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HS Code |
442976 |
| Chemical Name | 4,4'-Dibromooctafluorobiphenyl |
| Cas Number | 1806-11-9 |
| Molecular Formula | C12Br2F8 |
| Molecular Weight | 463.92 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 106-109°C |
| Density | 2.14 g/cm³ |
| Solubility | Insoluble in water |
| Synonyms | 4,4'-Dibromo-2,2',3,3',5,5',6,6'-octafluorobiphenyl |
| Pubchem Cid | 64409 |
| Smiles | C1(=C(C(=C(C(=C1F)F)Br)F)F)-C2=C(C(=C(C(=C2F)F)Br)F)F |
| Inchikey | XCHKAEMHYNQFME-UHFFFAOYSA-N |
As an accredited 4,4'-Dibromooctafluorobiphenyl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 10-gram amber glass bottle, tightly sealed, labeled "4,4'-Dibromooctafluorobiphenyl, ≥98% purity," with hazard and handling instructions. |
| Shipping | 4,4'-Dibromooctafluorobiphenyl should be shipped in tightly sealed containers, protected from moisture and light. It is classified under hazardous chemicals; handle according to local, national, and international regulations. During transport, ensure secondary containment and appropriate labeling. Use suitable personal protective equipment when handling, and avoid exposure to heat or direct sunlight during shipping. |
| Storage | 4,4'-Dibromooctafluorobiphenyl should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect it from moisture and direct sunlight. Ensure appropriate chemical labeling and restrict access to trained personnel. Store at room temperature or as specified by supplier recommendations. |
Applications of 4,4'-Dibromooctafluorobiphenyl in Industrial Manufacturing4,4'-Dibromooctafluorobiphenyl provides specialized performance in advanced materials, electronics, and specialty polymer processing. As a direct manufacturer, we support industrial producers with precise grade consistency for various high-value downstream sectors. 1. Liquid Crystal Display (LCD) Intermediate SynthesisDisplay material manufacturers rely on this intermediate for OLED and advanced LCD formulations. The compound introduces enhanced electron mobility and thermal stability essential for next-generation displays. Its halogenated biphenyl structure becomes part of complex syntheses where purity and physical property control impact pixel uniformity and device reliability. Our technical support aligns with mass production QC protocols in this highly competitive sector. Industry compliance standards
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2. Specialty Fluorinated Polymer ProductionHigh-end fluorinated polymer manufacturers use this material as a comonomer or building block for engineering plastics with targeted thermal and dielectric properties. Its structure improves creep resistance, dimensional control, and fire retardancy in aerospace and electronics polymers. Our process control ensures batch consistency and impurity profiles meeting international standards for demanding end uses. Industry compliance standards
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3. Electronic Materials for Printed Circuit Board (PCB) LaminatesProducers of high-frequency laminate resins use this item for its dielectric stability and chemical durability. When incorporated in prepreg formulations, it helps achieve low dissipation factor and moisture uptake, which are critical for 5G and advanced server PCBs. Direct supply from our plant supports strict batch traceability and cleanroom requirements. Industry compliance standards
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4. Advanced Flame Retardant SystemsChemical formulators use this compound as a key intermediate or additive to meet strict non-halogenated and ultra-low smoke emission standards. Its high bromine and fluorine content delivers effective flame suppression with reduced migration compared to traditional systems. We deliver grades matched to polymer blending and extrusion protocols found in consumer electronics and public safety applications. Industry compliance standards
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5. Chemical Vapor Deposition (CVD) Precursors for Specialty CoatingsProducers of high-performance surface coatings and thin films utilize this substance as a fluorinated source in the CVD process for microelectronics or anti-corrosive applications. It helps achieve uniform film coverage and tailored surface energies required for chip packaging and high-reliability sensors. As the original manufacturer, we maintain ultra-high purity specifications for low particulate and organic residue. Industry compliance standards
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As chemists who focus on highly specialized fluorinated aromatics, we spend a lot of time delving into molecules that only make sense once you get close enough to see their real-world effects. 4,4'-Dibromooctafluorobiphenyl is one of those chemicals. Its name might sound intimidating, but it’s a staple for advanced materials researchers and process engineers who need reliability down to the molecular level. We manufacture this compound directly, so every batch reflects our investment in refining the process right from the choice of raw materials to the conditions of purification that make or break performance in a customer’s application.
Having made this compound for years, we recognize the wear and tear that comes from handling highly fluorinated biphenyls with reactive halogen substituents. Not every aromatic with bromines and fluorines behaves the same, and the differences show up during reaction set-up, scale-up, and purification. Octafluorination stiffens the biphenyl skeleton, so you start with an electronically starved structure compared to non-fluorinated analogues. This changes everything from solubility profiles to reactivity windows. More than a synthetic curiosity, those factors affect yield and downstream functionality.
During bromination, placement precision matters. We aim for full para-substitution—on both rings, at the 4 and 4' positions. Impurities from partial fluorination or mis-substitution can act as poisons in subsequent reactions. This influences not just the chromatography but also the long-term supply to users who don’t want to risk unpredictable side reactions in their own processes.
Experienced chemists looking at our product tend to ask first about purity and physical form. The pure compound usually presents as a white crystalline solid. In our facility, we watch for off-odor, discoloration, or clumping, which can signal contamination or hydrolysis—nearly invisible problems unless you know what to expect from the chemistry. Maintaining vacuum-dried conditions and using fluoropolymer lined containers lowers loss during storage and transit. Users looking to prepare intermediates or activate the biphenyl for polymer integration see a direct benefit here.
We manufacture 4,4'-Dibromooctafluorobiphenyl to a high-purity grade, targeting trace-level control of other halogenated biphenyls, and ensuring less than 99.5% major component is never tolerated. Melting points remain sharp, as loss of crystalline order flags poor separation; this ties back to years spent tightening our solid-liquid extraction steps. We routinely analyze by NMR and GC-MS, confirming full disappearance of starting octafluorobiphenyl and ruling out ortho- or meta- isomers, which, from experience, become evident long before a batch could be packaged.
Our users rarely employ 4,4'-Dibromooctafluorobiphenyl for simple transformations. In most requests, the compound serves as a high-value intermediate for functional polymers, especially those looking for thermal or chemical inertness matched with the flexibility to add other groups precisely. In our lab, we’ve customized the product for clients developing liquid crystal displays, high-end electrical insulation, and even medical imaging substrates, all of which lean heavily on the rigidity and electronic character brought by a fluorinated biphenyl. The dual bromine groups at the 4,4'-positions enable site-specific cross-coupling or substitution, giving chemists a precise handle on subsequent modifications without the unpredictable behavior found in less symmetrical molecules.
Contrast that to broader-used or more-regulated biphenyl derivatives. For example, PCB contaminants from various non-fluorinated or irregularly-substituted biphenyls create headaches in electronic or analytical applications. We purposefully eliminate lower brominated or partially fluorinated side products, so results are consistent whether a batch goes into a pilot plant reactor or gets sent for analytical calibration. With many customers, feedback has circled back on just how much time gets saved by not troubleshooting unexplained secondary peaks in GC or UV traces.
We only ship after full internal qualification because every experienced organic chemist knows that even trace contaminants—especially those structurally close to the target—can derail a synthesis or degrade a material’s performance. On scale-up runs, minor temperature fluctuations or delays on filtration can produce elusive by-products that don’t show up in bulk melting point but pop up midway in a downstream coupling reaction. SOPs that skip thorough up-front analytical testing almost always end in bottlenecks for everyone.
Decades of production have led us to integrate double chromatographic and crystallization purifications, not because it's standard but because clinging to the minimum spec leads to regression over time. This extra scrutiny pays off especially for customers in semiconductor or advanced coatings research, where even low-level interfering species can trigger a six-month project delay.
There’s no shortage of biphenyls with varying halogen substituents. Some labs improvise with hexafluoro- and tetrafluoro-biphenyls or substitute iodine or chlorine in place of bromine. Each brings its own baggage. Brominated, fully-fluorinated biphenyls like our 4,4'-Dibromooctafluorobiphenyl strike the best balance for most process chemists. The bromine substituents, sitting at opposite ends of a rigid, nonpolar scaffold, present optimal leaving groups for palladium-catalyzed couplings. Chlorinated analogues often require harsher conditions or deliver lower yields due to their poorer leaving group characteristics. Iodine variants, while highly reactive, often give undesired side reactions under coupling conditions and degrade more readily, creating storage headaches.
From what we’ve seen in process troubleshooting meetings, hexafluorinated or non-symmetrical biphenyls often introduce isomeric complexity, which means longer clean-up downstream. Full octafluorination makes the rings highly electron-deficient, pushing reactivity where many cross-coupling partners fail to approach, yet the symmetry simplifies both modeling and NMR characterization. This avoids the ambiguity engineers face when batch data shows unexplained peaks or unexpected reactivity.
Our experience with larger customers in coatings R&D confirms the value in using a consistent, fully-fluorinated para-dibrominated biphenyl structure. They report more predictable flame resistance and stability in harsh solvent regimes compared to either unsubstituted or partially-substituted fluorinated aromatics. These outcomes underscore why we never cut corners on separation from isomeric impurities or incomplete bromination side-products.
Scale brings headaches in any fine chemical operation. In multi-kilogram lots, we’ve learned that unchecked exotherms during bromination or incomplete drying at the final stage can wreck purity standards established in smaller batches. Routine process tweaks—adding staged additions, revamping jacket cooling, or fine-tuning vacuum levels—respond to feedback from process monitoring. Instead of maximizing every run for the highest tonnage, we prioritize reproducibility, as deviation in this structural class almost always feeds back to client complaints or, worse, real-world material failures. Our line operators routinely share the latest chromatograms and endpoint verifications, passing on knowledge so that learning from past production missteps doesn’t get lost.
Over the years, our chemists have seen that environmental management plays a role, too. Fluorinated compounds present persistent toxicity concerns if handled carelessly, which is why we continuously invest in safer containment, waste treatment, and exposure monitoring infrastructure. Regulatory compliance isn't a box-checking exercise—it stems from wanting our staff and customers safe, and our environmental footprint minimized, because breaches ripple out to raise costs and reputational risk long after a batch leaves the gate.
Development pipelines for advanced technologies force us to stay nimble. Customers in electronics and high-performance coatings expect reliable, traceable chemical histories and consistent batch performance. Their chemists often ask to visit production lines or view in-progress data, and we encourage this, since our confidence in the product matches what rigorous users require. Supply interruptions, tracing back to unpredictable intermediates or outages among upstream halogenation suppliers, have taught us to diversify raw material sourcing and keep safety stock prepared for critical user needs.
From talking directly to technical leads at Fortune 500 firms and university groups, we've noted that flexibility in packaging and shipping sometimes trumps small savings off unit cost. No customer gains from saving pennies if product degradation or contamination sneaks in during long-haul shipment. We partner with carriers familiar with hazardous and sensitive organofluorine logistics, preferring shipment timing and bulk containerization that matches the user’s turnaround expectations.
Leading applications continue to surprise us. Many companies order 4,4'-Dibromooctafluorobiphenyl to support their R&D for high temperature and chemically inert polymer backbones. One group told us their new fluorinated polyimide, built from our biphenyl core, pushed operating windows in aerospace environments by another 50 degrees, reducing system failure rates. These aren't isolated results; the structure provides a rare blend of thermal stability and chemical resistance that few other aromatic cores match.
Another use case involves lithography and semiconductors. Because fully-fluorinated, highly symmetrical biphenyls resist photodegradation, they're valued in extreme ultraviolet (EUV) patterning processes. Our discussions with research teams show they prefer our material over less defined alternatives because it presents lower outgassing and remains inert under radical conditions—key for building thinner, more reliable resist layers.
Liquid crystal and optoelectronic R&D teams often build their custom mesogens or spacers with our biphenyl as a platform. The electron-withdrawing nature of the fluorines tunes both dielectric constant and alignment, lending predictability not found in methyl- or chlorine-substituted cores. These teams rely on batch-to-batch predictability, trusting our demonstrated control over both halogen content and crystalline structure.
Making and delivering complex halogenated aromatics uncovers supply chain and process risks that never show up with basic commodity chemicals. Intellectual property theft, market disruptions after geopolitical events, and rare impurities from specialty reagents have all forced us to refine our business practices. Working in this industry means planning for uncertainties—stockpiling critical starting materiaIs, investing repeatedly in employee safety and analytical updates, and adapting to shifting logistics rules.
Our commitment to in-house R&D and open communication with end-users lets us spot potential problems early. New regulatory actions in key export markets matter to us, since delay or transit bans on brominated organics can upend delivery. We've built relationships with compliance consultants and customs brokers so we can reliably interpret shifting requirements, adapting documentation and labeling before pain is felt down the chain.
Chemists thrive off experimentation. From our bench scale batches to kilogram orders, we keep close ties with academic collaborators, integrating their feedback as they tweak reaction protocols or probe unexpected results. Their findings sometimes influence our manufacturing windows; shifts in acceptable impurity levels or new coupling technologies might push us to adjust purification or drying steps. Our door remains open to technical feedback, whether it’s a request for increased surface area, lower trace water, or faster shipment for a critical path experiment.
Across multiple sectors, the drive for better, safer, and more functional products, using 4,4'-Dibromooctafluorobiphenyl as a starting point, continues to grow. We see real-world improvements in device longevity, energy efficiency, and resistance to harsh conditions. Working closely with both experienced R&D users and newcomers ensures we continually refine every stage, from reactor cleaning protocols to long-term archive sample storage.
The lessons we accumulate on the floor mean more accurate guarantees about chemical structure and quality. Retailers and traders focus on moving boxes, but only someone on the reactor deck knows what happens if agitation stops unexpectedly or cooling is too slow. Our teams catch the earliest signs of trouble before a product lands in regulatory crosshairs or a client’s multi-million-dollar processing run is derailed by unseen contaminants. Even small changes—such as vessel material upgrades or new in-line analytical checkpoints—become difference makers in a specialty chemical landscape dominated by technical precision.
It’s experience that lets us answer customer queries with detailed run history, anticipate where a novel application could face an unknown interaction, and support both niche and mainstream users without risk. Owning the process, from raw materials to shipment, elevates not just our own product, but the quality of every synthesis, device, and application built with our 4,4'-Dibromooctafluorobiphenyl.
Technological demands keep changing, pushing us to re-examine how we manufacture and deliver specialty biphenyls. We draw on decades of hard-won expertise dealing with sensitive, highly engineered molecules. It’s not enough to rely on yesterday’s methods if we’re to help customers create tomorrow’s advanced materials. We constantly revisit purification, packaging, and quality benchmarks to ensure our 4,4'-Dibromooctafluorobiphenyl does exactly what is demanded, right out of the bottle, batch after batch.
From a manufacturer’s bench, this blend of chemistry, experience, and open technical exchange is what secures both sustained quality and innovation for downstream users. This compound opens more doors than it closes, and our commitment runs beyond any single sale—it’s about evolving with our partners and the ambitious projects they chase. The journey doesn’t end at the warehouse—it continues every time someone picks up a vial from our latest run and pushes the boundaries of what’s possible.