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HS Code |
264819 |
| Chemicalname | 2-Bromopyridine-4-Carboxylic Acid |
| Casnumber | 7499-47-6 |
| Molecularformula | C6H4BrNO2 |
| Molecularweight | 202.01 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 180-184 °C |
| Solubility | Slightly soluble in water, soluble in polar organic solvents |
| Purity | Typically ≥98% |
| Smiles | C1=CN=C(C=C1Br)C(=O)O |
As an accredited 2-Bromopyridine-4-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-Bromopyridine-4-Carboxylic Acid, sealed with a screw cap and labeled with hazard warnings. |
| Shipping | 2-Bromopyridine-4-carboxylic acid is shipped in sealed, chemically-resistant containers with clear labeling. It is transported in accordance with local, national, and international regulations for hazardous materials. Proper cushioning, secondary containment, and documentation ensure safe delivery. Storage and handling instructions are provided to minimize risks during transit and upon receipt. |
| Storage | 2-Bromopyridine-4-carboxylic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect it from moisture, heat, and direct sunlight. Use only in chemical fume hoods and handle with appropriate personal protective equipment to prevent skin and eye contact. |
Applications of 2-Bromopyridine-4-Carboxylic Acid in Industrial Manufacturing2-Bromopyridine-4-Carboxylic Acid serves as a specialist intermediate in a select range of high-value chemical manufacturing environments. Our factory focuses exclusively on supplying this material to B2B users in established downstream segments, supporting production efficiency by ensuring precise composition and traceable compliance at every stage. 1. Pharmaceutical API Intermediate SynthesisIn pharmaceutical manufacturing, this compound is demanded as a critical intermediate during the multi-step synthesis of several anti-viral and anti-infective active pharmaceutical ingredients. Leading downstream formulators leverage its unique brominated pyridine structure during palladium- or copper-catalyzed cross-coupling reactions for selective functionalization of complex molecules, frequently in the late stage of synthetic development. Close control of raw material quality and addition is necessary to maintain batch-to-batch consistency and comply with regulated impurity thresholds in the final API. Industry compliance standards
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2. Agrochemical Intermediate for Pyridine-based Herbicide FormulationsMajor agrochemical producers utilize 2-Bromopyridine-4-Carboxylic Acid as an advanced intermediate during the manufacturing of select pyridine-derived herbicide actives. Its chemical structure enables precise bromine-to-amine or bromine-to-alkyl substitutions under alkaline and amination conditions, supporting the construction of active herbicide backbones. Continuous process monitoring is mandatory to ensure complete conversion and prevent persistence of residual starting material in the technical concentrate. Industry compliance standards
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3. Specialty Chemical Synthesis for Chiral Ligand Production2-Bromopyridine-4-Carboxylic Acid finds application in the synthesis of chiral ligands and catalysts for asymmetric hydrogenation and cross-coupling processes. Specialty chemical manufacturers employ this raw material at key substitution steps to introduce specific functional groups under controlled reaction atmospheres, permitting the production of high-purity ligands with tight chirality specifications demanded by downstream catalytic process users. Strict adherence to reaction stoichiometry and analytical characterization at each stage supports reproducible chiral performance in end-use applications. Industry compliance standards
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4. Electronics Material Intermediate in Liquid Crystal Display (LCD) ManufacturingElectronics material manufacturers incorporate 2-Bromopyridine-4-Carboxylic Acid during LC material development, especially for synthesizing highly substituted pyridine derivatives that serve as key performance enhancers in nematic and smectic liquid crystal blends. The introduction of bromine functionality enables further controlled modifications for tuning dielectric and optical properties, which are essential for large-format flat-panel display production. Process integration requires minimized metallic and halide contaminants due to high purity demands of the electronic sector. Industry compliance standards
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In our experience running a chemical manufacturing line, certain fine chemicals show up again and again because industry demands reliability, clean downstream chemistry, and transparent sourcing. 2-Bromopyridine-4-Carboxylic Acid, a pyridine derivative, stands as one of those trusted tools. The market for heterocyclic intermediates keeps growing, and this particular compound offers some clear advantages, both in synthesis efficiency and end-use scope.
We take pride every time we complete a run of 2-Bromopyridine-4-Carboxylic Acid. For us, quality starts early — beginning with checked raw materials. At full-scale, the process needs attention to detail. Each batch sits under close watch during bromination and carboxylation, since trace impurities can derail downstream reactions for the pharmaceuticals and materials that rely on this intermediate. Yield and purity make a difference, not just yield alone. We automate analytic measures for every lot: High-performance liquid chromatography (HPLC) and NMR confirm target purity, which we set above 98%. Most partners in pharma request nothing less. If a batch misses the mark, we isolate the problem, and we never pack off substandard product.
Consistency matters in the fine and specialty chemicals field. Pharmaceutical users demand not only purity but also batch-to-batch reproducibility. From our own runs over months and years, only tight process controls can guarantee that each lot will behave just like the last. Little things like reactor temperature ramps and solvent quality play a role, so we keep a detailed operations log and retrain every technician who joins the team.
2-Bromopyridine-4-Carboxylic Acid falls into a group of designer halogenated pyridines. As a solid, it comes off the line as off-white or faintly yellow crystalline grains. It’s not just a cosmetic observation — that color tells an experienced eye a lot about residual reactants and trace side products. We pack it only after full drying and screening to eliminate clumping, since a free-flowing solid makes dosing and reactivity far more predictable downstream.
Melting point measurements typically clock in above 180°C. That thermal stability makes for easy transport and storage, compared with more volatile or sensitive pyridine analogs. Material stays workable through common air exposure, meaning formulators or process chemists have fewer containment headaches to handle. Its moderate solubility in both organics and some aqueous systems helps open up flexible synthesis routes, which matters to research labs as well as larger production outfits.
Plenty of pyridine derivatives line a catalog’s shelves, but selective bromination at the 2-position and the 4-carboxylic acid substitution unlock meaningful differences. The position of the bromine atom — adjacent to the nitrogen — offers reactive access for Suzuki couplings and other palladium- or copper-mediated cross-coupling reactions. Often, competing products with alternative bromination patterns behave less predictably and deliver lower conversion rates in coupling chemistry.
Choosing 2-Bromopyridine-4-Carboxylic Acid means you avoid another headache that workers on the bench know well: unwanted isomers. The precise regiochemistry of this intermediate saves time downstream, which can cut out the need for laborious purification or chromatography steps. In pharmaceutical development where each unplanned step bills against a project timeline, the right choice of starting material can erase days of avoidable troubleshooting.
Many of our partners in pharma and materials chemistry seek this acid primarily for its role in constructing complex pyridyl scaffolds. It plugs into cross-coupling reactions, amide formations, and more adventurous custom syntheses. The strong activation at both the 2-bromo and carboxylic acid centers enables site-specific edits that would be far trickier with generic pyridine acids or with 3- or 5-substituted alternatives.
We hear from drug discovery scientists who count on this building block to introduce functional handles or linker arms. Medicinal chemistry depends on reliable introduction or modification of halide and carboxyl groups; misplaced bromines — or impure material — only add risk to high-stakes syntheses. We also supply researchers building coordination complexes, where the combination of the acid and bromo groups brings unique electronic effects, valuable in catalyst or ligand design.
Our records show steady interest, not only in high-purity research grades but also in modest-volume lots destined for pilot-scale production lines. Chemical engineers operating kilo labs choose 2-Bromopyridine-4-Carboxylic Acid because its behavior scales from flask to reactor vessel with little drama, especially when compared to less stable or more hygroscopic halopyridines.
Years back, we noticed too many lots of heterocyclic acids from commercial sources arriving with yellow tints or minor by-product peaks. Instead of letting those impurities become another industry headache, we overhauled our own process. Feedback from several long-term customers pushed us to refine the bromination and improve mother liquor separation. A bit of back-and-forth with our synthetic team led us to adjust extraction solvents, which cost more up front but delivered acid with higher recovery and cleaner spectra.
Every time we walked the plant floor during these early runs, real-time feedback mattered. No automated control can spot color drift or subtle texture changes in a drying pan quite like a technician who’s made a hundred batches. Collaboration across our chemists and operators closed the gap — purity issues dropped, and fuss over downstream chromatographies eased up.
Now, established customers notice faster, more robust product releases. We don’t promise every run will look identical, but we share test data transparently and readily take in-house feedback to make lab-scale and scale-up work easier.
Some manufacturers offer lower brominated pyridine carboxylic acids or analogs with substitutions at the 3- or 5-position instead. In our lab and in our customers’ feedback, these alternatives show different reactivity profiles. The true 2-bromo, 4-carboxy pattern provides an extra edge in coupling and functionalization because it directs both nucleophilic and electrophilic chemistry more cleanly. No one wants to risk a run of expensive coupling reagents only to learn the intermediate carried excess positional isomers or residual halides. Precedents in published syntheses assign value to this structure for its predictability and tuneable reactivity.
In contrast, competing acids with multiple halogenations or mixed substitutions can complicate reaction planning. Those choices may seem attractive on paper due to slight cost reductions, but more process development time and unpredictable separation problems often wipe out those savings. Our team has spent years answering technical support queries from researchers stalled by off-the-shelf analogs. The take-home lesson: the right structure up front usually means less trouble all the way down the process.
Production chemists recognize the difference between a material that keeps its properties over months and one that degrades, absorbs moisture, or yellows badly in standard storerooms. Our batches of 2-Bromopyridine-4-Carboxylic Acid maintain integrity in double-bagged, closed containers without specialty refrigeration. The crystalline granularity and air stability allow for accurate dispensing. We have users storing kilos through multi-month campaign runs without signs of caking or decomposition, assuming they keep to basic chemical hygiene and avoid exposing it to strong bases or reducing agents outside controlled reactions.
We offer direct pointers to teams developing new formulations or transferring from bench to pilot scale. Field experience indicates that proper sealing and segregation from incompatible substances is enough to maintain chemical and physical attributes, avoiding headaches common to more highly substituted halopyridine analogs. Several of the legacy compounds in this class—especially those with additional reactive groups or less desirable halogen positions—prove finicky and unpredictable outside very tight storage conditions. Our acid’s stability often resolves common logistical challenges in just-in-time production settings.
Talking price gets personal because every chemist and engineer knows the pain of blown budgets and delays. We run direct sourcing at every step—avoiding multi-tier brokers—so costs remain predictable and supply chain shocks less likely. Still, brominated building blocks can swing in price as elemental bromine and pyridine bases shift on the market. We buffer with in-plant reserves and deep relationships with raw material suppliers, so customers face fewer delays.
Order histories show most buyers plan projects on long timelines, specifying monthly or quarterly lots. For preclinical and scale-up programs where stop-and-go orders are riskier, we recommend block scheduling so material arrives in step with campaign milestones. Few things anger a production team more than holding up a reactor line for lack of a single intermediate; we’ve helped many partners avoid these jams.
Customers value not just a product, but the security of knowing every lot comes with provenance and open communication. We track every batch through digitized logs, process signatures, and third-party analytic checks whenever a customer needs added assurance. Every time a research chemist reports unusual observations, we investigate and improve. This open-door approach comes straight from recognizing how much future work rests on the consistency of our output. In one instance, a small discrepancy in UV absorbance flagged by a downstream user led us to audit our drying cycle timings — we updated SOPs and shared findings across our customer base, helping eliminate nagging issues in a few persistent syntheses.
Technical support matters just as much as reliable logistics. Many of our regulars bring us feedback from their ongoing projects. It’s not uncommon for us to field requests for alternate particle sizes, micronization, or custom blends, which we honor where process development timelines allow. Sometimes even a small tweak—like changing sieving mesh—helps solve dispensing headaches or brings about cleaner filtrations in pharmaceutical labs.
Beyond performance and price, questions about sustainability keep growing alongside regulatory pressures for greener chemistry. Our synthesis pathways now use brominating agents and solvents with improved recovery and low-waste protocols. We work to minimize energy input and solvent loss at every step, and we routinely revisit third-party environmental audits. Whenever possible, we consult published life cycle analyses for the pyridine sector, and we keep communication lines open with buyers who want to track their supply chain footprint.
Process improvements in the last few years already reduced total solvent use per kilogram of material produced, and we’re exploring continuous flow bromination as a way to further cut waste and lower reaction times. Each innovation that translates to a cleaner, safer process gets passed along as part of our responsibility to both clients and the chemical workforce. Many users in pharma—a highly regulated industry—need documentation tracking sustainability efforts, which we provide openly.
2-Bromopyridine-4-Carboxylic Acid sits among those specialty intermediates that bridge lab discovery and commercial process realities. Having made, packed, and shipped thousands of kilos, we’ve seen how reliable sourcing and upfront transparency help avoid wildcards as projects move through development phases. The specificity of this building block supports precise chemistry and dependable results.
Whether you’re handling rapid small-molecule screens or assembling scale-up protocols for a next-generation material, quality-controlled and data-supported intermediates like this one lay the foundation. After years on the bench and in the plant, no marketing spin substitutes for rigorous production controls and honest technical feedback. Our ongoing goal is to supply not just another pyridine derivative, but a solution that helps move real chemistry forward, batch after batch.