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HS Code |
915545 |
| Chemicalname | 4-Bromo-2,6-Difluorobenzonitrile |
| Casnumber | 57381-51-6 |
| Molecularformula | C7H2BrF2N |
| Molecularweight | 218.00 |
| Appearance | White to off-white solid |
| Meltingpoint | 58-62°C |
| Purity | Typically ≥98% |
| Density | 1.74 g/cm³ |
| Solubility | Slightly soluble in organic solvents (e.g., DMSO, DMF) |
| Smiles | C1=C(C=C(C(=C1F)Br)F)C#N |
| Inchi | InChI=1S/C7H2BrF2N/c8-5-1-4(3-11)2-6(9)7(5)10/h1-2H |
| Storageconditions | Store at room temperature, tightly closed |
| Hazardclass | Irritant |
As an accredited 4-Bromo-2,6-Difluorobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g package is a sealed amber glass bottle with a white label detailing chemical name, formula, hazard symbols, and supplier information. |
| Shipping | 4-Bromo-2,6-Difluorobenzonitrile is shipped in tightly sealed containers, protected from moisture and light, and labeled according to hazardous material regulations. It is transported via certified carriers, following all safety and environmental guidelines for handling chemicals, including compliance with relevant local, national, and international shipping laws and documentation requirements. |
| Storage | Store 4-Bromo-2,6-difluorobenzonitrile in a tightly sealed container, in a cool, dry, well-ventilated area, away from direct sunlight, moisture, and incompatible substances such as strong acids or bases. Keep away from sources of ignition and oxidizing agents. Ensure proper labeling and secondary containment, and avoid prolonged exposure to air. Use appropriate personal protective equipment when handling. |
Applications of 4-Bromo-2,6-Difluorobenzonitrile in Industrial Manufacturing4-Bromo-2,6-difluorobenzonitrile serves as a key intermediate in several advanced chemical manufacturing sectors, supporting precise synthesis demands in pharmaceuticals, crop protection, and materials science. Manufactured and quality-assured in-house, we supply this material for high-purity applications where tight specification control is required for downstream processing. 1. Pharmaceutical Active Ingredient SynthesisThis compound acts as a core building block in the synthesis of advanced pharmaceutical intermediates, especially in the production of targeted kinase inhibitors and central nervous system (CNS)-active molecules. Multi-step process routes often require its integration at an early stage, where halogenated and fluorinated aromatics are essential for optimized biological activity profiles. Our sites manufacture and test this material according to stringent control protocols for use in API synthesis pathways. Industry compliance standards
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2. Agrochemical Intermediate ProductionOur material is integrated into advanced crop protection molecule synthesis, supporting the assembly of pyridine and pyrazole derivatives with halogenated aromatic backbones. Leading agrochemical groups use it for next-generation herbicide and fungicide actives, where both fluorine and bromine substitutions are critical for field efficacy and regulatory compliance. Industry compliance standards
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3. Liquid Crystal Display (LCD) Material SynthesisDisplay technology manufacturers utilize 4-bromo-2,6-difluorobenzonitrile for synthesizing advanced liquid crystal monomers with high dielectric anisotropy and chemical stability. Reactivity of the halogen and nitrile groups in this material enables the construction of rigid-rod or biphenyl LC structures, enhancing pixel switching speeds and display clarity in modern TFT-LCD panels. Industry compliance standards
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4. Advanced Polymer Synthesis for Specialty CoatingsChemical processors use this material in the polymerization of high-performance engineering resins and specialty fluorinated polymers. The inclusion of both cyano and halogen functionalities allows for controlled copolymerization, delivering improved chemical resistance and thermal stability to downstream coating and film applications in electronics and automotive sectors. Industry compliance standards
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5. Custom Fine Chemical SynthesisContract synthesis organizations and custom research groups require this aromatic nitrile for the preparation of patented intermediates or research-only molecules. Its dual halogen and nitrile functionalities support diverse coupling, cross-coupling, and nucleophilic substitution reactions essential for rapid prototyping and SAR studies in chemical innovation pipelines. Industry compliance standards
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Competitive 4-Bromo-2,6-Difluorobenzonitrile prices that fit your budget—flexible terms and customized quotes for every order.
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At our production facility, we have worked hands-on with halogenated aromatics for years, and 4-Bromo-2,6-Difluorobenzonitrile stands out in our lineup for its reliability and purity. Every batch that leaves our reactors reflects both the routine and the discipline that come from years of scaling up aromatic nitrile synthesis. In the world of advanced organic intermediates, this compound gets more attention than some may expect. That comes down to reproducibility, and to the consistent, crisp profile this molecule brings to synthesis sequences in the labs and plants of our clients worldwide.
The chemical backbone—C7H2BrF2N—offers a unique interplay between the electron-withdrawing effects of bromine, the pair of fluorines, and the nitrile. The substitution pattern sharpens its reactivity profile. A chemist who has worked through benches stacked with benzonitriles, benzaldehydes and their halogenated cousins knows how a pair of fluorines in the meta positions and a large para bromine tip the electronic balance. It is this exact setup that often gives 4-Bromo-2,6-Difluorobenzonitrile a significant edge over other benzonitrile isomers in coupling and substitution chemistry.
In our facility, batches are manufactured in high-purity form. The structure allows it to be provided as a white or nearly white solid, crystalline and free-flowing after appropriate drying and sieving. Flash point, melting point, and other thermophysical properties closely follow established literature values, but each lot is checked with in-house spectra and chromatographic records. Our QC lab runs regular GC, HPLC, and NMR analyses; this remains the only way to maintain the confidence that you, and our own process chemists, expect. In actual practice, the handling experience is straightforward—minimal dustiness, predictable solubility in common organic solvents, and a stable shelf presence when moisture and heat are kept away.
Let’s take a look at practicalities. Powders that cake quickly or clump after short storage spells can create bottlenecks in production. Over the years, our experience with controlling solvents and drying parameters has produced a solid that resists caking even in humid climates, making both sampling and transfer easier for operators. Waste minimization occurs naturally when you can weigh and dispense material without half of it sticking to every metal scoop along the way.
Since we are directly involved in production, the bulk of our output travels to customers in fiber drums and HDPE pails with security seals. Drum sizes and packing materials have evolved over time, shaped by feedback from downstream processors working with automated feeders or batch reactors. Some partners requested specialized liners to avoid static charge or material adherence. These requests are simple for us to accommodate since packing happens next to synthesis rather than at a third-party warehouse. We have tweaked our drying and cooling steps to limit static charging, so powders do not become airborne or migrate when drums are filled or emptied. These small details can make the difference between a smooth shift and hours of cleanup on a plant floor.
On the ground, operators appreciate that our product pours easily and rarely forms lumps, even after a few weeks in a warehouse. That is not an accident. A lot of attention goes toward the final milling and screening stages; as a manufacturer we have more control over these aspects than traders and resellers. When you deal directly with the factory, you avoid the problems caused by multiple rounds of repackaging or long, uncontrolled periods in bulk transport.
4-Bromo-2,6-Difluorobenzonitrile found its place predominantly as a coupling partner and intermediate for diversified syntheses. Production chemists who have to scale up palladium-catalyzed cross-couplings often prefer this molecule, since it delivers robust yields and fewer by-products compared to similar monofluorinated or unsubstituted benzonitriles. The reactivity stems from the driving influence of the electron-withdrawing substituents—chemists reach for this intermediate in the pursuit of fluoroaryl motifs that remain stable under harsh process conditions. In our direct conversations with formulation chemists, structural features like these usually mean fewer surprises in downstream steps.
Pharmaceutical developers often draw on this intermediate for custom aryl building blocks. We see repeated orders from process development labs exploring scalable synthetic routes for kinase inhibitor scaffolds or niche agrochemical actives. The aromatic ring’s balance between electron density and bromine availability makes it a smooth starter for preparing biphenyls, diarylethers, and other complex motifs through Suzuki-Miyaura and Buchwald-Hartwig reactions. Our R&D team worked in close communication with process chemists from several multinational firms to optimize pathway yields for molecules requiring difluorination, where other benzonitriles failed to deliver high selectivity or enough stability.
Customers often ask how 4-Bromo-2,6-Difluorobenzonitrile stacks up against its mono-substituted cousins or other fluorinated benzonitriles. Based on results from both pilot and full-scale production, the combination of ortho fluorines with the para bromine creates a distinctive balance: enhanced reactivity while holding on to enough stability that material loss is minimal during purification. In physical property terms, purity remains high, and color stays acceptable. Other halogenated benzonitriles, particularly those with only a single fluorine or without bromine, have sometimes proven too reactive or, conversely, insufficiently active, leading to more side reactions and less predictable results in cross-coupling.
As a manufacturer, one of the most telling distinctions appears in actual throughput and reproducibility. The difluoro configuration decreases the risk of unwanted electrophilic substitution in subsequent steps, so impurities are easier to clean out with standard work-ups. In less engineered nitriles, our clients have reported batch-to-batch drift in reaction kinetics, impacting both yield and safety. With 4-Bromo-2,6-Difluorobenzonitrile, those differences narrow, especially as operators gain experience with its handling profile.
Security of supply for key inputs like bromine and specialty fluorinating agents matters more than ever. Direct manufacturing gives us an edge here—we control upstream sourcing, and build redundancy by long-term agreements with regional chemical consolidators. Through regular site audits, we confirm the quality and consistency of our input streams. When the market for specialty aromatics tightens, that position lets us buffer customers from price shocks and persistent shortages. More than once, downstream producers have called us with last-minute increases in needed output; our control of both feedstock and output has enabled us to deliver during difficult times.
The approach to waste management also differentiates manufacturing from repackaging. Over half a decade, we have overhauled our scrubbing systems, and installed new capture columns for acidic and halogenated waste. All transfers remain closed, so off-gassing or exposure never put workers or neighbors at risk. As one of the chemists directly responsible for reviewing HSE reports, I have seen how design changes such as secondary containment pay dividends. The days of open-drum transfer and deferred clean-up belong in the past. Investing early in process safety and environmental control brings process reliability and keeps our reputation intact with every shipment.
Our factory’s process engineers know that regulatory documentation adds another layer to specialty intermediate production. We provide analytics, batch records, and impurity profiles that match the traceability standards of both pharma and agrochemical firms. Every certificate you receive with your order reflects batch-specific test records, not boilerplate sheets copied from the internet. Customers want details, not broad claims. That transparency builds partnerships, since research and commercial teams on the other side of the world can use our data to make real-time process modifications without waiting for second-hand answers.
The most tangible evidence of trust comes from multi-year supply agreements. Those only come after months, sometimes years, of joint troubleshooting and specification refinement. Bench chemists and plant managers give us pointed feedback—sometimes about solubility, particle size, or compatibility with specialized carrier solvents. We incorporate those requests far more quickly than traders, since changes don’t require multiple layers of approvals or relabeling across distant warehouses. That’s one of the distinct advantages of buying direct from a production source.
The journey to an improved 4-Bromo-2,6-Difluorobenzonitrile process did not come from textbook recipes alone. Over many campaigns, our operators logged differences in solubility, stability, and reaction exotherms in real time. It took more than one cycle of failed dryer runs to achieve a repeatable powder consistency. We learned to keep both process and packaging close together. Our operators now monitor ovens and drum filling lines located side by side on the same floor, which reduces the lag between synthesis and packing, helping us bypass moisture pick-up and static build-up. It is these details—visible only on the factory floor and not in sales slides—that build the product experience into every delivery.
Input from different industries spurred process upgrades, too. A few years ago, a pharmaceutical customer pointed out that their batch yields saw slowdowns with excessive fine particles near the bottom of a drum. We went back, upgraded sifting equipment, and added a supplemental blender on the drum line. Soon, we heard from the same customer that their filter beds were running cleaner and the yield uptick paid for itself. Such results do not emerge from generic spec sheets—they arise through direct feedback, frequent dialogue, and the willingness to experiment and implement new approaches.
As an aromatic nitrile with halogen functionality, this compound requires clear logistics planning—especially given customs scrutiny and transit regulations in multiple markets. Freight forwarders, customs compliance teams, and receiving warehouses all look for up-to-date labeling and hazard communication, which we issue directly. Having managed dozens of international bulk shipments each season, our staff know the pitfalls of winter container condensation and summer heat waves. We pack for the conditions—not just the regulations spelled out in codes—and keep extra padding and barrier liners on hand for high-humidity or long-haul destinations.
Storage challenges led to another practical tweak. Past experiences demonstrated that uncontrolled storage produces caked, yellowed, or even partially hydrolyzed material, especially near the warehouse floor or against thin walls in hot climates. We implemented recommendations from storage engineers to keep drums in shaded racks and off the ground, reducing the risk of temperature cycling that spoils color or purity. For customers close to the equator or in snowy northern climates, we share this information, since getting pristine material to an end user sometimes depends as much on warehouse condition as on synthesis skill.
Working close to the raw process—rather than through layers of wholesalers—produces steady, quantifiable differences in the handling and use of 4-Bromo-2,6-Difluorobenzonitrile. Every adjustment to particle size, drum liner, or final drying method happened after production teams and end-users compared notes. We do not rely on speculation, but on test results and feedback sent straight from the field. Such a feedback loop outpaces the generic offerings typical of bulk intermediates traded via catalogues. The end result: faster changes, timely supply, and fewer unknowns for researchers scaling up.
As a producer, the relationship with clients doesn’t end when a shipment departs. Problems reported by customers translate into rapid process adjustments and better long-term product performance. In the chemical industry, word spreads quickly about which sources of aromatic nitriles maintain consistent color, melting point, and reactivity. Over the years, our reputation for quality and adaptability stands as an outcome of engineering choices, experienced operators, and the trust placed in us by companies around the world.
Among fluorinated aromatic nitriles, 4-Bromo-2,6-Difluorobenzonitrile’s value comes not from theoretical selectivity but from hundreds of campaigns proving its utility in high-value pharma, agro, and specialty material syntheses. Every lot produced at our site carries lessons from previous runs—adjusted reactor setpoints, additional filtration steps, and real-world observations from talented operators. The feedback loop from production floor to user’s bench guides every refinement, and the results show up in cleaner reactions, easier handling, and fewer hang-ups during scale-up.
Working directly with the manufacturer offers advantages that a reseller cannot touch. Control of raw materials, production protocols, and logistics ensures that the compound arrives clean, dry, and with up-to-date documentation. Our commitment to supplying 4-Bromo-2,6-Difluorobenzonitrile exceeds basic compliance; it is rooted in a culture of technical rigor and response to customer needs, built up over years on the floor of a working chemical plant.