|
HS Code |
180396 |
| Chemical Name | 2-Chloro-3-cyano-4,6-dimethylpyridine |
| Molecular Formula | C8H7ClN2 |
| Molecular Weight | 166.61 |
| Cas Number | 1119-73-3 |
| Appearance | Light yellow to brown solid |
| Melting Point | 60-63°C |
| Density | 1.19 g/cm3 (estimated) |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | CC1=CC(=NC(=C1Cl)C#N)C |
| Inchi | InChI=1S/C8H7ClN2/c1-5-3-6(2)11-8(9)7(5)4-10/h3H,1-2H3 |
| Purity | Typically >98% (commercial samples) |
| Storage Conditions | Store in a cool, dry place, tightly closed |
As an accredited 2-Chloro-3-cyano-4,6-dimethylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram sample of 2-Chloro-3-cyano-4,6-dimethylpyridine is sealed in an amber glass bottle with a tamper-evident cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 12 MT packed in 240 fiber drums, each containing 50 kg of 2-Chloro-3-cyano-4,6-dimethylpyridine. |
| Shipping | **Shipping Description:** 2-Chloro-3-cyano-4,6-dimethylpyridine is shipped in sealed, chemically resistant containers under ambient conditions. It should be labeled according to chemical safety standards, with proper hazard identification. The package must be protected from moisture and handled by trained personnel, complying with all local and international hazardous material transport regulations. |
| Storage | Store 2-Chloro-3-cyano-4,6-dimethylpyridine in a tightly sealed container, in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and moisture. Keep separate from incompatible materials such as strong oxidizers and acids. Properly label the container and use secondary containment if necessary. Access should be restricted to trained personnel following appropriate chemical safety protocols. |
| Shelf Life | 2-Chloro-3-cyano-4,6-dimethylpyridine is stable for at least 2 years when stored cool, dry, and tightly sealed. |
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Purity 99%: 2-Chloro-3-cyano-4,6-dimethylpyridine with purity 99% is used in pharmaceutical intermediate synthesis, where high product yield and minimal impurity formation are achieved. Melting point 102°C: 2-Chloro-3-cyano-4,6-dimethylpyridine with melting point 102°C is used in solid-phase organic reactions, where stable handling and consistent reactivity are ensured. Particle size <10 μm: 2-Chloro-3-cyano-4,6-dimethylpyridine with particle size less than 10 μm is used in fine chemical formulations, where enhanced dissolution rate and uniform dispersion are obtained. Moisture content <0.2%: 2-Chloro-3-cyano-4,6-dimethylpyridine with moisture content below 0.2% is used in moisture-sensitive synthesis steps, where side reactions are minimized. Stability temperature up to 80°C: 2-Chloro-3-cyano-4,6-dimethylpyridine with stability temperature up to 80°C is used in heated batch processing, where compound integrity is maintained during reaction. HPLC assay ≥98%: 2-Chloro-3-cyano-4,6-dimethylpyridine with HPLC assay of at least 98% is used in agrochemical precursor manufacturing, where formulation consistency and efficacy are supported. Residual solvent <500 ppm: 2-Chloro-3-cyano-4,6-dimethylpyridine with residual solvent content under 500 ppm is used in API production, where regulatory compliance and product safety are enhanced. |
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In the world of heterocyclic building blocks, 2-Chloro-3-cyano-4,6-dimethylpyridine stands as one of those compounds that has quietly enabled a wide range of modern chemical syntheses. Producing it is no simple step: there’s satisfaction in tackling its synthesis, optimizing purity at every stage, and reliably supplying a chemical that forms the foundation of many pharmaceutical and agrochemical paths. Commercial application means a lot more than just batch consistency or hitting published purities. What we repeatedly see is that quality at scale saves trouble later, and this kind of compound has earned a reputation precisely because of its reliability.
Let's talk about the molecule itself. With both a chloro and a cyano group attached to a dimethylpyridine core, this compound offers unique nucleophilic and electrophilic potential. The 2-chloro group opens up the ring to selective substitutions, which synthetic chemists appreciate when they’re building more complex molecules downstream. The cyano group at the third position enhances its reactivity and unlocks new reaction options—especially for heterocycle expansion or specialized coupling. Placing the methyls at the four and six positions may seem like a detail, but this arrangement has a direct impact on both steric protection and electronic influence, improving selectivity for certain synthetic routes.
We have worked for years to perfect our production model for 2-Chloro-3-cyano-4,6-dimethylpyridine. Current standard lots offer a chemical purity that consistently surpasses 98%, with residual moisture staying firmly below 0.5%. Most commercial customers ask us for the high-purity, off-white or pale yellow crystalline form. We routinely check for all possible contaminants, not just those typically noted in reference monographs. Customers sometimes request a slightly damp solid; more often, they ask for very low volatility and a product that stays stable during transport across seasons and continents.
Many in the market focus on meeting the most basic numbers for color, melting point, or purity. Years of customer feedback taught us to pay close attention to invisible details—trace metals, controlled particle size for reproducibility, and minimizing chlorinated byproducts. These aren’t extras; they make the difference between a straightforward downstream application and hours wasted troubleshooting unwanted side reactions. The result is a reliability our team feels proud to stand behind.
In practice, this pyridine derivative rarely gets used in isolation. Its real value shows up in the hands of pharmaceutical R&D, crop protection developers, and specialty chemical producers. Many leading pharmaceutical syntheses use it as an intermediate for constructing more complex ring systems or introducing functional groups that would otherwise be challenging to install. Several antiviral agents, kinase inhibitors, and plant-protection agents start with this scaffolding. With the cyano and chloro groups perfectly positioned, chemists achieve site-specific substitutions and cyclizations that define newer, more targeted therapies.
We’ve watched customers use it to establish selectivity for halide exchange, take advantage of the active cyano for amidine or amine formation, and leverage the dimethyl substitutions both to tune reactivity and to block unwanted nucleophilic attack. If you scan current literature, you’ll spot it as a backbone in custom ligands, antiviral screens, and active pharmaceutical ingredient precursors. Every year, new uses for this scaffold turn up, driven by chemists who find small improvements to reaction protocols because the raw material itself remains predictable year in, year out.
You could reach for plenty of pyridine derivatives, but very few hit the balance that’s possible with both cyano and chloro reactivity plus the shielding of dual methyl groups. Standard 2-chloropyridines or simple cyanopyridines just don’t offer the same selectivity. In our view, that selectivity in subsequent reactions is the key reason many R&D teams keep returning to this specific intermediate. Unwanted side reactions or product mixtures cost far more over time than small up-front savings; our product’s precise substitution pattern streamlines nearly every step from scale-up to purification.
Comparisons often come up with 2,6-dichloropyridine or 3-cyanopyridine, both of which are routine in chemical catalogs. Chemically, these lack the unique balance of both electron-withdrawing and electron-donating influence found in 2-Chloro-3-cyano-4,6-dimethylpyridine. For instance, in nucleophilic aromatic substitution, our product enables much milder reaction conditions—saving reaction time, cutting back on harsh reagents, and improving environmental profiles for finished pharmaceutical or agrochemical products. End users frequently see higher yields and fewer chromatographic headaches. We hear this from both small custom synthesis teams and the production lines of established bulk manufacturers.
Formulation experts and purification chemists notice the difference—products made from our compound are more consistent in crystallinity and less likely to harbor persistent minor impurities. These seemingly minor benefits mean less need for repeated purification cycles, smoother scale-ups, and more robust process validation.
Every batch receives a careful focus on logistics and storage stability. The product stays dry, packaged in chemically inert liners, and moves through controlled environments that match the season and shipping destination. Over the years, we’ve optimized packaging upgrades after seeing real-life challenges. Exposure to ambient humidity caused early batches to develop clumping or minor color changes—improvements in our process and logistics now prevent most of those headaches. Only a chemical maker who has seen and solved these issues at scale can share best practices, such as minimizing air headspace, using high-density barrels, and confirming batch integrity even after long ocean transit.
We learned from practical experience that customers want a product that stands up to months in storage without degradation. Our QC team tracks stability profiles closely and regularly shares data with long-term partners. Those pursuing regulated drug intermediates value this documented shelf life; for agricultural innovators, it eliminates worries about seasonal or product launch delays.
One challenge still under debate in the industry involves the recycling and reuse of transport containers to reduce environmental footprint without compromising chemical quality. This is an area we’re actively exploring, as reducing single-use plastics aligns with operational sustainability goals, but always gets weighed carefully against product safety.
Raw material choices matter—sourcing high-quality starting materials directly impacts both purity and yield. Over years of scale-up work, we put together a network of suppliers that provide documented, contaminant-controlled inputs. We see some competitors cut corners with recycled intermediates or poorly controlled bulk materials. From experience, those shortcuts never pay off. Problems show up later in downstream impurity profiles, or even worse, in the stability of the finished product itself.
We believe advances in pyridine chemistry should support responsible practices as well. Many of our process steps now use less harsh solvents or are run under improved energy conditions thanks to continuous flow setups and targeted catalyst use. Reducing chemical waste, capturing solvent streams, and upgrading cleaning routines have not only helped maintain purity but also keep the work in step with environmental and regulatory priorities worldwide. Working with customers whose end products face strict regulatory review taught us the value of full traceability—not just in paperwork but in practical, day-to-day plant operations.
Manufacturing at scale tests every detail of a chemical process. We deal firsthand with the jump from hundred-gram pilot lots to multi-ton annual production. Small changes in temperature ramps or solvent selection turn out to matter a lot; one missed impurity can throw off an entire batch downstream. Batch-to-batch reproducibility depends on both skilled operators and well-maintained analytical instruments. We routinely invest in in-process controls, frequent calibration of GC and HPLC systems, and targeted sampling at critical points. This approach ensures the product delivered today matches the one delivered six months ago, which in turn matters for regulated applications—and for any downstream partner building up an archive of process validation data.
One recurring challenge for 2-Chloro-3-cyano-4,6-dimethylpyridine comes from controlling chlorinated and nitrogenous byproducts. These minor components require careful monitoring. We don’t just rely on traditional limit tests. Instead, we sample for a wider range of impurity classes, using NMR, LC-MS, and detailed trace analysis. Over time, investing in this level of control has saved countless hours on the customer end, as unpredictable impurity spikes can derail weeks of expensive synthesis further down the line.
Shipping and handling protocols were not always so rigorous; early on, we saw a clear link between poorly controlled transit and minor but frustrating impurity profile changes. Since then, we’ve created a feedback loop—customers tell us about unexpected findings, and we adapt batch control documentation and transit processes. This kind of responsiveness is only possible when the people who make the material also own the responsibility for its journey, from plant to client.
Manufacturing pyridine derivatives means dealing with materials that demand respect for safety and regulatory demands. We draw directly on experience working with auditors and customer QA teams preparing for inspection. Complete and accurate batch traceability has become a standard, not an afterthought. Proper classification under hazardous goods regulations, provision of in-depth certificate of analysis, and batch-level impurity mapping aren’t optional in our view. Feedback from customer safety reviews regularly leads to updated handling instructions and fresh training for shipping partners.
Auditors and regulatory bodies focus hard on documentation, but what matters most to users is real-world chemical stability and known impurity profiles. End-users developing regulated end products—whether pharmaceuticals in clinical pipelines or crop protection agents under review—depend on this transparency. We build long-term trust by sharing analytical data and remaining open about the process modifications that take place after scale-up. We also note that many downstream regulatory submissions now require source statements and full trace impurity data; consistently meeting these evolving standards calls for active engagement, not just a static set of test results.
One of the things that makes this compound a favorite among chemists is how dependable it has remained over changing research priorities. Years ago, customers ordered mostly for pilot-scale pharmaceutical intermediates and academic research. In the last several years, we’ve supplied growing quantities for crop science projects, flavor and fragrance innovation, and experimental materials with tailored charge properties.
Many breakthroughs in synthesis rely on having a stable supply of a core building block. We’ve advised on scale-ups where a team uncovers a new variant of cyclization or a regioselective substitution based on this pyridine framework. Each project that succeeds on our raw material adds something to the collective toolbox of organic synthesis. Every tough downstream challenge—tackling impurities, developing greener protocols, meeting ever-rising regulatory hurdles—makes our product and process better.
Collaboration with end users—especially when problems arise—has done more to shape our production philosophy than any textbook or reference monograph. Years of experience in troubleshooting: those cycles of listening, testing, and iteration have improved not only product performance but also packaging and logistics.
A recent example involved a customer scaling a new precursor synthesis. They ran into issues with unexpected color development and solubility shifts. Our technical team ran parallel batch assessments, shared real impurity data, and jointly reviewed every stage from storage to end use. Working with the chemists, not just supplying them, uncovered a minor but crucial shipping condition issue. Fixing that problem improved performance not only for them but across every downstream process using the same batch. Those shared wins are some of the most satisfying aspects of the job.
Partnerships with both established multinational groups and smaller research teams have shown us that no two projects look the same. Some customers care most about scale-up stability and bulk delivery; others focus on extremely tight impurity profiles for complex small-molecule drug programs. The diversity of real-world use cases—from grams in the lab to tons on a factory scale—fuels process improvements that eventually benefit the entire market.
We focus on producing a reliable, reproducible chemical that doesn’t just meet the lab’s minimum specifications, but actually helps chemists move their projects forward. Every batch is built on lessons learned, both from our own experience and from working closely with our user base. Over time, our product’s balance between reactivity, purity, and predictable downstream outcomes has become its real value. The difference comes not from published standards, but from a hands-on commitment to making a better solution for diverse and demanding applications.
For those working at the frontier—developing the next generation of pharmaceuticals, agricultural actives, or functionalized materials—the confidence that comes from a stable supply of a trusted intermediate is priceless. In our view, it is this ongoing, direct engagement with our partners that allows us to offer both product and insight, supporting advances in chemistry that reach far beyond our own doors.