Anhui Liwei Chemical Co., Limited
Products

Phenol, 4-Bromo-3-Methyl-


    • Product Name Phenol, 4-Bromo-3-Methyl-
    • Alias 4-Bromo-m-cresol
    • Einecs 221-472-2
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    960166

    Cas Number 2650-64-8
    Molecular Formula C7H7BrO
    Molecular Weight 187.04
    Iupac Name 4-bromo-3-methylphenol
    Appearance White to off-white solid
    Melting Point 64-68°C
    Boiling Point 263°C
    Density 1.58 g/cm³
    Solubility In Water Slightly soluble
    Synonyms 4-Bromo-3-methylphenol, 3-Methyl-4-bromophenol

    As an accredited Phenol, 4-Bromo-3-Methyl- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 4-Bromo-3-Methylphenol, tightly sealed with a screw cap and labeled with hazard warnings.
    Shipping **Shipping Description:** Phenol, 4-Bromo-3-Methyl- should be shipped in tightly sealed containers, protected from light and moisture. It must be clearly labeled and handled as a hazardous material, with relevant UN numbers (such as UN2821). Transport in accordance with local, national, and international regulations for toxic and corrosive chemicals.
    Storage Phenol, 4-Bromo-3-Methyl- should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers. Protect from moisture, direct sunlight, and heat. Properly label the storage container and keep it away from food and drink. Use secondary containment to prevent spills or leaks.
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    For samples, pricing, or more information, please call us at +8615380400285 or mail to sales2@liwei-chem.com.

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    Tel: +8615380400285

    Email: sales2@liwei-chem.com

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    Certification & Compliance
    More Introduction

    Phenol, 4-Bromo-3-Methyl-: A Manufacturer's Perspective

    Direct Insights into Production

    Working hands-on in the synthesis of Phenol, 4-Bromo-3-Methyl-, I have witnessed the raw transformation from basic precursors to a refined compound carrying precise functional groups. Every stage, from choosing the brominating agent to guiding the methylation step, shapes the purity and reaction profile. Each batch demands careful attention, since even a trace difference in process temperature can influence color, melting range, or by-products. We monitor these parameters closely, documenting changes in real time, because tight control gives customers the reliability they seek. Routine gas chromatography and mass spectrometry checks allow us to confirm each lot’s authenticity before moving forward.

    The product we generate meets specifications for laboratory and industrial research, but more importantly, it presents a solution to the challenges our partners face in selective synthesis. The 4-Bromo group acts as a versatile site for further substitution, while the 3-Methyl moiety tailors reactivity for specialty applications. Researchers have consistently chosen this molecule as a bridge to more elaborate aromatic systems, or as an intermediate in the design of bioactive agents, photographic chemicals, and specialty materials. The subtle difference in substitution pattern compared to 2-bromo or unsubstituted phenol completely alters electron density and activation energy, which we know from decades of bench experience leads to sharper selectivity in downstream reactions.

    Quality Creates Confidence

    No two synthesis campaigns are entirely alike, and the world outside the laboratory rarely shifts to accommodate textbook procedures. Humidity fluctuates. Raw material lots exhibit hidden quirks. Equipment, even under routine maintenance, demands periodic recalibration. Each shipment of Phenol, 4-Bromo-3-Methyl- carries a report detailing moisture content, purity (typically exceeding 98%), melting point, appearance, GC trace, and residue analysis to provide transparency. We routinely welcome customer audits and technical tours, demonstrating sample extraction and real-time analytics. Our technicians document each batch with digital logs and hold reference samples, so post-sale analysis can track any reported anomaly back to its source. Over the years, I’ve seen that the best way to catch tiny inconsistencies is through regular side-by-side comparisons—a method that spotlights even faint color shifts invisible to most protocols.

    Complex Chemistry in Action

    Our formulation involves sequential bromination and methylation routes, rooted in classical organic methods but updated for safety and scale. We source bromine and cresol through established channels governed by audit trails, rejecting off-spec raw materials at the receiving dock. Monitoring during bromine addition, using in-line Raman spectroscopy, confirms the electrophilic substitution has completed prior to quenching. In our methylation reactor, layered agitation assures even distribution, as we’ve learned from older batch records that stagnant zones result in underperforming yields. At each junction, we diamond-paste filter the intermediate and track color, as incomplete removal of spent catalysts visibly changes the finished product after storage.

    Phenol, 4-Bromo-3-Methyl-, structurally distinct from its 2-bromo or para-methyl counterparts, offers pronounced stability under ambient conditions. The para-bromo substitution resists oxidation compared to more reactive ortho arrangements. This lets the compound maintain its utility over longer storage periods—a quality valued by researchers stocking libraries of aryl precursors. Fewer peroxides form, waste is lower, and shelf-life stretches well beyond a year in sealed drums when humidity remains below 45%. We’ve received feedback from polymer chemists switching from non-methylated analogues who observed markedly easier purification post-coupling, a practical impact of the methyl group’s electron-donating effects. These subtle real-world advantages stem from hands-on problem-solving and iterative batch improvements, rather than abstract theoretical models.

    Addressing Real-World Usage

    Customers often ask about the difference between our 4-Bromo-3-Methyl-Phenol and more common phenolic derivatives. In routine cross-couplings or nucleophilic aromatic substitutions, our product's precise electronic characteristics change how it behaves compared to, say, symmetric halophenols or simple methylphenols. The bromo group at the para position minimizes unwanted side reactions, especially in Suzuki or Buchwald–Hartwig protocols. This leads to both higher yields and less problematic purification. Methylation at the meta spot draws electron density, stabilizing the aryl-oxygen bond for improved shelf and process stability.

    Our experience shows electronic effects directly impact how these molecules behave inside a reactor. For instance, we routinely see improved selectivity for aryl-aryl couplings relative to non-methylated competitors, which can form isomeric or over-reacted byproducts. In fine chemical and pharmaceutical R&D, even small increases in yield save weeks of work and reduce the need for repeated runs. One customer in agrochemical intermediate synthesis explained that switching to our 4-Bromo-3-Methyl-Phenol dropped their average purification time by nearly 30%, reducing overall manufacturing costs measurably.

    Customizing Production Without Compromise

    Every producer faces pressures to maximize volume and minimize cost. Through continuous feedback loops with our users, we've developed multi-ton processes that focus sharply on both safety and environmental performance. All our reactors are equipped for closed handling and vapor recovery. This reduces bromine emissions, protects workers, and shrinks our environmental footprint. Solvent recycling systems running in parallel with workup stages further trim operational waste. By prioritizing in-house control of each reaction phase, we have learned where shortcutting quality backfires—sometimes in the form of polymeric tars that ruin entire batches, other times as failed customer syntheses that waste weeks of project time.

    Many newcomers to our sector underestimate how subtle process changes affect downstream applications. Holding solvent ratios constant, filtering earlier, or altering batch temperature just a few degrees can shift product behavior once it leaves our gates. Our staff shares observations with key customers, and some partners even request small deviations for custom runs. These collaborative tweaks—adding a pre-chill, changing a quench rate, or pre-filtering through finer glass frit—lead to measurable performance improvements without requiring full process redesigns.

    Fulfilling Evolving Application Demands

    Demand for fine-tuned intermediates such as 4-Bromo-3-Methyl-Phenol grows with the spread of targeted synthetic chemistry in pharmaceuticals, dyes, and complex materials. Our clients often work at the innovation front, testing pathway hypothesis only once per project stage, meaning intermediate failures carry disproportionate costs in both research and capital. In biosynthesis precursor development, for example, the difference between para-bromo or ortho-bromo substitution can mean the difference between a working or non-working pathway, or a dramatic variance in toxicity during trials. Our approach stays grounded: we document user successes and failures, using them as input for ongoing refinements in process temperature, quench schedules, and storehouse humidity.

    We have worked hand-in-hand with dye manufacturers needing sharply defined aromatic intermediates for chromophore extension. Their feedback prompted tighter color and residue specifications. Pharmaceutical users demand high lot-to-lot reproducibility, so we have set up archive retention samples, available two years after shipment for any back reference. We treat each application as its own learning curve, whether the end use involves polyaryl ether formation, liquid crystal intermediates, or small molecule lead optimization.

    Safe Handling Built into the Process

    From years of plant operation, we know that safety and quality are inseparable. Our team has faced the realities of severely exothermic runs, minor raw material contamination, and near-miss spills, each of which led to updated internal procedures and improved PPE standards. Finished Phenol, 4-Bromo-3-Methyl- remains stable in sealed packaging, but transfer and open-drum operations call for double-layer nitrile gloves, safety eyeglasses, and chemical apron—a regimen we enforce for warehouse and dock crews alike. All staff receive periodic training grounded in real incidents from past operations, not just theoretical risks.

    We also invest in air monitoring at storage and shipping points. Automated VOC detection stations signal if breakthrough contamination rises above safe thresholds. Regular scrubber and ventilation maintenance protects both our people and local environment. Our insurance audits have noted the consistent drop in reportable incidents as we increase cross-shift communication—lessons learned from earlier years, when small solvent leaks could go unnoticed until a larger problem developed.

    Data-Driven Continuous Improvement

    Nothing substitutes for on-the-ground knowledge. We compile extensive process and customer support data, not only to meet regulatory requirements but because close tracking shows trends and unexpected patterns that catalyze further process development. Years ago, we added an extra filtration step after chromatographic separation. This single move slashed visible residue and halved complaints related to crystallization in customer handling. By following up with every report of off-spec color or odor, we have built a timeline of process tweaks and their direct impacts—data that consultants rarely see and that has materially improved output consistency.

    Clients have provided valuable long-term feedback, pointing to minor tweaks that increased yield or improved performance in subsequent reactions. For instance, swapping to a slightly different drum liner lowered static buildup and dust accumulation, reducing particle aggregation in sample withdrawal. These seemingly small changes reflect the culture of incremental, practical improvement that permeates every level of our organization. The knowledge accrues with every complaint, every returned sample, and every successful customer project.

    Serving a Diverse R&D Base

    Working directly with end-users rather than intermediaries has taught us how varied the requirements for Phenol, 4-Bromo-3-Methyl- actually are. Some labs ask for microbatches to validate new synthetic pathways, while established manufacturers request bulk shipments for regular campaigns. Each presents its own challenges: for small-lot requests, purity can often be raised even higher using slow crystallization and manual residue checks. In scaled runs, focus stays on maintaining uniform color and melting range batch after batch. We use separate storage for critical lots to prevent cross-contamination with more reactive halogenated or multi-methylated phenol stocks.

    A large share of our product now supports pharmaceutical R&D, where gradual changes in global regulations mean more extensive documentation and retention samples. We routinely supply detailed batch histories, analytical logs, and spectrographic overlays confirming lot lineage. These real-world demands drive deeper process scrutiny, not just during initial syntheses but through each phase of purification, packaging, and shipping.

    Environmental Responsibility in Practice

    Every chemical plant carries a heavy responsibility not just to the customer, but to the community and broader environment. By optimizing both core reactions and downstream workups, we’ve cut bromine use by nearly 15% compared with legacy protocols. Recovered solvents are distilled and re-circulated within the plant, leaving a fraction of the original organic waste compared to a decade ago. A dedicated environmental team audits discharge and vent streams, and we have equipped each reactor bay with spill management and containment kits. For us, responsible chemical manufacturing means ensuring no by-product or emission ever leaves the site untreated.

    Both local inspectors and external auditors walk our shop floors several times yearly, making unannounced visits. This direct oversight has fostered a culture of vigilance that extends beyond compliance into voluntary improvements, such as early adoption of zero-discharge wastewater systems. Responding to these real pressures enables the business to supply fine chemicals at scale while retaining the confidence of our partners, neighbors, and regulatory bodies.

    Closing the Loop with Stakeholder Communication

    The most valuable innovations have come not from strategic planning meetings, but through regular, open dialogue with the laboratory teams using our 4-Bromo-3-Methyl-Phenol. We maintain regular calls and site visits with key clients, comparing application feedback with our own process data. This living feedback cycle informs batch scheduling and triggers preventive adjustments even before customer requests. Responding directly to customer pain points—whether a solubility issue in a screening campaign or an unforeseen side reaction during scale-up—has proven far more effective than relying on generic process optimization.

    For example, one research group involved in advanced OLED synthesis required us to explore custom purification regimes to minimize trace halide contamination. Through a mix of customer-run trials and in-house microfiltration experiments, we developed a process that retained high product throughput while reducing trace impurities by an order of magnitude. This ability to respond with specific, solution-oriented changes, grounded in both customer reports and internal trial data, continues to define our approach.

    Why Substitution Patterns Matter

    From the earliest lab-scale batches to multi-metric-ton shipments, we have seen firsthand that even a single substitution on the phenol ring can drastically change both manufacturing approach and application value. The 4-Bromo-3-Methyl- arrangement, selected for both electrophilic activation and steric effects, influences color, melting behavior, stability, and even how downstream users experience the product in their own reactors. These differences often go undocumented by distributors. As direct manufacturers, our constant observation—coupled with analytical rigor—unlocks process improvements that benefit any end user who cares about reliability and downstream efficiency.

    Looking Ahead

    As synthetic complexity rises year by year, demand for intermediates such as Phenol, 4-Bromo-3-Methyl- increases. Every new customer request brings unforeseen challenges and lessons, each of which helps us refine sourcing, production, and delivery practices. Our approach, honed by real experience rather than generic protocols, prioritizes hands-on control, data-driven process adaptation, and continuous engagement with users. For us, each drum and bottle not only represents a batch of chemical product, but also a cycle of accumulated experience, improvement, and partnership—all built to meet the expanding ambitions of chemical researchers and industrial innovators worldwide.