|
HS Code |
657022 |
| Name | 2-Cyano-4-methylpyridine |
| Cas Number | 35546-65-3 |
| Molecular Formula | C7H6N2 |
| Molar Mass | 118.14 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 233-235 °C |
| Density | 1.085 g/cm3 |
| Refractive Index | 1.535 |
| Solubility In Water | Slightly soluble |
| Flash Point | 94 °C |
| Smiles | CC1=CC=NC(=C1)C#N |
| Pubchem Cid | 68580 |
As an accredited 2-Cyano-4-methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Cyano-4-methylpyridine is supplied in a 100g amber glass bottle with a tamper-evident cap, labeled with safety information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-Cyano-4-methylpyridine: Standard 20-foot container, securely packed in drums or bags, total weight ~16-18MT. |
| Shipping | 2-Cyano-4-methylpyridine is shipped in tightly sealed containers to prevent leaks or contamination. It should be stored in a cool, dry, and well-ventilated place, away from incompatible substances. During transit, it is classified as a hazardous chemical, requiring proper labeling and handling according to local and international regulations. |
| Storage | 2-Cyano-4-methylpyridine should be stored in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and protected from light. Store at room temperature, avoiding excessive heat or moisture. Proper labeling and secondary containment are recommended to prevent spills or accidental exposure. Use appropriate chemical storage cabinets if available. |
| Shelf Life | 2-Cyano-4-methylpyridine has a shelf life of at least 2 years when stored in a cool, dry, and tightly sealed container. |
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Purity 99%: 2-Cyano-4-methylpyridine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and impurity-free API production. Melting point 98°C: 2-Cyano-4-methylpyridine with melting point 98°C is used in fine chemical manufacturing, where it offers process reliability and controlled crystallization. Particle size <100 µm: 2-Cyano-4-methylpyridine with particle size less than 100 µm is used in catalyst formulation, where it promotes uniform dispersion and improved catalytic efficiency. Stability temperature up to 150°C: 2-Cyano-4-methylpyridine stable up to 150°C is used in high-temperature organic transformations, where it maintains chemical integrity throughout the reaction process. Water content <0.05%: 2-Cyano-4-methylpyridine with water content below 0.05% is used in moisture-sensitive synthesis steps, where it prevents hydrolysis and guarantees consistent product quality. |
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2-Cyano-4-methylpyridine hasn’t always turned heads in the world of specialty chemicals, yet it plays a quiet but important role in the laboratory. The underlying chemistry fascinates me, not just because of the way this molecule threads together a pyridine ring with a cyano group at the second position and a methyl group at the fourth. It’s small shifts like these in structure that open up new possibilities for synthesis and end uses. Whether you’re a scientist scaling up for industrial output or a researcher piecing together a pharmaceutical compound, the versatility of this compound stands out in real-world applications.
At its core, 2-Cyano-4-methylpyridine is a derivative of pyridine—a backbone for so many modern molecules. Adding a cyano group at position 2 doesn’t just modify the ring’s reactivity; it can shift the whole range of available reactions. That methyl at position 4 further tweaks electronic properties, making the molecule both more stable in some reactions and more labile in others. I’ve seen these subtle changes create major ripple effects in the lab, especially when precision counts. Sometimes the difference between success and wasted effort hinges on which derivative lands in your reaction flask.
Seeing a product spec sheet rarely captures the value of purity and consistency, but in my experience, these aspects matter more than we let on. No one wants to trouble-shoot a failed reaction and discover trace impurities in their starting materials. High-purity 2-Cyano-4-methylpyridine—often achieving assays above 98%—lets you focus on the reaction outcome rather than second-guessing your ingredients. The crystalline powder is typically off-white or light yellow; even these color differences can hint at subtle impurities or drying issues that sometimes fly under the radar. Those labs chasing electronic or pharmaceutical-grade results know how much easier it is to optimize a process with a lot where every gram behaves the same.
Medicinal chemistry has a long-standing relationship with pyridine derivatives, and 2-Cyano-4-methylpyridine is right in the mix. It’s a solid choice for building pyridine-based drugs or intermediates, where the cyano group opens doors for later functionalization. I’ve seen teams use it to anchor side-chains in newer classes of active pharmaceutical ingredients—those small changes often yield big improvements in solubility or metabolic stability. Beyond pharma, dyes, agrochemicals, and specialty polymers have all benefited from the more reactive cyano group, which can undergo cyclization, nucleophilic substitution, or reduction without disturbing the rest of the molecule. This reliability stands out especially in multi-step synthesis, where single-pot yields depend on reagents that won’t hijack unrelated sites on a molecule.
To appreciate 2-Cyano-4-methylpyridine, it's important to understand where it sits among its peers. Plain pyridine offers that basic ring structure, but lacks the added flexibility that a functional group brings in. Move to 2-cyanopyridine, and you get enhanced reactivity thanks to the electron-withdrawing group, but without that methyl group, some reactions run too hot or too cold. Toss in a methyl at a different position, say the third or fifth carbon, and the molecule’s reactivity pattern shifts yet again, sometimes in ways that don’t help with target synthesis. In the lab, I’ve noted that this particular substitution pattern—cyano at two, methyl at four—strikes a balance between manageable reactivity and selective activation, making it ideal for stepwise transformations where most intermediates need survival through challenging conditions.
No data point speaks quite like experience. I watched a colleague navigate a tough route to a heterocyclic pharmaceutical intermediate. The path looked like a straight shot on paper, but trouble set in when using generic pyridine derivatives. By turning to 2-Cyano-4-methylpyridine, and leveraging its stability during nitration steps, she saved weeks of column purification and batch-to-batch headaches. From my own experience with demanding Suzuki coupling reactions, this compound gave more predictable yields with fewer side reactions—especially when moisture crept into the process. Stability in the presence of minor contaminants is a practical blessing, particularly in industrial and scale-up runs where perfection is rare.
Working with specialty chemicals, you quickly realize there’s no shortcut around tight standards. The reliability of 2-Cyano-4-methylpyridine can ease audits and nods from regulatory agencies when purity is documented batch after batch. These days, with so much riding on raw material consistency—especially as pharma and electronics put more emphasis on traceability—sources offering current certificates of analysis, analytical data, and physical property profiling back up their claims with real evidence. In my view, that’s the cornerstone of trust in a supply chain thick with variables.
Global supply chain issues have affected nearly every specialty chemical, and 2-Cyano-4-methylpyridine isn’t exempt. Any researcher who’s spent late nights searching for substitutes—or faced price spikes from a supplier—knows the consequences firsthand. Sourcing has become a strategic consideration, not just about price but about consistency and lead time. Labs with backup suppliers or the ability to validate multiple lots maintain productivity while others scramble. If you’re setting up a new process, building in flexibility with sourcing early on saves time and frustration down the line.
Chemists know the drill: respect the reagents and they’ll often return the favor. 2-Cyano-4-methylpyridine, like most nitrile-containing aromatic compounds, calls for careful storage in airtight containers and cool, dry spaces. Exposure to air and moisture can provoke degradation, which means your best work sometimes pivots on a forgotten lid or a slow desiccator. Having spent long hours prepping for sensitive reactions, I pay attention to the little things—dedicating bench space, minimizing transfer steps, and using proper labeling. Safety goggles and gloves aren’t optional; while this molecule doesn’t boast acute toxicity like some industrial chemicals, it’s smart to protect against unexpected splashes or spills.
Chemical responsibility extends beyond the reaction flask. Waste management for compounds like 2-Cyano-4-methylpyridine is a key topic in labs and regulatory circles alike. Used solvents, rinsate, or excess product must find their way to proper disposal streams, not down the drain. I’ve seen sustainable practices take root where teams plan for waste minimization and solvent recovery from the start. Shifting to closed systems and reducing unnecessary solvent use goes a long way, both for the environment and the bottom line.
Innovation in the chemical industry often depends on the reliability of the building blocks. 2-Cyano-4-methylpyridine’s track record for purity and dependable reactivity has made it a preferred reagent in both academic and industrial settings. In drug discovery, this predictability can shave months off development when every trial counts. I saw one med-chem group test candidate after candidate, reaping the rewards of clean mass spec and NMR spectra with each use. For process chemists, fewer byproducts and less troubleshooting translate into smoother product release schedules.
With demand growing for more targeted drugs and sustainable agrochemicals, chemists keep searching for molecules that offer unique reactivity or selectivity. 2-Cyano-4-methylpyridine finds itself as a useful intermediate for creating nitrogen-containing heterocycles and even functioning as a ligand in transition metal catalysis. In some recent applications, I’ve seen research teams tweak reaction conditions and leverage the electron-withdrawing cyano group to drive regioselective transformations. It’s these subtle advantages that spark innovation in downstream products, from crop protection to smart materials, where every synthetic shortcut saves effort and resources.
Time after time, scaling up from milligram to kilogram exposes the limits of poorly characterized materials. The predictability of 2-Cyano-4-methylpyridine acts as a stabilizer when processes are pushed from benchtop to pilot plant. In my early days, I underestimated how minor tweaks during small runs—switching between lots or slight variations in humidity—could throw entire production batches into chaos. Consistent material from a trusted supplier means fewer sleepless nights for process engineers and greater confidence for the QC team signing off on released lots.
Given the thousands of pyridine derivatives available, narrowing down the best option isn’t always straightforward. Leaning on experience, I’ve found 2-Cyano-4-methylpyridine excels when the target compound requires a balance of stability and reactivity at distinct ring positions. Its unique substitution pattern suits steps where other derivatives either overreact or yield unwanted byproducts. Drawing clear lines between options on paper helps, but nothing substitutes for hands-on trials and direct feedback from process runs. At the end of the day, the best molecules are those that deliver under pressure, with minimal fuss and maximum results.
All too often, the gap between a successful small-scale reaction and an efficient industrial process comes down to impurity control. Trace levels of unreacted starting materials or side products can confound analytics, paint a misleading picture of yield, or simply gunk up downstream operations. Well-prepared 2-Cyano-4-methylpyridine sidesteps many of these pitfalls with documented impurity profiles and support from reputable vendors. Scaling up also introduces the need for equipment that can safely handle nitriles and pyridine derivatives—reliable extraction systems, careful temperature management, and vigilant sampling make the difference between smooth runs and costly downtime.
Analytical chemistry stands as the backbone of effective process control. For 2-Cyano-4-methylpyridine, routine use of HPLC, GC-MS, and NMR ensures real-time insight into quality, purity, and contaminants. Having audited labs that take shortcuts, I’ve seen productivity drop just from missed low-level contaminants. Keeping a sharp eye on analytics doesn’t just satisfy paperwork—it builds confidence for the scientists running complex syntheses or regulatory reviewers looking for ironclad evidence of compliance.
More often than not, the relationship with a chemical supplier counts as much as the quality of the raw material. Reliable suppliers offer more than a datasheet—they back up their product with technical support, current testing reports, and the willingness to troubleshoot when a process goes sideways. In my own experience, finding a partner who understands the stakes can turn a wall of chemical jargon into practical advice and successful outcomes. Scalable, documented production keeps things above board, and honest disclosure about any changes or shortages sets the stage for long-term collaboration.
As research moves steadily towards targeted synthesis and sustainable manufacturing, intermediates like 2-Cyano-4-methylpyridine fill the gap between broad-access commodity chemicals and designer molecules. Each new frontier—be it pharmaceuticals, crop science, or electronics—demands molecules with tailored properties and assured quality. I see increasing value in transparently sourced and well-characterized materials; they allow for innovation while keeping environmental and regulatory concerns in check. Leveraging these compounds for greener syntheses and reduced waste flows will define the next decade of chemical manufacturing.
Reducing chemical waste and environmental impact doesn’t mean slashing productivity. Small steps—like optimizing reaction parameters to cut down on excess reagents and byproducts, or cycling solvents and minimizing hazardous stream production—have made a difference in the labs I’ve worked. These best practices gain momentum when reinforced by transparent supply chains and third-party verification. To go further, integration of digital tools—AI-led prediction of reaction outcomes, real-time analytic feedback, and inventory management—will help push specialty chemicals like 2-Cyano-4-methylpyridine toward a more sustainable future.
As scientific research takes on digital transformation, chemists handling intermediates like 2-Cyano-4-methylpyridine need more than just technical know-how. Sharpening data literacy, learning to interpret signals from smart lab systems, and understanding the environmental implications of every step add new layers of responsibility and possibility. Training sessions, clear protocols, and access to up-to-date documentation make it easier for both new and experienced chemists to adapt and excel.
At the end of the day, the prevalence of 2-Cyano-4-methylpyridine in high-value chemistry stems not only from its chemical merits but from a combination of trustworthy sourcing, reliable quality, and real-world understanding of what users need. Matching user demand with expert technical service and transparent quality validation provides a platform for progress that benefits the entire chemical supply chain. Whether deploying this molecule in an R&D setting, fine-tuning a pilot plant, or overseeing sustainability benchmarks, knowing the story behind each bottle helps ensure the next breakthrough is built on solid ground.