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HS Code |
222036 |
| Iupac Name | 6-Chloro-2-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine |
| Molecular Formula | C7H3ClF3N3 |
| Molar Mass | 225.57 g/mol |
| Cas Number | 101152-94-7 |
| Appearance | White to light yellow powder |
| Melting Point | 142-144 °C |
| Solubility In Water | Poorly soluble |
| Smiles | C1=NC2=C(N1C(F)(F)F)C=CC(=N2)Cl |
| Inchi | InChI=1S/C7H3ClF3N3/c8-4-1-2-13-5(3-4)14-6(12-13)7(9,10)11/h1-3H |
| Pubchem Cid | 156777 |
| Storage Conditions | Store in a cool, dry place and keep container tightly closed |
As an accredited 6-Chloro-2-(trifluoromethyl)-3H-imidazo(4,5-b)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g package features a tightly sealed amber glass bottle, labeled with the chemical name, structure, purity, and safety information. |
| Container Loading (20′ FCL) | 20′ FCL loads approximately 12 MT of 6-Chloro-2-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine in securely sealed fiber drums. |
| Shipping | 6-Chloro-2-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine is shipped in tightly sealed containers under ambient or refrigerated conditions, depending on sensitivity. Packaging complies with chemical safety regulations to prevent leaks or contamination. All shipments include safety documentation and labeling according to international transport and hazardous materials guidelines. Handle with appropriate personal protective equipment. |
| Storage | 6-Chloro-2-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine should be stored in a cool, dry, and well-ventilated area, tightly sealed in a chemical-resistant container. Protect from light, moisture, and incompatible substances such as strong oxidizers. Store at room temperature or as specified on the product label, and follow standard chemical hygiene practices to ensure stability and safety. |
| Shelf Life | Shelf life of 6-Chloro-2-(trifluoromethyl)-3H-imidazo(4,5-b)pyridine is typically 2-3 years when stored in cool, dry conditions. |
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Purity 99%: 6-Chloro-2-(trifluoromethyl)-3H-imidazo(4,5-b)pyridine with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal side reactions and maximized yield. Stability temperature 180°C: 6-Chloro-2-(trifluoromethyl)-3H-imidazo(4,5-b)pyridine with stability temperature 180°C is used in high-temperature coupling reactions, where thermal robustness maintains compound integrity. Particle size 10 µm: 6-Chloro-2-(trifluoromethyl)-3H-imidazo(4,5-b)pyridine with particle size 10 µm is used in fine chemical formulations, where uniform dispersion enhances reactivity and product homogeneity. Melting point 210°C: 6-Chloro-2-(trifluoromethyl)-3H-imidazo(4,5-b)pyridine with melting point 210°C is used in solid-state organic electronics, where consistent melting behavior supports stable device fabrication. Moisture content <0.5%: 6-Chloro-2-(trifluoromethyl)-3H-imidazo(4,5-b)pyridine with moisture content <0.5% is used in moisture-sensitive catalyst development, where low water content prevents catalyst deactivation. |
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For those of us deeply rooted in heterocyclic chemistry, 6-Chloro-2-(trifluoromethyl)-3H-imidazo(4,5-b)pyridine offers a toolbox for constructing new possibilities. Drawing from countless runs through our reactors and purification columns, this compound stands out whenever a reliable and structurally robust scaffold is required. Our in-house teams value it as a building block when developing advanced pharmaceutical intermediates and custom molecules for crop protection.
We know from experience that the presence of both chlorine and trifluoromethyl groups on the imidazo[4,5-b]pyridine core gives this molecule stability during harsh reaction conditions. Our plant engineers favor this compound because it resists unwanted side reactions even in extended heating and during exposure to a range of strong reagents. This reliability comes from a backbone that is less susceptible to hydrolysis, oxidation, or nucleophilic attack than related pyridine derivatives. Production teams get enhanced yields and fewer headaches in downstream purification—an advantage not always achieved with standard, less substituted pyridines.
Our daily work aims to deliver consistent, high-purity batches, typically exceeding 98% HPLC purity. Powder form ensures ease of weighing and precise dosing into reaction vessels. No flow agents or unnecessary fillers disrupt the performance. Every jar and drum gets filled under controlled humidity because researchers have told us moisture sensitivity impacts reactions. These fine details are not afterthoughts; they arise from years of feedback and active lab experience.
Chemists in our research partnerships come back to 6-Chloro-2-(trifluoromethyl)-3H-imidazo(4,5-b)pyridine for good reason. The electron-withdrawing trifluoromethyl group at the 2-position tweaks the electron density, making it more reactive in certain cross-coupling reactions. Medicinal chemists appreciate this modification, which can improve metabolic stability and tweak biological activity profiles. On the agrochemical side, the compound’s aromatic rigidity and halogenation open doors to new modes of action against resistant pathogens.
We have seen this molecule serve as an effective core in kinase inhibitor libraries and potential anti-infectives. Its compatibility with Suzuki and Buchwald-Hartwig couplings allows rapid diversification, which accelerates hit-to-lead timelines in medicinal chemistry. Our technical team always monitors for impurities that might interfere in such sensitive reactions, relying on robust analytical methods—LC-MS, NMR confirmation, and rigorous batch release tests—to avoid setbacks in both large and small-scale research projects.
6-Chloro-2-(trifluoromethyl)-3H-imidazo(4,5-b)pyridine distinguishes itself from the typical pyridine or imidazole derivatives. Compared against simple 2-substituted pyridines, for instance, the imidazopyridine core brings increased rigidity and unique hydrogen bonding patterns. This means it’s favored for stacking interactions in enzyme binding pockets or layered crystal lattices. Applying it in fragment-based drug design campaigns delivers higher “developability scores”—a term we’ve heard echoed by multiple pharma partners.
Chlorine substitution at the 6-position isn’t a cosmetic change. It facilitates subsequent halogen-lithium exchange or palladium-catalyzed functionalizations, giving synthetic chemists more attachment points and flexibility in scaffold elaboration. In practice, this means research projects move more rapidly from small-scale analog design to scalability and process development. Over the years, we have compared it to non-halogenated analogs and have consistently observed cleaner downstream modifications—less by-product formation, smoother chromatography profiles.
Unlike products sourced from trading houses, our material comes off the line with process traceability that goes all the way back to raw materials. We know which batches experience minor deviations in crystal form, monitored in real time by laser particle size measurement. Any spurious color or off-smell triggers a full analytical workup. Long-term, this attention to process control means researchers experience fewer surprises, whether scaling up for a pilot campaign or running exploratory mg-scale experiments.
Improved isolation methods, adapted from trial runs, now limit the formation of side-products like the di-chloro impurity. We learned early on, during several multi-week syntheses, that a small change in solvent composition or catalyst lot can tip the balance between a clean product and one requiring repeat purification. Direct communication between our plant chemists and our end-users fosters continued improvements—if a customer’s process falters, we hear about it and adapt.
We know chemical manufacturing creates responsibility for both our people and the planet. Over the last decade, our approach to waste minimization during production of 6-Chloro-2-(trifluoromethyl)-3H-imidazo(4,5-b)pyridine has shifted. Closed-loop solvent recovery, safer handling protocols, and batch-wise emission tracking arose from both regulatory trends and genuine concern from floor managers. No one wants to work with uncontrolled emissions or hazardous exposures. Operators receive regular training not just in compliance, but in practical hazard recognition unique to halogenated intermediates.
The chloro and trifluoromethyl features demand special storage—high-density polyethylene containers ensure chemical compatibility, and airtight seals prevent both cross-contamination and degradation. These aren’t just regulatory duties, they stem from memos written by the very people lifting bags and monitoring drums during midnight shifts.
One element we keep hearing from our customers: “The consistency is baked into every drum.” That reputation came from exhaustive QC work and listening when a researcher describes issues that may not show up on a batch certificate. Our own R&D group regularly experiments with new reaction conditions, ensuring the product stands up to variations in base strength, temperature, and catalyst selection.
Analytical chemists on our team have mapped out the UV-Vis and MS profiles of every expected by-product, so unexpected peaks trigger swift troubleshooting. If a new customer raises a unique application—for example, scaling up a continuous flow process—we will often pull a handful of technical staff from production to consult directly. Sharing these data directly often preempts quality issues further downstream.
Although official specifications don’t feature solubility profiles in every solvent, years of hands-on experience help guide practical use. We have tested this compound’s compatibility with DMSO, polar aprotic solvents, and common non-polar organics. We have watched as ether-rich solvents caused precipitation issues, while acetonitrile provided robust dissolution, especially for preparative HPLC loads. Tracking these outcomes reduced lost time and batch-to-batch surprises in our partners’ labs.
Every batch’s journey is mapped, from choice of starting material—often a halogenated nicotinic acid—to the final filtration and drying. Our operators monitor every stage, manually inspecting filtrates for clarity and color. GC and HPLC analysis follows before each pail is closed and labeled. This vigilance catches those rare misformed crystals that create headaches later on and weeds out the unpredictable trace impurities.
We have also tailored our post-processing based on feedback from regular customers. Some request finer powder for automated dispensation; others prefer coarser granulation for ease of transfer in larger glassware. We handle these requests internally, drawing from a sizable inventory maintained in atmosphere-controlled rooms.
Watching a new molecule go from kilo lab to commercial scale changes the way a manufacturer thinks about quality and reproducibility. A few misplaced grams, a shift in lot purity, or a misinterpreted spectral readout can turn weeks of work into a setback. That’s why we never stop collaborating with those who work at the bench. We’ve refined both our technical offerings and reporting based on stories from research teams—those who work late hours, juggling parallel syntheses, pressured for time and accuracy. Their input shapes our process more than any textbook or off-site specification committee ever could.
Every pilot batch, every metric ton, carries the testaments of operators who have run this product line for years. Their feedback, paired with careful record-keeping, has brought about improved batch reproducibility. Chromatography runs get recorded for retention time shifts; spectral fingerprints are built up across hundreds of batches, capturing the subtle changes that can affect both bench-level and plant-wide outcomes.
Automated reaction monitoring and advanced purification equipment at our site don’t replace the attentive eyes and hands of our crew. The nuanced scent of a batch, the feel of a properly dried powder, or the exact shade of off-white—these are skills that only develop with time spent on the production floor. Blending this expertise with robust analytical data boosts confidence for those receiving our shipments. It means fewer distractions and more time spent advancing science.
Our laboratory network feeds data and samples directly into our quality management system, using protocols we’ve iteratively developed for fast and clear defect reporting. Problems don’t linger across multiple production cycles. Everyone involved, from incoming raw material inspectors to shipping crews, has a direct line to production leadership to push for improvements.
Experienced buyers cite regulatory scrutiny as a growing challenge. We’ve responded with auditable records of every significant handling point that 6-Chloro-2-(trifluoromethyl)-3H-imidazo(4,5-b)pyridine encounters in our facility. Certificate of analysis data tie back to original batch sheets and, if needed, sample reserves. Our regulatory staff works closely with compliance officers to ensure both data integrity and defensible process documentation. Batch recall drills aren’t theoretical—they’re practiced, ensuring traceability right down to individual containers.
Over time, it’s become clear what truly differentiates 6-Chloro-2-(trifluoromethyl)-3H-imidazo(4,5-b)pyridine from other intermediates. Chemically, it’s the fusion of properties—reactivity, steric environment, and resistance to common side reactions. Practically, it’s the steady reliability through multiple campaigns, even with changes in scale or equipment. As a manufacturer, we’ve seen projects hinge on these details. Subtle features, such as its response to strong base or the ability to selectively activate the core for further derivatization, make it a choice component in advanced syntheses.
Dialogue with those who ultimately work with our product guides nearly every improvement. Whether a recurring customer reports issues with filterability, or a new researcher describes an unanticipated reaction quirk, these insights reach the core of our process control. There’s no substitute for regular, candid communication. Many troubleshooting sessions have led directly to process adjustments, from improving filtration rates to refining drying protocols for better storage stability.
Many on our production team come from laboratory backgrounds. They recognize the difference between an academic “certain purity” and bench-reproducible consistency demanded in real-world projects. Training new team members emphasizes practical problem-solving as much as adherence to protocols. It’s not enough to hit a minimal specification; the target is a product that delivers for end-users, project after project, because it’s made with shared hands-on experience.
Peer mentorship on the floor has sped up not just onboarding, but the pace of practical innovation. Instead of waiting for batch failures, our teams actively chase down bottlenecks and inefficiencies noted by users. This approach gives those handling and preparing 6-Chloro-2-(trifluoromethyl)-3H-imidazo(4,5-b)pyridine every day a voice in shaping its future iterations.
Our work as a chemical manufacturer draws on the expertise of many participants—operators, analytical chemists, process engineers, and researchers at the bench. 6-Chloro-2-(trifluoromethyl)-3H-imidazo(4,5-b)pyridine represents a synthesis of chemical design and day-to-day practical judgment. Achieving quality at scale requires more than technical knowledge; it takes open feedback channels and flexibility in problem solving.
Improvements rarely come top-down; more often, they come from small suggestions voiced by those who troubleshoot problems directly. As this compound continues to open new opportunities in pharmaceuticals and beyond, its quality and utility reflect the lessons gathered through real-world challenges—encountered, tackled, and solved at every stage of its manufacture and use.