|
HS Code |
680345 |
| Chemical Name | 1,2-Dibromotetrafluorobenzene |
| Molecular Formula | C6Br2F4 |
| Molar Mass | 307.86 g/mol |
| Cas Number | 327-89-1 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 173-174 °C |
| Density | 2.25 g/cm³ |
| Refractive Index | 1.546 |
| Smiles | C1=C(C(=C(C(=C1F)F)Br)F)Br |
| Inchi | InChI=1S/C6Br2F4/c7-1-2(8)4(10)6(12)5(11)3(1)9 |
| Solubility | Insoluble in water; soluble in organic solvents |
| Pubchem Cid | 11763 |
As an accredited 1,2-Dibromotetrafluorobenzene 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 1,2-Dibromotetrafluorobenzene, labeled with hazard warnings, CAS number, and manufacturer details. |
| Shipping | 1,2-Dibromotetrafluorobenzene is shipped as a hazardous chemical, typically in tightly sealed containers made of compatible materials. It must be clearly labeled, protected from physical damage, and transported according to relevant regulations for brominated organics. Proper documentation, including Safety Data Sheets (SDS), and appropriate hazard signage are required during shipping. |
| Storage | **1,2-Dibromotetrafluorobenzene** should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it separate from incompatible substances such as strong oxidizers or bases. Clearly label storage containers, and ensure access is restricted to trained personnel using proper personal protective equipment (PPE). |
Applications of 1,2-Dibromotetrafluorobenzene in Industrial Manufacturing1,2-Dibromotetrafluorobenzene plays a critical role as an intermediate in several advanced material production processes, providing reliable chemical properties essential for downstream synthesis. Our manufacturing expertise ensures consistent quality and technical support for demanding industrial applications. 1. Advanced Agrochemical Intermediate SynthesisIn the crop protection sector, manufacturers utilize this compound as a key halogenated intermediate for synthesizing fluorinated and brominated herbicides. Its dual functionalization enables controlled modification during elongation or coupling reactions, which is essential for introducing specific aryl groups or for subsequent nucleophilic substitutions aimed at increasing biological efficacy and stability in harsh field conditions. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Synthesis of Liquid Crystal Display (LCD) MonomersThe electronics industry incorporates this halogenated benzene derivative to introduce precisely spaced bromine and fluorine atoms during monomer design for high-performance liquid crystal compounds. Downstream formulators value its unique electronic effects, which enhance the alignment and response times of final liquid crystal mixtures, directly influencing panel clarity and low-voltage operation. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Pharmaceutical Building Block for API SynthesisThis compound serves as a strategic halogenated intermediate in pharmaceutical fine chemical synthesis, used in the preparation of specialty aryl fluorides and bromides required for non-standard API scaffolds. Medicinal chemistry teams rely on its high purity and reactivity for routes needing chemo-selective substitution, often in steps that form core units for anti-cancer or CNS drug candidates subject to complex regulatory review. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Manufacture of High-Performance Specialty PolymersProducers in the advanced materials sector utilize 1,2-dibromotetrafluorobenzene for synthesizing specialty fluorinated and brominated polymers with elevated chemical resistance and unique physical properties. Its controlled reactivity allows incorporation into fluoropolymer backbones, facilitating the fabrication of membranes and films used in harsh chemical environments or as dielectric materials. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Fine Chemical Synthesis for Photolithographic MaterialsSemiconductor manufacturers source this molecule as an intermediate for synthesizing specialty aryl compounds used in photoresists and antireflective coatings. It provides tunable halogenated structures that influence the solubility and pattern transfer properties critical for sub-90nm lithography, and its high purity specification ensures low trace contaminant levels during final resist formulation. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 1,2-Dibromotetrafluorobenzene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Every day in the plant, production lines hum to the careful rhythm of established quality controls and chemical transformations that demand more than just technical knowledge. As the team responsible for creating 1,2-Dibromotetrafluorobenzene, we recognize that value in specialty chemicals starts with experience and a close look at how purity, process repeatability, and safety track through every batch.
Our approach stands on deep understanding, not simple repetition. 1,2-Dibromotetrafluorobenzene, with its recognized CAS number and molecular structure, tells a specific story: two bromine atoms and four fluorine atoms distributed on a benzene ring in ortho configuration. This design defines the character and reactivity of the material, shaping where and how it’s used from advanced synthesis labs to industrial-scale steps for specialty polymers and electronics intermediates.
Our internal codes distinguish between various grades—be it high-purity, intermediate, or technical—because one customer's requirements for trace metals, halide balance, and moisture tolerance can differ sharply from the next. For advanced material synthesis, like compounds destined for OLED applications or certain pharmaceutical intermediates, a clear cut-off for impurities will determine yield, side reactions, and downstream costs. Models without well-managed impurity profiles have been known to generate persistent troubles: ghost peaks in chromatograms, reduced yields, or interaction with catalysts.
From production side, handling the halogen balance is no small matter. Excess bromine or poorly managed fluoride levels can influence everything from shelf life to compatibility with planned reactions. By controlling parameters such as process temperature, solvent selection, and distillation cut points, we deliver consistent outcomes. Repeated analytical checks drive down batch-to-batch variability, supporting confidence for formulators or process chemists deciding whether to scale up or switch suppliers.
Compared with generic bromofluorobenzenes, our 1,2-dibromo-tetrafluorobenzene stands apart in the field because of its reproducibility and confidence in specifications. Many competitors run most of their quality checks at the start or end of production; we sample through key steps. This strategy cuts down the chance for unexpected cross-contamination or late-stage surprises that risk whole batches or laboratory investment.
Every lot report that leaves our lab isn’t just a piece of paper—it's a summary of weeks' worth of process vigilance. In the handling and formulation of 1,2-dibromo-tetrafluorobenzene, nothing exposes quality gaps faster than downstream blending or synthesis. When our product meets customer facilities, clarity on specification—such as GC purity, water content by Karl Fischer, and residual acids—proves its value, not in theory, but in batch efficiency and predictable conversion rates.
Small-scale users sometimes ask why laboratory-grade may come at a premium compared to technical-grade. From our experience, laboratory syntheses often involve sensitive steps—Pd-catalyzed couplings or halogen-lithium exchange, for example—where even parts-per-million levels of side impurities have triggered failed lots. The ability to deliver true 98-99%+ purity with low halide ion and moisture content has saved customers both time and money, sparing them rework and salvage chemistry.
For those in industrial manufacturing, the story shifts slightly. High throughput reactors and automated systems favour bulk packs and stable flows. Here, control over particle size distribution for solid shipments, homogeneity, and low caking tendency reduces unexpected downtime or maintenance. Our ongoing collaboration with downstream engineers identified packaging solutions and inert-atmosphere fills that preserve material integrity months after delivery.
In our work with electronics manufacturers, the core trait that makes 1,2-dibromotetrafluorobenzene appealing is its combination of robustness and selectivity during fluorination or arylation. Fluorinated benzene rings serve as stable, electron-withdrawing scaffolds. The ortho-bromine configuration makes this compound a suitable precursor for further coupling or substitution, showing higher reactivity in cross-coupling settings compared to some isomers or less-halogenated congeners.
In real-world practice, some customers turn to this molecule as a building block for more complex, high-value targets: specialty monomers, certain agrochemical intermediates, or constructing ligands for catalysis. For these steps, consistent bromine positioning and the electronic nature of the ring structure prove crucial for selectivity and repeatable process conditions.
Some new users have equated 1,2-dibromotetrafluorobenzene with other halogenated benzenes, but the reactivity window can shift dramatically—especially when using metal–halogen exchange conditions. Our technical collaboration sessions highlighted several instances where switching from one isomer to the next led to significant changes in by-product profiles or yields due to altered electronic effects. Being there to dissect these outcomes, not just sell product, allowed our partners to reach their targets faster.
1,2-Dibromotetrafluorobenzene shares similarities with its closely related isomers and congeners, yet displays a unique blend of reactivity and selectivity. The precise placement of bromines at adjacent positions influences its behavior distinctly from the 1,3- or 1,4-isomers. In applications where regioselective coupling or ortho-functionalization is critical, such structural features distinguish it from alternative offerings.
Users sometimes inquire about the differences between dibromo-tetrafluorobenzene and less-fluorinated analogs. Extra fluorines in the ring impact everything: solubility, volatility, reaction kinetics, and stability under both storage and processing. Chemicals with lower fluorine content often react more aggressively, increasing the risk of side reactions, especially in cross-coupling. The heavy fluorination of our material balances chemical inertness with just enough reactivity, streamlining complex syntheses and cutting down the troubleshooting hours our team used to spend consulting with customers back when they worked with mismatched products.
Even small process alterations—temperature, catalyst choice, solvent—prompt different results between this compound and others in its group. That’s why our plant invests both in document-backed specifications and boots-on-the-ground troubleshooting. We study where deviations in halogen loading or trace metals could lead an entire scale-up astray, drawing on lessons from every setup trial and customer feedback session.
Over years, we’ve watched the demand profile shift from small, specialized requests to larger, multi-ton batches for integrated supply chains. Early adopters often came from academic or pilot-scale environments, looking to build out the next phase of a molecular platform. Today, growth comes from broader industries: electronics, specialty polymers, and intermediate producers seeking reliable repeat supply at scale.
We learned quickly that applications push our material to its technical limits. Where some buyers sought it for direct use in halogen exchange chemistry, others pivoted towards free-radical reactions, or Suzuki and Stille couplings in the construction of extended aromatic systems. Each reaction exposes strengths and stress points. In cross-coupling, for instance, slow-release packaging to avoid clumping played a tangible role in cutting downtime for automated feeders. Where reactions called for higher solubility, we improved drying protocols and granulation practices to avoid batch failures.
Because many of our customers integrate this compound into regulatory-bound finished goods, our internal compliance and traceability run deep. Batch documentation, storage condition monitoring, and recall readiness don’t just assure audits—they protect production partners from setbacks and delays, which we have witnessed during times of upstream disruptions.
Challenges crop up in every plant, not just in the lab. We’ve seen impurity spikes due to upstream solvent fluctuations, or run-ins with caking issues during humid months. Solving these didn’t come from a template—our people tested different drying agents, rotated through inert gas fills, and dialed in upstream filtration to drive down problem ions. Each step reflected hours on the plant floor, not just consulting a standard handbook.
To keep moisture at bay and avoid unpredictable reactivity, we supply material in low-permeability drums or sealed glass, with nitrogen overlays. Tracking shelf stability, even across international shipments, prompted us to work closely with partners in logistics to monitor temperature and humidity in transit. These details aren’t side concerns—they dictate whether a month of hard work in a supply chain gets lost to a single uncontrolled variable.
The benefit of acting as a manufacturer, not a trading intermediary, is the direct feedback loop. Customer reports on handling properties have led us to change not just bags and drums, but to revisit process points in chemical refinement. When a complaint surfaced about fines buildup during powder transfer, in-plant trials led to equipment upgrades and procedural shifts. Each improvement comes back to the same idea: moving challenges from downstream to upstream leaves customers free to innovate, not firefight.
Product data are not just reference values for us; they function as checkpoints against real-world failure. Our in-house analytics scan each batch for halide distribution, water content, and trace organic contaminants using methods validated against reference standards. Not every batch sees the same test slate—feedback from customers and our own incident reviews sometimes prompt additional scrutiny for specific contaminants or secondary products.
Where other suppliers rely heavily on generic certificates, our reports match the way customers actually use the data. For instance, a user planning for nickel- or palladium-catalyzed functionalization may focus on background levels of sulfur or phosphorus. We tailor our reporting so critical performance indicators get spotlighted right away, rather than buried in pages of uninterpreted numbers.
Operational safety remains central at every node, not just on paper. Our staff’s exposure-monitoring results and regular environmental audits have fed directly into supplier selection for solvents and reagents, helping drive down both hazardous waste generation and time spent on event response. Changes made here ripple outward, giving our partners a larger safety margin and reducing total lifecycle impact for everyone involved, not just the people on our own team.
Clear distinctions set 1,2-dibromotetrafluorobenzene apart: its capacity for controlled reactivity, its traceable purity, and the repeatability we bring batch after batch. We’ve picked up countless stories from customers finding improved yields, cleaner spectra, or more stable product shelf life after making the switch from less-disciplined sources. Each lesson comes directly from walking the tightrope of industrial reliability and academic curiosity.
For some formulators, even the minor aspects of handling—aromatic odor, color shift after extended storage, or packing density in bulk shipments—drive process design. Our openness to reviewing small complaints, from equipment compatibility to handling practices under variable site conditions, shapes a cycle of improvement. It’s not about chasing the fastest route to market, but ensuring each shipment meets standards built on in-plant, daily vigilance.
No single product or plant sets the pace for the entire field, but standing as a direct manufacturer gives a responsibility to support the community of users. We see firsthand how regulatory scrutiny, cost pressures, and technical demands keep rising. By focusing on long-term partnerships, quality transparency, and hands-on support, we help our partners navigate these currents rather than just survive them.
It can be easy to treat specialty chemicals as commodities—just one more drum among thousands—but in truth, 1,2-dibromotetrafluorobenzene carries its own nuanced set of expectations. From the moment raw halogens move into our reactors to the final tamper-proof seal before shipping, the question isn’t whether the product matches an ideal, but how close we can get to an evolving real-world standard shaped by practice, not just paper protocols.
Other voices may speak from spreadsheets or procurement contracts; we speak from the vantage of actual plant experience. The story behind every batch isn’t just a celebration of chemistry, but of practical problem-solving—the bumps and quick fixes that never make it to sales brochures. This kind of insight, built up from years of running, stopping, and repurposing lines, embeds itself in every drum or bottle of 1,2-dibromotetrafluorobenzene we ship. For those who stake their projects or products on these specialty chemicals, we know every detail counts and commit to being an ongoing part of that success—not from a distance, but right alongside those still building and refining tomorrow’s chemical innovations.