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HS Code |
657376 |
| Cas Number | 90-05-1 |
| Iupac Name | 2-Methoxyphenol |
| Common Names | Guaiacol |
| Molecular Formula | C7H8O2 |
| Molar Mass | 124.14 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 205 °C |
| Melting Point | 28 °C |
| Density | 1.12 g/cm³ |
| Solubility In Water | 17 g/L (20 °C) |
| Flash Point | 82 °C |
| Smell | Distinctive smoky odor |
As an accredited 2-Methoxyphenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 500 mL of 2-Methoxyphenol, tightly sealed with a screw cap and labeled with safety and hazard information. |
| Shipping | 2-Methoxyphenol (Guaiacol) should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Transport it in accordance with local, national, and international regulations. Label containers appropriately with hazard information and handle with care, as it is flammable and may irritate skin and eyes. |
| Storage | 2-Methoxyphenol (Guaiacol) 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 and acids. Protect from direct sunlight and moisture. Properly label the container and keep it away from heat and strong bases to ensure stability and safety during storage. |
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Purity 99%: 2-Methoxyphenol with 99% purity is used in pharmaceutical synthesis, where it ensures high yield and minimal impurities in drug intermediates. Melting point 85°C: 2-Methoxyphenol with a melting point of 85°C is used in cosmetic formulation, where a controlled solidification profile enhances formulation stability. Molecular weight 124.14 g/mol: 2-Methoxyphenol with a molecular weight of 124.14 g/mol is used in analytical standards, where accurate quantification and calibration are achieved. Boiling point 205°C: 2-Methoxyphenol with a boiling point of 205°C is used in flavorant production, where thermal stability enables consistent aroma release. Solubility in ethanol 40 g/L: 2-Methoxyphenol with solubility in ethanol of 40 g/L is used in fragrance manufacturing, where it provides efficient dissolution and homogeneous blending. Stability under UV light: 2-Methoxyphenol with UV stability is used in polymer additives, where it prevents discoloration and maintains product appearance. Viscosity grade low: 2-Methoxyphenol with a low viscosity grade is used in ink formulations, where improved flow and printing quality are achieved. Particle size <20 μm: 2-Methoxyphenol with particle size below 20 μm is used in coated tablet processing, where uniform coating and rapid disintegration are ensured. Stability temperature 120°C: 2-Methoxyphenol with a stability temperature of 120°C is used in resin synthesis, where it maintains chemical integrity during high-temperature reactions. Reactivity index high: 2-Methoxyphenol with a high reactivity index is used in antioxidant production, where enhanced free radical scavenging leads to increased product shelf life. |
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Life in a lab, a wood shop, or a factory hinges on quality raw materials. One compound that keeps showing up wherever folks care about both results and reliability is 2-Methoxyphenol, often recognized by its everyday name, guaiacol. Guaiacol finds demand in everything from syrups to synthetic flavoring labs, from fragrance factories to chemical research. Some might call it just another aromatic organic compound, but draw closer and a pattern emerges: this little molecule keeps showing up where real work happens.
2-Methoxyphenol comes with a chemical formula of C7H8O2. It has a molar mass of about 124.14 g/mol, which means you can measure it with ease, whether blending in a beaker or setting up a new pilot reaction. Pay attention to its appearance — a clear to pale yellow liquid, sometimes forming crystals if you get the temperature low enough. Boil it gently and it’ll go from liquid to vapor at around 205 degrees Celsius, so there’s space to play with simple distillation or recovery work, if needed. Mix it up with water, and you’ll notice it’s only slightly soluble; in ethanol or ether, it goes right in, which backs up its value in both industrial and research settings where versatility means saving time and avoiding gridlock.
You’ll notice its distinctive, smoky aroma — I’ve always associated that smell with the “bite” of smoked foods or traditional medicines. That signature odor isn’t just a quirk, but a reason folks reach for it in food processing, pharmaceutical batches, and fragrance design. The density settles in close to 1.1 g/cm³ at room temperature, so transporting and blending doesn’t need specialized equipment.
I remember working in a flavor lab that kept a carefully labeled bottle of 2-Methoxyphenol at the front of the cold storage. One small pipette would introduce a smoky note to syrups and sauces that no “natural smoke” copy ever quite matched. This compound, extracted in the past from guaiacum wood, now largely comes from synthetic or semi-synthetic routes, which means consistent results batch after batch. With more chefs, perfumers, and doctors seeking cleaner, reproducible ingredients, guaiacol earns its shelf space with reliability.
Chemists also value it as a key intermediate. Its methoxy group and free phenolic hydrogen let you tweak the core structure into all sorts of valuable byproducts — like vanillin (the backbone of vanilla flavor), or antioxidants used in preservatives. In pharmaceutical work, researchers lean on 2-Methoxyphenol to build expectorants or antiseptics. In one cough syrup batch, a dash of guaiacol helps thin mucus, making recovery a bit more comfortable for the patient.
If you ever open a beaker and get that familiar smoky whiff, there’s a fair chance 2-Methoxyphenol just went into the recipe. That signature aroma has real practical value; it’s the core character in the smoky edge of whiskey, the “cooked” note in certain cheeses, and even the essence of some traditional Asian grilling techniques. Compared to other smoky flavor compounds, guaiacol arrives clean, with a recognizable and steady profile. For a chef hunting for dependable results, this predictability matters every time.
It’s common to stack up 2-Methoxyphenol against other aromatic chemicals like cresols, eugenol, or even simple phenols. Chemists know that swapping a methoxy group for something bulkier or more reactive changes everything. Take eugenol, the dominating flavor in cloves; it shares part of the structure but comes with heavier notes, showing up stronger in perfumes or orthopedic medicines. Cresols bring higher antiseptic action, but at the expense of odor control and handling problems. Standard phenol, sharp and almost acrid, leaves little room for fine-tuned flavor or scent design.
I’ve stood over a bench, swirling samples, and the usability differences become clear fast. 2-Methoxyphenol blends smoothly and with less volatility in heated conditions — handy if working with warm solutions or continuous processes in factories. Simple phenol, in contrast, evaporates quickly and can bite the nose, which complicates both handling and downstream product scent. Safety routines also differ: guaiacol, though handled with care, isn’t nearly as notorious as some cresolic mixtures for skin and vapor hazards. That doesn’t give chemists a license for carelessness, but it changes the day-to-day risk profile for teams in flavor, fragrance, or pharmaceutical industries.
If you need to modify molecular structures, guaiacol holds up as an accessible building block. Researchers take advantage of the methoxy group to route toward a wide range of derivatives with little need for harsh activation steps. This means faster, more efficient synthesis; the bottleneck isn’t chemical stubbornness, but rather planning and testing the new molecules. Lab teams report fewer side reactions, fewer clean-up headaches, and lower energy demands. It’s not just about what flavor lands on store shelves — it’s about how much time and material gets spent behind the scenes to get there.
Years of experience tinkering with food science taught me how tricky it can be to chase a specific flavor or aroma profile. Some compounds seem to fade or morph under heat, but 2-Methoxyphenol hangs on longer. That’s why barbecue sauces, smoked cheeses, and meats often rely on guaiacol when a robust, recognizable smoke note is non-negotiable. Its thermal stability means fewer recipe surprises during baking, roasting, or smoking.
The rise in “natural” labeling has many food brands returning to guaiacol sourced from wood or lignin. This isn’t just about marketing; it’s also about traceability and understanding exactly what goes into every batch. Unlike more complex smoke flavor systems that contain dozens of unknown chemicals, pure guaiacol lets producers list a single, well-understood item in the recipe. That transparency builds trust, not just with regulators but with kitchen professionals and savvy consumers.
Aging processes, whether in cheese caves or whiskey barrels, also benefit from guaiacol’s character. Natural aging develops a wide bouquet of flavors, but sometimes a batch falls short. Using guaiacol to boost or “fill in” certain sensory notes can save both the product and the producer’s plans. Its compatibility with ethanol and other common solvents keeps it easy to work into processes that require extraction, blending, or controlled infusion.
Working under fluorescent lights and pipette in hand, it’s easy to see how a couple drops of guaiacol at the right stage can make or break a pharmaceutical run. Its most common role sits in expectorant mixtures, helping loosen mucus and make cough remedies do what they promise. It’s gentle enough for repeated dosing yet potent when you need results in the middle of flu season. Over-the-counter products still hark back to guaiacol or its derivatives as the backbone of mucolytic solutions.
This molecule’s history isn’t new. Medical records dating back over a century mention guaiacol as an antiseptic and a mild anesthetic — the sort of medicine handed out in dusty glass bottles or stashed in battlefield kits. What’s changed is the ability to manufacture it with higher purity and tighter controls, so patients and doctors can rely on batch-to-batch consistency without surprises. Doctors appreciate knowing a compound has a long record of use, and modern manufacturing tools provide that peace of mind.
Ethical manufacturers focus on removing contamination and byproducts. The risk of impurities, if left unchecked, ranges from allergic reactions to unpredictable interaction with other drugs. I’ve seen the extra investment in purification pay dividends: fewer regulatory hurdles, smoother approvals, and more confidence all around. Sourcing remains a challenge if producers cut corners; the right supplier stays focused on quality, not just volume.
Analytic chemistry thrives on reliability. Pull up lab records and you’ll spot researchers using guaiacol as a calibration standard for certain kinds of spectroscopy or as a starting reagent for more advanced synthesis. Because its chemical reactivity is well-mapped and understood, researchers avoid the costly trial-and-error phase that less familiar compounds can spring.
Organic synthesis students learn early how guaiacol’s methoxy and hydroxyl positions offer unique entry points for transformation. Whether simple methylation or crafting more exotic derivatives such as vanillin, the process runs smoother because the groundwork is already well-established in literature. In my experience, using guaiacol means relying on a playbook already fine-tuned by decades of chemists who've come before.
Not every chemical on the shelf pulls this double duty — advancing research and supporting practical applications. In teaching labs, a bottle of guaiacol might help a new student master TLC (thin-layer chromatography) or test out new preservation systems for food or biological samples. With its mid-range boiling point and modest volatility, it’s not a safety headache, yet it gives students respect for procedure and careful handling.
Sustainability means more than recycling pipette tips or switching to LED lab lights. The chemical industry feels pressure from public health advocates, regulatory groups, and everyday citizens who want fewer risky toxins getting out into the world. 2-Methoxyphenol, especially when sourced as a byproduct of lignin breakdown in paper mills or biomass operations, fits better with these goals than many synthetic alternatives. Using what used to be waste brings new value and keeps more resources in play.
Moving toward greener chemistry platforms, I’ve seen companies tweak their guaiacol supply chain to favor natural extraction or use renewable feedstocks. Environmental audits back up the claim: lower total emissions, less hazardous waste, and a path toward circular processes that don’t just end in the landfill. For smaller or mid-sized producers, this sort of sourcing adds up to big competitive advantages. You can trace your supply all the way back to the forest or field, and that’s not something every flavor or fragrance ingredient can say.
Not all chemicals are equal in safety and comfort at work. From my years at the bench, one detail stands out: 2-Methoxyphenol, while potent, can be handled safely with ordinary lab precautions. Well-ventilated workspaces, gloves, and basic splash protection keep risks in check. Its pungent odor serves as a built-in warning system — few techs will linger with a spill or open container. Extensive use in labs and production settings maps out its health profile, and thousands of safety data sheets echo similar points: treat it with respect, but you won’t face the dramatic hazards of more aggressive phenolic agents.
Some workers will get mild skin or respiratory irritation if exposed too often. Good training and straightforward labeling solve most issues before they occur. The relatively low toxicity compared to many phenolic analogs means that, in the grand sweep of research and production-grade chemicals, guaiacol stands out for practical, user-friendly handling. Still, good storage habits — cool, dry cabinets, secure lids — extend shelf life and keep both quality and safety standards high.
Getting the best from 2-Methoxyphenol requires attention at every step — sourcing, storage, mixing, and waste handling. Greedy suppliers might cut corners with incomplete purification, leading to off odors or sticky residues in finished batches. I’ve seen teams solve this by introducing robust QC protocols, demanding spectral analysis, or batch-traceable paperwork from vendors. Avoiding contamination isn’t just a matter of paperwork; it’s about time saved, products rescued, and fewer headaches at audit time.
Waste streams involve another layer of work. While guaiacol itself doesn’t present the highest disposal risk, any washed-out glassware or expired stock still deserves proper treatment, not a trip down the drain. Integration into an active waste minimization plan — with solvent recycling and neutralization steps — prevents legacy issues and aligns with modern environmental standards. Manufacturers in both food and pharma sectors can benefit from setting clear internal rules: proper labeling, strict shelf dating, and routine inspections.
Supply chain risk isn’t unique to guaiacol, but the rise in global demand means sourcing must be set up with fallback plans. If one factory goes offline, or a supplier shifts to less sustainable material sources, having active relationships and backup vendors ensures production continues without a hitch. Strong relationships and open channels keep the market stable — and keep panic off the production floor when orders jump or deadlines loom.
Chemical innovation rarely involves just running new reactions or playing with fancy equipment. In the real world, adapting to client needs, shifting regulations, or evolving market demand often starts with a handful of core ingredients that have built trust over decades. 2-Methoxyphenol remains one of those foundations. More clients want cleaner flavor labels, faster batch cycles, and environmentally safer processes. Guaiacol’s versatility gives R&D teams space to tinker, iterate, and scale up with less risk of product recalls or regulatory stumbles.
Technological progress has made it possible to extract guaiacol more efficiently and with a lower carbon footprint than ever. Fermentation tech, improved lignin breakdown, and smarter purification all feed into more cost-effective, sustainable supply chains. Smart companies look upstream, not just at finished product benchmarks, and adjust raw material standards to fit both consumer values and technical requirements.
On the branding side, storytellers now draw a straight line between traditional smoked foods and the molecular backbone that delivers that experience. Producers who lean into this narrative find new fans among chefs, bartenders, and home cooks — all eager for reliability and traceability in the flavors they use and serve.
Decades ago, someone in a crowded lab or bustling kitchen found 2-Methoxyphenol added the right spark to their product or process. Since then, this compound’s staying power has been built on real-world proof: it can take heat, stand up to repeated blending, and offer a reliable signature, often at a lower price point than flashier options. Folks who care about flavor, fragrance, or function return to guaiacol because it does the job, every time.
It pays to keep a close eye on where and how your guaiacol gets made, with a commitment to responsible sourcing and safe handling. Standards evolve, markets shift, but quality holds value. In a business where every batch can make or break a season or a reputation, that steady, proven backbone has never mattered more.