|
HS Code |
228909 |
| Name | 2-Bromopentafluoropropene |
| Chemical Formula | C3BrF5 |
| Cas Number | 428-57-9 |
| Appearance | Colorless liquid |
| Boiling Point | 33-35°C |
| Density | 1.9 g/cm3 |
| Refractive Index | 1.317 |
| Solubility In Water | Insoluble |
| Flash Point | Non-flammable |
| Smiles | C(=C(Br)F)C(F)(F)F |
| Pubchem Cid | 11084 |
| Melting Point | -110°C |
| Odor | Sweet, ether-like |
As an accredited 2-Bromopentafluoropropene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100-gram amber glass bottle, tightly sealed, labeled "2-Bromopentafluoropropene," with hazard symbols, lot number, and safety information. |
| Shipping | 2-Bromopentafluoropropene is shipped as a hazardous chemical and should be packaged in approved, tightly sealed containers under an inert atmosphere. Transport must comply with international regulations, typically as a flammable, toxic, and environmentally hazardous substance. Handle with care, avoiding heat, ignition sources, and physical damage during shipping. Proper labeling is required. |
| Storage | 2-Bromopentafluoropropene should be stored in a cool, dry, and well-ventilated area, away from heat sources, moisture, and incompatible substances such as strong bases and oxidizers. Keep the container tightly closed and properly labeled. Store in a corrosion-resistant container, preferably made from materials compatible with halogenated compounds. Use secondary containment to avoid accidental leaks or spills. |
Applications of 2-Bromopentafluoropropene in Industrial Manufacturing2-Bromopentafluoropropene serves as a key fluorinated building block in a variety of advanced industrial sectors. Owing to its reactive bromine and pentafluoropropene structure, this intermediate enables targeted functionalization for next-generation polymers, specialty refrigerants, agrochemical actives, and electronic materials. Explore the principal application scenarios where our direct manufacturing capabilities integrate this raw material into downstream processes. 1. Fluorinated Elastomer Monomer SynthesisDownstream producers of specialty elastomers incorporate this material directly into the monomer synthesis step to introduce high-fluorine content and enhance chemical resistance. The reactive bromine moiety enables controlled copolymerization with other fluoro-olefins and vinylidene fluoride derivatives, facilitating the production of fluoroelastomers suited for automotive, semiconductor, and aerospace sealing applications. Industry compliance standards
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2. Refrigerant Intermediate SynthesisProducers engage this molecule in multi-step synthesis as a key halogenated intermediate for low-GWP refrigerants. The material’s pentafluoropropene backbone and reactive bromo substituent enable downstream transformation into hydrofluoroolefins (HFOs) featuring environmentally preferred combustion and pressure performance. It supports feedstock streamlining for phasedown-compliant refrigerant families. Industry compliance standards
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3. Agrochemical Active Ingredient SynthesisAgrochemical manufacturers utilize the compound for introducing highly fluoroalkylated portions into crop protection molecule scaffolds. Its high electronegativity and reactivity drive specific substitution or coupling reactions, with the resultant actives showing enhanced environmental stability and targeted molecule reactivity essential for modern pesticide formulations. Industry compliance standards
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4. Electronic Grade Fluorochemical PrecursorThe electronics sector draws on this raw material for synthesizing specialty fluorochemical intermediates used in the fabrication of semiconductors and advanced display panels. The unique profile allows formation of surface modifiers and etchants with ultra-low metal and nonvolatile residue levels, which are critical to photolithography and wafer-clean processes. Industry compliance standards
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5. Pharmaceutical Fluorine Introduction IntermediatePharmaceutical ingredient developers select this compound for the regioselective introduction of fluorine into small molecule actives. The pentafluoropropene structure opens access to specific fluorinated analogs, supporting modifications that enhance bioavailability, metabolic stability, and physicochemical profiles of candidate drugs under development. Industry compliance standards
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Our journey manufacturing 2-Bromopentafluoropropene, known in the field by its CAS number 422-56-0, began after demands increased for high-purity, selective reagents in fine chemical synthesis and specialty polymers. Decades in fluorine chemistry lab work have revealed one lesson after another about handling perfluoroalkyl halides efficiently and safely, recognizing the unique role a compound like this plays both as a strategic intermediate and as a tailored reactant.
Molecular formula C3BrF5, or, for some, 1-bromo-2,3,3,3-tetrafluoropropene, occupies a solid niche among fluoroolefins. Its structure—an unsaturated three-carbon chain, one terminal double bond loaded with electron-withdrawing fluorines, and a single bromine—provides reactivity one rarely finds in other halogenated alkenes. During batch distillation, the way pentafluoropropene’s vapor pressure interacts with the bromine atom can give headaches, so practical operational experience counts more here than theoretical knowledge.
Scaling up from hundreds of grams on a bench top to metric tons in a reactor hall highlighted certain peculiarities. For our process, maintaining vigilance over temperature profiling avoids polymerization and excessive side-reactions. Atmospheric control matters: once, a slip in system tightness almost led to an uncontrolled release—luckily, pressure monitors caught it early. Handling isn’t suited for general-purpose glassware; fluorinated olefins and bromides test every O-ring, gasket, and operator’s attention to detail.
We target a minimum 99% purity in the finished product. Each drum or cylinder moves through rigorous GC-MS and NMR analysis: contamination can disrupt subsequent synthesis or even cause hazardous byproducts down the value chain. Over the years, impurities—especially unreacted bromine or C3F6 byproducts—proved troublesome for customers. Feedback led us to install in-line purification and more robust cold traps, especially since trace acids corrode steel over time.
Most buyers use 2-Bromopentafluoropropene as a key intermediate in fluoroaromatics and active pharmaceutical ingredients. In the field, you rarely see it on its own—chemists reach for it as a building block. Selectivity matters in cross-coupling reactions: our experience confirms that bromine’s leaving group potential allows for wider functionalization compared to non-halogenated pentafluoropropenes. Metal-catalyzed processes, especially those targeting high-value trifluoromethylated scaffolds, lean heavily on this compound to introduce perfluoroalkyl groups. It also underpins various hydrophobic polymer backbones, where stability and weatherability surpass that of hydrocarbon olefin analogs.
In polymer synthesis, use in copolymerization with vinylidene fluoride or hexafluoropropylene delivers materials that resist both acids and bases, making them ideal for chemical-resistant coatings and membranes. Customers specializing in chemical processing have reported improved membrane life—and that outcome justified the investment in additional analytical steps. In basic research, the double bond remains a point of attack for various functionalizations; we see many requests from specialty labs working to build out new solvolytic or biradical pathways.
Unlike more stable, perfluorinated aliphatics, 2-Bromopentafluoropropene engages actively in reactions that demand a well-placed bromine or unsaturation site. Most commercially available fluoroolefins lack this coupled reactivity, as one often finds in either fully saturated, more inert molecules or more reactive yet less selective analogs.
Experience reveals 2-Bromopentafluoropropene stands apart from related compounds like 1,1,1,2,3,3,3-heptafluoropropane, chlorotrifluoropropene, or trifluoropropene, not just in chemical structure, but in practical handling, reactivity, and end-use utility. Bromine offers a strategic balance: compared to chlorine, it confers higher selectivity and milder reaction conditions when employed as a leaving group.
We have seen customers initially attempt to substitute with less expensive chlorinated variants, only to circle back because yields, particularly in palladium or copper-catalyzed reactions, lagged far behind. The steric and electronic influence of five fluorines starkly contrasts against difluoro- or trifluoro-olefins. Our documentation and customer feedback sheets overflow with references to the higher regioselectivity obtainable in SN2′ substitution and cross-coupling.
From a safety and storage perspective, 2-Bromopentafluoropropene’s lower reactivity compared to fully unsaturated or sulfur-functionalized analogs reduces the risk profile in warehouse environments. Long-term compatibility demands regular rotation of stock: over three years, we noted potential for gradual hydrolysis—prompting shifts in our packaging materials to fluorinated polymers and select stainless alloys.
Handling the compound, no one misses the faint, sharp odor typical of five-fluorinated molecules. Storage is less challenging than it is for acid fluorides and chlorofluoroolefins which corrode most vessels, though the product does require prevention from contact with strong bases and nucleophiles. The bromine atom, while ready to depart under catalytic guidance, sticks tight under ambient storage, which is a blessing for both shipping and long-term warehouse management.
Adhering to strict analytical protocols has built strong bridges with downstream users. Issues occasionally emerge where residual unreacted feedstock interferes with precise applications—these highlight the importance of ongoing quality audits. We maintain regular dialogue with formulation chemists and process engineers at customer facilities, sharing best practices about product dilution, secondary containment, and even custom packaging solutions.
Some end-users seek assistance tuning their reaction conditions: our technical support draws in part on data from our own quality control laboratories. Adjustments in catalyst loading, temperature ramp, and solvent choice make a marked difference in both operational throughput and yield. Once, a client synthesizing an agrochemical precursor struggled with low conversion rates; after swapping out a standard ligand, based on our in-house organofluorine experience, the process optimized and throughput tripled over three campaigns. We treat such collaboration as an extension of the manufacturing process itself—and continual feedback guides our own synthetic upgrades.
Supply chain volatility, especially during pandemic-era logistics, tested every plant’s flexibility. By phasing in local storage of key raw materials and diversifying reactor batch scheduling, we have prevented bottlenecks from impacting contractual supply agreements. Years ago, inadequate contingency planning caused a brief production halt—since then, monthly drills ensure everyone understands how to handle both mechanical and chemical emergencies on the floor.
Documentation tailored to individual regulatory environments further eases movement internationally: from customs declarations to compliance with international shipping codes, our team assembles everything origin-to-destination, removing paperwork headaches for customers. A strong foundation in technical documentation, paired with decades of direct experience, streamlines import into Europe, North America, and East Asia.
As the discussion of per- and polyfluoroalkyl substances (PFAS) grows in public and regulatory circles, manufacturers face questions about stewardship throughout the entire lifecycle of fluoroorganic products. We continuously review upstream and downstream emissions, seeking to minimize both fugitive losses in production and downstream persistence. Fluoroolefins, including 2-Bromopentafluoropropene, break down more readily under UV radiation than their alkane relatives, and that difference points to responsible use where low-global warming-potential chemistries remain a priority. We have upgraded to closed-system reactors, enhanced fume scrubbers, and formal disposal partnerships for every shipment.
By working closely with national environmental agencies and voluntary industry groups, we help shape realistic handling, containment, and end-of-life standards that meet or exceed current guidelines. Our zero-waste mindset leads to continual re-examination of solvent selection, distillation protocols, and byproduct recovery. Reclaiming residual HF from reactions and tracking the fate of brominated byproducts feed back into real-time process improvements on the factory floor.
For buyers dealing primarily with paper descriptions and brochures, differences between 2-Bromopentafluoropropene and its relatives rarely jump off the page. Those of us who have spent years in production know that the fine distinctions—impurity profile, handling ease, shelf life, adaptability across reaction types—drive actual value far more than technical jargon suggests. Conversations with operators, researchers, and regulatory officers continue to shape both product and practice, always anchoring priorities to real-world outcomes.
Decisions in sourcing and scaling have given us both wisdom and battle scars. Unplanned halts due to supply disruptions taught us the hard way to invest in predictive maintenance and local stockholding. Feedback from polymer labs, especially complaints about inconsistent vaporization during feeding, pointed out issues in drum pressure stabilization we would’ve missed otherwise. These insights shift routine into progress, and push the entire team toward continuously better outcomes.
Most buyers, after a few cycles, discover the value in genuine manufacturer support. Things go wrong—a cylinder arrives too cold and doesn’t dispense, or a batch’s GC report shows a 0.1% impurity spike. Addressing these quickly, with transparency, means keeping customers’ production lines moving and, as importantly, learning ourselves what really matters at the point of use.
Our role doesn’t end at the loading bay. We make sure each customer understands not only the product specifics, but also optimal storage and handling tips, typical shelf life under local conditions, and fallback procedures for atypical events. Offering both experience and real-time workplace data means no surprises, and fewer costly interruptions down the chain.
2-Bromopentafluoropropene delivers much more than a chemical name or a CAS number. For supply partners working in advanced materials, specialty pharmaceuticals, or custom synthesis, the value lies in consistent quality, robust technical partnership, and flexibility rooted in manufacturing reality. Fluoroalkyl chemistry continually evolves: each production run uncovers new nuances—be it in catalyst compatibility, in reaction cleanup, or in regulatory adaptation—that strengthen both science and trust.
We believe in bringing both hard data and hard-earned experience to the table, solving challenges before they cascade, and sharing insight that only comes from hands-on production and close customer relationships. As research in specialty chemicals for tomorrow’s needs breaks new ground, we keep refining process, product, and partnership, ensuring that 2-Bromopentafluoropropene continues to set benchmarks for reliability, application breadth, and long-term value in the chemical manufacturing landscape.