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HS Code |
423272 |
| Iupac Name | 4-Bromopyridine-2-carboxylic acid |
| Molecular Formula | C6H4BrNO2 |
| Molecular Weight | 202.01 g/mol |
| Cas Number | 63006-18-4 |
| Appearance | White to off-white solid |
| Melting Point | 205-210°C |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=NC=C1Br)C(=O)O |
As an accredited 4-Bromopyridine-2-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "4-Bromopyridine-2-Carboxylic Acid, 25g." Tamper-evident seal; hazard symbols and handling instructions are present. |
| Shipping | 4-Bromopyridine-2-carboxylic acid is shipped in secure, chemical-resistant packaging, clearly labeled with hazard information. It is transported in compliance with relevant regulations for chemical safety. The container is sealed to prevent leaks, and accompanied by a Safety Data Sheet (SDS). Handle and store in a cool, dry, and well-ventilated area. |
| Storage | 4-Bromopyridine-2-carboxylic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep it separate from incompatible substances such as strong oxidizing agents. Store at room temperature and avoid exposure to excessive heat. Ensure all containers are properly labeled to prevent accidental misuse or contamination. |
Applications of 4-Bromopyridine-2-Carboxylic Acid in Industrial ManufacturingAs a direct manufacturer of 4-Bromopyridine-2-Carboxylic Acid, we connect with leading industrial users across pharmaceutical, agrochemical, and specialty chemical sectors. This section showcases the practical deployment of our material in critical downstream processes. Each application focuses on genuine industry needs, compliant practices, and precise integration into modern manufacturing flows. 1. API Intermediate in Antiviral Drug SynthesisMany pharmaceutical companies utilize this acid as a building block for nucleoside analogue synthesis, particularly in antiviral API development where the bromo and carboxyl functionalities enable selective transformations. Our material serves as a key intermediate in the early-stage diversification of pyridine scaffolds, supporting high-value product lines subject to stringent regulatory and analytical requirements. Industry compliance standards
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2. Agrochemical Herbicide PrecursorMajor agrochemical formulators employ this molecule as a modular building block for synthesizing selective herbicides. The pyridine core, with its electron-withdrawing bromo and carboxyl groups, is instrumental in generating heterocyclic systems with targeted pre- and post-emergent weed control properties. Industry compliance standards
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3. Specialty Fluorinated Pyridine Compound ManufacturingFluorochemicals manufacturers leverage this pyridine derivative as a key halogen-exchange substrate for the production of fluorinated intermediates. The electron-poor aromatic system permits regioselective fluorination, which is foundational for downstream use in fluorinated active ingredients in both crop science and specialty chemical segments. Industry compliance standards
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4. Advanced Dye Intermediate for Electronic DisplaysOur material is incorporated by advanced colorants manufacturers in the synthesis of functional pyridine-based dyes for LCD and OLED displays. Its structural features facilitate targeted coupling and cyclization, ensuring defined electronic configurations for stability and chromatic performance under device operation conditions. Industry compliance standards
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5. Research-Grade Building Block for Custom Ligand SynthesisSpecialty chemical labs and technology enterprises select this compound for custom ligand fabrication due to its reactivity profile and substitution pattern, which support coordination chemistry and next-generation catalyst design. Academic groups and high-tech R&D units utilize such raw materials to optimize ligand motifs for transition metal catalysis and fine chemical transformations under rigorously controlled conditions. Industry compliance standards
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Working in chemical manufacturing day in and day out, you gain an appreciation for the quirks and challenges of every compound that travels through the plant. 4-Bromopyridine-2-carboxylic acid, model 1039-09-8, brings those challenges in spades and stands apart from the crowd—both for its structure and for the ways it supports modern science and industry. It’s a pale, crystalline substance you come to know by its sharp odor and its tendency to settle in the bottom of the reaction flask if you’re not careful, but over time, you see beyond that into the role it plays out beyond these walls.
First-hand, chemists look for a compound like this not for its own sake, but for what it brings to the table in drug discovery, material science, and synthesis projects. The bromine at the four position on the pyridine ring offers a level of synthetic versatility that pure pyridine carboxylic acids can’t match. In the lab, it acts as a dependable building block—a starting point that accepts transformations without buckling under normal conditions. Researchers rely on the functionality combination: a carboxylic acid that withstands manipulation and a bromine atom that serves as a handle for cross-coupling and substitution chemistry.
Manufacturing 4-bromopyridine-2-carboxylic acid at scale takes careful control and an eye for unexpected batch-to-batch quirks. The compound forms off-white to faintly yellow crystals, not unlike many halogenated heterocycles. Our reactors keep moisture under control to stop unwanted hydrolysis, especially when working above 60 degrees Celsius. Most projects call for material at 98% or greater purity. In pharmaceutical research, even a trace impurity can throw an entire synthetic campaign off track, so purification receives constant attention. Column chromatography works on small scale, but recrystallization and solvent optimization dominate in real world production.
We focus on particle size and moisture content for easier weighing and transfer. Fine crystalline powders tend to clump and cake in humid environments, but our facility keeps dry rooms to ensure the material flows and fills packaging smoothly. A batch can run several hundred kilos, destined for research labs, scale-up pilot projects, and larger process chemistry collaborations. The color, melting point, and spectral fingerprints (NMR and HPLC) go through QA checks before a drum leaves the plant.
Countless synthetic pathways start with a molecule like 4-bromopyridine-2-carboxylic acid, especially in medicinal chemistry and the hunt for new catalysts. The bromine position lets chemists forge new carbon–heteroatom or carbon–carbon bonds using established Suzuki, Buchwald-Hartwig, and Stille couplings. The carboxyl group stays intact through most transformations, ready for later amidation, esterification, or decarboxylation as needed.
Teams in pharma lean on this intermediate for its reliability when building kinase inhibitors, antibiotics, and small-molecule probes. The acid functional group sticks to standard coupling protocols, forming amide bonds with a wide scope of amines. The bromine can switch out for aryl, vinyl, or alkynyl partners, letting chemists build complexity late in a synthetic sequence. Construction of ligands for transition metal complexes often starts here, as does exploration of pesticidal and herbicidal agents in the agrochemical field. We have customers who run combinatorial libraries from the parent acid, exploring structure–activity relationships by preparing dozens of analogs with different substituents.
Material scientists approach it for similar reasons, working from the unique geometry and reactivity profile. We’ve seen projects where surface-active compounds, specialty dyes, and organic semiconductors all start from this acid. Each cycle through the plant can support a dozen separate projects outside our doors—applications we rarely hear about again until a formula number or synthetic route comes across an order spreadsheet, matched to an end product.
It’s worth discussing what sets 4-bromopyridine-2-carboxylic acid apart for practitioners who weigh many options. You see pyridine-2-carboxylic acid itself show up as a standard intermediate, but the hydrogen at position four limits what you can do downstream. Substitution on the ring—adding a bromine in this case—opens up halogen metal-exchange chemistry as well as straightforward cross-couplings. Chlorinated and iodinated analogs do pop up in requests; bromine hits the sweet spot for lability and cost. Chlorine sits tighter on the ring, less reactive in palladium-catalyzed reactions. Iodine swaps faster than bromine in Sonogashira and Ullmann reactions but pushes the price up and can complicate purification.
We’ve fielded orders for the methyl, ethyl, and other smaller acids, where the aim is tuning the electronics or solubility. The bromo acid holds its own, especially when selectivity or downstream reactivity matter more than sheer availability. Customers balancing raw material cost with productivity find brominated pyridines pragmatic—safer to store than their iodo siblings and easier to handle at volume than their nitro variants. The byproduct profiles also favor the bromo, since it avoids some of the dense, hard-to-remove residues that build up from other halogenations.
Looking even at raw material handling, the bromo version powders with consistent bulk density and suffers less from static charge on transfer lines compared to the more polar acids in this family. Repacking and sampling go faster, with fewer issues routing through glass and stainless.
Scaling a compound like this up highlights issues you miss in glassware. Impurities have nowhere to hide in even a hundred-liter batch. Even subtle changes in reaction solvent, brominating agent, or pH drift can leave you with off-specification acid. Our process engineers work closely with QC to learn each source of trouble—sometimes a trace of copper in the water supply shows up as a green tint, or a small variance in addition rate leaves a higher-melting byproduct.
We’ve switched solvent systems at the pilot scale, shifting from traditional acetonitrile setups to greener alternatives like methyl ethyl ketone or water–miscible alcohols for better safety and waste stream management. Between environmental calls for lower solvent use and our own operators’ preference for easier cleaning, finding the right balance keeps everyone engaged.
Customers requesting higher-volume shipments of 4-bromopyridine-2-carboxylic acid expect consistent quality, so we stick with validated analytical HPLC and GC methods for every lot. For years, this deep knowledge has made the difference between a product that arrives ready for a quick reaction and one that stalls an entire batch campaign in pharma research.
The journey for a product like ours doesn’t end at shipping. We work closely alongside R&D chemists troubleshooting new reactions, sometimes fielding early morning calls about unexpected TLC results or purity drops. Our technical team draws from both academic and industrial backgrounds, translating between the needs of small-lab research and pilot-plant process chemistry.
A customer developing enzyme inhibitors once relied on our acid for side chain elaboration. Their project nearly derailed after switching to a competitor with a higher percentage of a closely eluting isomer. Rapid troubleshooting and a batch rework delivered the needed purity, putting their timeline back on track without a costly delay. Such cases remind us that behind every drum or carton lies a project deadline and an investment in people’s hopes and work.
Getting the material formulated for use in solid-phase peptide synthesis or combinatorial libraries often requires extra drying steps, so we keep options open for low-moisture or micronized forms. Over time, our batch designs built up a set of parameters for reproducible quality that slows only when unusual requests arise, such as customizing particle size for automated dispensing robots or running additional metal analyses for stringent biopharmaceutical projects.
Demand for 4-bromopyridine-2-carboxylic acid has shifted with waves of new therapeutic targets and advances in catalysis innovation. Five years ago, requests surged as new pyridine-based kinase inhibitors hit the literature. We saw another uptick during the onset of organic LED development, as researchers hunted heteroaryl intermediates that could survive harsh device fabrication steps. Price swings for starting materials like 2,4-dibromopyridine can tighten margins and prompt a rethink about inventory and waste management.
Our strategy relies on transparent supply chain tracking and early communication about lead times. When the pandemic disrupted bromine logistics, we built up a buffer inventory and adjusted forecasts, helping customers avoid major gaps. Being in contact with freight partners and raw material vendors matters more than ever with international regulatory pressure and shipping delays. Investment in storage and climate control gives us a way to bridge short-term shortages, while routine audits keep every drum accounted for.
4-bromopyridine-2-carboxylic acid demands a practiced eye for safety. All steps, from charge-in to packaging, take extra care, since accidental skin contact or inhalation can trigger irritation or respiratory discomfort. We invest in sealed transfer lines, glove boxes, and local scrubbers, along with PPE protocols that get drilled every quarter. Our team also flags courses in chemical spill management and safe waste handling—brominated organics need careful tracking before heading to incineration or reclamation.
The question of sustainability weighs heavy in the plant management meetings. Halogenated compounds require more robust wastewater treatment, and keeping losses low improves both safety and environmental metrics. Upgrades over the last decade led to more closed-loop systems for wash solvents and separation lines, as well as continuous monitoring for trace organic release. We train operators to spot leaks and deviation early, since quick intervention saves both product and environment.
The real measure of quality comes from the people. Machine upgrades and SOP refinements matter, but a keen operator catching something off by sight or smell can prevent hours of lost time. We’ve fostered a work culture where reporting near-misses and process deviations brings praise and investigation, not hassle. It’s this boots-on-the-ground knowledge that keeps our reputation steady among clients who count on getting what they order, batch after batch.
Developments in catalysis and materials science continue to push new uses for metallo-organic intermediates, where 4-bromopyridine-2-carboxylic acid provides a reliable entry point. We talk regularly with partner labs investing in automated synthesis, where the need for batch-to-batch consistency outweighs the drive for the absolute lowest cost. Increasingly, companies want greener profiles and less residual halide in downstream applications, nudging us to trial alternate purification and brominating agents.
We’re expanding analytics to monitor both trace metal and halide residue, giving downstream users in pharma and electronics confidence in their own compliance. As European and North American regulatory environments tighten on halogenated waste, we’re testing more in-house recovery systems and solvent recapture options than ever before. Internal R&D projects now compare legacy production with newer, less wasteful methods to stay ahead in both efficiency and compliance.
Collaborative development projects with academic groups have become common. We support ongoing projects testing cross-coupling with new palladium and nickel catalysts, and feedback from small pharma and biotech pushes us to keep purity and reproducibility standards above the norm. Whether the end use lands in an agricultural product, a screens display, or as the basis for new therapeutics, this acid continues to serve as a vital building block.
Every batch of 4-bromopyridine-2-carboxylic acid leaving our facility carries the marks of many hands and minds. We know which purification cut yields the best downstream conversions, which container lines block sunlight most effectively, and which production lots bring an extra degree of dryness that helps peptide chemists succeed. We’ve fielded urgent requests for custom packaging, last-minute analytic documentation, and more than a few rounds of regulatory paperwork. Our role—day after day—is to keep refining our process, listening to those working at the bench and in formulation, and supporting industries that rely on chemical intermediates doing exactly what they’re supposed to, again and again.
With the progress in synthetic methodology and growing appetite for innovation in pharma, electronics, and materials, working with a flexible, responsive manufacturing partner is more vital than ever. Our team stands behind every drum, every lot, and every shipment of 4-bromopyridine-2-carboxylic acid sent on its way—eager to meet the next challenge that comes with this versatile compound, and the next discovery waiting around the bend.