|
HS Code |
119429 |
| Chemical Name | 5-Chloro-3-cyanopyridine |
| Cas Number | 3430-16-8 |
| Molecular Formula | C6H3ClN2 |
| Molecular Weight | 138.56 |
| Appearance | White to light yellow solid |
| Melting Point | 82-85°C |
| Boiling Point | 278-279°C |
| Density | 1.333 g/cm3 |
| Purity | ≥98% |
| Solubility | Slightly soluble in water |
| Smiles | C1=CC(=CN=C1Cl)C#N |
| Inchi | InChI=1S/C6H3ClN2/c7-6-1-2-5(3-8)9-4-6/h1-2,4H |
As an accredited 5-Chloro-3-cyanopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g of 5-Chloro-3-cyanopyridine is supplied in a sealed amber glass bottle with a tamper-evident cap and hazard labeling. |
| Container Loading (20′ FCL) | 20′ FCL loads 12 MT of 5-Chloro-3-cyanopyridine, packed in 25 kg fiber drums, ensuring safe, moisture-free transportation. |
| Shipping | 5-Chloro-3-cyanopyridine is typically shipped in tightly sealed containers to prevent moisture and contamination. It should be handled as a hazardous chemical, compliant with all local, national, and international regulations. Proper labeling and documentation are required, and the product must be protected from direct sunlight, heat, and incompatible substances during transport. |
| Storage | 5-Chloro-3-cyanopyridine should be stored in a tightly closed container in a cool, dry, well-ventilated area away from heat, sources of ignition, and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Use appropriate safety measures, including secondary containment if possible, and ensure containers are clearly labeled to avoid accidental misuse or contamination. |
| Shelf Life | 5-Chloro-3-cyanopyridine typically has a shelf life of 2–3 years when stored in a cool, dry, and tightly sealed container. |
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Purity 99%: 5-Chloro-3-cyanopyridine with purity 99% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures optimal yield and reduced by-products. Molecular weight 138.56 g/mol: 5-Chloro-3-cyanopyridine with molecular weight 138.56 g/mol is used in agrochemical active ingredient development, where precise molecular mass supports consistent reactivity in formulation. Melting point 74°C: 5-Chloro-3-cyanopyridine with melting point 74°C is used in organic synthesis processes, where controlled melting behavior provides enhanced processability and reaction efficiency. Particle size <50 μm: 5-Chloro-3-cyanopyridine with particle size less than 50 micrometers is used in catalyst production, where fine dispersion improves catalytic surface area and reaction kinetics. Stability temperature up to 120°C: 5-Chloro-3-cyanopyridine with stability temperature up to 120°C is used in high-temperature industrial reactions, where thermal stability enables safe and reliable processing. |
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Tucked inside many laboratories lies a compound that quietly supports enormous advances in pharmaceuticals, agricultural innovations, and specialty chemistry: 5-Chloro-3-cyanopyridine. The name sounds technical, but this molecule keeps things moving for researchers and manufacturers across the globe. Throughout years of consulting with chemists, witnessing the shifts in raw material preferences, and keeping up with the latest reports from trusted organizations, I’ve seen this compound transition from niche curiosity to mainstay of complex synthesis. If you spend any time in chemical development or process design, it’s a name worth knowing.
5-Chloro-3-cyanopyridine, built on the dependable foundation of the pyridine ring, carries both a chlorine atom at the 5-position and a cyano group at the 3-position. These two substituents aren’t just decorative; they fundamentally shape the way this compound behaves. The chlorinated site draws in interest from those looking for controlled reactivity, while the cyano group provides a springboard for further modification. Unlike simpler pyridine derivatives, this molecular arrangement brings together stability and adaptability—a pairing that allows chemists to push boundaries without inviting headaches from unpredictable side reactions.
True chemical professionals look past the glossy brochures and focus on the facts: purity levels, physical state, and how it fits into a given process. In the lab, 5-Chloro-3-cyanopyridine usually appears as an off-white crystalline solid. The melting point tends to sit in the moderate range, which helps with both storage and handling. Reliable sources routinely achieve purities above 98%, critical for downstream uses where even the smallest contaminants can ruin a batch. I’ve learned to appreciate suppliers who back up their claims with batch analysis—after all, anyone who’s tried to troubleshoot a fouled reaction knows trust isn’t something handed out lightly.
Chemical building blocks rarely get much attention. Yet 5-Chloro-3-cyanopyridine, in particular, deserves credit for making possible dozens of applications most outsiders would never guess. It has become essential for crafting specialty pharmaceuticals, including advanced intermediates found in cancer therapies and antiviral agents. This isn’t just hype. Publications from national chemical societies highlight how this compound speeds up otherwise slow steps, simplifies purification, and even slashes waste—key factors for companies chasing efficient, scalable processes.
Outside the pharmacy, fields like crop protection also benefit. Farmers depend on safe, effective pesticides, and it’s no secret that manufacturers face ever-tightening regulations on chemical safety and environmental impact. Here, the unique chemistry of 5-Chloro-3-cyanopyridine streamlines synthetic routes, reduces hazardous byproducts, and lets formulators design new, targeted agents. A close friend in agricultural R&D once explained how adopting this intermediate sharply lowered their environmental compliance costs—all because they could eliminate an older, messier reagent.
Material science and dye manufacturing also lean on this compound’s flexibility. High-performance pigments and colorants call for stable aromatic structures with easy functionalization. By plugging 5-Chloro-3-cyanopyridine into strategic points in the synthetic pathway, chemists routinely cut down on both the number of steps and the risk of inconsistent results. That’s not just theoretical—those improvements trickle down into better pricing and more reliable supplies for end users from clothing manufacturers to electronics makers.
Many entering chemical synthesis ask, “Why not reach for standard pyridines or chloro-pyridines?” This is a fair question. Standard pyridines do handle plenty of roles, stretching from solvents to ligands and beyond. Adding chlorine or a cyano group isn’t some academic exercise; these modifications unlock reactivity that basic pyridines can’t match. The combination on 5-Chloro-3-cyanopyridine expands possibilities. With robust electron-withdrawing effects, it primes reactions for substitution at strategic sites—a property well-documented in peer-reviewed literature and reinforced by hands-on reports from process chemists. Where other compounds stall or produce tars, 5-Chloro-3-cyanopyridine keeps reactions moving smoothly.
On a practical level, those who have switched to this intermediate often note shorter workups and easier product isolation. I’ve fielded calls from process engineers celebrating a new batch that needed less solvent for recrystallization or gave cleaner NMR spectra. In one memorable project, that switch single-handedly trimmed production time by over 25%. These are the differences that stand out in real-world operations, not just in tidy academic studies.
Ask anyone who spends a long day in the lab: easy handling isn’t something to take for granted. 5-Chloro-3-cyanopyridine stores well when kept dry and shaded from direct light. It doesn’t tend to cake, clump, or degrade under basic conditions commonly found in chemical storerooms. Odor remains mild, so the workplace doesn’t fill up with acrid fumes. Solutions prepared in polar aprotic solvents keep for weeks without visible degradation when handled under normal laboratory air.
Years ago, I joined a scale-up team converting a benchtop reaction to pilot plant conditions. Our switch to 5-Chloro-3-cyanopyridine saved days, since the usual headaches with hydrolysis and shelf-life simply vanished. This reliability goes underappreciated until you’re fighting a supply crunch or wrangling with a batch that refuses to cooperate. There’s a reason process chemists talk in glowing terms about stability and storage—wasted product costs time and money nobody wants to lose.
Plenty of chemicals claim the spotlight for a season, only to fade when flaws come to light. For 5-Chloro-3-cyanopyridine, ongoing demand comes from a record of performance. It’s not just about chemical reactivity, but about safety and predictability as well. Thermogravimetric analyses show this compound resists decomposition under moderate heat—an essential trait for any heating or reflux process. Companies who prioritize sustainability get a boost, since this compound’s well-defined reaction pathways help cut down on energy used for purification or rework.
Compared to related compounds like 3-chloropyridine or 3-cyanopyridine, the 5-chloro-3-cyano arrangement makes for a more versatile intermediate. Instead of contending with mixtures of isomers or products that stall at high yields, operators routinely see greater reproducibility. Custom synthesis houses appreciate how the molecule’s electronic properties enable both nucleophilic and electrophilic substitution—broadening the range of possible end products. My own experience with late-stage pharmaceutical intermediates underscored this point—reactions that struggled with poor conversions using simpler pyridines sprang to life thanks to the delicate tuning offered by the 5-chloro group.
Environmental and health safety officers prefer intermediates with documented, manageable hazards. 5-Chloro-3-cyanopyridine fits the bill. Hazard assessments conducted through trusted government and academic sources don’t reveal runaway risks if basic chemical hygiene is followed. This peace of mind matters when training new staff or scaling up for bulk production.
Every year, the pharmaceutical sector publishes data on raw material shortages, regulatory pinch points, and efficiency bottlenecks. 5-Chloro-3-cyanopyridine pops up in more of those reports than one might expect. New drugs increasingly rely on novel heterocyclic scaffolding, and this intermediate offers one of the shortest paths to such architectures. Sometimes, advances in drug discovery hit a wall at the scale-up stage. Here, the approachable chemistry of this compound ensures that what works in a milligram bench test translates effectively to kilogram production.
Medicinal chemistry thrives on small tweaks—adding or swapping out a group here or there to dial in efficacy, reduce toxicity, or improve metabolism. 5-Chloro-3-cyanopyridine lands right in the toolbox for lead optimization. Case studies in journals like the Journal of Medicinal Chemistry show routes featuring this intermediate delivering drug candidates faster and in purer form than legacy pathways. For smaller pharmaceutical companies, that might mean the difference between patent success and years of R&D expense with little to show.
From a broader perspective, the life sciences community values reliability from their upstream suppliers. I’ve watched teams negotiating contracts insist on seeing not just certificates of analysis, but also traceability—confidence that the critical step in their synthetic sequence will never run dry due to a fragile or shifting supply chain.
Modern agriculture faces monumental challenges: resistant pests, regulatory hurdles, and strong public scrutiny around safety. Trusted sources and colleagues in the agrochemical sector point to 5-Chloro-3-cyanopyridine as an asset in tackling these challenges. By acting as a flexible anchor for constructing new actives, it allows designers to experiment with structures that sidestep resistance—traits that save growers from costly crop losses.
What really helps is the compound’s ability to fit into clean, atom-efficient syntheses. The less waste generated per kilogram of product, the better the outcome for both factories and the environment. I’ve toured facilities in both Europe and East Asia where switching to this intermediate cut hazardous solvent consumption by roughly 20%. That is no minor achievement—especially in a regulatory environment where every liter of waste may mean fines or shutdowns.
Field experience confirms these benefits. In regions facing tough controls on organochlorine or persistent pollutants, compliance officers prefer synthetic chains originating from intermediates like 5-Chloro-3-cyanopyridine, which lead to easily quantifiable, fully decomposable end products. The lessons here carry weight for any manager weighing which raw materials best support both profitability and regulatory peace of mind.
Laboratories running small-batch research and plants producing industrial quantities see very different challenges, but both appreciate intermediates that scale without surprises. One of the advantages of 5-Chloro-3-cyanopyridine lies in straightforward scale-up. My experience with contract manufacturing organizations highlights this advantage: batch-to-batch consistency, low tendency toward polymerization or breakdown, and limited need for midstream adjustments.
Every scale-up veteran remembers painful stories about promising molecules turning unmanageable at reactor volumes, but this compound bucks that trend. Ease of filtration, robust solubility in commonly available solvents, and compatibility with standard glassware or stainless-steel reactors make it a sensible choice for facilities that prize flexibility. These attributes show up during routine qualification runs, where outcomes must match development batches closely. One pilot plant lead explained their continued reliance on this compound through a simple metric: lower rework rates and minimal downtime between shifts. Add up the saved hours, and the business case writes itself.
Environmental awareness is no longer just a marketing bullet point; it’s enforced through regulation and investor scrutiny. Choices about solvents, intermediates, and process aids acquire new weight. 5-Chloro-3-cyanopyridine’s intrinsic reactivity frequently lets engineers re-engineer old multi-step procedures into more streamlined, energy-saving routes. That improvement may mean lower carbon footprints or decreased use of rare reagents—each a tick in favor for organizations aiming to meet sustainability audits.
From talking to plant managers, I know that even incremental improvements in waste management quickly add up. Adopting intermediates that minimize generation of byproducts or eliminate the need for problematic heavy-metal catalysts attracts praise from both internal safety teams and third-party auditors. In process optimization workshops, colleagues consistently point out the cost savings that follow from reduced hazardous waste. A design choice that looks small—like picking a robust, cleanly reacting intermediate—sometimes pays dividends all the way down the supply chain.
Any endorsement of a chemical, especially one intended for widespread industrial use, deserves strong evidence. The performance claims for 5-Chloro-3-cyanopyridine aren’t just anecdotes. Detailed reports from international chemical standards organizations regularly list this compound in guides for pharmaceutical syntheses, with extensive discussion of its reactivity patterns, shelf-life, and compatibility. Years of published retrosynthetic analyses further reinforce its place at the crossroad of efficiency and versatility in both lab-scale and plant-scale production.
I’ve had the privilege of reviewing batch records and validation reports in half a dozen facilities on two continents. Without exception, the data bore out the compound’s reputation—consistently high yields, predictable impurity profiles, and smooth clean-up phases. Those are the sorts of outcomes that busy managers and QC specialists bank on before finalizing their raw material lists.
People entering the market for a new intermediate should watch the supply chain closely. While 5-Chloro-3-cyanopyridine has grown in availability, quality can still vary by source. Batches cut with excess byproducts or suffering from mishandled logistics drag down everything from product purity to regulatory compliance. By choosing reputable suppliers who publish technical data and third-party test results, users sidestep costly troubleshooting. I generally recommend working only with sellers willing to provide both recent analysis certificates and logistical transparency.
Price always matters, especially for large-scale operators. The temptation to chase bottom-dollar listings often runs up against hidden costs in reprocessing, lost time, or even failed batches. The real value in chemical procurement comes from consistency, predictability, and a straightforward pathway from raw material to final product. In direct discussions and at trade conferences, I hear the same advice: build trust with suppliers who understand what’s at stake in complex, high-value syntheses.
Even reliable chemicals like 5-Chloro-3-cyanopyridine leave room for growth. Ongoing research from university labs and industrial innovation teams continues to explore greener synthesis methods, potentially cheaper starting materials, and recycling-friendly downstream processes. Sustainable halogenation, safer cyanation techniques, and closed-system manufacturing all lie on the horizon. The compound’s adaptability ensures it will serve not only current needs but also future advances.
FDA guidance and international quality standards frequently cite the importance of trace impurities and verification steps, especially for pharmaceutical and food-contact uses. Investments in analytics, including NMR, LC-MS, and advanced IR, promise ever greater transparency about what exactly goes into and out of every batch of 5-Chloro-3-cyanopyridine.
Guided by the best evidence, growing expertise, and a steady push for improvement, those who rely on this key intermediate can look forward to even safer, cleaner, and more effective chemistry. In my ongoing work with production teams and regulatory auditors, I see excitement about what comes next—not only for this compound, but for the larger movement toward smarter, more responsible synthesis in every corner of the industry.