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HS Code |
384884 |
| Productname | 6-Bromo-4-Methylpyridine-2-Amine |
| Casnumber | 914223-43-9 |
| Molecularformula | C6H7BrN2 |
| Molecularweight | 187.04 |
| Appearance | Off-white to light brown solid |
| Meltingpoint | 97-101°C |
| Purity | Typically >98% |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
| Smiles | CC1=CC(=NC(=C1)N)Br |
| Inchi | InChI=1S/C6H7BrN2/c1-4-2-5(7)9-6(8)3-4/h2-3H,1H3,(H2,8,9) |
| Storageconditions | Store at -20°C, protected from light and moisture |
As an accredited 6-Bromo-4-Methylpyridine-2-Amine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | |
| Shipping | |
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Every field has its essential tools. For synthetic chemistry, 6-Bromo-4-Methylpyridine-2-Amine brings more than just a name worth memorizing. Chemists with years at the bench know this is the kind of intermediate that expands what’s possible in drug discovery, material science, and beyond. So what sets it apart from a sea of other halogenated aminopyridines? A good starting point is the molecular formula—C6H7BrN2. There’s enough subtlety in its structure to open up selective transformations, enough reliability to support high-stakes syntheses.
Many industries chase molecules that unlock new paths. In the labs I remember, scouting for something like 6-Bromo-4-Methylpyridine-2-Amine usually meant someone was serious about targeting a specific active site or looking to modulate aromaticity without sacrificing reactivity. The bromo group at the 6-position acts as a convenient handle, letting chemists run reactions that turn this amine into something specialized, something meaningful. The methyl at the 4-position acts differently—it’s small, yet it shifts electron density in understated ways. These two modifications set this molecule apart from more run-of-the-mill aminopyridines.
In person, 6-Bromo-4-Methylpyridine-2-Amine usually arrives as an off-white to pale brown powder. That slight tint already tells a story about the raw material and its purity. High-performance labs pay attention to color shifts; sometimes, that’s an early signal about impurity profiles, which can throw off sensitive syntheses. Chemically, this compound keeps a solid—often sharp—melting point, indicating robustness in formulation. This makes a real difference when downstream steps demand temperature-sensitive operations.
There’s a reason researchers keep reaching for this molecule. Its dual functionality opens up cross-coupling reactions, like Suzuki or Buchwald-Hartwig, with more ease than some other aminopyridines. The amine group at the 2-position lends itself to selective modifications, while the bromine can swap out cleanly for more elaborate groups. My own sessions in the lab taught me that this saves time and can shave off a whole reaction step compared to working with a precursor that lacks the bromine or the methyl. Fewer steps mean fewer chances for things to go wrong.
Some molecules frustrate chemists because their reactive sites are too similar—they don’t allow selective manipulation. With 6-Bromo-4-Methylpyridine-2-Amine, the substitution pattern means the chemist has a clear map. The amine lends nucleophilicity, the bromine marks a spot for activation, and the methyl acts as a subtle shield. This is more than just theory—during scale-up, I’ve watched this feature translate to higher yields and fewer tough-to-purify side products.
You find this compound in projects that aim to generate kinase inhibitors, antifungal scaffolds, or high-value ligands for catalysis. Drug designers often go for this building block because novel pyridine derivatives often sit at the heart of patentable pharmaceuticals. In agrochemistry, modified aminopyridines play their part in pesticides and crop protectants. What’s remarkable is that a tweak at the 4 or 6 positions, using this molecule as a base, can give agrichemicals improved selectivity and environmental persistence. In real-world applications, those subtleties matter—a more selective pesticide can protect the crop while sparing pollinators.
Any chemist who’s ever developed a synthetic route learns quickly that impurities are more than a nuisance. Even a fraction of unreacted halogenated aminopyridine can throw off spectroscopic analysis and force extra rounds of purification. I remember a project where inconsistent batches led to lost weeks because the highlighting NMR shifts came from residual starting material. Trusted sources of 6-Bromo-4-Methylpyridine-2-Amine maintain purity levels above 98%. When lots come with clear chromatography traces, it makes work more efficient. That level of consistency can save hours, if not days, especially in deadline-driven projects.
Not all aminopyridines behave the same. Moving the methyl or bromo group changes the game entirely. For example, 2-bromo-4-methylpyridine or 4-methylpyridine-2-amine won’t offer the same outcome in a synthetic sequence. The position of the bromine influences selectivity in cross-coupling; a shift can drop yields or force different conditions. In one project, switching to 6-bromo placement improved the ortho-selectivity and gave higher regioisomeric purity in the next transformation. Little changes in ring substitution can translate into large practical differences at scale.
With a bromo and an amine both in play, the options multiply. It opens the door to building bipyridine ligands used in catalysis, or to crafting heterocyclic cores that underpin advanced functional materials. From my own work, I noticed pharmaceutical chemists favor these motifs when tackling antibiotic-resistant targets. The capacity to tune the core skeleton means researchers can respond to new biological findings without rebuilding their libraries from scratch.
Supply chain issues have always haunted chemical development, especially for niche building blocks. Labs sometimes chase multiple vendors and still run into quality variations. For 6-Bromo-4-Methylpyridine-2-Amine, reputable suppliers provide clear analytical data—NMR, HPLC, and mass spec confirmations. Problems arise when a batch falls outside standard specs. During one period of disruption, I heard from colleagues who received lots with off-odors or discoloration. In fast-moving projects, such surprises can derail timelines. Working with a consistent source not only builds trust, it saves money—downtime in a synthetic lab quickly adds up.
Solubility always shows up in research decisions. 6-Bromo-4-Methylpyridine-2-Amine, being a heteroaromatic amine, dissolves well in most polar organic solvents, making it a sensible option for standard reaction setups. In my lab days, the ability to run reactions in DMF, DMSO, or even acetonitrile offered flexibility you don’t always get with more hydrophobic alternatives. It also means this intermediate handles routine purification—column, crystallization, even trituration—without heroic measures. This can matter in pilot scale-up, where small tweaks in isolation have big impacts on overall process time.
No compound is used in a vacuum. Modern research laboratories expect chemicals to come with clear safety data. For 6-Bromo-4-Methylpyridine-2-Amine, proper handling calls for gloves, eye protection, and well-ventilated hoods. Like most small-molecule intermediates, it avoids high reactivity in aqueous systems but doesn’t create dangerous exotherms in standard use. Disposal still follows local regulations and waste protocols, since halogenated compounds must not end up in ordinary waste streams. Companies have leaned toward greener protocols in recent years, pushing for recovery and recycling where possible. In my own experience, keeping a clear MSDS on file and regular training sessions smooth out most hiccups before they start.
Long-term storage decisions shape how reliably a compound serves its purpose. Most research facilities keep 6-Bromo-4-Methylpyridine-2-Amine in cool, dry environments, shielded from light and sources of moisture. Over months, well-sealed containers prevent degradation. I once saw a batch degrade after a cap was left loose over a summer holiday—it ended up sticky, and chromatography later confirmed changes in purity. Lessons like this reinforce why basic storage habits form the backbone of laboratory reliability.
The science matters, but so does tracking the compound’s journey in the lab. Analytical reports—NMR, HPLC, LC-MS—become just as important as the powder itself. Documentation builds confidence that subsequent steps use a material fit for purpose. This is especially true in regulated sectors like pharmaceuticals or crop science, where every parameter can become subject to later audit. I’ve watched as diligent record-keeping prevented launches from stalling, and the same approach helps smaller teams run more efficiently. Clarity in paperwork prevents headaches down the line.
Innovation comes from building on the right foundation. In drug research, modifying the aminopyridine scaffold with halogens gives rise to fresh classes of kinase inhibitors, targeted cancer therapeutics, and antimicrobial candidates. The flexible core of 6-Bromo-4-Methylpyridine-2-Amine supports SAR (structure-activity relationship) exploration on tight timelines. In materials science, fields as diverse as OLED displays and battery research benefit from new heterocyclic ligands based on this core. Collaborations between chemists and engineers often start from these tailored building blocks—sometimes a shift in functionality opens unexpected properties, leading to patents and new markets.
Challenges abound, of course. The path from small-molecule benchwork to a true product involves surprises in both process chemistry and logistics. When a key building block like this is stuck in customs or subject to fluctuating tariffs, research teams scramble to redesign syntheses. Three years ago, I watched a team pivot away from a bromo intermediate when global bromine shortages threw pricing out of reach. Revising routes slowed the project by months. One potential solution calls for forging tighter relationships with suppliers who understand specialty needs—regular dialogue about lead times and batch customization serves everyone better in the long run.
It’s easy to underestimate the little hurdles that show up with routine use. Trace impurities in 6-Bromo-4-Methylpyridine-2-Amine sometimes stem from incomplete halogenation, leading to regioisomeric products. Savvy chemists rely on TLC, HPLC, and other techniques to spot these before they cause problems downstream. In my time overseeing process validation, routine troubleshooting meant flagging anomalous peaks and working with producers on corrective measures. Some labs even partner directly with suppliers to tighten up production specs. These hands-on solutions prevent headaches at the purification stage and build a culture of shared problem solving.
Every field faces mounting pressure to innovate more sustainably. For intermediates like 6-Bromo-4-Methylpyridine-2-Amine, that means scrutinizing supply chains for solvent choice, energy usage, and waste production. Some manufacturers have begun shifting away from harsher reagents, exploring catalytic routes or using renewable energy sources in synthesis. As a result, the carbon footprint of this compound keeps shrinking, even as demand rises. In one university partnership, pilot projects optimized microwave-assisted reactions and solvent recycling, slashing waste by half. Industry-wide, simple steps—recovering solvents, using lower-energy purification—translate into meaningful savings for all parties.
Students or early-career researchers often start out intimidated by molecules with names like this. Once you recognize the leverage offered by dual functional handles, though, you see why senior chemists turn to it so often. As research groups search for new targets and properties, this compound offers flexibility without forcing the learner into lengthy, convoluted setups. From a teaching perspective, introducing students to reactions involving 6-Bromo-4-Methylpyridine-2-Amine helps them grasp fundamental principles—selectivity, functional group manipulation, and purification—better than more inert starting points.
Modern innovation never lives in isolation from regulation. Pharmaceutical, agricultural, and technology sectors all operate under strict oversight. Reliable data packages for compounds like 6-Bromo-4-Methylpyridine-2-Amine play into rapid approvals and compliance reviews. Documentation that covers traceability, analytical results, and batch consistency supports fast turns on projects bound for clinical trials or commercial application. A handful of times, I watched regulatory hurdles stall launches, all because minor details—batch history, analytical anomalies—hadn’t been handled. Teams who prioritize full documentation for each shipment avoid these pitfalls and protect their research investment.
Some of the most impactful breakthroughs come from teams that cross boundaries—bringing together chemists, biologists, and engineers. Compounds like 6-Bromo-4-Methylpyridine-2-Amine provide the common ground for these efforts. A process chemist might use the molecule to tweak pharmacokinetics, while a biologist screens for new binding profiles and an engineer tailors manufacturing steps. These collaborations, based around the flexibility offered by smart intermediates, speed up real-world advances. From my own years in a multidisciplinary team, I saw how a well-chosen synthetic intermediate could open up unexpected routes and new ways to solve problems.
The path from grams to kilos isn’t just a matter of order size. Batch reactions for 6-Bromo-4-Methylpyridine-2-Amine can uncover new bottlenecks—solubility limits, heat management, or isolation snags. Larger reactors sometimes expose previously minor exotherms or crystallization quirks. One client’s multi-kilo run hit a snag when unexpected byproducts insisted on forming, unrelated to bench-top control. Teams solved it through iterative tweaks—minor changes in stirring rate, temperature, and work-up volatiles. This ability to adapt on the fly is the calling card for teams familiar with the quirks of advanced building blocks.
The environment surrounding specialty chemicals never stays still. The next few years likely bring continued movement towards more sustainable sources, clearer supply channels, and expanded application spaces. New computational tools could drive better predictive models for both synthesis and end-use, revealing fresh uses for established intermediates. In my own network, colleagues constantly seek building blocks that anticipate regulatory trends or consumer attitudes—halogenated aminopyridines with well-documented safety and environmental performance stay at the front of the line.
People might not realize that their medicines, electronics, or even the health of their food supply often rely on specialty chemicals like this. It’s not about making the biggest waves, but about providing sturdy, reliable rungs on the ladder to discovery. My own respect for these household-name intermediates comes from seeing small changes in molecular design open entire new chapters in research—whether it’s an improved therapy, a greener process, or a new set of electronic materials.
No one lab or company acts alone in shaping progress. The widespread use of 6-Bromo-4-Methylpyridine-2-Amine tracks the growth of coordinated global networks, as chemists and suppliers learn to anticipate needs and navigate challenges as partners. Training, collaboration, transparency in sourcing, and clear documentation all feed into faster, safer, and more effective research. It’s a patchwork ecosystem—one that depends as much on reliability in raw materials as ingenuity in research.
Decades of experience in applied chemistry taught me to value versatility and consistency above everything. 6-Bromo-4-Methylpyridine-2-Amine brings both in ample measure. Whether you’re setting out to build a novel drug candidate, improve a material’s properties, or simply support the next round of experimentation, this compound deserves a place in the discussion. It’s not flash or hype, just honest-to-goodness utility, built on years of practical feedback from those who work closest to the problems that matter.