|
HS Code |
500982 |
| Chemical Name | Phenol, 3-Bromo-4-Methyl- |
| Cas Number | 18909-37-2 |
| Molecular Formula | C7H7BrO |
| Molecular Weight | 187.037 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 80-84°C |
| Boiling Point | 263°C |
| Density | 1.62 g/cm3 |
| Solubility In Water | Slightly soluble |
| Structure | Bromine at position 3, methyl at position 4 on phenol ring |
| Synonyms | 3-Bromo-4-methylphenol; 3-Bromo-p-cresol |
| Pubchem Cid | 344853 |
As an accredited Phenol, 3-Bromo-4-Methyl- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 25g of Phenol, 3-Bromo-4-Methyl- is a sealed amber glass bottle with a tamper-evident screw cap. |
| Shipping | **Phenol, 3-Bromo-4-Methyl-** should be shipped as a hazardous material in compliance with local, national, and international regulations. Use tightly sealed, chemical-resistant containers and package with absorbent materials. Label with appropriate hazard warnings and ship at ambient temperature, avoiding extremes. Ensure proper documentation and safety data accompany the shipment. |
| Storage | **Phenol, 3-Bromo-4-Methyl-** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and bases. Protect from light and moisture. Use appropriate chemical-resistant shelving, label clearly, and restrict storage to authorized personnel. Store at room temperature, following all safety regulations. |
Competitive Phenol, 3-Bromo-4-Methyl- prices that fit your budget—flexible terms and customized quotes for every order.
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Every chemical that leaves our facility carries the mark of our process know-how and the real effort that goes into its creation. Phenol, 3-Bromo-4-Methyl-, with the molecular formula C7H7BrO, isn’t one of the most glamorous molecules in the broad family of fine chemicals, but it’s one that brings its own value to specialty applications. From the ground up, crafting this compound takes careful attention, and not just because of the bromination step—we know from experience that the quality difference hinges on more than just purity on paper.
At the heart of this compound’s relevance lies a specific substitution pattern: bromine at the 3-position, methyl at the 4-position, both on a phenol ring. This specific layout produces properties that distinguish it from other brominated or methylated phenols. A simple ring change alters reactivity, solubility, and the types of derivatives you can make. Whether you’re formulating intermediates for pharmaceuticals, working on agrochemical research, or developing custom monomers, this molecule doesn’t behave like a straight-up bromophenol or toluenol. That subtle difference defines its performance in both bench chemistry and scaled-up processes.
On paper, synthesizing 3-Bromo-4-Methylphenol looks neat and tidy. In a clean, controlled lab, you could follow a textbook route, but scaling this up shows the devil in the details. At larger scale, bromination throws challenges—by-products, exothermic reactions, and the need for continuous monitoring. Methyl group placement affects the selectivity of the bromination; a batch that ran for five hours instead of four transforms yield and purity metrics. Our reactors do the heavy lifting, but our crew’s experience makes the difference. Temperature management, careful reagent feed, and our in-house purification combine for a batch-to-batch consistency that a bench chemist rarely sees. Material is finished as a white to off-white crystalline solid, indicative of controlled production and effective purification.
Everyone asks about specifications—purity, melting point, moisture, color. These details might look technical, but for folks working downstream, those are the numbers that keep a process from going sideways. Our standard production batches of Phenol, 3-Bromo-4-Methyl-, consistently feature purities above 98% by GC and minimal trace contaminants. Targeted melting points typically fall between 74 and 77 degrees Celsius; it’s not just academic, but the marker we watch on our crystallization step to flag potential off-ratio isomers or over-bromination. Residual solvent content stays below food-grade trace levels, well under 0.2%, and color checks ensure the absence of yellowing that could hint at oxidation or side-products. End-users come to expect these specifics because they translate to more predictable yields in their own syntheses—whether looking for coupling efficiency in Suzuki reactions or reliable performance in resins.
We’ve seen Phenol, 3-Bromo-4-Methyl- exit our loading docks for a spectrum of use cases. Pharmaceutical researchers often use it in routes toward nonsteroidal scaffolds and advanced intermediates; the bromine and hydroxyl provide orthogonal handles for further modification. Agricultural teams incorporate it into the synthesis of crop protection molecules—its selective activation supports the installation of diverse functional groups. Polymer chemists, too, tap into its dual substituent pattern when seeking reactivity balance between nucleophilicity and steric effects. A seasoned formulator wants predictability and potency; this molecule offers both through its defined functionalization pattern. Each lot might land in a different sector, but the needs echo: fast, clean coupling, clear analytics, and seamless process scale-up.
Understanding what sets 3-Bromo-4-Methylphenol apart from related phenols starts with experience at the pilot plant. Introduce the methyl group at position 4, and you shift both electron density and steric layout compared to the simpler 3-bromophenols or 4-methylphenols. This seemingly small change can make a world of difference in cross-coupling and substitution chemistry. In Suzuki or Heck reactions, for example, our experienced partners report higher selectivity and cleaner conversions when using the 3-bromo-4-methyl variant. The methyl group tends to block undesirable ortho reactions, enhancing product isolation and sidestepping purification headaches. Some alternative bromophenols, especially those lacking the methyl group at the para position, show broader, dirtier chromatographic signatures after reaction, which slows down scale-up and increases solvent load. Our production team noticed that even trace differences in ring substitution led to marked changes in flask color, aroma, and ease of post-reaction workup—the seasoned chemist in me always keeps a nose out for the faint, slightly sweet, woodsy note of a right-run batch.
Multiple years in chemical manufacturing teach you to respect consistency. The biggest asset we invest in isn’t just in reactors or software, but in the lived experience of handing batches the same way, every time. Every lot of 3-Bromo-4-Methylphenol gets run through a full panel: purity by gas chromatography, water content by Karl Fischer, spectroscopic finger-printing by NMR or FT-IR, and routine checks against in-house color and melting point standards. Analytical chemists and plant operators trade notes every shift: a faint difference in retention time or crystal size can alert us to upstream process nuances few others catch. The approach keeps customer processes running smooth, limiting the unexpected stops caused by hazy material or shifting parameters. In return, our customers often share their own data with us, which feeds right back into our process improvements.
On a practical note, working with this compound, both bromine and the phenol group highlight worker safety and ventilation in our design choices. The fumes from brominated phenols have a distinct character; one missed closing of the vent and you’ll know it. Adequate extraction, gloves that don’t degrade, and dedicated storage for both raw materials and finished product keep the risks at bay. Before product leaves the plant, on-site tests ensure it meets the strict standards necessary for downstream users. We’ve learned over the years that attention to detail—lockers, ventilation, tracked batch codes—ends up mattering more than any poster on the wall.
Shipping specialty chemicals isn’t just about throwing drums on a truck. The compound travels in HDPE or glass-lined containers, inerted if necessary, and labeled to align with international transit rules. We’ve invested in data logging for sensitive lots, so temperature and humidity get tracked in real time. Customers tell us the difference this makes if a product takes a long route or gets delayed—a solid batch of 3-Bromo-4-Methylphenol ought to perform just as well after a few weeks in transit as when it left our site. In the rare event something seems off, we work with clients directly, pulling archived snapshots of production and packaging to trace every step. This keeps downtime low—that matters more than just words like “traceability” on a spec sheet.
Process chemists learn respect for the downstream impact of what comes out the side of a reactor along with product. Bromination by-products and spent solvents might look routine until you scale up. Years back, we revised our quenching and neutralization process to knock harmful emissions and corrosive wastes down to a small fraction of what older practices generated. Close looped solvent recovery pulls off reusable fractions, which become feedstock for other synthesis campaigns or, when feasible, outside partners needing high purity solvents. The methyl group source (usually toluene or derivates depending on lot) gets scrutinized to prevent halogenated impurities from going anywhere near the wastewater stream. Local agencies check our batch data; our own audits run monthly. The approach pays off with a stronger relationship to the region, fewer regulatory surprises, and better downstream process water for us all.
Over the years, we’ve supplied Phenol, 3-Bromo-4-Methyl- to labs and plants on five continents. Feedback from formulation chemists, process scale-up teams, and R&D scientists shapes our process improvement loop. One group working on pharmaceutical leads highlighted the clean SNAr substitutions they achieved, thanks to the compound’s reactivity—less need for repeated chromatography, less waste, and more reliable kinetic data. Agrochemical developers care more about stability in long-term storage. They’ve sent us detailed reports on product behavior under variable humidity; in response, we adjusted packaging liners, reducing surface static and caking. Onsite users in resin companies flagged odor and trace contamination—our team tweaked the distillation cut points, leaving residuals down to trace ppm. Each of these interactions brings home the importance of open channels between manufacturing and user sides, where real-life issues drive actual process refinements far more than any formal spec revision alone.
Our longest-serving shift leads teach that high-quality chemical manufacturing means never assuming outcomes based on the last good run. Every batch comes with its own quirks—humidity changes, aging catalysts, different feedstock lots bring subtle changes. In our plant, each operator documents minute-to-minute temperature, pressure, color, and odor. Even a slight orange tint or the way a freshly crystallized product smells can be a sign that something’s off or just right. We’re not afraid to shut things down and rework material if anything seems off from the standard. Anything less puts the whole supply chain at risk, and that isn’t acceptable to anyone counting on the next drumful for a critical production run. Over the years, our approach turned up unexpected findings—a tweak in solvent mix shaved a full hour from drying time, a change in inert blanket for storage doubled shelf-life for certain customers. Each improvement arrives through real-world practice and the willingness to collaborate up and down the supply chain.
Customers often ask why pulling from a direct manufacturer beats sourcing through layers of brokers or distributors. Having built this chemistry from raw material up, the answer is transparent: access to immediate technical support, honest discussion about issues, and the capacity to respond quickly when orders need adjusting or troubleshooting. When a customer runs into an unexpected result at scale or wants to try a novel reaction condition, our product development chemist and plant manager are on the same call, offering insights based on the last five years’ worth of run data. No abstract promises—real numbers, real fixes, tailored to match what’s actually exiting the reactor, not just what’s on a Certificate of Analysis.
Of course, every compound faces hurdles. Market fluctuation in bromine and methyl precursors can send ripples down the production plan. There have been years where a bulk supplier’s shutdown changed global prices overnight. Instead of passing uncertainty downstream, we carry forward inventory while exploring alternate supply chains for stability. Logistical hiccups during international transit—border closures, regulatory reviews—can disrupt delivery. Our response? Early packaging, dynamic routing, and constant, transparent customer updates. Add to that the realities of environmental regulations tightening every year. To keep up, our technical and EHS teams upgrade containment, adopt greener solvents, and work with regulatory bodies to stay a step ahead.
Phenol, 3-Bromo-4-Methyl-, keeps finding new endpoints as research evolves. We see promising signals from advanced polymer groups and next-generation medicinal chemists exploring the unique properties behind the compound’s dual substitution. Our commitment remains the same as ever: hands-on oversight, direct customer engagement, and a culture where every hired hand gets to understand both the molecule and its impact in the real world. From chemistry to logistics, from environment to final end-use, a quality product only goes so far without the attention and openness to keep improving with every run and every customer touchpoint.