|
HS Code |
892296 |
| Chemical Name | 2-bromo-3-(trifluoromethyl)pyridine |
| Molecular Formula | C6H3BrF3N |
| Molecular Weight | 226.99 g/mol |
| Cas Number | 43177-19-1 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 206-208 °C |
| Density | 1.70 g/cm3 |
| Smiles | C1=CC(=C(N=C1)Br)C(F)(F)F |
| Inchi | InChI=1S/C6H3BrF3N/c7-5-4(6(8,9)10)2-1-3-11-5/h1-3H |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Refractive Index | 1.498 |
As an accredited 2-bromo-3-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-bromo-3-(trifluoromethyl)pyridine, sealed with a red screw cap, labeled for laboratory use. |
| Container Loading (20′ FCL) | 20′ FCL can carry about 12,000–14,000 kg of 2-bromo-3-(trifluoromethyl)pyridine, packed in drums or IBCs. |
| Shipping | 2-Bromo-3-(trifluoromethyl)pyridine is shipped in tightly sealed containers, protected from light and moisture. Transport complies with all relevant hazardous material regulations, ensuring safety and labeling accuracy. Typically shipped by air or ground with appropriate documentation, it is handled as a hazardous, corrosive organic compound in accordance with international chemical transport standards. |
| Storage | Store 2-bromo-3-(trifluoromethyl)pyridine in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition, strong acids, bases, and oxidizing agents. Avoid direct sunlight and moisture. Ensure proper labeling and secondary containment, using compatible chemical storage cabinets if possible. Handle under inert atmosphere if required, and follow all relevant safety protocols. |
| Shelf Life | **Shelf Life:** 2-Bromo-3-(trifluoromethyl)pyridine is stable for at least 2 years when stored tightly sealed, cool, dry, and away from light. |
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Purity 99%: 2-bromo-3-(trifluoromethyl)pyridine with purity 99% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures enhanced yield and reduced byproduct formation. Melting point 50°C: 2-bromo-3-(trifluoromethyl)pyridine with a melting point of 50°C is used in organic electronics development, where precise phase control supports consistent material deposition. Molecular weight 226.98 g/mol: 2-bromo-3-(trifluoromethyl)pyridine with molecular weight 226.98 g/mol is used in heterocyclic compound manufacturing, where accurate mass balance improves formulation reliability. Particle size ≤10 µm: 2-bromo-3-(trifluoromethyl)pyridine with particle size ≤10 µm is used in catalyst preparation, where fine dispersion enhances catalytic surface area. Stability at 25°C: 2-bromo-3-(trifluoromethyl)pyridine with stability at 25°C is used in laboratory reagent storage, where long-term shelf life maintains reagent effectiveness. Water content ≤0.2%: 2-bromo-3-(trifluoromethyl)pyridine with water content ≤0.2% is used in moisture-sensitive reactions, where minimal water content prevents hydrolysis and degradation. Residual solvents <500 ppm: 2-bromo-3-(trifluoromethyl)pyridine with residual solvents less than 500 ppm is used in agrochemical intermediate fabrication, where low solvent residue meets regulatory safety standards. Appearance (white crystalline solid): 2-bromo-3-(trifluoromethyl)pyridine with appearance as a white crystalline solid is used in high-throughput screening libraries, where solid-state purity aids in automated handling and dosing. Boiling point 220°C: 2-bromo-3-(trifluoromethyl)pyridine with a boiling point of 220°C is used in process development, where thermal stability allows for robust reaction conditions. |
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Production of specialty chemicals such as 2-bromo-3-(trifluoromethyl)pyridine requires commitment, precision, and a steady investment in technology and quality systems. This compound, best known by the molecular formula C6H3BrF3N, appears as a pale to light yellow solid or liquid, depending on its storage temperature and batch age. Its molecular weight rides around 241.99 g/mol. In daily work, our team recognizes this compound by its distinctive – though not overpowering – chemical odor, and its well-defined crystalline appearance fresh from synthesis.
The value of 2-bromo-3-(trifluoromethyl)pyridine shows up in multiple research, development, and industrial processes. Our manufacturing teams routinely see demand from agrochemical, pharmaceutical, and advanced material innovators. Over the years, we've noticed that development chemists gravitate toward this compound when they pursue efficient syntheses of target molecules that require both a pyridine core and functional sites capable of supporting substitution or coupling. The trifluoromethyl group, directly attached to the pyridine ring, sets it apart from simpler halopyridines. What results is not only higher chemical reactivity at the 2-position, but also substantial changes in electronic properties — factors that chemists leverage to improve yield or introduce selectivity in downstream processes.
The bromo substituent does more than serve as a reactive handle. With expert handling, it supports Suzuki, Sonogashira, and Buchwald-Hartwig couplings, bridging easily from lab-scale reactions into pilot and production runs. Feedback from process development colleagues shows its crystalline form handles well under dry conditions and can be weighed or transferred with minimal dust or loss — a feature that often gets overlooked during laboratory project scoping, yet pays real dividends once processes scale up. Years of experience have taught our operators that consistency in particle size, color, and purity ensures fewer surprises for analytical quality control, and fewer headaches for our clients.
We design our processes for 2-bromo-3-(trifluoromethyl)pyridine around efficiency and reproducibility. This product arrives from our reactors at minimum purity of 98 percent by HPLC and NMR — a standard that supports most R&D and industry requirements without need for custom purification. The remaining two percent consists mainly of related synthetic impurities or trace solvents, both of which we work to control below recognized thresholds, since even low-level contaminants can derail certain downstream reactions. Specialist users regularly request expanded certification, ranging from trace metal analysis to GC-MS, as their applications move toward regulated environments.
Practical details matter a great deal during storage and use. Our staff avoids repeated freeze-thaw cycles and prolonged exposure to air or moisture, which tend to degrade shelf life and cloud appearance. We standardize internal batch testing so that what arrives at your loading dock matches the stated physical parameters — color, melting range, and solution clarity. We pack the product under inert gas when requested, and favor HDPE or glass containers sealed with moisture barriers to protect the chemical structure. Even slight variations in physical quality can prompt R&D teams to question data reliability, so we eliminate batch variations wherever possible.
Through years of operation, we’ve accumulated practical insights into what makes or breaks a high-purity halopyridine product. Stability, precision of analysis, and process reliability carry more weight than catalog promises or headline purity. New users often ask what distinguishes our offering from generic or poorly-documented batches on the market. The answer owes a lot to the trust and transparency we bring to collaborations with R&D and production teams worldwide.
Chemical structure underpins utility. The combined influence of trifluoromethyl and bromo groups at defined positions supports site-selective transformations. This cannot be achieved by simple mixtures of monofunctional pyridines; it depends on controlling both regioselectivity in synthesis and purity in the finished product. In our runs, we have refined multi-step processes to drive conversions to completion — reducing unwanted isomers and minimizing the risk of introducing byproducts that could complicate regulatory filings.
Safety and health standards guide every step from pilot plant to bulk shipment. Unlike more volatile or malodorous pyridine derivatives, 2-bromo-3-(trifluoromethyl)pyridine rarely triggers acute health complaints under standard laboratory handling, provided usual containment and ventilation measures remain in place. Our shift supervisors monitor exposure by periodic air sampling and scrupulous adherence to chemical hygiene methods. We avoid false assurances, and publish batch-exact testing data so users understand what’s present in every package shipped from our facility.
Most users reach for this product at transition points in a synthetic sequence — especially when scaffold diversification or route flexibility matters. It appears regularly as a precursor in heterocyclic chemistry, helping to construct next-generation pharmaceuticals and crop protection molecules. The bromo substituent, especially when combined with the electron-withdrawing effect of trifluoromethyl, promotes reliable cross-coupling even at low catalyst loadings. These properties lower risk of failed reactions and unpredictable scale-ups.
Pharmaceutical chemists on our customer advisory panel have clarified that the compound’s CF3 group can enhance metabolic stability and membrane permeability in analogues — a fact that gets repeated in scientific publications. Several discovery chemists have confirmed that the presence of both bromo and trifluoromethyl in a single pyridine offers a shortcut to motifs otherwise accessible only through much longer, less predictable routes. In actual use, this translates to cleaner reactions, simplified purification, and faster project timelines.
Material science engineers occasionally request custom grades of this product to support development of specialty polymers and advanced coatings. The distinct combination of halogen and fluorine content modifies surface energy and adhesion properties in final applications, extending use beyond classic pharmaceutical and agricultural targets. By keeping our process flexible, we accommodate unique packaging or impurity requirements that sometimes arise in fast-moving industrial research.
As a matter of practice, scale-up from benchtop synthesis to multi-kilogram runs brings a fresh set of challenges for storage, blending, and safety. Reliable physical form, tight bulk density control, and well-documented batch analytics permit safer, more predictable transitions through kilo labs and pilot suites. The experience of seeing a process through from a single flask to metric ton production grounds every decision about which raw materials and intermediates to rely upon, and 2-bromo-3-(trifluoromethyl)pyridine has earned its spot on that short list.
Clear differences separate 2-bromo-3-(trifluoromethyl)pyridine from other, often less expensive, pyridine derivatives. Standard 2-bromopyridine offers only a halogen at the 2-position and typically lacks the electronic characteristics imparted by a trifluoromethyl group. By contrast, mono- or difluoromethyl-substituted pyridines tend to show diminished reactivity or yield in many coupling or nucleophilic substitution reactions. The three fluorines in the CF3 unit amplify both the inductive effects and the physical properties that lead to favorable biological and materials performance. Customers in need of that formation of highly stable C–F bonds will not find an easy substitute in monofluorinated analogs.
Cost-conscious buyers often wonder about the price-to-performance ratio. In our experience, the direct downstream impact on selectivity, process reliability, and regulatory package completeness outweighs any initial premium. The long-term savings — fewer failed batches, reduced need for multi-step purification, and improved regulatory confidence — are widely documented by clients in both the pharmaceutical and agrochemical sectors. This justifies the continued investment in developing supply chains exclusive to high-quality trifluoromethylated pyridine intermediates.
A word about process byproducts. Inexpensive, low-quality material often drags along persistent odor, off-color, or undetected positional isomers, and troubleshooting these issues during process validation costs orders of magnitude more in lost time and regulatory filings than a few cents saved per gram up front. With our compound, each batch arrives with batch-level documentation and traceable origin records. In-house process chemists confirm identity and isomeric purity, keeping focus on the downstream applications instead of backtracking on material quality.
We’ve fielded requests for side-by-side comparisons with other pyridine-based building blocks, including simple methyl, ethyl, or chloro analogs. Feedback from polymer chemists and pharmaceutical innovators has been consistent: none achieve the same performance in demanding conditions, whether in pilot reactors or late-stage medicinal chemistry screens. The synergy between bromine and trifluoromethyl on a single aromatic ring gives a distinct edge in exploratory and production settings, whether aiming for better electronic communication, improved target molecule properties, or streamlined synthetic access to key motifs.
Delivering reliable product quality, free from batch-to-batch swings or regulatory headaches, takes ongoing effort. We’ve invested in process controls that track every step, from raw material handling to final drum filling. Strong supply chain relationships with vetted upstream producers help keep critical raw inputs in spec. We verify reagent provenance and regularly audit internal and third-party labs that conduct quality analytics. Occasionally, even small gaps in documentation have led to extended production reviews, reinforcing the lesson that tight controls from start to finish pay dividends for downstream safety and regulatory filings.
Waste minimization deserves attention. Pyridine chemistries often create aqueous and organic byproducts that require careful management. Our plant design includes separation, collection, and treatment systems that follow national and international best practices. We engineer our reaction steps to maximize conversion and limit hazardous byproduct formation. Scrubbers, solvent recovery, and waste stream monitoring keep both our neighbors and our operational risk teams at ease. Over the years, positive environmental audits and near-miss tracking have built a workplace culture confident in both safety and sustainability.
Handling hazardous properties with practical controls avoids surprises for everyone on our team. The bromo and trifluoromethyl groups add some handling complexity, but our crew uses closed transfer systems, vapor containment, and personal protective gear tailored to specific roles. Regular training keeps safe practices top of mind. We’re candid about the reality that 2-bromo-3-(trifluoromethyl)pyridine, like many halopyridines, needs sensible respect and compliance with workplace standards. Safe handling is not simply a regulatory hurdle, but a means to keep experienced workers and process teams productive in the long haul.
Manufacturing this product has underscored the central role of regulatory knowledge. Each year brings more detailed expectations about impurity profiling, solvent residuals, and shipping safety. We’ve aligned batch records and traceability systems with global regulatory expectations. Our analytical team maintains certifications in line with global authorities, and we conduct periodic proficiency studies to stay sharp. Chemical customers have shared that such transparency simplifies later filings and inspections, saving weeks or months in project timelines when questions arise.
We keep product innovation in focus as well. Process improvements, continuous-flow adaptations, and solvent exchange updates all seek ways to reduce cycle time and waste. Our technical partnerships with process development teams have yielded fresh ideas — use of greener solvents, adjustments in catalyst loading, and in-depth impurity tracking all contribute to measurable gains across the product life cycle. We share process learnings across our manufacturing, quality, and customer service teams because cross-discipline communication consistently drives improvement.
Supply chain resilience draws attention too. Markets shift, political events disrupt shipment routes, and raw material prices fluctuate. We have bolstered dual-sourcing strategies and strategic inventories at multiple production sites, lessening the impact of isolated outages or global market volatility. For customers, this delivers the assurance that their critical materials pipeline stays open, whether they’re in early discovery or full-scale launch mode. The feedback we receive from procurement managers and supply chain analysts affirms the value of continuous investment in reliability.
Partnership with users matters just as much as technical features of a molecule. Chemical manufacturing, even with advanced automation, runs best with open technical dialogue — troubleshooting issues, clarifying requirements, and seeking continuous improvement. We treat every batch as a conversation with the end user, ready to adapt our process to both process challenges and new regulatory priorities. This approach keeps our knowledge up to date and keeps quality rooted in real practice, not theoretical benchmarks alone.
Our perspective on 2-bromo-3-(trifluoromethyl)pyridine grows out of deep practical engagement, steady improvement, and honest communication with downstream users. The streamlining of manufacturing, batch testing, and delivery cycles has delivered consistent results for clients in demanding industries. This compound’s unique attributes — structural, electronic, and practical — meet a set of needs that simpler or off-brand derivatives cannot match. Through hands-on management, robust documentation, and adaptive production technology, we stand by each unit delivered as a tool for innovation. And while regulatory, safety, and market demands keep evolving, commitment to product integrity remains the key factor that bridges chemistry from laboratory idea to successful scale-up.