|
HS Code |
659030 |
| Chemical Name | 2-Methyl-4-Bromophenol |
| Cas Number | 13532-16-6 |
| Molecular Formula | C7H7BrO |
| Molecular Weight | 187.04 g/mol |
| Appearance | White to light brown solid |
| Melting Point | 78-81°C |
| Boiling Point | 263°C (estimated) |
| Density | 1.6 g/cm³ (approximate) |
| Solubility In Water | Slightly soluble |
| Smiles | CC1=CC(=CC=C1Br)O |
| Inchi | InChI=1S/C7H7BrO/c1-5-4-6(9)2-3-7(5)8/h2-4,9H,1H3 |
| Refractive Index | 1.585 (estimated) |
| Synonyms | 4-Bromo-2-methylphenol |
As an accredited 2-Methyl-4-Bromophenol 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-Methyl-4-Bromophenol, tightly sealed, labeled with hazard information and chemical identification. |
| Shipping | 2-Methyl-4-Bromophenol is shipped in tightly sealed containers, protected from light and moisture, in compliance with hazardous materials regulations. It is transported with appropriate labeling and documentation, ensuring safety during transit. Handling guidelines recommend shipping at ambient temperature, avoiding direct sunlight, and using secondary containment to prevent leaks or spills. |
| Storage | 2-Methyl-4-Bromophenol should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers. Keep in a cool, dry, well-ventilated area, ideally in a chemical storage cabinet designed for hazardous chemicals. Ensure proper labeling, and avoid sources of ignition, heat, or direct sunlight. Access should be limited to trained personnel. |
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Work with aromatic fine chemicals has always brought an interesting mix of science and challenge. 2-Methyl-4-Bromophenol—with the molecular formula C7H7BrO—stands out among our portfolio for its unique substitution pattern on the phenolic ring. Our engineers have consistently found that adding a methyl group at the ortho position and a bromine at the para position impacts both physical properties and chemical behavior.
On the manufacturing floor, we observe how these structural specifics affect everything from solubility to reactivity. The methyl group tweaks the electron density of the ring, influencing the way this compound interacts with other reagents. The bromine not only adds mass and changes the volatility but also brings notable reactivity in substitution and coupling reactions, which our downstream customers appreciate when they need a reliable halogenated building block.
We synthesize 2-Methyl-4-Bromophenol through controlled electrophilic aromatic substitution routes, always choosing routes that minimize impurities and allow us to recover solvents for recycling. Years of bench and pilot plant work taught us that reaction temperature, brominating agent concentration, and timing matter just as much as purification steps. Any shortcut in washing or phase separation leads to stubborn byproducts or sticky residues, which our team deals with directly—no abstract protocols, just practical chemistry.
Handling this compound presents distinctive challenges. Its volatility is lower than unsubstituted phenol but higher than longer-chain analogues. The methyl group means a lower melting point compared to 4-bromophenol, which changes how it behaves in chillers or jacketed tanks. We keep our batches dry and protected against light and air, which avoids discolored or off-spec material that would slow down a customer's synthesis.
Specifications aren’t just numbers on a sheet for us. The purity we deliver—usually above 98% by GC—translates directly to fewer purification steps for our customers. We keep residual solvents well below 0.5%, verified with headspace GC, because residue can ruin a catalyst or downstream coupling reaction. Particle size and density don’t apply much, as this product is a crystalline solid, but our QA checks confirm consistent flow and pourability.
Water content affects shelf stability and reaction reproducibility. We aim for less than 0.2% water by Karl Fischer titration because experience shows that higher water loads lead to unpredictable nucleophilicity and unwanted hydrolysis problems in synthesis. Every bottle we fill at our plant meets this limit, because every failed run wastes time and money both for us and for you.
Over the past decade, we’ve seen a steady increase in orders for 2-Methyl-4-Bromophenol from both pharmaceutical and agrochemical companies. The bromine atom opens up cross-coupling opportunities, making this compound a popular choice for Suzuki or Buchwald-Hartwig reactions. Researchers report that the ortho-methyl group provides a steric twist, funneling selectivity in complex molecule formation.
Several of our customers design antibacterial or antifungal agents by exploiting the phenolic OH. Our product’s high reproducibility in phenol content and halogenation purity matter; even ppm levels of unrelated halides can throw off biological testing. In our view, the methylated version allows fine-tuning of physiological properties compared to plain 4-bromophenol—modifying lipophilicity and altering metabolic stability. Custom applications in UV-absorbing polymers and specialty resins come from smaller development labs, who rely on our lot-to-lot data to avoid costly re-optimization.
Anyone who has worked with halogenated aromatics knows that small changes to the ring bring large changes in downstream chemistry. Unsubstituted phenol oxidizes more readily and reacts unselectively without extra protection—its volatility creates safety headaches in a plant environment. 4-Bromophenol, lacking the methyl, has a higher melting point and somewhat sharper odor, while also being less chemically flexible for some applications because the ortho position is unblocked.
On the other hand, 2-Methylphenol (o-cresol) is easier to work with in terms of odor profile and melting/boiling point, but it doesn’t offer the reactivity needed for halide-driven coupling. Adding a methyl group to 4-bromophenol leads to a distinct melting range (often around 62–66°C, based on our latest batches), giving a solid that stores and weighs more conveniently at room temperature than some of its oily cousins.
From formulation to complex scaffold assembly, comparing products side by side on the bench reveals differences that don’t show up in spec sheets. Handling losses, ease of reaction, and byproduct profiles all shift when switching from 4-bromophenol to the 2-methyl version. New customers often share that their reaction yields jump or side-products fall when they try our 2-Methyl-4-Bromophenol. These practical details sway research and production managers more than any marketing pitch ever could.
Every batch of 2-Methyl-4-Bromophenol we send out passes through hands-on scrutiny at the plant: TLC spot checks before bulk charging, GC-MS overlays for final eluents, and a sniff test that comes from years on the job. Any trace of an off-odor, or faint coloration, raises alarms—a reliable sign of oxidative side reactions, which we have traced back to equipment or atmospheric oxygen leaks in the past.
Our QA team holds onto reference standards from early batches, using them as internal benchmarks. There’s no room for batch drift: as soon as a lot strays in melting point or headspace, we halt release. This unwavering approach comes not from paperwork, but from hard-won lessons—customers don’t forget process upsets that could have been avoided with better QC. Shipments under 20kg often go to academic labs, where reproducibility decides whether a grant-funded project succeeds. All product is handled in high-density, lined HDPE bottles that stand up to repeat opening in even the most hurried lab.
Managing halogenated waste remains a challenge for us as much as for customers. We’ve built solvent recovery loops into our process—each liter of toluene or methanol we reclaim reduces both emissions and cost. Our distillation columns run under reduced pressure to capture volatile bromides and prevent their release. Containment isn’t just a paperwork box to check; neighbors and regulators watch closely, and every emission threshold keeps us accountable.
We work to minimize bromine use and recover everything feasible; spent reaction mixtures head to certified handlers where safe incineration procedures neutralize the residuals. Internally, every operator cycles through hazmat refreshers and emergency drills. Our track record has improved each year, and we’re making progress on closing the loop for container reuse—customers now return clean drums to the plant, cutting our net plastic use.
Sourcing reliable bromine and making sure its purity doesn’t waver presents an ongoing headache. Commodity markets change quickly, and every swing creates budget uncertainty. We hedge by maintaining a mix of local and overseas suppliers, and we keep backup stocks in dedicated, ventilated storage to avoid disruptions in production. Global regulations shift as well, with import controls tightening for both brominated and phenolic compounds.
Quality documentation requests have multiplied. Each client needs custom COAs, traceability documentation, and ever more detailed impurity profiles. That workload drives up the cost of compliance, but our team has learned to respond efficiently—templates help, but responsiveness matters more. We don’t send robotic emails when a researcher asks about a contaminant risk—we pull the batch records, look for trends, and talk through mitigation directly.
A fresh wave of research in pharmaceuticals and electronics brings new interest to molecules like 2-Methyl-4-Bromophenol. Functionalized organic scaffolds for OLEDs, advanced intermediates for kinase inhibitors, and additive blends in specialty coatings all depend on the predictable reactivity delivered by this compound’s structure. Discovery chemists keep us updated on the unexpected results—sometimes, a slight tweak of the methyl orientation means a difference in yield or spectral clarity.
Recent conversations with R&D teams emphasize the growing need for halogenated phenols with precise purity and known physical properties. Newer regulations further restrict allowable trace metals and unwanted halides, so we keep refining crystallization and washing steps. Now, demand for kilogram-scale lots comes as much from development-stage biotech as from industrial bulk users. We stay tuned to these shifts, adjusting equipment and workflows to keep pace with where the science moves.
Close contact with end-users teaches us what works in practice, not just in theory. Once, a customer had trouble with scale-up yield in a Buchwald coupling—our tech support reviewed their chromatograms, suggested drying agents, and together we pinpointed a trace moisture issue. That fix stuck, and their yield bounced back. Stories like that make a difference to our entire shop floor team.
Regular customer feedback tells us whether any given lot meets expectations, from crystal habit to ease of handling. We take those insights to refine our grinding and packaging techniques, always sharing lessons learned with our partners. For every innovation in our line, there are rounds of in-person training and back-and-forth troubleshooting. Those conversations build trust, and that trust builds return business year after year.
We have manufactured 2-Methyl-4-Bromophenol for years, relying on technicians who know the minutiae of phenolic halogenation. Raw material pre-qualification, real-time in-process controls, and an unwavering focus on traceability make the difference between smooth delivery and a warehouse of unsellable product. Our history includes learning from small missteps, catching a subtle glycol carryover one year that caused yellowing and odor issues during scale-up. Those moments drove process changes and deeper staff training, benefitting all our later batches.
Selecting a producer, rather than a repackager or trader, means getting chemistry backed by first-hand quality assurance, and by a team that understands both the molecule and its uses. We handle every step—from sourcing, through synthesis and purification, to final shipping. That direct control supports stable supply, flexible order sizes, and consistent product, even as market forces shift.
We see more customers integrating 2-Methyl-4-Bromophenol at the earliest stages of molecule design. Preclinical researchers planning a late-stage functionalization step account for sterics and electronics right up front, knowing our product lands within the GC and NMR specs they expect. Academic partners sometimes ask for extra data—MS fragmentation patterns, crystallographic parameters, absorbance maxima “just in case”—and our in-house analytical team delivers.
Process development chemists appreciate that our sample scale matches their pilot scale: grams for the hood, kilos for the kilo lab, drums for the first production run. On our side, we keep watch on reactivity tests: boronic acid coupling, base stability, even alternate routes to downstream sulfides or ethers. That level of real-world testing on our line shortens the troubleshooting cycle and cuts surprises for anyone picking up a drum for the first time.
Making high-purity 2-Methyl-4-Bromophenol isn’t about automated reactors or routine batch logs. It’s shaped by every batch chalked up on our whiteboards and by every mistake we correct on the filling line. Each lot we produce reflects the input of hands-on chemists and operators who treat batch deviation as a call to investigate, not conceal.
For customers looking to scale new chemistry or validate a process, relying on a direct manufacturer brings reassurances that paperwork alone can’t provide. We stand by every bottle, every drum, and every conversation with the labs who choose our product. From bench chemistry to plant delivery, we strive for accountability and open lines—experience, transparency, and a true knowledge of the chemistry at stake.