|
HS Code |
103323 |
| Chemical Name | 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine |
| Molecular Formula | C6H2BrF4N |
| Molecular Weight | 243.99 g/mol |
| Cas Number | 881674-58-0 |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically ≥ 97% |
| Density | Approx. 1.7 g/cm³ |
| Smiles | C1=CN=C(C(=C1Br)C(F)(F)F)F |
| Inchi | InChI=1S/C6H2BrF4N/c7-4-2-12-6(8)3(1-4)5(9,10)11 |
| Solubility | Soluble in organic solvents (e.g., DCM, THF) |
As an accredited 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled “3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine, 5g.” Includes hazard symbols, batch number, and supplier details. |
| Container Loading (20′ FCL) | 20′ FCL container loaded with securely sealed drums of 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine, compliant with chemical safety regulations. |
| Shipping | 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine is shipped in tightly sealed, chemical-resistant containers, typically under ambient temperature conditions. Proper labeling, including hazard identification, accompanies the package. Transportation must comply with local regulations for hazardous materials, ensuring protection from moisture, heat, and physical damage to preserve chemical stability and safety during transit. |
| Storage | **Storage for 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine:** Store in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances like strong oxidizers and acids. Protect from moisture, heat, and direct sunlight. Recommended storage temperature is 2-8°C (refrigerator). Use suitable chemical-resistant containers and clearly label them. Handle under inert atmosphere if sensitive to air or moisture. |
| Shelf Life | 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine typically has a shelf life of 2 years when stored cool, dry, and sealed. |
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Purity 98%: 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield target compound formation. Melting Point 45–47°C: 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine with a melting point of 45–47°C is used in fine chemical production, where it enables controlled solid-phase reactions. Molecular Weight 260.97 g/mol: 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine at molecular weight 260.97 g/mol is used in agrochemical research, where it allows accurate analytical dosing. Stability Temperature up to 80°C: 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine stable up to 80°C is used in catalytic reaction processes, where it maintains structural integrity under reaction conditions. Particle Size <100 microns: 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine with particle size less than 100 microns is used in automated manufacturing systems, where it improves dispersion and consistent mixing. Water Content ≤0.5%: 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine with water content ≤0.5% is used in moisture-sensitive organic synthesis, where it reduces side reaction risk and increases product purity. Residual Solvent <200 ppm: 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine with residual solvent level below 200 ppm is used in regulated chemical manufacturing, where it meets stringent quality compliance for end-use. Color Pale Yellow: 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine with a pale yellow color is used in dye intermediate fabrication, where it facilitates color consistency in final products. |
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Years in the pyridine derivatives sector offer a unique vantage point for understanding the demands around 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine. In our line, attention to every variable in the synthesis process becomes routine, not just expectation. Achieving a consistent batch rests on deep familiarity with the reactivity of heterocyclic aromatics and the robust tendencies of bromine and fluorine substitution. Many in-house chemists have spent late nights observing the nuances of halogen exchange, crystallization rates, and stability in different storage conditions.
Our model for this compound has evolved, not through rote optimization, but by dealing directly with pragmatic hurdles from scale-up—pressure fluctuations in the vessel, incomplete substitution, or handling of volatile intermediates. Every kilogram has shown us something new about controlling temperature profiles, tailoring purification steps, and protecting staff. Analytical chemists have verified each lot on finely calibrated NMR and GC-MS equipment, catching minor byproducts the untrained eye might miss. Learning the exact fingerprint of a clean 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine sample takes more than a spec sheet—it's a matter of deep hands-on repetition.
The core of this pyridine ring—substituted with a bromine, fluorine, and a trifluoromethyl group—delivers reactivity combinations not found in standard halopyridines. In our shop, the significance appears in every order and research inquiry: some colleagues need the bromine site left untouched for Suzuki couplings, others ask for tips on using the trifluoromethyl position in medicinal lead development. The bromo and fluoro groups lie in positions that encourage selective transformations, especially for chemists aiming to elaborate more complex scaffolds.
We're often asked how this compound stands in relation to simpler analogs such as 4-bromopyridine or 2-fluoropyridine. The added electron-withdrawing power of the trifluoromethyl group, placed at the 4-position, reshapes both reactivity and solubility. While standard halogenated pyridines see wide use in material science or as basic intermediates, medicinal chemists gravitate toward 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine for new investigational drug targets, thanks to the extra fluorination’s impact on metabolic stability and binding specificity.
A typical bromofluoropyridine may seem similar on a casual glance, but substituent effects can either hinder or open up routes for next-step reactions. One memorable customer learned the difference while switching to our material: a reaction that barely yielded product with plain 3-bromopyridine achieved robust conversion with the trifluoromethyl compound. Minutes after confirmation by TLC, they called back in pure delight. That experiment cemented how transformative seemingly small changes in substitution really are.
From our earliest lots, research groups worldwide have shared success stories involving 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine. The pharmaceutical sector often drives demand, with teams exploring new kinase inhibitors or optimizing pharmacokinetic profiles in preclinical candidates. In these environments, small differences in building block purity and impurity profile quickly impact performance downstream. A few years ago, we heard about a major synthesis that stalled due to a trace impurity from an alternative source—a story that prompted us to revisit our purification sequence and reinforce our ongoing dialogue with process teams. Honest discussion with buyers about their real-world problems has provided more insight than any textbook.
Chemical research rarely runs a straight line. We have seen how delays in securing tightly specified pyridine intermediates can bottleneck entire projects. A customer working in contract synthesis shared that, after introducing our 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine, the reactivity window shifted, yielding a more manageable process with less stalling over side-products. Hearing these reports helps us refine upstream processes, anticipate upcoming needs, and spot consistent pain points—sometimes as subtle as trace metal contaminants, other times as concrete as improving lot traceability.
Owning the entire manufacturing chain offers opportunities—and responsibilities—unavailable to intermediaries or traders. At kilogram scales, reactions that once looked straightforward on paper develop personalities: agitation speed may influence local concentrations, temperature gradients form, and exotherms behave differently. We learned years ago that each batch of 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine must be watched and steered with more than just instrumentation. Field teams report back to technical experts, and sometimes, it takes face-to-face troubleshooting on the shop floor to understand an anomaly.
We have always chosen equipment with containment and environmental safety as primary criteria. Some byproducts of halogenated pyridines demand care in capture and disposal; we had to overhaul vent scrubbing systems twice after identifying subtle leaks. Conversations with downstream users also sharpened our focus on packaging—for example, the compound reacts unfavorably to certain plastics, spurring us to switch to high-grade fluoropolymer or amber glass for storage and shipping.
Internal teams receive thorough, regular training amid tight procedural controls—practical approaches that do not show up on a spec sheet. The aim is to send out every drum and bottle without surprises or unknowns. Over years of operation, mistakes served as the best training: managing a situation with off-spec product or halting a run after seeing worrying pressure readings drove home the need for vigilance and respect for the chemistry itself. That same vigilance supports customers, since it is easier to spot genuine material based on its behavior—smell, color, reaction response—when you have been there from start to finish.
We also help bridge the knowledge gap for end users who may not routinely handle complex halogenated pyridines. Technical support extends to in-depth analysis, not only authentication by NMR, IR, and LC-MS, but a consultative approach—translating analytical fingerprints into practical feedback. The utility of 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine often depends on its ability to open up new synthetic spaces; end users sometimes need more than just a bottle and a certificate of analysis. We've hosted lab visits where researchers walk the floor to see quality control first-hand, or hold troubleshooting calls to decipher why a familiar reaction stuttered in a scale-up.
Both industrial and academic clients appreciate more than just purity; insight on storage or minor degradation paths can be just as critical. The compound's volatility and sensitivity call for tight control from the moment it leaves the reactor. Some researchers work in remote settings where solvent choices or required ancillary reagents shift based on local regulations—sharing our lessons about compatible solvents, filtration aids, or pH adjustments ensures the compound delivers its intended results no matter the setting.
Over the years, the pressure to improve environmental outcomes has sharpened our own approach. Handling halogenated intermediates responsibly requires more than checking boxes. Real safety comes in the details: managing effluent, capturing halide residues, and monitoring worker exposure. We have committed to minimizing energy use and switched to less hazardous cleaning solvents where possible. In multiple plant upgrades, investments in improved fume extraction and better PPE for staff came before expansion or maximizing production. Risk mitigation isn't theoretical—it keeps teams healthy and the business sustainable.
The commitment to transparency with environmental disclosures has deepened as well. We release actual emissions figures publicly and welcome audits from partners—too many communities have been burned by companies hiding behind vague assurances. Our experience demonstrates that clarity and accountability bring better long-term partnerships, especially as more customers prioritize ethical sourcing. It is not simply a response to regulation, but a matter of earning trust batch after batch.
The dialog between manufacturer and end user remains a major catalyst for product innovation. Requests for gram samples of 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine often grow into multi-kilo campaigns. Sometimes, this resulted in new demand for alternative pack sizes or the introduction of paperwork supporting compliance in restricted markets. Our regulatory team collaborates with legal and logistics departments to anticipate these shifts, like registering molecules for customs in new territories or prepping dossiers for pharmaceutical pre-approval inspections.
Creative solutions to logistical challenges flow from experience. At one point, high humidity in remote storage locations compromised certain shipments. Standard desiccants weren’t cutting it, so packing was redesigned to prevent any ingress. Other times, customers wanted express shipments for time-sensitive research; new relationships with specialist carriers meant faster delivery with preserved quality.
Seasoned production staff always look ahead to prepare for fluctuations in demand or regulatory scrutiny. We run pilot trials for alternative synthetic routes—sometimes driven by supply constraints on starting materials, other times for cost reduction. Results can be uneven, and what works in the flask may need rework at plant scale. But the willingness to repeat, refine, and learn from each turnaround ensures improvement. Even incremental changes often ripple downstream, whether in improved batch consistency, better yield, or ultimately fewer headaches for users.
The reality of chemical supply today calls for rapid adaptation to shifting regulations, freight logistics, and raw material availability. This has become especially apparent as international standards tighten, forcing stricter documentation and audit-readiness. Staff respond to requests for full batch traceability and impurity profiles from multinational buyers, and occasionally work with customs officials to explain legitimate use cases in drug discovery or materials research.
Trade disruptions and interrupted logistics chains can lead to supply gaps, especially for niche products like 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine. We have worked to maintain buffer stocks of critical reagents, and reinforced direct lines of communication with all suppliers. Diversification avoided bottlenecks more than once. On more than one occasion, a regular supplier’s force majeure nearly froze production, but contingency stocks and backup vendors helped us keep our promises.
Handling halopyridines on the manufacturing side ingrains habits and instincts that cannot be replicated in a trading company or distribution warehouse. Staff memorize subtle differences in aroma, texture, and even the way product behaves during dissolution, all of which point to underlying purity and profile. That hands-on, daily involvement with actual materials differentiates us; quality assurance takes root in the factory, not on a commodity spreadsheet.
As manufacturers, each order serves as both obligation and feedback. If a run performs beyond expectations, customers let us know. If a customer reports an issue, technical staff retraces each step of the batch, scouring logs for anomalies, and updating procedures if a process improvement emerges. Learning is continuous, not episodic. The ability to directly adapt and improve process controls keeps the entire team keyed into both chemistries and people behind the molecules.
End users feel that commitment, whether embedded in the reliability of the product or in the responsiveness of support. Everything is traceable back to first-hand practice: knowing which cleaning agents won’t interact with residue, forecasting shelf life in varied climates because you tested it deliberately, or reminding research teams to check for solvates in every fresh shipment.
Chemical manufacturing never stands still. As demand for advanced pyridine building blocks like 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine intensifies—especially for use in high-precision pharmaceuticals and next-generation materials—the onus to innovate grows, too. Old production lines see new software upgrades, reactor fleets expand, and analytical capacity widens. By working closely with both the research and business sides of the industry, the manufacturer remains ahead of shifting needs—not simply by scaling up, but by eliminating friction points for end users.
Current waves in the market tilt toward efficiency and green chemistry principles. We have begun re-examining traditional solvent systems and exploring new catalytic routes. Early trials indicate the promise of lower-waste regimes, improved atom economy, and smarter resource utilization. The motivation goes beyond regulatory obligation—it is a matter of pride in the profession, and a reflection of how real-world manufacturing must advance to meet the pace of scientific discovery.
Feedback from colleagues in laboratories around the globe shapes continued refinement. As more researchers share ideas, send reaction snapshots, and push the limits on what this molecule can do, the manufacturer’s experience loop becomes richer. Direct collaboration breeds more dynamic improvement—process tweaks, better documentation, and more tailored troubleshooting in response to new synthetic challenges.
Reflecting on years managing 3-Bromo-2-fluoro-4-(trifluoromethyl)pyridine—a niche molecule that draws out specialized skill—reinforces the unique role dedicated manufacturing plays. Rather than settling for standard supply-chain practices, we focus on the human element, layer technical insight with hard-earned lessons, and treat every challenge as a learning moment. Whether for the seasoned process chemist or the early-career researcher, the discipline, pride, and expertise poured into every batch show through, from first drum to latest innovation.