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HS Code |
330075 |
| Chemical Name | 2-Bromo-4-Methylphenol |
| Cas Number | 15859-08-2 |
| Molecular Formula | C7H7BrO |
| Molecular Weight | 187.04 g/mol |
| Appearance | White to off-white crystalline solid |
| Melting Point | 66-70°C |
| Boiling Point | 256°C |
| Density | 1.62 g/cm³ |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Synonyms | 2-Bromo-4-methylphenol; o-Bromo-p-cresol |
| Smiles | CC1=CC(=C(C=C1)Br)O |
| Inchi | InChI=1S/C7H7BrO/c1-5-2-3-6(8)7(9)4-5/h2-4,9H,1H3 |
As an accredited 2-Bromo-4-Methylphenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-Bromo-4-Methylphenol, sealed with a screw cap, labeled with safety and chemical information. |
| Shipping | 2-Bromo-4-Methylphenol is typically shipped in sealed, chemical-resistant containers to prevent leaks or contamination. It is transported according to hazardous materials regulations, ensuring proper labeling with hazard warnings. The package is protected from heat and incompatible substances, and accompanied by a Safety Data Sheet (SDS) for safe handling and emergency procedures. |
| Storage | Store **2-Bromo-4-Methylphenol** in a tightly sealed container in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect it from light and moisture. Handle using gloves and appropriate protective equipment. Properly label the storage container and keep it away from sources of ignition or heat. Ensure storage area has spill containment measures. |
Applications of 2-Bromo-4-Methylphenol in Industrial ManufacturingAs a specialized manufacturer of 2-Bromo-4-Methylphenol, we support downstream sectors with high-purity intermediates engineered for advanced formulations. The following are key industrial application scenarios where this material serves critical roles in downstream value chains, strictly focusing on real deployment and compliant practices. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisIn the pharmaceutical sector, 2-Bromo-4-Methylphenol functions as a core intermediate for synthesizing antibacterial and antifungal API derivatives. It contributes specific aromatic structures through nucleophilic substitution and cross-coupling processes, enabling the efficient construction of core pharmacophores while maintaining strict impurity profiles required by drug master files. Its integration facilitates the synthesis of advanced molecules where positional bromination is essential for downstream activity, ensuring optimal conversion rates under regulated conditions. Industry compliance standards
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2. Synthesis of Agrochemical Actives (Herbicides and Fungicides)In agrochemical manufacturing, this phenol-bromo compound provides a reactive feedstock for the synthesis of crop protection agents. Its brominated aromatic core enables tailored modification of bioactive molecules, especially those designed for broad-spectrum crop protection. Downstream synthesis exploits the phenolic and halide functional groups for coupling with amine or carboxyl components, supporting resistance management strategies through structural diversity. Efficient process controls and batch traceability are maintained to address regulatory obligations for agricultural chemical production. Industry compliance standards
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3. Industrial Biocidal Additives for Paints, Coatings, and Wood Preservatives2-Bromo-4-Methylphenol acts as a core biocidal ingredient in industrial formulations tasked with microbial and fungal control in construction materials. When formulated into paints, marine coatings, or wood preservatives, it replaces traditional chlorinated phenols, providing high fungicidal activity at reduced application levels. Its stability under alkaline and UV-exposed environments adds to its value in rigorous outdoor conditions, and the integrated compound is designed for compliance with biocidal product directives while keeping application-specific residues within regulated safety limits. Industry compliance standards
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4. Specialty Chemical Intermediate for Electronic and Polymer MaterialsIn the electronics and advanced polymer sectors, this compound serves as a precision intermediate in the synthesis of high-performance polymers and specialty resins. Precise bromination and methyl substitution enable the downstream generation of monomers and oligomers with defined dielectric, thermal, and flame-retardant properties. The compound often enters processes such as oxidative polymerization or nucleophilic aromatic substitution, facilitating the build-out of functional groups fundamental to electronic substrate and circuit insulation materials for next-generation devices. Industry compliance standards
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5. Intermediate for Synthesis of Aroma and Fragrance CompoundsIn aroma and fragrance manufacturing, this compound is deployed as a key aromatic building block for the preparation of specialty chemicals conferring phenolic and woody olfactory notes. Its role focuses on facilitating targeted etherification or esterification reactions in highly controlled batch environments to deliver unique molecular structures for perfumery within regulated concentration thresholds. Strict adherence to purity, traceability, and absence of unwanted halogenated by-products is maintained for safe downstream blending. Industry compliance standards
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Over the past decades, new demands have continued to shape the fine chemicals industry. One compound that has quietly but steadily drawn increasing attention from chemists and manufacturers alike is 2-Bromo-4-Methylphenol. Marked by its chemical formula C7H7BrO and identifiable as a pale, off-white to light brown crystalline solid, this compound reflects both the precision of our craft and the strength that comes from continued investment in process control.
Our team has been producing 2-Bromo-4-Methylphenol at commercial scale for years, supplying research laboratories and specialty chemical users who look for reliability batch after batch. This compound sits among the class of substituted phenols with a bromo group para to a methyl group on a benzene ring structure. As simple as this substitution pattern might appear to some, the underlying chemistry asks for care at every stage. Our experience with halogenation and the downstream purification steps has repeatedly shown just how sensitive yield and purity can be to variables others might dismiss.
Chemists often compare this molecule with other brominated phenols or methyl-substituted phenol derivatives. From a synthetic perspective, the presence of both a bromine and a methyl group on the aromatic ring shifts its reactivity beyond what either single substitution would do. For example, introducing the bromine at the ortho or para position changes both electron density and steric profile. In practice, this has downstream consequences. When using 2-Bromo-4-Methylphenol as a starting material or intermediate, we find it opens routes in fine chemical and pharmaceutical synthesis that are not so readily available using more basic halophenols or cresols.
The methyl group in the four position activates the ring in ways that become clear during coupling reactions. In Suzuki and other palladium-catalyzed couplings, the bromo functionality offers solid leaving group ability, often allowing for selective transformations that avoid overreaction or unwanted byproduct formation. We've tuned our bromination and isolation conditions so that each batch meets high standards—usually upwards of 99% by HPLC, as confirmed in-house—without the colored side-products that often linger in less carefully controlled operations.
We manufacture 2-Bromo-4-Methylphenol to strict specifications. Particle size, crystal morphology, and moisture control play critical roles. Customers tend to focus on purity, and understandably so, but the devil is as often in those less obvious details. Large, stubborn crystals hamper dissolution and can drag down throughput in automated dosing systems. Fine powders come with their own headaches, from dust formation to static cling inside glassware and hoppers. Finding the middle ground has driven us to adjust crystallization rates using both classical and newer methods, so our material pours easily yet dissolves rapidly. Water content remains below 0.3% w/w by Karl Fischer, minimizing the risk of hydrolysis or decomposition during long-term storage.
A lot of effort has gone into how we prepare this compound for shipment. Over-purified material may sound like a good idea, but stripping away trace stabilizers sometimes renders the product too reactive in customers' hands, especially in humid climates. Our approach achieves consistent content and a shelf life of at least two years under ambient conditions, as demonstrated by our own ongoing retention sample analysis.
Lab manuals and catalog entries tend to reduce chemical intermediates to bullet-points. We know, though, that the real world is rarely so tidy. 2-Bromo-4-Methylphenol found an early niche in the synthesis of agrochemical building blocks, including specialized herbicide intermediates and certain fluorescent probes. Today, pharmaceutical groups use it in stepwise multi-component reactions—sometimes for classic carbon–carbon bond formation, and sometimes to introduce oxygen- or sulfur-containing moieties by displacement.
Manufacturers often remark on the improved regioselectivity and chemical yields seen with this product compared to the more commonly available 4-methylphenol or para-bromophenol. The two substituents—bromine and methyl—change not only reactivity but also solubility and melting point, which in turn affects purification options for subsequent intermediates. For example, brominated phenols tend toward higher melting points and sometimes require stronger solvents, but the presence of a methyl group in the para position offsets both.
In our own pilot and production-scale runs, we've documented that the coupling reactions involving this compound proceed faster under milder conditions compared with analogs. That means less downtime and energy use for our customers—something that’s grown in importance as environmental regulations tighten. Fewer solvents and simpler downstream separations also translate to less waste, aiding efforts to meet internal and external sustainability goals. The benefits are not hypothetical; our technical support logs are filled with stories of processes that worked the first time using our material, after months of troubleshooting with alternate sources.
An important question often comes from our customers: why 2-Bromo-4-Methylphenol and not something simpler, like pure bromophenol or just cresol? The answer isn’t just about having two groups instead of one. For many processes, specificity saves money. For instance, in multi-step synthesis for specialty drugs, each additional control point—be it in purification, selectivity, or downstream functionalization—can shave weeks and tens of thousands of dollars off a research or scale-up project.
Bromophenols are routinely used in flame retardants, dyes, phenolic resins, and several pharma synthesis pathways. But not all isomers give the same result. Ortho-bromo methylphenols, for example, often show decreased reactivity in nucleophilic substitution, leading to incomplete conversion or complex purification steps. Mono-substituted methylphenols rarely provide the combination of lipophilicity and leaving group power achieved in the 2-bromo-4-methyl arrangement. That’s why we stuck with this particular structure, reaffirming its position for target compounds requiring both controlled reactivity and predictable handling.
Users working on new ligands or catalysts find the increased electron density from the methyl group paired with the bromine’s activation effect creates unique reactivity, opening opportunities for synthesis that aren’t possible with plainer analogs. For these applications, nuances matter—it's not just swapping out a bottle on the shelf, it's avoiding months of dead ends and the expense that comes with them.
Many specialty chemicals begin life as research curiosities, and 2-Bromo-4-Methylphenol was no exception. Over time, demand for reproducibility has transformed its role from rare intermediate to mainstay across several markets. Our production history mirrors this change. Early runs were done on a bench scale, typically for research or custom synthesis houses. The need for higher throughput and batch-to-batch repeatability led us to redesign reactors and invest in more robust analytical methods.
By monitoring every phase of synthesis, including post-reaction workup, we’ve built a track record of tenacity—recovering high purity at scale, while actively checking for notably problematic impurities such as dibrominated compounds or phenolic tars. Customers tell us they rely on the absence of these side products, especially in applications with tight specifications like pharmaceuticals or electronic-grade compounds. The result is a product line that meets practical needs rather than theoretical ideals.
Regulatory regimes worldwide encourage chemical manufacturers to innovate safer, cleaner processes. 2-Bromo-4-Methylphenol isn’t exempt from scrutiny, and our facilities have had to adapt. Reducing brominated byproducts and minimizing waste effluents are both technical and ethical imperatives. By fine-tuning reaction temperature, feed rates, and reagent quality, we cut undesirable side reactions to levels below regulatory thresholds—not because guidelines demand it, but because mistakes in these areas get expensive and can slow down client R&D cycles.
We’ve reconfigured our water usage and installed advanced scrubbing systems to capture low-level bromine vapors. These upgrades didn’t just drop emissions, they cut long-term maintenance and improved operator safety. Our own process engineers were the first to see the results first-hand: longer equipment life and lower rework rates, which ultimately translate into better pricing and reliability for end-users.
Sourcing raw phenolic feedstock carries supply chain risk as well. To buffer against fluctuating availability or quality, we’ve developed alternative supplier channels and qualifying tests that reject inconsistent shipments. This in-house vigilance offers both continuity and the added benefit of knowing every drum leaving our gate starts with raw materials we’d use ourselves.
Experience has shown that 2-Bromo-4-Methylphenol behaves predictably under common storage conditions if the basics are respected. Airtight packaging, low humidity, and protection from direct sunlight go a long way. Our standard drums and kegs keep the material away from environmental contaminants, preventing discoloration or clumping during months of storage or transit. Where possible, clients who store this product for longer terms benefit by maintaining temperatures below 25°C, though we’ve seen stable results up to 30°C with material that stays sealed and dry.
Bulk handling raises questions of static charge and dust. Our materials handling team long ago switched to anti-static liners and dedicated flow stations, reducing workplace risk and product loss. We apply these same standards in filling, sealing, and labeling, helping ensure customers receive what we’ve seen in our own internal inventories.
Stability testing runs concurrently with every lot release, and current retention samples trace back over five years. In that period, we haven’t logged a single instance of degradation or potency drift in unopened containers, which means users downstream draw from fresh material every time.
What sets 2-Bromo-4-Methylphenol apart in our experience isn’t simply its chemical profile, but the way users have leveraged its strengths and reported back. Our customers in academic research continue to publish new routes using this compound, especially in the creation of heterocyclic scaffolds and novel ligands for catalysis. Industrial chemistry groups, meanwhile, cite its reliable performance in high-throughput syntheses—where a poorly behaving intermediate can derail whole project timelines.
Over dozens of site visits and technical exchanges, our technical service team has worked alongside user chemists to optimize reactions based on live feedback. In several cases, process chemists ran initial screens using competitors’ material and saw lower purity, slower reaction times, and sticky residues that held up filtration steps. Field tests using our product reversed those trends, often allowing yield increases without equipment upgrades. These stories feedback both ways: we use that information to update process specifications and offer advice to others troubleshooting similar reactions.
Having a reliable supply of specialty intermediates allows end-users to focus on improving their own products instead of troubleshooting quality issues. Our model for 2-Bromo-4-Methylphenol reflects that: every batch is backed by analytical data, archived records, and support from staff who understand both upstream production and downstream applications. The compound’s physical and chemical characteristics aren’t left to chance, but are shaped by years of incremental process development—a practice that’s made easier by constant feedback from both internal use and customer case studies.
As regulatory and market pressures continue to favor minimized waste, reduced energy use, and improved worker safety, we see 2-Bromo-4-Methylphenol positioned as a go-to intermediate for complex molecule construction. The synthesis and downstream integration of this compound demand not only technical skill, but willingness to adjust to new challenges as markets evolve.
We continually monitor changing technical requirements and regulatory trends—not because they always demand it, but because staying ahead of these shifts ensures our partners never scramble in the face of new rules or technical snags. That involves not only improving lab and plant routines, but investing in research that explores alternate synthetic routes and greener process chemistry. More than one time, adopting a new bromination or work-up procedure has cut both byproduct load and energy demand at scale, with direct benefits for users downstream.
Direct feedback loops and openness to field results set the tone for our operation. When one pharma sector partner realized improved crystallinity allowed a key filtration step to run twice as fast without new downstream equipment, this quickly became our new performance benchmark. Evolution in our process never stands still; we treat the chemical as a living product, always ready to advance when our clients push their own boundaries.
We believe 2-Bromo-4-Methylphenol will keep gaining ground, not just as a reliable workhorse but as an enabler for creative synthetic chemistry. The right intermediate doesn’t just meet an immediate need; it offers a foundation for innovation, risk reduction, and forward planning. The conversations with our partners drive subtle but important changes to our methods, packaging, and technical support. That means challenges—both expected and unexpected—are met with solutions formed by real production data, shared experience, and mutual trust.
Building quality into each batch of 2-Bromo-4-Methylphenol is an ongoing endeavor. Every improvement, whether in purity, packaging, or process adaptation, is rooted in lessons learned through daily practice on the line and in the lab. For customers facing demanding synthesis timelines, new product development, or unexpected bottlenecks, this compound offers not only molecular functionality but decades of expertise in each shipment.
The road from raw feedstock to finished specialty chemical rarely runs straight. For us, the journey is measured in small, constant gains—each crystallization, every analytical run, all the technical conversations that clarify what matters most for those counting on us. In making 2-Bromo-4-Methylphenol, we don’t just deliver a compound; we deliver the certainty earned through years of getting things right, from lab bench to bulk drum and beyond.