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HS Code |
118881 |
| Product Name | Methyl 5-Bromomethylpyridine-2-Carboxylate |
| Cas Number | 98475-07-1 |
| Molecular Formula | C8H8BrNO2 |
| Molecular Weight | 230.06 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Boiling Point | Decomposes before boiling |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
| Smiles | COC(=O)C1=NC=C(C=C1)CBr |
| Inchi | InChI=1S/C8H8BrNO2/c1-12-8(11)7-6(5-9)3-2-4-10-7/h2-4H,5H2,1H3 |
| Storage Temperature | Store at 2-8°C |
| Synonyms | 5-(Bromomethyl)nicotinic acid methyl ester |
As an accredited Methyl 5-Bromomethylpyridine-2-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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Chemistry doesn’t always get the fanfare it deserves. Some compounds make headlines because they touch our daily lives, showing up in new medicines, battery technology, or environmental innovations. Others go unnoticed, even though whole sectors rely on their steady performance. Methyl 5-Bromomethylpyridine-2-Carboxylate—bit of a mouthful, granted—belongs to the second group. It doesn’t win any popularity contests, but those in the business of synthesis or specialty chemicals have seen how a small detail like a bromine atom on the right spot transforms a whole process.
Handling complex synthesis often comes down to having the perfect starting ingredient. With its distinct five-membered ring, nitrogen, and that eye-catching bromomethyl group, this particular chemical gives chemists flexibility. The carboxylate moiety on the ring helps balance reactivity, often turning up in pharmaceutical intermediates where precision is critical. The addition of a bromine to the methyl position is more than just a decorative twist. From experience, anyone who has run a tough substitution knows how much easier it gets having an accessible leaving group.
If you work in a research lab or an API (Active Pharmaceutical Ingredient) manufacturing line, you’re already familiar with the way certain building blocks smooth out or complicate your day. Even a small difference—a bromine instead of chlorine, methyl over ethyl—can snowball as the synthesis progresses. This product, with its specific arrangement, often finds itself at the crossroads of medicinal chemistry projects, especially for folks exploring heterocyclic scaffolds or optimizing reaction series for patent strategies.
I’ve watched teams grind through weeks of trial reactions searching for a path that won’t waste expensive catalysts or leave a tangle of impurities. The appeal of Methyl 5-Bromomethylpyridine-2-Carboxylate often lies in solving a particular headache: getting the right bromine placement with a stable, easy-to-handle ester. It doesn’t constantly off-gas, you don't have to treat it like dynamite, and storage demands aren’t absurd. Chemical producers appreciate its shelf life and stability under standard conditions. Researchers, in turn, value it as a reagent that doesn’t throw nasty surprises midway through a sequence. That may not sound glamorous unless you’ve lived through a failed oxygen-sensitive reaction or mystery by-products ruining a week’s worth of set-up.
Unlike more volatile compounds in the same family, this molecule typically comes as a crystalline solid or viscous oil, making it straightforward to weigh and measure. The bromomethyl group opens the door to all sorts of transformations: Suzuki couplings, Buchwald–Hartwig reactions, nucleophilic substitutions—the kind of chemistry that keeps the life sciences pipeline moving. With that flexible nitrogen on the ring, chemists play with hydrogen bonding and ring-locking strategies, setting up further functionalization with a broad palette of reagents.
Product quality matters, and here it’s more than a buzzword. Every synthesis professional I know checks the certificate of analysis before even uncapping a bottle. With this compound, typical purities run upwards of 97%, and residue limits are critical. Even a smidge of leftover solvent or related structure can mess with a multi-step process. Impurities, especially similar pyridine derivatives, sneak through if a producer cuts corners. In that sense, established suppliers who monitor every batch with NMR, HPLC, and GC earn respect and repeat business. Personally, I’d rather pay a little extra for peace of mind than debug a stuck reaction with no obvious explanation.
The nitty-gritty—melting point, moisture tolerance, packaging integrity—tends to matter more here than in “commodity” chemicals with broader specs. In drug discovery labs, a handful of milligrams might fuel assays that shape million-dollar decisions. On pilot lines, a kilogram-scale mishap turns into real money. Stories circulate about off-color solutions, unidentified peaks on chromatograms, and how a revamped purification process turned an unreliable batch into a linchpin for a new route. Quality control doesn’t always grab an audience, but those checks decide who moves forward and who starts over.
The chemical market isn’t short on pyridine carboxylates or halogenated methyl derivatives. There’s a temptation to swap one for another, but close only counts for horseshoes. I’ve watched new process chemists try to substitute with a chloromethyl version—hoping for a better price or availability—only to find reactivity drops, yields fall, or a minor change magnifies downstream issues. The unique value of the bromo group rests in its reactivity profile: it’s enough of an activating group to invite nucleophilic attack or cross-coupling, but rarely so overzealous that it creates an explosion risk or complicates isolation.
You’ll see methyl 5-chloromethylpyridine-2-carboxylate and even the iodo analog hanging around the catalogues. The iodo form promises the best leaving group for conventional nucleophilic substitution, but it tends to drive up cost and can demand special storage. The chloro is cheaper, but its reactions typically run sluggish unless you pump up the temperature or coax it with strong catalysts—and that's not always a trade-off process engineers want to make.
Comparing to non-halogenated methylpyridine-carboxylates strips away the synthetic flexibility altogether. Less reactivity, fewer pathways for transformation, more time (and money) spent chasing after the next intermediate. In a world where speed and adaptability mean market advantage, picking the right version shapes how quickly new compounds reach development.
Drug discovery and contract manufacturing turn to intermediates like this not just for their chemistry, but for supply chain reliability. Regulatory authorities demand full documentation on raw materials, which pushes companies to stick with established, well-characterized ingredients instead of rolling the dice on less-proven variants. Over the last decade, the need for reproducibility has only grown. Every regulator wants a paper trail, every QA auditor reads chromatography curves like a storybook, and every customer expects consistency whether they order a gram or a hundred kilos.
This product doesn’t typically wear a warning label more intense than basic lab chemicals, but getting labels right—lot, batch, handling instructions—still fuels smoother audits and fewer compliance headaches. I’ve sat in on many project meetings, and you always hear the sigh of relief when sourcing lands a reliable compound that just works, sparing the R&D team from drama that has nothing to do with their science.
Plenty of chemists think about green chemistry and sustainability beyond just buzzwords. This compound holds up fairly well in that regard. Manufacturing routes rely on scalable, established reactions with moderate environmental impact. Waste streams do include bromides, so most large operations install scrubbers or neutralization protocols. These aren’t overly burdensome compared to the alternatives. It helps that the carboxylate function doesn’t require extreme conditions to protect, and final purification rarely involves persistent organic solvents if the upstream work is clean.
On the safety side, this isn’t a compound that sets off red flags, but personal protective equipment, hood operation, and proper waste disposal are still a given. Long days in synthesis labs have taught me it only takes one sloppy weigh-up to introduce unwanted variances or, worse, a reactant cloud where there shouldn’t be one. The product’s stability at room temperature reduces the headache factor, a clear advantage over compounds demanding cold-chain logistics.
Custom synthesis keeps the wheels turning for drug discovery and materials science. This product often figures into multi-step schemes where speed and predictability make the difference between a promising candidate hitting testing windows or falling behind. Companies that specialize in high-purity intermediates rely on compounds like this to keep clients coming back. In my own work sourcing specialty chemicals for new project launches, I’ve seen how a dependable supplier for this building block becomes a trusted partner, not just a name on a catalog.
Some teams push production into pilot plant territory, needing reproducibility at 10 kg and beyond. For others, it’s about smaller-scale work, enabling diverse analog screening. Either way, having a solid grasp on the performance profile and supply chain realities shapes smarter planning. Those with experience know the pain of a delayed delivery or a “new and improved” batch that turns out to be neither.
The price tag on Methyl 5-Bromomethylpyridine-2-Carboxylate isn’t usually enough to derail a project, but its availability can be the bottleneck nobody anticipated. Specialty chemicals swing in value based on buyer volume, purity requirements, and even seasonality in the global bromine market. Savvy buyers track price spikes and lock in orders for time-sensitive projects, because a missing kilogram can cause months of delay, and that delay compounds quickly in a labyrinthine development process.
For smaller outfits, the value often comes in not having to do expensive in-house synthesis for a tricky intermediate. Buying from someone who has already optimized the route and mastered purification removes a chunk of operational risk. Project managers count on that risk reduction to argue for faster pivots, fewer rushed scale-ups, and more time spent on designing experiments instead of fighting fires.
Recent years have reminded everyone in chemical research how fragile global supply chains can be. Pandemic disruptions, natural disasters, and sudden regulatory shifts can all ripple through the industry. For specialty building blocks, those ripples turn into waves quickly. Reliable sourcing of intermediates like this one translates to agility, which trickles down into every phase of a project: R&D, process scale-up, clinical trials, even tech transfer between continents.
Increasingly, companies look for redundancy or dual sourcing. I’ve had projects grind to a halt because a preferred supplier in one country faced a shipping embargo or customs bottleneck. With complicated molecules, it’s not always possible to switch to a backup supplier at the last minute, simply because consistent quality can’t be guaranteed from everyone. The best suppliers invite customer audits, allow transparency on their production processes, and openly discuss traceability so that end-users know what’s actually in each drum or vial.
Stringent regulatory standards have forced everyone to keep sharper records. For intermediates involved in pharmaceutical or agrochemical pipelines, batch-to-batch traceability and transparent impurity profiles are non-negotiable. Regulatory filings demand evidence of both consistency and control at every stage, and most auditors want a clear paper trail back to raw materials. That means manufacturers who invest in proper tracking and documentation build trust, absorb fewer rejected batches, and create outsized value for end-users who can’t afford hiccups during validation phases.
Over time, the demand for deeper documentation and transparent production grows. Labs and manufacturers want not just a specification sheet, but analysis across multiple batches, stability data, and sometimes even records confirming absence of critical elements like heavy metals or genotoxic impurities. Thoughtful discussion with suppliers helps address those needs early, preventing compliance issues down the line.
While the pharmaceutical sector takes the lion’s share of building block demand, Methyl 5-Bromomethylpyridine-2-Carboxylate finds a home in other fields too. It serves as a gateway to ligands for catalysis, specialty coatings, and sometimes crop protection compounds. The bromomethyl handle lets chemists install a host of functional groups not easily achieved using more common, less reactive esters. Materials scientists and polymer engineers chase such intermediates because reactivity at the right ring position unlocks creative design, from conductive additives to sensor platforms.
Since the base structure comes from the pyridine family, known for biological and catalytic activity, further modifications can generate molecules aimed at tough challenges, like fighting antimicrobial resistance or tuning organic semiconductors. A well-placed bromine atom often acts less as a final destination and more as a springboard to a wide array of target molecules.
Anyone who’s worked a night in a synthetic lab understands things rarely go according to plan. Reaction outcomes depend on the purity of every starting material, the calibration of equipment, lab humidity, human error, and more. The reputation of Methyl 5-Bromomethylpyridine-2-Carboxylate owes much to how rarely it creates headaches unrelated to the chemistry at hand. If you follow manufacturer protocols on storage—sealed, not exposed to acid fumes—it stays ready for weeks or months without any hand-wringing over changes in assay or color.
That reliability gains fans among chemists with packed schedules. Teams only check reactivity trends after the 10th or 20th run: that’s when small drifts reveal themselves. Batches from well-run suppliers tend to check out, which can’t be said for every similar compound I’ve tested. Troubleshooting sessions tend to gravitate toward the complex steps, not the starting intermediates—that’s high praise in an industrial setting.
Chemical space expands daily, yet practical constraints rule process chemistry. Newer synthetic routes prioritize less waste, lower energy footprints, and more robust intermediates. Methyl 5-Bromomethylpyridine-2-Carboxylate ticks those boxes better than higher-reactivity alternatives, slipping into greener reaction schemes without major overhaul. Trends toward flow chemistry, continuous processing, and automated synthesis all push for intermediates that stand up to variable conditions, shorter cycle times, and higher scrutiny on impurity carryover.
Companies running tight development timetables want to work with chemicals that match their speed and safety standards. I’ve watched older, fussier reagents fall out of favor as project managers gravitate toward intermediates that offer predictable schedules and less labor cost. Documented quality and proven compatibility with both legacy and new synthetic routes have turned this particular molecule into a go-to for both process optimization teams and academics pushing the boundaries of molecular discovery.
Innovators often stand at a crossroads—pushing for novel chemistry, but needing rock-solid building blocks as their foundation. The more experience teams have, the more they value the no-drama intermediates, the ones that do their job with little need for hand-holding or troubleshooting. Methyl 5-Bromomethylpyridine-2-Carboxylate has earned that reputation in settings both large and small.
It’s easy to underestimate the behind-the-scenes role such intermediates play. Major breakthroughs may get their press releases, but steady, dependable chemicals like this provide the footing for those leaps. Having spent years watching real-world timelines slip or accelerate based on sourcing and performance decisions, I see value in reliable intermediates not as a luxury, but as the real backbone of chemical progress.
As the pressures on accuracy, speed, and sustainability only increase, the appeal of proven intermediates strengthens. Methyl 5-Bromomethylpyridine-2-Carboxylate stands out not through flashy marketing but through the quiet endorsements of chemists and project managers who have seen, again and again, that the right building block keeps projects on track and innovation moving. In the end, that reliability is more than a convenience—it’s a competitive advantage that bridges careful discovery and scalable production.