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HS Code |
283370 |
| Product Name | 2,6-Dibromo-4-Fluorophenol |
| Cas Number | 180163-82-4 |
| Molecular Formula | C6H3Br2FO |
| Molecular Weight | 285.89 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 85-89°C |
| Density | 2.16 g/cm³ (estimated) |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥98% |
| Smiles | C1=C(C=C(C(=C1Br)O)Br)F |
| Inchi | InChI=1S/C6H3Br2FO/c7-3-1-4(8)6(10)5(9)2-3/h1-2,10H |
| Synonyms | 2,6-Dibromo-4-fluoro-1-hydroxybenzene |
| Storage Conditions | Store at 2-8°C, dry and well-sealed |
As an accredited 2,6-Dibromo-4-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 2,6-Dibromo-4-Fluorophenol, sealed with a screw cap and labeled with hazard information. |
| Shipping | 2,6-Dibromo-4-Fluorophenol is shipped in secure, sealed containers to prevent exposure and contamination. It is transported according to regulations for hazardous materials, with clear labeling and safety documentation. Temperature and moisture controls may be applied to maintain product integrity during transit. Handle with proper personal protective equipment upon receipt. |
| Storage | 2,6-Dibromo-4-Fluorophenol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition or incompatible substances such as strong oxidizers. Protect from light and moisture. Store at room temperature and avoid excessive heat. Use appropriate chemical labeling and ensure access is restricted to trained personnel. |
Applications of 2,6-Dibromo-4-Fluorophenol in Industrial ManufacturingAs the original manufacturer of 2,6-Dibromo-4-Fluorophenol, we supply high-purity material directly to production facilities across multiple advanced synthetic industries. Below, we outline key downstream application routes, referencing actual quality standards, applied formulation ratios, practical process sites, and specific types of finished goods by sector. 1. Pharmaceutical Intermediate for API SynthesisThe compound acts as a halogenated phenol building block in multi-step synthesis of select pharmaceutical actives, especially advanced intermediates for next-generation anti-infective and oncology drug candidates where precise halogen placement affects molecular binding and metabolism studies. Researchers and process chemists introduce it after aromatic substitution sequences and before key cyclization or condensation operations, with formulation optimization tightly controlled based on target molecule design and scale-up batch consistency. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisThis halogenated phenol finds frequent use in the agrochemical industry as a core intermediate for the production of specialty herbicides and selective fungicides. The molecular structure enables designers to tune efficacy and environmental degradation profiles in the final crop protection product. It is commonly added during the early stage aromatic ring assembly, followed by acylation, alkylation, or additional halogenation based on the required biological activity spectrum. Industry compliance standards
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3. Electronic Chemical Precursors for Photoresist ManufacturingAdvanced microelectronics fabrication integrates the material into custom photoactive resin formulations used in pattern transfer for semiconductor wafers. Photolithography suppliers rely on precise substitution and electron-withdrawing patterns provided by this intermediate to improve contrast, sensitivity, and process latitude. It enters the process during the synthesis of photoacid generators or as a modifying phenolic component in resin backbone extension steps. Industry compliance standards
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4. Specialty Material for Liquid Crystal Display (LCD) Alignment LayersFormulators in advanced display manufacturing utilize this compound as a modifier in polyimide alignment layer production, benefiting from its regioselective halogen groups to impart improved anchoring energy and thermal stability for liquid crystal cells. These processing advantages enable producers to achieve higher uniformity in alignment and reduce image retention in final devices, with the material joining the matrix during the imidization stage of polymer synthesis. Industry compliance standards
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5. Intermediate in Veterinary Drug SynthesisProducers of specialized veterinary pharmaceuticals integrate this input during multistep synthesis of certain topical antimicrobials and feed additive intermediates where specific halogenation patterns contribute to bioavailability and spectrum of activity. Reactions involve site-directed coupling or oxidative cyclization using the phenolic substrate, followed by purification to veterinary-grade GMP requirements before blending into final dosage forms. Industry compliance standards
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Working with 2,6-dibromo-4-fluorophenol comes down to understanding what chemists and formulators actually need in the lab or plant. Every decision on the floor, from how we control temperature on the reaction kettle to which grade of bromine source we use, affects the quality and consistency of this compound. As a team who manages the process from raw material selection to the final crystallization stage, we see firsthand the critical details that influence performance and downstream compatibility for end users.
The model often requested by research labs and manufacturing partners is based on the molecular formula C6H3Br2FO. Our own batches typically reach purity levels above 98%, which gives our customers flexibility whether they are scaling syntheses or conducting scientific research. No batch leaves our facility without going through ^1H NMR and HPLC verification; we know that assurance matters, especially for those who depend on reproducibility and trace impurity tracking.
There is a reason research teams and production lines seek out 2,6-dibromo-4-fluorophenol over other halophenol variants. The dual bromines in the ortho positions, flanking the phenolic oxygen, shift the electronic character of the ring. Combined with the fluorine at position 4, this arrangement stabilizes the molecule in unique ways. Reactivity, solubility, and even the way the product behaves under light or heating all trace back to this structure.
Some customers ask about the functional difference between this compound and something like 2,4-dibromo-6-fluorophenol or even simple 4-fluorophenol. From our experience, the steric protection imparted by the ortho-bromines plays a huge role in reducing unwanted polymerization and sidereactions during further stages of synthesis. The fluorine atom at the para position provides selective activation, making this compound work better as a versatile intermediate, especially in pharmaceutical and agricultural chemistry where precision counts.
Consistency is not optional. Our facility is equipped to deal with moisture control, which matters since halophenols like this one show sensitivity to atmospheric water. We package in sealed, inert containers shortly after purification, keeping the material dry and stable until it’s in the customer’s hands. There is little tolerance for error here — a trace of water or even a minor contaminant alters downstream yields or activity in target products. The lessons learned on the production line become material facts for those who use our product, so we keep tight process records and provide full traceability on every lot.
Most requests come from industries seeking reliable phenolic intermediates for the development of specialty pharmaceuticals, agrochemicals, and exploratory material sciences. The unique halogenation pattern of 2,6-dibromo-4-fluorophenol makes it a favorite for those looking to introduce both bulk and selective reactivity into their aromatic system. Medicinal chemists, for instance, pursue this structure for core modifications — not just for its own sake, but because it serves as a solid building block in synthesizing fluorinated or brominated APIs. Testing batches for reactivity with various acylating or alkylating agents, we’ve noticed how standard protocols behave differently depending on trace impurity levels and crystal form, so we work with process researchers to optimize each production run, dialing in exactly what they want.
Agrochemical developers rely on sharp batch-to-batch reproducibility. As any farmer or supplier in the agricultural supply chain knows, consistent outcomes are essential. A single off-spec batch of phenolic intermediate not only derails formulation but risks regulatory approval downstream. By tightly controlling process parameters — such as solvent ratios and temperature staging — we supply a product that formulators can trust in their herbicidal or fungicidal pipelines.
There have been growing trends in the use of halogenated phenols for new material development. Specialty polymers and coatings use 2,6-dibromo-4-fluorophenol for its ability to introduce electronic modulation in polymer backbones. For material scientists in need of performance coatings or advanced electronic materials, the combination of high-purity phenol and precise halogen substitution unlocks new functionalities. Few substitutes deliver the same balance of reactivity and thermal stability, and we’ve seen this first-hand in customer pilot projects.
Making 2,6-dibromo-4-fluorophenol is not as simple as just dosing bromine into the reaction flask with a fluorophenol precursor. Over-bromination, for example, introduces heavy impurities that are devilishly hard to remove downstream. The right solvents, reaction timing, and workup steps are crucial to avoid producing mixed isomers or over-substituted side products. On the production line, our chemists spend more time on analytical characterization than some might expect. Each parameter — from cooling gradients to solvent evaporation rates — has been fine-tuned over years based on what we’ve learned in practice.
Filtration, crystallization, and drying each carry their risks. Vacuum levels influence residual solvent content, so we record every deviation. Overly aggressive drying can lead to decomposition or loss of the phenolic OH group, shrinking yield and degrading quality. No generic process from literature ever fits exactly; every aspect of our procedure has been walked, step by step, by our own team to match what end users truly require.
Cleanup after synthesis is as important as the chemistry itself. After a run, the reactor and pump lines see a full solvent purge with organic and aqueous washes to prevent cross-contamination. For some, these steps might look excessive, but we’ve seen how a seemingly invisible residue can come back to haunt later batches. Recordkeeping and lot tracking mean that if a customer calls about anything unusual, we can trace back not just the materials, but who ran the batch and on what date.
After years in chemical manufacturing, the differences between 2,6-dibromo-4-fluorophenol and more common halophenol derivatives become clear. Many phenolic building blocks—take 2,4,6-tribromophenol or 4-fluorophenol for instance—target broader applications. Their higher reactivity can be an asset, but this also means chemists fighting with unpredictable byproducts, difficult purification, or poor selectivity.
2,6-dibromo-4-fluorophenol brings a blend of steric hindrance and specific activation that isn’t easy to replicate. The ortho-bromines protect the phenolic OH while still allowing for targeted derivatization through the para-fluorine. This means synthetic chemists can pursue more selective cross-coupling or alkylation reactions without sacrificing stability. Downstream, these features reduce waste, improve final purity, and save time—assets that matter for both research and large-scale manufacturing.
Our skeptical customers often compare halogenated phenols by real-world factors: melting point, handling stability, byproduct profiles, and, sometimes, even odor or material color. 2,6-dibromo-4-fluorophenol stands out for its crystalline form, ambient shelf stability when dry, and a solid melting point that aids in solid-handling processes. Its lower volatility, compared to simpler phenols, means safer, more predictable handling through both pilot and commercial manufacturing.
Scale-up of halogenated phenols always brings surprises. Thick slurries, exothermic reactions, and sensitive washing steps test equipment and operator skill. On larger reactors, heat transfer and mixing become less forgiving than in the small-batch pilot stage. Our team has spent years refining agitation speeds, feed rates, and extraction protocols to avoid both incomplete reaction and physical blockages.
Disposal and emission control take on new significance at ton-scale. Bromine emissions, spent acid waste, and halogenated byproducts are tracked and neutralized at our facility using multi-stage scrubbing systems and chemical neutralization. Environmental compliance is not an afterthought; every lot leaves our plant with documented waste treatment records, both for our peace of mind and for customers facing their own regulatory reviews.
Sourcing reliable raw materials—especially high-purity bromine and fluorinated phenols—often limits supply. We maintain supplier relationships measured in years, not months, and regularly audit incoming materials. In-house QA brings confidence, sparing customers from headaches caused by undetected batch variance.
For many in R&D or production, technical support is crucial. Our chemists provide direct insights on handling, solubility, and compatibility with other process components—knowledge drawn from running the same reactions ourselves. We recognize the difference between desk research and hands-on troubleshooting. Some customers encounter sticky residues after filtration or observe unexpected exotherms in pilot scale; we’ve faced the same hurdles, so our advice goes beyond generic troubleshooting.
Whether it’s optimizing for flow chemistry, minimizing solvent usage, or improving reaction selectivity, collaboration with downstream partners only strengthens outcomes. Several joint projects with pharmaceutical innovators led to modified isolation conditions, improving both purity and overall process yield. Our facility supports these collaborations by providing small-scale evaluation samples or adapted batch sizes, so customer teams can test and adjust before committing to larger orders.
Every manufacturing stage comes with safety checks, not just because regulations say so, but because our own teams handle these chemicals daily and expect the same standards for their safety as any end user would. The work involved in managing brominated and fluorinated aromatics can’t be understated—skin and respiratory sensitivity, combined with the need for solvent control and thorough ventilation, lead us to over-build our facilities with containment and air handling in mind.
Minimizing waste is more than a talking point. Solvent recovery systems allow us to re-use a significant portion of organic solvents in subsequent batches, stacking both cost savings and environmental benefit. As we track new developments in waste minimization and energy-saving synthesis routes, there’s ongoing investment in improving yields, reducing wash volumes, and recycling process streams. These are not always easy fixes, but the incremental improvements build up over years.
Feedback from long-term customers has reshaped how our team approaches everything from raw material inspection to the design of packaging. Listening to complaints about shipping damage or receiving caked material led us to redesign both our containers and our post-drying protocols. Now, most shipments of 2,6-dibromo-4-fluorophenol leave our plant double-sealed, with desiccant and tamper-evident closures. This isn’t a marketing move—losses from shipment problems add cost and waste, and the lessons learned investing in better presentation show up in fewer support calls and improved customer trust.
Meeting customer expectations, especially when tight delivery schedules abound in the life science and specialty chemistry industries, means putting extra eyes on both the paperwork and the finished goods. Every supply contract brings a new set of expectations, and we tailor storage and delivery according to each partner’s feedback. Rush orders, batch certifications, post-delivery analysis—it’s part of the work that goes with being a true manufacturer.
We see new research driving further demand for 2,6-dibromo-4-fluorophenol, not only for the standard applications, but in emerging areas like complex organic frameworks, photostable polymers, and electronic materials. Researchers developing these materials face new challenges: tighter impurity specs, demand for greener synthesis, or the need to support scale transitions from bench to bulk. As manufacturers, it’s our responsibility to adapt both our process technology and our quality management systems to support these advances.
Process intensification—whether continuous-flow synthesis, in-line purification, or automated sampling—remains an active area in our facility. Early results show better yields, lower solvent waste, and shorter turnaround times. We work directly with equipment vendors and academic partners to incorporate these capabilities, aiming to deliver not just better product, but smarter, more efficient processes across the supply chain.
Knowledge sharing forms a big part of our value. Open communication with partners—whether for analytical methods, stability studies, or waste management—sets us apart as a manufacturer, not just a supplier. Trust grows in these dialogues, translating into shared success, fewer surprises, and a smoother path from reactant to finished product for everyone involved.
Years of making and shipping 2,6-dibromo-4-fluorophenol have taught us what customers require: consistency, transparency, problem-solving acumen, and respect for the realities of daily laboratory and facility life. Beyond meeting the spec sheet, we strive to provide guidance, address challenges, and keep improving both product and process.
For anyone seeking high-purity, reliable, and thoughtfully-manufactured 2,6-dibromo-4-fluorophenol, we commit ourselves every day to deliver the kind of value we expect as chemists, and as partners. The combination of technical depth, real-world experience, and open communication defines how we do business. From raw material intake to final shipment, every detail counts—and nobody is more invested in your successful application of this product than those who craft it from the ground up.