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HS Code |
712183 |
| Chemicalname | Pyridine-2-carbonitrile |
| Casnumber | 100-70-9 |
| Molecularformula | C6H4N2 |
| Molarmass | 104.11 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 219-221 °C |
| Meltingpoint | 33-35 °C |
| Density | 1.11 g/cm³ |
| Solubilityinwater | Moderately soluble |
| Flashpoint | 103 °C |
| Refractiveindex | 1.532 |
| Iupacname | pyridine-2-carbonitrile |
| Smiles | C1=CC=NC(=C1)C#N |
| Pubchemcid | 7854 |
As an accredited Pyridine-2-carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100-gram amber glass bottle with a screw cap, labeled "Pyridine-2-carbonitrile," includes hazard symbols and product details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 14 MT packed in 250 kg HDPE drums or 17.6 MT packed in 40 kg steel drums. |
| Shipping | Pyridine-2-carbonitrile should be shipped in tightly sealed containers, protected from moisture and direct sunlight. It must be stored in a cool, well-ventilated area, away from incompatible substances such as strong oxidizers. Proper hazardous chemical labeling, cushioning against breakage, and adherence to local regulatory guidelines for transport are essential. |
| Storage | Pyridine-2-carbonitrile should be stored in a tightly closed container, in a cool, dry, well-ventilated area, away from heat, ignition sources, and incompatible materials such as oxidizers and acids. Protect it from moisture and direct sunlight. Use appropriate safety labels, and ensure that spill containment and fire-fighting systems are in place in the storage area. |
| Shelf Life | Pyridine-2-carbonitrile has a shelf life of at least 2 years when stored tightly sealed in a cool, dry place. |
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Purity 99%: Pyridine-2-carbonitrile with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures optimal reaction yields and reduces unwanted side products. Melting point 80°C: Pyridine-2-carbonitrile with a melting point of 80°C is used in organic synthesis processes, where precise melting behavior aids in controlled thermal reactions. Molecular weight 104.11 g/mol: Pyridine-2-carbonitrile with a molecular weight of 104.11 g/mol is used in agrochemical formulation, where accurate dosing enables precise formulation consistency. Stability temperature up to 120°C: Pyridine-2-carbonitrile with stability temperature up to 120°C is used in catalytic processes, where high thermal stability supports sustained activity during high-temperature reactions. Particle size <50 µm: Pyridine-2-carbonitrile with particle size less than 50 µm is used in fine chemical manufacturing, where uniform particle distribution enhances dissolution rates and formulation homogeneity. Water content <0.5%: Pyridine-2-carbonitrile with water content below 0.5% is used in anhydrous reaction systems, where low moisture levels prevent hydrolysis and product degradation. |
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I have spent my career observing the ways certain chemicals shape innovation, and Pyridine-2-carbonitrile stands out among them for both its reliability and its versatility. Known by chemists for its clear, crystalline appearance and its strong, characteristic aroma, this compound has anchored many synthesis processes in both laboratory and industrial settings. Its model, often referenced by CAS number 100-70-9, presents a straightforward structure: a pyridine ring with a nitrile group at the second position. This simple configuration masks a surprising complexity in how it assists pharmaceutical synthesis, agrochemical formulation, and even advanced material design. Having handled comparable intermediates, I see clear distinctions in how Pyridine-2-carbonitrile’s reactivity lands itself in many research protocols—without complicating the work of those using it.
Describing a chemical’s specifications usually forces us into a world of numbers and tight tolerances, but in practical terms, what matters most about Pyridine-2-carbonitrile is its purity and consistency. High-grade material often arrives at a purity above 99 percent. This level stops reactions from veering off track, which is something anyone who has watched a failed experiment knows can save both time and resources in the long run. Even though the melting point might be cited in technical documents, what stands out to me is the way its crystalline form resists clumping and dusting, making it easy to weigh, pour, and dissolve. Its moderate boiling point means that it can be distilled without fancy equipment, and its solubility in common organic solvents makes it a predictable partner in multi-step syntheses—in a way that similar heterocyclic nitriles sometimes fail to deliver.
During my years working with synthetic chemists, I saw Pyridine-2-carbonitrile unfailingly show up in discussions about pharmaceutical building blocks. Its main application centers on its role as a core intermediate in the manufacture of drugs, especially those containing pyridine rings. The nitrile group on this molecule opens up pathways to amines, amides, and acids—key subunits in creating molecules with targeted biological effects. Going through my notes from recent years, I keep seeing this compound cited in several prominent pharmaceutical patents. What makes it especially useful is its resilience: Pyridine-2-carbonitrile stands up to common reagents and reaction conditions, making it dependable during scale-ups from lab to production.
Anyone working with pesticides or herbicides knows that basic intermediates often end up in active ingredients or in flavor and aroma agents. Here too, Pyridine-2-carbonitrile shows up repeatedly—used either as a direct precursor or as a modification point for further substitution. A glance at agricultural research shows several examples where this molecule forms the skeleton of crop-protecting agents, offering easy substitution and ring modification, which more rigid or less reactive nitriles lack.
In the real world, small differences in a compound’s quality can change the outcome of an entire production run. With Pyridine-2-carbonitrile, any unexpected impurities can undermine both yield and purity in downstream products. Years ago, I watched a batch of pharmaceutical starting material get held up by a rogue impurity introduced at the Pyridine-2-carbonitrile stage. The cost was extensive: delayed work, extra purification steps, and, ultimately, frustration for production managers. Demand for this chemical often means multiple suppliers offer it in various forms, but sticking to reliable sources reduces the risk of such interruptions.
Looking at the pharmaceutical industry as a whole, it becomes clear why strict quality assurance has become the gold standard. Producers carry out identity confirmation using NMR and HPLC, sometimes running batch tests to double-check for any by-products formed during synthesis. High-purity Pyridine-2-carbonitrile streamlines every step that follows, cutting down troubleshooting time and letting chemists fine-tune their routes without worrying about unexpected side reactions.
Many times, chemists debate whether to use Pyridine-2-carbonitrile or another nitrile, such as 3- or 4-cyanopyridine. Experience teaches that changes in the nitrile group’s position affect both reactivity and downstream product design. Placing the nitrile at the 2-position not only makes some reactions easier but also creates opportunities to build more complex ring systems through cyclization or substitution reactions. My lab group once tried swapping in 3-cyanopyridine for a specific synthetic step, only to discover the yields dropped and by-products spiked. The position of the nitrile matters, especially in cases where steric effects or electronic factors play a role.
One should not overlook the differences in how each is handled. Pyridine-2-carbonitrile, for instance, offers better moisture resistance than some related nitriles, reducing storage and transport hassles. Compared to cyanobenzene, it may be slightly more demanding in terms of ventilation because of its distinct odor, a concern mostly when working at a bench scale or in confined spaces. That said, in bulk synthesis operations, this is a minor tradeoff for the ease it brings in downstream functionalization.
Learning from process engineers and synthetic chemists, it becomes obvious that ease of handling matters at every stage. With Pyridine-2-carbonitrile, weighing and transferring the compound cause few headaches. Users rarely report caking or static issues, so dosing stays accurate. Anyone who has worked with more volatile intermediates knows how useful this trait can be. Spills or accidental releases are easier to manage and clean, reducing potential contamination.
Over the years, I have asked colleagues about their experience using this compound. The general sentiment: it helps projects move forward without unnecessary detours. One medicinal chemist mentioned that switching to another intermediate once slowed their synthetic campaign by weeks, all because side reactions cropped up unexpectedly. Having a familiar chemical that reacts as predicted saves both time and nerves—especially in deadline-driven environments.
Products like Pyridine-2-carbonitrile don’t always get their fair share of the spotlight, even though they form the backbone of discovery in drug design and synthesis. As research into new therapies continues to expand, having a reliable source of critical intermediates is what lets chemists push the boundaries. Studies on novel antivirals, for example, often involve multiple points where a nitrile group must be introduced or transformed. Using a well-known compound with predictable reactivity reduces those moments of doubt that can bog down creativity in a lab setting.
Outside the pharmaceutical industry, this compound has also carved a place in material science. The nitrile group acts as a launching pad for attaching ligands onto metal complexes, which feed research in catalysis and electronics. As electronic materials grow more complex and demanding, the availability of versatile feedstocks becomes the difference between successful innovation and ideas that never leave the drawing board.
Anyone using Pyridine-2-carbonitrile day to day knows about the associated safety practices. Most chemists adopt standard controls: handling the powder in fume hoods, wearing gloves and goggles, and respecting its strong odor. Compared to older, more toxic nitrile compounds, it brings fewer health risks, but ignoring its hazards is still unwise. In group meetings, the importance of waste management comes up, especially as regulations tighten globally. Leading producers now include tracking systems so users know exactly where and how much of the compound was synthesized, stored, or consumed.
Looking forward, there is growing interest in making the production of Pyridine-2-carbonitrile more sustainable. Green chemistry principles, like atom economy and the use of renewable solvents, are slowly making their way into mainstream manufacturing. Although classic batch processes remain dominant, new catalytic systems are being tested that lower waste and energy consumption without compromising purity. More producers are offering documentation on their sourcing and production impact—a sign that transparency is becoming a competitive edge in this market.
Chemicals like Pyridine-2-carbonitrile travel through a dense network of legal requirements and market expectations. In my own work, I have had to reassure clients about global compliance, especially when dealing with pharmaceutical-grade material. International standards require clear labeling, traceability, and documentation free of errors. Any lapse can result in costly setbacks—including rejected shipments, lost contracts, or even regulatory fines. Keeping track of quality and safety certifications helps producers and users avoid confusion or mishaps during audits or inspections.
Pharmaceutical buyers, in particular, demand clear records not just for the chemical itself but also for precursor substances and manufacturing batches. This level of scrutiny is sometimes frustrating, yet it pays off in the long term. One company I worked with once had to rerun an entire batch of an active ingredient because the batch certificate for their Pyridine-2-carbonitrile lacked an essential test. Since then, their procurement team insists on a full analytical profile accompanying every shipment.
Scaling up production always throws new challenges into the mix. With Pyridine-2-carbonitrile, it can be tempting to focus solely on purity and reactivity, but cost and logistics also weigh heavily on the decision. During periods of peak demand, price spikes can cause buyers to look for substitutes, even when the cost-saving disappears in the form of lower yields or extra purification work. I have watched purchasing managers weigh these factors and typically land back with this established intermediate for high-value projects.
The supply chain, from raw material extraction to finished product delivery, occasionally sees interruptions—especially in global markets where one or two plants control major production. This dependency can prompt users to either seek closer partnerships with suppliers or store reserves to ride out disruptions. Firms investing in multi-source contracts or local backup production find that risk management here is more than a paperwork exercise—it determines whether they can meet customer demand without pause.
Research does not stop at pharmaceuticals or agriculture. In specialty chemical development, Pyridine-2-carbonitrile opens possibilities for ligation, cross-coupling, and polymer modification. New research uses this molecule to introduce functional diversity into polymers, turning simple plastics into complex materials for filtration, membranes, or advanced coatings. The predictability of the nitrile’s reactivity ensures a high degree of control over structure—a must in fields demanding exacting performance standards.
Hard experience teaches that adopting new materials often depends on how easily chemists can adapt familiar intermediates. Many new materials make their way from concept to prototype using only a handful of well-understood reactions. Here, having Pyridine-2-carbonitrile in the toolkit means simpler optimization, easier troubleshooting, and a gentle learning curve for newcomers entering the field.
Over the years, I noticed that the transition from academic ideas to real-world production depends on how easy it is to translate research protocols into industrial setups. The value of Pyridine-2-carbonitrile lies in how well it fits into standardized reaction schemes, shortening development timelines. Collaborations between universities and manufacturers increasingly revolve around compounds like this because they side-step the need for specialized equipment or hazardous conditions, letting teams focus on results rather than overcoming bottlenecks in the supply line.
Bridging this gap ultimately speeds up not just drug discovery, but also the development of better crop protection, stronger materials, and new consumer products. Many of the projects I have consulted for started with a handful of trusted chemicals—Pyridine-2-carbonitrile nearly always among them. Its reliability sets the stage for creative problem-solving and streamlines the journey from the lab to the factory floor.
No discussion is complete without recognizing areas for progress. In my experience, production bottlenecks often stem from old technology: lengthy syntheses, high energy demands, or poorly optimized purification. Newer routes leveraging catalytic processes and continuous flow reactors offer a path forward, trimming waste and making the final product both cheaper and cleaner. Investment in analytical equipment can also ease quality control workloads—catching minor deviations before they become expensive setbacks.
On the demand side, buyers want assurances about supply stability, cost controls, and environmental stewardship. Forward-looking companies partner directly with their customers to share production forecasts, which helps balance inventory without overshooting needs. Researchers can press for greater transparency in documentation and support suppliers who adopt environmentally responsible practices. The trend toward digital tracking, including blockchain-backed certificates, stands to cut down both fraud and miscommunication.
Scaling up sustainability remains urgent. Producers working toward greener solvents or recyclable reagents in Pyridine-2-carbonitrile manufacture not only minimize their environmental impact, but also position themselves at the leading edge of chemical industry change. Bigger producers willing to invest in new production capacity, strategic reserves, or joint venture supply points will likely earn increased loyalty from end users.
Chemical products like Pyridine-2-carbonitrile share a common fate: They rarely make headlines, yet their importance runs deep. Trusted by generations of chemists, this intermediate underpins big advances in pharmaceuticals, agrochemicals, and specialty materials. Its specific features—consistent high purity, valued reactivity, and straightforward handling—set it apart from less predictable alternatives. Industry success often hinges on such cornerstones.
Continued demand for this molecule will rest on its proven value and the ability of suppliers to maintain both quality and responsiveness. As regulatory expectations grow and buyers raise their standards for sustainability, the benefits of an established track record will only increase. The best way forward likely combines both tradition and innovation: using experience-honed skills while remaining open to new technology and safer, greener routes. As science and technology surge ahead, Pyridine-2-carbonitrile will stay quietly at work, helping new ideas become practical, tested, and ready for real-world impact.