|
HS Code |
711325 |
| Chemicalname | 2-Bromo-5-Methyl-Phenol |
| Casnumber | 4911-49-1 |
| Molecularformula | C7H7BrO |
| Molecularweight | 187.04 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 65-69°C |
| Boilingpoint | 267°C at 760 mmHg |
| Density | 1.64 g/cm³ |
| Solubility | Slightly soluble in water |
| Refractiveindex | 1.583 |
| Flashpoint | 128.2°C |
| Smiles | CC1=CC(=C(C=C1)Br)O |
As an accredited 2-Bromo-5-Methyl-Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 grams, tightly sealed with a screw cap, labeled "2-Bromo-5-Methyl-Phenol" including hazard and handling instructions. |
| Shipping | 2-Bromo-5-Methyl-Phenol is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. It is classified as hazardous and is transported according to relevant regulations, using appropriate labeling and documentation. Personal protective equipment is recommended during handling to ensure safety and prevent exposure during transit. |
| Storage | 2-Bromo-5-methyl-phenol should be stored in a cool, dry, and well-ventilated place, away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed and protected from light. Store at room temperature and avoid excessive heat and moisture. Properly label the container and use appropriate personal protective equipment when handling the chemical. |
Competitive 2-Bromo-5-Methyl-Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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In chemical manufacturing, details matter. Over the years, I’ve seen customers return not just for a specific material, but for predictable results batch after batch. 2-Bromo-5-Methyl-Phenol, with the model identifier 23488-38-2, gives that reliability. Through hands-on production and feedback from chemists, we gradually learned which factors actually drive quality in intermediates like this one. Unlike with trading or reselling, the experience of making every batch carries knowledge that gets built into each drum and bag shipped out of our doors.
This compound carries a distinct core: a phenolic ring substituted with a bromine at position 2 and a methyl at position 5. It’s often requested in the form of a pale crystalline solid, offering notable purity and easily handled in production settings. Through direct feedback from formulation chemists, we’ve come to understand that one of its key draws remains selective reactivity. The presence of both a phenol and a brominated aromatic site opens up routes for Suzuki couplings, protective group strategies, and the construction of biaryl systems.
When customers approach us for this molecule, they typically focus on either pharmaceutical intermediate applications or specialty chemical synthesis. Many of the largest volume requests originate from teams investigating new antibacterial agents, building unique dye molecules, or pursuing agrochemical scaffolds. Reliable supply of this compound often means researchers can batch their reactions with less risk of variable impurity levels.
Model number 23488-38-2 represents more than a registry—it’s the output of repeated optimization. Early on, our production lines turned out only modest lots of 2-Bromo-5-Methyl-Phenol, and the main challenge came from residual organic impurities from bromination. Over several years, repeated fine-tuning let us drive the purity above 99 percent in routine batches, verified by GC and HPLC. We heard from customers that even small proportions of tribrominated or demethylated byproducts could affect downstream yields in medicinal chemistry, so removal of these side products became routine QC rather than an afterthought.
To ensure practical usability, we keep the moisture content below 0.5 percent and residual solvents less than 0.2 percent. Our operators prefer lots that form manageable, free-flowing crystals; to that end, we developed a specific crystallization technique that minimizes caking while keeping particle size within a narrow range. These tweaks, born from hours on the shop floor, rarely appear in specification sheets but often make a difference when unloading at a lab or plant site.
Anyone who has spent time in chemical synthesis knows that consistency doesn’t just happen. Our operators run batch records that go back years, recording every slight change in temperature profile, addition rate, or washing solvent. It wasn’t unusual during early scale-up to lose entire batches due to runaway exotherms during the bromination step. Even now, every yield swing is investigated—on countless occasions a subtle variation in impeller speed or jacket cooling explains a difference in product quality. These logs and habits become second nature, and it’s part of why the material we send out today shows tight control from batch to batch.
Regular engagement with users, especially when something unexpected shows up in their chromatography results, has forced us to keep improving. Unlike traders, we can look up a batch by its code and trace it to the shift schedule, the lot of bromine, even the exact cooling water temperature at time of addition. Transparency leads to trust, and that’s tough to imitate without direct production experience.
From a practical standpoint, users value that 2-Bromo-5-Methyl-Phenol ships easily and stores well under standard conditions. Purity drops only when exposed to strong UV or reactive vapors, so routine warehouse storage requires only a sealed container kept away from direct sunlight. Feedback shows our material’s shelf stability routinely surpasses two years in a closed system. For pilot plants and labs where downtime translates to lost work, that reassurance supports uninterrupted progress.
Physical handling drew closer scrutiny after a few user complaints years ago about clumping during humid summer months. We changed our packing protocol to use double-sealed HDPE drums and adjust dessicant amounts, which nearly eliminated those issues. It’s little challenges like these—ones that never appear on material safety data sheets—that set suppliers with factory floor experience apart from middlemen who cannot adapt.
Most of the requests for 2-Bromo-5-Methyl-Phenol fit two main categories: medicinal chemistry and materials science. On the pharma side, it serves as a key step toward aryl ether or biaryl formation, usually as part of a multi-step program toward an active pharmaceutical ingredient or advanced intermediate. Downstream yields hinge on the selectivity of the bromination; unwanted substitution at other ring positions complicates purification and can spoil entire campaigns. We adapt our process to minimize ortho, para, or polysubstitution, delivering a compound that lets customers work faster through their own synthetic routes.
In the colorant and coatings sectors, formulators seek aromatic phenol derivatives that offer both stability and tuneable reactivity. 2-Bromo-5-Methyl-Phenol becomes a useful handle for making complex dyes and UV absorbers, providing sites for further modification while withstanding heat and light exposure better than unsubstituted phenols. In our earliest years, several polymer manufacturers reached out with detailed application questions; the lessons we learned shaped our material’s specification and processing instructions.
Not all phenols are interchangeable in practice. Substitution at the 2 and 5 positions in this molecule alters its reactivity and the types of transformations it supports. Many aromatic bromides suffer from multiple halogenations that trigger side reactions or from poor reproducibility during scale-up synthesis. By sticking to a highly controlled halogenation protocol, our 2-Bromo-5-Methyl-Phenol delivers a single major product, making it an attractive building block for those who must avoid unnecessary downstream complications.
We keep hearing about issues when users try similar halogenated phenols from unverified sources. Some blends have poorly controlled melting points, color impurities, or react inconsistently. Years of feedback led us to reinforce our purification regime with extra distillation and filtration steps. For customers, that consistency translates to cleaner reactions, higher yields, and fewer column partitions. These small edge cases—like how the methyl group alters solubility in specific solvents or how phenolic hydroxyl’s location impacts Selectfluor coupling—grow out of hands-on collaboration, not just textbook knowledge.
In complex synthesis, minor structural changes often matter more than the uninitiated expect. Several customers tried closely related analogs, like 2-Bromo-4-Methyl-Phenol or 2-Bromo-5-Ethyl-Phenol, but the methyl at the 5 position hits a performance sweet spot. The electronic effects stabilize reaction intermediates for some Suzuki and Ullmann couplings, giving better conversion and selectivity. Substituting ethyl or shifting the methyl’s position, based on real user trials, produced more side reactions or required entirely different purification workflows. Over the years, this exact compound evolved into a “standard” for certain segments in dye chemistry and pharma intermediate development, due mostly to its performance in challenging multi-step protocols.
In earlier production campaigns, we noticed suppliers from indistinct channels offering what looked like similar brominated phenols—until side-by-side comparison in UV-vis or HPLC revealed a universe of difference. Some compounds, despite similar paperwork, introduced reactive debris into finished API synthesis or failed to dissolve cleanly during coupling. That consistent gap between production-grade and trader-grade material is only visible through repeated use, which is why many customers demand manufacturer-traceable material for customer-facing projects.
Contaminant control has driven many process improvements. Technical staff in our plant have learned, sometimes the hard way, that uncontrolled bromination introduces hard-to-remove dibromo or tribromo byproducts. Several years of minor setbacks, including an entire campaign scrapped by a key customer due to unacceptable impurity content, led us to optimize our cooling and dosing sequence. Now, every batch undergoes double analysis—once at the end of crystallization, and again after primary drying. Small steps like adding a packed filtration column or extending vacuum drying make a measurable real-world difference.
Long-term customer relationships revolved around trust in our traceability. A few years ago, a deviation in a third-party-sourced solvent caused color impurities in one product batch. While traders might quietly substitute lots or blame user error, we traced the source, overhauled our procurement, and implemented in-house solvent pre-screening. Repeat customers know that batch-to-batch trace assurance and retention sampling help them catch—even before they commit downstream—anything that could veer off course. That engagement isn’t just a slogan. Every growth step came because a chemist called our Q.C. lab, not because a broker relayed a complaint.
End-users often cite the need not just for purity but for robust technical support. Our own technical team works directly with R&D chemists to share process optimization tips, such as best solvents for recrystallization or guidance on handling phenolic residues after coupling reactions. Sometimes a new user will discover that a slight tweak to their existing workup, suggested by our own operators, cuts hours from their project timeline or significantly boosts final yield. That hands-on knowledge has become part of the value we deliver; it grows every year we stay on the factory floor and in touch with those who actually run reactions.
We’ve become acutely aware of environmental and safety implications. As regulations on halogenated phenol intermediates evolve, adaptation becomes a constant. A few years back, wastewater streams became a compliance challenge, especially with brominated residuals. Several upgrades to our effluent treatment and recovery systems allowed us to reduce brominated effluent and cut raw water demand by double digits. We share lessons from these projects with customers who need to fulfill their own sustainability mandates.
Looking ahead, the demand for high-quality intermediates like 2-Bromo-5-Methyl-Phenol shows no sign of waning. Research teams continue to explore more complex targets, which increases the pressure on material suppliers to keep technical standards high. Expanded capacity, tighter process automation, and ongoing partnerships with formulation groups mean we keep learning, adapting, and passing on those improvements in every batch. By staying directly connected to every step—from raw materials through final packaging—we bring customers both material and peace of mind. Every improvement in manufacturability only proves itself through the next synthesis, not on paper.
Being a direct producer of 2-Bromo-5-Methyl-Phenol means carrying every lesson, every near-miss, and every customer success story into each run. The difference between bench-scale success and commercial scale delivery crystallizes over months and years in hundreds of refinements—most invisible to the untrained eye, but felt instantly by an experienced user. This compound stands as a case study in how feedback cycles, practical chemistry, and commitment to real-world usage make a difference. Our containers may ship around the globe, but the trust in each shipment is earned one batch at a time, through careful production and real dialogue with those who count on dependable intermediates.