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3-Bromo-3,3-Difluoropropene

    • Product Name 3-Bromo-3,3-Difluoropropene
    • Alias 3-Bromo-3,3-difluoro-1-propene
    • Einecs 'EINECS 259-250-7'
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    657671

    Product Name 3-Bromo-3,3-Difluoropropene
    Cas Number 431-72-5
    Molecular Formula C3H3BrF2
    Molecular Weight 156.96
    Appearance Colorless liquid
    Boiling Point Celsius 69-71
    Density G Per Cm3 1.616
    Refractive Index N20d 1.410
    Smiles C=CC(Br)(F)F
    Inchi InChI=1S/C3H3BrF2/c1-2-3(4,5)6/h2H,1H2
    Solubility Insoluble in water
    Storage Conditions Store at 2-8°C
    Synonyms 3-Bromo-3,3-difluoro-1-propene
    Vapor Pressure Mmhg 132 (at 20°C)

    As an accredited 3-Bromo-3,3-Difluoropropene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 3-Bromo-3,3-Difluoropropene (25g) is packaged in a sealed amber glass bottle with a secure, chemical-resistant screw cap.
    Shipping 3-Bromo-3,3-Difluoropropene is shipped as a hazardous material in compliance with international regulations. It is packaged in tightly sealed containers, typically under inert gas to prevent decomposition. Shipping requires proper labeling, documentation, and handling by certified personnel, ensuring safety and environmental protection throughout transit. Temperature control may be necessary, depending on quantity and destination.
    Storage 3-Bromo-3,3-difluoropropene should be stored in a cool, dry, and well-ventilated area, away from heat, sparks, open flames, and incompatible substances such as strong oxidizers. Keep the container tightly closed and properly labeled. Store in a chemical-resistant container, preferably glass or compatible plastic. Avoid exposure to moisture and direct sunlight. Follow all relevant safety and regulatory guidelines.
    Application of 3-Bromo-3,3-Difluoropropene

    Applications of 3-Bromo-3,3-Difluoropropene in Industrial Manufacturing

    As an experienced chemical raw material manufacturer, we supply 3-Bromo-3,3-Difluoropropene for targeted industrial applications in pharmaceutical, agrochemical, fluorochemical, and specialty intermediate syntheses. The following downstream segments demonstrate its practical use, technical incorporation, and compliance with international production requirements.

    1. Pharmaceutical Intermediate Synthesis

    This difluorinated bromoalkene sees extensive use as a building block in active pharmaceutical ingredient (API) production. Synthetic chemists employ its unique halogen-fluorine pattern to introduce difluoropropenyl groups into heterocyclic systems, enabling downstream functionalizations such as Suzuki or Heck couplings under GMP environments. During the API manufacturing chain, careful control of the halide/fluoro ratios enables precise structural innovation for next-generation therapies.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP EudraLex Volume 4
    • FDA cGMP 21 CFR Part 210/211
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • Typically 0.6–1.2 equivalents relative to core heterocyclic or aromatic substrates, with adjustment based on yield optimization and downstream purification requirements

    Downstream process integration

    • Charged directly into the step requiring difluoropropenyl introduction, followed by in situ transition metal-catalyzed coupling reactions, with residuals removed during workup and chromatographic purification

    Final product types

    • Antiviral and anticancer drug intermediates
    • CNS-active fluorinated pharmaceuticals
    • Specialty peptidomimetic APIs containing fluorine motifs
    • Advanced intermediates for patented small molecules

    2. Agrochemical Active Ingredient Development

    Research and development teams utilize 3-Bromo-3,3-Difluoropropene as a core intermediate for synthesizing advanced agrochemical actives. This compound serves in the construction of fluorinated side chains that enhance bioavailability and target selectivity for herbicides and fungicides. Rigorous process validation and safety assessment occur under supervision of the responsible authorities to ensure safe handling of halogenated precursors and compliance with relevant environmental and chemical legislation throughout production stages.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • ISO 17025 Accredited Laboratory Analysis
    • REACH Regulation (EC) No 1907/2006
    • Globally Harmonized System (GHS) for labeling and packaging

    Typical usage ratio

    • Integrated at 1.0–1.5 equivalents during key steps for active ingredient core assembly, adjusted based on target molecule substitution pattern in multi-step synthesis

    Downstream process integration

    • Added as a halogen/fluorine synthon during late-stage molecule construction, typically in protected laboratory reactors, monitored by in-process HPLC or GC for impurity control

    Final product types

    • Difluoralkylated triazole fungicides
    • Selective herbicide bases with enhanced lipophilicity
    • Next-generation insecticidal intermediates
    • Soil treatment and plant protection actives

    3. Fluoropolymer and Fluoroelastomer Modification

    Manufacturers of specialty fluoropolymers and fluoroelastomers employ this raw material to introduce difluorinated allylic moieties, impacting crosslinking behavior and final product elasticity. The addition frequently occurs during the pre-polymerization functionalization, where small-scale pilot operations determine batchwise ratios. Integrators document traceability from raw material lot through finished goods, supporting high-performance product lines for pulp, wire & cable insulation, and chemical-resistant linings with defined release properties.

    Industry compliance standards

    • ASTM D2116 Standard Specification for Fluoropolymer Products
    • ISO 9001:2015 Quality Management
    • UL 94 Flammability Rating for cable materials
    • RoHS Directive (2011/65/EU) for electrical applications

    Typical usage ratio

    • Recommended loading of 0.2–0.8 mol% relative to main monomer feed, optimized to balance mechanical strength and desired fluorine incorporation

    Downstream process integration

    • Added at the oligomer or comonomer stage before reactor charge, facilitating post-functionalization or as chain-end modifier in melt-phase polymerization, followed by blending and extrusion as required

    Final product types

    • High-performance FKM elastomers
    • Electronically insulative fluorinated tubing
    • Release liners and gaskets
    • Fluorinated specialty films

    4. Advanced Chemical Synthesis for Crop Protection Safeners

    Process chemists employ this intermediate in crop protection safener research, targeting selective reactivity patterns to moderate herbicide toxicity. Introduction of difluoropropenyl and bromo functionalities enhances metabolic stability, with careful adjustment per substrate. Scale-up from laboratory to pilot batch applies stringent documentation and Environmental, Health, and Safety (EHS) oversight, adhering to agricultural chemical directives and traceability from raw input to formulated concentrate.

    Industry compliance standards

    • OECD Guidelines for Testing of Chemicals
    • ISO 14001 Environmental Management Systems
    • Chemical Facility Anti-Terrorism Standards (CFATS)
    • Good Laboratory Practice (GLP)

    Typical usage ratio

    • Scale-up synthesis uses 0.5–1.0 equivalents, adjusted by target safener yield and substrate functionality to prevent by-product formation

    Downstream process integration

    • Fed during the key phase for carbon-bromine/fluorine bond introduction in the core molecule, followed by isolation and staged purification for safety and environmental compliance

    Final product types

    • Crop protection safener molecules
    • Herbicide antidote precursors
    • Metabolic enzyme modulators for plants
    • Integrated plant protection blends
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    Certification & Compliance
    More Introduction

    Introducing 3-Bromo-3,3-Difluoropropene: Meeting Real Industry Challenges

    Our years of hands-on experience in fluorochemical manufacturing have taught us that the success of a synthetic route depends as much on reliability as it does on innovation. 3-Bromo-3,3-difluoropropene, known in some lab circles as 3-BDFP, stands out in the catalog for people designing or modifying pharma intermediates, crop protection compounds, and other specialty fluorinated structures. We’ve produced and validated this molecule under a range of conditions that parallel how it gets used in real-world processes, so this is not just another bottle on the shelf—we consider it a building block for teams that need straightforward reactivity, purity, and scale-up support.

    Key Characteristics and Specifications

    Our typical production runs deliver 3-Bromo-3,3-difluoropropene with a purity of at least 98 percent, verified by GC and NMR. We keep moisture and acidity low, well below thresholds that might kick off side reactions during sensitive couplings or fluorination steps downstream. Over time, requests from researchers and production chemists have led us to optimize for stability in storage and shipping. The clear, nearly colorless liquid flows and dispenses easily—no waxy residues or separation headaches. Most batches test for halide levels and non-volatile residue, because routine checks catch issues before they interrupt your process. Our fluorine and bromine content is confirmed for every lot; those that work with multi-step syntheses know that tighter controls in each feedstock can pay off by reducing byproducts in the finished molecule.

    Why 3-Bromo-3,3-Difluoropropene Makes a Difference in Synthesis

    Chemists who work with modern drug scaffolds or agrochemical actives demand halogenated intermediates that bridge new ideas with practical manufacturing. This specific propene strikes a balance between reactivity and handle-ability. The bromine atom sits on a terminal carbon, making it a reliable leaving group for SN2 substitutions—especially useful for N- or O-alkylation reactions in heterocycle formation. The difluoromethylene keeps the compound electron poor around the double bond, making it more resilient to polymerization or hydrolysis compared to many other unsaturated bromide or fluoride analogues. We regularly hear from partners that this reduces waste during scale-up and helps avoid expensive re-purification steps. Not every halopropene will keep its shape for months in normal storage conditions; we have long-term data demonstrating our product resists yellowing or decomposition, which minimizes risk across inventory cycles.

    Direct Differences: How Our 3-Bromo-3,3-Difluoropropene Stacks Up

    It’s easy to lump all bromodifluoropropenes together on paper, yet subtle formulation and process changes matter a lot once you leave the design stage. We see several practical differences between our product and similar molecules. For one, earlier generations of brominated, unsaturated fluoroalkyls could bring in higher levels of dialkylated impurities—a headache for reactions looking for strict selectivity. Our finishing and isolation sequence cuts out those ghost peaks, so you’re not scrambling with extra chromatography after the fact. Also, chemists that tried switching to trifluorovinyl or non-brominated difluorinated alkenes noticed that replacements introduce issues with volatility, thermal stability, or less predictable substitution profiles. The difluoropropene backbone works with a range of catalysts—especially palladium and copper setups—while still allowing for simple aqueous workups in many cases. That kind of operational ruggedness means more predictable outcomes in the hands of production teams operating at tens or even hundreds of liters.

    Applications Where Consistency Matters

    The biggest value-add for this intermediate shows up in settings where each lot needs to perform the same every time. We’ve supported teams building propenyl-linked drug molecules, especially where the bromine acts as an entry point for further fluorination or cross-coupling. One customer working on a novel seed treatment compound used our 3-Bromo-3,3-difluoropropene as the central alkene in a late-stage introduction, which allowed them to increase overall yield by simplifying the isolation steps—less time chasing impurities, more time analyzing real product. Crop science groups come back for it, since many newer herbicidal or fungicidal actives have shown improved field persistence or selectivity by tuning the ratio of bromine and fluorine in the core skeleton. The stability offered by the difluoromethylene pattern, compared with unsaturated monofluoro or non-fluorinated analogs, offers better resistance to hydrolysis and weathering during storage and application.

    Supply Chain Lessons Learn on Fluorinated Intermediates

    Several years ago, volatility in the global fluorochemical supply chain underscored the importance of backwards integration. Our dedicated process line for 3-Bromo-3,3-difluoropropene doesn’t rely on spot purchasing of upstream fluorinated agents; instead, we generate precursors in-house, including direct handling of HF-based starting materials all the way through bromination and distillation. Along the way, analytical teams monitor impurities, since trace metals or extraneous halides can catalyze undesired pathways during your transformation steps. We respond directly to feedback from synthetic chemists who have tried off-brand or re-bottled material, many finding increased batch rejections due to unexpected byproducts. Ensuring traceability—from drum fill back to kilo-lot receipt—has eliminated most “mystery failures” during scale-up. As regulatory and environmental surveys intensify, our process meets internationally accepted best practices for emissions, waste, and occupational safety, leveraging local investments over import dependency.

    Feedback from Real-World Deployment

    Labs and plant teams return to this molecular unit because it lets them simplify steps that, with other building blocks, would need extra time for rework or purification. Take a high-throughput route to a fluorinated heterocycle: substitution proceeds to high conversion, and aqueous phase separations yield product without sticky emulsions typical of former approaches with trifluoromethylated alkenes. The physical profile of our 3-Bromo-3,3-difluoropropene—liquid at room temperature, low viscosity, and minimal odor—fits consistently into automated addition systems. This matters to engineers and operators aiming to keep batch times short and labor requirements reasonable. It reduces error rates versus powders or sticky semi-solids, and waste removal can be managed through existing solvent recovery infrastructure.

    Environmental and Regulatory Outlook

    Environmental safety and regulatory pressures around halogenated intermediates keep evolving year-by-year. Ongoing dialog with authorities and customers ensures our product documentation, shelf labeling, and waste transfer arrangements fit current rules for most major markets. We don’t use stabilizers containing banned substances; production streams recycle excess solvents, and gas-phase byproducts are scrubbed in-line. The result: you know exactly what you’re working with, and you document compliance for every lot. Reports on residuals, shelf life, and DfE data are made available, including studies on hydrolytic and photolytic breakdown. Storage for extended periods matches well with the practical realities of research and production schedules—no unexpected pressure buildups or shelf-life surprises.

    Process Support from Manufacturer to User

    Partnership with our team means direct communication with chemists that built and improved this compound from pilot scale up. Over the years, scale-ups in kilo- and ton-level batch reactors have led to refined handling instructions, startup routines, and finish protocols. This kind of practical insight gets built into every delivery, including straightforward advice for temperature control, materials compatibility, and quenching or neutralization. When route holidays or technical challenges arise, feedback and observations from others in bench, kilo-lab, and commercial settings get incorporated into process recommendations. Practical support helps avoid work-stopping pitfalls, and colleagues from QC share tips on expedient assay techniques that fit the main analytical setups—GC, HPLC, NMR—found in industry labs.

    Ongoing Improvements and Future Readiness

    The next wave of chemical applications is already pressing for tighter controls and narrower impurity bands. Over the last few quarters, we’ve upgraded our analytical validation routines, including improved methods for detecting low-level halogenated oligomers and better quantitation of trace organics. Lot release standards now include review of trace residual solvents by GC-MS, following concerns voiced by several active pharmaceutical ingredient producers. We experiment with alternative purification techniques—fractional distillation under custom atmospheric conditions, targeted charcoal treatments—to further extend shelf stability and minimize reactivity with atmospheric oxygen or trace acids.

    Continuous review of process analytics helps retain an edge, especially as demand grows for bespoke fluorinated intermediates or as end-users propose new routes connecting to larger, more complex API or fine chemical families. Our technical team works directly with downstream formulators to assess whether small tweaks in the bromination or finishing step bring broader process benefits, easier regulatory documentation, or reductions in waste volume. We also support transition studies from batch to flow chemistry, owing to increased interest in continuous manufacturing among our key partners.

    Direct Comparisons and Typical Substitution Issues

    We understand research groups and process development teams often weigh cost, availability, and reactivity against each other. Some experiment with trifluoropropene homologs in search of more aggressive substitution, but these frequently run into thermal control puzzles, higher VOC emissions, or stubborn end-group instability. Monofluorinated or chlorinated analogs trade down on selectivity, often boosting downstream purification costs. Our 3-Bromo-3,3-difluoropropene’s place on the balance beam comes from its use in forming libraries of new molecular entities using cross-coupling and alkylation schemes. Feedback has come in from both north and south hemispheres detailing how certain alternative sources, especially reprocessed or resold batches, introduce low-boiling point ghost peaks on scale. Mistakes here cost more than just material—they disrupt scheduling and regulatory audit timelines. Our approach, grounded in direct synthesis and unbroken QC oversight, shuts down such cycle-wasting problems before they start.

    Customers often ask about storage or handling differences with other halopropenes. Ours handles long-term storage without discoloration or clumping, and pressure fluctuations are minimal under recommended conditions. Handling and transfer in typical chemical glovebox environments carry little risk of fume build-up or sticky residue, which earlier analogs often suffered. Purity holds up whether the application is pharmaceutical or agricultural, reducing re-screening or pre-processing steps before your main reactions. It also demonstrates compatibility with a wide range of solvents and reagents, from polar aprotic environments to traditionally non-polar workflows. These measurable, practical outcomes build confidence in every transfer, every batch, every run.

    Learning from Real Use: User Reports and Field Insights

    We listen to feedback from regular users—plant chemists, pilot engineers, researchers—about everyday handling and process integration. One team, moving from kilo-batch to multi-ton scale, found that the absence of side product formation led to more stable crystallizations and clearer endpoint detection. Their move from a less refined, third-party intermediate to our direct-manufactured 3-Bromo-3,3-difluoropropene cut stepwise processing times by over a day per campaign. Reports from another crop-protection formulator focused on shelf-life: extended storage without loss in converted material, which meant orders could be staged well in advance without wastage or unplanned downtime. These insights shape our own process updates—not just meeting order specs, but anticipating new bottlenecks. Regular customer visits, open-lab trials, and cross-team QA/QC reviews all feed into iterative improvements. When partners report issues—cloudiness over time, inconsistent halogen content, decreased yield in tandem reactions—we trace back to raw-input tuning and small-batch trials, close the loops that caused delays, and validate changes before the next full-scale campaign.

    Commitment to Reliable Supply and Trusted Results

    Long-term partnerships grow on dependability. We invest heavily in vertical supply for critical fluorochemicals like 3-Bromo-3,3-difluoropropene, insulating end-users from price spikes and unexplained disruptions. Sourcing is local or regional whenever possible, with backup routes and tested supplier networks for key feedstocks. Large-volume users get priority tracking and surge capacity in case of industry upswings. Because we’ve walked the same ground as our customers—waiting for delayed shipments or puzzling over unexplained purity drops—we focus not only on making the product but also on keeping logistics smooth. Regular lead time reviews, coordinated staging, and prompt response to urgent re-stock requests all reinforce the trust needed for multi-year collaboration. Our technical team tracks every production run, supports validation audits, and logs all user feedback for fast follow-up and continuous improvement. This sort of reliability can make the difference between a process staying on track or hitting unforeseen snags.

    Sharing Real-World Learning and Collaboration

    The role of 3-Bromo-3,3-difluoropropene in modern chemical synthesis continues to expand. Unique bond arrangements bring tunable reactivity without overshooting volatility or creating handling headaches. As more end-users explore green chemistry adaptations and automation, the importance of stable, clean, and accessible intermediates only increases. We deepen our knowledge base through weekly project reviews, post-campaign debriefs, and strategic partnerships with academic and industry groups. Whether refining an existing project or helping explore a novel route, the direct manufacturer’s perspective brings a blend of technical control, supply chain resilience, and user-centered learning to the table. That’s the difference you’ll see with each order, every batch, every time feedback asks for another adjustment in line with evolving application needs.