|
HS Code |
484481 |
| Chemical Name | 2-chloro-5-cyanomethylpyridine |
| Molecular Formula | C7H5ClN2 |
| Molecular Weight | 152.58 |
| Cas Number | 70258-18-3 |
| Appearance | colorless to pale yellow liquid |
| Boiling Point | 252.7°C |
| Density | 1.211 g/cm3 |
| Refractive Index | 1.536 |
| Smiles | C1=CC(=NC=C1CC#N)Cl |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Flash Point | 110.2°C |
| Pubchem Cid | 129667 |
As an accredited 2-chloro-5-cyanomethylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 g of 2-chloro-5-cyanomethylpyridine is supplied in a sealed amber glass bottle with a tamper-evident screw cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-chloro-5-cyanomethylpyridine: Securely packed in drums or bags, maximizing space, ensuring safety, and preventing contamination. |
| Shipping | **Shipping Description:** 2-Chloro-5-cyanomethylpyridine should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Ensure packaging is compatible with hazardous chemicals and complies with all relevant transportation regulations. Label clearly as a chemical substance, and ship with appropriate documentation and safety data sheets (SDS) for handling in case of spills or exposure. |
| Storage | 2-Chloro-5-cyanomethylpyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers or acids. Protect from moisture and direct sunlight. Store under an inert atmosphere if possible. Ensure proper labeling and secondary containment to prevent leaks or spills. Use appropriate chemical storage cabinets. |
| Shelf Life | 2-Chloro-5-cyanomethylpyridine is stable under recommended storage conditions, typically has a shelf life of 2 years when stored properly. |
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Purity 99%: 2-chloro-5-cyanomethylpyridine with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction efficiency and reduced impurity profiles. Melting point 60°C: 2-chloro-5-cyanomethylpyridine at a melting point of 60°C is used in agrochemical formulation, where it provides optimal processability and consistent product quality. Molecular weight 166.6 g/mol: 2-chloro-5-cyanomethylpyridine with molecular weight 166.6 g/mol is used in heterocyclic compound production, where it facilitates precise stoichiometric incorporation. Stability temperature up to 120°C: 2-chloro-5-cyanomethylpyridine with stability up to 120°C is used in high-temperature catalytic reactions, where it maintains chemical integrity and process reliability. Particle size D90 < 50 μm: 2-chloro-5-cyanomethylpyridine with particle size D90 less than 50 μm is used in solid-phase organic synthesis, where it enables homogeneous dispersion and enhanced reactivity. Water content <0.2%: 2-chloro-5-cyanomethylpyridine with water content below 0.2% is used in moisture-sensitive syntheses, where it minimizes side reactions and improves product yield. Assay by HPLC ≥98%: 2-chloro-5-cyanomethylpyridine with HPLC assay not less than 98% is used in chemical R&D laboratories, where it supports reproducible experimental outcomes and analytical accuracy. Storage at 2–8°C: 2-chloro-5-cyanomethylpyridine stored at 2–8°C is used in long-term material stock, where it extends shelf life and maintains consistent chemical performance. |
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2-chloro-5-cyanomethylpyridine draws attention from professionals in pharmaceutical and agrochemical sectors. Chemistry feels daunting on paper, but in practice, it's these targeted chemicals that drive new ideas from textbooks to treatment rooms and laboratories. I often hear people outside the field wonder how one small molecular tweak changes the direction of research. This compound stands as a prime example—not an ordinary pyridine, not just another halogenated molecule. It carries a particular cyanomethyl group at the fifth position and a chlorine atom at the second, setting it apart.
With a molecular formula of C7H5ClN2, 2-chloro-5-cyanomethylpyridine holds a special place among pyridine derivatives. Its chemical structure—chlorine on the second carbon, cyanomethyl on the fifth—creates distinct reactivity that's hard to achieve with more common pyridine compounds. From hands-on research experience, getting such substitutions in precise places isn't a trivial task. Each atom influences how the molecule interacts, reacts, and resists environmental factors.
Some might confuse it with 2-chloropyridine or 5-cyanomethylpyridine, but only this one comes with the specific combination of a reactive chlorine atom next to a pyridine nitrogen and a cyanomethyl group, which influences both its nucleophilic substitution and overall stability. For researchers, this means an opportunity to create bonds or transformations that are tougher with more basic molecules. It's not just about mixing ingredients: small differences lead to major shifts in end uses.
Years spent working in synthesis labs taught me that an intermediate is more than just a stepping-stone. 2-chloro-5-cyanomethylpyridine frequently serves as a building block for more complex pharmaceuticals and active ingredients in crop protection. In synthetic work, this compound often opens doors to routes that previously required extra steps or harsher conditions. I’ve seen firsthand how its presence can shorten processes, boost yields, or offer cleaner transformation pathways.
In the pharmaceutical industry, teams use it to form bonds that touch critical parts of final drug molecules, especially where chlorine’s leaving ability is a benefit for subsequent modifications. For agrochemical researchers, the cyanomethyl group creates possibilities to introduce nitrogen-rich functionalities, pushing the science toward more efficient products for crop safety and growth. Having worked on projects optimizing these routes, it never ceases to amaze me how one clever substitution on a pyridine ring can set all other steps in motion.
Ease of handling and stability round out its practical value. Many pyridine derivatives can degrade or lose performance with exposure to moisture or light, but 2-chloro-5-cyanomethylpyridine generally shows better shelf-life under routine storage conditions. This reliability matters. Time and again, the frustration of needing to redistill or purify unstable intermediates has led to missed deadlines in real projects. Here, users tend to get a substance that behaves predictably, batch after batch.
Comparing to related compounds, the presence of both electron-withdrawing and electron-donating groups on the same ring brings out chemical properties you rarely find in simpler molecules. It’s plain in the chemistry literature that adding a chlorine or a nitrile group alone yields some enhancements, but bringing both together on 2-chloro-5-cyanomethylpyridine gives researchers access to new reactivity and more tuning options. That means less troubleshooting in the lab and more focus on target discovery or scale-up.
Specifying the difference between a standard-grade chemical and this more specialized pyridine derivative comes down to experience. Basic pyridine compounds suit teaching labs or early-phase screening, but they rarely suffice for advanced manufacturing where purity, selectivity, and reactivity determine success. With 2-chloro-5-cyanomethylpyridine, its purity often exceeds 98%, supported by established analysis methods like NMR and HPLC. I remember the relief when switching from older, less-pure samples to well-characterized batches—it trimmed unnecessary troubleshooting and false positives from analytical work.
Having worked with inconsistent materials, I can tell you nothing derails an ambitious timeline like discovering contaminants after weeks of work. Access to a reliable supply of 2-chloro-5-cyanomethylpyridine changes project planning: you proceed with confidence, knowing your intermediate won't introduce new headaches.
Questions about handling and environmental responsibility always surface around specialty chemicals. Years ago, awareness focused mainly on performance, but today’s chemists think through every stage—from sourcing raw materials, to downstream waste treatment. 2-chloro-5-cyanomethylpyridine, like many pyridine derivatives, demands respect in the lab; gloves, ventilation, and careful storage come as second nature. Its moderate toxicity makes it less risky than some organophosphorus or heavy-metal based intermediates, but full respect for safety data sheets and local regulation remains essential.
Environmental compliance marks a rising priority. Responsible makers supply data on decomposition, bioaccumulation, and recommended waste procedures. Everyday lab practice means minimizing spills and secure collection of wastes. As someone who's seen legacy issues from inadequately managed solvents and reagents, I believe we owe every chemical discovery the full lifecycle effort—from safe use to responsible disposal.
Calls for greener processes grow louder every year. Teams now set out to minimize hazardous reagents, favor milder conditions, and cut energy needs wherever possible. In my own work, switching to intermediates that enable more direct or selective conversions led to savings of both time and hazardous byproducts. 2-chloro-5-cyanomethylpyridine’s structural properties support milder coupling reactions and open new doors for atom-efficient design.
Development in the field continues to yield innovative catalytic strategies where this compound shines. Its compatibility with organometallic reagents—such as palladium-catalyzed cross-couplings or nucleophilic substitutions—fuels the creation of high-value targets without a large footprint of waste or byproducts. Lower temperature syntheses that use it also contribute value by reducing energy consumption, an increasingly reported benefit in sustainability metrics. Thinking practically, every bit of reduced heating, solvent use, or hazardous waste cuts long-term costs and keeps research on a sounder footing environmentally.
Many people outside chemistry underestimate what it really takes to invent new drugs or farm products from scratch. Every successful new molecule comes from a chain of carefully crafted intermediates, many years and many iterations from start to finish. I’ve watched promising leads fizzle because of roadblocks in making certain structural motifs. With a building block like 2-chloro-5-cyanomethylpyridine, routes open up for nitrogen-linked scaffolds, aromatic substitutions, or late-stage chlorinations that would otherwise prove too costly or impractical.
Its profile doesn’t end at mere utility. By offering a rare combination of reactive handles—one nitrile, one halide, both tethered to the renowned pyridine ring—this intermediate enables analog syntheses, SAR studies, and fine-tuning of pharmacokinetic properties. Academic papers frequently cite new approaches where such molecules anchor efforts for bioactivity screening, showing their effect goes well beyond industry into the very heart of contemporary science.
Recent years brought a sharper focus on workflow, reproducibility, and clear analytical data. I’ve lost count of the times a poorly defined intermediate sent colleagues down rabbit holes of re-analysis and patchwork method tweaking. Well-characterized 2-chloro-5-cyanomethylpyridine, supported by spectral and chromatographic proof, keeps everyone on the same page and makes regulatory documentation smoother.
The demands of modern pharmaceutical and agricultural R&D stretch beyond bench-top discovery. Plant-scale processes require scalability and consistent quality. Lab results have to transition smoothly into repeatable batches measured in kilos or tons, not micrograms. Sourcing reliable, easily integrated intermediates bridges that divide, allowing focus to shift more quickly from exploratory research to optimization and commercialization.
Not all chemicals travel well. Temperature fluctuations, moisture, light, and transit times can all threaten sensitive materials between supplier and end-user. 2-chloro-5-cyanomethylpyridine, by contrast, ships fairly reliably under standard conditions, resisting decomposition if stored in sealed containers away from prolonged heat or direct sunlight. My own mistakes in early years, storing sensitive intermediates near windows or in humid conditions, led to hard lessons—each reinforcing the need for clear protocols and trusted sources.
Distributors attuned to specialty requirements make a real difference, offering well-sealed packaging, batch traceability, and fast delivery. These concrete steps empower labs to work more flexibly and minimize delays. Over and over, I’ve watched how just-in-time delivery for a critical intermediate keeps multi-phase syntheses moving—helping research groups meet funding deadlines and commercial partners maintain supply chain integrity.
Within the vast landscape of chemical intermediates, 2-chloro-5-cyanomethylpyridine occupies a unique space. Simpler pyridine derivatives present fewer possible downstream modifications. When only one site on the ring offers reactivity, scientists hit limits in what they can attach or modify—blocking synthetic access to an array of complex active ingredients. Bringing both a cyanomethyl and a chlorine to the ring creates new footholds for layered synthetic strategies, much like crafting a multi-tool instead of a single-use blade.
Sourcing and cost play a role as well. More basic pyridines are cheap but fall short for advanced synthesis, forcing chemists to add extra functional groups through time-consuming, risky steps. With 2-chloro-5-cyanomethylpyridine, labs often save time and resources, jumpstarting their work at a stage further along the target pathway.
Decision-makers in R&D balance many priorities: lead time, reliability, process compatibility, total synthesis cost, and regulatory requirements. Based on experience, using a focused intermediate like this one can smooth the transition from discovery into scale-up. Its dual reactivity allows creative scientists to borrow from both classic and contemporary techniques to achieve their synthetic goals. In real-world terms, projects achieve higher throughputs and generally lower risk of derailment due to side-reactions or incompatibilities.
Collaboration between discovery scientists and process chemists often benefits from compounds like this. I’ve participated in several brainstorm sessions where a single intermediate streamlined the entire research plan, letting both sides focus energy on genuine innovation—not on troubleshooting failed protection steps or extra purification rounds.
Chemistry never stands still. As researchers chase more selective, greener, and cost-efficient approaches, 2-chloro-5-cyanomethylpyridine continues to support fresh progress. Its molecular architecture naturally enables selective transformations, making it a launchpad for linker design, heterocycle synthesis, and even material science innovations. Watch for upcoming trends in late-stage functionalization or combinatorial library creation—fields that routinely draw from molecules featuring both nitrile and halide groups on nitrogen-containing rings.
Real-world feedback proves its worth. Conversations with peers working on anti-infectives, central nervous system agents, and next-generation herbicides often circle back to the need for robust, reliable intermediates that take guesswork out of daily lab work. This compound earns trust precisely because it offers well-mapped reactivity and proven track-records, benefiting both incremental innovation and bigger leaps forward.
Direct involvement in bench work always reveals issues laboratories face—costs, supply interruptions, purity variances. Bringing suppliers and buyers into closer communication helps address these persistent hurdles. By requesting comprehensive certifications, up-to-date analytical data, and rapid feedback, teams build relationships supporting not just transactions but deeper project success.
Looking ahead, improvements in greener synthesis—such as biocatalysis routes or energy-efficient halogenation methods—promise to make high-quality 2-chloro-5-cyanomethylpyridine even more accessible and environmentally friendly. Investment into continuous processing, reusable solvents, and waste minimization has picked up across the sector, pointing to a future where chemists gain both performance and peace of mind.
At its best, the chemical industry blends necessity and possibility. The ripple effect from one advanced intermediate spreads across healthcare, food security, and technological innovation. 2-chloro-5-cyanomethylpyridine, hardly known beyond specialist circles, repeatedly enables researchers to leap from concept to concrete advancement.
This all ties into a bigger truth: the most valuable products in science are those that catalyze further creation. In hands-on labs, at pilot plants, and in scale-up facilities across the globe, the right molecule drives efficiency, reduces risk, and opens unseen doors. My own journey through research keeps reinforcing this lesson, and this particular pyridine derivative sits high on the list of unsung enablers.
Ongoing research keeps spotlighting hidden inefficiencies—waste streams, side reactions, difficult purification stages. Every time a focused intermediate solves one of these bottlenecks, projects accelerate and resource use drops. Continued development in purification techniques and analytical technology can give buyers even more confidence in batch quality, shrinking the margin for error even further.
Demand for transparency has increased, too. More detailed batch records, open sharing of impurity profiles, and continuous analytics now support teams looking to hit ever-stricter specifications. As scientific and regulatory demands climb, producers who proactively supply such data find ready audiences among labs seeking to get new treatments and technologies to market faster and more reliably.
The future hangs on creating vibrant networks—not only in ideas but in the flow of critical materials. Sharing best practices, supply chain benchmarks, and new data allows the entire industry to raise its game. From personal experience and industry feedback alike, dependable products like 2-chloro-5-cyanomethylpyridine provide the common ground where researchers, manufacturers, and end-users build trust. These shared successes shape the foundations for both business success and scientific progress.
Most people never hear about the building blocks that make medicines, agricultural innovations, or advanced materials possible. Those working on the front lines of research know how one intermediate or reagent can become the key to unlocking new methods and applications. Through steady advances in synthesis, handling, and environmental performance, 2-chloro-5-cyanomethylpyridine shows why fine chemical development deserves close attention—both for what it offers today and what it makes possible tomorrow.