Anhui Liwei Chemical Co., Limited
Products

2,6-Dibromo-4-Fluorophenol


    • Product Name 2,6-Dibromo-4-Fluorophenol
    • Alias 2,6-Dibromo-4-fluoro-1-hydroxybenzene
    • Einecs 259-992-2
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    362872

    Productname 2,6-Dibromo-4-Fluorophenol
    Casnumber 28442-09-5
    Molecularformula C6H3Br2FO
    Molecularweight 285.90
    Appearance White to off-white solid
    Meltingpoint 82-86°C
    Boilingpoint No data available
    Density 2.13 g/cm³
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    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
    Refractiveindex No data available

    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 & Storage
    Packing Amber glass bottle containing 25 grams of 2,6-Dibromo-4-Fluorophenol, sealed with a screw cap, labeled with hazard and identification information.
    Shipping 2,6-Dibromo-4-Fluorophenol is shipped in tightly sealed containers, compliant with international regulations for hazardous chemicals. It should be protected from moisture, heat, and incompatible substances. Proper labeling and documentation are required, and it must be handled by trained personnel, ensuring safety during transportation. Store in a cool, well-ventilated place.
    Storage 2,6-Dibromo-4-fluorophenol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect it from light and moisture. Clearly label the storage area and ensure restricted access to authorized personnel. Use chemical-resistant shelves or cabinets specifically designed for storing hazardous organic compounds.
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    Certification & Compliance
    More Introduction

    2,6-Dibromo-4-Fluorophenol: Practical Insights from a Chemical Manufacturer

    Understanding 2,6-Dibromo-4-Fluorophenol in Real-World Manufacturing

    2,6-Dibromo-4-fluorophenol holds a distinct value in our lineup, forged through precise halogenation and fluorination steps that rely on clean, controlled environments. Having run multi-ton batches in stainless-lined reactors, I can confidently say few intermediates give as consistent results when stringently handled. This compound, known in the lab as 2,6-DBFP, brings together the stability of two bromine atoms and the electronegativity of a single fluorine on a phenolic ring, making it more than a specialty item for niche research. Over years of direct feedback and field testing, several patterns of successful deployment stand out, especially in pharmaceutical intermediate synthesis and advanced material fabrication.

    Specifications That Actually Matter to Our Clients

    From our own continuous process testing, the technical benchmark for 2,6-DBFP emerges from batch-to-batch reproducibility. Purity measured by HPLC has moved past the 99% mark in nearly every scale-up I’ve supervised. Moisture and elemental analysis come back tight—typically below 0.3% water content and within a narrow window for residual free halides. In daily use, these physical scores aren’t just lab numbers; they decide how smoothly our customers’ next reaction stage will run. Our in-house team saw too many headaches from contaminants or off-white batches during early production trials. Learning from these, our current method spins up bright, off-white crystals that filter and dry quickly, with melting points consistently matching literature values.

    Most requests land between 100g and 25kg, packaged moisture-proof before handoff. Larger reactors let us respond quickly if a client scales up unexpectedly—we’ve done triple-digit kilo lots on short notice during API rollouts. Packaging integrity isn’t an add-on, it’s the direct answer to hydrolysis risk that ruins phenolic stocks left exposed just a few days too long. The best batches I’ve run leave no unpleasant odor, minimal dust, and hit target specs on first test—those are the lots our returning customers name in their project notes.

    What Usage Looks Like in the Lab and at Scale

    Here’s what often gets missed: The phenolic function in 2,6-DBFP really shines as a chemical handle. Most buyers we talk to aren’t just chasing a unique ring—they need something reactive enough for cross-coupling and protection schemes, stable enough for prolonged storage. Solubility profile tends toward organic solvents—DCM, chloroform, and EtOAc—making it straightforward to run extractions and clean isolations after coupling or substitution steps. We’ve watched both pharma innovators and agrochemical developers pull yields above 95% during their screening when the starting DBFP is clean and dry from our plant.

    I’ll never forget a customer visit where we watched a few grams go through a Suzuki coupling. The chemist ran with a standard air atmosphere, minimal base, and saw conversion hit completion fast, thanks to the electronic effects driven by the two bromines and one fluorine. That trifecta gives this intermediate its edge: the bromines activate the ring for further substitution, while the fluorine tames undesired side reactions, especially compared against dihalophenols lacking the electron-withdrawing punch of fluorine. Where requests come in for halogenated phenols that can survive aggressive metal-catalyzed steps, I recommend 2,6-DBFP every time—not because it’s a catch-all, but because our own in-house chemistry confirms its versatility.

    Comparing 2,6-DBFP to Other Halogenated Phenols

    Direct comparison comes up often, especially when users look at 2,6-dibromophenol, 4-fluorophenol, or broader mixed halides. Our own data—pulled straight from GC-MS and NMR results—puts 2,6-DBFP in a narrower impurity window, with a better balance of reactivity and shelf stability. If you line up a group of similar phenols, most with two bromines but lacking fluorine develop brownish tints or degrade faster under light. Those with more than one fluorine, or more complex halide patterns, see poor yields in Suzuki or Buchwald-Hartwig couplings, based on side-chain elimination or inactive ring positions.

    Fluorination at the 4-position doesn’t just tweak electronics; it suppresses ortho/para migration and stabilizes the intermediate against both oxidation and unwanted dimerization. I remember a specific pilot run of non-fluorinated 2,6-dibromophenol: we fought off-color formation and odd resonance peaks on NMR because phenolic hydrogen migrated under stress. Plugging in the 4-fluoro, as nature sometimes dictates in halogenated natural products, locked the structure and cut wasted effort chasing down byproducts.

    Another concern from our scale-up clients centers on ease of purification. Other options, especially bulkier mixed halogen phenols, resist standard silica filtration or tend toward emulsions. 2,6-DBFP routinely gives sharp melt points and smooth separations, even when you process crude product directly from quench. Our in-house safety team appreciates the lowered volatility and milder hazard profile, since off-gassing of brominated or over-fluorinated phenols complicates handling on open benches. This creates fewer bottlenecks in kilo-scale runs, reducing both PPE burden and engineering controls.

    Improving Supply Consistency in Response to Real-World Challenges

    Quality and consistency follow from deep process control, not just paperwork or outside audits. Early batches forced us to rethink our stoichiometry, especially managing bromination runs that drifted due to minor temperature fluctuations. Adding in-line monitoring—UV and IR sensors—caught the deviation in real time, letting us dial in smaller temperature gradients and avoid over-bromination. Supply chain squeezes in bromine and specialty fluorinating agents almost always ripple into pricing or availability. Instead of waiting for market shocks, we diversified upstream raw suppliers and built a small in-house regeneration loop that reclaims and purifies solvent, minimizing both cost swings and environmental impact.

    Having worked shoulder-to-shoulder with R&D chemists and process engineers, I’ve seen firsthand the difference tight in-process controls make for complex aromatics. A batch lost because of uneven fluorination hits more than yield—it sets back development timelines for our buyers. Tracking every critical parameter, from halide feed rates to endpoint titration, we catch trouble before it leaves the tank. That level of detail lets us back what we ship, no matter if it’s destined for a gram-scale trial or a full-on production campaign.

    Supporting Customers Beyond the Drum

    Conversations with our customers don’t stop at product release forms. Process transfer data, solvent compatibility, recrystallization procedures—these often turn up as urgent calls weeks after initial delivery. We pull from our actual production archives to advise on solubility tweaks or alternate quenching agents when unexpected side products appear. There’s no substitute for hands-on knowledge covering trial runs, cleaning protocols, and scale transitions. More than once, sharing our own recovery and drying tips cut our client’s cycle times by hours, if not days.

    I see many buyers moving on to more complex phenol couplings, especially as fluorinated aromatics rise in drug development. The clean reaction profiles of 2,6-DBFP let scale-up groups avoid nasty downstream separations. We stay agile to adjustments—whether a customer needs a tighter sieve fraction or a different packaging size for their automated transfer lines, we take those requests as an opportunity to improve product delivery, not an afterthought. Every new feedback session, every in-person visit, shapes our batch documentation so future orders meet real—not hypothetical—lab needs.

    Product Reliability Rooted in Hands-On Process Control

    So many challenges in phenol production surface far from the safety of academic design-of-experiment charts. Outgassing, color drift, recovery losses—these pave the way for subpar intermediates that stall development downstream. We haven’t just studied these effects—we’ve wrestled with them under pressure. Take a poorly controlled bromination: color drifts, side products stack up, and the main peak on GC starts losing area. We address these realities long before material ships to a customer. It’s this kind of hands-on troubleshooting that makes the final material more than a just a catalog number, turning it into a dependable tool useful even under harsh synthetic protocols.

    Process robustness shows up clearest on the receiving end. Process chemists tell us again and again that 2,6-DBFP from our lot handles well with glovebox techniques, doesn’t stick to stainless, and resists hydration in both HDPE drums and foil-lined sacks. The fine particulate profile means less breathing hazard during transfer, another overlooked safety plus. Oddly, the same attributes that challenge us in drying and grinding become selling points: consistent particle size and flowability cut lost mass and make gravity transfers painless.

    Troubles We’ve Faced—and How They Guide Continuous Improvement

    Troubleshooting batch failures pointed to truths that no handbook predicts. We lost two entire campaigns early on to poorly calibrated peristaltic pumps—leading to runaway fluorination, sticky residues and months of lost work. Patched seals on glass reactors allowed ambient moisture and tainted more than one kilo lot. Both incidents led to investment in new monitoring equipment and tighter SOPs. It feels easy to write off lost time as the cost of doing business, but every setback complicated a downstream customer’s campaign for weeks.

    Cross-contamination sometimes occurs if older lines aren’t vapor-purged or if impeller blades go uncleaned after similar halides. We turned this into a training case for our new operators—using real contaminated samples to highlight trace impurities under GC. Now, a scheduled cleaning protocol follows every switch, no exceptions.

    Another lesson came from international shipping restrictions. During one recent global disruption, several shipments sat in customs for weeks, risking polymerization of sensitive material. Our logistics crew quickly swapped to smaller-pack formats and ramped our insulated warehousing to keep product within tolerances. We see this as our job: preventing small logistical hitches from turning into process headaches halfway around the world.

    Why 2,6-DBFP Keeps Its Place Amid Changing Regulations and Emerging Needs

    Regulatory agencies now flag more halogenated organics for long-term review. 2,6-dibromo-4-fluorophenol still passes all major regulatory screens for purity and hazard labeling, and we track all updates on both RoHS and REACH list status. Whenever regulations tighten or new reporting expectations emerge, we update labeling, SDS, and test protocols to relay changes proactively. Our in-house compliance officers coordinate directly with buyers to avoid last-minute surprises, particularly for scale-ups in pharma where timing drives bottom line costs.

    Material traceability takes front stage in audits these days. We push all analytical reports, batch records, and test results into a customer-accessible database, so any process check or repeat run can track back to the exact day and lot the sample came off our drying trays. If a production issue arises—with an impurity, a drift in melting point, or a delayed shipment—real traceability lets us solve that problem for the next batch, not just patch it for the current order.

    Looking Forward to New Applications and Feedback Loops

    Interest keeps rising in fluorinated intermediates that can stand up to complex coupling chemistry without creating side reactions or regulatory flags. Our development partners explore new ligation techniques, greener coupling routes, and advanced performance plastics using classic phenol frameworks like 2,6-DBFP. Every new method we pilot, every innovative process our partners share back, feeds a growing body of know-how that strengthens future production and introduces efficiencies on both sides of the transaction.

    Nothing replaces eyes-on-lab experience. Partners and competitors alike echo a simple truth—real production stories, documented by hands on the shop floor, dictate the learning curve for every new intermediate. No catalog entry can anticipate problems like persistent clumping after storage or incomplete dissolution in low-polarity solvents. Through continued process analytics, side-by-side pilot trials, and debrief calls with clients, we adapt our product for both legacy and emerging apps. Suggestions—from antistatic packaging to finer-tablet grinding—show up as adjustments in the very next round of production, not shunted to the background.

    Staying close to customer teams speeds innovation on both ends. We send technical representatives to on-site troubleshooting whenever a customer hits an unfamiliar reaction snag with DBFP. Results from these collaborations jump straight back to plant management and process engineers, so incremental improvements make their way into regular production, sharpening each batch and deepening trust.

    Putting Experience to Work for Better Chemistry

    Manufacturing 2,6-dibromo-4-fluorophenol takes more than a recipe: it draws on years of collective wisdom about raw materials, equipment quirks, and customer needs. Every batch, every feedback loop, strengthens the reliability of the end material. Those planning downstream syntheses, whether in pharma, specialty materials, or advanced research, stake their timelines and budgets on starting intermediates that behave the same way time after time. We keep open communication, double down on training, and monitor every metric, so the material that leaves our door delivers the same results run after run. In a field where minor deviations in input create huge swings in output, attention to real-world issues—never just theoretical specs—separates a trusted partner from just another supplier.

    We encourage every user of 2,6-dibromo-4-fluorophenol to share back lab hurdles, innovative uses, or unexpected side reactions. What we learn together won’t just support continuous improvement for one plant—it seeds best practices for the wider technical community, advancing practical science everywhere this unique intermediate travels. Our ongoing goal: keep chemicals flowing seamlessly from synthesis through process and application, so the innovators using our material can focus on progress, not troubleshooting supply.