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HS Code |
336177 |
| Chemical Name | 1,2-Dibromo-4-Fluorobenzene |
| Molecular Formula | C6H3Br2F |
| Molecular Weight | 253.89 g/mol |
| Cas Number | 573-57-9 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 220-222 °C |
| Density | 2.062 g/cm3 at 25 °C |
| Refractive Index | 1.605 |
| Flash Point | 95 °C |
| Solubility In Water | Insoluble |
| Smiles | Brc1cc(F)ccc1Br |
As an accredited 1,2-Dibromo-4-Fluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "1,2-Dibromo-4-Fluorobenzene, 99%, 100 g" with hazard symbols and tightly sealed screw cap. |
| Shipping | 1,2-Dibromo-4-fluorobenzene should be shipped as a hazardous chemical in compliance with international transport regulations. It must be packaged in secure, leak-proof containers, labeled appropriately, and accompanied by a Safety Data Sheet (SDS). Avoid exposure to heat and direct sunlight. Only trained personnel should handle the shipment. |
| Storage | 1,2-Dibromo-4-fluorobenzene 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 away from strong oxidizers and incompatible materials. Store in a chemical safety cabinet, preferably designed for hazardous or organic chemicals, and label storage containers clearly. Handle using proper protective equipment. |
Applications of 1,2-Dibromo-4-Fluorobenzene in Industrial ManufacturingAs a specialist in the synthesis and supply of 1,2-Dibromo-4-Fluorobenzene, we support a focused range of downstream industrial sectors where this compound delivers proven molecular advantages for process efficiency and final product quality. Listed below are the principal application areas based on established industry practice. Each scenario details compliance guidelines, recommended usage ratios, integration into downstream workflows, and representative finished goods. 1. Pharmaceutical Intermediate for Active Ingredient SynthesisAPI manufacturers use this aromatic halide intermediate for precise molecular modifications in complex drug synthesis. Its dual bromine and fluorine substituents provide essential reactivity handles required for the construction of core pharmaceutical scaffolds through cross-coupling, halogen exchange, and nucleophilic substitution reactions. The compound’s high purity and consistent halogen positioning support stringent batch-to-batch reproducibility demanded in regulated drug synthesis pipelines. Industry compliance standards
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2. Agrochemical Intermediate for Herbicide SynthesisProducers of modern herbicides and pesticide actives incorporate this compound to introduce both bromine and fluorine moieties on aromatic rings, leveraging its reactivity for subsequent functionalization stages. It serves as a controlled halogen source to achieve precise molecular architecture that defines crop-safety and field-stability performance in active agrochemical molecules. Industry compliance standards
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3. Advanced Liquid Crystal Material SynthesisSpecialty electronics and LCD panel manufacturers employ this compound as a structural building block in the development of high-performance liquid crystal monomers. The specific halogen arrangement enables tight control over molecular alignment, dielectric anisotropy, and thermal stability, which are critical for achieving clarity, response times, and operational voltage specifications in advanced display modules. Industry compliance standards
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4. Intermediate for Specialty Polymers and Performance MaterialsManufacturers in the advanced materials sector select this compound as a key intermediate for the synthesis of high-durability fluorinated polymers and specialty resin additives. Its precise functional group positioning allows for fine-tuning of polymer backbone properties, leading to increased thermal resistance, chemical inertness, and fire retardancy tailored to demanding industrial applications. Industry compliance standards
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5. Agrochemical Analytical Reference MaterialEnvironmental and regulatory laboratories utilize this compound as a stable, well-characterized analytical standard for multi-residue pesticide analysis. Its unique halogen structure supports calibration and validation of analytical methods—including GC-MS and LC-MS—applied in trace contaminant monitoring within complex agricultural matrices. Consistent physical and chemical properties ensure method reliability for compliance testing and product release. Industry compliance standards
Typical usage ratio
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Back in the early days of our production line, chemists valued clean, reliable halogenated benzenes for their accuracy and consistency in synthesis. Our 1,2-Dibromo-4-Fluorobenzene continues that tradition, refined through decades of scale-up, purification, and feedback direct from pharmaceutical and agrochemical development labs. With CAS number 1435-51-6, this compound appears as a clear, pale to colorless liquid under standard storage and can blend quickly into reaction schemes requiring selective halogenation and fluorine incorporation.
Experienced chemists know that precise placement of each substituent on a benzene ring gives a synthetic route its backbone. The 1,2-dibromo-4-fluoro arrangement opens opportunities for downstream transformations. That’s essential during the design of new actives where every step in the sequence can introduce risks of by-products, unreacted starting materials, or troublesome purification.
From the day we installed our closed-system halogenation reactors, we found that the interaction between temperature, catalyst choice, and reaction time directly influenced positional purity. A shift of even a small proportion toward para- or ortho- isomers changes performance in cross-coupling and metalation reactions. We have invested in analytical HPLC, GC-MS, and NMR screening for every batch, confirming that the final product delivers the expected reactivity profile: predictable, stable, with target selectivity for those who depend on it for further substitutions or coupling.
We have worked side-by-side with medicinal chemists and process engineers who need halogenated benzenes to behave exactly the same way every time, no matter the scale. Throughout our production cycles, our operators manually test the intermediate stages, often triple-checking batch blends before moving forward. This hands-on approach keeps the chemical clean and avoids trace metal or solvent residues common in less scrutinized syntheses.
Our model uses direct bromination of a selected fluorobenzene precursor, followed by fractional distillation and filtration. With a boiling point typically around 240°C, the liquid rests stable in glass containers under ambient conditions. Technicians note low volatility under normal lab air, though fume extraction is always recommended for open container work due to the sensitivity of brominated aromatics.
1,2-Dibromo-4-Fluorobenzene finds its way most often to synthesis teams focused on the next generation of small-molecule drugs, plant protection compounds, and specialty polymers. The two bromines and one fluorine on the benzene core let chemists insert new groups with high control, particularly using Suzuki, Stille, or Ullmann coupling.
We’ve seen this chemical act as a launching platform for complex, multi-step syntheses where every fraction of unreacted or mis-placed halogen can derail progress. Recent projects in the field of fluorinated agrochemicals have relied on our product to place a single fluorine into a later-stage molecule, often for the purpose of tuning bioactivity or improving metabolic stability. Polymers research also taps into the reliability, since downstream monomer derivatization can hinge on complete conversion at just one of the bromo positions while the fluorine remains untouched by milder nucleophiles.
Consistent performance comes from controlling purity to no less than 98.5%, confirmed by proton and carbon NMR and routine GC assessment. Minute quantities of unreacted precursor, isomeric contaminants, or downstream halogenation by-products don’t end up in the final vessel. Over the years, we refined our crystallization and distillation steps to address how traces of other dibromofluorobenzenes can ruin a batch run at the kilo scale.
Typical drums and bottles ship with tight capping and vapor barriers, since minimizing exposure to moisture or oxidizing air preserves stability. Every unit moves through pack-out with tamper evident closures and batch tracking, not just for compliance, but because a compromised container, in our experience, can throw off assay readings. Regular spot tests in receiving labs keep our team directly accountable to the scientists at the bench, who have told us what they expect: straightforward handling, no cloudy aliquots, no slow crystallization in the cold room, and no surprises.
Plenty of halogenated benzenes reach the market from bulk commodity producers, but few match the balance of reactivity and selectivity found here. Many standard products in this space suffer from a lack of regioselective functionalization. Products like 1,4-dibromo-2-fluorobenzene or 1,2-dibromo-3-fluorobenzene can drag along isomerization issues, which our process addresses head-on with carefully chosen reaction windows and post-reaction scrubbing.
Generic commercial halobenzenes also tend toward higher levels of trace impurities and can fluctuate in composition batch to batch. We encountered incidents early on where improper container linings, or recycled drum stoppers, added unwanted organic residues, creating issues for customers scaling up to pilot volumes. As manufacturers, we adapted by standardizing inert linings and by direct work with liner and cap suppliers, logging every material for potential cross-contamination. Few competitors can point to item-level accountability throughout the whole journey from reactor to bottle.
Several research partners working in nucleophilic aromatic substitution often call us with early-stage plans for a new route. Some projects require insight into optimal solvent loads or how best to separate mono- from di-functionalized intermediates. We maintain technical staff with both bench and process backgrounds who can spot subtle issues, such as incomplete phase transfer or unexpected retention during chromatography, which often result from vendor batch-to-batch inconsistencies. It’s the direct conversation with working chemists—sometimes after hours, sometimes at pilot scale—that sets our manufacturing approach apart.
Shipping logistics also matter. Some products originate from faraway places with long dwell times in customs or in uncontrolled warehouses, picking up unwelcome traces of water, dust, or sunlight degradation. We timed our own logistics chain to reduce each step, storing in climate-controlled facilities and confirming resins or seals used on every vessel stay inert. Our batch labels connect to a digital trail showing synthesis date, QC data, and shipping record by serial number.
It’s no secret that brominated aromatics call for strict respect on the bench and production floor. Our team wears full PPE and applies local exhaust ventilation during all decanting, aliquoting, and drum handling. Managers enforce routine air quality checks and issue change-out requirements for gloves and valve gaskets.
Years in the industry add up to certain rules of thumb: always decant slowly, collect residue for tested disposal, and rethink venting protocols if a sharp odor appears. The result is a clean work area and safe downstream blending. We maintain monthly training sessions so new operators learn precisely why corners cannot be cut, especially when brominated compounds demand close storage with desiccants and away from open electrical panels or exposed metal.
Process yields have always driven customer satisfaction. In previous decades, failures often traced back to solvents and packaging, so our process keeps sources minimal, using high-grade, single-use solvents where practical and expelling the rest with nitrogen stripping. We also keep nimble QC turnaround, so any out-of-spec batch gets flagged and withheld before release to the warehouse.
Group leaders from client labs frequently point out that halogenated intermediates like ours, when impure, can spark whole-sequence repeats. That leads to wasted time, resource loss, and, at scale, environmental impact through unnecessary waste disposal. Our manufacturing adjustments, including real-time online analytics and in-process sampling, directly target this pain point.
Supply stability influences research pipelines. Global events sometimes disrupt raw material pathways for crucial precursors. Years ago, we diversified our vendor base and built up secondary purification equipment to maintain product flow, preventing costly delays for our customers on tight launch deadlines. Our on-site labs hold retention samples for each batch cycle, so if a question arises, we review original spectral data and, if needed, re-run purity or moisture checks.
Technical specialists and procurement managers have shared direct feedback about the traceability and responsiveness they expect from a primary manufacturer. Avoiding the “black box” effect of resellers, we ensure that every inquiry lands on the desk of someone who actually knows the process. Sometimes, this has meant adapting fill sizes, shifting to higher-purity grades, or taking back returned stock with no argument—learning from experience always sharpens our future approach.
In collaborative development projects, especially those involving new fluorination or borylation chemistry, our technical liaisons and shift chemists will join in on regular update calls. We respond based on operational realities, balancing actual production schedules, downstream solvent availability, and real-world scale-up constraints with the pressures synthetic teams experience in the lab.
Manufacturers of halogenated aromatics work under tight regulatory controls. Rigorous documentation from sourcing, processing, and packaging moves with every batch to ensure compliance with evolving standards. Early on, our quality team learned to keep audit-ready records since spot inspections can arrive without notice.
Facility upgrades in waste air scrubbing and water treatment emerged as high priority, enabled by close work with local authorities and ongoing employee training. Hazard coding, spill response kits, and quarterly safety drills all become part of the workflow, not afterthoughts. Our ongoing R&D also addresses green chemistry alternatives wherever possible, minimizing the environmental loading by focusing on yield boosts, solvent recycling, and minimizing purge gas usage.
Hands-on involvement at each production step has taught us the value of relentless attention to the small details. Experienced operators take pride in knowing exactly how their reactor’s wall temperature or stirring rate can influence end-product quality. Certain batches come with unique quirks—a slightly different color, a bit more viscous, or a sharper smell—which only careful monitoring catches before a shipment leaves the plant.
Problems mean more than a failed batch or a returned drum. They carry consequences for critical research programs that can lose weeks retracing steps or troubleshooting unknown impurities. Our ongoing pursuit is to erase these headaches, delivering a compound that responds the same in every chromatograph or flask, time and again.
Years of dialogue with those working at the sharp end of synthesis drive our continuous process improvements. We tune reaction timings, test alternative brominating agents, and run repeated split-batch assessments to boost selectivity without ballooning costs. Facility investments aimed at better air handling, drum sanitation, and packing resilience often emerge from a single customer comment about a minor leak or a strange residue at the cap.
Pharma and agrochemical customers value options: Sometimes they require larger volumes for pilot programs, other times, just a single flask for bench-scale trials. We accommodate these requests by keeping modular filling capabilities and assembling a shipping system that scales up or down as needed. Operators seek feedback after every delivery, and technical support channels stay open whether issues arise immediately or after months of storage.
The landscape in specialty chemicals is always shifting, especially as new targets appear in pharmaceuticals, crop protection, and advanced materials. Machine learning applied to reaction prediction has increased the need for high-certainty, well-characterized starting materials. We look ahead to even tighter specifications, streamlined batch analytics, and speedier, more flexible order fulfilment in response to growing customer demands.
From conversations with synthetic organic groups, it’s evident the field is driving toward more sustainable, efficient, and tailormade molecular building blocks. The balanced reactivity and ease of substitution in 1,2-Dibromo-4-Fluorobenzene positions it well in the innovation pipeline. Continuous investment in purification, robust packaging, and after-sale technical guidance ensures labs get not just a chemical, but the confidence to push research one step further without hesitation.