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HS Code |
297966 |
| Productname | 4-Bromo-2,6-Difluorobenzyl Alcohol |
| Casnumber | 864070-88-8 |
| Molecularformula | C7H5BrF2O |
| Molecularweight | 223.02 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Smiles | C1=C(C=C(C(=C1F)Br)F)CO |
| Solubility | Soluble in organic solvents |
| Storagetemperature | 2-8°C |
| Inchikey | OMFUVXHMMFXAMZ-UHFFFAOYSA-N |
As an accredited 4-Bromo-2,6-Difluorobenzyl Alcohol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g of 4-Bromo-2,6-Difluorobenzyl Alcohol is packaged in a sealed amber glass bottle with a tamper-evident cap. |
| Shipping | 4-Bromo-2,6-Difluorobenzyl Alcohol is shipped in tightly sealed containers, protected from moisture and light. It is classified as a chemical reagent and should be handled with care, following all relevant regulatory and safety guidelines. Shipping is typically via ground or air transport, in accordance with applicable hazardous material regulations. |
| Storage | 4-Bromo-2,6-Difluorobenzyl Alcohol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, heat sources, and incompatible substances such as strong oxidizers. Keep the container clearly labeled and avoid exposure to excessive temperatures. Use proper protective equipment when handling and ensure storage complies with local regulations. |
Applications of 4-Bromo-2,6-Difluorobenzyl Alcohol in Industrial Manufacturing4-Bromo-2,6-Difluorobenzyl Alcohol plays a critical role as an intermediate in multiple high-value chemical industries, contributing precise molecular structure, functional reactivity, and strict batch consistency for sophisticated end-use formulations. Our direct integration into customer supply chains supports seamless compliance with global regulations and scalable process optimization. 1. Pharmaceutical Active Ingredient SynthesisThis raw material enters the pharmaceutical sector as a key building block for synthesizing advanced intermediates applied in drug manufacturing, especially for patent-protected small molecule APIs in oncology, antiviral, and CNS therapeutic classes. End users select this compound due to its halogenation pattern, which facilitates selective downstream substitution reactions, maintaining stringent impurity profiles critical to drug safety and quality control. Industry compliance standards
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2. Agroch emical Active Intermediate PreparationThe compound finds consistent demand in agrochemical manufacturing, serving as a functionalized aryl alcohol precursor for the synthesis of next-generation herbicides and insecticides. Its dual halogen substitution enables regioselective modifications, which enhance biological uptake and degradation profiles for active ingredient innovation focused on regulatory-mandated residue limits and environmental safety. Industry compliance standards
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3. Advanced Organic Electronic Material SynthesisManufacturers employ this alcohol derivative to construct specialized aromatic monomers incorporated in organic light-emitting diodes (OLEDs) and high-performance liquid crystal alignment layers. The alcohol group offers anchoring capability for subsequent etherification or esterification, while bromo and difluoro substitutions impart desired electronic characteristics, required for controlled charge transport and emission wavelength tuning. Industry compliance standards
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4. Specialty Fine Chemical Synthesis (Custom Intermediates)Research-driven chemical companies integrate this aryl alcohol into the synthesis of fluorinated and brominated specialty intermediates, customized for advanced material development, molecular diagnostics, or process analytical chemistry. The material's multifunctional structure supports modular attachment, which boosts flexibility in creating target compounds that often require tight impurity and trace element control, particularly in the context of multi-kilogram pilot campaigns. Industry compliance standards
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Among the broad palette of fluorinated benzyl alcohol derivatives, 4-Bromo-2,6-difluorobenzyl alcohol stands out for chemists looking to build more complex structures in the lab. Its molecular formula, C7H5BrF2O, and CAS number 241382-55-2 draw interest from synthetic organic chemists and the teams who supply them. In the manufacturing plant, handling this material goes beyond the routine, especially when scaling from kilo-lab to hundred-kilogram lots. Not every fluorinated benzylic alcohol with a bromine atom gets the job done in the same way, and the nuances arise in the details only the manufacturer experiences firsthand.
Adding a bromine atom at the para position on a 2,6-difluoro-substituted benzyl alcohol core doesn’t just look good on a blackboard—it matters for how it behaves in further chemistry. Over years of producing similar halogenated aromatics, certain quirks around purity and side-product profiles become familiar. That bromine, coupled with two strong electron-withdrawing fluorines, tunes the electron density on the ring and impacts downstream reactions. Fluorines in the 2 and 6 positions help conserve reactivity at the benzylic hydroxyl while suppressing unwanted side reactions on the aromatic core.
Other benzyl alcohols—swapping out those halogens for something else—often lead to lower selectivity or harder purification. These small changes affect yield, crystallization, and stability. Early on, we tried alternative routes with similar molecules, but the absence or rearrangement of fluorines or bromine built complexity into otherwise straightforward reactions.
Standard model numbers may serve the logistics team and procurement process, but in the plant, those numbers signify far more—consistent grade, particle attributes, and analytical benchmarks. 4-Bromo-2,6-difluorobenzyl alcohol typically emerges as a colorless to faintly yellow crystalline solid, with melting points and purity thresholds that matter for each batch. Analytical teams look for HPLC purity above 98% and NMR spectra without surprises. Water content, typically below 0.5%, prevents instability during sensitive reactions downstream. Residual solvents, especially from halogenated and aromatic solvents, require rigorous monitoring, as even trace amounts risk sabotaging the next synthetic step for our customers.
From a chemical manufacturer’s perspective, 4-Bromo-2,6-difluorobenzyl alcohol doesn’t leave much room for error in its journey from reactor to drum. Many of our customers use this compound as a key intermediate in the synthesis of complex pharmaceuticals or specialty agrochemicals. Its bromine and fluorine atoms lend themselves well to cross-coupling and nucleophilic substitution reactions. Medicinal chemists favor it for building up more advanced scaffolds where selective activation, especially on the benzylic position, is critical. It’s especially popular for preparing active pharmaceutical ingredient (API) intermediates that require strict traceability and batch reproducibility.
Compared to similar benzyl alcohols—such as those with only fluorine or chlorine substituents, or purely hydrocarbon cores—this compound opens up different reactivity profiles. Its dual fluorine substituents both shield the ring from unwanted side reactions and steer reactivity toward the benzylic position. The para-bromine creates a reliable handle for palladium-catalyzed cross-coupling. Once you handle enough halogenated intermediates, these small differences save days or weeks in the plant and lab.
Long before any shipment leaves the facility, quality assurance takes center stage. Lessons from early batches showed that trace by-products—sometimes barely traceable by TLC—could build up through subsequent steps and pollute a final API synthesis. With 4-Bromo-2,6-difluorobenzyl alcohol, controlling the exotherm during bromination and fluorination steps prevents overreactions and impurity formation. Analytical development continually tunes detection limits to spot even minute process deviations.
Without these controls, impurity profiles shift, and yield in next-step couplings or oxidations falls off. Chemists who’ve spent hours tracking down a rogue isomer from a poorly controlled batch know the cost firsthand. Over a decade of dialing in synthetic routes, adjusting agitation rates, and designing purification protocols, every modification serves the same goal: reproducibility, so that each shipment matches the last. That reliability doesn’t happen by chance.
Scaling haloaromatic compounds brings challenges—agitated vessels, exothermic additions, even the way you quench reaction mixtures requires a steady approach. Generating waste containing brominated and fluorinated by-products also poses environmental responsibilities. At the plant, these challenges aren’t abstract. Engineering controls and careful solvent recovery reduce the environmental footprint, and the waste treatment equipment’s performance features in operator meetings as often as throughput data.
Solvents like dichloromethane or toluene, common in these syntheses, get recycled in an on-site distillation loop. Though initial investment runs high, lowering the overall volume of halogenated waste saves cost and meets stricter compliance requirements. In the synthetic world, few things slow a line down faster than a red-tagged waste drum or a regulatory audit gone sour. By controlling emissions and minimizing hazardous runoffs, we align manufacturing with regulatory trends and societal expectations.
Not all production issues show up in a batch report. Packing materials for halogenated benzyl alcohols, for instance, matter more than most realize. Standard HDPE jugs don’t handle long-term storage well due to potential permeation and degradation, which affects shelf life and purity. Glass containers do the trick for the lab, but at scale, the risk of breakage and cost become prohibitive. We landed on fluorinated HDPE and specialized liners, avoiding leaching and permeability issues—solutions born from a line of ruined drums and customer complaints long before the right workflow matured.
Winter sometimes brings shipment delays and destabilization concerns during longer overland journeys. The balmy season offers its own headaches: tightly sealed drums expand, internal pressures climb, and the risk of seal breaches surfaces. Our logistics crew learned to factor these real-world complications into lead times and packaging decisions. There’s no textbook for discovering just when a compound like 4-Bromo-2,6-difluorobenzyl alcohol exceeds its thermal comfort zone in transit—those insights accumulate the hard way.
Having produced a parade of benzyl alcohol derivatives, the subtle differences drive home the importance of every atom. Early attempts with non-fluorinated or differently substituted analogs brought inconsistent reactivity, less stability, and, in some cases, tricky purification steps. With 4-Bromo-2,6-difluorobenzyl alcohol, the electron-poor aromatic ring ensures better shelf stability and less aerial oxidation than certain methyl- or chlorine-only analogs. This makes it less prone to discoloration or resin formation on storage.
The balance that this compound strikes between nucleophilicity on the benzylic hydroxyl and leaving-group capacity on the aromatic ring hits a sweet spot for Suzuki–Miyaura or Buchwald–Hartwig couplings. That’s more than a chemical property—it becomes an economic and workflow advantage in an active campaign, saving purification steps and reducing labor hours. Project managers appreciate fewer deviations and surprises on pilot-scale syntheses; for them, a more predictable benzyl alcohol directly impacts the path to the customer’s finished product.
Raw materials for halogenated and fluorinated intermediates rarely arrive trouble-free. Every lot of potassium fluoride or bromine source gets tested for trace contaminants that might later emerge in product impurity profiles. Sometimes, changes at a supplier—switching solvent grades, altering drying protocols, or swapping container types—show up as unexplained shifts in purity or color. For 4-Bromo-2,6-difluorobenzyl alcohol, years of sourcing diligence get compressed into every “in-spec” batch.
Sustainable sourcing, while a buzzword for many, touches the ground in our daily planning. A steady contract with a fluoride supplier, for instance, cuts the risk of last-minute shortages and price volatility. Our procurement and production teams coordinate to balance cost containment with long-term supplier relationships, understanding that any disruption echoes across the production schedule and ultimately to the end user.
Customer audits become commonplace with high-profile intermediates. Pharma and agrochemical clients expect more than a certificate of analysis—they often request end-to-end traceability and manufacturing records down to the equipment used. Internal audits, batch record reviews, and electronic lab notebook integrations have grown further entwined in our workflow. Acting on deviations before they cascade improves reliability and builds shared confidence across the supply chain.
We’ve learned that even something as small as a loosened process step or a delay in recording a titration end-point can lead to questions weeks later. Establishing digital traceability across raw material arrival, production, and quality control adds overhead, but now stands as standard practice in demanding markets.
Sometimes, routine feedback loops from customers—complaints about haze, odor, or solubility—spark deeper process investigations. In the past, switching a step to avoid residual pyridine didn’t just fix one company’s problem—it led to tighter control of the drying cycle and solvent purity. As regulations and applications evolve, so does our manufacturing. Even minor improvements to the carbon footprint matter in a world of expanded environmental scrutiny. Closed-loop solvent recovery, heat integration between process steps, and remote monitoring systems have become daily tools, not luxury options.
Improvement in yield over the past five years came from focusing on individual bottlenecks identified both by operators and automated controls. Transitioning to finer agitation during bromination, for example, shortened reaction times and reduced impurity formation. The plant team shares ownership in these solutions, innovating changes not just for efficiency but for a cleaner downstream process, shorter cycle times, and consistent product output.
Demand for 4-Bromo-2,6-difluorobenzyl alcohol continues to trend upward, fueled by wider adoption of fluorinated building blocks in drug discovery and pesticide formulation. These downstream industries face increasing pressures to deliver molecules with improved bioavailability, metabolic stability, and selectivity. The compound’s structure provides a versatile node for further derivatization—either by introducing new functional groups at the benzylic position or replacing the bromine through metal-mediated cross-couplings.
From our end, these trends translate to a need for flexible batch sizes, tighter analytical verification, and the capacity to respond quickly to changes in forecasted volumes. Increasingly, customers ask about supply chain security and site redundancy, urging chemical manufacturers to plan not just for regular operations, but for contingencies and surge demand.
Many of the recurring obstacles, such as unplanned shutdowns, scale-transfers, and raw material variations, lose their sting through relentless process documentation and routine risk assessments. On-site laboratories run parallel tests, sometimes analyzing the same batch multiple times to cross-verify data and forestall error propagation. Staff training, dating back to onboarding and extending through periodic review, ensures best practices stick around long after the consultant leaves.
Batch-to-batch consistency in halogenated intermediates like 4-Bromo-2,6-difluorobenzyl alcohol relies less on automation alone and more on retaining practical know-how. Sitting alongside new chromatography equipment are logbooks filled with handwritten notations, reminding everyone on the plant floor how frequently success leans on direct experience. It’s not about chasing perfection, but getting a little closer with every iteration.
Real-time monitoring of reaction progress, linked to control systems, reduces guesswork and enables proactive interventions. Several process upsets caught early via inline FTIR or NMR monitoring have prevented costly batch failures. Data capture doesn’t just help internal teams; when customers ask for deeper analysis—a chromatogram, an impurity profile, or a trending report—the required detail already sits waiting in the digital dashboard.
In the coming years, machine learning models may identify predictive markers in the process that even experienced chemists overlook. Combined with networked process control, future manufacturing can support more robust and transparent relationships with supply chain partners, minimizing the risk of disruption and supporting end-user confidence.
From the plant’s perspective, producing 4-Bromo-2,6-difluorobenzyl alcohol never comes down to hitting a purity number alone. Delivering this compound means providing reliability, traceable quality, and a clear path forward for the customer’s own synthesis needs. Our work doesn’t stop at the reactor or filling line, but extends into technical support and the capacity to troubleshoot issues as they arise in client laboratories.
The most successful supply relationships develop when both sides recognize the reality—chemicals like these aren’t commodities. They’re crafted tools, shaped by process improvements, day-to-day problem solving, and ongoing attention to detail. With every step, from raw material sourcing to packaging to shipment tracking, our plant’s focus remains locked on delivering a product trusted by chemists who know the fine difference every atom makes.