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HS Code |
996246 |
| Chemical Name | Methyl 2-bromopyridine-3-carboxylate |
| Synonyms | 2-Bromo-3-pyridinecarboxylic acid methyl ester |
| Cas Number | 120023-30-9 |
| Molecular Formula | C7H6BrNO2 |
| Molecular Weight | 216.03 |
| Appearance | Pale yellow to yellow liquid or solid |
| Boiling Point | 303.1°C at 760 mmHg |
| Density | 1.601 g/cm3 |
| Refractive Index | 1.582 |
| Smiles | COC(=O)C1=C(N=CC=C1)Br |
| Purity | Typically >97% |
| Solubility | Soluble in common organic solvents like DCM and methanol |
| Storage Conditions | Store at 2–8°C, tightly sealed |
| Hazard Classification | Irritant |
As an accredited Methyl 2-bromopyridine-3-carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 25g of Methyl 2-bromopyridine-3-carboxylate is supplied in a sealed amber glass bottle with a tamper-evident screw cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packed 160–180 drums or fiber cartons, each 200–250 kg, total 16–18 MT Methyl 2-bromopyridine-3-carboxylate. |
| Shipping | Methyl 2-bromopyridine-3-carboxylate is typically shipped in tightly sealed containers made of chemically resistant materials. It should be handled and transported according to international regulations for hazardous chemicals, protected from moisture, heat, and incompatible substances. Proper labeling and documentation must accompany the shipment to ensure safe handling and compliance. |
| Storage | Methyl 2-bromopyridine-3-carboxylate 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 oxidizers. Avoid exposure to moisture. Store the chemical at room temperature, and ensure proper labeling. Use appropriate safety measures, including secondary containment, to prevent leaks or accidental spillage. |
| Shelf Life | Methyl 2-bromopyridine-3-carboxylate typically has a shelf life of 2-3 years when stored tightly sealed, cool, and dry. |
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Purity 98%: Methyl 2-bromopyridine-3-carboxylate with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and consistent batch quality. Melting Point 75°C: Methyl 2-bromopyridine-3-carboxylate with a melting point of 75°C is used in fine chemical manufacturing, where reliable melting behavior aids controlled processing. Stability Temperature up to 120°C: Methyl 2-bromopyridine-3-carboxylate exhibiting stability temperature up to 120°C is used in catalytic coupling reactions, where it maintains molecular integrity during thermal procedures. Molecular Weight 216.03 g/mol: Methyl 2-bromopyridine-3-carboxylate with molecular weight 216.03 g/mol is used in agrochemical research, where precise mass facilitates accurate formulation and dosing. Moisture Content <0.5%: Methyl 2-bromopyridine-3-carboxylate with moisture content below 0.5% is used in custom synthesis, where low water content ensures minimal hydrolytic degradation. Particle Size <50 μm: Methyl 2-bromopyridine-3-carboxylate with particle size below 50 μm is used in solid-phase synthesis, where fine granularity enhances reaction kinetics and homogeneity. Assay by HPLC ≥99%: Methyl 2-bromopyridine-3-carboxylate with HPLC assay ≥99% is used in active pharmaceutical ingredient (API) development, where high analytical purity supports regulatory compliance. |
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On the production line, every kilogram of methyl 2-bromopyridine-3-carboxylate tells a story of careful material handling and strict quality targets. Our team has learned through experience that a good batch isn’t just about reaching the right purity on paper. It comes from supervised synthesis, stable storage, and honest testing. Methyl 2-bromopyridine-3-carboxylate (often referenced as its CAS number, 147513-32-2) draws interest from chemists who need a flexible intermediate. Its structure—halfway between simplicity and functional possibility—means it shows up in projects from pharma building blocks to advanced organic syntheses.
For some, the draw comes right from the pyridine ring, made more reactive by a bromine atom at the 2-position, and a methyl ester group at the 3-position. In the hands of research chemists, these features open paths that aren’t as easily accessed with unsubstituted pyridines or their chlorinated siblings. On our end, this has meant fielding questions about compatibility nearly every week: Does the product hold up under a range of temperatures? Can it be trusted for scale-up? Does it outclass similar compounds? Our reputation depends on those answers.
We’ve seen clients wrestle with batch-to-batch variation from questionable sources. That’s a headache. Pure methyl 2-bromopyridine-3-carboxylate should look almost colorless to pale yellow, with a clean NMR and HPLC trace, not a haze of impurities or faint off-notes. On our shop floor, even a light yellow tinge can prompt retesting, as it might point to partial hydrolysis or trace unreacted starting material. Methanol carries over easily if the final washes aren’t done right, and we spot-check it by GC before any drum goes out the door.
Research-stage customers tend to buy this molecule in fine-chemical grade, between 98% and 99% purity, as they want the ester intact for downstream transformations. In process development or pilot-scale production, chemists sometimes need larger volumes. Batch size affects the filtration and drying steps, and if those aren’t dialed in, the result is inconsistent melting point, off-smells, or persistent residual solvents. We catch these with real-world tests rather than relying on spec sheets alone. Too often, traders or resellers give vague answers when a client asks about crystallinity, batch processing history, or stability under humid air. As the manufacturer, we don’t have that excuse. We carry out ambient and accelerated stability testing—a lesson learned after an early customer had trouble storing an open bottle on a busy synthesis bay.
This molecule sits at an intersection of properties. Its bromine atom rests on a pyridine ring—an arrangement that leaves the ring activated to nucleophilic substitution, especially at ortho and para positions. We’ve supplied it to customers running Suzuki, Negishi, and other cross-coupling reactions, and we’ve seen methyl 2-bromopyridine-3-carboxylate outperform analogs where the reactive halide is on a benzene ring, rather than pyridine. Chemists sometimes ask whether the methyl ester survives aggressive reaction conditions. From the lab notebook to pilot plant, we have observed that the methyl group lends good resilience to hydrolysis up to modest base strengths.
Compared with 2-chloro- or 2-iodo-pyridine-3-carboxylates, the bromo compound hits a sweet spot on cost and reactivity. Bromides cost less per mole than iodides and activate the ring just enough—unlike chlorinated analogs, which force tougher conditions on the user. Green chemistry concerns drive users away from classic halogenated solvents, so we test the solubility of our product in safer alternatives. Methyl 2-bromopyridine-3-carboxylate dissolves in most standard polar organic solvents, and we double-check compatibility with industry-preferred DMF, DMSO, and acetonitrile.
The main use of methyl 2-bromopyridine-3-carboxylate traces back to its role as a synthetic intermediate. Many of our bulk clients turn it into pharmaceuticals, agrochemicals, or fine chemical derivatives. The molecule often acts as a lynchpin, connecting two or more building blocks through amide coupling, esterification, or nucleophilic substitution. Hazards multiply if a shipment arrives with impurities, as these can cascade through a multi-step synthesis, reducing yields or introducing tough-to-purge side products.
One research partner used this product for a new generation of kinase inhibitors, relying on its manageable reactivity and predictable behavior in Suzuki couplings. Another, in agricultural chemicals, built complex heterocyclic scaffolds by using this compound to anchor electron-withdrawing groups onto a pyridine ring for increased bioactivity. In both cases, feedback circled back to the consistency of melting point, purity testing against international standards, and the importance of even the small details—how dry the product stays after shipment, or how well the ester character holds up during storage.
Process engineers on our team keep an eye on how small impurities tested at ppm levels can tie up production downstream. For example, 2-hydroxy- or 2-unsubstituted pyridine derivatives must be kept at bay to avoid missteps in high-throughput screening programs. Each batch undergoes not just instrument checks, but deliberate wet chemical tests and repeat crystallizations. If the ester group shows any sign of partial saponification, it calls for a quick turnaround, not hand-waving.
Brominated compounds sometimes get a reputation for volatility or instability. Over the years, we learned that methyl 2-bromopyridine-3-carboxylate stores well enough in sealed, opaque containers away from heat. Our storage environment stays within 18–23°C—better than the high seasonal swings some clients report in their own warehouses. We always keep all moisture away, especially after running experiments that showed a slow climb in trace acid content during open-air exposure.
As the original manufacturer, our job continues past shipment. Clients return empty drums to us for quality investigations—even years after the fact. We test decomposition byproducts. We compare seasons of production against long-term stability, looking for shifts in color, odor, or melting range. Open collaborations with bench chemists have taught us not to rely on assumptions about shelf life. Experience forced us to add oxygen- and humidity-monitoring controls. For those storing large lots, we recommend layered storage (primary vessel, then outer drum) and strict first-in, first-out rotation, as high humidity damages this compound more through gradual ester hydrolysis than sudden breakdown.
Manufacturers see swings in bromine feedstock prices and regulatory tightening that traders and brokers seldom address openly. We balance raw material costs, careful allocations of labor and energy, and the pressure to maintain consistency even as input costs drift year to year. Over decades, we’ve invested in real-time analytics so that each furnace, each synthetic vessel, and each crystallizer gets instant feedback. By catching off-spec signals early, we avoid waste—and pass cost savings back to users through stable pricing on long-term contracts.
Scrutiny from regulatory bodies shapes our approach. Stringent inspections force us to keep an eye on batch genealogy and raw material traceability. Over the last decade, we’ve increased our transparency—sharing not just purity specs but full chromatograms and validation runs—because customers producing active pharmaceutical ingredients (APIs) ask for clear evidence. We keep that data in a format research teams can review and auditors can inspect in a single file.
Competitive products—like methyl 2-chloropyridine-3-carboxylate or the iodo analog—serve similar roles in reactive intermediate chemistry, but each comes with practical tradeoffs. Chlorides require higher-energy processes, often needing rounds of optimization to squeeze out usable conversion rates, especially in metal-catalyzed couplings. Iodides, more reactive, have higher cost and risk sudden volatility. Our bromide intermediate exhibits smoother kinetics over a broad set of reaction conditions, balancing cost and reactivity.
Some clients experiment with methyl 2-fluoropyridine-3-carboxylate, aiming for tighter control on downstream reactivity or metabolic stability. We have watched those syntheses demand stricter hazard controls and advanced purification—factors that upend most production time lines. The bromo intermediate, in contrast, allows wider process margins and safer handling. We don’t recommend mixing halide sources unless you’re running controlled optimization groups, as batch cross-contamination can sour entire synthetic plans.
Bench chemists often settle on the bromo compound once they audit their full costs: procurement, process yield, waste disposal, and time spent handling purification headaches. Over dozens of production campaigns, we have charted shorter process cycles and lower rejection rates compared to both lower- and higher-halogenated esters. This reflects on the bench and on the books.
No step in our process stays static. We reevaluate filtration, solvent recovery, and raw material inputs at each campaign. Analytical chemists audit impurity profiles with modern LCMS, flagging unknowns and co-eluters that broader screens miss. If a client’s downstream process flags a recurring impurity—even at marginal levels—we investigate synthesis parameters, carry out root-cause analysis, and adjust runs on the next lot.
Scaling up from gram-scale trials to multi-ton production reveals quirks that bench chemists seldom see: changes in crystal habit, subtle phase separation during quench, or rare dimerization if the batch spends too long in a reactor at low agitation. Our experience flags these process changes faster than outside labs. We don’t just hand off a product spec—we patch those learnings into the next run.
Material sourcing stays under careful watch, especially in the global market where supply disruptions have become routine. We lock in multiple bromine, pyridine, and methanol sources and audit each for compliance before ordering. Failures at any stage get investigated, not ignored. This matters every quarter, especially when higher-purity needs force rebalancing of procurement contracts.
End users ask pointed questions—about moisture pick-up, photostability, melting range, and adverse event history. Those who must clear strict regulatory reviews send formal questionnaires asking for every revision in analytical methodology. These audits have prompted us to tighten both batch documentation processes and internal review cycles.
Research clients often want to tweak downstream reactions and call on us for insights on product compatibility, solvent controls, or thermal reactivity. We share our own lab’s reaction logs and internal teams frequently run parallel test reactions, providing side-by-side yield and selectivity data on alternative halide intermediates. That feedback loop, running from lab bench to bulk production and back, sharpens the reliability of both our product and our customer’s process.
For a manufacturer, selling methyl 2-bromopyridine-3-carboxylate is more than meeting a written technical standard. We work side by side with process chemists scaling up from bench to production, and with research groups synthesizing new chemical entities. Our analytics track not only purity by HPLC but confirm lack of volatile or residual reagents, track moisture uptake over time, and benchmark optical clarity against internal standards.
The difference between a reliable supply of methyl 2-bromopyridine-3-carboxylate and a generic drum on the dock shows up in project timelines and cost control. Our focus remains fixed on getting the product right, responding to real-world use, and tuning each lot based on open conversation—not just data sheets. Integrity keeps the process honest, and hard-won experience behind the scenes sets the foundation for every downstream success.