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HS Code |
487915 |
| Cas Number | 91-10-1 |
| Molecular Formula | C8H10O3 |
| Molecular Weight | 154.17 |
| Iupac Name | 2,6-Dimethoxyphenol |
| Synonyms | 2,6-Dimethoxy-1-hydroxybenzene |
| Appearance | White to off-white crystalline powder |
| Melting Point | 97-101°C |
| Boiling Point | 273°C |
| Solubility In Water | Slightly soluble |
| Density | 1.21 g/cm3 |
| Smiles | COC1=CC(=C(C=C1)OC)O |
| Pubchem Cid | 6968 |
As an accredited 2,6-Dimethoxyphenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,6-Dimethoxyphenol, 25g, is packaged in a sealed amber glass bottle with a tamper-evident cap and clear labeling. |
| Shipping | 2,6-Dimethoxyphenol is typically shipped in tightly sealed containers, protected from light and moisture. It should be stored at room temperature in a well-ventilated area, away from incompatible substances. During transit, handle with care, follow relevant regulations, and ensure labeling for safe chemical transportation. Avoid exposure to heat or open flames. |
| Storage | 2,6-Dimethoxyphenol should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from sources of ignition and incompatible materials such as oxidizing agents. Protect it from light and moisture. Ensure the storage area is equipped for handling organic chemicals and is clearly labeled to prevent unauthorized access and accidental exposure. |
Applications of 2,6-Dimethoxyphenol in Industrial ManufacturingAs a direct producer of 2,6-Dimethoxyphenol, we supply this high-purity intermediate for established downstream industries where its phenolic and methoxy functionalities provide distinct technical and regulatory advantages. Below we outline specialized application scenarios in which our material supports compliance, formulation performance, and repeatable processing value. 1. Pharmaceutical Intermediates – Synthesis of Antiparkinsonian Agents2,6-Dimethoxyphenol serves as a key synthesis intermediate for producing dopaminergic medications targeting neurological disorders. Its selective reactivity allows for controlled O-methylation and phenolic coupling steps used in the manufacture of active pharmaceutical ingredients such as entacapone. Strict in-process controls and consistent purity are critical to assure downstream reaction yields and final product regulatory acceptability. Industry compliance standards
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2. Fine Chemical Synthesis – High-Performance AntioxidantsDownstream specialty chemical producers employ 2,6-Dimethoxyphenol in the preparation of high-temperature-stable antioxidant additives used in elastomers and plastics. Its ortho-dimethoxy substitution pattern improves stabilization efficiency and compatibility with phenolic resin matrices, ensuring lasting protection against thermo-oxidative degradation in demanding end uses. Industry compliance standards
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3. Agrochemical Synthesis – Precursor for Protective Fungicide AgentsWithin agrochemical production, companies use 2,6-Dimethoxyphenol to synthesize certain phenolic fungicides. The compound’s methoxy groups confer increased stability and moderate water solubility to end-use molecules, optimizing distribution and leaf adherence in formulated crop protection products. Industry compliance standards
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4. Dye and Pigment Manufacture – Intermediate for High-Purity Triarylmethane DyesDye manufacturers utilize 2,6-Dimethoxyphenol as a key coupling agent in the controlled synthesis of triarylmethane-type dyes, where uniform substitution is crucial for color consistency and lightfastness. Its reactivity profile enables selective functionalization and minimized side product formation during colorant synthesis for inks and optical materials. Industry compliance standards
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Drawing from decades of hands-on experience in manufacturing phenolic derivatives, we’ve recognized 2,6-Dimethoxyphenol as much more than another laboratory curiosity. Known by some as syringol, this compound has carved out its own spot in the toolbox of chemists, biotech specialists, and polymer designers alike. The backbone of its appeal sits in the pair of methoxy groups at the 2 and 6 positions, while the hydroxyl at the 1 spot provides a unique entry point for modifications. Rarely do we see building blocks with such distinctive reactivity matched with relative chemical stability in the benzenoid series.
Our batches of 2,6-Dimethoxyphenol consistently exhibit purity levels exceeding 98%, a specification that we monitor rigorously each day. The demand from research labs and production lines doesn’t slow for any uncertainty about the input materials. Crystallizing the finished product correctly, eliminating by-products like monomethyl ethers or isomeric organics, and packing it to minimize moisture uptake have become routine measures.
Anyone who has worked directly with phenolic ethers knows that each structural tweak changes not just reactivity but also handling basics. Syringol turns most heads on the shop floor because of its sharp melting point. It comes off our crystallizers as white to off-white solid needles, as opposed to the sticky or oily nature of some other methoxy-phenol isomers. That clearly simplifies weighing and transferring—especially for scale-up. The faint, pleasant vanilla aroma is a dead giveaway for this compound, although our plant team always emphasizes the need to work in well-ventilated environments.
High purity also means our clients spend less time down the road cleaning up side reactions or separating impurities. In our own synthesis campaigns, we rarely see trace levels of residual solvents and minimize colored impurities by using precise fractional crystallization. Moisture content affects the downstream performance, so we seal finished syringol in moisture-barrier bags—an approach learned from years of product complaints in the early days before controlled environment packaging.
Labs and production engineers often ask about the best uses for 2,6-Dimethoxyphenol versus its many cousins. Its value shows up most clearly in oxidative coupling and polymer chemistry. For example, in our own R&D division, we noticed that the extra methoxy group at the ortho position raises electron density, making electrophilic substitution more efficient than in the standard guaiacol or hydroquinone. Lignin-modeling studies in academic partnerships use syringol to emulate the guaiacyl and syringyl units of natural lignin. Here, the two methoxy groups closely mirror those in real biomass—a feature single-methoxy analogs can’t provide.
If you’ve ever explored the synthetic routes for natural flavors, fragrances, or medicinal precursors, you know that certain reactions run more cleanly with 2,6-Dimethoxyphenol as a starting material. The yield improvements stem directly from the molecule’s electron-rich aromatic ring and the relatively unhindered hydroxyl group. This combination allows for selective functionalization, and as operators of multipurpose reactors, we’ve found batch reproducibility stays high, even across different campaigns.
Our team has handled a broad swathe of methoxyphenols, from guaiacol to vanillin and syringaldehyde. Where guaiacol offers only a single methoxy, 2,6-Dimethoxyphenol reliably produces greater activity in oxidative enzyme studies or laccase-based polymerizations. That’s not an abstract claim—it tracks to better mimicry of lignin’s actual makeup and greater solubility in some nonpolar media, as we observed in side-by-side production trials for resin additives.
Vanillin has a more powerful, lingering scent and a reactive aldehyde group, often chosen for applications in food and fragrance. Yet vanillin’s aldehyde is even more susceptible to unplanned side reactions, especially in oxidative settings. Syringol remains inert under many such conditions, broadening the processing options for resin and coating chemistries. Comparing with catechol or pyrogallol, which oxidize rapidly to colored quinones, syringol’s dual methoxy substitution provides useful stability across a wider pH and oxidation window.
In over twenty years manufacturing and blending phenolic intermediates, nearly every major application of syringol has passed through our process lines or customer support desks. One of the earliest requests came from a flavor and fragrance house developing smoky notes for barbecue and whiskey flavorings. Syringol forms a backbone in the composition of natural wood smoke, and it delivers both a smooth aroma and chemical authenticity in processed food products. Not surprisingly, we regularly see it included as flavor standard in analytical reference libraries for complex aroma identification in food research.
On the fine chemicals side, our samples have played roles in buffer systems and advanced antioxidant cocktails. The dual methoxy substitution slows down unwanted oxidation, making it a reliable stabilizer in sensitive matrices. Several of our clients in Japan and Western Europe use syringol as an intermediate for synthesizing syringaldehyde. Syringaldehyde itself is a node in the synthetic routes for ligands and specialty polymers, so controlling the purity of this precursor is mission-critical.
The pharmaceutical industry often requires aromatic building blocks for heterocycle syntheses. Syringol’s regular supply ensures no batch delays in scale-up or pilot runs. Similarly, academic researchers exploring oxidative catalysis or enzyme selectivity trust syringol because it reliably shows the intended activity in published laccase activity studies. This builds a base of confidence for scientists relying upon our materials to stand up to peer review and regulatory scrutiny.
Consistent product quality doesn’t materialize by accident. Any phenolic product line that pays lip service to purity but fails to control every process variable will see bad lots, field complaints, or unexpected downtime. From our earliest days, we invested in automated temperature and pH controls for the methylation and demethylation steps. Reactions get monitored by GC and HPLC, not kitchen timers or uncalibrated thermometers.
Each time contaminants such as m-dimethoxyphenols or residual anisoles creep into a batch, our yield drops and downstream users suffer headaches. Early learning cycles taught us not to rush crystallization, even if it meant slowing down a line. Feedback from a polymer manufacturer—frustrated with off-color batches in 2009—motivated us to rework our purification steps. We introduced multiple recrystallizations and invested in packaging solutions that block moisture, because phenolics absorb water and spoil shelf life.
Fielding queries from customers worldwide has made it clear: academic data sheets don’t always predict industrial processing outcomes. We routinely guide customers away from less robust grades when their process demands tighter melt range or lower ash. That direct feedback makes its way back to our chemists and operators—looping real-world lessons into our everyday production ethos.
Having spent years on the factory floor, I know what happens when a raw material comes in off-spec. Equipment gets cleaned again, schedules slip, and supply chains get tied up. We invest in process controls with traceable records not just for regulatory audits, but to guarantee that product leaving our warehouse works the same in Shanghai as it does in Stuttgart or São Paulo.
For 2,6-Dimethoxyphenol, this extends to checking water content on leaving each filling station, running FT-IR fingerprint confirmation, and logging every melting point. Our quality assurance lab staff know that end-users pick up the consequences of even minor process changes. Weighing and sampling protocols keep cross-contamination with related isomers in check, because even a fraction of a percent makes purification downstream a headache most labs would rather avoid.
While 2,6-Dimethoxyphenol most famously arises from synthetic protocols, interest in renewable sourcing has led us to support several biomass breakdown research initiatives. As part of a consortia looking into valorizing lignin waste from pulp or biorefinery streams, our technical leads supplied reference standards and monitored the small-scale recovery of syringol from pyrolyzed wood. This line of research aims to link a circular approach to specialty chemical manufacturing—both for economic and environmental gains.
Internally, we recover solvents and minimize energy use in both the synthesis and recrystallization stages. The plant engineering division reviews process energy consumption yearly, correcting any spikes traced to cooling water or steam use. That same attention to resource flows finds echoes in how we formulate shipping and storage—using drums designed for repeated refilling and close-coupled logistics partners who value transit integrity as much as we do.
Direct feedback from users often leads down entirely new avenues. In 2017, after a joint project with a co-polymerization specialist, we validated syringol-based epoxy resins in niche elastomer blends. The finished parts showed resilience and easier processability than the old systems based on single-methoxy precursors. Soon after, a coatings team demonstrated clear UV-filter effects using syringol derivatives, showcasing the value of dual methoxy substitution for light stability in transparent films.
Field leads and applications chemists collaborate with our manufacturing staff to match delivered product to experimental intent. For low-ash batches demanded by biochemical assay manufacturers, we install dedicated lines and avoid raw material cross-use. The result is a chain of trust—bonded not to generic product codes, but to measurable, process-backed familiarity with 2,6-Dimethoxyphenol. That reliability powers innovation downstream, from molecular diagnostics to advanced sensors.
The path from raw aromatic feedstocks to a pure, crystalline final product isn’t linear. Early runs in our plant generated more colored tars and hard-to-filter solids than marketable product. We tuned batch pH profiles and set up continuous separations to push impurity profiles below the levels seen globally. We now measure sulfate and heavy metal residue in every batch, not because minimum legal thresholds require it, but because research and pharma users demand extra mile vigilance.
One structural challenge comes from global supply inconsistencies for anisole and methylating agents. Sourcing high-integrity reagents with reproducible purity takes constant vendor screening and negotiation. When supply tightens, we draw on pre-qualified secondary sources, having validated those vendors through actual pilot trials rather than paper compliance. Our logistics operation also maintains safety protocols for handling powdered phenolic products. Moisture ingress during transit or customs delays can ruin an otherwise flawless batch, so we work closely with freight partners and receive real-time package integrity alerts.
Waste management can’t be an afterthought in any rigorous chemical operation. Methanol and other solvent by-products from 2,6-Dimethoxyphenol production are captured, distilled, and reintroduced into compatible processes. Solids filtered from reaction or washing steps get packaged for specialized disposal or recycled where viability exists. This closes loops not just for cost management, but for responsible stewardship of environmental impacts.
Our safety specialists train staff to respect the vapor-phase transfer risks associated with aromatic ethers. Syringol’s relatively mild odor doesn’t signal its full hazard profile—so containment protocols must match those written for less agreeable phenols. Industrial hygiene monitors keep workplace air within controlled levels, and our partnership with PPE vendors guarantees a pipeline of appropriate gloves and goggles.
Dust management also sits high on our risk register. In dry rooms or filling stations, we install localized extraction and HEPA filtering not because regulations threaten penalties, but because our own incident reports from earlier years proved the effectiveness of layered controls. In customer advisory sessions, we recommend segregated storage, given that even minimal cross-exposure can compromise both reactivity and long-term shelf life.
Each drum, sack, or flask that leaves our site embodies hundreds of process touchpoints—each one recorded and retraced from raw material register to end-user signoff. The people who blend, test, package, and ship syringol build upon years of gradual improvement, adapting not just for regulatory compliance, but to anticipate the next wave of customer requirements.
As synthesis strategies evolve to favor renewable sources and low-waste processes, molecules like 2,6-Dimethoxyphenol stand to play an ever-wider role. They support designing greener polymers, next-wave pharmaceuticals, and more sustainable flavors and fragrance chemistry. Our job as manufacturers goes beyond filling orders; it extends to educating partners, driving quality, and resolving the inevitable obstacles between the lab bench and industrial reality.
Any successful integration of 2,6-Dimethoxyphenol today starts not with specs on a sheet but with listening—something we do constantly as a manufacturer. From production tech to research scientist to process scale-up engineer, feedback drives product integrity, fuels our technical team’s motivation, and cements reputation as a trusted supplier. That’s the tradition we stand by and the future we help shape.