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HS Code |
299140 |
| Product Name | 6-Bromopyridine-2-Carboxylic Acid Methyl Ester |
| Cas Number | 63500-71-6 |
| Molecular Formula | C7H6BrNO2 |
| Molecular Weight | 216.03 |
| Appearance | White to off-white solid |
| Melting Point | 54-58°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
| Smiles | COC(=O)C1=NC(Br)=CC=C1 |
| Inchi | InChI=1S/C7H6BrNO2/c1-11-7(10)5-3-2-4-6(8)9-5/h2-4H,1H3 |
| Storage Temperature | Store at 2-8°C |
| Synonyms | Methyl 6-bromopicolinate |
As an accredited 6-Bromopyridine-2-Carboxylic Acid Methyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a sealed 5-gram amber glass vial with a tamper-evident cap and a printed product identification label. |
| Shipping | 6-Bromopyridine-2-Carboxylic Acid Methyl Ester is shipped in tightly sealed containers, protected from light and moisture, and handled as a hazardous chemical. It is packaged in accordance with international transport regulations and shipped with proper labeling, documentation, and safety precautions to ensure secure and compliant delivery to the destination. |
| Storage | 6-Bromopyridine-2-Carboxylic Acid Methyl Ester should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and incompatible substances such as strong oxidizing agents. Store at room temperature or as specified on the product label. Always follow proper chemical storage protocols and use in a fume hood if necessary. |
Applications of 6-Bromopyridine-2-Carboxylic Acid Methyl Ester in Industrial ManufacturingAs an original manufacturer, we supply 6-Bromopyridine-2-Carboxylic Acid Methyl Ester for advanced intermediate synthesis across regulated sectors. The following application fields in fine chemical, pharmaceutical, agrochemical, and specialty materials production represent established downstream channels based on real world use, regulatory frameworks, and supply chain integration. 1. Pharmaceutical Active Ingredient Synthesis (API Intermediate)This compound is a key intermediate for the multi-step manufacture of selective kinase inhibitors, antihypertensives, and antiviral drug molecules. API manufacturers use it in the pyridine ring-building stage and for introducing bromine functionality during the synthesis of complex heterocyclic drug scaffolds. Process engineers focus on achieving regulatory-grade purity and traceability throughout the batch. Product integration requires compliance with pharmaceutical QC standards, precise stoichiometry, and validated purification steps to support global drug registration dossiers. Industry compliance standards
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2. Agrochemical Synthesis (Pyridine-based Herbicide Building Block)Pesticide and crop protection producers employ this material as a synthetic block for constructing brominated pyridine intermediates used in highly regulated herbicides and fungicides. The compound enables selective halogen placement within pyridine rings, essential for molecular design of crop-selective actives. Downstream procedures demand adherence to agrochemical registration dossiers, robust environmental controls, and impurity profiling per global agricultural standards. Industry compliance standards
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3. Specialty Electronic Material Intermediate (OLED and Functional Dye Precursors)Manufacturers in the electronic chemicals sector incorporate this compound as a precise precursor for high-performance materials such as organic light-emitting diodes (OLEDs) and specialty luminescent dyes. Controlled bromine and ester groups within the molecule enable downstream customization of electron mobility and color tuning required in display technologies. The specialty segment mandates high-purity lot control, advanced analytical validation, and demonstrable consistency per tech industry standards. Industry compliance standards
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4. Fine Chemical Synthesis (Pyridine-Containing Catalyst Precursors)Specialty catalyst manufacturers apply this compound during the synthesis of ligand systems and organometallic catalyst frameworks exploiting its brominated pyridine motif. The reactivity profile supports selective cyclization, coupling, or nucleophilic substitution routes essential to advanced polymerization catalyst manufacture. The fine chemical field emphasizes batch reproducibility, verified catalytic activity, and trace impurity elimination prior to shipment. Industry compliance standards
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5. Veterinary Drug Intermediate (Antiparasitic Synthesis Route)Veterinary active pharmaceutical ingredient (VAPI) producers leverage the compound for construction of pyridine scaffolds used in modern antiparasitic agents. Integrated as a brominated ring block, it streamlines further diversification in multi-step reaction sequences. The veterinary supply chain highlights adherence to VICH and regional regulatory protocols for API impurity management and cross-contamination controls. Industry compliance standards
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Drawing from decades of experience navigating batch synthesis for fine chemicals and pharmaceutical intermediates, it’s clear that not all heterocyclic esters respond the same in the lab. 6-Bromopyridine-2-carboxylic acid methyl ester, a product we have produced on multi-kilogram scales, distinctly sets itself apart through a balance of reactivity, handleability, and purity. Many in the chemical market might not immediately distinguish between the half-dozen pyridine esters with similar ring substitutions, but subtle differences quickly reveal themselves on the bench or in the pilot plant.
Our process always pushes for consistency in yield and physical characteristics. 6-Bromopyridine-2-carboxylic acid methyl ester, with its defining methyl ester group at the 2-position and bromo at position 6, directs regioselectivity during subsequent synthetic steps. The methyl ester avoids the volatility and hydrolysis risks seen in ethyl esters, especially when handling open vessels under varying humidity. This product crystallizes in pale, free-flowing form; we reach HPLC purity of 99% in all production-scale lots without resorting to chromatographic clean-up. Anyone who has tried to separate regioisomers by column chromatography appreciates what it means to start with pure material.
Product consistency shapes how process chemists design and troubleshoot. With a melting point reliably measured within a narrow band and a controlled, low water content from vacuum drying, end-users in agrochemicals and pharmaceuticals find that their reactions proceed as planned batch-to-batch. From our own facility, we maintain trace-level metal residues and minimal halide contamination, answering calls from partners across API and specialty materials manufacturing. The methyl ester configuration resists unwanted transesterification, meaning you gain both shelf stability and confidence during prolonged campaigns.
Large-scale brominations, especially on pyridine substrates, can run into unpredictable side reactions and overbromination. Early in our manufacturing journey, we saw that purification regularly became a bottleneck—impurities stuck around and caused headaches for analysts and downstream chemists. Over years of method development, we engineered tailored crystallization steps, tight process controls, and real-time monitoring by in-line IR and NMR to preempt byproduct formation. The process’s robustness ensures a confidence that is earned, not assumed.
Solvent management matters. We optimized to avoid chlorinated waste and cut down volatile emissions that cause headaches during reaction work-up. Purified product arrives with consistent bulk density, a fact often overlooked by newcomers to chemical manufacturing until caking or clumping halts a process. Working with metric-ton shipments, each hazard—from dust to static—multiplies, so scaling up carries risks that demand expertise. Our product’s texture ensures ease of portioning and dissolution. Whenever we shifted to other esters in pilot batches to match customer requests, shelf life tended to become unpredictable, dusting increased, and yields varied more widely. Years in the plant taught us not to discount these practical details.
Not all pyridine carboxylic acid derivatives blend seamlessly into automated reactor lines, especially in modern flow chemistry. Customers using 6-bromopyridine-2-carboxylic acid methyl ester as a core scaffold for active pharmaceutical ingredients often look for reliable solubility and predictable behavior in DCM, DMF, and common aprotic polar solvents. In hands-on QA sessions with our customers’ technical teams, we’ve tested custom dissolution protocols side-by-side. Our trials have repeatedly shown that the NMR and GC-MS spectrum remain consistently aligned with specification, without spike failures or off-color batches. The methyl ester’s unique interaction with nucleophiles means it resists spontaneous hydrolysis—crucial during multi-step syntheses at scale where losses compound quickly.
Sometimes end-users press for even tighter impurity spectra—especially those working with sensitive catalysts downstream. Over our years in chemical processing, we’ve received regular requests for custom extended testing: high-resolution LC-MS, trace halide assay, or elemental analysis panels. Our manufacturing workflows have adapted, using in-process data collection and real-time feedback to fine-tune every parameter, from raw material vendor qualification to the sequence of solvent stripping in downstream evaporations. It takes a committed operations team, not just a lab-scale recipe, to achieve these metrics at multi-hundred-kilo throughput.
Chemists familiar with pyridine scaffolds know how minor changes echo through an entire synthesis plan. The 2-methyl ester, compared to 3- or 4-substituted versions, steers reactivity toward defined couplings with high regioselectivity, particularly when used as a coupling partner in Suzuki, Buchwald-Hartwig, or amidation reactions. We have seen firsthand that opting for a carboxylic acid, or a bulkier ethyl ester, led to slower kinetic profiles or stubborn impurity bands during scale-up. In collaborative projects with pharmaceutical partners, our 6-bromopyridine-2-carboxylic acid methyl ester enabled shorter routes and fewer chromatographic separations—in one case, reducing a three-step process to two under continuous flow.
Unlike its nitro- or chloro-containing relatives, the bromo-pyridine ester’s selective reactivity in metal-catalyzed cross-couplings saves time in synthetic route scouting. That single distinction has made or broken project viability from our perspective, especially in contract manufacturing settings with razor-thin margins. For those accustomed to dealing with more recalcitrant intermediates, the switch to our pure 6-bromo ester product frees up reactor capacity and labor hours, resulting in actual reductions in production costs, not just paper savings.
It’s tempting to view this ester as just another numeric entry in a catalog, but developing and producing material for stringent API use repeatedly proves the product’s critical value. One partner, aiming for a new anti-infective drug lead, used our material over an eighteen-month campaign with zero lot rejections—not an easy feat by any standard. Their analytical team found the batch-to-batch NMR matched perfectly with their in-house records. Failures at this stage trigger months-long delays and regulatory headaches no team wants to face.
We also support electronic materials manufacturers with this compound—users who expect fine control over substitution patterns. Year after year, reports come back showing that off-target reactions, sometimes triggered by unseen impurities in supplier materials, simply did not occur at previous rates after switching to our standardized product. Not every producer offers the same confidence, especially at scale, underscoring that a genuine manufacturer’s insight at every stage pays dividends for end users.
Unlike traders or brokers, we stand by every step in the production, from kilogram to metric ton. Our process development scientists exchange feedback with partners directly and regularly host site visits for technical audits. All analytical work, from qNMR to Karl Fischer titration, takes place in our in-house QC facility—not farmed out nor run on mismatched instruments. Customers rely on honest, technology-driven answers to formulation or scalability concerns, not empty assurances or boilerplate certificates.
Regulated end-users, especially those filing DMFs or planning global registrations, appreciate our traceability. Each drum comes attached to an unbroken documentation pipeline, going back to raw material origins, synthesis cycle logs, and analytical results. Our records, both batch and analytical histories, stand open to customer review—a practice endorsed by our internal quality team after reviewing best practices drawn from extensive supplier-auditing experience.
Synthetic chemistry only answers one part of the equation. Material that clumps, cakes, or dusts off uncontrollably frustrates technicians and causes meters to misread, which introduces unreliability and, at scale, generates serious losses. Our engineering staff optimized the drying process to lock in the correct residual moisture while keeping the granules stable. Storage stability for months under typical warehouse conditions has been field-tested repeatedly. Many substitute products from traders or toll manufacturers arrived with hidden caking after just six weeks in inventory—a reality that ended up costing years of process optimization back downstream.
Waste streams enter consideration for every kilogram produced. Brominated aromatic wastes, if mismanaged, saddle operations with hazardous byproducts or local regulatory troubles. We reengineered effluent streams and process emissions, catching and removing volatile organics at the condensing stage to minimize environmental burden. Responsible process development does not just satisfy a certification—reducing brominated load in plant discharge changed our standing with regulators and earned us access to more exacting supply chains.
Working up from small-scale lab protocols to industrial scale, our team encountered issues with thermal instability and isomeric byproducts—a common pitfall in early literature preparations. Multiple iterations improved on the isolation steps, built analytical sign-offs right into intermediate stages, and cut down cycle times for greater throughput. The process now leverages continuous real-time monitoring, avoiding the batchwise blind spots that hampered older manufacturing runs.
Continual dialogue with regular customers identified pain points—innocuous-looking specification lines that, in practice, spelled out real delays. Adjusting particle size distribution, backing up packaging robustness, and setting clear expiry labeling have lowered complaint rates to near zero. In direct feedback sessions, end users remarked on the difference in process reliability compared to prior vendors’ inconsistent supply.
While most production focuses on medium- to high-volume contracts, research groups and custom synthesizers demand flexible packing and batch size. Our technical team regularly works with these groups, adjusting for their specific solvent compatibility or downstream transformation requirements. This sort of feedback loop—the chance to troubleshoot or modify specifications based on concrete lab results—feeds back into our large-scale production, closing gaps that more removed suppliers overlook.
Not all suppliers can pivot to a special request—to eliminate traceable latex or silicone impurities, for example, or supply sub-batch samples drawn directly from line drumming. Direct control over plant and process means we back these requests with actual process adjustments, not just a new product code sticker.
Experience manufacturing brominated pyridine esters teaches hard lessons about what analytical and batch uniformity mean to downstream success. Where others outsource or dilute responsibilities through a chain of intermediaries, we bear direct accountability for each step. Our product has earned its position after years of iterative improvement, operational discipline, and a refusal to ship sub-par lots. Customers facing regulatory or commercial deadlines depend on this assurance—facing FDA or REACH scrutiny brings risk best borne with a supplier who knows the stakes on every drum shipped.
Actual knowledge grows not in clean conference rooms but on the plant floor and in the lab. We have learned that keeping the lines open with both customer process teams and internal QA drives long-term improvement. Product launches or changes to specifications are always tested against years of stability and performance data drawn from our own records. In our experience, ongoing effort to meet and anticipate market needs determines the difference between a short-term supply contract and a real manufacturing partnership.
Anyone who has stood at the interface between lab-scale innovation and industrial delivery appreciates the value of an ester intermediate that delivers, not just on a data sheet, but in the actual churn of a plant or research lab. We have seen how small lapses lead to real losses or missed opportunity, and how real gains emerge from deliberate process investment. 6-Bromopyridine-2-carboxylic acid methyl ester finds value in this context—not only as a molecule but as the result of a long-standing, hands-on approach to chemical production and supply. The satisfaction comes from seeing customers trust the difference and invest their own work in compounds we know inside out.