|
HS Code |
620920 |
| Name | 4-Chloro-5-methylpyridine |
| Cas Number | 70258-18-3 |
| Molecular Formula | C6H6ClN |
| Molecular Weight | 127.57 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 191-193 °C |
| Melting Point | -13 °C |
| Density | 1.169 g/cm3 |
| Refractive Index | 1.535 |
| Flash Point | 73 °C |
| Solubility In Water | Slightly soluble |
| Smiles | CC1=CN=CC(Cl)=C1 |
| Pubchem Cid | 2755134 |
As an accredited 4-Chloro-5-methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 4-Chloro-5-methylpyridine is supplied in a sealed amber glass bottle with hazard labeling and secure screw cap. |
| Container Loading (20′ FCL) | 20′ FCL can load about 14 MT of 4-Chloro-5-methylpyridine, packed in 200 kg drums, palletized or non-palletized. |
| Shipping | **4-Chloro-5-methylpyridine** is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It should be transported under ambient conditions, labeled according to hazardous material regulations. Standard shipping precautions for flammable, toxic, or irritant chemicals apply. Ensure compliance with local, national, and international transport regulations for safe delivery. |
| Storage | 4-Chloro-5-methylpyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible materials such as strong oxidizers. Avoid contact with moisture. Keep the container clearly labeled and protected from physical damage. Ensure storage area follows appropriate chemical safety regulations and restrict access to authorized personnel only. |
| Shelf Life | 4-Chloro-5-methylpyridine 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%: 4-Chloro-5-methylpyridine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimized by-product formation. Melting Point 46°C: 4-Chloro-5-methylpyridine with a melting point of 46°C is used in agrochemical formulations, where it facilitates controlled solid-state handling and processing. Stability Temperature 120°C: 4-Chloro-5-methylpyridine with stability up to 120°C is used in high-temperature catalytic reactions, where it maintains chemical integrity and consistent reaction efficiency. Moisture Content ≤0.2%: 4-Chloro-5-methylpyridine with moisture content ≤0.2% is used in API synthesis, where it reduces unwanted hydrolysis and ensures product purity. Molecular Weight 129.57 g/mol: 4-Chloro-5-methylpyridine with molecular weight 129.57 g/mol is used in heterocyclic compound construction, where it provides precise stoichiometry control in multi-step reactions. Particle Size ≤50 µm: 4-Chloro-5-methylpyridine with particle size ≤50 µm is used in fine chemical blending, where it enables homogeneous mixing and accurate dosing accuracy. |
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Chemistry unlocks new possibilities every year, and 4-Chloro-5-methylpyridine quietly stands among the lesser-known but highly dependable starting points for progress in labs and manufacturing floors. I first learned about this compound in a chemistry lab packed with busy researchers—some deep in the hunt for new agrochemical solutions, others trying to tailor molecules for drug development. At a glance, its structure looks straightforward: a pyridine ring with a chlorine atom at the four position and a methyl group at the five. This small change compared to unmodified pyridine gives it different qualities, making it useful for a range of applications that require precise molecular tinkering.
Working in research, the difference between compounds can come down to a single atom’s position, shaping everything from how a raw material handles reactions to how the final product behaves. 4-Chloro-5-methylpyridine’s makeup brings unique reactivity, letting chemists build more complex molecules for specialty applications. Several years back, a colleague used it preparing building blocks for an active pharmaceutical ingredient. Using the right variant cut unnecessary steps, saving time and minimizing waste. There’s real satisfaction finding a tool that delivers on reliability and fits the job at hand.
In research and production, consistency takes priority. A compound like 4-Chloro-5-methylpyridine often appears in a clean, crystalline or liquid form, depending on temperature and humidity, with purity reaching over 98 percent in quality-controlled batches. Most reputable suppliers ensure the material contains only trace impurities. Purity levels matter because they affect the yield and safety of downstream products—something that’s hard to appreciate until you’re running trial reactions at scale. A few years ago in a pilot plant, I saw technicians examine each incoming lot using NMR and GC analysis to weed out anything that could spoil a carefully calibrated process. With thousands of dollars of material riding on a sequence of steps, even a subtle hitch shows up fast. 4-Chloro-5-methylpyridine usually drops into a workflow without drawing attention—a sign it’s the right tool.
Its chemical properties set the tone for safe and effective handling. With a molecular formula of C6H6ClN and molecular weight of roughly 127.57 g/mol, its structure resists breakdown in air and light under normal storage conditions, reducing waste. It carries a distinctive, slightly pungent odor, which seasoned hands quickly recognize in the lab. Safety data points to it being less hazardous than more reactive pyridines, but personal protective equipment and good ventilation remain part of best practice. Personally, I’ve always stored it in airtight glass containers, away from strong acids and oxidizers, to avoid any unplanned reactions.
In my experience, 4-Chloro-5-methylpyridine rarely finds itself in the consumer spotlight, yet it quietly supports big advances behind the scenes. It earns its keep as an intermediate—a critical stepping stone—in making more complex chemicals. For instance, several years ago, we needed a reliable way to produce a key precursor for crop protection products. Related pyridine derivatives couldn’t match 4-Chloro-5-methylpyridine’s selectivity. Its reactivity enables smooth substitution or coupling with various functional groups, lowering the risk of unwanted side-products.
Beyond crop protection, the pharmaceutical sector frequently leans on this compound. Medicinal chemists use it as a scaffold while developing new drug candidates, especially where selectivity and stability can save weeks of tedious trial and error. I recall it acting as a bridge compound while designing small molecule inhibitors—an example that sticks because removing even a single purification step shaved costs considerably and sped up delivery to clinical collaborators.
This molecule isn’t limited to the lab. Industrial chemists look for intermediates that shoulder scale-up without buckling under higher temperatures or reaction speeds. In one industrial setting, the smooth conversion of 4-Chloro-5-methylpyridine into specialty dyes stood out. Its controlled reactivity reduces side-product formation, allowing for a more streamlined purification process. Colleagues in the materials science space have mentioned its use to insert functional groups in polymers for electronics—areas where custom building blocks help meet strict quality targets.
Not all substituted pyridines pull their weight the same way. Over time, I’ve worked with a variety of chlorinated and methylated pyridines. Modest as it seems, moving either substituent to a new position radically alters the reactivity. For example, 2-chloro-5-methylpyridine proved trickier under nucleophilic substitution, derailing what looked like a promising reaction pathway. Replacing the methyl group with bulkier substituents changed the melting point and made the compound less predictable during scale-up.
Compared to other pyridine derivatives, 4-Chloro-5-methylpyridine often comes with a smoother reaction profile. Academic and patent literature supports this: its electronic configuration steers reactivity toward desired products with fewer side steps. Colleagues have noticed that 3-chloro-5-methylpyridine tends to produce higher levels of undesired byproducts, which increases downstream purification demands. One process engineer once mentioned weeks lost to troubleshooting byproduct removal until they settled on the 4-chloro isomer.
Taking cost into account, this compound hits a sweet spot. Specialty pyridines with more demanding synthesis require extra work and price themselves out of reach except for niche uses. 4-Chloro-5-methylpyridine, sitting between the basic and heavily modified options, gives enough flexibility for further modification, letting researchers balance cost, scalability, and performance. In my experience, the result is a compound preferred by both bench scientists and process engineers.
Looking at current trends, sustainability and responsible sourcing shape almost every purchase. This compound’s robust stability and modest hazard profile can help reduce both environmental impact and supplier risk. Several suppliers now follow voluntary standards for reduced-waste production and more transparent documentation, making audits and certifications less painful on the receiving end. In some labs, reliable batch-to-batch consistency frees up time for teams to focus on product development rather than routine troubleshooting.
My own projects have benefited from fewer reaction failures after switching to this intermediate for specialty heterocycle construction. Organic transformations such as Suzuki–Miyaura coupling or nucleophilic aromatic substitution have gone more smoothly, with product purities high enough to skip extra purification. Cost savings add up—in some cases, smaller teams can handle complex syntheses previously out of reach. This trickles down to more groups being able to compete and innovate, widening the field.
Despite its many strengths, working with 4-Chloro-5-methylpyridine isn’t free from hurdles. Some large-scale processes still generate byproducts, and capturing every last trace adds costs in energy, labor, and waste management. Post-synthesis handling requires trained staff who understand chemical safety—not all users have access to proper ventilation or disposal services. I’ve seen new staff struggle with correct weighing and dispensing, so hands-on training and clear labeling stay essential.
Sourcing still throws up complications, especially for small-scale users or in regions outside established chemical supply networks. Global supply disruptions—weather, regulatory shifts, or transport bottlenecks—can choke availability or lengthen lead times. Direct, long-term contracts with trusted suppliers reduce headaches, but smaller labs don’t always have the bargaining power to secure these deals. Once, a delayed shipment of this compound set a whole project back by a month, underlining the importance of supply chain resilience.
Regulation continues to tighten on hazardous chemicals, but 4-Chloro-5-methylpyridine’s moderate risk profile allows it to stay accessible to research groups and manufacturers. Updates to chemical inventories and international agreements might change that landscape. Regular reviews of storage, documentation, and disposal procedures help organizations stay up to speed. In larger organizations, compliance teams make a real difference, but individual researchers also benefit from up-to-date chemical management systems that flag expiring stocks or regulatory shifts.
Building a more resilient chemical workflow means thinking about both immediate and future needs. For teams relying on 4-Chloro-5-methylpyridine, practical solutions include staff training, regular safety audits, and closer collaboration with suppliers. Keeping an eye on process improvements can help cut down on solvent waste and reduce overuse of hazardous reagents. When I set up new reaction protocols, I aim for smaller batch sizes during trial runs, minimizing losses if unexpected results turn up.
Investment in better ventilation and personal protection lowers exposure risk—not only for 4-Chloro-5-methylpyridine, but for the host of chemicals typical in a working lab. Clear procedures for accidental spills speed up response times, and detailed labeling goes a long way in reducing everyday mishaps. Leadership plays a big part here: promoting a safety-minded culture translates into lower accident rates and long-term savings. Bringing in fresh perspectives from environmental engineers or sustainability consultants can spot overlooked improvements in chemical management.
On the sourcing side, moving beyond a single-supplier mindset reduces risk. Diversified networks, with backup agreements and clear performance metrics, buffer against unexpected delays. Leveraging digital inventory systems, I’ve found, makes tracking consumption rates and expiration dates less tedious. In one particularly busy quarter, better tracking allowed us to anticipate shortages and adjust orders before production slowed.
Researchers and producers can benefit from working with educators, regulators, and suppliers to keep best practices current. Colleges and technical schools integrating chemical safety, regulatory, and green chemistry modules into their curriculums equip the next generation to make smarter choices. Industry partnerships open doors for students to see how a compound like 4-Chloro-5-methylpyridine plays into large-scale projects, from new medicine development to innovative crop protection.
Technical forums and industry groups open opportunities for peer-to-peer learning. Sharing case studies about process failures and successes builds collective experience, reducing avoidable mistakes. Colleagues swapping tips on purification methods or recycling spent solvents can nudge broad improvements. Community-driven data platforms also help track supply trends, price fluctuations, and regulatory updates—resources that were rare just a decade ago.
A practical approach to regulatory change proves helpful. Instead of waiting for new rules to catch up with best practice, proactive organizations review and update their processes regularly. Lukewarm adoption of these steps leads to unnecessary risk, but teams championing compliance usually see better safety records and higher product quality. Staying ahead of the curve isn’t just about ticking boxes; it means products make it safely to end-users, whether in pharmaceuticals, agriculture, or high-value materials.
Though 4-Chloro-5-methylpyridine rarely appears in headlines or marketing brochures, its role supports countless innovations hidden from view. Reflecting on my years handling and working with this compound, the biggest value lies in its quiet dependability. Whether speeding up a reaction, unlocking a new drug candidate, or slashing production downtime, every small gain adds up.
Colleagues across industries value intermediates that behave predictably, scale cleanly, and open doors to new discoveries. 4-Chloro-5-methylpyridine carries these traits. As research and development continues to push boundaries, tools like this one show how humble starting materials can unlock new solutions for medicine, sustainable agriculture, and material science. Progress often depends less on bold breakthroughs and more on reliable partners—whether that’s a trusted compound or a well-trained team at the bench.
Looking ahead, building safer, more responsible chemical handling practices and resilient supply chains will set apart the leaders from the rest. Small changes—better labeling, improved protocols, or strategic sourcing decisions—make every batch of 4-Chloro-5-methylpyridine serve broader goals. My own experience bears out that success in research and manufacturing comes from sweating these details, learning from others, and never losing sight of the big picture.