|
HS Code |
786892 |
| Iupac Name | 2-[2-(3-methoxyphenyl)ethyl]phenol |
| Molecular Formula | C15H16O2 |
| Molecular Weight | 228.29 g/mol |
| Cas Number | 3130-73-2 |
| Physical State | Solid |
| Melting Point | 63-67°C |
| Boiling Point | 390.4°C at 760 mmHg |
| Appearance | Off-white to light yellow solid |
| Solubility In Water | Slightly soluble |
| Density | 1.14 g/cm³ |
| Flash Point | 161.6°C |
| Smiles | COC1=CC=CC(=C1)CC2=CC=CC=C2O |
As an accredited Phenol, 2-[2-(3-Methoxyphenyl)Ethyl]- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25-gram amber glass bottle with a secure screw cap, labeled with product details and safety instructions. |
| Shipping | Phenol, 2-[2-(3-Methoxyphenyl)ethyl]- should be shipped in tightly sealed containers, protected from light and moisture. Store and transport at cool temperatures, following all relevant chemical safety regulations. Ensure appropriate labeling and documentation as per local and international shipping guidelines for chemicals, and handle with care to avoid spills or exposure. |
| Storage | Phenol, 2-[2-(3-Methoxyphenyl)ethyl]- should be stored in a tightly closed container, in a cool, dry, well-ventilated area. Keep away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from light and moisture. Proper labeling and secure shelving are essential to prevent accidental spillage or misuse. Use secondary containment if appropriate. |
Competitive Phenol, 2-[2-(3-Methoxyphenyl)Ethyl]- prices that fit your budget—flexible terms and customized quotes for every order.
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Quite a few years have passed since we started working with substituted phenols, and every introduction of a new compound brings along its own learning curve. Phenol, 2-[2-(3-Methoxyphenyl)ethyl]- stands out as more than just an organic intermediate. In the day-to-day operations at our manufacturing plant, we've observed how even tiny modifications in molecular structure shift the way a molecule behaves in both lab and plant environments.
As chemical manufacturers, consistency and purity steer every process step. We produce this compound for customers who need reliability batch to batch, and who notice even the smallest deviation in trace impurities or melting point. There’s no shortcut to building that trust with long-term customers; it comes from hard-won lessons at scale-up, methodical QC, and regular review.
Chemically, Phenol, 2-[2-(3-Methoxyphenyl)ethyl]- revolves around a phenolic core bearing a 2-(3-methoxyphenyl)ethyl side chain at the ortho position. We see an increasing demand for these ether-substituted aromatic derivatives in our client feedback, especially when downstream synthesis calls for flexibility in reactivity or further substitution. The addition of a methoxy group onto the phenyl ring not only shifts the electron distribution but also leaves a mark on solubility, viscosity, and sometimes even the compound's smell in the plant.
You’ll often find this molecular scaffold in segments of agricultural chemistry and pharmaceutical research. From direct experience, research teams using it in structural analogue libraries report high substrate compatibility and reliable behavior with brominating agents and oxidative reagents. The ortho position on the phenol can offer an anchor point for further functionalization, something synthetic chemists discuss often when optimizing routes for more complex targets.
Our technical teams have noted that in upscaling from pilot to production, careful temperature control prevents unwanted side reactions at the methoxy-substituted ring. Routine spectral inspections (NMR, HPLC, GC-MS) keep our analytical work transparent with clients, supporting efficient troubleshooting if anomalies appear. Compared to more basic substituted phenols, this compound’s molten behavior during crystallization can be uneasy for new operators, but years of experience on the floor have taught us to recognize the right visual cues before moving to filtration.
Our product model for Phenol, 2-[2-(3-Methoxyphenyl)ethyl]- focuses on both analytical standards and repeatable manufacturing. Each production lot follows an established synthetic route, starting from high-purity phenol and a carefully sourced 3-methoxyphenylethyl precursor. Even seemingly small decisions—solvent selection, time at reflux, workup pH—leave a big mark on yield and purity. Production consistency runs deeper than meeting an assay threshold; over the years we’ve learned that stable performance only comes by keeping a sharp eye on every raw material that enters the facility, and double-checking every step with in-process QC.
Far from just blending ingredients, running these syntheses relies on timing, temperature, and the work ethic of experienced operators. From tank cleaning to actual charging, every step must meet internal protocols. Months of testing and validation, not just for the target product but also for possible side-products, have built our confidence in this process.
Usage cases for this compound often include research-driven synthesis of advanced intermediates for both small-scale pharma and agrichem projects. Our most frequent users share that the ortho-substitution pattern allows for a flexible approach toward more advanced ring modifications. This flexibility simplifies route selection when time-to-market pressures rise. The methoxyphenylethyl group, with its own unique reactivity, provides opportunities for stoichiometric control in further derivatization.
Teams working with fine chemicals use this product to open up pathways toward eventual active ingredients for herbicides and fungicides. Our interactions show that both early-stage medicinal chemistry programs and process development teams value stability at ambient storage and predictable shelf-life, which helps when planning long-term projects.
It’s interesting hearing from contract research organizations who mention this compound provides a “problem-solving” benefit thanks to its specific substitution—not always obvious in retrosynthetic planning, but soon apparent in bench-top trials. We keep close contact with clients during development and scale-up stages because it’s always easier to adjust a process before full-size batch runs, instead of after. From customizing particle size distributions after seeing customers’ downstream handling issues, to helping brainstorm safer solvent swaps, the collaboration often leads to process improvement on both sides.
A decade back, pure phenol was the norm for general synthesis, but the industry has shifted toward specialty phenols to meet the demands of complex molecular targets. Difference pops up fast the moment you introduce a 2-[2-(3-methoxyphenyl)ethyl]- substructure. Our own bench and plant data show clear steps up in selectivity during oxidative coupling reactions, and changes in solubility profile that can strongly benefit formulations with restricted solvents. Operators working with the standard mono-alkyl substituted phenols notice the improved thermal stability during exothermic reaction steps—the methoxy group and extended side chain alter the heat transfer profile, which helps when scaling past 50L reactors.
Another distinguishing factor comes up during purification: basic phenols often run into sticky residues or hard-to-remove contaminants. This particular derivative consistently produces cleaner filtrates, according to our plant records, so operations run smoother with less backtracking. We have reduced overall column recycling and solvent washes compared to similar processes run with non-methoxy analogs, cutting hours off post-run clean-up time.
We keep a library of reference spectra for both Phenol, 2-[2-(3-Methoxyphenyl)ethyl]- and several close analogues. This data set has proven its worth every time a question arises about trace impurity origin or possible cross-contamination. Testing new lots side by side highlights that minor tweaks in ring substitution bring out non-trivial changes in crystallization, melting point, and even the compound’s ultraviolet absorbance curve—details that matter to formulation chemists working on complex mixtures.
Producing Phenol, 2-[2-(3-Methoxyphenyl)ethyl]- on commercial scale takes more than just following a textbook protocol. Real-world manufacturing brings up issues you just don’t see on paper. Early batches failed to meet the color and clarity requirements for some clients using the material in optical chemistry, so we invested in a multi-stage filtration and color-removal system. What looked simple on the bench changed when iron content in reactor vessels created off-odors in the product—remedied through improved vessel passivation and extra inline carbon filters.
Improving yields while keeping down run time has been a constant aim. By running root cause analyses on occasional low-yield batches, we traced the biggest culprit to start-stop temperature shocks in heating cycles. After revising control loops and adding multi-point thermocouples, we now see tighter reproducibility lot after lot. Every improvement adds up, driving operational efficiency and a more predictable cost structure.
Waste minimization also impacts how customers see our product. We recycle spent solvents whenever in-house analytics confirm no adverse build-up of non-volatile impurities, cutting both disposal costs and our environmental footprint. As regulations about industrial organics tighten, those details increasingly draw attention in customer audits, so we put in the time for rigorous verification and traceability all along the supply chain.
Nothing gets closer to the heart of manufacturing than addressing quality complaints and using them to drive better processes. One client flagged a batch due to unexpected darkening in storage. Instead of brushing it off, we launched a full investigation, running accelerated stability studies, and involving both QC and plant team leads. We widened our shelf-life tracking and now include non-destructive predictive oxo-content analysis before bottling, a direct outcome from listening to real-world user experience.
Being receptive to feedback, especially from labs taking the product through demanding synthesis steps, builds more than just good rapport. Our technical documentation over the years has grown thicker, not through repetition, but by capturing those minor but vital notes—everything from ideal drying times, to handling advice for minimizing static, and common signals to look for during recrystallization.
A strong supplier relationship should always include both sides. We have open dialogue around unexpected outcomes; chemists regularly share protocol adjustments that could give safer or cleaner conversions when using our product. If there’s room to tune the process, we’re open to piloting it together with clients—whether that means switching to a greener solvent, adjusting packaging formats, or even testing alternate drying methods to fit highly specialized end-use needs.
Transporting Phenol, 2-[2-(3-Methoxyphenyl)ethyl]- brings along a unique set of questions. Some clients need temperature-controlled shipping because prolonged heat exposure affects long-term color and purity. To manage this, we’ve standardized double-layered packaging and include tamper evidence to assure both confidentiality and quality retention.
Storing this compound at scale means keeping moisture and airborne contaminants away. We recommend sealed, UV-protective drums for bulk users, based on shelf-life analysis and ongoing storage stability studies. Facilities with automated powder handling systems see best results if they limit batch transfers by pre-portioning material into intermediate bulk containers before opening, based on feedback and our site trials on dust minimization.
Regulatory scenarios have shifted in recent years, introducing new hurdles for production of substituted phenols. We track all new REACH updates, limits on possible byproduct residues, and provide full transparency on impurity profiling. A recent audit from a multinational client resulted in zero nonconformities thanks to trace documentation and material traceability posted both ways. Like any regulated business, anticipation of new compliance standards forms a daily part of operational prep.
Looking back at our product archives and order histories, demand for methoxy-substituted phenols has moved steadily up. Pharmaceutical chemists in particular value the differentiation possible with electron-rich aromatic groups. Catalogues from twenty years ago barely touched these compounds, but constant improvement in resin purification and automated process handling opened possibilities. As synthetic strategies in drug and crop protection research evolve, molecules like Phenol, 2-[2-(3-Methoxyphenyl)ethyl]- now claim a spot in several patents for complex frameworks, particularly where precise ortho and para functionalization matters.
We keep our ear to the ground through client discussions and trade group meetings. There’s constant pressure to squeeze out extra purity or shorten routes, and we use those market findings as lead indicators for changes to our own internal SOPs. Storage stability and micro-impurity levels now come up far more often than ten years ago—these trends give us plenty of motivation to refine both analytical processes and production layout.
As manufacturers, we sit at the crossroads connecting early R&D with large-scale production realities. Clients routinely share early syntheses or process changes, seeking manufacturer insight into what’s achievable outside the lab. Our technical services team isn't just a troubleshooting hotline. Internal know-how grows through direct plant experience: which purification schemes really scale, how to troubleshoot batch-to-batch variability, and how to spot issues before they balloon into costly disruptions.
Our long partnerships have grown out of that blend—honest sharing of plant data, willingness to pilot unfamiliar procedures, and an eye for translating research-stage syntheses up to full truckload or multi-ton scale. Reflecting on years of producing advanced phenolic intermediates, I’ve learned never to underestimate the value of a tightly run plant, nor how much innovation comes from trusted customers teaching us new perspectives.
Many chemical companies chase technological improvement as an end in itself, but from our view inside manufacturing, improvement always starts from listening: to operators working the lines, to plant engineers building new safety layers, and to end-users testing the product under harshest conditions. Phenol, 2-[2-(3-Methoxyphenyl)ethyl]- shows the results of decades of that close attention—it’s not just another catalog number, but a compound whose real value emerges through hands-on care, feedback, and a commitment to making every batch a bit better than the last.