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HS Code |
858065 |
| Chemical Name | 6-Chloro-2-methyl-3-nitro-pyridine |
| Molecular Formula | C6H5ClN2O2 |
| Molecular Weight | 172.57 g/mol |
| Cas Number | 54794-00-4 |
| Appearance | Yellow to brown solid |
| Melting Point | 84-88°C |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥ 98% |
| Storage Conditions | Store at room temperature, keep container tightly closed |
| Synonyms | 2-Methyl-6-chloro-3-nitropyridine |
| Structure | Pyridine ring with methyl at position 2, chlorine at position 6, nitro at position 3 |
| Hazard Class | Irritant |
As an accredited 6-Chloro-2-methyl-3-nitro-pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 6-Chloro-2-methyl-3-nitro-pyridine is supplied in a sealed amber glass bottle with a tamper-evident screw cap. |
| Container Loading (20′ FCL) | 20′ FCL holds about **14 MT** of 6-Chloro-2-methyl-3-nitro-pyridine, packed in 25 kg fiber drums, safely palletized. |
| Shipping | 6-Chloro-2-methyl-3-nitro-pyridine is shipped in sealed, chemical-resistant containers to prevent leakage or contamination. It must be handled as hazardous material, complying with relevant regulations (such as DOT, IATA). Shipping is typically by ground or air, with clear labeling and appropriate documentation to ensure safe, compliant transportation. |
| Storage | 6-Chloro-2-methyl-3-nitro-pyridine should be stored in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers and reducing agents. Keep the container tightly closed and properly labeled. Protect from direct sunlight and moisture. Use appropriate chemical-resistant containers, and limit access to trained personnel only. Store at recommended temperature, usually ambient. |
| Shelf Life | 6-Chloro-2-methyl-3-nitro-pyridine typically has a shelf life of 2-3 years when stored in a cool, dry place. |
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Purity 98%: 6-Chloro-2-methyl-3-nitro-pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced by-product formation. Melting Point 92°C: 6-Chloro-2-methyl-3-nitro-pyridine with a melting point of 92°C is used in agrochemical manufacturing, where it provides optimal thermal stability during formulation. Molecular Weight 174.56 g/mol: 6-Chloro-2-methyl-3-nitro-pyridine with molecular weight 174.56 g/mol is used in heterocyclic compound development, where it enables precise stoichiometric calculations and reproducible results. Particle Size <50 µm: 6-Chloro-2-methyl-3-nitro-pyridine with particle size less than 50 µm is used in advanced material sciences, where it promotes uniform dispersion in composite matrices. Moisture Content ≤0.2%: 6-Chloro-2-methyl-3-nitro-pyridine with moisture content ≤0.2% is used in fine chemical synthesis, where it minimizes hydrolytic degradation and ensures product consistency. Stability Temperature up to 120°C: 6-Chloro-2-methyl-3-nitro-pyridine with stability temperature up to 120°C is used in industrial reaction processes, where it maintains structural integrity under heat stress. Assay ≥99%: 6-Chloro-2-methyl-3-nitro-pyridine with assay ≥99% is used in analytical reference standards, where it guarantees accurate quantification and traceability. |
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There’s a quiet sort of revolution going on in chemistry labs and manufacturing hubs. It doesn’t always get headlines or buzzy acclaim, but it powers pretty much every field that relies on complex molecules turning into useful products. In that world, 6-Chloro-2-methyl-3-nitro-pyridine rises as a valuable workhorse, pushing discovery forward in ways that might go overlooked. Anyone who’s spent time puzzling over reagent shelves or evaluating synthesis pathways learns which compounds reliably deliver. This one has found a real reputation among process chemists for good reason.
People might see a chemical like 6-Chloro-2-methyl-3-nitro-pyridine and just skim over it—another name in a catalog. For those who’ve worked with it, the appeal comes down to the way its functional groups open doors to creative chemistry. The chloro, methyl, and nitro groups each offer distinct reactivity, turning this pyridine derivative into a versatile synthetic intermediate. From pharmaceuticals to agricultural innovations, many final products build on molecular frameworks like this one. Years ago, I watched a team wrestling with multi-step syntheses for a crop protection agent. When they landed on this compound, it made their pathway leap forward. The gains were clear: higher yields, easier purification, predictable results even during scale-up. For researchers and process engineers, that kind of consistency matters a lot more than flashy statements on a label.
Choose two different nitro-pyridines off a supplier’s list, and the devil’s in the details. Each position on that aromatic ring changes how it behaves. 6-Chloro-2-methyl-3-nitro-pyridine stands apart because its three functional groups are placed to strike a balance—they’ll resist hydrolysis under physical processing, but come alive when chemists target specific reactions. That means less time correcting failed reactions or cleaning up impossible separations. Folks in the lab talk about “problem children” among their reagents, but this is the reliable sort.
If you compare this compound with, let’s say, 4-nitro-pyridines or simple methyl-pyridines, the differences aren’t just academic. The methyl at the 2-position and the bulkier nitro at 3-direct both impact not just reactivity but solubility and isolation. In pharmaceutical synthesis, that sort of profile means you can often use milder conditions and waste less starting material—an everyday concern in both R&D and manufacturing. Seasoned chemists watch for those subtle improvements, which over thousands of batches can save a fortune and countless work-hours.
Out in the academic world, 6-Chloro-2-methyl-3-nitro-pyridine pops up in literature as a respected scaffold. In my years teaching undergraduates advanced organic synthesis, I noticed students gravitate toward real-world challenges: new antibiotics, herbicides, or specialty dyes. Every time you push a new bioactive compound through the pipeline, you search for reliable building blocks that let you bolt on complexity without losing control. This pyridine fits because it brings together three different chemical handles. You can try reduction, halogen exchange, or nucleophilic substitutions—hot topics in modern medicinal chemistry. Anyone developing an enzyme inhibitor or a nervous system probe wants something robust that also allows for further tuning. Products with fewer modifiable sites often box you in before the fun even starts.
Move downstream, and production chemists appreciate the repeatable performance. You won’t find yourself guessing batch to batch; the routes remain as straightforward in a beaker as in a reactor. Making active pharmaceutical ingredients (APIs) can bring surprises, but this building block rarely throws unpredictable curveballs when handled with reasonable precautions. That makes it an easy recommendation for anyone concerned about scale-up hiccups.
Everyone who handles specialty reagents learns quickly: some products demand constant troubleshooting. Some batches degrade in storage, others respond poorly to heat or solvents. Over time, I’ve seen products with the same chemical name from different sources behave differently, because trace contaminants or unpredictable stability creep in. 6-Chloro-2-methyl-3-nitro-pyridine, when verified by consistent suppliers, delivers on purity and longevity. I’ve found this compound keeps its quality during reasonable storage—months, not days—which lends confidence to project timelines. There’s a peace of mind that comes from knowing you won’t have to recalibrate protocols with each order.
Transparency matters more now than in the past. Enforced by tightening regulations and growing quality audits, documentation and traceability allow a lab to operate smoothly even as requirements toughen. With this compound, anyone sourcing it from a reputable supplier finds an audit trail from production facility through to the customer. For those in highly regulated industries, the value can’t be overstated. It’s not just about passing inspections—it’s also about protecting patient safety and ensuring ethical research. It surprised me when, in my early years at a pharmaceutical start-up, I saw a lead project grind to a halt because a previous compound lacked proper records. Lessons like these leave a mark, shaping future choices. By sticking with ingredients underpinned by sound documentation and analytical support, chemists keep projects on track, even as expectations keep rising.
In the daily practice of chemistry, trust often grows from the tools that prove themselves. The punch list for a quality building block isn’t long: purity, consistency, safe handling, and meaningful documentation. 6-Chloro-2-methyl-3-nitro-pyridine checks these boxes, so it finds its way onto reorder lists and lab shelves again and again. On more than a few occasions, I’ve seen procurement teams default to the known good, thanks to its strong performance record. In universities as well as startups, those decisions shape the pace of discovery. It’s not glamorous, just dependable—the unsung hero of successful multi-step reactions.
The commercial landscape for chemical intermediates never stands still. Markets shift as new therapies and agrochemicals arrive, and with them come changing demands for precursor compounds. This is where 6-Chloro-2-methyl-3-nitro-pyridine keeps proving its worth. Rather than being trapped by narrow utility, it stays relevant across sectors—pharmaceutical, crop science, even specialty coatings. Production volume and supply flexibility also matter. It’s no good having a promising scaffold if you can’t source enough or need to pay outrageous prices. Whether you work in a big pharma company or a lean start-up, forecasting reliability becomes a real concern. Fortunately, this compound benefits from a mature supply chain, thanks to sustained demand and well-established synthesis methods. That helps avoid procurement bottlenecks and spot shortages—problems that have tripped up plenty of projects over the years.
Applications are broad but specific at the same time. Beyond the big headlines around pharmaceuticals, chemists turn to this compound to create heterocyclic libraries or assess new catalysts. In industrial research, using 6-Chloro-2-methyl-3-nitro-pyridine opens the door to faster development cycles, because every reaction step runs smoother—less stuck in troubleshooting, more time spent advancing the actual science. This is the practical advantage that experience brings, and it's worth remembering for anyone picking up responsibility for process optimization.
For anyone unfamiliar with the ins and outs of laboratory work, it might seem like all reagents look the same on a spreadsheet. My own years at the bench revealed a different truth: Some steps get derailed by inconsistent batches, tricky solubility, or unpredictable reactions. Plenty of colleagues have traded horror stories over coffee about reagents that seemed fine on paper but created headaches in practice. With this compound, those headaches rarely surface. It dissolves predictably in common solvents, letting users avoid creative gymnastics to persuade it into solution. Handling it rarely introduces risk under normal laboratory protocols—good for seasoned professionals and trainees alike. Over time, this reliability generates its own kind of trust. Knowing you can reach for a compound and expect it to behave means more than presentation slides often admit.
No chemical product arrives without challenges. Supply chain shocks, geopolitical tension, or raw material price hikes sometimes threaten predictability. I’ve lived through moments of sudden scarcity, when a beloved reagent briefly vanished as demand outstripped supply or a key facility went offline. For chemists, these interruptions aren’t just a blip—they may delay launches or force revalidation at huge cost. Companies and research groups can mitigate these risks through strategic sourcing and by partnering with suppliers who back up their products with transparency about capacity and raw material origins. Pre-purchasing or collaborative stockpiling sometimes offer a buffer against supply gaps. Over the next few years, expanding domestic production capacities, encouraging greener manufacturing, and nurturing multiple supply relationships will become even more important. For stakeholders, these steps form the backbone of resilience and ensure essential compounds like 6-Chloro-2-methyl-3-nitro-pyridine remain available when needed most.
Seasoned chemists develop a feel for suspect material—clumping powders, strange off-hues, or drifting analytical results all hint at bigger problems. With 6-Chloro-2-methyl-3-nitro-pyridine from verified sources, those red flags are rare. Analytical support, such as batch-specific HPLC or NMR data, arm researchers with confidence to proceed. Any lab—industry or academic—relies on those traceable analyses to catch issues before expensive scale-up stages. While trust isn’t built overnight, repeated positive experience with a product builds a quiet loyalty. I learned this firsthand managing a portfolio of synthesis projects. The difference between running late-night chromatography on a clean product versus fighting unknown side-products can mean the difference between a productive week and a stretch of wasted effort.
Sustainability concerns now carry practical and ethical weight in chemistry. As new regulations emerge and customer expectations grow, eco-friendlier manufacturing becomes more than just a buzzword. The production of pyridine derivatives—including 6-Chloro-2-methyl-3-nitro-pyridine—increasingly relies on greener pathways, using less toxic reagents, minimizing solvent use, and recycling waste whenever possible. Manufacturers who invest in cleaner processes see fewer workplace hazards, less hazardous waste, and a tighter grip on costs. For buyers, asking questions about how these compounds are made isn’t just window dressing; it impacts company reputation and compliance, especially in pharmaceuticals where green chemistry initiatives can even accelerate regulatory approval. From my own consulting work with sustainability teams, I’ve seen how switching to suppliers with robust stewardship programs often pays back in public trust and smoother business operations.
Global rules around hazardous chemicals grow stricter almost every year. Labs and companies need products fully compliant with current safety, transport, and waste handling standards. The burden falls not just on suppliers, but all the way down to end-users tracking compliance documentation, safety data, and risk assessments. With a well-supported product like this, those essentials are included without drama. Some suppliers even help clients keep safety documentation up to date as rules evolve, meaning fewer compliance worries for busy lab managers. Those in charge of regulatory filing and site audits know just how valuable such peace-of-mind can be. It’s not enough for a product to work in the chemistry; it must fit into frameworks for health, safety, and environmental norms.
Even among trusted reagents, not all store equally well. Some degrade quickly, especially when exposed to humidity or light. For the industry-standard 6-Chloro-2-methyl-3-nitro-pyridine, proper storage—cool, dry, and well-sealed—preserves the product across substantial timelines. This property becomes crucial during extended projects or long shipping routes. I recall one university team that ran into trouble using a less stable analog that decomposed during an unusually humid summer. They lost weeks tracing the error to poor storage compatibility. Since then, labs that handle larger quantities check packaging, re-test over time, and keep material out of unsuitable environments. Experience proves that up-front discipline pays off with less downtime and reduced rework.
Teamwork often drives fresh breakthroughs. A single compound can serve as a bridge between specialties—synthetic chemists, analytical scientists, application developers, and regulatory managers all bring distinct perspectives to a product’s use. A versatile intermediate like 6-Chloro-2-methyl-3-nitro-pyridine inspires collaboration, because it integrates readily with other synthetic strategies. In joint projects I’ve witnessed, materials scientists relied on this scaffold to attach functional polymers, while drug discovery teams pivoted it toward novel pharmacophores. Its multi-functional nature allows for creative tweaking, and in a well-run research environment, it brings together many hands toward building better molecules. As pressure to innovate grows louder across industries, the connectivity and adaptability provided by robust intermediates become more than mere conveniences—they enable the entire cycle of invention to keep moving.
From the teaching lab to full-scale industry, the value of a compound like 6-Chloro-2-methyl-3-nitro-pyridine rests on daily experience and proven utility. Any scientist who juggles deadlines, budgets, and unpredictable experiments would recognize the comfort and efficiency that comes from a tried-and-true building block. The compound’s unique structure lets chemists branch out or double down, supporting changing project needs. Regulatory backing, traceability, and sustainable practices deepen that trust and keep doors open for the next scientific leap. For those not yet familiar with the time-worn wisdom of using tested intermediates, the story of this pyridine stands as real evidence that good chemistry comes from choosing dependable tools. Through countless experiments and many collaborative successes, it remains a quiet backbone, letting innovation continue without unnecessary friction.