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HS Code |
849143 |
| Product Name | 4-Bromo-2-Chloro-6-Fluorophenol |
| Molecular Formula | C6H3BrClFO |
| Molecular Weight | 225.45 g/mol |
| Cas Number | 852140-74-0 |
| Appearance | White to off-white solid |
| Melting Point | 55-59°C |
| Purity | Typically ≥ 97% |
| Solubility | Slightly soluble in organic solvents |
| Density | Approximately 1.8 g/cm³ |
| Synonyms | 2-Chloro-4-bromo-6-fluorophenol |
| Smiles | C1=C(C=C(C(=C1Cl)F)Br)O |
| Storage Temperature | Store at 2-8°C |
| Hs Code | 29081990 |
As an accredited 4-Bromo-2-Chloro-6-Fluorophenol 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 4-Bromo-2-Chloro-6-Fluorophenol, tightly sealed, with hazard labeling and tamper-evident cap. |
| Shipping | 4-Bromo-2-Chloro-6-Fluorophenol is shipped in tightly sealed containers, protected from light and moisture. Packaging complies with hazardous materials regulations, including appropriate labeling and documentation. Shipments are handled by certified carriers and are tracked during transit to ensure safe delivery. Storage at ambient temperature is recommended unless otherwise specified. |
| Storage | **4-Bromo-2-Chloro-6-Fluorophenol** should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers or bases. Keep it in a cool, dry, and well-ventilated area, preferably in a designated chemical storage cabinet. Ensure proper labeling and avoid exposure to heat and ignition sources. Use appropriate personal protective equipment when handling. |
Applications of 4-Bromo-2-Chloro-6-Fluorophenol in Industrial ManufacturingAs the original manufacturer, we supply 4-Bromo-2-Chloro-6-Fluorophenol for industries that require precise halogenated intermediates to achieve stringent technical, quality, and regulatory objectives. Below, we outline how major downstream sectors integrate this raw material into targeted workflows, providing details for regulatory compliance, practical formulation specifics, manufacturing process stages, and resulting end products. 1. Pharmaceutical Intermediate SynthesisThis halogen-substituted phenolic compound functions as a critical intermediate during multi-step synthesis of select APIs in oncology and antiviral medication pipelines. The chemical structure enables key biaryl coupling and halogen exchange reactions central to target molecule assembly, satisfying high-purity demands in regulated pharmaceutical manufacturing pipelines. Industry compliance standards
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2. Agrochemical Building BlockDownstream agrochemical manufacturers use this specialty phenol to achieve precise substitution in the synthesis of advanced herbicide actives. Its combination of bromine, chlorine, and fluorine enables effective tailoring of reactivity profiles in key coupling and cyclization steps, supporting the molecular innovation that drives higher crop protection selectivity and environmental compliance. Industry compliance standards
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3. Specialty Dyes and Pigment PrecursorsAdvanced dye and pigment producers exploit the trifunctional halogen attributes to generate high-performance pigment intermediates suitable for electronics, imaging, and specialty coatings. The structure delivers both chromophore extension and improved fastness properties crucial for downstream coloration performance in strict technical environments. Industry compliance standards
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4. Advanced Material CoatingsSelective incorporation into the formulation of engineered surface coatings leverages the phenolic and halogen substituted structure to enhance adhesion and chemical durability. Coating manufacturers utilize this raw material in precision applications demanding high resistance to solvents, acids, and atmospheric degradation—requirements typical in electronics, optics, and specialty glass processing lines. Industry compliance standards
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Working hands-on with halogenated phenols, the subtle variations in each molecule change not just the chemistry but the whole approach to the synthesis and application. 4-Bromo-2-Chloro-6-Fluorophenol, known in shorthand by its CAS number 142073-30-1, has become an integral part of our product lineup for a reason—one rooted in real experience and persistent feedback from formulation teams.
This compound offers more than a string of halogen atoms stuck to a ring. Its precise substitution pattern leads to an interplay in reactivity not found in more commonly used phenols or simple monohalogenated versions. Every group on that aromatic ring—bromo at the 4-position, chloro at the 2-position, and fluoro at the 6—modulates both stability and reactivity toward downstream synthesis, influencing how we build more complex molecules or intermediates.
We have learned not to just follow specifications but to shape them in line with laboratory and factory realities. Our 4-Bromo-2-Chloro-6-Fluorophenol comes as a crystalline solid, crafted for low moisture and consistent particle size. Our typical batches feature assay levels above 97%, with each lot confirmed by NMR and HPLC. Residual solvent content stays below thresholds required for advanced pharmaceutical synthesis, and trace metal content is monitored at every step.
Color alone often tells a story before formal analytics kick in. Clean, off-white or faintly pale crystals show proper handling and purification—dull or discolored stocks point to oxidation or hydrolysis, which we check after every synthesis. This vigilance surfaced over years of batch improvements and customer evaluations.
Shelf stability under dark, dry storage reaches well past a year, which eliminates nervousness during shipment delays or project slowdowns. Our experience with international clients, especially in hot and humid regions, led us to focus on stability with double-sealed containers and humidity indicators. These might seem like small details, but any chemist reading this knows firsthand the frustration of unplanned hydrolysis halfway through a synthesis.
Few aromatic compounds deliver so much flexibility in such a compact structure. Straight from feedback in the plant and the lab, here’s how manufacturers, especially those in pharmaceuticals and agrochemicals, use this molecule. Each group on the ring gives a tailored handle for further transformation. Nucleophilic aromatic substitution runs more efficiently, especially on the fluorinated position, as the electron-withdrawing effect of the bromo and chloro subtly activates the ring. Aromatic halogens also serve as excellent leaving groups or points for palladium-catalyzed cross-coupling reactions.
In the hands of experienced organic chemists, 4-Bromo-2-Chloro-6-Fluorophenol becomes the cornerstone of synthesis for substituted phenol derivatives. Reactions worked out on small scale quickly reach kilogram scale in our reactors, thanks to predictable behavior—no foaming, no runaway side reactions, and consistent yields during etherification, esterification, or Suzuki-Miyaura coupling.
Agrochemical developers appreciate the selective reactivity, utilizing it for building blocks in seed treatments and growth regulators. For active pharmaceutical ingredients, the trifecta of halogens enables the construction of sterically demanding, metabolically robust intermediates. We have received requests from several multinational companies looking to leverage this exact substitution pattern to build in metabolic stability into their candidate drugs or fine-tune their bioactivity profiles.
Many newer, high-potency actives coming to market trace their origins back to versatile building blocks like 4-Bromo-2-Chloro-6-Fluorophenol. In custom synthesis, this product consistently ranks among the preferred starting materials for crafting more complex halogenated rings and heterocycles. Medicinal chemists value how this molecule opens doors to rapid analog generation, especially where selective dehalogenation or directed ortho metalation is required.
Compared to phenols with a single halogen, the tri-halogenated structure resists unwanted oxidation far better, especially during storage and workup in batch reactors. We handled cases where single-chloro or mono-fluoro phenols degraded or discolored over time, leading to off-spec batches. The presence of bromo and chloro next to fluorine increases both shelf life and reliability under a wider range of storage and process conditions.
During reaction scale-up, predictable melting and crystallization prove essential. This model rarely throws plant operators for a loop—instead, operators get clear dissolutions, reproducible filtration, and easy wash-downs after the shift. That means fewer headaches, less wasted solvent, and less lost time.
Those working in fine chemical synthesis will spot the difference in halide substitution. Mono-halogenated phenols leave you with limited scope on cross-coupling or nucleophilic substitution, especially as you introduce sensitive substituents. With this molecule, the three halogens open up sequential substitution strategies that don’t call for much extra protecting group manipulation. That saves both steps and waste, an issue that comes up often in process meetings where time, yield, and regulatory cost matter equally.
On an analytical level, this compound provides sharper, more easily interpreted NMR and mass spectra. Our analytical team, having reviewed samples from dozens of suppliers, consistently notices that the tri-halogen pattern delivers clearer, more distinct peaks, which helps ensure every batch meets its intended spec.
Over the years, working closely with operators and analytical chemists, we’ve dialed in our process to avoid the three most frequent production issues we saw in the early days: solvent inclusion, halide scrambling, and batch carry-over. We chose synthesis steps that prevent rearrangement and minimize environmental footprint—no excess halogen usage, just enough for conversion, and built-in scavenging.
Our drying routine reflects lessons learned the hard way. We made investments in low-temperature vacuum drying, which prevents unwanted color formation and retains the mild odor profile customers expect from a high-purity tri-halogen phenol. Each production batch follows the same script—synthesis, quench, crystallization, repeated water washes, solvent stripping, and drying with real-time monitoring. We focus on keeping dissolved inorganic salts below 0.2% weight, ensuring both compatibility in process and excellent filterability.
No matter how optimized the process, solvent traces sneak in. Over time, we homed in on which solvent residues mattered most. Now, every batch sees a full GC profile before release, and residual DCM or THF consistently runs far below both ICH and local requirements for pharmaceutical intermediates.
Since we ship globally, we prioritize neutral pH, no visible particulates, and low static charge on the product—small details, but the sort that signal attention to quality to every receiving QC lab.
Requests for custom sizing and packaging grew alongside the popularity of this molecule, not as an afterthought, but as a direct response to process engineers and chemists looking to reduce manual handling and dust formation. In scaling up for bulk orders, we started vacuum-packing at the source and offering multiple drum sizes. The result: much less risk of environmental contamination and batch-to-batch transfer loss.
Feedback from formulation chemists has shown that the compound’s solubility in non-polar and mid-polar solvents speeds up integration into typical process flows—no need to adjust entire batch protocols just to accommodate one tricky starting material. Once it hits the reactor, solid dispersion completes quickly; plant operators reported faster clean-out times, shorter processing windows, and consistently less downtime.
Our discussions with partners and users have repeatedly brought up how easy it is to scale up from gram scale to over a hundred kilograms. This sort of feedback, directly from project managers and technical directors, led us to invest further in batch reproducibility and more robust distillation trains for mother liquor recovery. It’s surprising how much smoother regulatory filings and audits go when every drum matches its COA, and customers experience zero surprises in downstream formulations.
Quality in specialty chemicals rarely comes down to just analytical specifications. We spend just as much time listening to pain points: unexpected crystallization, filter clogging, batch discoloration after heat treatment, or problems integrating with automated dispensing systems. These aren’t just “nice-to-fix” issues. They are the realities that drive decision-making at every stage, from plant trials to full-scale commercial runs.
For 4-Bromo-2-Chloro-6-Fluorophenol, direct relationships with formulation teams and bulk handlers revealed unexpected benefits. Enhanced handling characteristics reduced clean-out times, and fewer complaints about dust exposure let us improve not only quality but worker safety. Small changes to drum liners, the addition of tamper-evident seals, or the use of static-dissipative packaging added up to fewer rejected shipments and more consistent customer satisfaction scores.
Over the past decade, one trend has become undeniable: increasing scrutiny over halogenated chemical production. Regulatory agencies worldwide continue to press for lower halogen emissions, better waste treatment, and full traceability for each step in production. As a manufacturer, this goes beyond simply meeting local laws. It shapes our everyday decisions.
By adopting closed-loop waste solvent systems, we cut halogen emissions in our plants by nearly half. Investing in better catalyst capture and recycling systems has kept precious metals out of both waste streams and downstream product, turning what would have been regulatory headaches into operational improvements. Rather than treating compliance as a cost, we see it as a challenge that can drive smarter chemistry.
Many of our customers in regulated segments—agrochemicals, pharmaceuticals, custom synthesis—have insisted on full lot genealogy out of legal and ethical necessity. That pushed us to track every source material, every reaction vessel, and every cleaning protocol. This transparency feeds directly into environmental, social, and governance scoring by external audit teams, a trend we see growing from North America to East Asia.
Energy input remains another major consideration. Traditional synthesis of tri-halogen phenols required either high-pressure reactors or energy-intensive halogenation. Drawing on feedback from factory engineers, we switched to milder reaction conditions wherever possible, integrating heat recovery between consecutive process steps and automating temperature control to avoid both overprocessing and wasted cooling cycles.
We don’t shy away from the challenges associated with scale. Every ton of product carries with it the cumulative impact of these decisions, and our approach has been to stay open to customer feedback and regulatory guidance. Each improvement, whether in waste reduction, raw material traceability, or packaging safety, has come from real conversations with lab managers, technical directors, and frontline operators.
The true differentiator isn’t always apparent to those outside the plant walls. But for a chemical with this structure, we have found the combination of purity, reactivity, and stability rarely encountered together. Both the trifecta of bromo, chloro, and fluoro groups and the knowledge baked into our process set it apart from similar compounds.
Looking beyond lab analysis, strict quality routines and deep integration with receiving labs up and down the supply chain reveal real performance advantages. A well-made batch saves days worth of troubleshooting, regulatory rework, and laboratory adjustment. It reduces waste and prevents accidents—especially critical as more chemical plants move toward heightened safety regulations and operator protection.
Our product goes to teams working on everything from next-generation crop protectants to cancer treatments. Practical concerns dominate every conversation we have with end-users—cost per unit of transformation, safe handling under heat and pressure, and reduction of side reactions when used with sensitive catalysts. Stable performance from batch to batch means less recalibration and more confidence, whether you’re working at bench scale or feeding a multi-ton reactor.
Whether crafting a single milligram sample for R&D or filling trucks for commercial scale, every improvement reflects a direct encounter on the plant floor, a lesson learned, or a customer requirement met. This ongoing cycle of feedback and improvement underlines the value of experience—chemistry executed with consistency at scale, supported by proof, not promises.
Our history with the 4-Bromo-2-Chloro-6-Fluorophenol process has taught us that ongoing engagement with customers, regulatory groups, and internal teams builds a better product than tight specs alone. The best measures of progress come from customer success in downstream synthesis, reliable batch release, and a continuous stream of challenges from those working on the frontlines of chemical development.
Solving new problems keeps us moving forward: how to push purity boundaries, further minimize environmental impact, or package more safely for global transit. Each improvement—driven by practical necessity, not just compliance—turns up as better processing, less waste, and smoother workflows for the chemists and operators counting on our products.
Trust built over years does not come from generic promises or abstract virtues but from getting into the details—batch by batch, shipment by shipment, problem by problem. We keep showing up, learning from each production run, and letting every lesson shape the next step in chemical manufacturing.