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HS Code |
554762 |
| Product Name | Methyl 5-bromo-2-chloropyridine-3-carboxylate |
| Cas Number | 887410-31-3 |
| Molecular Formula | C7H5BrClNO2 |
| Molecular Weight | 250.48 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically >98% |
| Melting Point | 76-80°C |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
| Smiles | COC(=O)C1=CN=C(C=C1Br)Cl |
| Inchi | InChI=1S/C7H5BrClNO2/c1-13-7(12)5-4(8)2-3-10-6(5)9/h2-3H,1H3 |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Synonyms | 5-Bromo-2-chloro-3-pyridinecarboxylic acid methyl ester |
As an accredited Methyl 5-bromo-2-chloropyridine-3-carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 10 grams, sealed with a screw cap, labeled with chemical name, CAS number, hazard pictogram, and handling instructions. |
| Container Loading (20′ FCL) | 20′ FCL can load 12MT of Methyl 5-bromo-2-chloropyridine-3-carboxylate, packed in 25kg fiber drums or as customized. |
| Shipping | Methyl 5-bromo-2-chloropyridine-3-carboxylate is shipped in tightly sealed containers, protected from light and moisture. It is transported in compliance with relevant hazardous material regulations. Appropriate labeling is used to ensure safe handling, and shipping is typically by ground or air through authorized carriers, depending on destination and regulatory requirements. |
| Storage | Store **Methyl 5-bromo-2-chloropyridine-3-carboxylate** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep the chemical at room temperature, protected from moisture. Use secondary containment and ensure proper chemical labeling. Authorized personnel should handle and store this compound following standard laboratory safety protocols. |
| Shelf Life | Methyl 5-bromo-2-chloropyridine-3-carboxylate is stable for 2 years when stored in a cool, dry, and dark place. |
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Purity 98%: Methyl 5-bromo-2-chloropyridine-3-carboxylate with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield reactions and minimal impurities. Melting Point 95°C: Methyl 5-bromo-2-chloropyridine-3-carboxylate with a melting point of 95°C is used in controlled crystallization for agrochemical manufacturing, where it promotes consistent batch quality. Particle Size <10 μm: Methyl 5-bromo-2-chloropyridine-3-carboxylate with particle size less than 10 μm is used in fine chemical production, where it enables uniform dispersion in formulations. Moisture Content <0.5%: Methyl 5-bromo-2-chloropyridine-3-carboxylate with moisture content less than 0.5% is used in solid-state synthesis operations, where it reduces risk of hydrolytic degradation. Stability Temperature up to 110°C: Methyl 5-bromo-2-chloropyridine-3-carboxylate with stability temperature up to 110°C is used in high-temperature organic transformations, where it maintains integrity under process conditions. |
Competitive Methyl 5-bromo-2-chloropyridine-3-carboxylate prices that fit your budget—flexible terms and customized quotes for every order.
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Day after day on the factory floor, the focus rests on reliability—not only in production volumes, but also in pinpointing the right building blocks for modern active pharmaceutical ingredient (API) discovery. In our experience, Methyl 5-bromo-2-chloropyridine-3-carboxylate stands out as one of those compounds that both chemists and process engineers circle on their lists. They look for tight control: clean halogenation, unmistakable pyridine integrity, no drifting by-products. So, we put the effort where it counts—on refining every step, from the initial bromination through the final filtration.
Working in an environment where each step in a synthetic route gets scrutinized, we’ve seen firsthand how a subtle impurity or a shift in moisture content can propagate problems downstream. Our batches reflect the cumulative lessons from countless process iterations, not a one-off approach. Using direct halogenation under monitored conditions, coupled with column purification, our plant delivers consistent Methyl 5-bromo-2-chloropyridine-3-carboxylate, batch after batch. A freshly tested GC trace always brings a little satisfaction; the peaks look right, the spectrum matches the archive, and the residual solvents measure below detection limits.
A few years ago, custom synthesis projects drove our initial focus on this specific bromochloro carboxylate. We recognized that no matter how niche a pyridine intermediate looks on paper, it often becomes a core node in drug discovery. Medicinal chemists prize this ester because the electron distribution across bromine, chlorine, and the ester makes it a prime candidate for cross-coupling reactions. It’s not about generalized versatility, it’s about clearly-thought reactivity. The ortho halogens open the door for both Suzuki and Buchwald-Hartwig couplings.
Bench chemists tell us the difference when using our material in their pilot runs. The story repeats: reactions proceed smoothly, extended purifications become unnecessary, and teams meet their project milestones. These outcomes come from getting the critical details right—kiloliter glass reactors that maintain steady temperature, robust phase separation at scale, and full transparency in each Certificate of Analysis. If a project demands an iterative hydrogenation or high-dilution cross-coupling, they have confidence our material won’t be the weak link.
Talking specifications might sound clinical, but this is where the line gets drawn between research frustration and production reliability. Purity always comes first on our list. We target a minimum of 98% by HPLC, reflecting what we actually find in in-house runs, not a marketing number. Water content rarely exceeds 0.3%, as measured by Karl Fischer titration under controlled conditions, which cuts back on downstream hydrolysis. Residual solvents raise red flags at routine checkpoints.
Particle size and flow properties, often skipped by competitors, receive direct attention in our plant. Early on, some customers reported clumping during transfer or erratic dosing from drums. By optimizing filtration and oven drying steps, we achieve a free-flowing crystalline product that fits automated weighing and handling equipment. High-shear mixing tests confirm the bulk density you see on the COA matches what you get in your workflow. This approach saves rework, and it lets larger operations run leaner without surprise downtime.
Product teams in pharmaceuticals, specialty agrochemicals, and fine chemical research seek this compound not because it’s generic, but because it triggers precise transformations that standard pyridine derivatives can’t match. Bromination adds a heavier, more polarizable site for selective substitutions, while the 2-chloro orientation resists spontaneous hydrolysis during storage. This means lower reactivity towards atmospheric moisture and better shelf life. Materials that lose potency sitting in a drum just complicate scheduling and cost planning. Here, our compound holds up.
Inside our plant, documentation systems track every raw material lot, so traceability isn’t an afterthought. Bi-weekly reviews by our analytical chemists catch any trend shifts over time, an extra layer that process auditors and procurement managers recognize when visiting our sites. Each year, as customers stretch the reactivity window and scale-up limits, our technical team fields new questions—about batch reproducibility, about regulatory traceability, about residual metals after production. Working side by side with users, we address these requests in real time, compacting feedback into our quality system.
Discussion around Methyl 5-bromo-2-chloropyridine-3-carboxylate gets sharper when users lay it next to related molecules. Standard methyl pyridine carboxylates lack the duo-halogen features that chemists turn to for fine-tuned substitution. Substituting only bromine or chlorine at meta positions cuts down options for further elaboration. Our own R&D teams routinely find that the pairing of bromine at the 5-position and chlorine at 2 grants better selectivity for cross-coupling reactions—less side-chain scrambling, fewer ring-opened byproducts, more route flexibility.
We’ve heard from scale-up chemists that simple pyridine-3-carboxylates with a single halogen resist certain C–C couplings, producing lower yields or forcing the use of more aggressive catalysts. This methyl ester, with both the bromo and chloro substitutions, unlocks pathways that would otherwise stall at small-batch scales. During qPCR probe synthesis and advanced material projects, these dual halogen sites bring about functional handles, making complex modifications feasible without reworking the core scaffold.
Every kilo of Methyl 5-bromo-2-chloropyridine-3-carboxylate gets delivered to users aiming to build something consequential—new candidate drugs, high-value fine chemicals, custom reagents for R&D. Their feedback drives our refinements. For one custom API partner, the dual-halogen pattern allowed for late-stage amination and rapid halide exchange, cutting weeks from their synthetic route compared to older single-halogen carboxylates. They finished validation runs with higher overall yield, less column work, and with no troublesome trace chlorination at off-target positions.
In agrochemical research, the compound has aided enzyme inhibitor discovery, bringing lead optimization timelines down. Cascade reactions that used to suffer low conversion found better site-selectivity and cleaner mass-spec profiles when the substrate carried both bromine and chlorine in the right spots. Our chemists engage directly with these teams, tweaking process variables and sample preparation protocols so these benefits become routine, not occasional lucky breaks.
Manufacturers with multi-layered supply chains often run into trouble: delays, lost documentation, shifting specs. Our team controls the process from raw input—pyridine derivatives and halogens—all the way to finished, tested product. We don’t move material through trading houses or contract repackagers. Each lot aligns with the reference chromatogram stored in our internal library. When a user needs supporting spectral data or process details, the answer comes directly from the plant manager or analytical lead responsible for that lot.
Over years of production, we invested in plant upgrades—dedicated halogenation reactors, advanced filtration units, and custom drying ovens. Tracing a lot number back means no stalling, no confusion over where or how a given drum was produced. This direct model prevents headaches when regulatory authorities examine procedures for cGMP or multi-compendial compliance. It’s a point of pride among production staff who know that every operator’s choices show up downstream—there’s no one else to point at if something goes off-script.
Nobody gets the process perfect from the start. Scaling this molecule from bench synthesis to plant volumes brought surprises. Initial plant runs showed hydrochloric acid fume formation that stressed downstream filtration cartridges. By adjusting temperature ramp rates and adding venturi scrubbers, we contained emissions and cut cartridge wear. Subsequent runs reached target throughput without excessive filter changes.
Process development in a live plant environment also surfaced lessons around solvent choice and workup. One scale-up batch suffered from persistent emulsion formation during aqueous wash. Through joint sessions between lab and plant teams, we revised mixing stages and selected cosolvent mixtures that broke emulsions rapidly. Batch test records now confirm that clarity point in every lot. By closing the feedback loop, we spot issues before they escape into shipped material—and make sure new fixes stick.
Meeting customer and agency expectations for transparency becomes easier with a short, accountable supply chain and thorough records. Each year, environmental teams from our site update process hazard analyses, focusing on halogen management, solvent recovery, and emissions control. Local wastewater norms demand responsible effluent handling, so our process water passes through multi-stage neutralization before discharge. Pre-treatment logs, pH records, and halide content levels stay available for review.
Regulatory audits, whether for pharmaceutical customers, specialty intermediates, or internal EH&S teams, proceed smoothly because process records and QC data flow directly from a single source—our plant. We benefited by adopting electronic batch records and in-house archival for all analytical methods. No duplicate data entry, no confusion about current specs, nothing left to “interpret.” Everyone from the line chemist to the regulatory compliance lead can trace each container’s journey.
Supplying this complex intermediate isn’t enough if researchers operate in the dark. Our technical team fields questions not just on product properties, but on fit for use in specific reactions—common catalysts, predicted coupling partners, known side reactions. We share hints from our process chemistry team on optimizing yields and avoiding common pitfalls with the molecule. Sometimes, sharing failures saves users weeks of trial and error. One client, citing unexplained color formation during scale-up, worked with our team to adjust base addition sequence, stabilizing the reaction and preventing loss of product.
We keep tabs on trends where new research pathways open. Increasingly, groups experiment with tandem coupling or late-stage functionalization leveraging the dual-halogen motif. By supplying not just reliability in each drum but technical depth and current best-practices, our company grows alongside cutting-edge research, keeping chemical invention moving consistently forward.
Every drum dispatched carries more than a tracking label; it reflects the people on the floor who commit themselves to doing things right, shift after shift. Our operators call out irregularities, our lab analysts watch for data drift, and our management expects to answer customer questions directly. We listen as users describe emerging needs—tighter specs, new testing protocols, or support for evolving green chemistry standards. The feedback doesn’t gather dust on a shelf—it returns to process adjustments, equipment upgrades, and ongoing staff training.
We recognize that research chemists, process scale-up teams, and regulatory auditors all scrutinize each intermediate’s profile. So, we invite partners to audit our process—physically or through data. Our model isn’t built around one-off sales, but around repeat runs that prove the value of hands-on manufacturing, deep technical experience, and mutual trust with end users. When the needs change, we adapt alongside, grounded by the lessons from every production cycle, every feedback session, and every milestone reached with our clients.
Walking the production line, sights and sounds remind us of the responsibility that comes with crafting a key intermediate like Methyl 5-bromo-2-chloropyridine-3-carboxylate. Whether mixing a new batch, checking the chromatogram, or reviewing a new client’s application of the product, the commitment stays the same. Attention to detail, clear communication, and a willingness to improve drive each day’s successes. Serving ambitious chemists and serious research teams, we aim to be more than just a vendor—we’re a partner in progress, grounded in experience and the real demands of modern chemistry.