|
HS Code |
676321 |
| Cas Number | 607-47-2 |
| Molecular Formula | C6H3ClN2 |
| Molecular Weight | 138.56 g/mol |
| Appearance | White to pale yellow crystalline powder |
| Melting Point | 67-70 °C |
| Boiling Point | 305 °C |
| Density | 1.29 g/cm³ |
| Synonyms | 2-Chloro-6-pyridinecarbonitrile |
| Solubility In Water | Slightly soluble |
| Smiles | C1=CC(=NC(=C1)Cl)C#N |
| Refractive Index | 1.600 (estimated) |
| Purity | Typically ≥98% |
| Flash Point | 138 °C |
As an accredited 2-Chloro-6-cyanopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g package of 2-Chloro-6-cyanopyridine comes in a sealed amber glass bottle with a tamper-evident screw cap. |
| Container Loading (20′ FCL) | 20′ FCL can typically load about 13–16 metric tons of 2-Chloro-6-cyanopyridine, packed securely in drums or bags. |
| Shipping | 2-Chloro-6-cyanopyridine is shipped in tightly sealed containers, protected from moisture and direct sunlight. It should be handled as a hazardous material, following all relevant safety and regulatory guidelines. Suitable labeling and documentation are required for transport, with precautions taken to avoid spills, leakage, and exposure during handling and transit. |
| Storage | 2-Chloro-6-cyanopyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong acids and bases, oxidizers, and moisture. Protect from light and sources of ignition. Ensure the storage area is labeled and restrict access to trained personnel. Follow all applicable safety guidelines and regulations for hazardous chemicals. |
| Shelf Life | 2-Chloro-6-cyanopyridine has a shelf life of 2–3 years when stored cool, dry, tightly sealed, and protected from light. |
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Chemistry as a field thrives on thoughtful detail and inventive connections. One often overlooked yet impactful compound in research laboratories and industrial settings is 2-Chloro-6-cyanopyridine. Chemists frequently pursue new ways to unite science and application, and this molecule quietly supports their efforts. Studying pyridine derivatives leads to a handful of essential intermediates, and this specific compound has found a meaningful niche.
2-Chloro-6-cyanopyridine looks simple on paper: a six-membered pyridine ring, marked by a chlorine atom at the second position and a cyano group at the sixth. Such a structure might suggest straightforward answers, but its real-world roles extend far beyond paper and ink. Combined halogen and nitrile functionalities do more than increase chemical complexity—they open the door for a range of synthetic strategies. The electronic effects of the chlorine and cyano groups shape its reactivity, steering how this compound interacts with reagents in both laboratory syntheses and scaled-up processes.
Most of the time, when folks talk about pharmaceuticals or crop protection, focus tends to rest on the end product rather than all the careful building blocks behind the scenes. 2-Chloro-6-cyanopyridine rarely gets headline attention, but the work it makes possible deserves closer inspection. Its dual functional groups turn it into a tool for chemists shaping complex molecules. In pharmaceutical research, it contributes to the synthesis of active pharmaceutical ingredients (APIs), especially where a pyridine core features prominently in a drug’s structure. Its role doesn’t stop at medicine either; those in agrochemical development often use it to form new pesticides or herbicides that can improve crop yields while navigating regulations and safety standards.
Talking about pyridine derivatives means entering a crowded field. 2-Chloropyridine and 2-cyanopyridine, for instance, both show up regularly, each offering their specific reactivity profile. On its own, 2-chloropyridine lends itself to nucleophilic substitution reactions thanks to that reactive chlorine. 2-cyanopyridine’s nitrile group welcomes transformations, especially hydrolysis or reductions, that install useful functional groups one at a time. Yet, neither matches the particular balance of reactivity that 2-chloro-6-cyanopyridine brings to the table. The simultaneous presence of both substituents on the same ring broadens the pathway map, allowing sequential or selective reactions that let chemists control the creation of new compounds with greater precision.
Working chemists always ask: what does the actual product look like when it comes off the shelf and into the flask? High purity matters for reproducibility and safety, especially in pharmaceutical and pesticide routes. Purity above 98 percent signals reliability, though any trace impurities or remaining solvents might impact sensitive processes. Color varies from white to pale yellow, a clue to its condition and the absence of degradation. The crystalline powder form gives it stability and makes it easy to handle in standard laboratory operations.
Its molecular weight, melting point, and solubility all factor into day-to-day handling. At 152.56 g/mol, the molecule falls into a comfortable zone; it isn’t too heavy for accurate weighing, nor so light as to present unique handling difficulties. The moderate melting point, ranging around 78-80°C, means it can be weighed, transferred, and stored at room temperature in most climates without worry. Solubility in common organic solvents like dichloromethane, ethyl acetate, or acetonitrile smooths the way for mixing and reaction set-up. Anyone who’s tried to dissolve an insoluble powder in vain knows the frustration that a recalcitrant intermediate can cause; in this respect, the chloro-cyano combo offers welcome cooperation.
Sitting in a lab surrounded by countless bottles, each with a complicated name or cryptic code, many reactants look interchangeable. Sorting through them, the winner usually becomes whichever one performs with the least fuss and the greatest yield. 2-Chloro-6-cyanopyridine, though unassuming, backs up its presence with proven versatility. In my own time spent over clinking glassware and swirling reaction mixtures, a compound like this often becomes the lynchpin in a synthetic sequence. Take palladium-catalyzed cross-coupling as an example: the chlorine atom activates the pyridine ring for Suzuki, Buchwald-Hartwig, or Stille coupling, letting a whole range of partners attach cleanly at that position.
Once the coupling finishes, the cyano group doesn’t just tag along for the ride—it becomes the jumping-off point for further changes. Chemists who need a new amide, carboxylic acid, or amine can transform the –CN group with strategies ranging from acid- or base-catalyzed hydrolysis, to catalytic hydrogenation, to reduction with lithium aluminium hydride. With these options, the synthesis plan grows more flexible. Experience shows that reducing the need for multi-step protection and deprotection saves both time and materials; fewer steps mean fewer chances for error.
As chemical production rises to industrial scale, every little detail in a synthetic plan gets magnified. A student in a university lab can get away with losing a pinch of product down the drain, but manufacturing hundreds of kilograms leaves no room for slippage or unreliable material. 2-Chloro-6-cyanopyridine’s appeal partly comes from its clean reactivity—but for factories, consistent particle size and non-hygroscopic properties also matter. Powders that cake, clump, or draw in moisture present major headaches for automated processing and filling.
Another aspect in industrial circles: supply chain reliability. Access to well-documented, audited sources matters much more for buyers in pharmaceutical or agricultural markets who face regulatory scrutiny at every turn. If material properties drift from batch to batch, or unwanted byproducts show up, the risks multiply—whether to process safety, downstream reproducibility, or finished product quality.
Chemists often walk a fine line between performance and safety. The reactivity that makes 2-Chloro-6-cyanopyridine so appealing can also demand heightened attention to material handling. Compounds with halogen or nitrile groups, for example, can irritate skin or eyes, so physical barriers—gloves, goggles, proper fume hoods—aren’t simply recommended, but expected as baseline practice. Companies are increasingly mindful of environmental stewardship as well; waste generated from cleanups, spills, or routine disposal can’t be tossed out of mind. Research on greener synthesis methods—shorter pathways, lower energy demand, minimal byproducts or toxic reagents—frames the next set of industry advances.
Looking at the marketplace, supply chain transparency is no longer a luxury; it’s an expectation from partners, end users, and regulators alike. Regulatory environments, especially those set by agencies like the US Environmental Protection Agency (EPA) or the European Chemicals Agency (ECHA), continue to sharpen requirements around traceability, purity, and potential impurities. Countries that serve as major producers or exporters of pyridine derivatives must regularly update documentation and testing standards. Facilities need robust internal tracking and rigorous analytical testing to ensure that each kilogram matches customer and regulatory expectations.
Ethical sourcing should be another lens for assessing chemical intermediates. For something like 2-Chloro-6-cyanopyridine, the responsibility stretches backwards along the supply chain to the raw materials and forward to the products that depend on it. Chemists, suppliers, and buyers can all play a part by supporting transparency and preferring production routes with lower environmental impact and fair labor conditions. Projects aimed at recycling waste streams or developing greener pathways matter not only for technical performance, but for broader stewardship of shared resources.
Whether working on a small molecule drug or designing a new pesticide, the hurdles of synthesis pile up fast. Some reactions look simple, but the cleanup and purification demand hours at the bench. 2-Chloro-6-cyanopyridine, with its dual reactive groups, offers rare flexibility, but it’s not invincible to practical frustrations. Sometimes the starting material sits solid but stubborn, refusing to dissolve in the solvent you want; other times, side reactions claim too much of the yield, carving unplanned detours into the path. Through trial and error, chemists learn to pick solvents, temperatures, and workup conditions that minimize headache. More advanced techniques—using automated flow reactors, or in-line monitoring via HPLC—help scale up efficiently and catch problems before they snowball.
One lesson stands out: cut corners on material quality or react too quickly to cut costs, and the process almost always comes back to bite. Working with high-quality, well-characterized 2-Chloro-6-cyanopyridine can save hours of reprocessing or failed experiments. Over time, the upfront investment in premium reagents pays off in both reliability and output.
Pharmaceutical and agrochemical firms, facing ever-tougher regulations and a tighter focus on purity, motivate suppliers to refine their production and testing protocols. Increasingly, laboratories adopt advanced analytical tools for quality control: chromatography for purity, spectrometric methods for identity, and moisture analyzers for stability. These steps provide the documentation and assurance necessary to satisfy auditors—and keep consumer trust high for the medicines and products that eventually reach market shelves. Inconsistent batches, out-of-spec characteristics, or the slightest hint of contamination stop production until the problems resolve.
Global trade shifts also affect where companies source intermediates. Geopolitical issues, environmental disasters, and transportation bottlenecks can all strain supply lines, especially for specialty chemicals. Firms that once depended entirely on single-source suppliers now invest in more diverse networks or closer regional partners. Having contingency plans in place—to qualify backup suppliers, pre-validate materials, and strategize for unexpected shortages—helps avoid production slowdowns or costly project delays.
Methods that were once considered advanced have become routine. Chemists now explore palladium-catalyzed couplings and other cross-coupling techniques not just for ease, but for atom economy and reduced waste. 2-Chloro-6-cyanopyridine fits these reactions well, allowing new molecular architectures with less waste, energy, or risk. Designing reactions that work in water or with bio-based solvents moves the industry closer to environmental goals.
Attention has also turned to continuous flow synthesis—an approach that limits exposure and works well for reactive intermediates. By feeding ingredients through small, closed channels, chemists speed up reactions and gain tighter control over temperature, mixing, and safety. 2-Chloro-6-cyanopyridine responds well in such set-ups, powering more efficient production lines and better containment for hazardous emissions or spills.
For those in the trenches, the need to innovate sits alongside repeatability and regulatory compliance. One clear step forward involves ongoing research into alternative synthetic routes that minimize hazardous reagents or byproducts. Hotspots for improvement include catalyst recycling, process intensification, and green solvent selection. Some groups experiment with biocatalysts—engineered enzymes that steer transformations with the speed and specificity nature intended, while sidestepping heavy metals or toxic solvents.
On the purchasing and regulatory front, digital tracking and blockchain-style authentication systems offer a way to confirm the origin and history of each batch of 2-Chloro-6-cyanopyridine. That helps allay concerns from brand-name drug manufacturers, strict government regulators, and even end customers. Connected databases make it easier to verify compliance, flag anomalies, and enforce rapid response in the event of a recall or contamination scare.
No one group holds all the answers—industry, academia, regulatory agencies, and end users all bring different priorities and expertise. Chemical manufacturers see the pressure to drive cost down, but can’t ignore safety or environmental impact. Pharma and ag companies demand reliability and reproducibility. Regulators watch for potential health impacts, persistent pollutants, or emerging safety concerns. Branching out from siloed approaches, shared knowledge accelerates improvements. Partnerships between university labs, specialty chemical makers, and manufacturers have enabled pilot runs of innovative synthetic strategies before companies scale up.
Across the field, best practices now spread rapidly: early-adoption of greener catalytic systems, better documentation, tighter process controls, and smarter waste handling. Training the next generation of chemists—teaching hands-on practical skills and a mindset of responsibility—ensures that smart progress sticks, instead of slipping back under profit pressure.
Some might say all intermediates blur together, just as another off-white powder ready for storage. That thinking misses the real nuance of chemical progress. 2-Chloro-6-cyanopyridine shines not for glamour or brand name, but for solving the sorts of problems every chemist faces. In my work, success often hinges as much on choosing the right building blocks as on talent or clever tricks. A compound that’s pure, predictable, and supports clean reactions means shorter development timelines, more reproducible outcomes, and fewer headaches down the line.
Mistakes aren’t cheap. Skipping thorough QC or buying low-grade intermediates has hidden costs—failed reactions, wasted hours, lost samples, or even hazardous events requiring expensive clean-up. The longer I work with fine chemicals, the more I value suppliers who treat small details as seriously as the headline performance. That covers everything from honest documentation to responsible packaging to responsive support when challenges arise.
Science marches ahead at a restless pace. New drugs, smarter crop protection, next-generation battery materials—all depend on a complex web of reliable, advanced intermediates. 2-Chloro-6-cyanopyridine remains a dependable choice not because it’s flashy but because it continues to enable controlled, stepwise molecular innovation. As researchers build ever more complicated structures, the call for reliable reagents only grows louder.
While much of its story unfolds out of public view, those in the know recognize the contribution it makes. The silent workhorses—like this pyridine derivative—keep the doors open for real breakthroughs. In a world where demands for accountability, safety, and environmental protection are only rising, the track record and proven performance of such molecules matter more than ever.
Experience at the bench shapes judgment. Choosing a solid intermediate like 2-Chloro-6-cyanopyridine reflects a respect for both science and the chain of hands that move material from bottle to finished product. Preserving this dedication to quality and innovation ensures that the next generation inherits a toolkit ready for anything, and a world made safer and more sustainable by smart choices today.