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HS Code |
650470 |
| Cas Number | 22059-81-8 |
| Iupac Name | 1,2-Dibromo-3,3,3-trifluoroprop-1-ene |
| Molecular Formula | C3HBr2F3 |
| Molecular Weight | 255.84 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 109-110°C |
| Density | 2.088 g/cm³ (at 25°C) |
| Melting Point | -72°C |
| Refractive Index | 1.4350 (at 20°C) |
| Solubility In Water | Insoluble |
| Synonyms | CF3CH=CHBr2 |
As an accredited 1,2-Dibromo-3,3,3-Trifluoropropene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,2-Dibromo-3,3,3-Trifluoropropene is packaged in a 500 mL amber glass bottle, tightly sealed with hazard labeling. |
| Shipping | 1,2-Dibromo-3,3,3-Trifluoropropene should be shipped in tightly sealed containers, away from heat, sparks, and open flames. It must be clearly labeled as hazardous, and transported in accordance with local, national, and international regulations. Use secondary containment to prevent leakage and ensure handlers wear appropriate chemical protective equipment. |
| Storage | 1,2-Dibromo-3,3,3-Trifluoropropene should be stored in a tightly sealed container in a cool, dry, well-ventilated area away from direct sunlight and sources of ignition. Avoid storage near heat, oxidizing agents, acids, or bases. Properly label the container and ensure it is compatible with the chemical. Use secondary containment and follow all local regulations for storage of hazardous chemicals. |
Applications of 1,2-Dibromo-3,3,3-Trifluoropropene in Industrial ManufacturingAs a specialized manufacturer, we supply 1,2-Dibromo-3,3,3-Trifluoropropene (DBTFP) to critical industrial sectors where its chemical reactivity, selectivity, and halogen content provide high-value transformations. The following established downstream applications highlight how producers integrate this molecule for advanced material synthesis, agrochemical intermediates, refrigerant development, pharmaceutical actives, and specialty polymer modification. 1. Agrochemical Intermediate SynthesisProducers of modern herbicides and insecticides employ DBTFP as a key intermediate, exploiting its fluoroalkylation and bromination functionality to construct highly active molecules. Plant protection chemical plants react this compound with nucleophiles, introducing trifluoropropenyl and dibromo motifs into new actives, where strict residue and environmental benchmarks govern every step of production. Integration occurs during the core-step halogenation or alkylation sequence. The fine-tuning of molar ratios hinges on the specific crop-protection target and downstream structure-activity relationship optimization, ensuring regulatory alignment and process consistency. Industry compliance standards
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2. Pharmaceutical Intermediate ManufacturingPharmaceutical fine chemical production facilities use DBTFP as a fluoroalkyl and dihaloalkene donor during multi-step synthesis of APIs, notably those needing metabolic stability enhancements or CNS penetration. Its halogenation versatility allows selective functional group modification under cGMP environments. Implementation occurs at the specific alkylation or halogen exchange stage of the process, after stringent raw material ID and under full traceability controls. The input ratio adheres strictly to stoichiometric balance and risk assessments to meet impurity thresholds for ICH Q7 and relevant pharmacopoeial monographs. Industry compliance standards
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3. Refrigerant and Halon Precursor ProductionRefrigerant and halon producers use DBTFP in the synthesis of environmentally safer hydrofluoroolefins (HFOs) and fire suppressant blends. The molecule’s dibromo and trifluoropropene groups allow its conversion to advanced HFO refrigerants via hydrodehalogenation, dehydrohalogenation, or Grignard cross-coupling routes, a critical operation for compliance with low-GWP mandates. Input level is calculated as a tight stoichiometric match to maximize conversion and minimize unreacted bromide, with downstream separation of side-products and gas-phase distillation for purity assurance. Industry compliance standards
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4. Advanced Specialty Polymer ModificationManufacturers of specialty fluoropolymers and engineering plastics leverage DBTFP as a functional monomer precursor or polymer end-group modifier. The reactive propenyl and halogenated structure enables precise introduction of trifluoro and dibromo functionality, which enhances heat resistance, hydrophobicity, or chemical barrier properties of finished polymers. Process input matches specific copolymer recipes or chain-end modification targets, considering polymerization initiator activity and desired performance upgrades. Dilution in selected organic solvents and in-line metering support effective reaction control in continuous or batch processes. Industry compliance standards
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The push for better, safer, and more adaptive building blocks in chemistry keeps shaping the work we do every day. In our own journey with 1,2-Dibromo-3,3,3-Trifluoropropene (commonly, DBTFP), the story has grown past a line in a product catalog. Our plant’s reactors have produced dozens of halogenated intermediates over years, but there’s something distinctly robust about DBTFP: ease of control during synthesis, purity that tracks tighter than many older alternatives, and properties that help downstream users cut downtime and waste.
Leveraging extensive quality management protocols, every batch we complete triggers a chain of checks that starts with raw material validation and ends with bottled liquid that meets tight chromatographic specs. In practice, we keep the bromine and trifluoromethyl sources under constant watch, since even slight deviations can create difficult-to-trace byproducts. Take our DBTFP, catalogued as Model 1233TF–DB for reference. It consistently clocks in above 99.5% by GC, with moisture and non-volatile matter held well under thresholds accepted by major agrochemical, pharmaceutical, and specialty chemistry partners. For producers downstream, minute differences in purity or isomeric content can drive up costs or slow production—something we don’t pass on.
A product like 1,2-Dibromo-3,3,3-Trifluoropropene doesn’t travel lightly: it has a distinct, sharp odor, moderate volatility, and a clear, nearly colorless appearance. Colleagues often ask, during plant tours or training sessions, about the fumes escaping when a drum briefly opens. Even at room temperature, DBTFP can lose integrity if left uncapped, so we’ve worked at length to improve our filling, venting, and downstream packaging. Drum walls, seals, and even the pallet stretch—everything is chosen to keep the product as fresh on day thirty as it was at bottling.
Out in the field, some customers report that switching out DBTFP from another halogenated propene takes less than half an hour, since the viscosity and reactivity align closely with others in the family. Our founding team includes process engineers who spent their early careers in fine chemical plants, so we aim to remove hurdles in clean-in-place protocols and feeding lines. Not every product maintains stability to this degree during short-term storage or transport, and comparative studies in our own lab confirm shelf life over several months under dry, inert gas—far longer than many isomers or structural analogs.
Questions about the product’s identity surface often. How does DBTFP distinguish itself from close relatives, such as 1,3-dibromopropene or other trifluoropropenes? The answer lies in its molecular effects. The presence of both terminal bromines and a trifluoromethyl group creates a tricky balance in reactivity. Compared to mono-fluorinated propene derivatives or fully saturated versions, DBTFP stands out for its role as both an alkene synthon and a halogen source. Several industry collaborators have found yield improvement and cleaner work-ups when running nucleophilic additions, due to the electronic “pull” exerted by the trifluoromethyl and dibromo units. You don’t get this same effect from the more traditional 1,3-dibromopropene, which often reacts with broader selectivity and leaves more waste to manage.
Another key differentiator comes during dehydrohalogenation and elimination steps. We once watched an operator test three related halogenated propenes in parallel applications for a medical intermediate. The DBTFP reaction completed hours ahead, cutting solvent use and sidestepping side-product formation that normally required column clean-up. Some of this comes from the way the fluorines interact with the double bond, shifting reactivity and selectivity just enough to simplify downstream work.
Not every chemical spends its life rotating quietly in a storage tank. DBTFP stands as a backbone in major syntheses—especially active ingredient design for crop protection, veterinary chemistry, and selected pharmaceuticals. Colleagues developing newer pesticidal platforms routinely update us with feedback: intermediates built on DBTFP show lower halogen loss during coupling reactions, and form cleaner, more predictable profiles in pilot trials than alternatives. There’s no accident in these observations—the compound’s balanced halogen load and electronegative features help teams scale up safer and more efficiently.
Pharmaceutical R&D groups occasionally invite our chemists to advise on nucleophilic substitution strategies, since DBTFP’s reactivity profile fits tightly with a handful of scaffolds that other halogenated propenes can’t emulate. The pre-installed trifluoromethyl group has an impact on pharmacokinetics, often impacting metabolism rates in experimental APIs under study. We’ve worked with several partners to redesign step sequences, harnessing DBTFP’s properties for better yield, lower environmental load, or easier purification. Tracking these partnerships over years, we notice cycles: early adoption, minor process adjustments as quirks surface, then gradual standardization as the product proves itself robust in diverse scenarios.
Years of manufacturing DBTFP have made hazards and safe handling deeply familiar. Brominated and fluorinated intermediates impose specific safety obligations. Short, well-regulated inhalation events have clear action plans at our site: quick air exchange, constant monitoring for overexposure, and extensive training for line staff and lab personnel. One incident from several years back—a faulty transfer hose—set off a lesson that persists today: no shortcut exists for engineering controls and careful PPE selection. This isn’t a matter of meeting compliance: it’s about real, lived experience in a busy, chemical-rich facility where seconds count if something turns sideways.
Across partners, we see a broad range of handling infrastructure. Some specialty chemical sites boast multi-layer glove boxes, in-line scrubbers, and local exhaust, while others operate in basic drum rooms. We share our own process audit criteria freely when asked, since we’d rather build safe, repeatable systems than respond to emergencies later. Our operations team continues to update protocols, feeding lessons learned back to our own suppliers and packaging partners, since a safe, predictable supply chain serves everyone involved—whether that partner runs an R&D bench or a multi-ton production line.
Environmental regulators in recent years have raised the bar for fluorinated and brominated substances. Not long ago, routine calls with partners centered on legacy halogenated solvents or process waste. Nowadays the questions are sharper: what off-gases during use, how much persists in effluent, and how sustainable can we make disposal and recycling? We sit on technical committees alongside other manufacturers and contribute data on DBTFP to support a broader understanding of environmental profiles. Out of respect for both colleagues and the planet, we proactively invest in analytical testing, tracing even trace residues from process lines and test reactors to help limit unintended releases.
Our own R&D department pilots green chemistry substitutions each year. DBTFP earns its place because, with careful process design, it minimizes halogen load in side streams, and purification typically results in recoverable byproduct streams, not unrecyclable hazardous waste. Among routine conversations, we discuss options for abatement and reclamation with downstream users, occasionally working side-by-side to improve yield and cut down emissions and aqueous byproduct loads. This hands-on engagement lets us stay a step ahead in anticipating what next-generation sustainability rules may demand from synthetics like DBTFP.
Industrial partners using DBTFP don’t face the same challenges, so our approach refuses the one-size-fits-all mindset. On one project, an agrochemical team scaled a new active ingredient using our 1233TF–DB, and a bottleneck in liquid transfer set off a round of troubleshooting. Their tank farm wasn’t built for high volatility compounds, so we worked together to design a vented, pressure-equalizing set-up tailored to DBTFP’s vapor pressure and hazard class. Feedback arrived in days—a massive reduction in transfer loss, and much calmer operators, who now face less exposure risk and fewer spill close calls. That practical approach reflects our entire ethos: identify friction, consult openly, and chase better outcomes with end users in every link of the supply chain.
Elsewhere, a pharmaceutical partner experimented with alternate halogenated propenes but circled back to DBTFP because of sharp batch-batch reproducibility and a drop in off-color byproducts. Their prior candidate required two added purification steps per kilo—labor and solvent costs added up quickly. The process switch trimmed both, not by chance but due to DBTFP’s stability and selectivity profile. These gains aren’t unique—each winning process springs from thousands of small learnings, feedback rounds, and chemistry that actually listens to what users need on the ground.
Other manufacturers may treat their supply chain as remote, but our company’s culture revolves around hands-on engagement with every stage of production and delivery. Engineering, R&D, operations, and logistics meet weekly to surface process improvements, quality issues, or bottlenecks noticed out on the plant floor. More than once, a minor impurity trend noticed by a QC chemist has sent us back upstream to refine temperature ramps or raw bromine purification. Every year, external audits, customer QA teams, or regulatory visitors open our books. We value this close scrutiny because it makes the end product stronger and helps to maintain the tight purity range expected by long-standing customers.
For us, sourcing raw materials ranks just as important as refining output. We secure starting bromine and trifluoropropene under strict traceability systems, with contract language built around consistency and sustainability. This close relationship with suppliers means fewer surprises and a clearer record for every shipment. Many of the improvements customers see—lower impurity profiles, better storage stability, and fewer customer complaints—trace directly to this mentality: build reliability from the ground up, don’t just impose it at the final filter.
In our business, trust doesn’t come from marketing claims. Clients gauge us by the habits they witness—speed of problem-solving, transparency with documentation, willingness to admit error and fix it, and capacity to apply practical wisdom on every production run. For DBTFP, these moments often emerge when partners try something unexpected: pushing a reactor a few degrees out of spec, storing product a little longer than advisable, or scaling up on short notice. We document every deviation, create corrective protocols, and feed this data back to customers so each partner sits on a bedrock of shared knowledge.
Our technical support team includes chemists with hands-on plant experience. We commit resources to field visits, process troubleshooting, and sharing advances from our own continuous improvement efforts. Long-term customers receive regular updates—process chemistry notes, regulatory insights, and lessons learned in real time rather than annual data dumps. This direct, honest communication matters more than polished presentations. Fewer unmet needs, clearer answers, and better performance in the field—these benefits flow straight from how closely we stand with users at every stage.
The regulatory climate keeps shifting, sometimes quicker than industry can adapt. When new hazard classifications, exposure limits, or chemical registration rules arise—especially for halogenated intermediates like DBTFP—we review each one actively. Our compliance group liaises with government and international organizations, ensuring conforming packaging, labeling, and transport. Customers keep us on alert for country-specific rule changes, and we often pre-empt regulatory hurdles by providing new testing data or documentation before clients know they need it. This isn’t reactive, hands-off compliance; it becomes a continuous loop of anticipation, action, adjustment, and feedback, benefiting everyone who handles DBTFP across its lifecycle.
In practical terms, recent changes have called for updated transport hazard labeling and fresh exposure monitoring data. We allocate lab resources every month to test both original and stored product samples, maintaining robust data streams that assure both our team and our customers of consistent chemical integrity and regulatory conformity. Such steps are non-negotiable in building lasting business partnerships and in keeping the industry’s license to operate free from future risk.
Manufacturing specialty molecules like 1,2-Dibromo-3,3,3-Trifluoropropene is an exercise in daily learning. No process stays still for long. Each fresh batch, customer report, regulatory revision, or process tweak reveals unplanned details. Over the years, our chemical engineers and plant operators have introduced upgraded distillation systems, refined temperature control, and improved drum sealing—all based on active observation, not theoretical analysis. Site visits to customers close the loop, often uncovering handling or application insights invisible from behind the factory fence.
Not all advances are grand. Sometimes the story is a minor adjustment: a better valve, a more accurate purity test, new maintenance for filling lines. Step by step, these tweaks add up to smoother supply, fewer complaints, and greater trust. The ongoing education shared between our technical and operational staff means continual progress translates directly to every drum labeled with our DBTFP code. In the end, industry moves forward not by resting on one success, but by turning every challenge into practical, granular solutions anyone in the supply chain can act on.
Looking ahead, 1,2-Dibromo-3,3,3-Trifluoropropene sits in a strange position: widely adopted in many fields, yet always subject to new demands from industry, regulators, and society. Each year brings new questions. Which other synthetic routes can gain from its selectivity? How will regulatory pressure shape its lifecycle, especially as environmental science matures? Will green chemistry unlock related compounds that perform even better? We keep these conversations alive both in-house and with partners, knowing that only by confronting practical, real-world problems head-on can we maintain DBTFP’s relevance and value long into the future.
The journey hasn’t been simple. Over two decades, our own understanding of DBTFP’s unique quirks and strengths has deepened. Many challenges that once seemed daunting—impurity control, shipping hazards, best storage practice, regulatory alignment—now count as routine. Yet every change in market need, every request from a chemist trying to shave hours or costs from a process, every incident review or compliance challenge, reminds us of the stakes. What matters most remains constant: safe, reliable, chemistry-driven supply built by people willing to learn, adapt, and respond directly to users, day after day.