|
HS Code |
175002 |
| Iupac Name | ethyl 5-bromopyridine-2-carboxylate |
| Molecular Formula | C8H8BrNO2 |
| Molar Mass | 230.06 g/mol |
| Cas Number | 53159-44-1 |
| Appearance | pale yellow to brown liquid or solid |
| Melting Point | 48-52 °C |
| Boiling Point | 326.5 °C at 760 mmHg (estimated) |
| Density | 1.51 g/cm3 (approximate) |
| Solubility In Water | low |
| Smiles | CCOC(=O)C1=NC=C(C=C1)Br |
| Inchi | InChI=1S/C8H8BrNO2/c1-2-12-8(11)7-6(9)4-3-5-10-7/h3-5H,2H2,1H3 |
| Refractive Index | 1.566 (estimated) |
| Logp | 2.0 (estimated) |
| Pubchem Cid | 4436618 |
As an accredited ethyl 5-bromopyridine-2- carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 25g of ethyl 5-bromopyridine-2-carboxylate is packaged in a sealed amber glass bottle with a printed safety label. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for ethyl 5-bromopyridine-2-carboxylate: Securely packed, sealed drums or bags, compliant with safety regulations, maximizing container efficiency. |
| Shipping | Ethyl 5-bromopyridine-2-carboxylate is shipped in tightly sealed containers, protected from moisture and light. It is transported according to chemical safety regulations, typically under ambient conditions. Proper labeling, documentation, and handling as a laboratory chemical—avoiding contact with incompatible substances—are ensured to maintain product integrity and ensure safe delivery. |
| Storage | **Ethyl 5-bromopyridine-2-carboxylate** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and direct sunlight. Keep it separate from incompatible substances such as strong oxidizers and acids. Store at room temperature, and ensure the chemical is clearly labeled. Follow all relevant safety protocols and local regulations. |
| Shelf Life | Ethyl 5-bromopyridine-2-carboxylate is stable for at least two years if stored tightly sealed, dry, and protected from light. |
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Purity 99%: ethyl 5-bromopyridine-2-carboxylate with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and contamination-free reactions. Melting Point 90-93°C: ethyl 5-bromopyridine-2-carboxylate with melting point 90-93°C is used in solid-state organic synthesis, where it facilitates precise thermal processing and crystallization. Molecular Weight 244.04 g/mol: ethyl 5-bromopyridine-2-carboxylate with molecular weight 244.04 g/mol is used in API development, where consistent batch-to-batch quality is maintained. Stability Temperature up to 150°C: ethyl 5-bromopyridine-2-carboxylate with stability temperature up to 150°C is used in heated reaction protocols, where structural integrity is preserved under elevated temperatures. Particle Size <50 μm: ethyl 5-bromopyridine-2-carboxylate with particle size less than 50 μm is used in fine chemical formulation, where superior dissolution and reactivity are achieved. Moisture Content <0.5%: ethyl 5-bromopyridine-2-carboxylate with moisture content below 0.5% is used in moisture-sensitive syntheses, where unwanted hydrolysis is minimized. Reactivity: ethyl 5-bromopyridine-2-carboxylate with high bromine reactivity is used in cross-coupling reactions, where selective halogen exchange and efficient product formation are enabled. Solubility in DCM: ethyl 5-bromopyridine-2-carboxylate with high solubility in dichloromethane is used in organic extraction processes, where enhanced phase transfer and recovery are achieved. |
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As a manufacturer, we don’t just list chemicals on paper. Each compound comes with real challenges, stories, and direct experience. Ethyl 5-bromopyridine-2-carboxylate stands out in our own catalog, and not just for its complexity. Here, we take you inside what it means to work with this product, why its characteristics matter in practical terms, and how it differs from similar molecules in the pyridine family.
Ethyl 5-bromopyridine-2-carboxylate is more than a tongue-twister or a list of numbers. Its structure—an ethyl ester of 5-brominated pyridine-2-carboxylic acid—starts with selecting the right grade of bromine and sourcing pyridine carboxylic intermediates. Materials need batch-to-batch consistency. For those unfamiliar, this compound carries a bromine atom at the 5-position, which is not just a small structural detail; it shifts both reactivity and handling compared to more common pyridine esters.
We typically produce it as a high-purity crystalline solid, pale in color, with well-controlled moisture content. Our team keeps water levels low, as this ester hydrolyzes faster than unbrominated analogs if exposed to high humidity. The production lab tolerates no shortcuts—each batch passes GC and HPLC purity testing, focusing on maintaining the pyridine ring's integrity. Sensitive detection limits matter for our partners, especially those scaling to bulk synthesis from pharmacy up to manufacturing scale.
Unlike warehouse traders, we handle the material freshly off the reactor or after the rotary evaporator. Bromine’s presence in this molecule means higher attention to skin and eye protection, along with precise venting. The team doesn’t underestimate the dust—operators suit up even for sampling, as trimmed fingernails carry residues into spreadsheet logs if protection slips for just a moment. In our packing room, stability data guides shelf life, and we store finished lots in dedicated cabinets.
Our largest volumes of ethyl 5-bromopyridine-2-carboxylate go directly into pharmaceutical intermediates. Medicinal chemists, particularly in solid tumor research, prize this building block for two main reasons. First, the bromine atom at the 5-position acts as a useful point for further functionalization—Suzuki, Heck, or other cross-coupling routes open pathways to complex heterocycles or diaryl linker segments. Second, the ester group’s moderate reactivity enables chemoselective transformations: skilled chemists can convert the ester to acids, amides, or alcohols under controlled conditions, with less risk of unwanted side products than with methyl esters or acids directly.
In agrochemical R&D, teams chasing next-generation herbicides experiment with this compound for scaffold hopping and structure-activity studies. It slots easily into synthetic schemes for nitrogen-heterocycle-based products. Fine chemical research uses it as a launching point for creating ligands or corrosion inhibitors, and we’ve even had inquiries from polymer chemists exploring novel pyridine-based copolymers.
On every run, there are moments that separate experienced hands from newcomers. Alkylation and bromination demand careful calibration of temperature and mixing speed. One winter batch, an unseasonably cold morning cooled the reaction flask short of our standard base temperature, slowing the kinetics and forcing us to adapt with gentle steam heating. Small variations in atmospheric moisture alter crystallization. We learned not to rush the filtration just because the shift clock was ticking—fine particle morphology can clog the filter cake, lengthening process time by hours.
Compared to plain ethyl nicotinate, the bromo group changes solubility and melting profile. Workers observe subtle differences even in smell and dustiness, which newcomers might miss. That is further proof that, in chemical manufacturing, no molecule is just “like” another—physical traits and reactivity shift in ways no desk-bound theory predicts. Each batch becomes a new lesson, reinforcing methods and trimming inefficiencies.
Ethyl 5-bromopyridine-2-carboxylate doesn’t act like raw 2-pyridinecarboxylic acid esters or their methyl relatives. In purification, brominated esters show a higher tendency for low-temperature precipitation, and workers see denser, less porous crystal beds. This may seem minor, but large-scale crystal formation affects filtration times and yield loss. The compound’s increased molar mass and bromine’s electronic effects make it more polarizable. In practice, this tweaks NMR signals, making quality control more reliable but pushing us to calibrate our instruments for sharper detection.
When compared to 3- or 4-substituted analogs, we notice that the 5-bromo positional isomer resists substitution and hydrolysis in some reactions, especially under basic conditions. This resistance lets researchers carry out multi-step syntheses with fewer side reactions, but also calls for longer reaction times during downstream manipulations. Cost calculations reflect bromine’s market volatility; production scale-up hinges on reliable, pre-booked halogen supplies.
We tolerate no compromize at the purification stage. Minute impurities line shelves with returned barrels if customers spot an off-spec peak in their chromatogram. Teams run repeated TLC and HPLC checks—investing time and solvent to catch the last traces of colored by-products or unreacted starting material. We once fielded a quality complaint straight from a pilot plant engineer whose team saw an unexpected UV absorbance. After a night’s comb-through, the culprit turned out to be a carry-over impurity from a reactor gasket change. Ever since, we add a pre-release batch check after every scheduled maintenance.
Researchers tell us that even minor impurities in this compound influence catalyst performance during cross-coupling. That’s not just hypothetical; we saw a client’s Suzuki reaction yield drop 20 percent until we reforged our purification regime. Fine-tuning the process lifted overall satisfaction, saved rework hours, and protected our customer’s tight timeline.
Supplying chemists means locking in not just what shows on the COA, but what doesn’t. Steady impurity profiles, direct feedback loops from buyers, and hands-on tweaks to process parameters distinguish manufacturers from traders. Over years, we have learned small shifts in bromine supplier lot can show up as minuscule differences in by-product distribution. Tracking and cataloging those shifts, even when not strictly required by regulations, spares many headaches downstream for formulation or scale-up engineers.
Batch consistency also depends on investments in training. Our team doesn’t leave new operators unsupervised with this compound for at least several runs. Brominated organics require real familiarity with their quirks—residues cling to glassware, subtle odors linger, and spill response means real practice. Every missed drip on a benchtop can compound into hours of cleaning, recalibrating, and repeated environmental testing.
Real-world production brings externalities. Sourcing bromine calls attention to sustainability—our purchasing team favors suppliers reporting lower overall process emissions per ton. Waste streams from bromination remain tightly monitored, with our plant matching regional and international requirements for halogenated waste disposal. We reclaim solvents where possible and track the fate of each kilogram that enters or leaves our compound’s process system.
Supply chain resilience came into sharp focus during global transport disruptions. With specialty chemicals, especially halogenated intermediates, gaps in storage and logistics stretch fulfillment from weeks to months. We address this by pre-purchasing raw materials during market lows and storing in climate-controlled warehouses, cushioned by frequent communication with both upstream and downstream partners. It’s bitten into margins in tight times, but kept our long-term relationships running when others could not deliver.
Direct interaction with scientists outside our factory gates reveals both their priorities and their pain points. We’re regularly asked how quickly we can turn custom-gram lots to kilo-scale. Pilots want to know if our compound stands up under pressure or when run alongside different base promoters. We supply real samples and run parallel reactions ourselves to spot differences in yield, isolation, or by-products. Joint problem-solving sometimes uncovers hidden issues, like solubility miscalculations or unintended crystallization during storage at low temperatures.
Over years, our technical support has flagged two main concerns: stability under ambient conditions and compatibility with common solvents. We tackled the first with stabilized packaging—double-bagged liners, neutral-pH cushioning, and temperature logging stickers that flag excessive heat during shipping. For solvent use, we run extra control reactions in-house, sharing observations with customers about which solvent mixtures yielded clearer solutions or more consistent coupling yields.
Real feedback loops go both ways. We once received a set of reaction vials from a client, post-failure. Their in-house analysis blamed the substrate, but our team’s repeat of their process (using our own material) showed high reactivity if water content came in below certain ppm. This guided a tweak to both our own drying step and their laboratory technique. The result was fewer failed runs and less wasted material on both sides.
Progress in chemical manufacturing is never static. Each time vendor supply chains tighten, raw material specs shift or regulations change, we reevaluate long-standing assumptions about our process. Experience tells us that innovation’s practical side depends on feedback from buyers, regulatory auditors, and line workers. Documentation improves only if practitioners communicate gaps.
For ethyl 5-bromopyridine-2-carboxylate, several opportunities constantly arise. One is optimizing crystal size for faster filtration in large runs, which cuts downtime and reduces solvent use. We have invested in small-scale pilot reactors with real-time particle size analysis for this very reason.
Another focus involves tracking trace levels of metals and other potential catalyst poisons. As more pharmaceutical clients move toward continuous flow and highly sensitive catalytic systems, our detection limits must surpass baseline requirements, avoiding arbitrary cutoffs and instead providing complete data on residual palladium, copper, or other transition metals.
Enhanced automation, with more advanced dosing and monitoring systems, helps us maintain tight reaction control, and minimizes human error. We partner with automation engineers to fit our reactors with smarter sensors. These changes reduce batch variation and improve yield predictability, but also present new challenges when recalibrating processes after small hardware upgrades or software patches.
No manufacturer survives on machines and chemistry alone. Years of direct relationships have shown us trust grows from short, honest answers and quick adjustments to shifting needs. Clients with long development timelines rely on regular updates: logistics, COA changes, even early warning if a raw material cost will impact their long-term projections. We ship test lots, not marketing samples. Our reputation depends on matching product description with the substance that arrives at the loading dock—every time.
Transparency also means admitting limits. Sometimes a requested purity proves unworkable, or a synthetic route reaches physical constraints. Rather than over-promise, we share technical hurdles openly and work toward workable compromise. Partnerships with analytical labs and synthetic consultants help us address issues sooner, saving all stakeholders time and resources.
Ethyl 5-bromopyridine-2-carboxylate is more than a line in a catalog. Its manufacture demands precision, adaptation, and continuous learning. Fielding real-world requests and failures keeps our methods honest. The compound attracts researchers because of what its unique structure makes possible in the lab—efficient couplings, reliable transformations, and a robust starting point for more complex pharmacophores. We witness firsthand how even minor tweaks to synthesis, storage, or packaging ripple through entire R&D pipelines.
Our factory teams know this compound’s quirks in the same way a craftsman knows their tools: spectral signatures, handling properties, and all those subtle cues that never appear in a standard description. Communication bridges the distance between factory and user, reinforcing that chemistry is fundamentally a collaborative, human business.
By staying grounded in process knowledge and open exchange, we not only meet expectations set by regulatory bodies and industrial partners, but help researchers push boundaries further. Ethyl 5-bromopyridine-2-carboxylate is a case study in how close collaboration—from bromine sourcing to finished batch delivery—improves outcomes for innovators and end users alike.