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HS Code |
922814 |
| Product Name | Acide 4-bromopyridine-3-carboxylique |
| Synonyms | 4-Bromopyridine-3-carboxylic acid |
| Cas Number | 6358-67-6 |
| Molecular Formula | C6H4BrNO2 |
| Molecular Weight | 202.01 |
| Appearance | White to off-white powder |
| Melting Point | 220-225°C |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=CN=C1Br)C(=O)O |
| Inchi | InChI=1S/C6H4BrNO2/c7-5-1-4(6(9)10)2-8-3-5/h1-3H,(H,9,10) |
| Storage Conditions | Store at room temperature, tightly closed |
As an accredited Acide 4-bromopyridine-3-carboxylique factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Acide 4-bromopyridine-3-carboxylique, 5g, is packaged in a sealed amber glass bottle with a tamper-evident cap and label. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packs Acide 4-bromopyridine-3-carboxylique in sealed drums/cartons, ensuring safe, compliant international shipment. |
| Shipping | Acide 4-bromopyridine-3-carboxylique is shipped in secure, airtight containers to prevent contamination and moisture exposure. It is labeled according to hazardous material regulations and transported under controlled conditions, with appropriate documentation and handling instructions to ensure safety and compliance with chemical shipping standards. |
| Storage | 4-Bromopyridine-3-carboxylic acid should be stored in a tightly sealed container in a cool, dry, and well-ventilated area. Keep away from sources of ignition, heat, and direct sunlight. Store separately from incompatible substances such as strong oxidizers and bases. Ensure proper labeling and secondary containment to prevent leaks and spills. Use only with appropriate personal protective equipment. |
| Shelf Life | **Shelf Life:** Acide 4-bromopyridine-3-carboxylique is stable for at least 2 years when stored in a cool, dry place. |
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Purity 98%: Acide 4-bromopyridine-3-carboxylique of purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield of target compounds. Melting Point 210°C: Acide 4-bromopyridine-3-carboxylique with melting point 210°C is used in high-temperature organic reactions, where it provides thermal stability during processing. Molecular Weight 216.01 g/mol: Acide 4-bromopyridine-3-carboxylique with molecular weight 216.01 g/mol is used in drug design studies, where it allows precise stoichiometric calculations. Particle Size <50 µm: Acide 4-bromopyridine-3-carboxylique with particle size less than 50 µm is used in solid-state formulation processes, where it supports uniform dispersion and reactivity. Stability up to 80°C: Acide 4-bromopyridine-3-carboxylique with stability up to 80°C is used in accelerated stability testing for research, where it minimizes thermal decomposition. Water Content <0.5%: Acide 4-bromopyridine-3-carboxylique with water content below 0.5% is used in moisture-sensitive syntheses, where it reduces byproduct formation and maintains product integrity. |
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As a manufacturer with years at the production line, seeing the shift in demand for precision intermediates has shaped the way we approach products like Acide 4-bromopyridine-3-carboxylique. In the early days, purity targets hovered at the edge of 97%. These days, with life science and fine chemistry pushing the envelope, batches—ours included—routinely reach 99% and above. Meeting these numbers needs discipline through each stage, from crystallization to rigorous impurity checks. To keep consistency, every reactor, every wash, and every dry box needs hands-on attention, not just automated tracking.
The model we currently produce achieves this by leveraging a multi-step protocol built directly from feedback in our own pilot projects and long-term collaboration with custom synthesis groups. Chromatographic analysis after synthesis picks up even trace byproducts, which can make a difference in downstream reactions. Trace halogenated impurities, often ignored by less experienced outfits, catch our chemists’ eye—an approach shaped by real laboratory headaches caused by undetected contaminants.
In our sector, this molecule rose from the periphery due to its pivotal role in coupling reactions. Year after year, our clients—often medicinal chemistry units or materials science innovators—circle back to this acid for two primary reasons: its clean bromo-positioning and the reactivity window offered by the pyridine ring. Synthetic flexibility rests on the specifics of substitution; the carboxylic acid at the third position and bromine at the fourth together open routes not possible with alternatives like 2-bromo or 5-bromo-derivatives.
Unlike generic halopyridines harvested from typical batch runs, our compound’s narrow impurity profile means less troubleshooting for scientists. In drug project sprints, wasted weeks spent tracking down unexpected side products can derail timelines. By keeping halide impurities and regioisomers in check, we help keep the synthesis pipeline unclogged.
For years we produced to a baseline, but end-users kept reporting on what really mattered: solubility in key organic solvents, melting point reproducibility, performance as a coupling partner, and stability against decomposition. Armed with that, our in-process testing focuses squarely on LC-MS and NMR verification, batch stability tests under various storage conditions, and routine assays for moisture uptake. Spec readers might expect to see basic physical data, but a blind eye to subtle features—volatile impurities, for example—costs real money in downstream development. If a researcher wants to drive palladium-catalyzed couplings or esterifications at scale, these details shape the process far more than simple numbers on a data sheet.
In our facility, the development chemists often bring bench-scale stories straight to production. A recent round of Suzuki and Buchwald–Hartwig coupling assessments showed this acid’s edge in arylation sequences. Our raw material behaves smoothly in these cross-couplings because it avoids the latent side reactivity sometimes unlocked by misplaced halides or stray methyl groups. During scale-ups, poor quality intermediates can hamstring a synthesis sequence, making purification a practical nightmare. The current model’s consistent bromo and acid substitution lets scientists confidently push towards scale, with minimal surprises during work-up or crystallization steps.
Colleagues working in crop-protection chemistry and electronics noticed similar advantages. When introducing 4-bromopyridine-3-carboxylic acid into building block libraries for agrochemical candidates, the precise functionalization allows for molecule optimization without rerunning extensive purification protocols. Organic electronics teams, always on the lookout for fine-tuned heterocycles, combine its structural motif with other aromatic systems, banking on both electronic and spatial influence for superior material properties.
Not all pyridine derivatives work the same. Through side-by-side scale-ups on our own line, we have tracked comparative rates and selectivities under identical conditions. Compared with 3-bromopyridine-4-carboxylic acid, for example, our product consistently gives tighter melting ranges, stronger shelf life, and notably higher yields in carbon–carbon coupling scenarios. In practice, yields can jump by 5-15%—not an academic difference, but a significant factor in costs and time for any project with tight deadlines.
Some manufacturers cut corners during isolation. Our in-house teams once struggled with material from traders who overlooked residual solvent washing; the result—a persistent, faint aromatic taint in NMR signals. Residual solvents like DCM, methanol, or even unexpected acetone can linger, shifting reaction profiles and leaving production engineers chasing avoidable ghosts. With our current protocol, extensive vacuum treatment and multi-stage recrystallization have nearly eliminated recurrent solvent contamination, a detail born out of hands-on frustration.
Process tweaks start with the very chemists who run into those obstacles on the shop floor. Each improvement, whether it’s an extra filtration pass or a shift in crystallization temperature, gets stress-tested and logged by our QC team. When early batches revealed that some older filter media were leaching trace minerals, we worked with a local supplier to bring in cleaner equipment—real-time changes decided right at the plant level.
Another innovation involved reducing the risk of thermal decomposition. By monitoring each heat stage not just for target temperature, but for ramp rate and hold time, we changed loss rates from significant to trace. Improvement took several quarters to stabilize but now runs as standard. This kind of adjustment doesn't stem from a manual or outside suggestion, but from repeated cycles of troubleshooting and observation in our own workflow. A small efficiency on the reactor floor means lower cost and waste for everyone in the downstream chain.
Our earliest experience with outsourced material taught us more than a decade’s worth of hard lessons. Once, during a critical customer project, an unnoticed spike in iodine contamination nearly triggered a six-figure loss. Cleanup and re-validation chewed through a month of unbudgeted labor. The mistake forced us to tighten monitoring for halide profiles and brought home the reality: overlooked trace elements sabotage entire compound libraries. Chemists, not trained to play detective with every shipment, rely on upstream diligence. As the originating producer, the obligation falls to us.
Years of working at scale showed us that moisture control makes or breaks lot performance. Pyridine derivatives especially attract and hold water in unpredictable ways. Even after vacuum drying, one rainy week caused containers to leach measurable water content, impacting coupling efficiency downstream. In response, our facilities added redundant humidity control in both packaging and short-term storage—solutions created from relentless after-action reviews, not a checklist.
Customers often ask about supply chain stability and confidence in traceability records. As makers, not mere brokers, we keep logbooks tracing each critical raw material’s batch. Each block, from precursor halopyridine to final acid, ties back to our on-site stores. This level of transparency means when a partner runs into an unexpected reactivity issue or a registry number mismatch, we can pinpoint where deviation might have happened—sometimes within hours. It takes commitment to continuous improvement, keeping records that don’t just tick boxes, but serve the chemist facing a time crunch.
Unlike commodity products passed between trading houses, every output from our reactors holds a direct record trail back to source compound, synthetic pathway, and analytical confirmation. It’s not just about regulatory compliance; it’s about keeping projects on target, especially when collaborations extend across borders or involve multiple R&D sites.
Some projects grind to a halt over minor irregularities invisible on paper. Over months, we tracked a pattern: clients returned with complaints about “inconsistent behavior” in coupling steps. Internal review connected these problems to trace transition metal residues, a legacy of re-used catalyst beds. The solution took more than a single cleaning cycle; it demanded a complete overhaul in catalyst management and in-line monitoring, a shift only practical for a manufacturer with hands-on oversight. Follow-up batches, subjected to parts-per-billion screens, cleared persistent byproduct formation and restored confidence in rapid delivery contracts.
Similar collaboration led to modified packaging after discovery that some solvent-resistant liners leached minute plasticizers into sensitive compounds during summer transit. Direct input from process chemists brought about rapid upgrades to our packing room infrastructure. By involving stakeholders straight from the bench-top, we've streamlined the entire supply workflow.
Resellers often lack access, both to the production line and to feedback loops from end users. As the group responsible for actual molecule assembly, we’ve watched how slight operational variations—crystallizer rpm, filtration pressure, extended purge times—shift product quality in meaningful ways. Our end customers work at the sharp end, under budget and schedule pressures where minor variances spell the difference between success and repeat work. Learning from real process incidents, we tailor both synthesis and QC methodology to actual use cases—lab findings inform plant adjustments, in a cycle that wholesalers rarely witness.
Direct communication lines mean problems come straight to engineers familiar with both the chemistry and real-world applications. This builds trust looped around expertise, not marketing gloss. Chemical manufacturing thrives on such honest conversations, where production headaches, delivery bottlenecks, or scalability limits surface early. Feedback from the field has pushed us to refine cycle times, customize packaging volumes, and run extra stress tests—all changes impossible to pursue through arms-length intermediaries.
Across projects, what stands out isn’t only high delivered purity, but the reliability of consistency under repeat order cycles. Clients reach out for more of our Acide 4-bromopyridine-3-carboxylique because, batch to batch, these key metrics hold steady: clean IR and NMR profiles, reproducible melting and solubility data aligned with their most demanding reaction conditions. The result: fewer failed runs, faster troubleshooting, and reduced waste.
Over decades, our logbooks fill with product return rates, deviation reports, and corrective actions, each entry a lesson. Recurring patterns signal both opportunity and risk, and we push improvements based on documented feedback. Precision, less visible than headline purity figures, comes out most in side-by-side process trials—how the molecule performs not on paper, but in glassware and reactor. That feedback tightens our controls and keeps us focused on end-purpose utility.
Accountability matters from more than just a compliance perspective. With tightening industry standards and new environmental rules, we invested in closed-loop solvent recovery, energy monitoring, and byproduct reclamation on our line. These aren’t just for regulatory box-ticking; minimizing off-spec material, water usage, and hazardous waste cuts downstream operational risk for every customer in the chain.
Production teams track the environmental impact and actively overhaul steps vulnerable to excess waste or emissions. One such change—switching from an older high-solvent crystallization process to a more efficient, greener protocol—lowered waste barrels by more than half per ton produced over the last year. Conversations with industrial partners led us to adopt green chemistry metrics, translating into more sustainable delivery for everybody who designs around our compound, whether for medicinal chemistry or specialty materials.
Beyond analytical reports and certificates, the value rests with our people—synthetic chemists, production managers, and QC staff—who recognize the link between molecule and finished application. The tradition here is practical: solutions come from lab and plant, not only from deskwork. Competitive edges result from hands-on synthesis and unfiltered response to setbacks: from improved filtration protocols, humidity control improvements, down to the selection of personal protective equipment geared for these specific production runs.
Every detail matters. From the way the acid is dried and packed—protected against both ambient moisture and direct sunlight—to the monitoring of each lot’s journey from our site to doors worldwide, the end-user benefits from an unbroken chain of responsibility. This molecule earned its place over repeated, hard-won successes and course corrections, with each improvement marked by real, measurable results.
Our experience manufacturing Acide 4-bromopyridine-3-carboxylique brings home an ongoing lesson. Materials shape real science when produced and delivered in partnership with those who put them to the test daily. The difference between a functional raw material and a chronic source of trouble in the lab often starts long before shipment—at the intersection where process chemist, QC analyst, and production lead share responsibility for outcomes, not just outputs.
We welcome discussions based on feedback and open books, because the only way to refine performance is with a direct line of communication. With every lot leaving our plant, expectation matches reality—not due to chance, but from years of persistent learning and focused production practices. That story, not a glossy product list, forms the real backbone of our commitment as a chemical manufacturer.