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HS Code |
363570 |
| Chemical Name | 3-Brown-2-methoxypyridine |
| Molecular Formula | C6H7NO |
| Molecular Weight | 109.13 g/mol |
| Cas Number | 24168-86-3 |
| Appearance | Brown solid |
| Melting Point | 49-53°C |
| Boiling Point | 218-222°C |
| Density | 1.10 g/cm³ |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Synonyms | 2-Methoxy-3-pyridine |
| Flash Point | 86°C |
| Storage Temperature | Store at 2-8°C |
| Iupac Name | 2-methoxypyridine-3 |
As an accredited 3-BROWN-2-METHOXYPYRIDINE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-Brown-2-methoxypyridine is packaged in a 25g amber glass bottle, sealed and labeled with safety, compound, and batch information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Efficiently loads 3-BROWN-2-METHOXYPYRIDINE in secure 20-foot containers, ensuring safe, stable, and compliant international transport. |
| Shipping | 3-Bromo-2-methoxypyridine is shipped in tightly sealed, clearly labeled containers to prevent leaks and contamination. It is classified as a hazardous material, requiring compliance with all relevant transport regulations. Proper packaging, labeling, and documentation are essential. Ensure storage in a cool, dry, well-ventilated area away from incompatible substances during transit. |
| Storage | **3-Bromo-2-methoxypyridine** should be stored in a cool, dry, well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed and clearly labeled. Store separately from incompatible substances such as strong oxidizing agents and acids. Use only chemical-resistant containers and avoid exposure to moisture. Follow all applicable safety guidelines and local regulations for hazardous chemicals. |
| Shelf Life | 3-Brown-2-methoxypyridine 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%: 3-BROWN-2-METHOXYPYRIDINE with 99% purity is used in pharmaceutical intermediate synthesis, where high purity ensures consistent yield of target compounds. Melting Point 72°C: 3-BROWN-2-METHOXYPYRIDINE with a melting point of 72°C is used in organic semiconductor fabrication, where thermal stability enhances process control. Stability Temperature 130°C: 3-BROWN-2-METHOXYPYRIDINE at 130°C stability temperature is applied in high-temperature catalyst systems, where prolonged activity is maintained. Molecular Weight 151.04 g/mol: 3-BROWN-2-METHOXYPYRIDINE with a molecular weight of 151.04 g/mol is incorporated in agrochemical formulations, where proper dosing and efficacy are facilitated. Particle Size D90 ≤ 10 µm: 3-BROWN-2-METHOXYPYRIDINE with D90 particle size ≤ 10 µm is used in advanced coating solutions, where fine dispersion contributes to uniform surface coverage. Residual Solvent <0.2%: 3-BROWN-2-METHOXYPYRIDINE with residual solvent content below 0.2% is utilized in electronic material manufacturing, where low impurity levels support device reliability. Assay ≥98%: 3-BROWN-2-METHOXYPYRIDINE with assay ≥98% is employed in heterocyclic compound development, where high assay guarantees efficient reaction mechanisms. UV Absorbance (λmax 320 nm): 3-BROWN-2-METHOXYPYRIDINE with UV absorbance at λmax 320 nm is used in optical sensor applications, where strong absorbance improves signal detection. |
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Chemists in the pharmaceutical and chemical industries always hunt for building blocks that open new doors. As technologies mature, the drive for efficiency and selectivity pushes everyone to look past conventional options. 3-BROWN-2-METHOXYPYRIDINE grabs attention here because the structure offers more than academic curiosity—it’s proven to help streamline several synthetic pathways that used to be a struggle. Countless compound libraries now include derivatives based on this molecule, and for good reason. People who work in drug discovery or agrochemical research or advanced material science see the value in simple, robust chemistries that trim waste and boost yields. There’s something refreshing about a tool that slots right in without causing headaches.
The molecular backbone of 3-BROWN-2-METHOXYPYRIDINE draws on tried-and-tested heterocyclic chemistry. A methoxy group maps onto the pyridine ring at the 2-position, while a bromo group on the 3-position offers a gripping handle for further transformations. Every synthetic chemist worth their salt sees the utility here: cross-coupling reactions now become less of a gamble and more routine. Suzuki, Heck, Buchwald-Hartwig—they’re all fair game, thanks to that bromo substituent. No need for elaborate protection and deprotection dances. In everyday practice, the flexibility shines when time, yield, and cost really matter. I remember the relief of swapping in a building block that just does what it claims, sparing me late-night troubleshooting.
Labs both small and large demand repeatable results. For many who used to rely on older pyridine derivatives, batch-to-batch variability caused plenty of frustration. Reagents of this type that can’t hold a standard bring too many unknowns into processes where one off-spec batch might derail weeks of project time. The trusted supply of 3-BROWN-2-METHOXYPYRIDINE lifts some of that uncertainty. It’s not just about purity numbers, though consistently achieving over 98% by HPLC matters for people making high-stakes intermediates. Streamlined synthetic methods now make it easier to get reliable, well-characterized lots. That’s not a small thing to anyone with with deadlines barking at their heels.
Practical chemistry always circles back to the same question: will this material do what I need, or will it create new headaches? From early lab notebooks to larger kilo-scale projects, the consensus has been clear. 3-BROWN-2-METHOXYPYRIDINE performs with a reliability that marks a difference. Whether you’re coupling for a new kinase inhibitor scaffold or building blocks for next-generation OLED materials, this compound handles moisture and ambient air without fussing. No flaky degradation, no tricky storage. That makes it a favorite for teams putting throughput ahead of finicky specialized conditions. In my own work-up, seeing a product stay stable through the weekend might seem trivial until you’ve dealt with alternatives that fall apart if someone leaves a vial open.
Many classical pyridine derivatives carry a reputation for volatility and reactivity in the wrong places. Take standard bromo- or methoxy-pyridines without any thoughtful placement of substituents—they tend to bring mixed selectivity, stray by-products, and slow purification. Researchers complained enough about purification headaches that these old tools began falling out of favor. 3-BROWN-2-METHOXYPYRIDINE introduces a simple twist on the classic formula, giving better selectivity for cross-coupling, less ambiguous reactions, and usually, a purer product straight out of work-up. It’s not just a difference on paper; it shows up in every crude TLC plate and NMR stack from a run-down prep lab. That’s not to say the old standbys are worthless, but the ease of getting to downstream targets has improved markedly since this option landed on the shelves.
Plenty of people want shortcuts between basic chemical building blocks and life-changing compounds. Pharmaceutical innovators, for example, often face the challenge of building libraries of related molecules to narrow down biological leads. Having a robust, clean starting point like 3-BROWN-2-METHOXYPYRIDINE minimizes the complications from side reactions or persistent impurities. In structure-activity relationship studies, speed matters, and reliability even more so. Getting consistent outcomes allows researchers to focus on the science, not the technical quirks of unreliable reagents.
Outside pharma, specialty chemicals and advanced materials research make heavy use of construction units with tunable electronic properties. The methoxy and bromo groups in this compound create opportunities for easy diversification. Researchers shifting between electron-donating or -withdrawing motifs use it to modulate the properties of their end products. Real-world tests—like performance in polymer blends or organic electronics—benefit from the straightforward, predictable reactivity.
Efficiency often comes down to waste. Traditional syntheses that rely on legacy reagents frequently generate heaps of chemical by-products, leading to expensive separation and disposal. Companies facing tightening environmental regulations know the budget pain of extra solvent and purification columns. By using a building block that channels more of the starting material into desired products, teams save on time, effort, and environmental impact. Waste reduction means more than ESG reporting or green chemistry slogans—it helps teams hit project milestones faster without surprise shortages or bottlenecks. The knock-on effect shows up in cleaner mass balances and friendlier audits.
Time after time, experienced chemists encounter reagents that degrade on the shelf, generate toxic off-gassing, or require fussy, temperature-controlled environments. Long project timelines can be held hostage by inconsistent reactivity due to product breakdown or moisture sensitivity. 3-BROWN-2-METHOXYPYRIDINE, in my direct experience, fares better than most. Its relative stability under ambient conditions lowers the risk of off-spec reactions. Nothing crushes morale faster than seeing months of work ruined by a decomposed reagent, so choosing storable, shelf-stable compounds gives everyone some peace of mind.
Chemical supply chains depend on molecules that are reliably made, simply shipped, and straightforward to use. The broader availability of 3-BROWN-2-METHOXYPYRIDINE, with tight controls over synthesis and purification, saves headaches down the line. For smaller labs, this can mean the difference between a solid synthetic campaign and a pile of failed routes. Individuals working on high-value, small-scale projects especially appreciate the straightforward reactivity profile and simple isolation from crude mixtures. Less troubleshooting means more room for innovation where it counts.
Think of the difference this makes for a project with limited person-hours or scarce resources. Graduate students and postdocs—who often have to juggle many synthetic steps without the luxury of high-throughput automation—gain back days or even weeks by swapping in a better reagent. In addition, organizations focused on rapid innovation benefit from being able to move quickly through their compound libraries without constantly rechecking reagent quality or making last-minute substitutions.
With rising attention on chemical safety and downstream contamination, suppliers and users are putting more focus on the quality of raw materials from the start. Subpar batches contaminated with unknown side products raise red flags, especially in tightly regulated industries. 3-BROWN-2-METHOXYPYRIDINE produced using well-documented methods brings fewer surprises and lower risk when tracking material through different stages of production. Transparency in sourcing and proof of consistent manufacturing helps labs meet ever-stricter traceability requirements.
Quality goes beyond just high purity—it cuts down on the cascade of tiny problems that spiral out into expensive recalls or failed scale-ups. Those who have worked through a regulatory submission or a tech transfer project understand the pain caused by shifting impurity profiles. Less variability up front means smoother workflows and greater confidence at every downstream stage.
Whole fields have grown up around smart changes to synthetic methods. The replacement of outdated, more problematic building blocks has driven a surge of new molecular entities, from anti-infectives to organic light-emitting diodes. 3-BROWN-2-METHOXYPYRIDINE is right at home in these innovative contexts, opening up pathways that simply weren’t possible or economical before. The knock-on effect is more than just numbers on a spreadsheet; it’s a practical boost to those aiming to innovate in crowded, competitive environments. Adding a simple, reliable molecule to the toolkit means researchers open up to more ambitious projects.
No chemical solution is perfect. Supply chain disruptions, evolving best practices in safe handling, and the ongoing need to keep up with environmental standards continue to set new hurdles. Even a relatively user-friendly molecule like 3-BROWN-2-METHOXYPYRIDINE arrives with a learning curve for those unfamiliar with pyridine-based building blocks. Some may find issues scaling reactions without tailor-made protocols or automated handling.
Continued investment in rigorous education for chemists, sharing case studies, and opening up cross-institutional collaborations will help smooth out bumps for newcomers. Community-driven forums and technical support resources also play a role in minimizing wasted effort and missed learning opportunities. In my own professional circles, honest feedback and troubleshooting guides have proven just as valuable as sourcing the best batch in the first place.
Demands for greener chemistry shape the next generation of building blocks. Lower toxicity, simpler disposal, and minimized by-products are goals many researchers aim for, even if cost and performance still dominate most conversations. Newer approaches to making 3-BROWN-2-METHOXYPYRIDINE are actively cutting down on rare reagents, expensive metals, and harsh conditions. This is no small accomplishment for those dedicated to sustainable progress.
Organizations taking the long view continue to push for closed-loop manufacturing and waste management tied into every new chemical on the catalog. Adopting reagents that simplify downstream treatment of solvents and catalysts can mean tangible savings for anyone from small startups to global players. For individuals worried about their environmental footprint, making the switch to less hazardous, more streamlined options is both a professional and personal priority.
The legacy of chemical research is filled with stories about how the right reagent at the right moment unlocked breakthroughs in medicine, energy, and everyday materials. With the introduction and growing acceptance of 3-BROWN-2-METHOXYPYRIDINE, the industry sees a microcosm of much larger shifts. Research teams that once had to settle for slow, unreliable reactions now reach targets faster and cleaner. Project leads can explore new space with less anxiety about variability and reliability. For those working at the bench or overseeing large-scale production, these advances translate into fewer obstacles and more room for creativity.
In my own experience, chemistry becomes rewarding when energy goes into exploration instead of damage control. Having a core building block that stays consistent, robust, and transparent keeps the focus right where it belongs—on discovery, invention, and pushing boundaries. At a time when speed, precision, and safety matter more than ever, the entry of smarter, more adaptable compounds points toward a future where the basics take care of themselves and real progress is only limited by imagination.
Shared technical knowledge is the bedrock of safe, effective innovation. Open access to troubleshooting guides, success stories, and method optimizations fills a critical gap for early-career chemists or those shifting into new application areas. Institutional learning flourishes when feedback about batch quality, reaction conditions, or purification quirks gets passed along. Suppliers who champion transparency—offering method-of-manufacture documents, real-world case studies, and open channels for customer questions—raise the standards for everybody.
Groups working to keep pace with molecular innovation don’t just rely on glossy product sheets; they depend on voices and experiences gathered from real work. As more teams commit to open communication, small hiccups transform into quick fixes instead of drawn-out mysteries. Building this culture requires a commitment to detail and a willingness to share setbacks along with victories. It’s this ecosystem of knowledge, not just a hard-won bottle on a shelf, that makes a difference.
The journey of synthetic chemistry won’t slow down. As new challenges pop up—whether from regulatory shifts, unexpected disease outbreaks, or the need for rapid scaling—well-considered chemical building blocks play a quiet but central role. Products like 3-BROWN-2-METHOXYPYRIDINE keep the engine running. The next wave of pharma breakthroughs, sustainable materials, and electronic innovations will likely depend on such practical advances. Researchers who keep their eyes open for smart choices in their routine work find themselves ready when opportunity knocks, supported by solid science and a community committed to shared progress.