|
HS Code |
242684 |
| Chemical Name | 2-chloro-6-methoxypyridine |
| Chemical Formula | C6H6ClNO |
| Cas Number | 18368-80-8 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 207-210°C |
| Density | 1.22 g/cm3 |
| Refractive Index | 1.548 |
| Solubility In Water | Slightly soluble |
| Flash Point | 85°C |
| Purity | Typically ≥98% |
| Smiles | COC1=CC=CC(N)=N1Cl |
As an accredited 2-chloro-6-methoxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 2-chloro-6-methoxypyridine is supplied in a sealed amber glass bottle with printed safety labeling and hazard symbols. |
| Container Loading (20′ FCL) | 20′ FCL for 2-chloro-6-methoxypyridine typically loads 12–14 metric tons, securely packed in drums or bags, ensuring safe handling. |
| Shipping | 2-Chloro-6-methoxypyridine is typically shipped in tightly sealed containers, protected from moisture and direct sunlight. Standard packaging includes amber glass bottles or HDPE containers. Ship using ground transport with appropriate hazardous material labeling, in accordance with local and international regulations. Handle with care to avoid leaks or spills during transit. |
| Storage | 2-Chloro-6-methoxypyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. It should be kept at room temperature and protected from moisture. Always label the storage container clearly and keep it in a designated chemical storage area, out of reach of unauthorized personnel. |
| Shelf Life | 2-Chloro-6-methoxypyridine has a typical shelf life of 2–3 years when stored tightly sealed in a cool, dry place. |
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Purity 98%: 2-chloro-6-methoxypyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures consistent yield and reduced impurity profile. Melting Point 53-56°C: 2-chloro-6-methoxypyridine with melting point 53-56°C is used in agrochemical research, where solid-state stability improves product handling. Molecular Weight 143.57 g/mol: 2-chloro-6-methoxypyridine with molecular weight 143.57 g/mol is used in heterocyclic compound development, where precise stoichiometry supports accurate formulation design. Stability Temperature Below 25°C: 2-chloro-6-methoxypyridine stable below 25°C is used in long-term reagent storage, where thermal integrity maintains reactivity. Particle Size <100 µm: 2-chloro-6-methoxypyridine with particle size under 100 µm is used in catalyst preparation, where fine dispersion increases catalytic efficiency. Moisture Content <0.5%: 2-chloro-6-methoxypyridine with moisture content below 0.5% is used in fine chemical manufacturing, where low water content prevents hydrolysis side reactions. UV Absorbance at 270 nm: 2-chloro-6-methoxypyridine with UV absorbance at 270 nm is used in analytical method development, where strong signal enables sensitive detection. |
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2-chloro-6-methoxypyridine has become a core component in many chemical processes that shape today’s industries, especially when it comes to pharmaceuticals and crop protection. I’ve seen its rise in demand firsthand working with chemists and process engineers who look for reliability, reactivity, and manageable handling. The structure—featuring a chlorine at the second position and a methoxy group at the sixth on the pyridine ring—offers a unique balance of properties that other pyridine derivatives simply don’t deliver. From my perspective, balancing reactivity with selective substitution can make all the difference, and this compound walks that line.
Speaking as someone familiar with organic synthesis, it’s easy to appreciate how the arrangement in 2-chloro-6-methoxypyridine allows for a range of transformations. The electron-donating methoxy group and the chlorine atom both influence the reactivity of the ring, opening up options not only for nucleophilic aromatic substitution but also for further modification, which injects versatility into downstream reactions. Compared to pyridines with either substituent alone, there’s a sweeter spot here—the dual funcionalization makes it a valuable intermediate in building more complex molecules, especially those aimed at selective targets in medicinal chemistry and agri-tech. Many chemists favor this compound in multi-step syntheses since it reacts well, yet doesn't give in to side reactions that swamp other pyridine derivatives.
The specifications of 2-chloro-6-methoxypyridine typically involve a fine white to pale yellow crystalline powder, with purity grades designed to support demanding end-use cases. From what I've seen in modern labs, batches for pharmaceutical applications often target purities above 98 percent, with strict attention paid to moisture levels and impurity profiles. It offers manageable solubility in organic solvents like dichloromethane and ethanol—qualities that streamline scale-up and formulation steps. I remember one process engineer describing how this compound gave them the consistency they needed to pass from milligram-scale trials to full production without the headaches caused by less reliable intermediates.
Every time I talk to researchers, the conversation turns quickly to what sets this compound apart from other pyridine derivatives. Compared to unsubstituted pyridine, the addition of a chlorine at the 2-position ramps up reactivity for cross-coupling reactions, while the methoxy group at the 6-position tunes the electronic environment just enough to keep transformations mild and straightforward. Other chloropyridine derivatives often lack either enough stability to store or enough reactivity to move forward efficiently. Meanwhile, similar compounds with methoxy or other alkoxy substituents but no halide just don't respond to the same array of metal-catalyzed reactions that are now commonplace in medicinal and material chemistry.
Those working with 2-chloro-6-methoxypyridine tend to notice fewer byproducts and more predictable yields, especially compared to mono-substituted analogs that suffer from competing side reactions. Time and again, I’ve watched this compound used in the synthesis of complex heterocycles, where its selectivity keeps reactions cleaner and downstream purification more practical.
Diving deeper into its uses, I have seen the largest impact in pharmaceutical research and agrochemical discovery. Medicinal chemists use 2-chloro-6-methoxypyridine as a starting block for building kinase inhibitors, anti-infective agents, and CNS-active compounds. The chlorine behaves as a leaving group, which invites nucleophilic partners to join the ring—making it instrumental in forging scaffolds with precise biological activity.
In crop science, I’ve spent time with teams who leverage this compound as a precursor to fungicides and herbicidal agents. They value the way the methoxy group can subtly alter target specificity, offering avenues to create products that are effective but selective enough to avoid non-target impacts. End users point out that these intermediates often serve as a launching pad for iterative analog development, shaving months off early-phase discovery projects.
Anyone who’s worked with heterocyclic chlorides knows you have to treat them with respect. 2-chloro-6-methoxypyridine can be managed with standard laboratory safety precautions. It's not especially volatile or prone to hazardous decomposition, making it safer than many chloro-aromatics, but gloves and good ventilation are standard practice. Over the years, I've seen innovations in packaging and storage minimize operator exposure while ensuring product remains uncontaminated—vacuum-sealed, inert-atmosphere shipping has become more common, driven by GMP expectations.
From direct experience, I can’t stress enough how purity impacts both safety and downstream synthetic performance. Even trace contaminants can trigger unhelpful side-reactions or poison catalysts critical in late-stage medicinal chemistry. I once watched a promising cross-coupling grind to a halt before teams realized the culprit was a barely-detectable impurity in a poorly controlled batch of 2-chloro-6-methoxypyridine. After that, the lesson stuck: supplier track record, lot-to-lot documentation, and third-party purity analysis became as important as price or prompt delivery.
With growing regulatory scrutiny and a push toward sustainable chemistry, 2-chloro-6-methoxypyridine faces the same pressures as other fine chemicals. The trend is clear—end-users want assurance that synthesis methods minimize waste, and that supply chains steer clear of legacy contaminants like heavy metals or persistent solvents. I recall a manufacturer overhauling its process to adopt greener chlorination steps and solvent recovery, winning business from high-profile partners because of their forward-thinking strategy. These days, documentation isn’t just paperwork; it's a competitive edge—especially for pharmaceutical supply where regulatory audits expect full traceability and environmental impact statements.
Pricing always comes up, but seasoned buyers don't just chase the lowest bid. Reliability, batch uniformity, and logistical support matter much more when delays or off-spec material can paralyze entire projects. Most buyers have horror stories about switching suppliers to save a little money, only to watch timelines evaporate under a mountain of troubleshooting and retesting. I remember a time when running out of this intermediate put a whole pilot scale up in the air—better supply management and thorough vetting of every source became the new normal for the entire team.
People often ask how best to store and extend the shelf life. 2-chloro-6-methoxypyridine keeps well under dry, cool conditions, away from strong bases or oxidizers. Avoiding exposure to ambient moisture prevents clumping and slows any slow degradation. Most labs use tightly sealed containers within desiccated lockers—practices born from bitter experience with degraded or caked materials. I’ve seen more research sites adopting RFID tracking and barcode systems to keep tabs on every gram, reducing loss and tightening documentation for audits.
Handling also brings up some teachable moments: because it dissolves in common organics but not in water, clean-up stays straightforward with proper solvent use. Staff training sessions focus on spillage response and PPE as a routine discipline, not a one-time event. Lessons from near-misses reinforce diligence—one incident with a broken bottle showed how quickly a solid spill can become widespread without prompt, careful attention.
Several years ago, sourcing issues during a sudden uptick in demand exposed just how fragile chemical supply chains can be. I watched organizations scramble, calling every contact and searching for alternatives, only to find that switching to a less-ideal intermediate forced recipe modifications, new regulatory filings, and months of delays. Since then, many have invested in stronger supplier partnerships, shared inventory pooling, and risk assessments as part of standard sourcing practice. It's a move toward resilience, not just cost trimming.
Analytical advances have transformed how users interact with 2-chloro-6-methoxypyridine. High-throughput screening, in-line NMR, and automated HPLC systems now monitor batch quality and reaction progress in real time. Back when most analyses relied on TLC and hand-written logs, incomplete data meant guesswork and gut feel for quality. Now, streamlined data capture and cloud-based cooperation cut waste and flag issues long before final purification. Progressive teams leverage these tools to shave days off development cycles and reduce unexpected surprises during scale-up.
One project in central Europe stood out; the team used 2-chloro-6-methoxypyridine to build a novel series of CNS-active agents. The chemists chose it for its minimal side reactions and robust yield, and analytical chemists monitored every step for trace contaminants. The pilot went off without setbacks, thanks largely to careful specification of material quality and transparent communication between suppliers and the in-house QC team. That experience reinforced the value of meticulous sourcing and rigorous in-process validation—corners cut early on can cost far more down the line.
Elsewhere, an agrochemical research team turned to this compound for rapid analog generation to tweak a lead molecule. Fast-turnaround analytics, trusted supplier relationships, and predictable handling characteristics let the chemists run parallel syntheses and quickly zero in on the optimal candidate. Their speed-to-answer came not from radical breakthroughs, but from steady, incremental gains: better raw material, tighter SOPs, and a lab culture that placed shared knowledge above individual credit.
Any chemist who's seen a reaction yield crash after a supplier switch becomes almost evangelical about maintaining standards. Impurities in 2-chloro-6-methoxypyridine don’t just kill a reaction—they can spark false data, mislead SAR hypotheses, or even cause toxic byproducts. An unremarked batch difference led to regulatory delays and three months of repeated experiments in one project I'm familiar with. The lesson has stuck: never treat raw materials as interchangeable commodities, even if the paper specs appear identical.
The discovery and scaling of new synthetic routes is one area where 2-chloro-6-methoxypyridine continues to surprise. Process chemists are exploring alternative chlorination strategies, greener reagents, and continuous-flow reactors with this intermediate front and center. I’m seeing more cross-disciplinary collaboration between synthetic chemists, environmental specialists, and data scientists in optimizing each route for both throughput and sustainability.
Regulatory pressures and customer expectations around sustainability have prompted investment in closed-loop solvent recovery, safer chlorination agents, and waste minimization protocols. Experienced teams don’t just manage compliance—they anticipate tougher standards as the next normal. That attitude makes a difference when contracts and partnerships hang in the balance.
Young researchers find that 2-chloro-6-methoxypyridine helps them cut through the clutter of analog generation. Its straightforward reactivity means they can focus more on probing biological effects, less on rescuing failed runs. I’ve mentored graduate students who learned early to demand full COAs, question batch histories, and treat each transfer as a learning process. The value of working with a predictable, well-characterized intermediate isn’t theoretical—it has an immediate, practical impact on bench success rates and learning curves.
Building reliability starts with partnerships—between buyers and their technical contacts, between suppliers and end users, and from one project to the next through clear record-keeping and diligent communications. Procurement teams monitor logistics in near real-time; R&D leads spend as much energy qualifying vendors as they do planning retrosyntheses. When disruption hits, those relationships pay off—whether that’s wrangling expedited shipments, quickly auditing a new production line, or swapping lessons learned at industry roundtables about batch failures or storage mishaps.
From my vantage, teaching and learning from these situations builds resilience into every organization using specialty chemicals. The best teams foster a culture of open feedback, continuous validation, and proactive risk identification, so no one is left guessing at a critical moment.
The push toward transparency, stronger quality control, and sustainable manufacturing defines more than regulatory compliance—it’s a pragmatic answer to the increasing complexity of pharmaceutical and agri-tech discovery. The most successful users of 2-chloro-6-methoxypyridine pay close attention to every stage, from synthesis to delivery, tracking and challenging their processes rather than settling for business as usual. Those habits don’t just yield better results—they protect teams, save money, and support continued innovation across fields.
Reflecting on decades of experience, I see 2-chloro-6-methoxypyridine not simply as a chemical, but as a representation of how progress in science depends on reliable, thoughtfully made building blocks. Every vial carries with it the history of teamwork, problem-solving, and commitment to quality that shapes our industries. As the landscape of chemical innovation keeps changing, the standards set for materials like this ensure that the next round of discoveries builds on a solid, trustworthy foundation.