|
HS Code |
294045 |
| Cas Number | 656-99-9 |
| Molecular Formula | C4HBrF6 |
| Molecular Weight | 242.94 g/mol |
| Appearance | Colorless liquid |
| Boiling Point | 47-49°C |
| Density | 1.78 g/cm3 |
| Melting Point | -76°C |
| Refractive Index | 1.332 |
| Solubility In Water | Insoluble |
As an accredited 1-Bromo-2-(Trifluoromethyl)-3,3,3-Trifluoro Prop-1-Ene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with tamper-evident cap, hazard labels, holding 25 grams of 1-Bromo-2-(Trifluoromethyl)-3,3,3-Trifluoroprop-1-ene. |
| Shipping | **Shipping Description:** 1-Bromo-2-(trifluoromethyl)-3,3,3-trifluoroprop-1-ene should be shipped in tightly sealed containers under inert gas, protected from light and moisture. Transport in accordance with relevant hazardous materials regulations, typically as a flammable and potentially harmful chemical. Ensure adequate labeling, documentation, and use of secondary containment to prevent leaks or exposure during transit. |
| Storage | 1-Bromo-2-(trifluoromethyl)-3,3,3-trifluoroprop-1-ene should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, in a cool, dry, and well-ventilated area. Keep away from heat, sources of ignition, and incompatible materials like strong bases or oxidizers. Store at temperatures recommended by the supplier, typically under refrigeration or at room temperature. |
Applications of 1-Bromo-2-(Trifluoromethyl)-3,3,3-Trifluoro Prop-1-Ene in Industrial Manufacturing1-Bromo-2-(Trifluoromethyl)-3,3,3-Trifluoro Prop-1-Ene finds strategic value in specialized chemical synthesis, driven by its unique trifluoroalkyl ether structure and high bromine reactivity. As an original manufacturer, we support demanding applications within pharmaceutical intermediates, agrochemical actives, specialty fluorinated monomers, and advanced material modification workflows. Below we outline targeted industry scenarios based on verified manufacturing channels and procedures. 1. Pharmaceutical Intermediate SynthesisLeading pharmaceutical firms incorporate this compound as a fluorinated alkene building block in the construction of advanced APIs, especially for generating CF3-rich molecular frameworks. Chemists leverage its capacity to introduce trifluoropropenyl or bromotrifluoromethyl moieties in late-stage processes, supporting the synthesis of therapeutic candidates for oncology and metabolic disorders. Production requires strict adherence to validated batch records under GMP and traceable quality control, including direct halogenation routes responsive to regulatory inspection. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisSpecialty agrochemical companies utilize this compound for synthesizing trifluoromethylated active ingredients with improved lipophilicity and metabolic stability. Manufacturers rely on its brominated olefin structure for coupling with aromatic or heterocyclic scaffolds, supporting innovation in herbicide and insecticide development. Production protocols must follow national safety requirements for pesticide intermediates, including hazardous material management for both bromine and fluorine components. Industry compliance standards
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3. Fluorinated Polymer and Monomer ManufacturingPolymers and functional monomer firms incorporate the compound as a tailored monomer precursor for introducing high-density fluorine content into advanced materials. Fluorinated polymers require specialty vinyl or propene units derived via bromine-initiated polymerization, yielding resins with exceptional weatherability, low surface energy, and high dielectric stability. Tight raw material control and batch traceability apply for high-purity input to minimize defect rates in downstream extrusion, molding, and coating processes. Industry compliance standards
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4. Fluoroalkylation Reagents for Specialty Chemical SynthesisCustom synthesis operations apply this material as a core fluoroalkylating reagent enabling selective trifluoropropenylation of complex organic scaffolds. Fine chemical labs employ its high electrophilic bromine to introduce perfluoroalkyl chains, producing advanced intermediates for electronics, photoresist, and specialty surfactant applications. Quality assurance protocols call for batch-specific GC/HPLC analysis and robust personal protection during feed and waste handling. Industry compliance standards
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Competitive 1-Bromo-2-(Trifluoromethyl)-3,3,3-Trifluoro Prop-1-Ene prices that fit your budget—flexible terms and customized quotes for every order.
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We operate on the core principle that product integrity shapes chemical manufacturing. Working daily with halogenated intermediates, I see firsthand the demands from both R&D labs and established process lines for consistent and reliable building blocks. 1-Bromo-2-(Trifluoromethyl)-3,3,3-Trifluoroprop-1-Ene—often abbreviated by chemists as BTPTFE for clarity—stands out for several specific reasons that we’ve documented through bench, pilot, and full-scale output phases. This specialty compound doesn’t just fill another slot on a chemical list; it addresses tangible challenges in fluorine-based organic synthesis and advanced material creation.
Our batches of 1-Bromo-2-(Trifluoromethyl)-3,3,3-Trifluoroprop-1-Ene typically appear as colorless to pale yellow liquids, possessing a distinctive sharp odor with a noticeable volatility. Rigorous quality checks underscore our approach. Every liter undergoes GC analysis and refractive index validation, keeping impurity content below levels that would impact reactivity or product quality downstream.
We supply standard scale containers suitable for kilo to tonnage-grade buyers, all with COA transparency. Typical purity for contractual lots consistently reads above 98.5%, year-round and across production runs, since fluctuations create bottlenecks for customers performing scale-up or registration work. Moisture and acidity tests align with global benchmarks, and our facility’s investment in inert atmosphere storage cuts down on degradation incidents that sometimes appear with older, re-packed materials.
Much of the practical knowledge informing these checks doesn’t come from protocols on paper, but from process engineers gathering real output samples—paralleling the needs of chemists preparing library compounds or assembling pilot studies for new applications.
Our lab teams invest time comparing the performance of this compound to similar halogenated ethenes and propenes. It offers unique coupling reactivity because the bromo group sits adjacent to heavily fluorinated carbons. That configuration produces cleaner reaction profiles in many cross-coupling, elimination, and substitution steps, which is critical when margin for error is strictly limited.
From the start, we engineered the process with high selectivity to eliminate by-product contaminants—fluoroalkyl side chains and mixed halides—that complicate downstream purification for our customers. The molecular structure also tacks on enhanced thermal and chemical robustness, raising its compatibility with harsher reaction conditions that might degrade conventional bromo-alkenes. This holds value in organofluorine and specialty agrochemical R&D, where requests for ever-higher stability and reduced impurity loads never stop arriving.
Our production lines rely on carefully managed raw feedstocks and in-house designed reaction vessels, letting us maintain higher isomeric purity. We keep track of every lot, tracing each from synthesis through handling and filling, because end users expect not just consistent product but deep documentation for audits and process optimization.
Most buyers using 1-Bromo-2-(Trifluoromethyl)-3,3,3-Trifluoroprop-1-Ene come with very specific needs. Pharmaceutical development teams often pursue C–C and C–N bond-forming reactions where this compound offers both the reactivity of a bromoalkene and the electron-withdrawing punch of several fluorines. This enables chemists to introduce stable, bioactive motifs into lead compounds, expediting move from hit discovery toward IND filings. For industrial chemists building electronic or photonic materials, its fluorine load helps anchor properties such as chemical resistance, low dielectric constants, and unique interfacial behaviors in coatings or films.
In agricultural chemistry, some innovation projects pivot around fluorinated scaffolds to achieve better environmental breakdown profiles or pest resistance. The presence of a trifluoromethyl group—paired with the bromo leaving group—delivers constructs not easily created with more common bromoalkenes. Over the years, I’ve seen project managers benchmark this material against alternatives, focusing on yield, impurity footprint, and process adaptability. Rarely do they accept second-best, since downstream purification costs and regulatory filing requirements keep getting tougher.
Our chemists continually review alternative bromo and iodo-alkenes to address specific customer inquiries. We compare different routes (such as from 1,1,1,2-tetrafluoro-2-bromoethane or other perfluoroalkyl halides) and routinely see that mixtures with higher bromine content or lacking the trifluoromethyl “handle” perform unpredictably under harsh bases and catalysts. Substituting a typical vinyl bromide or a lower-fluorine bromo-propene gives lower conversion and higher unwanted by-products upon scaling, based on dozens of technical reports shared by buyers running kilo-lab reactors.
The head-to-head studies drive home that the additional trifluoromethyl group matters. Electron-withdrawing pull on the β carbon stabilizes reactive intermediates and cuts down on side-chain scrambling during coupling steps. Most standard bromoalkenes decompose more quickly or form polymeric residues, especially under palladium or nickel catalysis. We’ve fine-tuned our own purification trains—pressure distillation and multi-column chromatography—so customers receive a ‘plug-and-play’ intermediate, without needing to adjust entire workups or spike budgets with additional scavenging steps.
Consistency matters to every large-scale customer. This isn’t news to anyone who’s spent nights re-running a batch just because a subtle impurity slipped past. The experience taught us hard lessons in continuous process monitoring and quick troubleshooting. Investing in closed-loop distillation, vapor-tight vessels, and remote QC readouts each cut down on recall rates and customer complaints.
Shipping is just as critical as synthesis. The product remains sensitive to moisture and strong bases; even trace hydrolysis impacts downstream coupling efficiency. We use specialized coated drums, with nitrogen purge cycles during packaging, because experience proved standard drums let in too much moisture. Our own staff also completes basic compatibility checks with customer container types, preventing cross-contamination between lots and shipping delays that stall project timelines.
We do not outsource critical processes—handling remains supervised by trained staff inside the main facility only. Product lots include full batch records, impurity profiles, and, if requested, run residue analysis. We believe transparency and direct traceability matter far more than just quoting numbers from paper.
The surge in demand for specialized halogenated building blocks over the last decade didn’t happen in isolation. Most new agrochemical and pharma registrations require materials with a tighter impurity and origin profile, often tied to regional manufacturing codes. Cheaper, off-spec product from distributors or brokers bank on the end user making up the difference in the lab or plant. Our position from the manufacturing floor to the loading dock gives us full control over what leaves—every drum has genuine traceability back to the reactor, not just paperwork.
Supply chain disruptions can’t be predicted. We maintain contingency reserves of key raw materials, drawn from longstanding relationships with upstream producers sharing our standards for purity and reliability. Many customers have faced recall waves due to a single contaminated batch—these stories pushed us to refuse reselling repacked goods or untested lots. Maintaining a direct pipeline from synthesis line to loading dock has preserved delivery reliability for end users scaling new processes.
Custom adaptation forms a key part of why our 1-Bromo-2-(Trifluoromethyl)-3,3,3-Trifluoroprop-1-Ene earns repeat requests. Some partners approach us to supply milligram lots to support SAR studies, working with our chemists to map impurity profiles as reactivity changes. Other projects call for extra-tight impurity restrictions—sometimes as low as the low ppm range—to fit a specific specification for electronics or active ingredient production.
Drawing from dozens of development cycles, I’ve seen our R&D chemists rapidly modify crystallization or distillation steps to address customer feedback. Direct access to experienced staff saves external partners weeks (sometimes months) in troubleshooting: real-time solubility screening, stability assay adjustments, and impurity tracking get done alongside customer project managers. Time after time, collaboration at this level shortens scale-up steps and slashes wasted effort downstream.
We also cooperate directly on regulatory reviews, sharing all relevant production document sets to simplify new drug/chemical submissions under increasingly complex guidelines worldwide. The value stems not from bulk output alone but from a shared investment in reliability and scientific trust.
No chemical manufacturer can ignore the climate and environmental scrutiny now demanded by regulatory bodies, customers, and local communities. Our plant invested early in closed solvent recovery, on-site waste reduction, and air handling systems because halogenated emissions cannot just be “managed”—they must be controlled stringently. Routine audits and surprise inspections keep us honest, as do operator logs and third-party verifications of all treatment systems.
Every process update affecting 1-Bromo-2-(Trifluoromethyl)-3,3,3-Trifluoroprop-1-Ene runs through risk and footprint analysis, balancing innovation with plant safety and neighborhood impact. This includes feedstock sourcing: we connect with suppliers focused on minimizing fluorination by-products and disposing of spent reagents above minimum compliance. In many cases, changing a single solvent or pressure step cut hazardous waste volumes by half, confirming that day-to-day adjustments directly improve long-term sustainability.
Customers increasingly audit us not only for COA values but for waste logs and emission reduction performance. Our teams conduct regular in-house reviews ensuring that best practice isn’t just a buzzword—it’s a reality supported by every production run and shipment. This commitment reaches every aspect: from cooling water recycling to energy accounting, process Chemists and plant managers discuss sustainability in the same breath as yield or cycle time.
Being the actual source and not just a name on a bottle changes every aspect of how we approach this product. Years of real-world experience in synthesis, purification, and process troubleshooting give us a deep, practical perspective that can’t be matched by intermediaries. If there’s an issue or a goal requiring a change—tighter spec, slightly adjusted isomer ratio, or custom containers—we handle it immediately, without layers of approval or communication breakdowns.
Supplying directly to active R&D teams and production chemists means feedback loops back into process optimization for every batch, not just end-of-year summaries. Many fine details—solvent swaps to solve storage stability, or adjustments to moisture testing—come from conversations with actual users, not boardroom plans.
The past couple of years brought spikes in halogenated intermediate demand and forced us to rethink old batch scales and QA standards. Our flexibility comes from having full control of the synthesis process—so tweaks to instrumentation, reaction conditions, and packaging get implemented promptly, eliminating months of waiting and cutting back on troubleshooting cycles.
The evolution of 1-Bromo-2-(Trifluoromethyl)-3,3,3-Trifluoroprop-1-Ene reflects changing needs in pharma, agrochemicals, electronics, and advanced polymers. Ten years ago, demand centered mostly on custom syntheses from project labs. Today, multi-ton lots move through our shipping docks—to destinations where new regulations, property claims, and application challenges set the pace. The lessons learned from expanding production and tackling global disruptions shape every process tweak, from upstream sourcing to the way we check container linings.
As new requests emerge—sometimes for tighter isomeric profiles, sometimes for expanded impurity documentation, or for specialty stabilization packages—our approach stays rooted in technical expertise and customer feedback, not marketing gloss. We incorporate the latest analytics and safety improvements, because no claim means much without real process data and honest, rapid troubleshooting if an issue pops up.
Each kilogram of this compound represents a blend of chemistry, logistics, and a focus on partnership. Our team stays committed to pushing standards upward, making each batch and every delivery a reflection of real-world experience, direct responsibility, and a sharp awareness of both global and local impacts. Through close work with customers, transparent communication, and a hands-on approach at every stage, we put reliability and quality at the core of every lot that leaves our plant.