|
HS Code |
782157 |
| Chemical Name | 3-Chloro-4-methoxypyridine |
| Molecular Formula | C6H6ClNO |
| Molecular Weight | 143.57 g/mol |
| Cas Number | 3430-27-1 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 224-226°C |
| Density | 1.23 g/cm³ |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Flash Point | 103°C |
| Structure | Pyridine ring with chloro at position 3 and methoxy at position 4 |
| Smiles | COc1cccnc1Cl |
| Inchi | InChI=1S/C6H6ClNO/c1-9-6-3-2-4-8-5(6)7 |
| Refractive Index | 1.549 |
As an accredited pyridine, 3-chloro-4-methoxy- 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, tightly sealed, labeled with hazard warnings for pyridine, 3-chloro-4-methoxy-, with UN and CAS details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Standard 20-foot container, securely packed with drums or IBCs of 3-chloro-4-methoxy-pyridine, ensuring safe transport. |
| Shipping | **Shipping Description for Pyridine, 3-chloro-4-methoxy-:** Ship as a hazardous chemical, properly labeled as an irritant. Use tightly sealed containers made from compatible material. Protect against physical damage and segregate from oxidizers and acids. Follow all applicable regulations (such as DOT, IATA) and provide safety data sheet (SDS) with the shipment. Handle with appropriate protective equipment. |
| Storage | Store pyridine, 3-chloro-4-methoxy- in a tightly closed container, in a cool, dry, and well-ventilated area, away from heat, sparks, and open flames. Keep separate from strong oxidizing agents, acids, and bases. Avoid direct sunlight and moisture. Use in a chemical fume hood, and ensure proper labeling and secure shelving to prevent accidental release or spillage. |
| Shelf Life | **Shelf Life:** Pyridine, 3-chloro-4-methoxy- typically has a shelf life of 2–3 years when stored in a cool, dry, tightly sealed container. |
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Purity 98%: pyridine, 3-chloro-4-methoxy- with purity 98% is used in pharmaceutical intermediate synthesis, where high chemical yield and reduced impurity content are ensured. Melting point 36°C: pyridine, 3-chloro-4-methoxy- with a melting point of 36°C is used in organic reaction control, where precise phase management enhances reaction efficiency. Molecular weight 157.57 g/mol: pyridine, 3-chloro-4-methoxy- with a molecular weight of 157.57 g/mol is used in medicinal chemistry research, where predictable stoichiometry supports accurate compound design. Stability temperature up to 120°C: pyridine, 3-chloro-4-methoxy- stable up to 120°C is used in high-temperature synthesis, where thermal stability prevents decomposition under reaction conditions. Particle size <10 μm: pyridine, 3-chloro-4-methoxy- with particle size less than 10 μm is used in homogeneous blending processes, where uniform dispersion improves product consistency. Viscosity 2.5 mPa·s: pyridine, 3-chloro-4-methoxy- with viscosity of 2.5 mPa·s is used in liquid formulation systems, where optimal flow properties facilitate precise dosing and application. |
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Stirring a flask in an undergraduate lab, the curiosity for what makes a reaction tick often leads to unsung heroes like pyridine, 3-chloro-4-methoxy-. After years spent troubleshooting stubborn reactions or reviewing research papers, this compound keeps cropping up as a steady presence. At a glance, the name might seem like a mouthful. Break it down, though, and the structure—a pyridine ring carrying a chlorine at the 3-position and a methoxy at the 4-position—starts to tell its story.
Many think chemicals come straight out of textbooks, but discoveries in the lab show otherwise. Pyridine, 3-chloro-4-methoxy-, for example, serves a purpose that isn’t about flash but about backbone utility. Pharmaceutical labs look to it as a solid intermediate. It’s not a star on its own, but it often forms a key link in the chain leading to far more powerful molecules. Custom drug synthesis often demands this compound thanks to its very specific substitution pattern on the pyridine core, which guides transformations with reliability.
What sparks demand for this molecule among chemists often comes down to reactivity and selectivity. The chlorine on the ring gives you a handle for further coupling reactions, especially cross-coupling techniques like Suzuki or Buchwald-Hartwig. These methods have changed medicinal chemistry, letting researchers build complicated molecules piece by piece. The methoxy group, meanwhile, doesn’t just sit idly; it tunes the electron density, making the ring more amenable to certain transformations. Without tweaking like this, sticking to “generic” pyridines can mean dead ends or poor yields.
Every bottle on a lab shelf has a backstory, and pyridine, 3-chloro-4-methoxy- is no exception. Purity isn’t some abstract number here; in most labs, 98% or higher is a must, especially if the next steps involve sensitive catalysts or complex chiral synthesis. Even a 1% impurity can tank a project when working on multi-step synthesis or scale-up trials. Physical form counts, too. Most chemists expect this compound as a pale to light-yellow liquid. Small changes in how it pours and stirs can mean the difference between smooth production and lost batches.
Storage gets practical. Most storerooms keep it out of direct sunlight, in sturdy, sealed containers, away from oxidizers and acids. The smell alone—sharp, distinct, a bit like almonds—sticks in a memory bank, a reminder that proper handling keeps both process and people safe.
Standing at a lab bench, it’s tempting to wonder why not save money and use pyridine itself or some generic substitution. Real-world chemistry rarely rewards shortcuts. Substituting with a different derivative, or plain pyridine, can throw off an entire reaction route. The chloro and methoxy positions here are more than chemical trivia—they guide the molecule’s personality, dictating what reagents it plays nice with, how it weathers heat, and how reliably it delivers the desired product.
Discussions across research groups often highlight failed attempts with “close enough” alternatives. They rarely deliver, with side reactions and byproducts spiking costs and timelines. That’s why researchers stay loyal to the structure that works. This mosaic of chemical properties lets pyridine, 3-chloro-4-methoxy- fill a niche that other compounds can’t squeeze into.
Once you’ve tried to scale up a reaction based on textbook chemistry, you learn fast that not all fine chemicals are created equal. Impurities or off-color batches mean troubleshooting for days. That’s why, over years spent in both academic and industrial labs, a chemist comes to appreciate the reliability and predictability of reagents like pyridine, 3-chloro-4-methoxy-. Its stability under normal lab conditions keeps it from turning into an unpredictable wild card.
Technical writeups and lab meetings alike stress that one-size-fits-all doesn’t cut it. The drive for targeted, safer, and more effective medicines depends on starting with exactly the right building blocks. As regulatory scrutiny grows—driven by agencies across Europe, North America, and Asia—demand for traceable, high-purity intermediates rises. Every experiment and production run demands components that meet stringent standards, both for lab safety and ultimate patient outcomes.
Medicinal chemistry often starts with seemingly minor tweaks to a familiar scaffold. One methyl here, a chlorine there, and suddenly a molecule unlocks new activity or better bioavailability. Pyridine, 3-chloro-4-methoxy- enters the scene as a highly customized tool. It shows up in syntheses for anti-infectives, nervous system drugs, or even agricultural products, depending on where the research is headed. Patents often reference this molecule as a key starting point, proof of its established value. Its substitution pattern lets drug designers experiment with linked rings, heterocycles, or unique functional groups, pushing the boundaries of medicinal design.
Analytical chemists rely on benchmarks. Spectra—NMR, IR, mass spec—consistently match expectations with this compound. Chromatography runs smoother with fewer unexpected peaks, meaning reproducibility across labs. Scientists can spend their time exploring new questions, not untangling mystery impurities. By enabling consistent, reliable chemistry, pyridine, 3-chloro-4-methoxy- serves as an anchor in the sometimes-chaotic landscape of drug discovery.
Every chemical brings a trade-off. Pyridine derivatives, including this one, have their quirks—growing regulatory restrictions in some regions, safety protocols for handling, and always the drive to minimize waste and environmental impact. Labs that value sustainability keep a close eye on solvent use and reaction conditions. Process chemists tweak routes year over year, searching for higher yields and fewer byproducts.
Getting rid of residual chlorinated compounds at the end of synthesis can become a sticking point. Regulations increasingly push for greener chemistry, with both academic groups and industry giants publishing new protocols each year. In-house waste management teams focus on minimizing byproducts, aiming for cleaner reactions and smaller environmental footprints. Pyridine, 3-chloro-4-methoxy- isn’t immune to these changes, so ongoing research looks for more efficient, less polluting ways to make and use it.
Walk into a university chemistry department, and chances are a graduate student is pipetting this compound for a late-night run. The industrial sector, especially contract research and big pharma, also lean on it, sometimes at kilogram scales. Research labs prize its balance between reactivity and manageability, letting them try bold new routes without daily headaches about decomposition or unpredictable results.
Synthetic chemists have specific goals—maximize yield, minimize time, control every variable possible. For them, pyridine, 3-chloro-4-methoxy- isn’t an optional extra; it’s a foundation, trusted over years because it consistently delivers what’s promised. Analytical teams, meanwhile, count on its purity and traceability to avoid hours chasing down contaminant peaks. In production, predictability isn’t a luxury—it’s a requirement, and this compound delivers.
Experienced chemists tend to collect stories about failed syntheses and miraculous saves. Part of that comes down to picking the right intermediates. Compared to unsubstituted pyridine, pyridine, 3-chloro-4-methoxy- brings selective reactivity. The chloro substituent at the 3-position opens up cross-coupling options that simply don’t work on a bare pyridine ring. As for the methoxy group, it tilts electron density across the ring, changing how the molecule reacts with bases and nucleophiles—something you notice fast after a few rounds in the lab.
Other pyridines might offer a single functional group, but the special combination here gives options to chemists aiming for fine control. More complex transformations, like stepwise modifications or regioselective reactions, become feasible, with fewer surprises in the reaction flask and higher value in the final product. The outcome? Less time troubleshooting, more time advancing a project or meeting a deadline.
On the industrial side, big projects stand or fall on the consistency of their intermediates. In pharmaceuticals, agrochemicals, or specialty pigments, pyridine, 3-chloro-4-methoxy- helps deliver products that must meet ever-stricter purity and performance standards. Global supply chains depend on reliable sources that deliver clean, reproducible batches. Having a stable, predictable intermediate trims weeks or months off project timelines and removes the uncertainty that can frustrate both R&D and production teams.
From personal experience, watching pilot plant runs, having high-purity intermediates can spell the difference between a successful launch and costly, embarrassing recalls. Purity impacts not only chemical yields but also compliance, toxicity profiles, and shelf life. So, industrial chemists look for trusted sources, strong documentation, and chemistry that “just works.” Regulatory filings, whether to the FDA or EMA, hinge on demonstrating control at every step. Pyridine, 3-chloro-4-methoxy- consistently delivers, making itself indispensable in the sprint to market.
Chemists spend as much time worrying about health and safety as they do about reagents. Working with aromatic chlorides isn’t a casual affair. Gloves, goggles, fume hoods—these aren’t optional extras. The almond-like odor of pyridine, 3-chloro-4-methoxy- serves as a quick reminder of the care required. Chronic exposure issues, regulatory guidelines, and tighter Personal Protective Equipment standards are real concerns, especially as processes scale up from bench to pilot plant.
Training and experience bridge the gap between theory and safe practice. Younger researchers learn habits from mentorship and careful documentation—using the right containers, prepping quenching solutions, and running small-scale trials before committing to a full batch. Safety data sheets usually spell things out, but lived experience matters when it comes to managing spills, exposures, or emergency shutdowns. Responsible use ensures that chemistry moves forward without placing workers or the wider community at risk.
Where chemistry faces roadblocks, innovation steps in. Researchers keep hunting for greener synthesis routes, using less hazardous reagents and minimizing waste. Catalysis improvements let labs use smaller amounts of metals and solvents, reducing costs and environmental load. Continuous flow techniques, already adopted in several production facilities, offer better control and faster scale-up with less hands-on oversight.
Supply chain reliability drives home the need for secure, transparent sourcing. Covid-era disruptions taught the industry to value local suppliers and robust documentation. More labs audit their supply chains, track batch histories, and demand certifications from every supplier. The result: fewer surprises when scaling up, fewer batch failures, and a smoother regulatory path.
On the research side, the trend leans toward custom derivatization—designing closely related compounds with better activity, safer profiles, or easier breakdown in the environment. Green chemistry protocols, once a novelty, now appear in standard operating procedures worldwide. In this landscape, pyridine, 3-chloro-4-methoxy- keeps its place thanks to its reliability, but its future might also involve novel, more sustainable versions.
In an era of rapid innovation, reliability often turns into a rare virtue. Pyridine, 3-chloro-4-methoxy- holds onto its position by enabling new discoveries and supporting demanding industry standards. The balance of reactivity and manageability, traceable supply, and practical safety measures shapes its role as an unsung building block in chemistry’s ongoing evolution.
My own years of benchwork and production oversight have repeatedly shown how choosing the right intermediates paves the way for new therapies, cleaner processes, and more sustainable products. As chemists, we keep refining old methods and inventing new ones, but we always carry forward the value of trusted tools. Pyridine, 3-chloro-4-methoxy- isn’t glamorous, but its steady presence moves science and industry forward in meaningful, measurable ways.