimal point.
Chemically, 2,3-Dimethylhydroquinone doesn’t just mimic its simpler cousin, hydroquinone. The extra methyl groups at the 2 and 3 positions make substantial differences both in reactivity and performance. Most operators who’ve worked with standard hydroquinone notice right away that 2,3-dimethyl provides greater resistance to aerial oxidation in open systems. This means fewer surprises during storage and less concern about degradation if a container sits open in ambient air for a while. For large-scale synthesis, that extra stability matters, especially when a process makes use of strong oxidants.
We’ve seen formulators in the colorant and pigment industry lean toward 2,3-dimethylhydroquinone when they need more predictable coupling with diazonium salts or specific aromatic intermediates. As a reducing agent, it doesn’t just slow down the rate of undesired side reactions—it often prevents them altogether, which helps labs avoid the cost and hassle of extra purification steps. Because our plant controls particle size through proprietary milling, customers get a fine, uniform powder, making the material easy to disperse without caking or excessive dust.
Chemists, especially the ones working on pharmaceutical intermediates, tend to be specific about impurity profiles. Our 2,3-Dimethylhydroquinone sits at over 98% purity by HPLC, with typical byproducts (dimethyl-resorcinol and methylquinone) falling below 0.2%. Over the years, we’ve improved our purification process after dealing with clogged filters and poor downstream yields in scale-ups. These experiences underline a simple fact: impurities in hydroquinones often poison catalysts or trigger unpredictable side reactions. That forced us to shift from generic batch washes to multi-stage fractionation, all to meet our own standards for a product worth shipping.
The feedback loop from our customers—often harsh and direct—taught us about hidden challenges. Cosmetic pigment manufacturers reported color consistency issues until we tuned our neutralization and drying stages. Their color intensity improved, and batch-to-batch matching became less of a burden. We saw organic electronics researchers stretched out on purity; their yields for tanol-based devices rose only when trace contaminants finally dropped below their detection threshold. This came through persistent dialogue between their end-users and our plant, not from following a written spec blindly.
Practical experience beats speculation every time. Over the years, we’ve seen 2,3-Dimethylhydroquinone emerge as an intermediate in the synthesis of metolcarbamate derivatives and selective antioxidants. Not every reaction benefits from its use. In nucleophilic aromatic substitution, the presence of those two methyl groups can slow reactivity under certain conditions. On the other side, in radical-mediated reactions—or when a controlled rate of oxidation is critical—this methylation pattern often reduces competing side paths. Our technical support lines have walked more than a few process chemists through solvent swaps and temperature adjustments to harness these subtleties.
Contrast it to 2,5-dimethylhydroquinone or plain hydroquinone, and the edge stands out. Substituting at the 2 and 3 positions lowers the parent molecule’s acidity, allowing users to isolate intermediate adducts under slightly milder conditions. For battery manufacturers, this means avoiding saponification or excessive byproduct formation during charge/discharge cycles in flow battery electrolytes. We’ve collaborated with academic groups to test redox cycling, and this substitution came out slightly ahead in lifetime analysis, thanks to decreased over-oxidation in operational cells.
Lab staff and production managers often worry about what happens when a compound moves from a weigh boat to a barrel. Our operation supports both scales. For smaller R&D users, we supply sealed 1-kg drums, each batch bagged under inert gas. Installation of a new vacuum transfer system kept our lines free from cross-contamination—a lesson learned after an entire pallet once failed QA from exposure during transfer. On the industrial end, 25-kg drums with tamper-evident caps ship on heat-treated pallets. All large containers include individual batch certifications, because some customers’ regulatory teams require an original analysis on every drum.
Users working outside strictly controlled environments appreciate that 2,3-Dimethylhydroquinone’s smell is less pungent than unsubstituted hydroquinone. One pigment formulator told us this made a difference on a shop floor with minimal fume extraction. Direct feedback told us to keep investing in our drying and vacuum-sealing processes to preserve shelf stability even in high-humidity zones. In some climates, storage headaches come from ambient moisture, but our upgraded drum liners and slower cooling regime minimized caking and clumping.
Direct manufacturing means tackling challenges hands-on. Problems surface directly in our shop: an off-color batch, a persistent residual solvent, a poorly flowing powder. These are not abstract issues; they translate to lower process yields and frustrated chemists. We do not pass off quality problems to trading partners. Inventory is monitored in real time, and samples get pulled from every batch for retention and retesting. When a formula or process requires high consistency, we’ve seen our long-running customers benefit from single-lot supply for months at a time, enabling scale-up without mid-project specification drift.
Sourcing directly opens up dialogue. Troubleshooting a failed synthesis? Our plant managers and chemists know the quirks—how tweaks in solvent composition change particle properties, which batches deviate slightly by odor or hue, and why a subtle change from sheet to granular may impact filterability. We saw this happen in a customer’s dye plant: switching from hydroquinone to 2,3-dimethylhydroquinone reduced downstream filtration time and caused fewer cartridge changes, simply due to the absence of needle-like crystals common in other grades. Experiences like this inspire us to keep refining, not just meet specifications.
Buyers often face a choice between different methylated hydroquinones. Each brings its own set of physical and chemical quirks. Where solubility matters—especially in water—2,3-dimethylhydroquinone stands out with moderate aqueous solubility, especially compared to more heavily methylated variants like 2,5-dimethylhydroquinone or tetramethylhydroquinone. We’ve measured this repeatedly and kept detailed logs. Users manufacturing polymers for electronics found the intermediate solubility beneficial when prepping prepolymer blends—long before casting, the material would blend smoothly, and residual solidification nearly disappeared.
On the synthetic side, 2,3-dimethylhydroquinone frequently finds a role where oxidative stability is critical, and the methyl pattern achieves a sweet spot between steric protection and retained electron-donating ability. Many catalytic hydrogenation processes seek out this particular isomer to stabilize sensitive intermediates, limiting exposure to over-oxidation and keeping downstream costs manageable. Over the years, we’ve surveyed applications in lithography, antioxidant blends, and API intermediate pathways, and the same story repeats: the unique placement of those methyl groups provides just enough protection to get the job done without shutting down essential reactivity.
A common pain point comes from comparative bulk pricing. Standard hydroquinone often undercuts dimethyl variants, but repeated cost-benefit analysis by our customers illustrates how 2,3-dimethyl’s stability shaves time off downstream purification, keeps overall defect rates low, and lets them run fewer repeat syntheses. For high-value transformations, the premium recoups itself after only a few campaigns.
Our staff receives direct feedback not only on technical purity but also on practical handling. Some customers recall the headaches of earlier decades, when moisture pickup and color changes plagued batch consistency. We responded by tweaking our post-synthesis drying procedure and integrating faster cool-down phases to minimize condensation. Nobody likes to see a tan residue growing at the bottom of a drum after three months in storage. Stringent monitoring and routine stability trials now drive our shelf life claim, backed by our own retention sample testing. Reports from end-users have changed for the better since we tightened control at each post-processing step.
In both our local operation and at customer facilities, people handling 2,3-dimethylhydroquinone appreciate the relatively non-dusting, low-clumping profile of our powder, which comes from deliberate sieving and conditioning. This directly addresses safety, as airborne irritant dusts lower workplace satisfaction and trigger unnecessary PPE use. After installing closed transfer feeders, we cut visible dust by almost 70%, so workplace air samples shifted well within regulatory limits. These changes grew out of on-the-ground experience rather than stand-alone data sheets or consultant advice.
Being a chemical manufacturer involves more than production; it requires a close watch on global standards and environmental best practices. Over the years, regulatory requirements for substituted benzenediols have tightened, not just for toxicity but also for registration and waste management. We’ve adapted by maintaining a robust environmental dossier and providing full traceability for each outgoing lot. Customers request certificates of origin, and our records extend back over ten years—nothing gets shipped without matching records in our books. Some clients face RoHS and REACH requirements; our product is tested to supply these audits, and regular batch sampling ensures ongoing compliance.
Waste minimization also sits on our agenda. Solvent recovery hit 97% last year, and outlet streams are monitored by an in-house team. We’ve transitioned from wet to dry collection for spent filters and packaging, reducing landfill rates by over a third. Conversations with sustainability officers from our largest partners have guided process tweaks in real time, not as afterthoughts. These improvements have come at the prompting of users further along the supply chain who—facing their own audit challenges—asked for upstream documentation and proof that environmental burdens do not shift onto the end user.
Our journey with 2,3-dimethylhydroquinone underscores the importance of listening to what happens after the drum leaves our yard. Phone calls describing unexpected reactivity, clumping, or persistent off-odors turned out to be more useful than dozens of internal trials. One pigment manufacturer, struggling with filtration, sent us a full batch back for analysis—this prompted an overhaul of our packaging procedure. Pharmaceutical compounding labs demanded more detailed impurity profiles, so our analytics group invested in newer separation and detection technologies. These stories show how experience reveals more than any technical bulletin ever will.
Longtime customers develop a level of trust based as much on prompt troubleshooting as it is on published specs. We keep a dedicated channel open not just for order fulfillment but for collaborative improvement. More than once, a process engineer with unique reaction conditions explained how a seemingly minor tweak—like changing pellet size or optimizing surface finish—could boost yields or eliminate persistent fouling. These inputs feed back into our plant as real, tangible improvements to the next lot produced.
Decades in manufacturing have made it clear: 2,3-dimethylhydroquinone fills a vital place between simple hydroquinone and more exotic, heavily substituted relatives. Day-to-day experience—on the line and in the field—showed us that details matter. Every step in the process, from raw material selection, reaction monitoring, to finished product testing, carries lessons that translate directly into better product for real-world applications. The feedback from chemists, engineers, and technicians pushes us to refine, adapt, and deliver something more than “standard” chemical supply.
The successes and lessons learned in producing and supporting 2,3-dimethylhydroquinone have shaped not just our manufacturing philosophy but also our outlook on industry partnerships. We measure our work not by output volume alone but by the satisfaction and success of the scientists and operators who rely on each new shipment, whether for the first time or the hundredth.