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HS Code |
708096 |
| Chemical Name | 6-bromo-5-chloropyridine-3-carboxylic acid |
| Molecular Formula | C6H3BrClNO2 |
| Molecular Weight | 236.45 g/mol |
| Cas Number | 885276-71-1 |
| Appearance | white to off-white solid |
| Melting Point | 180-185°C |
| Purity | ≥98% |
| Solubility | sparingly soluble in water, soluble in DMSO and DMF |
| Synonyms | 6-bromo-5-chloro-nicotinic acid |
| Storage Temperature | Store at 2-8°C |
| Smiles | C1=C(C(=NC=C1Br)C(=O)O)Cl |
| Inchi | InChI=1S/C6H3BrClNO2/c7-4-2-5(8)9-3(1-4)6(10)11/h1-2H,(H,10,11) |
As an accredited 6-bromo-5-chloropyridine-3-carboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle, sealed with a tamper-evident cap, labeled "6-bromo-5-chloropyridine-3-carboxylic acid, high purity, for research use." |
| Container Loading (20′ FCL) | 20′ FCL loads 6-bromo-5-chloropyridine-3-carboxylic acid in sealed drums, palletized, moisture-protected, compliant with chemical transport regulations. |
| Shipping | 6-Bromo-5-chloropyridine-3-carboxylic acid is shipped in tightly sealed containers under ambient conditions. Proper labeling, documentation, and compliant packaging are ensured to prevent leaks or contamination during transit. Handle with care according to chemical safety regulations. Shipping typically adheres to international guidelines for non-hazardous laboratory chemicals. |
| Storage | 6-Bromo-5-chloropyridine-3-carboxylic acid should be stored in a tightly sealed container, protected from light and moisture. Keep it at room temperature, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Proper labeling and access only by trained personnel are recommended to ensure safety and maintain chemical stability. |
| Shelf Life | 6-bromo-5-chloropyridine-3-carboxylic acid remains stable for 2-3 years when stored in a cool, dry, tightly sealed container. |
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Purity 98%: 6-bromo-5-chloropyridine-3-carboxylic acid with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and consistent batch quality. Melting point 205°C: 6-bromo-5-chloropyridine-3-carboxylic acid with a melting point of 205°C is used in solid-phase peptide synthesis, where it maintains compound integrity during reaction conditions. Particle size <50μm: 6-bromo-5-chloropyridine-3-carboxylic acid with particle size less than 50μm is used in high-performance liquid chromatography, where it leads to improved solubility and homogeneous mixing. Stability temperature up to 120°C: 6-bromo-5-chloropyridine-3-carboxylic acid stable up to 120°C is used in agrochemical formulation development, where it offers reliable performance under process heating. Moisture content <0.5%: 6-bromo-5-chloropyridine-3-carboxylic acid with moisture content below 0.5% is used in API manufacturing, where it prevents hydrolytic degradation during storage and use. UV absorbance λmax 275 nm: 6-bromo-5-chloropyridine-3-carboxylic acid with UV absorbance λmax of 275 nm is used in analytical reference standards, where it enables accurate spectrophotometric quantitation. |
Competitive 6-bromo-5-chloropyridine-3-carboxylic acid prices that fit your budget—flexible terms and customized quotes for every order.
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Our journey with 6-bromo-5-chloropyridine-3-carboxylic acid starts on the production floor, not an office desk. This compound, best known by its structure—bromine at the six position, chlorine at the five, carboxyl at the three, all on a pyridine ring—represents precision and selectivity so often demanded by pharmaceutical innovators and fine chemical researchers. Its synthesis takes patience, careful feedstock selection, and a plenty of hands-on checking of every step. The chemical formula reveals more than numbers and symbols; it speaks to its real-world role as a functionalized building block.
What matters most after synthesis comes from reliable isolation. Our process delivers 6-bromo-5-chloropyridine-3-carboxylic acid as a pale, crystalline solid—no sticky residues, no off-smells. Over years of trial and error, we found that maintaining moisture control and tight pH windows during recrystallization leads to powders that meet the highest standards in both purity and ease of handling. Recently, stricter client demands for purity, usually hovering above 98%, have led us to optimize our chromatography steps. Each time, we send out product, it leaves our facility only after batch-specific HPLC and NMR analyses pass the benchmarks—not merely internal standards but also the ones confirmed by outside laboratories acting as external referees.
Lab chemists and process scale-up teams come to us because they want every single batch to perform the same way. In the early years, the variability in halogenated pyridines led to inconsistent reactions and weighed down yields—not only in-house, but when our customers scaled up their reactions. In response, we implemented integrated in-process checks, and built a culture where every technician double-checks their own runs using real chromatography data, not assumptions. Minor changes in moisture content, or surface area, can tip off unintended isomer formation or hydrolysis; we won’t ship a drum that hasn’t passed hands-on examination.
6-bromo-5-chloropyridine-3-carboxylic acid goes where simple pyridines or monosubstituted pyridines can’t. Each substitution, bromine and chlorine, brings a different kind of reactivity when coupling, acylation, or halogen-exchange reactions are required. Sourcing both halogens on a preactivated pyridine core, with the carboxylic acid, saves hours in process development labs and reduces risk. Some clients used to start with unsubstituted or monosubstituted pyridines, slogging through multiple synthetic steps, each adding cost and adjustment. The direct route this product provides dramatically reduces not only solvent waste and time but the headache of reproducibility challenges. The dual halogen pattern also gives medicinal chemists a chance to program orthogonal reactivity in late-stage diversification.
This compound doesn’t see use as a solvent, nor does it belong among basic intermediates churned out by bulk chemical plants. We see it ordered by gram and kilogram scale, destined for precise applications—usually as a starting point for heterocyclic drug fragments, specialty agrochemical actives, or sensor development. In the early 2010s, requests trickled in for single-comma-kilogram lots; in the last few years, we have been producing this at thirteen times that scale, driven by consistent demand from pharmaceutical custom synthesis groups. They rely on its selective reactivity to install new complexity, or introduce new ligand frameworks for catalyst design.
It matters how a compound holds up over months or during a bumpy shipment half a continent away. In our own experience, the 6-bromo-5-chloropyridine-3-carboxylic acid holds stable under ambient, dry conditions. Humidity, though, brings risk of slow hydrolysis and caking—less a theoretical concern and more a reality for anyone who has opened up a drum that left a loading dock in the rainy season. Our solution? We always package in double-sealed polyethylene liners inside rigid drums, with desiccant pouches, and monitor storage room humidity. For the labs that move only through a few grams a month, we provide vacuum-sealed bottles to lock out moisture and avoid product degradation. Long-term stability studies in our warehouse show less than 0.2% change in purity over a 24-month period under controlled conditions. This hands-on regimen protects not only shelf life but performance during critical reaction runs.
There’s a long list of halogenated pyridine carboxylic acids available on the market—so the question always returns: why choose this one? We spent years comparing its performance alongside 6-chloropyridine-3-carboxylic acid, 5-bromopyridine-3-carboxylic acid, and several dihalogenated analogs. Time and again, our collaborators have reported that this particular arrangement of bromine and chlorine delivers superior compatibility in Suzuki and Negishi couplings, especially in ligand-free conditions. In our own trials, side reactions and double dehalogenation tendencies decline sharply. There’s also a practical matter—other isomers sometimes show competing ring closures or require more stringent anhydrous handling, issues we have seen less frequently with this product.
With an exact molecular weight and formula, 6-bromo-5-chloropyridine-3-carboxylic acid doesn't leave much room for uncertainty. Chemists see its melting range (from our last dozen production runs, typically 194–198°C) as a real checkpoint—deviations from this range cue us to investigate impurities well before any shipment leaves the production area. From a physical handling perspective, the compound’s moderate solubility in polar aprotic solvents makes it a reliable player in modern coupling chemistry. Those details seem minor until a batch sits undissolved, holding up work on a deadline. We have tuned our crystallization process to keep the final powder easily dispersible, limiting fines so that lab staff can weigh and transfer quickly without endless scraping.
Manufacturing specialty halogenated pyridines raises safety, worker health, and environmental issues we tackle head-on. Earlier years saw higher waste volumes, especially mother liquors and wash solvents with persistent halogen content. These legacy issues motivated us to overhaul waste stream management, investing in multi-stage recovery and dehalogenation units, not just because of environmental compliance but because every liter saved brings down overall overhead. We trained up our staff—split between the reaction halls and the environmental unit—on the dangers of dust inhalation and correct PPE use, reporting no significant workplace exposure events since 2017. That bears out in smoother audits, but more importantly, keeps our own team and the receiving labs safe.
On the manufacturing end, the real headaches come with scale jumps. We started with flask syntheses, then scaled up to stirred reactor tanks, all while learning from batch to batch. Automated feeding and careful temperature controls help us match the quality from small runs to kilogram lots. Bottle-to-drum consistency comes from double-layered cleaning protocols, redundant raw material checks, and real-time data feedback loops. We’ve thrown out production runs—costly but necessary—rather than ship anything with suspicious purity drifts. Most clients request pilots before scaling up; we walk them through the same control points that govern our own processes, letting them compare lab to kilo scale outcomes directly.
Reliable supply means more than producing a stockpile. We source our feedstock halopyridines directly from vetted partners who meet our quality spec every time. Even a slight variation in precursor halide ratios can spell trouble downstream, causing off-colored residues or unpredictable melting points. Global logistics headaches—pandemic shutdowns, shipping delays, customs holds—prompted us to keep a rolling buffer inventory and to shift as much regional sourcing as possible. Direct communication with downstream formulators keeps their schedules aligned with our output. By trimming down unnecessary middlemen and building direct relationships, both sides see fewer surprises.
The most useful insights come from the bench—the researchers using 6-bromo-5-chloropyridine-3-carboxylic acid in iterative reaction screening. Every few months, we gather case studies and feedback from users: observations on dissolution times, on byproduct formation, on unexpected thermal sensitivities. Even small issues—such as minor dusting during weighing—feed back into our production workflow. Ongoing conversations with customers have, more than once, pushed us to recalibrate particle size, tweak drying protocols, or rethink packaging solutions. We’ve seen a direct payoff in lowered return rates and higher client retention as a result.
A common question from new partners involves handling and compatibility—can this molecule stand up to multistep chemistry, or will it throw off side products not listed on datasheets? Our own internal R&D teams combine published literature with proprietary runs to vet reactivity under common carbon–carbon or carbon–heteroatom coupling conditions. We maintain a rolling database, updated every quarter, referencing real-world yields, impurity profiles, and troubleshooting notes. Sharing that data, instead of quoting theory alone, helps our users fine-tune their methodology faster. We do not withhold raw observations, as we know open data exchange means greater reproducibility across labs.
Some believe that specialty chemicals like dihalogenated pyridine carboxylic acids belong to slow-evolving product lines. From the manufacturing side, nothing stays still. Yearly shifts in downstream chemical regulations, green chemistry mandates, and shifts in user needs push us to keep refining everything from packaging to purification. We have started integrating real-time process analytics and digital tracking, tying every lot to a traceable history of production steps, source batches, and analytical results. The aim is to minimize recall risk, but also to allow clients to audit their own regulatory compliance without guesswork. In a market gripped by supply chain instability and shifting standards, that traceability acts as a stabilizer.
We know that any chemical supplier can list specs, tout purity, or mention compliance, but years of hands-on records and ongoing feedback underline one point: consistent, batch-to-batch reliability matters most. Our investment in quality control, safety, and responsiveness begins with the raw materials and continues through to customer follow-up. Through cycles of regulatory and client-driven change, our commitment remains the same: provide a product that works the same every time it’s opened, from vial to drum, supporting those who create the next generation of pharmaceuticals, agrochemicals, and discovery chemistry. We don’t just ship product; we stand behind it, track its history, and listen to those who use it.