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HS Code |
646225 |
| Product Name | 6-Chloromethyl-2-Cyanopyridine |
| Cas Number | 10534-03-5 |
| Molecular Formula | C7H5ClN2 |
| Molecular Weight | 152.58 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 270-272 °C |
| Density | 1.23 g/cm3 |
| Refractive Index | 1.553 |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Storage Temperature | Store at 2-8°C |
| Smiles | ClCC1=NC=CC=C1C#N |
| Synonyms | 6-(Chloromethyl)picolinonitrile |
As an accredited 6-Chloromethyl-2-Cyanopyridine 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 6-Chloromethyl-2-Cyanopyridine, sealed, labeled with hazard warnings and chemical identifiers. |
| Container Loading (20′ FCL) | 20′ FCL container holds securely packaged drums or bags of 6-Chloromethyl-2-Cyanopyridine, ensuring safe bulk chemical shipping. |
| Shipping | **Shipping Description for 6-Chloromethyl-2-Cyanopyridine:** 6-Chloromethyl-2-Cyanopyridine is shipped in tightly sealed containers, protected from moisture and light. It should be handled as a hazardous chemical, compliant with relevant regulations (such as DOT, IATA, or IMDG). Ensure proper labeling, documentation, and segregation from incompatible substances during transit. Personal protective equipment is required for all handling. |
| Storage | 6-Chloromethyl-2-cyanopyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep it separated from oxidizing agents, strong acids, and bases. Store under inert atmosphere if possible to avoid moisture contact. Properly label the container and ensure access is restricted to trained personnel. |
| Shelf Life | 6-Chloromethyl-2-cyanopyridine should be stored cool, dry, and tightly sealed; typically stable for up to 2 years under proper conditions. |
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Purity 99%: 6-Chloromethyl-2-Cyanopyridine with a purity of 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Molecular Weight 152.57 g/mol: 6-Chloromethyl-2-Cyanopyridine with a molecular weight of 152.57 g/mol is used in agrochemical manufacturing, where it provides precise dosing and reaction control. Melting Point 60-63°C: 6-Chloromethyl-2-Cyanopyridine with a melting point of 60-63°C is used in custom chemical synthesis, where it allows process optimization under controlled temperature conditions. Stability Temperature up to 120°C: 6-Chloromethyl-2-Cyanopyridine with stability up to 120°C is used in industrial-scale reactions, where it maintains structural integrity throughout thermal processing. Particle Size <50 µm: 6-Chloromethyl-2-Cyanopyridine with a particle size less than 50 µm is used in solid formulation development, where it promotes uniform dispersion and improved reactivity. Water Content <0.5%: 6-Chloromethyl-2-Cyanopyridine with water content below 0.5% is used in moisture-sensitive reactions, where it minimizes the risk of hydrolysis and unwanted side reactions. |
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Modern chemical industries have seen remarkable shifts over the past two decades, especially in the field of pharmaceutical and agrochemical synthesis. I look at new intermediates with a mix of curiosity and practicality, always searching for that rare substance that creates genuine opportunities for improvement. Among a growing list of pyridine derivatives, 6-Chloromethyl-2-Cyanopyridine has cropped up with qualities both established and promising. Known by its CAS number 13444-24-1 and molecular formula C7H5ClN2, this compound steps forward for specialists eager to address nuanced research and manufacturing challenges.
Some may recall their first glimpse at the structure of 6-Chloromethyl-2-Cyanopyridine: a pyridine ring bearing a chloromethyl group at position six and a cyano group at position two. This particular arrangement invites further transformations; chemists can exploit both the reactive chloromethyl handle and the electron-withdrawing nitrile group. A typical batch comes as a white to light yellow crystalline powder, with a molecular weight of about 152.58 grams per mole.
Every flask or drum of this material speaks of careful handling and storage. During colder months in my previous laboratory, I learned not to underestimate the importance of well-sealed, light-tight containers to keep air and moisture from degrading the compound. Even routine weighing turns delicate when you deal with pyridine derivatives, given their potential to irritate if not treated with respect. There’s a slight, sharp odor some will recognize right away as characteristic of simple pyridine compounds.
For chemists, practical value always beats theoretical elegance. The combination of chloromethyl and cyano functions brings reactivity you rarely find together. At the bench, the chloromethyl group opens the door to a broad range of nucleophilic substitutions. If you’re working in medicinal chemistry, you can use it as a coupling partner with amines to create pyridylmethylamines, a class that populates multiple drug candidates. That cyano group shows its worth in further transformations—hydrolysis, reduction, or even addition reactions.
Colleagues working in agrochemical development have told me they depend on 6-Chloromethyl-2-Cyanopyridine for building more complex pesticide molecules. The path from starting material to final product often runs through this sharp-tasting powder, delivering reliable yields in a field where predictability matters a great deal. In pharmaceutical manufacture, developing lead compounds can mean days of trial and error with starting materials. The value of a pyridine intermediate, stable under storage but lively in the flask, can’t be overstated.
I’ve seen chemists debate pyridine derivatives late into the evening, each with opinions about optimal precursors. 3-Chloromethyl-2-cyanopyridine and 6-chloromethyl-2-cyanopyridine seem nearly identical on paper, yet their behavior diverges where it matters: reactivity, regioselectivity, and downstream product profiles.
A small shift in the chloromethyl group’s position can change the whole process. 6-Chloromethyl-2-Cyanopyridine tends to favor certain substitution reactions, steering products toward scaffolds favored in modern medicinal research. It forms the backbone of structures that 3-chloro analogs don’t reach efficiently. Nor does it overlap with simpler methyl- or cyano-substituted pyridines, which often require extra protective steps or show side reactions.
On a practical note, the stability and handiness of the 6-position derivative can reduce waste and streamline purification. That’s not academic theorizing—it translates to lower costs and fewer headaches, especially when scaling up. Some manufacturers lean on this intermediate because the crystallinity improves batch-to-batch consistency, an overlooked but important point if you’ve struggled with gummy reaction residues.
Talking to process development teams, you’ll hear about the real bottlenecks: raw material intake, reaction yield, ease of purification, and regulatory documentation. With 6-Chloromethyl-2-Cyanopyridine, these conversations simplify. Its primary claim to fame remains as an essential intermediate for multiple pharmaceutical and agrochemical syntheses.
In medicinal chemistry, the ability to drop a chloromethylpyridine moiety into an expanding scaffold can point toward antiviral, antibacterial, or oncological applications. Many pipeline candidates owe their existence, in part, to this compound’s dual reactive centers. Its presence in the route can reduce total step count for creating targeted therapies. For those engaged in hit-to-lead or lead optimization work, cutting redundant chemistry frees time and budget for more critical investigations.
Moving outside pharma, I’ve noticed agricultural R&D groups rely on it for semi-selective insecticidal agent synthesis. Used as a coupling partner, it performs well when you want consistent reactivity without unpredictable byproducts. Material scientists exploring functionalized organic layers have dabbled with this compound, exploring more specialized surface grafting thanks to the reactive chloromethyl arm. Every time a new application opens, supply chains and researchers benefit from its chemical resilience.
Many times I’ve seen a promising experiment go sideways due to inconsistent reagent quality. For 6-Chloromethyl-2-Cyanopyridine, purity level can make or break a synthesis. Impurities found at even small concentrations—such as unreacted precursors or side-chain contaminants—have the ability to poison sensitive downstream reactions. Reliable suppliers test every lot by HPLC and NMR, helping ensure what ships genuinely matches the product spec sheets, though even vigilant quality control isn’t infallible.
One overlooked issue lies in shipment and storage—particularly for those working far from central logistics hubs. Temperature swings and atmospheric moisture creep in unless you trust your packaging. I’ve received material past its shelf life, showing a distinct change in color and distinct lower reactivity. The realities of industrial-scale projects demand long-term stability and predictable behavior in chemical reagents, especially those at the heart of a synthetic route.
Handling protocols sit front and center. Getting this material on your gloves or accidentally inhaling small amounts can lead to quick respiratory or skin discomfort. Every lab with a bottle of 6-Chloromethyl-2-Cyanopyridine keeps clear safety directives and spill procedures visibly posted. In my early days, small lapses—rushed lab prep or lax attention to PPE—could cause bigger setbacks than just losing a few grams of product.
Sitting at the crossroads of utility and responsibility, producers and users of 6-Chloromethyl-2-Cyanopyridine must factor in environmental impact. Discharges, large or small, magnify when production volumes rise. Research into greener processing routes has been steady, with some manufacturers developing routes that limit chlorinated solvent use and cut down on hazardous byproducts. I’ve watched factories overhaul their waste-stream processes in response to tighter regulations, sometimes ahead of the deadlines, just to gain buyer trust and avoid problems that spiral out of control.
Those working in regulated industries—pharma especially—carefully track batch-level traceability for this intermediate. Audit trails, advanced documentation, and certifications often set apart suppliers in global trade. I remember one regulatory audit where the difference between smooth shipping and costly delay boiled down to a few pages of paperwork showing thorough material testing. Accountability keeps the entire sector honest, protecting both users and the wider community.
What keeps chemists and engineers reaching for 6-Chloromethyl-2-Cyanopyridine isn’t mere inertia or routine—it’s the intersection of reliability and creative promise. The last few years brought advances in cross-coupling chemistry and new catalysis strategies; now, chemists streamline routes to heterocyclic drugs and fine-tune agrochemical building blocks faster than before. I’ve seen collaborations sprout between universities and industry to harness these trends, pushing the boundaries of what a single intermediate can support.
I’ve watched colleagues experiment with blocked-isocyanate strategies, insert new payloads at the six-position, and modify pyridine rings for custom polymer systems—none of this possible without a robust, predictable intermediate. No one intermediate answers every research question, but this one’s run of solid performance, stability, and reactivity deserves its place on the shelf. It invites innovation rather than resisting change, helping new ideas reach the pilot plant stage and, sometimes, the market itself.
I remember years of scrambling to secure kilos for small-batch parallel experiments. Some suppliers only cared about ton-scale orders, leaving research teams to chase after small, fragmented lots. This can stunt homegrown innovation, forcing scientists to compromise or redesign routes around availability. Economic shocks, customs delays, and policy shifts keep the logistics teams on their toes, with the knowledge that a single missing shipment could halt critical work for weeks.
Larger buyers bring a different set of pressures—long-term contracts, reliability of access, and negotiable pricing. Building trust and open channels with core suppliers consumes extra time, yet it pays off with smoother inventory and less downtime. Some pharma and agri-tech leaders now diversify sourcing, holding multiple contracts to buffer against disruption.
We shouldn’t overlook the role of digitalization, either. I’ve worked with companies leveraging supply-chain tracking, automated reordering, and blockchain-backed traceability. These tools can’t guarantee smooth delivery for every batch, but they nudge the sector forward, making it more resilient and transparent for all players. Even small startups now participate more fully, with platforms letting them compare specs, batch results, and supplier track records before ever placing an order.
Sustainable chemistry grows out of daily habits more than grand pronouncements. Teams who regularly recycle spent solvents, minimize unnecessary waste, and design routes to maximize atom economy sow the seeds of longer-term health for their labs and the environment. Responsible use of 6-Chloromethyl-2-Cyanopyridine, from careful storage to complete records of use and disposal, forms part of that wider responsibility.
Those in academia don’t always have the resources for full-scale green chemistry programs, but they can still borrow good habits from industry—mixing batch sizes to match experimental scale, sharing surplus material, or investing in upgraded fume hoods. Students and younger researchers gain more than technical skills from handling specialty intermediates. They learn the habits and discipline of world-class labs, and carry those practices forward whether they land in industry, regulatory agencies, or education.
Markets respond to innovation, but only if the underlying supply chain supports forward momentum. Producers of 6-Chloromethyl-2-Cyanopyridine who anticipate tighter regulations or evolving end-use trends find ways to deliver higher-purity materials, invest in greener chemistry, or offer batch-specific customization at scale. Those are important steps if the sector wants to keep up with the demands of next-generation pharmaceuticals and crop science technologies.
Opportunities also open up for those investing in new process chemistry. I’ve seen pilot plants redesign their operations around water-based extraction or closed-loop solvent cycles, nudging the sector toward more sustainable growth. Research partnerships, sometimes even between small startups and global corporations, can drive the kind of transformation that benefits everyone—researchers, end users, and communities nearby.
For those working further upstream, every incremental gain in process efficiency compounds down the line, making it more feasible to try new approaches in product design. If we support a culture of responsible stewardship and practical experimentation, 6-Chloromethyl-2-Cyanopyridine will keep showing up in the stories we tell about real progress in applied science.
New entrants to this area face some hurdles, but optimism is warranted. Start by building direct relationships with vetted suppliers; those willing to provide current data on batch purity, stability, and handling protocols stand apart from the crowd. Invest in solid safety procedures and train staff on spill, fire, and inhalation hazards. Keep key documents retrievable and regularly reviewed, so no risk goes unchecked.
Don’t get drawn in by the lowest bid if it comes at the cost of shelf-life, documentation, or supplier responsiveness. The difference between a smooth synthesis and a failed batch often traces back to early buying decisions. For teams just establishing their research or production pipeline, build in time for quality checks and confirm you can scale procurement reliably before locking in any complex project.
Some gains also come from collaboration: reach out to peer labs, share tips, and check the latest literature for new applications. I’ve heard of scientists discovering new uses or solving bottlenecks just by reconnecting with colleagues they hadn’t spoken to in years. Modern science moves fast, yet relationships and routine best practices still make up the foundation of progress with specialty intermediates.
The impact of 6-Chloromethyl-2-Cyanopyridine extends past laboratory walls. Every kilogram delivered feeds into larger supply chains, stirring innovations in health, nutrition, and environmental safety. As chemical industries move toward more responsible growth models, each intermediate—no matter how specialized—plays its own part in the story. Responsibly sourced, tested, and handled, this compound adds value not only to finished goods but to the experimental culture that lies behind every breakthrough.
Sticking with good science and honest business practices, specialists, suppliers, and users keep this valuable tool working for progress that reflects not only technical achievement but a broad, thoughtful commitment to human betterment.