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HS Code |
897723 |
| Product Name | 2-Bromo-5-nitro-3-(trifluoromethyl)pyridine |
| Cas Number | 877399-50-3 |
| Molecular Formula | C6H2BrF3N2O2 |
| Molecular Weight | 288.99 |
| Appearance | Yellow to orange solid |
| Melting Point | 63-67°C |
| Purity | ≥98% |
| Solubility | Slightly soluble in organic solvents (e.g., DMSO, DMF) |
| Density | 1.85 g/cm³ (estimated) |
| Smiles | C1=CC(=C(N=C1C(F)(F)F)Br)[N+](=O)[O-] |
| Inchi | InChI=1S/C6H2BrF3N2O2/c7-5-3(6(8,9)10)4(12(13)14)1-2-11-5/h1-2H |
| Storage Conditions | Store at 2-8°C, dry and protected from light |
| Synonyms | 2-Bromo-5-nitro-3-(trifluoromethyl)pyridine |
As an accredited 2-Bromo-5-nitro-3-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass vial containing 5 grams of 2-Bromo-5-nitro-3-(trifluoromethyl)pyridine, with a tamper-evident screw cap and chemical label. |
| Container Loading (20′ FCL) | 20′ FCL: Typically loaded with 12–14 MT of 2-Bromo-5-nitro-3-(trifluoromethyl)pyridine, packed in 25 kg fiber drums. |
| Shipping | **Shipping Description:** 2-Bromo-5-nitro-3-(trifluoromethyl)pyridine should be shipped in securely sealed containers, protected from moisture and light. It must be labeled as a hazardous chemical, and handled according to relevant regulations, preferably under temperature-controlled conditions. Appropriate documentation, including safety data sheets (SDS), should accompany the shipment for safe transport and regulatory compliance. |
| Storage | **2-Bromo-5-nitro-3-(trifluoromethyl)pyridine** should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and incompatible materials such as strong bases and oxidizers. Protect from moisture and direct sunlight. Ensure proper labeling, and follow all relevant safety regulations for the storage of hazardous chemicals. |
| Shelf Life | Shelf life of 2-Bromo-5-nitro-3-(trifluoromethyl)pyridine: Stable for at least 2 years if stored sealed, cool, and dry. |
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Purity 98%: 2-Bromo-5-nitro-3-(trifluoromethyl)pyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction efficiency and minimal impurity incorporation. Melting Point 71-74°C: 2-Bromo-5-nitro-3-(trifluoromethyl)pyridine with a melting point of 71-74°C is used in organic electronics manufacturing, where controlled solid-state properties enable reliable thin film formation. Molecular Weight 272.97 g/mol: 2-Bromo-5-nitro-3-(trifluoromethyl)pyridine of 272.97 g/mol is used in medicinal chemistry research, where precise molecular targeting enhances compound screening accuracy. Solubility in Acetonitrile: 2-Bromo-5-nitro-3-(trifluoromethyl)pyridine with high solubility in acetonitrile is used in chromatographic separation processes, where it promotes rapid sample dissolution and efficient analyte detection. Stability Temperature up to 40°C: 2-Bromo-5-nitro-3-(trifluoromethyl)pyridine stable up to 40°C is used in agrochemical formulations, where it maintains compound integrity during storage and handling. |
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Our experience as a chemical manufacturer has taught us that some molecules quietly drive innovation. 2-Bromo-5-nitro-3-(trifluoromethyl)pyridine, more often known in lab conversations as a pyridine derivative with both halogen and fluorinated functional groups, is one of those behind-the-scenes players that support key steps across pharmaceuticals and specialty materials. On a technical level, this product showcases a blend of reactivity and selectivity, which has opened possibilities in synthetic routes not just inside our production lines, but also inside the facilities of our long-term partners.
The manufacturing of this compound requires more than textbook chemistry. Our technicians handle several controlled addition and temperature-sensitive stages. Each batch calls for consistency—especially since traces of unwanted isomers can complicate downstream modifications. In our reactors, the bromination and nitration steps come under careful observation, buffered to limit side reactions, followed by coupling with a trifluoromethyl reagent. Every operator in our facility recognizes that careful control keeps impurities low and color within expected limits. Gone unchecked, even slight trace impurities can shift a compound's behavior in later stages, hampering catalysis or requiring repeat purification work with expensive solvents.
The presence of the trifluoromethyl group and bromine atom on a pyridine ring means synthetic chemists access building blocks offering both electronic tuning and productive cross-coupling points. From our line operator’s perspective, this is more than just academic. Customers in pharmaceutical research often pursue small-molecule drug candidates with rigorous selectivity or metabolic stability requirements. The electron-withdrawing nature of the trifluoromethyl and nitro groups, paired with the activation achieved through bromine at the 2-position, shapes reactivity not just in theory, but in real-world process scalability.
We see firsthand the real effects of these substituents during pre-shipment analysis. No two production cycles unfold identically, so monitoring the product’s melting point, NMR spectra, and impurity profile ensures that outgoing shipments meet downstream performance targets. Sometimes, visible differences—slight changes in hue, dustiness, or stickiness—help us catch anomalies before QC screening. Direct operator observations remain valuable in identifying problems not immediately caught by automated systems.
We pack 2-Bromo-5-nitro-3-(trifluoromethyl)pyridine inside sealed HDPE containers lined for moisture protection, stowing them in well-ventilated, temperature-controlled rooms. Our workers know humidity or accidental sunlight can sometimes alter the apparent flow properties, causing caking or—very rarely—trace decomposition. Frequent warehouse checks, together with environmental monitoring, form a part of our regular routine. From our own warehouse crew, clear feedback loops help us adapt packaging through the seasons. In humid months, we double-check silica gel packets within each drum to keep uptake below critical thresholds.
Some newer entrants to the industry see packaging as an afterthought; our experience teaches caution. Flexibility in packaging size, based on client needs, can support smaller scale trials or bulk integration. Shipping long distances, particularly during seasonal temperature swings, can provoke unseen changes in crystalline structure that only regular QC at both sending and receiving ends can catch. Old hands in our shipping department still remember specific shipments where temperature loggers exposed minor excursions that, in turn, let us adjust container insulation for the next cycle.
Chemists like to say that every small tweak to a molecule’s functional groups can influence reactivity, but in practice, the differences between derivatives become pronounced only in application. We’ve produced both halogenated and fluorinated heterocycles without nitro groups, and the difference has shown up most clearly in cross-coupling and nucleophilic substitution steps. For example, the coexistence of a nitro and trifluoromethyl substituent raises the acidity of neighboring ring hydrogens and pushes certain coupling reactions toward preferable sites with reduced side formation. Explicitly, this allows medicinal chemists to dial in for structure-activity studies without relying on excess equivalents or elaborate protection/deprotection routines.
Other analogs, such as 2-bromo-3-trifluoromethylpyridine without nitro substitution, often underperform in late-stage functionalization. The nitro group’s strong electron-withdrawing effect assists downstream transformations—an impact often verified in our collaboration with process scientists. Many of our clients, after lengthy method development, see distinctive improvements in yield and purification ease, thanks to fewer polar byproducts generated under high-temperature conditions.
Our product largely heads into pharmaceutical research pipelines, but feedback from specialty agrochemical development groups continues to grow. For those working at the bench, this molecule serves as a robust cross-coupling partner—Suzuki and Buchwald-Hartwig couplings, for instance—where the bromine atom opens the door to further diversification. Over the last year, more process chemists share results demonstrating that the presence of the trifluoromethyl group delivers improved pharmacokinetic results for certain target molecules, while maintaining chemical stability through multi-step processes.
Occasionally we see orders directed solely for analytical reference, but the majority contribute to complex molecule assembly. We committed to supplying highly characterized lots, with detailed spectral and chromatographic data, knowing that even small deviations can derail long synthetic campaigns. Internal communication with client labs on best handling practices has reduced inadvertent batch losses and helped optimize their own purification strategies.
Scaling up from gram quantities to multi-kilogram output invites challenges that lab chemistry rarely addresses. Direct experience with solvent choice, base concentration, and phase separation underscores the practical difference between literature recipes and plant operation. Centrifuge fouling, reactor fouling, and filter cake behavior all play out in the course of a routine week on our shop floor. Our engineers have adapted reactor geometry and tailored agitation speeds to avoid local overheating, which can spike the rate of undesired dimer or tar production. Each plant modification over time draws directly from observed troubleshooting rather than from theorized improvements.
The reality of batch-to-batch variation emerges not just in yield but in how the product looks, flows, and even clumps. Changes in supplier APIs or microdifferences in raw material lots sometimes alter crystallization. The most experienced operators become keen at detecting subtle changes in product texture or drying behavior, reporting them for further lab QC checks—a critical contribution that can outpace lab instruments for speed and early detection.
Our customers often emphasize purity, but from our vantage, purity is not just about reaching a threshold. It’s about removing specific byproducts that threaten subsequent chemistry or complicate product registration. Analytical chemists in our team track specific potential contaminants—such as residual starting material or side-reaction isomers—using HPLC and GC-MS. Especially with this compound’s trifluoromethyl group, trace non-volatile residues could carry forward into high-throughput screening, impacting assay reliability. This real-world sensitivity drives our invested attention to both terminal assay and impurity profiling.
After trialing several purification and recrystallization methods, we settled on a protocol that balances efficiency with minimal thermal degradation. One memorable stretch during the summer heatwave drove us to reduce drying temperatures by nearly fifteen degrees, based on direct observation of product browning. Adjustments based on seasonal humidity have made our process more robust, delivering cleaner, easier-to-handle shipments to both domestic and international partners.
Every employee who handles 2-Bromo-5-nitro-3-(trifluoromethyl)pyridine comes to respect its properties through direct experience. Even though this molecule does not present extraordinary hazards, strict adherence to PPE and fume extraction remains standard. During loading or sampling, even a brief lapse can lead to discomfort or minor skin irritation—lessons reinforced through real-life 'near miss' events and regular safety briefings. Over years of continuous manufacture, periodic updates to local safety protocols, supported by outside audits, have led to better ventilation, improved spill control, and tighter storage records.
Shipping documentation and international labeling schemes demand detailed product data, translated across multiple languages. Our office staff can recite the ins-and-outs of evolving transport and hazard communication requirements from memory. One mislabelled shipment for export can bring costly delays—a lesson learned from prior years—with corresponding tweaks to our labeling and batch-release workflow.
Clients regularly ask about further modifications or derivatives. From our ongoing experience running kilo-scale batches, we recognize both growing demand and evolving applications. More process developers want direct trifluoromethylated frameworks that enable fewer synthetic steps and simpler purification regimes. In response, our R&D leads continue to probe selectivity and process efficiency metrics, focusing on routes that trim waste and deliver more predictable results. In-house experiments with alternative bromination and nitration agents have produced both wins and failures—each trial, success or setback, shapes the next iteration.
Increasingly, our partners care about the sustainability of raw materials. Pressure to move away from legacy chlorinated solvents and adopt green chemistry benchmarks continues to rise. Inside our production meeting rooms, debates over cost and eco-toxicity aren’t theoretical—they tie directly to our batch costs and the regulatory outlook of our largest customers. Some routes offer greener credentials but introduce process headaches; we draw on accumulated expertise to identify changes that meet both operational and environmental objectives, with input from every department, from QC to shipping.
Years of on-the-ground manufacturing brings a kind of learning that surpasses what most literature reviews can offer. Quality assurance, built on actual run data and corrections overtime, provides us with insights most apparent during troubleshooting or scale-up. We learned early on that fresh feedstocks—especially sensitive reagents for trifluoromethylation—must arrive quickly, cold, and with high purity. Delays and temperature abuse during transit directly impair both reaction rates and selectivity. Through trial and error, we built relationships with logistics partners who accommodate our refrigerated needs, keeping cycles smooth even through local weather challenges.
Our maintenance team adopts a forward-thinking approach to equipment calibration, checking not just for gross instrument deviations but for gradual shifts that could nudge reaction yields below contractual requirements. Analog batch logs and digital process records, reviewed at both daily shift changes and month-end meetings, reveal patterns and bottlenecks otherwise missed. Hospital-grade hygiene and zone separation in our filling rooms remains non-negotiable, with all staff involved in both upkeep and improvement. Unexpected inspection findings from years past prompted recalibration of our contamination controls; clean air handling remains part of our daily task roster.
Our technical service engineers stay in close touch with buyers, many of whom share details about new methodologies, unexpected difficulties, or even routine shipment feedback. Frequent conversations steer our in-plant improvements, whether in refining minimum drum sizes for bespoke R&D needs or adjusting internal documentation formats. On several occasions, clients provided real-time results from coupling or oxidation experiments, prompting us to examine whether micro-level manufacturing factors could be optimized.
Staff at our site invest equally in both documentation and hands-on support, offering real examples of troubleshooting oddities or adjustments made during process upsets. The entire workflow, from initiating a batch to packing and organizing shipment, benefits from everyone’s practical awareness. Employees at all levels—operators, lab analysts, and shipping clerks—view their part not in isolation but as a link in an ongoing partnership.
Knowledge transfer between shifts and across generations of operators gives us an edge. Monthly meetings set aside time for peer-to-peer discussion, with skilled veterans reminding newer team members of common trouble signs—a must, especially when scaling up. Lessons from past incidents, such as temperature overshoots or irregular flow rates during transfer, become woven into our standard operating practices. By encouraging staff to propose process tweaks, we foster continuous improvement rooted in real data.
Cross-training has enabled key staff to detect early signs of drift in product appearance or filtration timing—changes that could otherwise ripple down into client formulation processes. Operators empowered with shared responsibility find motivation in tracking not only yields but also client feedback on ease of handling or suitability for novel applications.
Every drum of 2-Bromo-5-nitro-3-(trifluoromethyl)pyridine that leaves our plant stands for more than the aggregated steps of a chemical synthesis. It reflects our ongoing work to support ever-evolving needs in the life science and specialty sectors, shaped as much by practical experience and detailed communication as by technical expertise. We maintain a far-reaching view, investing in both continuous product improvement and the daily, ground-level vigilance that keeps our standards high and our customer relations strong.