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HS Code |
768518 |
| Chemical Name | 5-Bromo-3-pyridinecarboxylic acid methyl ester |
| Molecular Formula | C7H6BrNO2 |
| Molecular Weight | 216.03 g/mol |
| Cas Number | 24162-79-0 |
| Appearance | White to off-white solid |
| Melting Point | 67-71 °C |
| Purity | Typically >97% |
| Solubility | Soluble in organic solvents (e.g., dichloromethane, ethanol) |
| Smiles | COC(=O)C1=CN=CC(Br)=C1 |
| Storage Conditions | Store at 2-8 °C, protected from light and moisture |
As an accredited 5-bromo-3-pyridine carboxylic acid methyl ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle with a screw cap, labeled “5-bromo-3-pyridine carboxylic acid methyl ester, 98% purity.” |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 5-bromo-3-pyridine carboxylic acid methyl ester: Packed in sealed drums, 10–12 metric tons per container. |
| Shipping | Shipping of **5-bromo-3-pyridine carboxylic acid methyl ester** must comply with chemical safety regulations. The compound should be securely sealed in appropriate containers, clearly labeled, and packaged to prevent leakage or contamination. Standard transport requires temperature and moisture control, adherence to hazardous material protocols, and provision of relevant safety data sheets (SDS) during transit. |
| Storage | 5-Bromo-3-pyridine carboxylic acid methyl ester should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of heat and moisture. Keep away from incompatible substances such as strong oxidizers. Avoid exposure to direct sunlight. Store in a chemical storage cabinet designated for organic chemicals. Always follow relevant local safety regulations and material safety data sheet (MSDS) guidelines. |
| Shelf Life | 5-Bromo-3-pyridine carboxylic acid methyl ester has a shelf life of 2 years if stored tightly sealed, protected from moisture, and light. |
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Purity 98%: 5-bromo-3-pyridine carboxylic acid methyl ester with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Melting point 60°C: 5-bromo-3-pyridine carboxylic acid methyl ester with a melting point of 60°C is used in solid-phase synthesis, where predictable crystallization enhances process efficiency. Molecular weight 216.03 g/mol: 5-bromo-3-pyridine carboxylic acid methyl ester with molecular weight 216.03 g/mol is used in medicinal chemistry research, where precise dosing and molecular design are required. Stability up to 40°C: 5-bromo-3-pyridine carboxylic acid methyl ester stable up to 40°C is used in reagent storage and handling, where reduced decomposition risk improves operational safety. Moisture content <0.5%: 5-bromo-3-pyridine carboxylic acid methyl ester with moisture content below 0.5% is used in high-purity organic synthesis, where minimizing hydrolytic degradation enhances reaction success. |
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In the business of manufacturing chemical intermediates, hands-on experience and understanding the intricacies of each reaction step shapes every decision we make in the plant. 5-Bromo-3-pyridine carboxylic acid methyl ester—also known in the lab by its CAS number 41034-25-9—presents a unique blend of reactivity and selectivity, often sought after for synthesizing pharmaceuticals and agrochemicals. Our process has been refined through years of batch runs, process controls, and direct feedback from QC.
We take pride in delivering this compound at a consistent purity above 98%, verified in our facility by in-house HPLC and NMR methods. The pale yellow crystalline powder maintains firm chemical stability in common transport and storage conditions. Clients have reported that our material handles well on a kilogram scale, minimizing dusting and static. We have spent considerable effort to minimize batch-to-batch variation, guided by lean manufacturing and real-world lab-scale to plant-scale trials.
Reliable supply starts in the reactor. Over several years supporting the evolving demands of pharmaceutical development, we have seen 5-bromo-3-pyridine carboxylic acid methyl ester serve as more than just a simple building block. Medicinal chemists count on this ester for introducing a controllable bromine handle, which creates opportunities for Suzuki and Buchwald-Hartwig couplings without the risk of forming unpredictable byproducts. The methyl ester group offers non-intrusive activation, making it straightforward to hydrolyze under basic conditions when a free acid is needed downstream.
Our process provides a high-isolation yield combined with a low contaminant profile, with attention paid to minimizing traces of starting materials like 3-hydroxy pyridine or methylating agents. The finished product flows directly into scale-up applications such as heterocycle library generation or the construction of advanced pharmaceutical actives. Researchers in toxicology synthesis programs have pointed to the compound’s versatility for late-stage functionalization, which cuts out redundant protection and deprotection steps.
Handling an aromatic ester often involves practical knowledge that textbooks skip. We have prioritized a product form that balances flowability with easy weighing in both research and manufacturing settings. At our sites, operators note this compound’s tight particle size distribution helps speed up recharging solid feed lines and reduces bridging or clumping in hoppers. Sampled containers retain their integrity under the standard climate range our customers see in Asia, Europe, and North America.
Oxidative stability has come up in client audits; our in-plant storage data show the brominated ester resists yellowing or forming odor even after several months in warehouse conditions, provided the product stays protected from direct sunlight and excess humidity. Transport teams appreciate the ruggedness of our sealed HDPE drums, which eliminates the risk of moisture ingress and cross-contamination.
Other suppliers frequently ask us why not supply just 3-pyridine carboxylic acid methyl ester or its plain 5-bromo analogues. Our experience on dozens of customer projects makes the answer clear. The 5-bromo-3-pyridine skeleton carries a uniquely balanced electronic profile; compared to bromination in other positions, this configuration favors more predictable downstream coupling, especially in cases requiring selective mono-arylation. Colleagues in process chemistry departments at API plants confirm that the para-bromo effect (relative to carboxylic methyl ester) plays a role in accelerating some cross-coupling routes while discouraging unwanted polymerization.
Some customers test alternatives like 5-chloro or 5-iodo derivatives. We see that while 5-iodo variants may bring increased reactivity for specific metal-catalyzed steps, they raise cost and pose increased sensitivity to light and air, complicating storage. The 5-chloro analog lags behind in overall yield for the same set of coupling reactions and often requires harsher activation. As a result, the 5-bromo-3-pyridine carboxylic acid methyl ester holds a practical midpoint between reactivity and stability—an advantage reflected plainly in lab yield and process safety metrics.
It takes more than technical knowledge to build a solid track record with demanding customers in fine chemicals. Our technical teams go through every kilo and every chromatogram. Each batch undergoes full analytical evaluation using HPLC for purity and NMR for structural confirmation. We focus on controlling related substances that can occasionally appear due to incomplete bromination or esterification, such as dibrominated or hydroxy-substituted impurities. Through repeated cycle optimization, our reactors run at tightly managed temperatures and residence times, and staff receive ongoing training to detect early signs of process deviation.
We also collect powder X-ray diffraction data on select lots to detect changes in crystalline structure, mainly if the compound is slated for solid-form screening by customers in preclinical studies. These data sets feed into our documentation, updated quarterly and accessible to all project leads. We operate a hybrid manual-automated record system to track each production run, reducing repeat errors and flagging intermediate stages for further QC review.
From day one, our compliance approach extends beyond local regulations. We have built our facility to operate under standards aligning with broad international requirements. In real terms, this means effluent from our bromination reactors is treated in three-stage scrubbing to remove trace organics and free bromide before hitting the final waste stream. Methylating agents that remain unreacted in the process are neutralized completely, tracked by on-site GC. Regular internal audits by our EHS supervisors keep us ahead of regionally evolving environmental expectations.
Feedback from partner audits, especially those prepared for regulatory filings in the US and EU, has helped us proactively adjust documentation and lot numbering practices, ensuring easy traceability for all customers managing regulatory portfolios. Our technical package includes full analytical certificates, reproducible retention times on HPLC, and detailed records for all lots shipped abroad, simplifying customer filings with local authorities.
Some of our earliest customers purchased this product for medicinal chemistry screening, where they found that the methyl ester not only performed reliably in microwave-assisted couplings but also showed compatibility with both aqueous and organic work-ups. Project chemists in larger pharma organizations have since shared their results using our compound to synthesize kinase inhibitor scaffolds, with a marked reduction in side reactions compared to similar 3-pyridine analogues lacking the bromo substituent.
Our technical support team works directly with client process chemists during scale-up, providing guidance on solvent swaps and quench conditions when handling this ester. Several contract manufacturers depend on our consistency during larger API campaigns; their feedback after production runs pointed to smoother purification versus non-brominated esters. The compound’s well-defined melting point enables rapid quality checks at receiving docks, saving weeks in batch release time for pharma clients pushing development timelines.
Based on first-hand experience supporting customers through both kilogram and multi-tonne orders, subtle differences in reagent quality can massively impact project timelines. Subpar material often produces unwanted byproducts or fails to pass specification on reactivity or purity, causing downtime on high-value production lines. Our main advice: verify consistency across lots, not just a single sample; confirm impurity profiles using orthogonal methods; and keep batch records accessible for audit at all steps.
We have encountered a few cases where customers assumed all 5-bromo-3-pyridine esters were interchangeable with benchmarks, only to discover compatibility issues with their specific catalysts or chromatography conditions. For example, recovery of active pharmaceutical ingredient precursors using automated centrifugal partition chromatography worked seamlessly when using our ester, but led to fractionation headaches with less robust analogues showing inconsistent particle size or color.
Long-term stability presents a real challenge in fine chemical storage, particularly in regions with fluctuating humidity. Our warehouse records show that, when kept in original sealed packaging and away from direct sunlight, the compound retains its specification for two years without detectable hydrolysis or decomposition. We routinely run accelerated aging studies under varied temperature and moisture conditions. These have shown no measurable loss in purity up to six months even at 40°C/75% RH, attributes favored by customers with intermittent production cycles.
Packaging design feedback comes directly from shipping teams: easy-pour, wide-mouth drums prevent bridging and speed up re-bagging for multiple process runs. Consistency in powder handling has reduced lost material and improved traceability during storage audits.
A manufacturer must never lose the habit of learning from users’ experience. We find that direct conversation with bench chemists, plant operators, and QA teams opens the door to details overlooked on paper. Customer sites have pointed out that our compound’s low static properties enable automated dispensing using existing gravimetric systems; this real-world usability distinguishes it against remotely manufactured alternatives, which often arrive too sticky or prone to bridging.
Toll and contract manufacturers also favor our trouble-shooting support, as they can contact our chemists directly for guidance on use and safe disposal. This practical partnership loops back to our own in-house process, driving improvements or batch reevaluations to head off potential issues before they materialize at our customer’s site.
The search for better routes to this methyl ester continues in our labs. We focus research efforts on greener oxidants, water-reducing reaction media, and alternative bromination strategies, aligning with sustainability targets. Chemists experiment with flow chemistry and continuous processing; these pilot projects have already trimmed energy costs while tightening product specs, reflecting a trend toward lower carbon footprints and higher yields per reactor hour.
Our technical team evaluates parallel formation of related esters, enabling customers to create compound libraries in one go. Feedback shows batch combo offerings reduce procurement overhead and shipping times, and in tech transfer meetings, researchers sometimes propose jointly developing custom derivatives on the 5-bromo-3-pyridine backbone. This spirit of partnership doesn’t just keep us ahead—it keeps the exchange of knowledge two-way, leading to better solutions for both sides.
Chemists in pharma, agrochem, and material science industries recognize this methyl ester as a specialty intermediate that enables synthetic creativity. The compound fills a niche, giving project leaders more control in intermediate and late-stage functionalization steps compared to generic pyridine derivatives. Over the years, demand for this chemical has not only remained stable but has also grown as new molecular targets require broader pyridine substitution patterns and more complex functional group interconversions.
In conversations with peers attending trade conferences, it’s clear that robustness—meaning how much abuse a material takes before changing characteristics—matters more than price or packaging. Project managers often mention the real cost of failure if an unreliable batch ruins a campaign or increases waste by even a few percent. Our internal focus has always stayed on robust and real-world readiness rather than theoretical purity alone.
All manufacturers of intermediates will tell you: supplying the same molecule that’s found on paper does not mean supplying the same value. We find that our long-term customers reward attention to process details and reliable communication. Every project, whether repeat or one-time, gives us new data points for improvement. Having walked the shop floor, watched the loading of drums, observed the care our staff take in matching up batch-specific paperwork to packed material, we know that the day-to-day grind of careful manufacturing pays off.
A keen understanding of reactivity trends, impurity risks, and the logistics of scale translate to stronger partnerships and dependability. For organizations ready to push the boundaries of reaction creativity, 5-bromo-3-pyridine carboxylic acid methyl ester continues to stand as a trusted tool—a platform for synthesis, backed by the reality of years in chemical manufacturing.