|
HS Code |
776704 |
| Productname | 2-Bromo-6-chloropyridine |
| Casnumber | 57966-95-7 |
| Molecularformula | C5H3BrClN |
| Molecularweight | 192.45 |
| Appearance | Colorless to pale yellow liquid |
| Meltingpoint | 22-26 °C |
| Boilingpoint | 225 °C |
| Density | 1.74 g/cm3 |
| Purity | Typically ≥97% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Flashpoint | 93.4 °C |
| Refractiveindex | 1.609 |
| Synonyms | 2-Bromo-6-chloro-pyridine |
As an accredited 2-Bromo-6-chloropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g bottle of 2-Bromo-6-chloropyridine is sealed in an amber glass container with a screw cap and hazard labeling. |
| Container Loading (20′ FCL) | 20′ FCL container loading of **2-Bromo-6-chloropyridine** involves safe, moisture-proof packaging in drums or bags for bulk export shipment. |
| Shipping | **Shipping Description for 2-Bromo-6-chloropyridine:** 2-Bromo-6-chloropyridine is shipped in tightly sealed containers to prevent leakage, stored in cool, dry locations away from ignition sources. Packages are clearly labeled according to hazardous chemical regulations and handled by trained personnel, complying with local and international transport rules for potentially harmful substances. |
| Storage | Store 2-Bromo-6-chloropyridine in a tightly sealed container, in a cool, dry, well-ventilated area away from heat, ignition sources, and incompatible materials such as strong oxidizers. Protect from moisture and direct sunlight. Use appropriate safety labeling and handle with chemical-resistant gloves and eye protection. Ensure storage area is equipped with spill containment measures and access is restricted to trained personnel. |
| Shelf Life | 2-Bromo-6-chloropyridine is stable under recommended storage conditions, with a typical shelf life of at least two years. |
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Purity 98%: 2-Bromo-6-chloropyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency. Melting point 48°C: 2-Bromo-6-chloropyridine with a melting point of 48°C is used in agrochemical active ingredient development, where controlled melting allows for precise formulation. Stability temperature up to 120°C: 2-Bromo-6-chloropyridine with stability up to 120°C is used in heterocyclic compound manufacturing, where it maintains chemical integrity during high-temperature reactions. Low particle size ≤50 µm: 2-Bromo-6-chloropyridine with particle size ≤50 µm is used in fine chemical production, where enhanced reactivity and dissolution are required. Moisture content <0.2%: 2-Bromo-6-chloropyridine with moisture content below 0.2% is used in electronic material synthesis, where minimal water content prevents unwanted side reactions. |
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2-Bromo-6-chloropyridine stands out for anyone who deals with specialty chemical building blocks. The combination of bromine and chlorine on the pyridine ring creates chemistry that opens doors for research, pharmaceuticals, and the fine chemicals sector. Historically, chemists sought more reactive pyridines but ran into problems with unstable materials or low yields during plant-scale production. With 2-Bromo-6-chloropyridine, you get a predictable molecule that fits seamlessly into Suzuki or Buchwald-Hartwig couplings—a statement grounded in both published literature and hands-on lab experience.
Every batch of 2-Bromo-6-chloropyridine brings purity backed by quality control, with CAS Number 39955-75-2 as its unique identifier. Chemists often talk about the importance of melting point and purity, especially around reactions where trace impurities sabotage intermediates or block catalysts. Here, the melting range falls between 51°C and 56°C, and most suppliers keep minimum purity at 98 percent or higher, using HPLC or GC validation. Consistency matters far more than a shiny technical data sheet—experienced hands always appreciate the predictable flow of a dry, off-white crystalline solid rather than sticky or clumpy powders that show up in other halogenated pyridines.
Packaged typically in secure amber glass or HDPE containers, shipments maintain stability and guard against degradation. Hygroscopic and light-sensitive compounds often lose quality during transport, but 2-Bromo-6-chloropyridine proves a relatively robust intermediate when stored in properly sealed bottles away from sunlight. We’ve all suffered a ruined reaction sequence because of exposure or moisture in the wrong container. This compound sidesteps those headaches when handled by an attentive team.
Chemicals like this don’t usually grab headlines, but they play a pivotal role behind the scenes in pharmaceutical and agrochemical research. Medicinal chemists gravitate to the 2-bromo and 6-chloro substitution pattern, looking to create molecules that modulate metabolic stability or receptor selectivity. You’ll find the compound on the route to kinase inhibitors, anti-infective leads, or crop protection molecules, often as a scaffold for further derivatization.
Experienced synthetic chemists appreciate this intermediate because both halogens interact differently with catalysts and nucleophiles. While you could pick a mono-halogenated pyridine, dual substitution offers unique options for regioselectivity. Bromine enables precise cross-coupling reactions with palladium catalysts—Suzuki and Stille reactions move forward efficiently under surprisingly mild conditions. The remaining chlorine can then anchor either direct amination, alkylation, or further halogen-lithium exchange. More flexibility in one scaffold means fewer supply chain headaches for downstream teams working on analog libraries or scale-up batches.
Many look for a tried-and-true synthetic partner that supports discovery work and pilot plant transition without retooling. This compound fits the bill. It’s common to see gram-to-kilogram order sizes in contract research or process R&D, where teams want seamless translation as a molecule moves from benchtop to production reactor. The option to leverage both bromo and chloro functions in a staged approach drives project efficiency—a lesson learned after navigating bottlenecks with less versatile halopyridines.
At first glance, most halogenated pyridines seem nearly interchangeable. Reality in the lab tells a different story. Mono-brominated or mono-chlorinated pyridines limit post-modification options and raise costs if you need orthogonal site selectivity. For medicinal chemists, subtle electronic effects from both halogens can nudge SAR outcomes by affecting hydrogen bonding or metabolic stability—sometimes steering a series away from cytochrome oxidation liabilities.
Process chemists, with one eye on yield and another on plant compatibility, run across problems using more reactive or less robust intermediates. Pyridine rings with only a chloro or bromo group often create mixtures or require harsher conditions, bringing headaches for scale-up or purification. In my experience, switching to 2-Bromo-6-chloropyridine at the early stages saves days of trouble in process development. Less time fussing with major byproducts or setting up tricky purifications means lower overhead for the project.
Some competitors tout similar compounds, like 2,6-dichloropyridine or 2,6-dibromopyridine. These don’t offer the same fine-tuned reactivity. The bromo substituent gets replaced more easily in cross-coupling, but the chloro group offers a slower, more controlled handle for further chemical elaboration. As a result, downstream transformations gain an extra layer of selectivity, reducing risk of off-pathway impurities. Having used each of these related molecules on actual discovery projects, nothing accelerates progress like a scaffold that minimizes unplanned surprises.
Long days in the synthesis lab teach you which reagents solve problems, and which create new ones. Early versions of halogenated pyridines often disappointed—fussy to handle, moisture-sensitive, and unreliable on scale. There’s nothing quite as frustrating as scaling up a reaction, thinking the chemistry is locked in, only to discover hidden reactivity or batch-to-batch impurities.
2-Bromo-6-chloropyridine marks a leap in reliability. Teams using it for cross-coupling or nucleophilic substitution quickly note the difference in work-up and downstream compatibility. I’ve seen chemists push beyond the typical med chem screen and bring this intermediate into flow chemistry or semi-batch processing, driven by the compound’s stability and reactivity balance. Routine analysis shows the product holds up to both classical washes and modern micron-scale flash purification. That level of durability can’t be underestimated—projects live or die by timeline, especially with competitive grants or tight production contracts.
No matter how advanced the toolkit, nobody wants a series of column runs or troubleshooting sessions caused by an unreliable intermediate. With 2-Bromo-6-chloropyridine, predictability in purification and performance frees up time for actual innovation. Anyone who’s spent hours troubleshooting obscure impurities knows how valuable this can be; focus shifts from problem-solving to data generation and faster “go/no-go” decisions.
All halogenated aromatics deserve respect in the lab, both for reactivity and for health. Experience tells me that 2-Bromo-6-chloropyridine creates a far safer working environment compared to old-school, volatile halopyridines. Fume hoods and gloves remain essential, not just as a formality, but to prevent skin and respiratory exposure. In decades past, pyridine derivatives often brought unexpected headaches—unpleasant odors, stubborn residues in glassware, and challenging waste streams.
This product, by contrast, cleans up easily and generates waste streams that most facilities can manage with established protocols. The crystalline form guards against dust, and lack of volatility makes for a less stressful flask setup, even in higher-throughput workflows. Still, every professional who handles it appreciates the clarity in published MSDS documents and regular updates from reputable suppliers. There’s wisdom in following well-established storage and transport precautions—something I always insist on with juniors in the lab. Keep it cool, dry, and capped, and you’ll avoid the pitfalls that plagued past generations.
Once reactions wrap up and the final product leaves the synthesis bench, 2-Bromo-6-chloropyridine’s influence spreads outwards. Drug development teams frequently reference the unique substitution pattern in research papers for kinase, GPCR, or anti-infective targets. In more than one case, building blocks like this shift SAR results just enough to tip a compound over the threshold for patentability or improved selectivity. With many companies looking to protect their intellectual property, single-atom adjustments—enabled by reliable intermediates—carry serious downstream value.
Beyond pharma, agrochemical teams tap this scaffold to build pesticide candidates that balance efficacy with environmental stability. The fine-tuned reactivity helps control breakdown rates in the field, sidestepping regulatory and ecological complications. In both fields, a robust intermediate keeps production lines moving, reduces downtime, and helps scientists move from whiteboard to real-world results.
Supply disruptions over the past decade taught the chemical industry that redundant sourcing and reliable documentation matter more than chasing the lowest price. 2-Bromo-6-chloropyridine often comes from plants with hard-earned quality credentials and full traceability. The move to green chemistry principles encourages auditors to ask tough questions about solvent use and waste reduction in halopyridine manufacturing.
Many makers report improvements in batch process efficiency and cleaner reaction work-ups—moves that align with evolving global standards for responsible manufacturing. While halogenated aromatics bring certain regulatory challenges, facilities that invest in recovery, containment, and downstream purification limit their environmental footprint. I’ve seen firsthand how plant changes in bases, solvents, or washing steps can cut waste and boost batch consistency. Sourcing from plants that prioritize sustainable methods means less uncertainty for chemists and a more resilient supply network.
No intermediate comes without hurdles. In some reactions, 2-Bromo-6-chloropyridine produces minor side impurities—chloride-driven byproducts can pop up if bases or solvents stray from recommended ranges. For newcomers, cross-coupling on the bromo-group needs precise temperature control and catalyst choice. But these aren’t insurmountable problems; in fact, experienced teams often prefer having a well-understood behavioral profile over gambling on exotic alternatives. Routine NMR or LCMS checks keep projects on track.
Looking ahead, opportunities arise from further reactivity tuning or improved regioselectivity using newly developed catalysts. With AI-driven reaction planning and automated platforms gaining traction, a reliable intermediate like this shortens the feedback loop, letting teams test routes and optimize in days instead of weeks. As a synthetic chemist, I welcome tools that free up more time for design and data interpretation—less trial and error, more productive cycles.
Scientists working with specialty chemicals value trust—not just in product quality, but in supplier transparency. Many suppliers now provide batch analytics, product histories, and rapid response to technical questions, much appreciated in tight timelines. Any yellowing, melting outside spec, or odd odor gets flagged and resolved, thanks to robust supplier channels. This kind of partnership gives peace of mind when the pressure’s on; having seen colleagues burn days trying to sort out mystery impurities copied from other supply chains, I understand why direct, honest information matters so much.
Niches like process chemistry or custom synthesis rely on intermediates that are not just pure, but whose origins and specs are clear. Regulatory authorities increasingly require documentation on everything from impurity profiles to analytical traceability. From the perspective of E-E-A-T—expertise, experience, authority, and trustworthiness—2-Bromo-6-chloropyridine repeatedly earns its place at the bench and in reports.
Feedback from working chemists provides a clearer guide than any brochure. Stories circulate about teams who struggle with off-brand pyridines, only to switch after seeing yield jumps with purer 2-Bromo-6-chloropyridine. Process specialists recount easier crystal crops and fewer run-ins with unexpected product discoloration or plant shutdowns for extra cleaning. These real-life experiences reinforce decisions to stick with proven sources.
Younger researchers gain valuable lessons from using quality intermediates out of the gate—spending time learning chemistry instead of chasing down mystery waste peaks. In my own experience, teaching grad students and post-docs, nothing cements good lab habits like a few cycles running on a reliable, well-characterized scaffold.
Companies facing issues with intermediates often jump straight to overhauling their synthetic route, but sometimes a smarter solution lies in adjusting upstream parameters or switching suppliers. Regular discussions with suppliers—clarifying purity needs, preferred packing, or technical support—keep problems at bay. Lab teams should dedicate some resources to periodic product comparisons or side-by-side tests, not just for initial validation but also as part of ongoing quality assurance.
For those scaling up, it pays to monitor reaction conditions tightly and rely on robust analytical support. Automated systems that sample reaction progress and track impurities help reveal trends that might otherwise go unnoticed until a batch goes off-spec. Investing in training and peer review of data closes the gap between what’s expected on paper and what happens when reactions scale. Sharing these lessons grows everyone’s skill set and tightens the feedback loop between bench and management.
At the end of the day, products like 2-Bromo-6-chloropyridine make a difference beyond technical stats. Their impact is measured by the hours saved, headaches avoided, and discoveries advanced. Over years working in both academic labs and industry, I have seen how the right intermediate streamlines entire projects. The choice affects everything down the chain—from analyst to process engineer, to the teams responsible for environmental compliance.
It’s easy to overlook the backbone molecules that drive innovation, but those who work with these chemicals day in and day out understand the value of a trusted, well-characterized product. As research and development push boundaries, tools like 2-Bromo-6-chloropyridine help teams cut through uncertainty and focus on science. That’s what keeps labs moving, ideas flowing, and new solutions appearing on the world stage.