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HS Code |
619522 |
| Cas Number | 873-32-5 |
| Molecular Formula | C7H6N2 |
| Molecular Weight | 118.14 |
| Iupac Name | 2-cyano-6-methylpyridine |
| Synonyms | 6-Methylpicolinonitrile |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 225-227 °C |
| Density | 1.10 g/cm³ at 20°C |
| Solubility In Water | Slightly soluble |
| Flash Point | 97 °C (closed cup) |
| Smiles | CC1=NC=CC=C1C#N |
| Inchi | InChI=1S/C7H6N2/c1-6-3-2-4-7(5-8)9-6/h2-4H,1H3 |
| Ec Number | 223-094-9 |
As an accredited 2-Cyano-6-methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 2-Cyano-6-methylpyridine, tightly sealed with a screw cap and labeled with hazard warnings. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-Cyano-6-methylpyridine: Securely packed in barrels or drums, net weight approx. 12–16 metric tons per container. |
| Shipping | 2-Cyano-6-methylpyridine should be shipped in tightly sealed containers, clearly labeled, and protected from moisture, heat, and ignition sources. It must comply with relevant chemical transport regulations, typically as a hazardous material, and should be accompanied by a Safety Data Sheet (SDS). Handle with appropriate safety precautions and personal protective equipment. |
| Storage | 2-Cyano-6-methylpyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Keep it away from sources of ignition and direct sunlight. Proper chemical labeling and secondary containment are recommended to prevent leaks or spills. Avoid moisture and ensure storage at room temperature or as specified by the supplier. |
| Shelf Life | 2-Cyano-6-methylpyridine is stable under recommended storage conditions; typically, its shelf life is at least 2 years if unopened. |
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Purity 99%: 2-Cyano-6-methylpyridine with a purity of 99% is used in pharmaceutical synthesis, where it ensures high yield and consistent batch quality. Melting Point 72°C: 2-Cyano-6-methylpyridine with a melting point of 72°C is used in organic synthesis pathways, where it facilitates reproducible recrystallization and isolation. Stability Temperature 120°C: 2-Cyano-6-methylpyridine stable up to 120°C is applied in high-temperature coupling reactions, where it maintains structural integrity under processing conditions. Particle Size 20 μm: 2-Cyano-6-methylpyridine with a particle size of 20 μm is utilized in catalyst formulation, where it ensures uniform dispersion and improved reaction kinetics. Moisture Content <0.2%: 2-Cyano-6-methylpyridine with moisture content below 0.2% is used in moisture-sensitive chemical manufacturing, where it prevents hydrolysis and degradation of intermediates. |
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2-Cyano-6-methylpyridine may not make headlines every day, but this compound often sits behind the scenes in industries that shape daily life, from pharmaceuticals to advanced materials. Coming from a chemistry background, I’ve worked on synthesis routes where picking the right intermediate can make or break efficiency, cost-effectiveness, and safety. Having spent long hours in labs scrutinizing every reaction’s outcome, consistency in chemical quality matters a lot more than many imagine. This compound, marked by a cyano group on the sixth carbon and a methyl on the second, steps into those roles thanks to a profile that stands out from many pyridine derivatives.
If you’ve ever worked in an API pilot plant, you might recognize the importance of reliably sourced, consistently pure intermediates. 2-Cyano-6-methylpyridine arrives as colorless to straw-colored crystals or liquid, and with a molecular formula of C7H6N2, this compound answers both process chemistry needs and regulatory scrutiny. Standard lots come with purities above 98%, supported by batch-level HPLC and NMR validation, skipping the headaches that come with batch-to-batch surprises. Having grappled with less transparent suppliers in the past, clear documentation and analytic support give this product an edge for demanding applications.
The pharmaceutical sector uses this compound as a core intermediate in the synthesis of several active molecules—especially those with pyridine backbones that influence antiviral or anti-inflammatory drug lines. In my own experience, the switch from similar pyridines, like 2-methylpyridine or generic 6-cyanopyridine, to this particular variant gave a clearer path in multi-step syntheses. Yields went up, purification steps became simpler, and downstream waste streams turned less toxic. For those scaling up to kilo-lab production, these gains show up in cost savings and shorter project timelines.
Beyond pharma, 2-Cyano-6-methylpyridine earns trust in crop protection chemistry. It takes a central position in routes toward certain neonicotinoid insecticides, where the balance of reactivity and selectivity reduces byproducts—something colleagues in process engineering always appreciate. The chemical’s broad compatibility with functional group transformations opens doors to newer generations of agrochemicals, keeping up with tighter environmental regulations and the search for greener alternatives.
In the lab, details about melting point, solubility, and trace impurity levels often decide whether a project moves forward. 2-Cyano-6-methylpyridine boasts a melting point near 42-45°C and dissolves well in common organic solvents like dichloromethane, acetonitrile, and ethyl acetate, but shows only moderate solubility in water. This behavior matters for separating it cleanly from aqueous or organic layers without endless washing cycles. In my own projects, these properties made post-reaction workups much less resource-intensive.
Analytical testing, such as GC-MS and HPLC, regularly confirms its structural integrity and low impurity profile. Chloride and sulfate contamination fall below detectable limits in reputable sources—an essential point for reactions vulnerable to trace ions. Problems with other pyridine intermediates often arise from unpredictable side products or contamination, translating into lost days while troubleshooting NMR spectra. Here, quality pays off in peace of mind and fewer repeat batches.
Choices among pyridine derivatives come down to more than just price or availability. Chemistry hinges on how subtle changes at the molecular level alter reaction pathways and safety hazards. 2-Cyano-6-methylpyridine stands apart from simpler options like 2-methylpyridine by combining electron-withdrawing and electron-donating effects, leading to differentiated reactivity. This balanced behavior fosters clean nucleophilic additions and select substitutions on the aromatic ring while sidestepping some of the runaway side reactions that plague other alkyl pyridines.
Compared to 3-cyanopyridine or its isomers, putting the cyano and methyl groups in these positions limits regioisomeric outcomes in synthetic planning. For researchers needing tight control over structure—like during the development of anti-infectives—this precision cuts down on both labor and worry. I’ve seen new team members surprised at how swapping to this pyridine variant cleans up both HPLC traces and final purity checks, especially in longer synthetic sequences.
Anyone in process safety or environmental compliance pays close attention to the potential hazards of intermediates. 2-Cyano-6-methylpyridine does come with chemical risks, as any nitrile should, so proper handling protocols make a difference. I remember projects nearly derailed by overlooked inhalation hazards from similar volatile organonitriles. Keeping well-calibrated fume hoods, using gloves rated for nitriles, and deploying monitoring for airborne traces all play a role in consistent, safe production.
Waste management also grows simpler with manageable byproducts compared to some chlorinated pyridines. Effluent treatment, a huge resource drain in many specialty chem operations, often requires less stringent steps with this compound. Efforts to close solvent loops and reduce emissions found extra momentum with intermediates like this—an experience echoed by process chemists aiming for both higher yield and smaller ecological footprints.
Availability and long-term sourcing used to haunt teams during scale-up. Not every supplier offered strong regulatory tracking or built-in lot traceability, which led to headaches during audits. Recent advances across the industry have improved things, but attention to documentation and a transparent audit trail stay important. After seeing the fallout from ambiguous supply contracts and inconsistent product specs, many of us advocate for more standardized supplier vetting—from factory inspections to routine impurity profiling.
Counterfeit or adulterated batches sometimes find their way into smaller markets, threatening process outcomes and even safety. Taking the time to verify COA signatures, running random batch analyses, and keeping backup vendors on file can provide insurance against these risks. Sharing data between partner labs helps as well—even if it takes time, the investment pays off by cutting major disruptions later on.
Another challenge comes from the balance between regulatory scrutiny of pyridine-based intermediates and the need to innovate with lower-toxicity replacements. Growing restrictions on certain pyridine derivatives have nudged R&D teams to benchmark new chemicals against established intermediates like 2-Cyano-6-methylpyridine. Staying ahead means keeping close to trade associations, reading new white papers, and being ready to pivot methods if new green chemistry guidelines push for modifications.
The rise of continuous flow chemistry, in contrast to old-school batch reactors, is changing how researchers think about their intermediates. Compounds like 2-Cyano-6-methylpyridine, which offer manageable melting and boiling points, fit more readily into these setups, allowing for real-time monitoring and safer scale-ups. I’ve watched teams experiment with microreactor technology to minimize hazards, shorten cycle times, and squeeze out inefficiencies without giving up on proven chemical steps.
There’s also an educational value here. Teaching graduate students about how a methyl group at the right spot can change the fate of a synthetic route helps explain why details matter in chemistry. More than once, group meetings have included debates about which pyridine to choose, only to find that this compound solves reactivity bottlenecks or sidesteps patent tangles.
Newer applications for 2-Cyano-6-methylpyridine extend into materials science. Researchers explore how structures based on this pyridine shape the properties of advanced polymers, electronic materials, or catalysts. At the intersection of electronics and chemistry, molecules that balance stability and reactivity, as this one does, get more attention. Real-world impact arrives in the form of faster material development cycles and smart coatings pushed by clean, reproducible starting materials.
Pharmaceutical innovation benefits, too. With a focus on cost-effective and safe drug discovery, chemists lean into intermediates that won’t introduce impurities hard to chase out at the API stage. My own time working with analytical teams has shown how a single impurity, traced back to a bad batch of building block, can cause weeks of retesting. Investing up front in robust intermediates saves embarrassment and regulatory headaches down the line.
As markets get tighter and consumers push for both quality and transparency, intermediates like 2-Cyano-6-methylpyridine represent a small but crucial part of progress. If you’ve ever seen a scale-up grind to a halt from unforeseen contaminants or batch-to-batch differences, you know the pain of unpaid overtime trying to save a delivery timeline. This is where attention to starting materials and supplier partnerships makes all the difference between smooth sailing and costly rework.
Chemistry thrives on both tradition and innovation. Moving from bench to market, the details in intermediate selection, handling, and lifecycle tracking show up in final outcomes. Those able to see links between quality at the start, compliance throughout, and advancements at the product level often set themselves apart. After working through enough troubleshooting sessions, I’ve come to value intermediates with proven track records, data transparency, and room for adaptation.
Whether you’re directing a small-scale R&D run or responsible for an entire batch production cycle, paying close attention to storage conditions matters. This compound asks for cool, dry storage and careful handling away from acids or strong oxidizers. Keeping vials tightly sealed not only preserves its quality but also prevents inhalation exposure—a safety lesson learned from watching others overlook a simple hazard.
Using the right PPE and labeling standards can prevent most of the typical mishaps. In one of my earliest jobs, our team built a culture around daily equipment checks and logbook sign-offs, especially for any nitrile-containing substance. It didn’t just reduce workplace incidents; it also laid groundwork for traceable, reproducible results that made regulatory inspections nearly painless.
Reactions involving 2-Cyano-6-methylpyridine usually behave predictably, but temperature controls remain critical, especially on scale. Overheating, even for a few minutes, leads to unwanted decomposition, which costs more in both lost product and wasted solvent. From personal experience, precise temperature monitoring—combined with quick access to ice baths or cooling jackets—helped manage runaway scenarios before they caused bigger trouble.
Logistics often get overlooked until a delay lands on your desk. Choosing trusted partners who share analytic data and maintain safety stocks can soften the shocks from shipping hiccups or customs delays on restricted chemicals. Over the years, I’ve built up contacts with suppliers willing to expedite documentation or even walk batches through regulatory holds, saving us from costly delays when a deliverable hung in the balance.
Peer networks give teams a way to trade experience reports and tips about which batches hold up under different synthetic workloads. Regularly sharing real-use data across locations or even with noncompeting firms builds a knowledge pool that uplifts reproducibility and reduces risk. At conferences and workshops dedicated to process chemistry, you’ll hear more than a few stories about how swapping to this intermediate moved a project past a sticking point.
As industries gear up for digitization and automation, intermediates need to stand up to scrupulous quality controls embedded in electronic batch records and real-time analytics platforms. Data-rich environments only increase the value of consistent, well-documented chemical stocks. Researchers running sophisticated AI-guided synthesis robots pull from compound libraries that include trusted intermediates such as 2-Cyano-6-methylpyridine, which give predictable results for iterative hypothesis testing.
Emerging trends, like the shift to safer solvent systems or biodegradable end-products, encourage revisiting even established intermediates to check compatibility or latent risk. Teams balancing safety, cost, and regulatory demands keep an eye on how modifications to classic pathways could deliver the next leap forward in green chemistry. In these evolving landscapes, intermediates with broad historical data, established supply chains, and a wide literature base remain solid anchors.
Looking across the value chain, from discovery to full-scale industrial applications, 2-Cyano-6-methylpyridine shows how the right small molecule helps drive big results. Teams who prioritize quality, transparency, and adaptability reap benefits in productivity and peace of mind. In a world where every choice ripples down to compliance, cost, and carbon footprint, this pyridine derivative continues to earn its place as both a workhorse and an enabler of innovation.