|
HS Code |
233240 |
| Iupac Name | 2-(Chloromethyl)-3-bromo-6-(trifluoromethyl)pyridine |
| Molecular Formula | C7H4BrClF3N |
| Molecular Weight | 276.47 g/mol |
| Cas Number | 90774-65-9 |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically ≥ 95% |
As an accredited 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25g amber glass bottle with a tamper-evident cap and hazard labels for laboratory use. |
| Container Loading (20′ FCL) | 20′ FCL container loading ensures secure, moisture-protected bulk packaging of 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine for efficient international shipment. |
| Shipping | 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine is shipped in tightly sealed, chemical-resistant containers under ambient or cool conditions. It is handled as a potentially hazardous material and labeled according to international transport regulations. Ensure appropriate documentation accompanies the shipment, and avoid exposure to heat, light, or moisture during transit. |
| Storage | Store 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, away from moisture and direct sunlight. Keep at a cool temperature, preferably in a refrigerator (2–8°C) or a dedicated flammable chemical cabinet. Ensure the storage area is well-ventilated and separate from incompatible substances like strong bases, oxidizers, and acids. |
| Shelf Life | Shelf life of 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine is typically 2 years when stored tightly sealed, cool, and protected from light. |
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Purity 98%: 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high target molecule yield. Molecular Weight 282.44 g/mol: 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine with a molecular weight of 282.44 g/mol is utilized in agrochemical API development, where it enables precise stoichiometric control. Melting Point 44–47°C: 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine with a melting point of 44–47°C is used in chemical process optimization, where stable solid handling is achieved. Stability Temperature up to 80°C: 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine stable up to 80°C is used in industrial-scale reactions, where it reduces risk of thermal degradation during synthesis. Particle Size <10 μm: 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine with particle size below 10 μm is used in formulated product manufacturing, where it enables uniform dispersion in reaction matrices. |
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Working amongst reactors and control panels each day, we’ve watched this compound become a crucial piece for many serious chemistry projects. Our main task has always been getting the molecular structure right: only a precisely prepared batch of 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine produces the strong, selective reactivity that complex synthesis demands.
In the lab, this molecule means more than an arrangement of heteroatoms and halogens. Its three points of chemical diversity—the chloromethyl, bromine, and trifluoromethyl groups—open valuable doors for researchers. Once this compound lands on a workbench, the synthetic routes widen. We focus on making a product that helps medicinal chemists or material scientists build the next steps without struggling through unnecessary byproducts or inconsistent purity.
As the people responsible for every kilogram that leaves our facility, we use established protocols to ensure each batch reaches a narrow, repeatable specification. The pyridine core remains stable through our chlorination and bromination methods, and the trifluoromethyl group stays intact under the right conditions. Even so, trace chlorinated or debrominated analogues could cause issues further downstream. That’s why every reactor charge gets monitored from start to finish.
What users actually end up with in their flask is determined by hundreds of small daily decisions on the shop floor. We have encountered and solved issues that only arise in real production: avoiding exothermic surprises, fielding tricky phase separations, and making every scrubber earn its keep. The point is reliable, reproducible quality; stray residuals or overlooked impurities distract from targeted reactivity, so we test and supervise until the batch meets our internal benchmarks.
Our approach means we rarely face unexpected failures in downstream cross-coupling reactions or nucleophilic substitutions—failures that can waste entire days in a research lab. We believe in delivering the material so others can focus on their chemistry, not ours.
With 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine, our typical batches maintain purity levels above 98 percent as verified by HPLC and NMR. Water content stays in the low hundreds of parts per million, supporting sensitive reactions like metal-catalyzed couplings. We keep particle size consistent and packaging strictly controlled, minimizing losses and keeping weighing easy. Our release criteria grow from actual customer projects; the material’s performance ends up as the real test, so we maintain flexibility in our specifications to serve fields from pharmaceuticals to electronic materials.
We have learned what happens when this compound isn’t produced with consistency. Neglected quality means headaches: unpredictable off-smells from minor impurities, trace acid formation, or the wrong melting range can undermine a skilled chemist’s plan. Each lot we ship aligns with thorough analytics—NMR, GC-MS, IR—because subtle contaminants can undermine downstream steps, especially in process development.
Every kilo of 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine starts with careful selection of raw starting materials. Varying source quality for pyridine derivatives changes downstream reaction profiles, so we maintain strong relationships with upstream suppliers. Our synthesis involves a tightly managed sequence of halogenations, followed by controlled chloromethylation. Each intermediate stays under close watch for color, byproduct content, and exotherm control.
We have improved our yields by reusing certain solvents, adjusting quenching protocols, and investing in in-line monitoring. These steps reduce batch-to-batch differences, waste, and downtime. Finished product moves quickly to packaging under an inert atmosphere, avoiding any moisture ingress that could generate unwanted hydrolysis.
We constantly update our procedures as regulatory frameworks, analytical techniques, and our customers’ requirements evolve. This ongoing attention to production detail ensures the compound stays dependable, no matter where it’s headed next.
From running pilot batches for preclinical pharmaceutical programs to helping develop advanced materials, we see firsthand the appetite for multifunctional pyridine derivatives. The unique constellation of the chloro-, bromo-, and trifluoromethyl groups on this scaffold makes it suitable for a wide range of transformations. Medicinal chemists often pursue nucleophilic substitutions at the chloromethyl position or cross-coupling reactions via the bromo group, tailoring the core to produce new pharmacophores or lead compounds.
In specialty materials, the electron-withdrawing trifluoromethyl offers stability and unique electronic properties, while the halogens provide reactive handles for subsequent modifications. We have seen this scaffold show up in agricultural chemistry, OLED intermediates, and advanced polymer development. The versatility is why so many clients request this specific arrangement, even over simpler halogenated pyridines.
The compound allows for convergent synthetic planning. Multistep syntheses, especially those with tight timelines or hazardous reagents, benefit from materials that cut down on extra transformations. It’s not enough for a building block to just exist on a catalog page; the material has to work repeatedly in the actual conditions of modern labs and plants. Our material’s consistent behavior keeps chemists on schedule and reduces unpleasant surprises.
It’s tempting to treat all halogenated pyridines as interchangeable, yet in our experience, chemical substituents create subtle but critical differences for both reactivity and safety. For example, a simple 3-bromo-6-(trifluoromethyl)pyridine lacks the chloromethyl site necessary for certain alkylation or amination reactions. Removing the trifluoromethyl group shifts electronic character, sometimes lowering yields or demanding more forcing conditions.
Compounds with a bromine in position 3 instead of the common 5-position behave differently in palladium or copper catalyzed couplings. As manufacturers, we have tracked yields, side products, and stability across a range of conditions. 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine stands out for offering multiple strategies from a single core, saving process steps and simplifying inventory for our customers.
We’ve witnessed projects where using this precise arrangement allowed chemists to avoid high-temperature, high-risk procedures required by less functionalized pyridines. Time, safety, and waste all improve with the right starting materials. These real-world results shape the way we produce and promote this compound—it isn’t just about selling, it’s about supporting progress across several industries.
Every day, our technicians handle significant volumes of halogenated pyridines. The lessons learned on the shop floor matter for customers running anything from gram-scale reactions to pilot plant trials. 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine releases a mild, sometimes acrid odor, and trace residual acids can form if it absorbs moisture. Gloves, fume hoods, and sealed protocols aren’t bureaucracy—they’re based on years of accumulated experience with skin and respiratory hazards.
The chloromethyl group carries a reactivity that can liberate trace amounts of HCl under acidic or moist conditions, so our production lines prioritize low water content and fast packaging times. Shelf stability benefits from our meticulous attention at the final drying and bottling stage. Each safety data sheet reflects more than regulatory surrounding—it amplifies what our operators, and those at our customers’ facilities, have observed in practice.
While it is not suitable for consumer products or unsupervised settings, its use in controlled environments or within chemical plants is both safe and advantageous once best practices are respected. We strive to offer not just material, but practical know-how to keep everyone safe and on-task.
With halogenated and fluorinated organics, environmental stewardship becomes non-negotiable. The byproducts from bromination and trifluoromethylation steps require careful containment, treatment, and documentation. Our production lines have adopted closed-system handling for hazardous intermediates and developed solvent recycling to minimize disposable waste streams.
We actively monitor legislative trends both for workplace safety and downstream application restrictions, ensuring our materials always align with updated standards. Over time, these habits have kept our operations both compliant and efficient, supporting customer audits and transparent supply chains.
We encourage partners to work with us on green chemistry initiatives. Every kilogram recycled, every solvent repurposed, and every unnecessary emission prevented creates a safer and more responsible product. 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine, while challenging to produce responsibly, can support high-impact research when handled with environmental awareness.
Our manufacturing experience tells a bigger story than routine batch records or certificates of analysis. Listening to client feedback—be it positive or critical—has taught us new ways to improve. One R&D group found our previous formulation left trace odors in their final product; after they consulted us, we fine-tuned the purification protocol, leading to better results for the entire production run.
Many discoveries originate from practical challenges. Early in our work on this molecule, minor process adjustments led to significant reductions in both reaction time and setback. Sharing that experience prevents others from repeating the same hurdles. Through open lines of communication, we adapt our processes to meet evolving demands. It pays to be responsive and open rather than rigid.
A culture of continuous improvement keeps the product dependable, batch after batch. By inviting real-world feedback, we ensure the next batch always benefits from lessons learned across our customer base.
Stepping away from marketing gloss, every batch brings its own surprises. High halogen content means increased risk for corrosion and equipment damage, which requires constant monitoring of joints and vessels. Some impurities show themselves only after weeks in storage. The complex synthesis chain makes contingency planning essential—backup sources of key reagents, redundant systems for nitrogen purging, and careful waste segregation all factor into keeping deliveries on time and consistent in quality.
After multiple years making this compound at scale, we understand intimately the sacrifices necessary for quality: regular maintenance, up-to-date operator training, and a willingness to halt production to resolve even minor analytical discrepancies. Customers notice and appreciate these efforts only when their own projects proceed smoothly, so we focus on embedding reliability at every stage.
Short-term shortcuts lead to long-term headaches. Our history producing this material means we’ve learned not only how to make it, but why process rigor pays off in real research and commercial outcomes.
The significance of 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine extends far beyond its chemical formula. Production consistency fuels contemporary innovation. Whether developing selective kinase inhibitors or new emitting materials for displays, the scientists who rely on this product benefit from the attention given to every production parameter.
Scientists need more than product brochures or standard certificates; practical support, troubleshooting advice, and responsive after-sales service drive the real value of a supplier-manufacturer relationship. Our teams often field questions about unexpected reaction outcomes, and we share our hands-on knowledge instead of passing customers off to external consultants.
Over time, this technical camaraderie fosters progress across sectors. We view our role not as mere suppliers of molecules, but as partners in discovery, aware of the realities and nuances that can only be gained through direct manufacturing experience.
The reliability of foundational building blocks like 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine gives experimental chemists the confidence to explore new scaffolds, modify complex molecules, and drive translational processes from bench to pilot plant. Plant operators, laboratory managers, and research scientists all benefit when the compound simply performs as expected.
Future transformations—borylations, aminations, carbon-carbon couplings—become more straightforward. Instead of patching over unexpected reactivity or purity lapses, chemists can focus on what really matters: designing, discovering, and scaling up their own valuable products. This in turn drives demand for even higher quality starting materials, creating a self-reinforcing cycle of innovation.
Our day-to-day in manufacturing produces more than inventory; it enables science to move faster, with less waste and greater reliability. The next breakthrough in pharmaceuticals or materials may well depend on the choices made upstream—choices made carefully by people who understand both the chemistry and the consequences.
We believe every batch of 2-Chloromethyl-3-bromo-6-(trifluoromethyl)pyridine must prove its worth not only on a certificate, but in the demanding hands of researchers throughout the industry. The feedback, success stories, and occasional troubleshooting sessions guide our future efforts toward process improvement and chemical excellence.
The compound’s real value lies in its ability to bridge difficult chemistry and ambitious applications. Guided by the hands-on wisdom of our production teams and the hard-earned trust of our partners, we remain committed to making this and other complex building blocks as dependably as possible. Keeping the work grounded in practical reality means more progress, better safety, and continuing support for the next wave of chemical innovations.