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HS Code |
218849 |
| Product Name | 1-Bromo-3,5-Dichloro-2,4,6-Trifluorobenzene |
| Cas Number | 185920-48-1 |
| Molecular Formula | C6BrCl2F3 |
| Molecular Weight | 282.87 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 165-170°C (estimated) |
| Density | 1.91 g/cm³ (estimated) |
| Purity | Typically ≥98% |
| Solubility | Insoluble in water, soluble in organic solvents |
| Smiles | C1=C(C(=C(C(=C1Br)F)Cl)F)Cl |
| Inchi | InChI=1S/C6BrCl2F3/c7-1-2(8)4(10)6(12)5(11)3(1)9 |
As an accredited 1-Bromo-3,5-Dichloro-2,4,6-Trifluorobenzene 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, sealed with a tamper-evident cap, labeled with chemical name, hazard symbols, and safety information. |
| Shipping | **Shipping Description:** 1-Bromo-3,5-dichloro-2,4,6-trifluorobenzene should be shipped as a hazardous chemical, packaged in tightly sealed containers, protected from moisture, heat, and incompatible substances. Label according to transport regulations (e.g., UN number, hazard class). Ensure compliance with local, national, and international shipping and safety requirements for halogenated aromatic compounds. |
| Storage | 1-Bromo-3,5-dichloro-2,4,6-trifluorobenzene should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from heat and direct sunlight. Store separately from strong oxidizers and acids. Ensure the storage area has appropriate spill containment and chemical labeling, and use secondary containment if possible to prevent accidental release. Wear suitable protective equipment when handling. |
Applications of 1-Bromo-3,5-Dichloro-2,4,6-Trifluorobenzene in Industrial Manufacturing1-Bromo-3,5-Dichloro-2,4,6-Trifluorobenzene is a specialized intermediate widely integrated across advanced synthesis processes within the agrochemical, pharmaceutical, and specialty material industries. The following sections provide in-depth application guidance for key downstream sectors, covering industry compliance, typical ratio, process position, and end-product output based on the established standards of real-world manufacturing. 1. Agrochemical Intermediate SynthesisMany major crop protection companies utilize this halogenated benzene derivative for introducing complex halogen patterns during the multi-step synthesis of selective herbicide active ingredients. The compound serves as a targeted aryl building block within nucleophilic aromatic substitution and palladium-catalyzed coupling reactions, critical for constructing scaffolds with required weed selectivity and bioactivity profiles. Industry compliance standards
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2. Pharmaceutical API Synthesis (Aryl Halide Coupling)Pharmaceutical manufacturers employ this benzene compound in protected, regulated synthesis streams to generate precisely-substituted aromatic rings essential for kinase inhibitors, neuroactive agents, and antiviral candidate development. Its unique halogenation profile supports regioselective Suzuki-Miyaura and Buchwald–Hartwig cross-coupling reactions required in modern medicinal chemistry for NCE discovery and scale-up. Industry compliance standards
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3. Fluorinated Liquid Crystal Material SynthesisProducers in the display and advanced optics industries rely on this highly fluorinated aromatic as a key structure-modifying intermediate for synthesizing high-purity fluorinated biphenyls and terphenyls, which determine phase transition behavior and alignment properties in high-performance liquid crystal formulations. The precision substitution enables tailoring of birefringence and viscosity vital for LCD applications including OLED panels and automotive displays. Industry compliance standards
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4. Advanced Electronic Chemical Manufacturing (Materials for Semiconductor Industry)Fabricators of microelectronic and photoresist materials utilize this trifluorinated, halogenated aromatic as a controlled-functionality intermediate in the synthesis of high-purity electronic-grade compounds. It is incorporated into molecular matrices to modulate dielectric properties, charge mobility, and wet etch resistivity of next-generation copper damascene photoresists and fluorinated polyimides for semiconductor interlayer insulation. Industry compliance standards
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Producing 1-Bromo-3,5-Dichloro-2,4,6-Trifluorobenzene means working with a molecule that showcases a careful balance of halogens on a benzene ring. The distinct arrangement of bromine, chlorine, and fluorine atoms makes this compound stand out among substituted benzenes in both structure and reactivity. This molecule, by its very nature, opens the door to synthetic transformations that fewer benzene derivatives can match. Over the years, chemists working on site with this compound have seen it anchor projects in electronic materials, advanced coatings, and pharmaceutical research.
Running a commercial process for this molecule relies on years of optimization. Reactions start with carefully protected feedstocks to ensure minimal contamination, since even slight impurities in halogenated intermediates cascade into downstream product quality issues. We work directly with bromine, chlorine, and fluorinated agents using high-integrity equipment, automated handling, and continuous environmental monitoring. Operating reactors for these precise aromatic substitutions involves not only managing exothermicity but also maintaining halogen ratios that preserve site-selectivity on the ring. After synthesis, multiple purification steps are run, not just to meet regulatory numbers, but because the downstream reactions that use this intermediate react poorly with leftover halogen donors or incomplete substitutions. There is no substitute for actual plant experience—despite a plethora of literature claims, minor changes in temperature or input grades always reveal themselves in GC and NMR data if corners get cut.
Spec sheets rarely tell the whole story with halogenated benzenes. The main figures—purity above 98 percent, water below 0.05 percent, and single-digit ppm for inorganic residues—set a minimum bar for workable material. We run batch-by-batch NMR scans and gas chromatography not only to confirm the mass balance, but to identify traces of isomeric by-products or the unreacted starting benzene. The most diligent customers care about what’s not on the datasheet: which peak in the GC-FID comes from the last run’s side-product, how the liquid’s faint yellow tint shifts after two weeks in transit, how tightly the melting point holds at each delivery. From our end, actual long-term partners ask for specifics on particle size after crystallization, solvent inclusions below detection limits, and what batch variability looks like over a three-year production window. Each new application prompts another layer of scrutiny, and this drives incremental improvements.
1-Bromo-3,5-Dichloro-2,4,6-Trifluorobenzene earns its place in a synthesis pipeline due to strategic substitution. Including both electron-withdrawing fluorines and blocky chlorine atoms means that the reactivity of the benzene ring drops, but select positions can still participate in cross-coupling reactions or nucleophilic aromatic substitutions. This means medicinal chemists see promise in functionalizing the remaining positions for target molecules, while electronics developers value the thermal and chemical robustness that all these halogens confer. In high-end liquid crystal and OLED intermediates, the ring’s symmetry and the exact placement of bromine and chlorine become a lever to fine-tune optical properties and stability. From the manufacturing floor, it is easier to track lot-to-lot consistency in properties like color, odor, and shelf life compared to less substituted ring systems, thanks to the predictable stabilization effect the fluorines bring.
Several years ago, we fielded requests to deliver similar compounds, substituting one or another halogen, to support rapid screening for new display materials. Purely difluorinated or monochlorinated variants proved easier to make but failed to deliver the same performance in many applications. In our experience, changing the degree and pattern of substitution—swapping fluorine for hydrogen on the ring, or shifting the bromine to another location—introduces unpredictability during scale-up. For instance, the melting and boiling points shift enough to challenge distillation at plant scale, or reactivity profiles no longer match expectations in cross-coupling pilot runs. The consistent feedback from real production lines has been that the trifluoro, dichloro, and single bromo arrangement produces the desired balance of electronic and steric effects, especially in intermediates meant for specialty polymers and advanced chemical synthesis.
This specific compound has become a familiar workhorse for our internal R&D and many collaborators. Over a decade, synthetic teams have used it to probe new methods in C–N and C–C coupling. The bromine’s leaving group ability supports clean reactions with Grignard and organolithium reagents, where less activated rings bog down in by-product formation. The chlorine pattern stabilizes intermediates, and fluorine atoms protect the core during oxidative steps. In one project, the compound’s resilience against hydrolysis allowed experimentation with aggressive catalytic systems in water-rich conditions where other aryl halides degraded outright. This mix of robustness and selective reactivity rarely emerges in less halogenated or over-substituted benzenes.
Getting this molecule from reactor to vial, then onto trucks for domestic and global shipments, taught us the importance of handling logistics as an integrated part of quality. Lower substituted benzenes lose material by evaporation or degrade under sunlight, forcing frustrating repackaging and returns. Our chlorinated and fluorinated benzene’s high stability means longer shelf life and reduced loss during transit, even in varying climates. We track each lot from synthesis through final packaging with QR-coded tracking, tying performance in client reactions back to specific runs and production conditions. True long-term consistency comes from analyzing every variable—air ingress, drum liner compatibility, fill volume, and even seasonal changes in storage humidity.
As operators deeply familiar with the practical realities of halogenated aromatic chemistry, we pay careful attention to emissions, worker safety, and waste management. Any process involving bromine or fluorinated agents raises the baseline for plant and environmental safety. Over the years, this meant investment in advanced scrubbing technology, dedicated closed systems for transfer, and full traceability on waste streams. On a plant floor, it becomes quickly apparent that any unplanned vent or minor leak—usually measured in single-digit grams—can create regulatory and safety headaches. We have found that continuous operator training combined with automated emergency controls limits exposure both for staff and the community.
In early years, suppliers often shipped halogenated intermediates with solvent inclusions or plant odors that interfered in scale-up. We overhauled crystallization and drying protocols, adding redundant solvent-stripping and headspace testing for residual volatiles. Another common issue was drum compatibility; the highly fluorinated ring can react with softer seals on standard barrels, so only certified liners and closures get used. Downstream users routinely report fewer batch-to-batch surprises since these adjustments took root. These are details that rarely make it into glossy presentations, but our plant teams see the cost of cutting corners every day. A few grams of off-odor or trace water content can wipe out weeks of synthetic work in a pilot plant, prompting deeper relationships with formulation chemists who rely on true-to-label specifications.
In manufacturing specialized aromatic intermediates, we follow not just required chemical registration standards, but their practical impact on long-term business sustainability. This means tracking not only country-level regulations but also the new requirements cropping up from large multinational customers with green chemistry programs. Every year, stores of retired plant samples and real shipment data feed into compliance dossiers for both customers and the regulatory side, smoothing progress during audits. By working upfront with hazard communication, responsible sourcing procedures, and responsive technical support, we lower the risk of unwanted surprises for everyone in the supply chain.
People who process our 1-Bromo-3,5-Dichloro-2,4,6-Trifluorobenzene in pilot and full production settings look for ease of handling, reliable dosing, and repeatable outcomes under varied conditions. Spotty consistency in physical properties—such as viscosity and solubility—has more to do with trace impurity contents than with published specifications. Years of cooperation with large and small firms reinforced that transparent communication about subtle lot differences is vital, especially during tech transfers or production scale-ups where small discrepancies can upset years of research. Our experience manufacturing this compound in high-purity form stems from ongoing dialog with researchers who respond quickly when something fails to meet expectations.
Lab-scale chemistry never fully prepares a team for what happens when hundreds of kilograms are being synthesized daily. Only hands-on production reveals how seemingly benign changes—like drum color or cooling water temperature—affect product appearance, delivery pressure, or end-use quality. Customers counting on just-in-time delivery for multi-step synthesis programs expect packaging and documentation tailored to their workflow. Over the years, engineers and operators at our facilities identified bottlenecks during drum charging, vapor control, and real-time QA that didn’t appear at gram scales. Sharing these lessons has helped our partners bring their own products to market faster, since they sidestep avoidable pitfalls.
Outside feedback drives the evolution of our processes and end product. Colleagues in pharmaceuticals report back when a residual solvent or off-color slows regulatory approval or triggers retesting. Polymer specialists focus on trace metal content that can poison catalysts. Over time, our in-plant teams developed rapid batch-testing for solvent carryover and tightly controlled the process water used in all cleaning cycles. These efforts spring from report backs on actual incidents in partner facilities, not abstract checklists or theoretical best practices. The most successful collaborations emerge through this ongoing, fact-based exchange.
There is always a temptation in the specialty chemicals sector to chase new applications on the basis of theoretical promise alone. Years of practice suggest that the most robust pathways start with a deep understanding of chemical structure and end-use requirements. Being able to handle difficult ring substitutions at an industrial scale has positioned this compound as a launchpad for innovation in several emerging technology areas. High-performance pigments and optoelectronic polymers built on halogenated aromatics depend on very specific impurity profiles and lot consistency—which our experience places within reach. Instead of relying entirely on literature precedent, we focus on empirical results: what each batch performs like in real-world synthesis.
No written guide captures fully the judgements formed by years on a production line or running synthesis in multi-ton reactors. Handling, purifying, and shipping 1-Bromo-3,5-Dichloro-2,4,6-Trifluorobenzene has taught our team that specification sheets form only the beginning of quality assurance. On-site audits and after-sales support form the backbone of reliability, reinforced by ongoing staff education and rapid turnaround for any technical query. We aim to set a standard grounded in practical application, real feedback, and a respect for chemical complexity. That is the difference experience makes—one batch, one client, and one continuous improvement cycle at a time.