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HS Code |
206264 |
| Chemical Name | 5-Bromopyridine-2-carboxylic acid methyl ester |
| Cas Number | 728919-27-1 |
| Molecular Formula | C7H6BrNO2 |
| Molecular Weight | 216.03 |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents (e.g., DMSO, methanol) |
| Iupac Name | Methyl 5-bromopyridine-2-carboxylate |
| Smiles | COC(=O)C1=NC=C(C=C1)Br |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
As an accredited 5-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 | Packaged in a 25-gram amber glass bottle with a secure cap, labeled with chemical name, purity, hazard warnings, and lot number. |
| Container Loading (20′ FCL) | 20′ FCL loads 5-Bromopyridine-2-carboxylic acid methyl ester securely in sealed drums or bags, maximizing space and minimizing contamination risks. |
| Shipping | 5-Bromopyridine-2-carboxylic acid methyl ester is shipped in tightly sealed containers, protected from moisture and light. It is transported as a chemical reagent, compliant with relevant safety and hazardous material regulations. Proper labeling and documentation accompany each shipment to ensure safe handling and delivery. Store at room temperature upon receipt. |
| Storage | 5-Bromopyridine-2-carboxylic acid methyl ester should be stored in a tightly sealed container, protected from moisture, light, and incompatible substances. Store at room temperature in a cool, dry, and well-ventilated area. Avoid sources of ignition and strong oxidizing agents. Ensure the storage area is appropriately labeled and access is restricted to trained personnel. |
| Shelf Life | 5-Bromopyridine-2-carboxylic acid methyl ester typically has a shelf life of 2-3 years when stored in a cool, dry place. |
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Purity 98%: 5-Bromopyridine-2-carboxylic acid methyl ester with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield coupling reactions. Melting point 64-66°C: 5-Bromopyridine-2-carboxylic acid methyl ester with a melting point of 64-66°C is used in organic synthesis protocols, where its defined phase transition enhances batch reproducibility. Molecular weight 216.04 g/mol: 5-Bromopyridine-2-carboxylic acid methyl ester with molecular weight 216.04 g/mol is used in medicinal chemistry, where it enables precise reagent stoichiometry. Stability up to 40°C: 5-Bromopyridine-2-carboxylic acid methyl ester with stability up to 40°C is used in multi-step syntheses, where thermal resilience reduces byproduct formation. Moisture content <0.5%: 5-Bromopyridine-2-carboxylic acid methyl ester with moisture content below 0.5% is used in anhydrous reaction environments, where it prevents hydrolysis and side reactions. Assay ≥ 98% (HPLC): 5-Bromopyridine-2-carboxylic acid methyl ester with assay ≥ 98% (HPLC) is used in chemical research laboratories, where it guarantees reproducible analytical results. Solubility in ethanol: 5-Bromopyridine-2-carboxylic acid methyl ester with good solubility in ethanol is used in solution-based reaction systems, where it enables homogeneous mixing and faster reaction rates. Controlled particle size (<75 μm): 5-Bromopyridine-2-carboxylic acid methyl ester with controlled particle size below 75 μm is used in catalyst preparation, where it facilitates uniform dispersion and increased surface area for reactions. |
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Every batch that rolls out of our plant draws on decades of hands-on work and an insistence on practical results. As chemical manufacturers, we work directly with raw materials, solvents, and reaction vessels—our understanding comes from the day-to-day trials of synthesis, purification, and scaling up. The product, 5-Bromopyridine-2-carboxylic acid methyl ester, stands out in our catalog not only because of its distinct structure but due to the steady, reliable quality we achieve by controlling the process from sourcing through packaging.
We do not believe in a one-size-fits-all mentality. In our facility, batch consistency and traceability drive our workflow. This compound, which some refer to as methyl 5-bromopicolinate, comes off our reactors at standard purities of ≥98% by HPLC, with targeted control of moisture and metal residues. That purity means whether you are building pharma intermediates, designing agrochemicals, or looking for a reliable scaffold for organometallic reactions, you can expect the same chemical to perform batch after batch.
Packing lines are set for a range of scales, with container choices based on stability and contamination risks. We keep samples back from every lot, so whatever leaves the warehouse can be verified later against retained reference material. We have found over the years that full transparency about quantitative testing results pays off. If something doesn’t meet our standards, it doesn’t go out the door—period.
Many research groups and production lines reach for this compound in their arsenal of pyridine derivatives. The methyl ester acts as a versatile functional group, allowing for gentle hydrolysis to the corresponding acid or keeping the molecule protected under milder conditions. The bromine at the five position activates the ring for further coupling steps—particularly useful for Suzuki or Buchwald-Hartwig reactions. Our production teams have worked directly with development chemists on several projects that needed tight control of ortho substitution. The consistent electronic properties of our material have led customers to report better yields and cleaner profiles during scale-up.
Unlike more common alkyl pyridine esters, the 5-bromo group brings added value, especially in pharmaceutical intermediate production. Many medicinal chemistry programs seek out aryl bromides for their cross-coupling compatibility and reactivity. During COVID-19, demand for viable heterocycle building blocks surged, and our 5-bromopyridine-2-carboxylic acid methyl ester played a quiet but essential role in several key syntheses.
Staying hands-on has taught us that moisture control can make or break the quality of pyridine derivatives. Even trace water during esterification or bromination steps changes the impurity profile and saponification risk. By running regular Karl Fischer analyses and tightening our drying protocols, we have been able to reduce hydrolysis challenges for our partners down the line. Sometimes the trickiest part lies not in the chemistry itself, but in housekeeping—cleaning reactors between batches to prevent cross-contamination, regularly checking seal integrity on storage drums, and never taking shortcuts with paperwork.
Our supply chain team works directly with trusted bromine and pyridine sources. Over the years, we have weeded out vendors who cut corners on purity or documentation. This might not sound glamorous, but it shields end users from the headaches of untraceable batch impurities or regulatory non-compliance. A single off-spec shipment from an upstream supplier can disrupt weeks of work. Through proactive ingredient testing and supplier auditing, we catch issues long before a production run backs up or a customer calls with a problem.
We also recognize regional differences in raw material quality. Some batches call for extra filtration, and some require a tweak in reaction temperature to compensate for minor variations in starting material grade. Our operators know that the machine never replaces the judgment of the chemist or technician watching for color changes, crystal formation, or subtle shifts in reaction behavior.
Not all pyridine methyl esters are the same, and our 5-bromo analog stands apart for several reasons. By introducing the bromo group at the five position—not the three or four position—the reaction pathway alters, as does the coupling potential. We have seen instances where a competitor's three-bromo pyridine ester failed to perform in metal-catalyzed processes, largely due to altered electron distribution and steric hindrance. For chemists building libraries of heterocycles, these fine details matter—switching to a five-bromo starting material can unlock better reactivity with boronic acids, amines, or alkynes.
In direct comparison to the acid form, the methyl ester gives extra flexibility. Direct hydrolysis of the acid can sometimes compromise sensitive substituents elsewhere on the ring, but the ester protects the carboxylic acid from aggressive reagents. This stability has opened up new pathways in both chemical biology and process chemistry.
One specific project comes to mind, where a client tried three commercial sources of a similar methyl ester and only our material met both purity thresholds and solubility targets for their coupling reactions. The lesson: empirical evidence always takes precedence over theoretical claims. We keep in touch with downstream users to hear about performance and tweak our process where necessary, closing the loop between the plant and the bench.
Nearly every order we fulfill goes toward building something bigger—a new drug candidate, a crop protection agent, or an assay probe. Our compound has passed through pharmaceutical GLP synthesis routes, agricultural screening hits, and scale-up kilo syntheses. Medicinal chemistry teams tell us they value tight control over both position and leaving group because it saves rounds of purification and troubleshooting.
Catalyst manufacturers have remarked that our consistency from lot to lot avoids headaches late in their production campaign. We keep a close watch on batch-to-batch variation because we know what it feels like to lose time and confidence due to ingredient drift. Our lab routinely cross-checks melting point, NMR purity, and reactivity, so downstream users see minimal surprises.
Years of environmental permitting and regulatory audits have brought home the impact of each choice we make in synthesis and waste handling. We have adopted solvent recovery and recycling wherever practical, and we enforce careful tracking of all hazardous material movements. Our operators receive ongoing training to spot safety risks, particularly around brominated intermediates, which can pose respiratory and skin hazards if mishandled. Experience shows that simple steps—such as improved ventilation, sealed transfer lines, and regular staff briefings—really do reduce incident rates.
For customers, our commitment to responsible chemistry adds assurance that the compound they receive is not only effective but produced with the community in mind. As more regulations tighten around persistent organic pollutants and hazardous intermediates, our focus on separated waste streams and minimized emissions becomes a competitive edge, not just a box to tick.
As with many pyridine esters, the material shows sensitivity to prolonged exposure to heat or base. In our earliest days, we encountered color changes and decomposition that traced back to packaging materials reacting with the ester. We shifted to lined containers and added desiccant packets based on actual field feedback rather than theoretical calculations. Every round of improvement sprang from tracking customer inventories and answering queries about appearance and stability. We saw that keeping the cold chain intact during shipping helped preserve the product through even protracted customs holds.
Questions sometimes arise about solubility in various solvents. We publish recommended solubility profiles from our own dissolution tests, rather than relying on secondary sources. In the rare cases of clumping or delayed dissolution, our technical staff work directly with client labs to pre-wet or pre-grind material as appropriate. Feedback loops like these help strengthen both our own protocols and downstream project outcomes.
Lab-tested purity guarantees more than compliance—it means the same method, yield, and physical outcome go from trial batch to final kilo run. We watch for even trace isomer formation or side-products that could affect the outcome of coupling, hydrolysis, or acylation reactions. Our process uses careful cooling and holding steps to avoid regioisomer contamination.
Accurate structural assignment starts with in-house NMR and mass spec confirmation, not just the vendor certificate. Our analytical team has seen their share of misidentified samples as result of ambiguous supplier documentation. By building our own in-house reference libraries, we correct these issues before they can propagate through a research project or production campaign.
Over time, we have found that customers value more than just specs—they appreciate knowledge sharing. Our team remains accessible to discuss not just reactivity, but also potential side-reactions, safe handling, and waste management specifics. Chemists integrating this compound into new syntheses want more than paperwork; they want insight into how subtle shifts in handling could impact large-scale success.
By sharing anonymized case studies and tested methods, we support partners in hitting their own targets. We find that closer relationships foster innovation as well as risk management. Sometimes, catching an issue early—like a shift in melting point or HPLC trace—prevents wasted effort on the customer’s end. These conversations also help us finetune future batches, based on actual use conditions.
Chemistry does not stand still. New synthetic routes, catalysts, and process intensification techniques keep emerging. We stay nimble by working closely with academic and industrial partners, reviewing new literature, and adopting advances where real value shows. Sometimes feedback leads us to refine extraction methods or test different crystallization solvents. Sometimes, it drives bigger investments such as flow chemistry or continuous processing. Improvements in yield also minimize waste downstream, reinforcing a culture of responsibility and cost-effectiveness that benefits both us and our customers.
We invest in practical innovation. A few years ago, a cooperative program with a university lab led to the adoption of safer, lower-temperature bromination methods, which increased yield and made plant operations safer. Implementing new technologies is not about chasing trends, but about finding what keeps our teams safe and our partners productive.
Market conditions shape pricing pressures across the global chemical sector. Holding the line on quality in times of raw material spikes calls for tough decisions—trimming back on non-essential expenses, renegotiating with suppliers, or finding efficiencies in plant runs. We have weathered cycles of volatility in the bromine market and have sometimes reduced margin to protect supply to key partners.
Investing in reliable supply pays dividends over time. We have learned that customers looking for bargain-basement pricing on specialty intermediates often pay more later in rework and troubleshooting. Our pricing might be modestly above the lowest on the market, but users often return after frustrating experiences elsewhere. The end-to-end quality, batch data transparency, and responsive technical support add value that cannot be measured simply in cents per gram.
By delivering 5-Bromopyridine-2-carboxylic acid methyl ester to labs and plants worldwide, we keep looking ahead—testing new batch technologies, adopting more predictive QC tools, deepening our understanding of impurity control, and training new generations of chemists and operators. Every improvement, small or large, starts with honest engagement and feedback. We stand by our commitment to integrity, safety, and open communication at every turn. Our experience shows that these principles keep project timelines on track, protect the end-user, and underpin successful partnerships in the ever-evolving chemical industry.