|
HS Code |
390107 |
| Cas Number | 4949-01-1 |
| Molecular Formula | C7H7BrO2 |
| Molecular Weight | 203.04 |
| Iupac Name | 3-bromo-2-methoxyphenol |
| Appearance | White to off-white solid |
| Melting Point | 54-57°C |
| Solubility In Water | Slightly soluble |
| Smiles | COC1=C(C=CC(=C1)O)Br |
| Inchi | InChI=1S/C7H7BrO2/c1-10-7-4-2-3-5(8)6(7)9/h2-4,9H,1H3 |
| Synonyms | 2-Methoxy-3-bromophenol |
| Storage Condition | Store at room temperature, keep container tightly closed |
| Pubchem Cid | 67333 |
As an accredited Phenol, 3-Bromo-2-Methoxy- 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 sealed 25g amber glass bottle with a screw cap, labeled with safety and identification information. |
| Shipping | Phenol, 3-Bromo-2-Methoxy- should be shipped in tightly sealed, chemically resistant containers, clearly labeled with hazard information. Transport must comply with local, national, and international regulations, avoiding heat, moisture, and incompatible substances. Use secondary containment and appropriate protective packaging to minimize risk during handling and transit. |
| Storage | Store **Phenol, 3-Bromo-2-Methoxy-** in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep container tightly closed and properly labeled. Segregate from incompatible materials such as strong oxidizers and acids. Use only in a chemical fume hood. Store in a corrosion-resistant container to avoid degradation and accidental release. |
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Stepping up to a reactor vessel with a batch of phenol, 3-bromo-2-methoxy-, I know exactly what I’m getting into. Years on the production line have shown me that every intermediate counts, especially one as purposeful as this. Chemically, my team produces this compound under carefully managed conditions, using bromination and methylation processes that maintain product consistency. The result feels less like just another bottle in the storeroom, and more like a tool that delivers specific benefits in multi-step syntheses.
I’ve watched demand for this molecule increase, especially from advanced organic synthesis labs and pharmaceutical R&D teams. There’s a reason behind it: the electron structure of the bromo- and methoxy- substitution on the phenol backbone opens up targeted reactivity. Synthesis routes that utilize this compound often aim for complex, functionalized aromatic targets. Our reactors handle volumes according to client scale—sometimes kilogram quantities for commercial runs, other times a few grams for developmental sampling. Every batch must pass spectral and chromatographic checks; we don’t send out anything until GC-MS and NMR results confirm identity and purity. Typical material comes clear to pale yellow, crystalline, and free from particulate contamination.
Talking to other chemists in the plant, comparisons with other substituted phenols often arise. For example, simple 2-methoxyphenol (guaiacol) lacks the selective reactivity offered by the bromine, making it less useful in halogen shuffle reactions. On the flip side, 3-bromophenol doesn't provide the electron-donating effect of the methoxy group, limiting the options for downstream methylation or cross-coupling.
Bromine in the 3-position brings unique directing effects in electrophilic aromatic substitution, while the methoxy at the 2-position increases nucleophilicity at precise sites. That combination pushes this phenol into a niche not easily filled by alternatives—even those with other halogen or alkoxy combinations. We’ve partnered with research chemists on pilot programs, providing insight into performance comparisons. For Suzuki and Buchwald-Hartwig coupling lines, our material reliably serves as an anchor for building out aryl systems, allowing for a cleaner reaction and less byproduct formation.
Making 3-bromo-2-methoxy-phenol is not a routine operation. Safety protocols around controlled bromination are strict, with fume extraction and containment mandated on the shop floor. I’ve had to train operators in stepwise addition and real-time monitoring, since over-bromination can generate unwanted side products that complicate purification. We rely on automated dosing systems, in-line IR, and temperature assessment to keep reactions within tolerance ranges.
The methylation step must use properly dried solvents and exclusion of moisture to prevent degradation or ortho-para mixtures that slow down isolation. My crew maintains validated cleaning procedures for all vessels, as even small residues throw off reaction yields. In downstream workup, activated charcoal and careful filtration help reach high clarity before distillation or crystallization. All waste streams, especially containing brominated organics, are neutralized and sent for solvent recovery, reflecting our commitment to safe industrial handling and environmental management.
Batch reproducibility has probably been our top focus. Each time we modify scale or customer specification, process chemists run test reactions, watching for purity shifts. During one recent order, a pharma customer requested sub-0.5% total impurity for an active ingredient synthesis. We had to reroute part of the workup, shifting the crystallization protocol and repeating drying steps. Without deep process familiarity and daily collaboration among team members, hitting that target wouldn’t have happened.
Across applications, 3-bromo-2-methoxy-phenol goes well beyond being a structure on a spec sheet. I regularly get requests from medicinal chemistry groups searching for better starting points for heterocyclic synthesis. The molecule’s dual functionality helps speed up library creation, particularly for generating diversified scaffolds where regioselectivity is crucial. Its solubility in organic solvents like DMF, DCM, and ethyl acetate means it integrates cleanly into multi-step reaction sequences.
I recall project feedback from a crop science customer trialing this phenol in fungicide precursor development. Their route demanded a phenolic substrate that could undergo direct bromo-cross coupling followed by amination, without requiring harsh reaction conditions that break down other protecting groups. Based on their data and what we observed in our own scale-ups, the starting purity and controlled substitution pattern made downstream reactions more predictable, minimized cleanup steps, and delivered higher yields of final product. Compared to 2,4-disubstituted analogs, we noticed cleaner chromatograms and less carryover of heavy-metal residues, cutting purification time in half for the customer.
There is a growing call from oligonucleotide and material science researchers for specialty monomers. Where they used to settle for less well-defined halophenols, switching to this product reduced batch rejections tied to side reactions from uncontrolled substitution sites. Over the past two years, as procurement teams ask for more detailed quality data, we’ve built up our record-keeping to include full traceability, from raw material lot tracing through each process parameter. That effort supports complex regulatory filings for our clients and cements our role as a source that understands what a working laboratory truly needs.
Chemistry isn’t just about specs written on a label. With every drum or packet that leaves our plant, I know the actual handling demands and storage needs. Despite being a relatively stable compound, 3-bromo-2-methoxy-phenol can pick up moisture in humid stockrooms. That’s why we recommend storing it in tightly sealed containers, away from light and in low-humidity areas. Periodic retesting assures customers that purity matches their documentation, which folks in validation labs appreciate, especially under GMP settings.
Reactivity can shift with storage age, especially if conditions slip and a sample absorbs water or volatile impurities. In my work, material stored for months in less-ideal conditions sometimes tests out at marginally higher acidity—a problem for those looking for exact stoichiometry in sensitive reactions. Catching such drift before dispatch or use keeps our reputation solid and customers on schedule.
Handling halogenated phenols comes with a heavy environmental responsibility. The last decade’s tightening regulations on brominated waste streams have shaped my daily workflow. Every outgoing shipment starts long before final QC, requiring dedicated waste treatment steps. Our operations involve solvent recovery and on-site remediation for effluents, minimizing the environmental footprint and guaranteeing traceability if auditors ever want to see our logs.
We lean into ISO and REACH compliance not by ticking boxes, but by embedding those expectations in every lab protocol and operator checklist. Each time industry standards change, our process engineers conduct hazard reviews, then train the line team to put the new guidelines into practice. That approach reduces incidents and supports customer guarantees—especially important for clients exporting finished products into regions with strict import controls.
Discussions with our partners underscore the value of up-to-date regulatory paperwork. Having immediate access to CoAs, SDS, and full batch lineage reduces downstream delays. Our proximity to the manufacturing step enables real-time information transfer; project leads can get updated analytical data in hours, not days, which speeds up both R&D efforts and routine production schedules.
Daily conversations with buyers and production chemists convinced me long ago that technical support must go beyond a hotline. Every time a new customer starts using 3-bromo-2-methoxy-phenol, our technical service team reviews their application notes and, if requested, shares guidance about solvent compatibility, temperature settings, and quenching options. During pilot trials at a biotech startup, our team provided alternate crystallization strategies to reduce solvent waste, based on nuances we’ve picked up running dozens of similar reactions. Sometimes, simply adjusting order of reagent addition or selecting anhydrous batches makes a difference in customer yields.
Customers launching new lines appreciate the chance to run small-scale lots before committing to scale-up. This reduces lost time and money from unforeseen complications. My colleagues regularly handle requests for tailored packaging, whether it’s amber glass for light-sensitive projects or inert-air sealed bags for bulk transit. We work closely with shipping teams to time deliveries so that sensitive shipments don’t wait out weekends or holidays in uncontrolled warehouses. That attention to detail helps clients maintain project momentum in tight timelines.
Lessons learned from running dozens of lots don’t sit in a binder. They go right back into process tweaks and, sometimes, full revalidation of equipment. Every chemist and operator here knows their hands-on experience improves the next batch. For 3-bromo-2-methoxy-phenol, ongoing fine-tuning of purification methods results in cleaner product and reduces solvent usage—a win for both safety and efficiency.
Analyzing customer feedback, recurring questions focus on trace impurities and options for further modifications. We’ve invested in better in-line analytical tools to provide profile snapshots for every shipment. This not only minimizes off-spec returns, but bolsters the confidence of formulation scientists who must meet higher internal standards or introduce the compound into tightly regulated programs.
Over the years, this process-driven approach strengthened our relationship with end users. Many project leads return for further technical consultation, knowing our on-site chemists have faced and solved the same issues they confront in their own synthesis work. Open channels for technical feedback mean we can adjust protocols to meet emerging needs without losing sight of the core production consistency our long-term clients depend on.
The global market for custom aromatic intermediates shapes our daily schedules more than any abstract pricing metric. In times of tight supply, priority goes to loyal customers, a policy born out of direct relationships rather than contract clauses. My team tracks holiday schedules, shipping lane volatility, and customs requirements, keeping buyers updated with realistic ETAs. We don’t overpromise on lead times, because in my view, transparency about production runs and actual inventory shields customer process teams from last minute rescheduling.
We commit to monitoring source quality not out of obligation, but because every unexpected turn in starting material purity can jeopardize a whole chain of syntheses. That vigilance led to long-term contracts with trusted suppliers and built-in options for parallel sourcing, so one hiccup in a bromine shipment or cresol feedstock doesn’t bring everything to a halt.
A few years ago, a surge in specialty chemical demand exposed weak points in standard distributor channels. We pivoted by expanding our in-house purification and small-batch packing capacity, stepping in for labs that used to depend on middlemen and faced weeks of delay in getting the right material. That lesson reinforced the benefit of closely managed, manufacturer-controlled supply chains, especially for low-volume, high-value compounds.
Working directly with labs on complex building blocks like 3-bromo-2-methoxy-phenol, our team sees first-hand where industry R&D is heading. That gives us the foresight to invest in next-generation intermediates, and to keep refining reaction conditions for new functional groups. Internal pilot programs explore alternate synthetic routes that generate less waste, tap renewable feedstocks, and simplify purification.
These investments are about more than cleaning up the plant or squeezing a bit more out of each run—they offer our clients new possibilities in method development and process safety. For instance, using greener bromination reagents might reduce quench waste, while continuous processing tech could cut exposure risks and batch failures. Each improvement comes from a cycle of experimentation, data analysis, and hands-on adjustments by people who understand both the theory and the reality of the manufacturing floor.
Colleagues often collaborate with academic groups, sharing anonymized process data to help develop safer, more robust reactions at the research level. These initiatives feed back into our process, keeping our chemistry relevant as needs shift from gram-scale to metric tons, and as regulatory demands evolve.
Every bottle of 3-bromo-2-methoxy-phenol tells a story—about technical hurdles, iterative improvement, and a relentless drive for reliability. Having stood at the reactor and wrestled with real-life process variables, I see every client project as an extension of our operation. That experience influences every piece of advice we share, each process change we enact, and the standards we impose on what we ship.
Long-term relationships with research groups and industrial partners aren’t built on catalog prices. They’re forged through shared challenges and demonstrable results. We don't rely on third-party assurances; our technical staff verifies every critical aspect, bridging the world between the lot code in the lab and the outcome in the customer’s finished product.
With every new project, we renew the commitment to close the informational gap between the plant floor and the research bench. Through transparent communication, focused technical collaboration, and a refusal to cut corners, our team stands behind the value and reliability of 3-bromo-2-methoxy-phenol for innovators at every stage of chemical development.