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HS Code |
172743 |
| Cas Number | 7145-41-3 |
| Molecular Formula | C11H16O4 |
| Molecular Weight | 212.24 g/mol |
| Iupac Name | 1,2,3,4-tetramethoxy-5-methylbenzene |
| Appearance | White to off-white solid |
| Melting Point | 106-108 °C |
| Boiling Point | 150-152 °C at 10 mmHg |
| Density | 1.15 g/cm³ |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | COc1cc(C)c(OC)c(OC)c1OC |
As an accredited 2,3,4,5-Tetramethoxytoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100-gram amber glass bottle of 2,3,4,5-Tetramethoxytoluene is securely sealed, labeled with hazard information and lot details. |
| Shipping | 2,3,4,5-Tetramethoxytoluene is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It is typically packaged in glass or plastic bottles, cushioned to prevent breakage. Standard safety and labeling regulations for organic chemicals are followed during transport. Shipment may be via ground or air, depending on destination requirements. |
| Storage | 2,3,4,5-Tetramethoxytoluene should be stored in a tightly sealed container, away from direct sunlight and moisture. Keep in a cool, dry, and well-ventilated area, separated from oxidizing agents and acids. Ensure proper labeling and avoid sources of ignition. Use storage facilities that comply with local chemical safety regulations to prevent contamination and minimize potential hazards. |
Applications of 2,3,4,5-Tetramethoxytoluene in Industrial Manufacturing2,3,4,5-Tetramethoxytoluene serves as a specialty intermediate in select chemical value chains due to its stable aromatic structure and methyl group reactivity. Our manufacturing clients integrate this compound in downstream transformation stages that require exceptional purity and specific functional group behavior. We outline below the documented use cases based on actual industry practice. 1. Fine Chemical Synthesis for Pharmaceutical IntermediatesMultiple pharmaceutical companies utilize this compound during the construction of advanced molecular scaffolds, especially as a starting material or protecting group in the synthesis of active pharmaceutical ingredients (APIs) like tetracycline analogs. Our high-purity grade supports stringent quality mandates during large-scale batch reactions, allowing for fewer downstream purification steps and higher yield in multi-step synthesis. Industry compliance standards
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2. Organic Electronic Materials PrecursorManufacturers specializing in organic light-emitting diodes (OLEDs) and organic photovoltaic (OPV) devices leverage the compound for selective methylation of polyaromatic cores. The material’s substitution pattern provides necessary electronic modulation, supporting tailored optoelectronic functionalities, especially where process control of charge-transport layers is critical. Industry compliance standards
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3. Dye and Pigment Manufacturing: Methoxybenzene DerivativesSelective downstream manufacturers employ this compound as a precursor for high-performance dyes and pigments, notably for the introduction of methoxy substituents that improve color intensity, solubility, and stability in textile and ink applications. The unique methylation pattern enables precise control of the chromophore properties, critical for advanced specialty pigment production. Industry compliance standards
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4. Fragrance Ingredient Intermediates for Aromatic CompoundsFragrance and aroma compound producers value this tetramethoxylated raw material for its utility in constructing complex musk and floral notes, often as a methylated aromatic intermediate. The controlled substitution pattern supports both olfactory profile development and the physicochemical stability required in fine fragrance compositions and premium consumer products. Industry compliance standards
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5. Specialty Resins and Polymer ModifiersProducers of high-gloss, specialty coatings occasionally integrate this tetramethoxy aromatic in resin modifier recipes to impart improved crosslinking density and chemical resistance. Its defined aromatic ether groups enable targeted performance tuning in coating resin matrices intended for high-value, decorative, or protective surfaces. Industry compliance standards
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Working hands-on with chemicals every day, it’s clear certain molecules shape modern industries far more than others. Among methoxytoluenes, 2,3,4,5-Tetramethoxytoluene (CAS 6309-51-9) draws attention inside our production floor due to its distinct set of properties and reliability for downstream synthesis. As a manufacturer, we pay close attention to details that sometimes get lost outside the plant: purity, trace impurities, recycling solvents, and safe, repeatable scale-up.
Chemists might see the structure as a simple methoxylated aromatic, but making a consistent batch, and supplying it in commercial quantities, calls for operational expertise. Our process uses selective methylation routes, confirmed by both GC and NMR. Instead of thinking of specifications as only numbers on a sheet, production teams see their practical effect. Inconsistent conversion or byproduct removal leads to inefficiency for a customer if it isn’t controlled here.
Most requests for this compound usually stem from two areas: as a key intermediate in complicated organic syntheses, or for use in advanced material development. Its structure, featuring four methoxy groups on a toluene backbone, provides both electron-donating strength for electrophilic substitution and resistance against harsh conditions. This combination of features supports a broad spectrum of transformations, including oxidative couplings, aromatic substitutions, and constructing more elaborate polyaromatic frameworks.
Research groups working on pharmaceuticals, dyes, or new polymeric materials have adopted this compound in many experimental designs. Its unique orientation of methoxy groups allows chemists to tackle structures that alternative isomers can’t yield efficiently. For example, in multi-step syntheses involving ortho-para substitution patterns, 2,3,4,5-Tetramethoxytoluene enables routes blocked to less substituted toluenes.
When our downstream clients discuss their struggles with unpredictable reactivity or possible contamination during scale-up, we recognize the issues. Lab-scale glassware doesn’t show the stress a vessel coating or an impure solvent can place on aromatic stability. As a result, our investment in high-throughput QA is real, and repeat analytical runs look for trace byproducts because just a few parts per million of unwanted side product can disrupt a catalyst-sensitive transformation.
Years of production and feedback have influenced how we view “regular” versus “high purity” specifications. For 2,3,4,5-Tetramethoxytoluene, most batch lots reach over 98.5% purity (by GC), and typical moisture content comes in under 0.1%. That’s not only for the numbers on a certificate but also for the reality of storage, process safety, and batch-to-batch consistency.
Handling large lots, we take care with bulk packaging materials. Polyethylene liners or glass bottles help avoid static or leaching, depending on the batch size. We avoid steel containers for this product regardless of food grade coatings, since metallic ions, even in trace amounts, influence certain organic reactions. Smaller orders for research use often leave our facility in flame-sealed glass under nitrogen, based on customer feedback about shelf-life stability.
Differences in grade make a tangible difference in a lab, and this comes from both raw materials and process controls. Our batches never mix recaptured solvents back without full analysis. Residuals such as dimethyl sulfate or acid catalysts see complete removal before crystallization and drying steps. Those process choices don’t just look neat on a release form; they protect our customers from mysterious “batch-to-batch drift”—a real headache for anyone who’s had unexplained failures.
Plenty of variations exist across the tetramethoxytoluene isomers. Placement of the methoxy groups seems a minor structural shift, but every experienced chemist knows even one change can upend entire synthetic schemes. The 2,3,4,5-isomer stands out for its balance: its symmetry makes it more predictable in para-chlorination or bromination, and its bulk slows down demethylation under acidic or basic conditions.
Other isomers, such as 2,4,5,6- or 2,3,5,6-, may see action in similar fields, but they follow different reactivity profiles. Electrophilic substitutions land at different rates, side chains react with varying selectivity, and oxidation suffers from more byproduct contamination. Through our manufacturing records, the 2,3,4,5- variant shows fewer resin formation issues in pilot-plant scenarios, leading to smoother scale-up for our partners.
The market does offer lower purity alternatives, sometimes from legacy producers not investing in modern purification. Those lower grades can work for simple research screening studies, but in API synthesis or material science, cleaner starting material proves its worth. Our plant tracks impurity profiles lot-by-lot and archives “library” samples for several years, so when a customer returns after seeing minor color changes in storage, we can review, test, and trace the cause quickly.
Making methoxy aromatics at scale has always faced two big realities: solvent handling and waste minimization. Traditional routes once used harsh methylating agents, generating large volumes of acidic or halogenated waste. Improvements in continuous-flow reactors and solvent recovery have shifted some of this burden. Our team focuses on solvent cycles with three passes and in-line distillation, reducing waste at source rather than merely disposing of it downstream.
We’ve seen improvements in yield with real changes—modifying reaction temperatures by just two or three degrees, or swapping out an old drum for a new cartridge filtration system. Reducing exposure to strong bases cuts down on minor saponification byproducts that never show up until a customer tries to run a high-resolution NMR. These factory-floor fixes, not just decisions from a spreadsheet, play the real role in consistent supplies.
For packaging waste, our shipments prioritize recyclable solutions when feasible. Clients ordering large drums see packaging designed for return and reuse. As global regulatory shifts demand still cleaner production, we continue to invest in batch tracking, green chemistry approaches, and staff training so both product and operations move in pace with social and industry expectations.
The largest usage share—according to both our observations and industry feedback—comes from innovation labs and specialty chemical producers. This compound often enters as a protected aromatic for selected functionalizations, acting as a linchpin for higher value targets. Some customers report use in producing specialty dyes, benefiting from stability under strong UV and resisting common atmospheric degradation.
Material science groups have highlighted unique thermal properties when small amounts blend into polymer matrices. Unlike many other methoxylated aromatics, this particular isomer gives a stable glass transition temperature and predictable reaction with aldehyde cross-linkers. We don’t just hear this in sales calls but also in returned samples that clients send for impurity testing. They often want confirmation that their observed material properties stem from our product and not unknown contaminants.
For some advanced pharmaceutical syntheses, 2,3,4,5-Tetramethoxytoluene becomes the precursor to demethylated catechols and even fully deprotected polyphenolic cores. Routine production with minimal aromatic halogens or residual acids remains important, since these would poison downstream catalysts or throw off drug purity assays. Our technical support team fields questions about potential re-reactivity or storage stability, offering practical guidelines based on observed degradation in warehouse tests rather than just theory.
Factories don’t run in a vacuum, and chemical supply chains today see pressures from raw material fluctuations, logistics delays, and new regulatory standards. We’ve seen situations where a missed methylating reagent shipment forces creative scheduling. In house, backup stocks and diversified sourcing for both solvents and toluene feedstocks keep production on a regular rhythm.
Unstable supplies create headaches downstream, not least for anyone building a new synthesis platform or scaling up drug intermediates. We hold inventory buffers, communicate directly with buyers facing sudden project surges, and batch plan based on seasonality of raw materials. Over years, this forward-planning changed from a cost-saving issue to a reliability guarantee, learned through experience rather than corporate policy handbooks.
Some markets call for custom grades—higher than our standard 98.5% purity, or pre-measured for automated batch feeders. We can produce these to order, but only because our plant runs full traceability from lot-to-lot. Each modified process documents change points, so if a feedback loop triggers a deviation, the team investigates root cause before approving release. Batch recalls used to be rare, but even the best teams occasionally see mislabeling, odd storage reactions, or minor container issues. Our transparency and record-keeping have led to improved trust and partnerships, not just quick fixes.
Anyone on the floor can share that working with 2,3,4,5-Tetramethoxytoluene calls for a few instincts. Moisture exclusion makes for longer shelf life and higher purity throughout shipment. We train staff to always double-seal containers and watch for signs of condensation or crystallization in cold storage. In bulk, temperature swings between truck transit and plant unloading lead to condensation above the material neck. Addressing this before shelf storage avoids agglomeration and caking.
For labs scaling from milligrams up to kilos, we recommend mandatory in-process checks—a quick GC or TLC scan rather than relying only on paperwork. These small steps catch unexpected shifts before they cascade into wasted time or lost product. Downstream, customers have changed project timelines just because earlier batches from other producers led them astray with hidden water or off-odors.
Direct conversations with clients matter. Pharmaceutical firms reported variable response in multi-step synthesis with legacy batches whose stability dropped after months on the shelf. We responded by introducing additional drying and baking before shipment, and switching all laboratory-scale glass to amberized vessels, entirely phasing out plastics for these pack sizes after repeated customer feedback about polymer leaching.
Batch uniformity remains an industry cliché, but in practice, teams track not just the key purity indicators but also minor analytes: color by Lovibond, melt point, and precise elemental analysis. This kind of granular attention sets our operation apart from commodity producers. It’s not about generating test reports to satisfy checklists, but truly following up so every drum leaves the plant as expected, ready for sensitive downstream work.
2,3,4,5-Tetramethoxytoluene serves its role well not because it’s exotic, but because producers can deliver reliable, well-characterized material batch after batch. Enthusiasm for its chemistry matches respect for the handling realities. By focusing equally on synthesis routes, purification, QA, and field use feedback, we’ve transformed this aromatic from a textbook intermediate to a staple in advanced research, fine chemical, and materials labs.
Our colleagues know the best way a producer sets itself apart involves responding to practical challenges as they arise, investing in both people and infrastructure, and building in regular customer engagement. Whether a client needs five kilos for a pilot run or five hundred grams for an entire project’s R&D phase, the production and quality control processes abide by careful preparation, follow-through, and a respect for the chemists and teams who depend on our consistency.