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HS Code |
296333 |
| Iupac Name | 5-bromo-6-hydroxypyridine-3-carboxylic acid |
| Molecular Formula | C6H4BrNO3 |
| Molar Mass | 218.01 g/mol |
| Cas Number | 63546-12-3 |
| Appearance | Solid (often off-white to light brown powder) |
| Solubility In Water | Slightly soluble |
| Structural Formula Smiles | C1=CC(=C(C=N1)C(=O)O)BrO |
| Pubchem Cid | 3255995 |
| Synonyms | 3-Carboxy-5-bromo-6-hydroxypyridine |
As an accredited 3-Pyridinecarboxylic acid, 5-bromo-6-hydroxy- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, with tamper-evident screw cap; label displays chemical name, hazard warnings, and lot number. |
| Container Loading (20′ FCL) | 20′ FCL (Full Container Load) safely loads 17 MT of 3-Pyridinecarboxylic acid, 5-bromo-6-hydroxy-, packed in 25kg fiber drums. |
| Shipping | **Shipping Description:** 3-Pyridinecarboxylic acid, 5-bromo-6-hydroxy- is typically shipped in a tightly sealed container, protected from moisture and light. It should be packed in accordance with local and international chemical shipping regulations, labeled as a laboratory chemical, and handled with care to prevent spills or exposure during transit. |
| Storage | Store **3-Pyridinecarboxylic acid, 5-bromo-6-hydroxy-** in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, moisture, and incompatible substances such as strong oxidizers and bases. Handle under fume hood if possible. Ensure proper labeling and keep away from sources of ignition. Avoid prolonged exposure and store at room temperature unless otherwise specified by the supplier. |
| Shelf Life | 3-Pyridinecarboxylic acid, 5-bromo-6-hydroxy- typically has a shelf life of 2-3 years when stored cool, dry, and sealed. |
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[Purity 98%]: 3-Pyridinecarboxylic acid, 5-bromo-6-hydroxy- with 98% purity is used in pharmaceutical intermediate synthesis, where high purity ensures optimal reaction yields. [Melting point 230°C]: 3-Pyridinecarboxylic acid, 5-bromo-6-hydroxy- with a melting point of 230°C is used in high-temperature organic syntheses, where thermal stability supports efficient processing. [Molecular weight 230.02 g/mol]: 3-Pyridinecarboxylic acid, 5-bromo-6-hydroxy- with a molecular weight of 230.02 g/mol is used in drug discovery research, where precise molecular profiling enables targeted compound screening. [Particle size <50 μm]: 3-Pyridinecarboxylic acid, 5-bromo-6-hydroxy- with particle size below 50 μm is used in formulation development, where fine granularity improves solubility and dispersion. [Stability temperature up to 140°C]: 3-Pyridinecarboxylic acid, 5-bromo-6-hydroxy- stable at temperatures up to 140°C is used in catalyst preparation, where thermal stability allows for consistent catalyst activity. [Moisture content ≤1%]: 3-Pyridinecarboxylic acid, 5-bromo-6-hydroxy- with moisture content not exceeding 1% is used in analytical reference standards, where low moisture enhances analytical accuracy. [UV absorbance λmax 310 nm]: 3-Pyridinecarboxylic acid, 5-bromo-6-hydroxy- exhibiting UV absorbance at λmax 310 nm is used in spectrophotometric assay development, where distinctive absorbance aids in sensitive detection. |
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Every successful introduction of a specialty chemical starts with genuinely understanding the needs in the lab, the plant, and the final end-use settings. After years working directly with pyridine-based intermediates in-house, handling their quirks, scaling up from small glassware to glass-lined reactors, and responding to batch-to-batch feedback from pharma and crop science R&D teams, our route to 3-pyridinecarboxylic acid, 5-bromo-6-hydroxy-, also known as 5-bromo-6-hydroxynicotinic acid, emerged out of practical questions: How clean can we make it; how reliably can we supply; and what structural features make this molecule worth the investment for our partners who need new options in heterocycle chemistry?
Specialty molecules like this don’t get a lot of attention in standard trade platforms, precisely because their users demand confidence beyond mere identification. So many stories in early-phase development involve a promising compound failing because a key intermediate couldn’t be sourced in time, or lacked the needed purity for a crucial condensation or coupling step. When industry projects come to us, the request is rarely generic; teams want reassurance that when they commit to a multi-kilo lot for synthesis or scale-up, they aren’t betting their project on a variable supply chain or inconsistent product behavior. Our approach is grounded in experience turning these requests into robust chemical processes and real reliability.
3-pyridinecarboxylic acid, 5-bromo-6-hydroxy- stands apart from other nicotinic acid derivatives in its versatile combination of chemical handles. The bromine substituent provides a key site for cross-coupling chemistry—especially Suzuki or Buchwald-Hartwig reactions—opening routes to generate new C–C or C–N bonds at the 5-position without unnecessary protection/deprotection steps. The 6-hydroxy group brings additional reactivity for etherification, esterification, or O-alkylation, and facilitates hydrogen bonding, which can shift solubility and interaction profiles in complex synthetic targets.
In practice, medicinal and agrochemical companies look for such hybrid functionality because it offers access to challenging heterocyclic scaffolds, often with significant patent space or biological relevance. This compound’s backbone builds off classical pyridine chemistry, but regulatory and commercial pipelines constantly push R&D teams to seek out modifications that increase activity, decrease off-target effects, or improve metabolic stabilities. We’ve seen requests from teams tuning lead candidates, developing enzyme inhibitors, or searching for new ligand frameworks that hinge entirely on their access to functionalized pyridinecarboxylic acids with clean, specific substitutions.
Making 3-pyridinecarboxylic acid, 5-bromo-6-hydroxy- at true manufacturing scale means more than quoting an assay on a COA. Down on the production floor, we deal with issues stacked up from process optimization. Bromination at the 5-position requires not only selectivity over the 3-carboxyl but careful control of exotherms and the minimization of over-brominated by-products. Introducing the 6-hydroxy moiety—especially ensuring regiochemical consistency—is a challenge that as a manufacturer, we address through repeated process validations and in-situ monitoring. Early pilots taught us to anticipate subtle color changes or downstream impurities that rarely show up in gram-scale academic runs, but can undermine commercial success if left unchecked.
Purity matters, but so does predictability in related compounds—especially those that might interfere with downstream reactions. By setting up analytical protocols combining HPLC, NMR, and mass spectrometry, we caught minor contaminants that could escape traditional methods. We learned quickly that some users pushing for high catalyst loading or using sensitive coupling partners hit hurdles even with minor residual halogenated by-products, so we set limits not just on the main compound, but also kept tabs on what could cause headaches later for their R&D groups.
We recognize that published minimum assay levels don’t always tell the story buyers need. Our in-house data shows that for a compound like 3-pyridinecarboxylic acid, 5-bromo-6-hydroxy-, a slightly higher moisture level or shifts in pH can change not only storage stability, but also reactivity as soon as the material moves into the first coupling step. Formulators and chemists working with these building blocks often ask for historical trend reports: how much did our melting point or residual solvent content shift over the last six batches; how does our GC headspace trace now compare to six months ago? These are questions only a manufacturer who runs the same reaction train, with the same cleaning regimes and solvent recovery, can answer with confidence. Our SOPs include batch release packages that go beyond minimal documentation, because feedback from users in scale-up and route scouting shows us what makes a difference once the project leaves the bench.
Having handled other brominated pyridines and matched them against our 3-pyridinecarboxylic acid, 5-bromo-6-hydroxy- side by side in real-world coupling reactions, we can say from practical experience these molecules do not behave identically—even when analytical data lines up. Downstream performance in cross-coupling or further modification often depends on small differences in trace impurity patterns, in polymorphic content, or on long-term storage characteristics. Feedback from multiple partners tells us they see fewer failed reactions and higher overall yields with our material because the process is highly tuned to reduce by-products that might deactivate Pd or Ni catalysts. Over the years, those savings in time and failed pilot runs have built up trust and repeat business.
Some people looking at the structural name might reach for whichever 5-bromo-nicotinic acid is on offer, but the interaction between the carboxy position, the bromine, and the hydroxy bears on reactivity and solubility behavior at every step from vitrification to chromatography purification. Our team has fielded calls about subtle precipitation issues or solvate formation, which we help debug because our chemists sit close to the process and document all observations across batches and seasons. With more off-patent intermediates and contract projects demanding deep technical support, we meet chemists where their challenges arise, not just with a bottle and a spec sheet.
Discussions with downstream innovators make clear that 3-pyridinecarboxylic acid, 5-bromo-6-hydroxy- isn’t just a commodity for inventory. It paves paths into diversified nitrogen-containing rings, fused components, and next-generation pharmaceuticals—not to mention its place in modern crop protection agents. Researchers rely on its dual functionalization to elegantly build up complexity without convoluted protecting group strategies. In agrochemical targets, the hydroxy and bromo handle lets formulators adjust molecular polarity and tailor environmental breakdown through synthetic control, meeting modern regulatory demands for both efficacy and biodegradability.
We’ve watched our material transition from gram-scale SAR campaigns to tens of kilograms supporting IND applications or new pesticidal candidates. In some cases, project chemists have looped back, sharing their results and unexpected observations, asking for tweaks (a slightly drier lot; different packing under argon) because our door remains open for discussion. Unlike generic listings that treat each intermediate as a line item, our operation is built for two-way feedback so we can improve both product and process.
Through years of scale-up work, we have learned how fine details affect ease of use. For example, slight lot-to-lot differences in granule size or density—from alternate crystallization solvents—can affect dissolution rates. A researcher seeking to dissolve a bulk supply for a hundred-litre reactor sees “flowability” not as an abstract ideal, but as a real-world bottleneck. In practice, user experience guides us to adjust drying times, sieve post-crystallization, or sometimes pack vessels with an eye to minimizing caking. A distributor or brokerage can’t offer these hands-on tweaks, but direct manufacturing carries the real incentive to keep buyers and downstream users happy, batch after batch.
As a lean manufacturer, we’re often pressed by external pressures—rising raw material costs, energy availability, and new environmental compliance demands. Each year tends to introduce a new challenge: restriction on halogenated waste streams, updated REACH registration, changing interpretations of hazardous shipment. We don’t treat these as obstacles for the customer to navigate, but instead deal with them day in, day out, so the compound arrives where needed, on time, and with the documentation teams require.
For us, scientific relationships take precedence over mere transactions. Chemists ordering this pyridinecarboxylic acid from a catalog may get the minimum they need, but rarely the certainty they want. Our plant runs the syntheses, handles each isolation and purification round, and confirms that not just the main peak, but the entire impurity profile, stays in line. Working directly with end users also surfaces recurring pain points—stray bromine, color stability, or issues upon re-crystallization after long storage. We address these at the root so they don’t become recurring themes in project delays.
During some recently completed multi-kilo campaigns with partners in Europe and Asia, we faced regulatory reviews that went deeper than the usual questions on origin. Notably, requests for “manufacturing traceability” and full analytical decks, including minor residual solvents and supply chain transparency, arrived months after initial shipments. Because we oversee the whole train from raw materials through shipping, not only could we furnish the full data package, we were able to share SOPs, analytical validation files, and even cross-lot variation analyses. Such comprehensive support is only possible at the manufacturing level, not as a feature of catalog re-labelers or intermediaries.
Sensible safety always comes down to direct experience. Some operators get lulled into complacency by familiarity; in our shop, repeated training and process hazard reviews back every batch. 3-pyridinecarboxylic acid, 5-bromo-6-hydroxy- demands respect for the brominated rings and carboxylic acid dust profile. We balance throughput targets with worker safety and environmental standards, addressing waste neutralization, air handling, and solvent recovery along the way.
Historically, many halogenated intermediates carried a significant environmental cost. We’ve revised our work-up protocols over time, implementing solvent recapture, reconfiguring some steps for lower-volume chlorinated solvent use, and, where possible, opting for aqueous or non-halogenated alternatives. Life-cycle thinking shapes product design from the earliest process chemistry right through to drum cleaning and loading into ISO containers. Partners who tour our site see firsthand how experience and cultural buy-in carries through from procurement all the way to warehouse release.
Producing laboratory-scale material remains an important part of innovation, but consistent scale-up is what drives results for industry. Our history working side by side with project leads as they move from bench to kilo to metric ton means we’re tuned into the subtle shifts that crop up at each scale. Reactor geometries, agitation, and heat-up rates all alter behavior of specialty heterocycles. Preventing runaway reactions, side-product formation, or loss of yield at larger volumes is as much art as science, and the only way to hone this is by running—and learning from—multiple campaigns.
Each delivery gives us another dataset. By monitoring not just release values, but also cycle time, analytical trending, and even handling differences in warehouse or at the dock, we give our customers both confidence and a collaborative edge. We keep clear lines with process chemists and formulation leads so problems can be fixed upstream, not just at the last minute.
A big part of our satisfaction comes from watching what innovators do with the intermediates we supply. In several pharmaceutical programs, our 3-pyridinecarboxylic acid, 5-bromo-6-hydroxy- has been built upon to launch exploratory SAR studies, then scaled into advanced intermediates supporting pilot plant syntheses. Our ties with academic teams offer insight into emerging uses, from ligand design to new materials chemistry. When questions about batch-to-batch fingerprints or analytical method transfers arise, we bring our own archives to address them, rather than leaving researchers to guess.
As new regulatory frameworks evolve and synthetic bottlenecks get tighter, companies and research groups turn to reliable manufacturing partners to ease pressure on timelines and project budgets. Handling regulatory paperwork, making timely improvements for purity or safety, and standing ready to troubleshoot technical queries all mean we’re partners, not just suppliers. Building trust with our peers leads to more open communication, shared learning, and smoother chemical innovation pipelines.
In our line of work, a specialty heterocyclic intermediate like 3-pyridinecarboxylic acid, 5-bromo-6-hydroxy- demonstrates its value not just by chemical structure, but by reliability, usability, and technical transparency. A compound may look similar on a spec sheet, yet perform very differently under real process conditions. Experience with the details—raw material sourcing, process controls, impurity removal, regulatory navigation, storage and shipment—cannot be tacked on at the last minute. It is built, batch by batch, by well-trained eyes in the lab and seasoned hands in the plant. Our role as manufacturers is not only to produce kilograms and tons, but to deliver confidence, adaptability, and insight to every partner who chooses to innovate with our products.