|
HS Code |
495033 |
| Chemical Name | 3-Chloropyridine |
| Molecular Formula | C5H4ClN |
| Molar Mass | 113.55 g/mol |
| Cas Number | 626-60-8 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 181-183 °C |
| Melting Point | -33 °C |
| Density | 1.181 g/cm3 at 25 °C |
| Solubility In Water | Moderately soluble |
| Flash Point | 75 °C |
| Refractive Index | 1.547 |
| Pka | 3.62 |
| Odor | Characteristic, unpleasant |
As an accredited 3-chlorine pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 500 mL of 3-chlorine pyridine, labeled with hazard symbols, chemical name, and handling instructions. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 3-chlorine pyridine involves securely packing drums or IBCs, ensuring safety, compliance, and efficient space utilization. |
| Shipping | 3-Chloropyridine is typically shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It should be clearly labeled as hazardous and handled with care, complying with local and international transport regulations. The shipping environment should be cool and dry, and packages must be protected from heat, ignition sources, and incompatible substances. |
| Storage | 3-Chloropyridine should be stored in a tightly closed, clearly labeled container within a cool, dry, and well-ventilated area away from sources of ignition. Keep it separate from strong oxidizers and acids. Protect from direct sunlight and moisture. Use appropriate chemical-resistant containers, and store at room temperature. Ensure access is restricted to trained personnel and follow all relevant safety and regulatory guidelines. |
| Shelf Life | 3-Chloropyridine typically has a shelf life of 2-3 years when stored in a cool, dry, tightly sealed container. |
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Purity 99%: 3-chlorine pyridine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal by-product formation. Molecular weight 114.55 g/mol: 3-chlorine pyridine of molecular weight 114.55 g/mol is used in agrochemical formulations, where it facilitates precise dosage calculations for effective pest control. Boiling point 171°C: 3-chlorine pyridine with a boiling point of 171°C is used in organic reaction processes, where it enables stable performance under elevated temperature conditions. Stability temperature 60°C: 3-chlorine pyridine with stability temperature of 60°C is used in storage of hazardous chemicals, where it reduces decomposition risk during warehousing. Melting point −39°C: 3-chlorine pyridine having a melting point of −39°C is used in liquid-phase synthesis routes, where it remains in the desired phase for continuous operation. Residual moisture ≤0.5%: 3-chlorine pyridine with residual moisture ≤0.5% is used in fine chemical production, where it delivers consistent reactivity and prevents unintended side reactions. Refractive index 1.535: 3-chlorine pyridine with refractive index 1.535 is used in analytical laboratories, where it allows accurate concentration determination in mixture analysis. |
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3-Chlorine pyridine appears as a pale liquid, often favored by those in chemical synthesis and pharmaceuticals. The molecular structure distinguishes itself through a chlorine atom at the third position on the pyridine ring, a detail that gives it qualities other pyridines lack. This relatively small change on the ring opens a world of possibilities in downstream reactions. Chemists tend to reach for this compound when other basic building blocks don’t quite fit the bill, especially in fine chemicals, crop protection agents, and active pharmaceutical ingredients. It’s a cornerstone in my workbench whenever I’m developing intermediates that demand precise modification of the aromatic ring.
You can hear from colleagues in the industry—this material finds a home in a surprisingly wide set of branches. In agrochemical labs, the structural twist of the chloro group helps craft selective herbicides and insecticides that might otherwise struggle to balance potency and breakdown time in soil. In the world of pharmaceuticals, it takes its place as a crucial intermediate. I’ve relied on its reactivity in nucleophilic substitution reactions, especially when introducing new side groups without disturbing the aromatic core. Medicinal chemistry teams value how this compound allows subtle tweaks in drug scaffolds, which can then play a role in optimizing drug performance or metabolic stability.
Unlike many off-the-shelf pyridine compounds, 3-chlorine pyridine doesn’t simply act as a base for other chemicals. Its reactivity with nucleophiles stands out, giving formulators creative room. Whether working in solvents like DMF or acetonitrile or using it as a precursor in Suzuki-Miyaura couplings, its track record speaks for itself. Tasks that demand careful halogen placement find few substitutes as effective. In my experience, its lower boiling point compared to heavier halogenated pyridines makes recovery more manageable, a factor you come to appreciate while scaling up lab work.
The world of chlorinated pyridines isn’t one-size-fits-all. While some might reach for 2-chloro or 4-chloro variants, everyone in a lab for long enough knows that the subtle differences determine the pathway of a synthetic route. For instance, 2-chloro pyridine shows higher reactivity at the second position, but it’s notorious for encouraging unwanted side reactions due to proximity effects on the ring. By contrast, the chlorine atom in 3-position offers a more predictable reaction pattern, helping to cut down on cleaning up side-products—a boon in any production run.
Another difference appears in environmental handling. 3-Chlorine pyridine’s physical behavior sets it apart from heavier-halogen substituted versions, which often linger longer in the environment. Environmental safety teams value how it can be monitored and handled with established methods, often reusing standard equipment without major hassle. This has practical impacts—even outside regulated labs—where easier treatment and containment sometimes means the difference between going forward or pulling back a promising development.
Every bottle of 3-chlorine pyridine should match certain standards, as anyone responsible for high-purity syntheses knows. I’ve worked with grades that show purity upwards of 99 percent, which helps ensure reactions don’t suffer from unpredictable yields due to impurity knock-ons. For those turning the knob from the kilogram to the ton scale, flash point and volatility jump up the priority list. Excess water spells disaster for most coupling reactions, so low moisture content always wins points. Transparent supply chains now support traceability, keeping track of key physical properties and batch histories that give peace of mind—especially after witnessing the trouble one stray impurity can cause in scale-up.
Researchers who value consistency often compare viscosity and refractive index readings from batch to batch, watching for odd shifts that might signal problems. On tougher syntheses, deviations in these specs point directly to process issues upstream. With 3-chlorine pyridine, what you see is often what you get, but inexperienced eyes can overlook how crucial it is to source material that matches precise spec sheets, especially for work that flirts with regulatory gating.
Demands on fine chemicals keep shifting, thanks to pressures from regulatory updates, new market needs, and better green chemistry practices. I’ve had to evaluate replacements for more persistent or hazardous halogenated compounds as green chemistry initiatives push for safer alternatives. 3-chlorine pyridine holds its own in these conversations, offering both versatility and manageable risk when used responsibly.
Process chemists and compliance teams now often work closer than before when approving raw materials. Documentation travels alongside the product: history of synthesis, waste mitigation, even the carbon footprint of sourcing. Every extra step helps catch batch-to-batch variation that might have gone unnoticed just a decade ago. I’ve seen labs switch from 2-chlorine to 3-chlorine pyridine, largely on the back of improved safety data and easier handling—factors that once seemed minor but now tip the balance on big projects.
Every chemical comes with its quirks, and 3-chlorine pyridine proves no exception. The material carries a noticeable odor and can sometimes affect the comfort of those not used to handling stronger-smelling reagents. Storage calls for tightly sealed containers in a cool, dry spot—a lesson learned after an accidental venting in an old chemical store left a persistent smell for weeks. Safety teams advise using gloves, goggles, and proper fume hoods, which those on the shop floor usually do without complaint, remembering the comfort that comes from not having to clean up after a spill.
Shelf life attracted little attention years ago, but after one incident involving degraded stock that led to weaker reaction yields, every shipment gets tested for freshness. Sensitive intermediates respond poorly to any breakdown in starting material, making frequent checks a smart routine. Waste disposal remains straightforward when compared to more exotic chemicals, though every facility sets its own guidelines. Easy compatibility with incineration or water treatment plants relieves the load on smaller labs where waste must move quickly and cleanly.
University researchers shared how 3-chlorine pyridine’s flexibility allows projects to go forward without the delays that come from needing specialized reagents. Independent start-ups join the ranks, looking to carve out greener safer routes to market. In my time, I’ve seen shifts in best practice move from single-use specialty intermediates to adaptable workhorses—3-chlorine pyridine now sits comfortably in this latter category, used in everything from pilot studies to final manufacturing steps.
Big players in agriculture and pharma depend on reliable supply chains. Anyone in procurement remembers the sting of bottlenecks caused by sudden policy shifts or factory slowdowns. 3-chlorine pyridine, thanks to established synthesis routes and wide production, weathers shortages better than many niche analogues. That reliability gives operational teams more confidence to build long-term product lines rather than scrambling for short-term fixes each sourcing cycle.
Environmental teams pore over reports and regulations, especially when a halogen atom sits anywhere on a molecule. Compared to some polychlorinated aromatics, 3-chlorine pyridine shows more predictable breakdown patterns. This keeps it in the running for companies competing in regulated markets. I’ve seen companies opt for 3-chlorine pyridine over some other chlorinated compounds not just for its chemical utility but for an easier time on the environmental assessment checklist.
Safety professionals emphasize proper training. I remember one incident in a shared university space where someone underestimated the fume risk during open transfers. Many labs responded by tightening procedures and investing in sniffers and proper hoods. These days, the learning curve is gentler but everyone appreciates a reminder about risks, proper ventilation, and labeled storage. Clearing up myth from fact on handling helps people new to chemicals develop good habits—the kind that head off both small headaches and big accidents.
Chemical supply is global, and market price changes keep everyone on their toes. Older supply routes relied on major chemical hubs, with wide swings in lead times and costs. Over the last few years, I’ve brought in 3-chlorine pyridine from both established and emerging vendors, watching lead times settle as more producers join the market. Bulk buyers often get breaks, but small and mid-sized labs now enjoy better access thanks to regional warehousing and faster customs processes.
As labs adapt to new regulations and unexpected supply shocks, 3-chlorine pyridine stands out for its stable pricing compared to more exotic or highly regulated alternatives. During COVID-19 disruptions, supply kept pace in most markets, underscoring its place as a reliable staple. That steady pricing lets research teams plan better—and any chemist knows the value of a stable budget.
Ongoing demand for greener approaches means suppliers work harder to reduce process waste, improve yield, and find less energy-intensive synthesis methods for 3-chlorine pyridine. Partners in production look at catalytic pathways and bio-based feedstocks, hoping to shrink the environmental footprint even further. Pressures from global regulators continue to shape where and how the molecules reach the market; as a result, technical teams collaborate more closely with suppliers to refine specs and robustly validate new sources.
Education remains a powerful tool. Young researchers in training programs benefit from early exposure to both practical chemistry and safety culture surrounding reagents like 3-chlorine pyridine. Open forums across industry lines help spread best practices for its use, waste management, and substitution in large-scale processes where feasible.
Having worked hands-on with 3-chlorine pyridine, I’ve noticed how the details—odor, volatility, or even labeling routines—shape day-to-day work. It’s not the sort of chemical likely to make magazine covers, but that doesn’t make its contributions smaller. Thoughtful sourcing, careful handling, and respect for downstream impacts, combined with solid preparation in the lab, make for smooth projects and safer outcomes.
Chemical innovation doesn’t just rest on brand-new breakthroughs. It benefits from flexible, reliable reagents that respond well to evolving needs. 3-Chlorine pyridine fits this bill by supporting a broad range of advanced syntheses, offering value through consistent supply and adaptable application. From the first small-scale test to the final stage of a scale-up run, my work—and the progress of those around me—owes more than a little to this versatile, modestly sized compound.