|
HS Code |
398805 |
| Chemical Name | 1,4-Bromophenol |
| Synonyms | p-Bromophenol, para-Bromophenol |
| Molecular Formula | C6H5BrO |
| Molar Mass | 173.01 g/mol |
| Appearance | White to light yellow crystalline powder |
| Melting Point | 64-66 °C |
| Boiling Point | 218 °C |
| Density | 1.65 g/cm³ |
| Solubility In Water | Slightly soluble |
| Cas Number | 106-41-2 |
| Smiles | C1=CC(=CC=C1O)Br |
| Ec Number | 203-397-0 |
| Flash Point | 109 °C |
As an accredited 1,4-Bromophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 1,4-Bromophenol, labeled with hazard symbols, chemical name, purity, and handling instructions. |
| Shipping | 1,4-Bromophenol is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. It is classified as a hazardous chemical and must be packed and labeled according to relevant regulations. Transportation should ensure minimal handling, with secondary containment to prevent leaks, and compliance with all local, national, and international shipping requirements. |
| Storage | 1,4-Bromophenol should be stored in a tightly closed container, away from light, heat, and incompatible substances such as strong oxidizers and bases. Store in a cool, dry, well-ventilated area dedicated to corrosive or toxic chemicals. Ensure proper labeling and keep away from ignition sources. Use secondary containment to prevent environmental release in case of spills or leaks. |
Competitive 1,4-Bromophenol prices that fit your budget—flexible terms and customized quotes for every order.
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Every batch of 1,4-Bromophenol tells a story rooted in both precision and diligence. For years, we’ve refined our synthesis, relying on a time-tested route that uses para-substitution to give high selectivity and substantial yield. Our teams handle sensitive intermediates daily, from halogenated aromatics through to the final phenolic compound. The core purity comes from anticipation at every checkpoint—small adjustments in temperature, gentle stirring rates, and extended purification cycles where needed. Each lot reflects this care. We never treat production as a checklist; we base our adjustments on chromatography runs and titration profiles collected batch by batch.
In the phenol derivatives space, margins for error run thin. Labs seeking a dependable source for 1,4-Bromophenol have often dealt with inconsistency from lesser-controlled material. Impurities—unreacted bromobenzenes, ortho-isomers, or trace metal residues—complicate applications in fine chemicals, especially in pharmaceutical intermediates. Our team prioritizes starting material scrutiny by sourcing bromine and phenol of high initial purity, minimizing carryover into the final product. Before packaging, we run spectroscopic analysis—typically 1H-NMR and IR—to confirm the compound fits its true fingerprint. The measured melting point, ranging close to its theoretical value, always falls within a narrow variance window due to this attention. This isn’t mere habit; it reduces customer lot rejection rates and fosters repeat projects with R&D teams working on tight deadlines.
1,4-Bromophenol stands out as an aromatic building block for more than its chemical profile. Many in the industry have seen variability in oxidative stability and reactivity from superficially similar suppliers. Those differences usually track back to manufacturing steps glossed over to cut costs: shortcuts in purification or insufficient moisture control. In our reactor halls, process monitoring takes center stage—condensation and distillation steps remain operator-attended, not left to chance. Finished powder undergoes controlled drying and is immediately sealed in lined drums to prevent hygroscopic uptake. We found that exposure, even for a few hours, leads to measurable degradation. Those measures lead to deeply consistent color, retention of free-flowing texture, and clear spectra, which matter in downstream chemistry.
Most customers request 1,4-Bromophenol as an intermediate for pharmaceuticals, agrochemicals, or specialty materials. Few end up using the compound unchanged. Typical syntheses harness its dual functional groups: the phenolic hydroxyl and para-bromine, enabling both nucleophilic substitution and cross-coupling. Drug discovery teams favor the molecule for Suzuki and Buchwald-Hartwig reactions, exploiting its reliability as a coupling partner. In crop science, it serves as a precursor for fungicide scaffolds; performance in this area links directly to batch purity—downstream catalysts don’t tolerate heavy metals or trace halides. Over the years, we’ve learned that even slight presence of ortho-isomers can throw off coupling yields, so we focus hard on eliminating these from the outset.
We identify our core product as 1,4-Bromophenol, with purity grades determined by high-performance liquid chromatography (HPLC) and other instrumental methods. For high-purity pharmaceutical research, we target 99% minimum, and internal records keep track of outlier runs. Color and odor matter, too—a pale white solid with the characteristic slight phenolic scent says much about its state. Bulk buyers, especially those feeding chemical syntheses at scale, need reliable melting point and controlled moisture. That’s why our drying lines see frequent upgrade, and warehouse storage stays climate-protected year-round.
Too many overlook subtleties in packaging aromatic compounds. The phenolic group and bromine atom make 1,4-Bromophenol both reactive and slightly hydrophilic, a combination that presents daily challenges for both ourselves and downstream users. Mistakes in sealing or extended contact with air rapidly introduce water—shifting melting points and opening doors for side-reactions in customer operations. Our drums use double sealing. Each unit gets inert gas backfilling to slow oxidation. While this raises costs, the long-term feedback has justified the investment. Returns and complaints over clumping or darkening fell to near zero once we instituted these steps; customer syntheses started with more reliable material, impacting process yields all the way to finished API or formulated pesticide.
Over the years, we’ve fielded questions about alternative products: “Would 2,4-Bromophenol fit our application?” or “Can’t we substitute a simple bromobenzene?” The structure-activity relationship can’t be ignored. The para-orientation of bromine and hydroxyl on 1,4-Bromophenol allows specific electronic behavior, crucial for transition metal catalysts and directed ortho-metalation. Ortho derivatives give different outcomes in cross-coupling. Simple phenol lacks the halogen, so doesn’t open the same pathways in palladium-catalyzed synthesis. Generic bromobenzenes fail to deliver in cases where hydrogen-bonding is needed or when extra activation is required on the aromatic ring.
Our technical team has worked alongside customer chemists in real time, optimizing catalytic runs or recommending pre-treatment when a project stalls. Differences in melting point, color, and spectroscopic signature between 1,4- and 2,4- isomers determine the route to downstream products, and feedback from these collaborations has pushed us to tighten fractional distillation and crystallization regimes in production. We measure our success not just in kilograms shipped, but in the number of formulation or pilot projects that reach scale without interruption.
We’ve built up a track record with customers working in very different environments. In pharmaceutical R&D, time kills projects, and only chemically reliable inputs keep development on pace. Our phenol derivative rarely becomes the active pharmaceutical ingredient itself, but forms the backbone of transition-metal catalyzed assembly, as seen in recent kinase inhibitor programs. In agroscience, manufacturers design generations of new agents that demand rapid turnaround of new intermediates. Here, analytical support—beyond minimum compliance—wins hearts. Sometimes, a new impurity crops up due to a change in a downstream process; we can troubleshoot by quickly running a GC-MS snapshot from retained samples, helping narrow down the culprit and save wasted scale-up time.
In electronics research, several teams push limits of organic semiconductors and polymer chemistry. 1,4-Bromophenol enters there as a monomer or pre-cursor for conducting polymers due to its head-to-tail orientation and functionalization options. Demands for electrical properties put greater scrutiny on ionic and metal contaminants. We upgraded our cleaning protocols on reactors and transfer lines following one such project, keeping sodium and calcium levels at new industry lows—sometimes under a few ppm—which directly translated to improved device yield for the customer.
Chemistry often comes with a significant environmental tail. Our own journey into minimizing impact started out of necessity. Early on, solvent use and bromine emissions challenged us with community pushback. We reworked scrubber systems, reducing atmospheric release contours to below measurable thresholds. Solvent recovery has become routine, with performance tracked weekly. Mother liquors, spent catalyst solutions, and phenolic byproducts all route to a closed-loop treatment system that produces re-usable output and slashes disposal bills by almost half. Regular site audits now combine with chemical mass balances, exposing us to third-party input that’s helped catch blind spots before they grow into regulatory issues.
Our teams recognize the importance of offering not only a reliable product, but one that comes from a responsible process. We now publish annual summaries—not only for compliance but to foster transparency that our industrial, academic, and R&D partners value. Sharing our mapped reductions in solvent use or energy demand gives others a chance to calibrate their own sustainability metrics, and draws in partnerships from buyers facing similar ESG demands.
Projects rarely stay in the same lane. A customer might start by purchasing a few hundred grams of 1,4-Bromophenol for early synthesis, then require hundreds of kilograms as the candidate molecule proves out. Scale-up brings unique challenges—mixing dynamics change, heat transfer profiles shift, and impurity profiles evolve. Our technical services group engages with scale-up chemists to match batch characteristics at every stage, sometimes producing custom grades, dried to bespoke levels or filtered to a unique micron level. Custom labeling and traceability certificates accompany each batch, so process validation, wherever in the world, won’t hit snags due to unexpected documentation.
We’ve shouldered tight lead-time demands from customers launching pilot production—sometimes delivering on timelines measured in days. Close partnerships with freight forwarders, and redundant raw material sources, let us respond to surges. Communication stays direct with the production floor. Delays in raw material or an unexpected technical snag prompts immediate customer notification, not a vague automated email. Accountability has kept relationships strong, and kept projects on track for all parties involved.
Operating in the specialty chemical arena means constant exposure to regulatory drift, supply chain disruption, and evolving customer demands. Brominated aromatics, in particular, face scrutiny over health and environmental hazards. We respond by maintaining active compliance records; employees undergo regular training not just to tick a box, but to engage with policy and real-world scenarios. Regulatory updates, from REACH to regional safety requirements, find their way into our process documentation almost as soon as they are published. Material Safety Data Sheets get overhauled with every significant change, including new labeling or transport restrictions demanded by authorities.
We also anticipate increased focus on particle size for advanced material projects. Several times, a shift in the distribution curve down by even a small margin made customer blending or dissolution unreliable. We’ve invested in finer milling and sieving, testing particle size by laser diffraction analysis to detect tail ends in the distribution. This close monitoring keeps end-use batches consistent over time and gives researchers a running start on new formulations.
Our plant isn’t just a set of reactors or a warehouse filled with drums. Each consignment forms the beginning, or continuation, of a partnership where knowledge and reliability blend to help customers innovate. We don’t treat customers as numbers; feedback loops go straight to the chemists and production staff responsible for every lot. It isn’t unusual for us to jump on a call with a chemist in Europe, troubleshooting a bottleneck in a cross-coupling step, pulling up our own analytics, and suggesting modifications that might speed up their route. Genuine conversation and collaborative problem-solving have powered several research breakthroughs. These relationships lead to incremental improvements in every facility run. Cases where customers need a modified drying profile or quick turn on a high-purity run get escalated without bureaucracy.
1,4-Bromophenol may seem basic amid a catalogue of novel reagents and fine chemicals, but the demands placed on its purity and consistency often outstrip more exotic compounds. Our plant teams feel this pressure. Small advances—like optimizing a crystallization step, or switching to a more robust chromatography resin—get tested and, if successful, folded directly into routine runs. We prefer clear, measurable improvements to just matching certificate values. Our aim stays set on creating a compound that serves as both reliable input and a vehicle for breakthrough—the kind of building block that speeds up reactions, reduces failed batches, and creates an edge for research and manufacturing customers alike.
Chemistry never stands still, and neither does our knowledge about 1,4-Bromophenol. Each project, every failed or successful lot, expands what we can offer and how we support our partners’ research. We track not just our internal output—yield, purity, physical state—but stay engaged with global trends that point to new uses and evolving regulations. Our staff attends technical conferences, collaborates with industry peers, and runs internal skill development focused on safety and state-of-the-art analysis. Through these activities, we aim to offer not just 1,4-Bromophenol, but ongoing value and peace of mind.
While we could list data points or offer up generic assurances, our real advantage lies in deep engagement with every stage of the process. From the raw materials to the final sealed drum, through to the customer’s bench or production line, our hands-on approach builds a track record you can trust. Whether your focus lies in life sciences, material synthesis, or custom chemistry, you'll find that attention to detail and a collaborative mindset define our offering. 1,4-Bromophenol, produced with this perspective, doesn’t just act as another chemical—it becomes an enabler of progress across countless research and production environments.