ethyl 2-bromopyridine-4-carboxylate

    • Product Name: ethyl 2-bromopyridine-4-carboxylate
    • Chemical Name (IUPAC): ethyl 2-bromoisonicotinate
    • CAS No.: 112898-00-7
    • Chemical Formula: C8H8BrNO2
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
    • CONTACT NOW
    Specifications

    HS Code

    726900

    Chemical Name Ethyl 2-bromopyridine-4-carboxylate
    Molecular Formula C8H8BrNO2
    Molecular Weight 230.06 g/mol
    Cas Number 62099-52-7
    Appearance Pale yellow liquid or crystalline solid
    Boiling Point 132-134°C at 15 mmHg
    Density 1.587 g/cm3
    Solubility Soluble in organic solvents (e.g., ethanol, dichloromethane)
    Smiles CCOC(=O)C1=CC(=NC=C1)Br
    Inchi InChI=1S/C8H8BrNO2/c1-2-12-8(11)6-3-4-10-7(9)5-6/h3-5H,2H2,1H3
    Refractive Index n20/D 1.564 (approximate)
    Purity Typically >97% (commercial samples)
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Synonyms Ethyl 2-bromoisonicotinate

    As an accredited ethyl 2-bromopyridine-4-carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle, sealed with a screw cap, labeled "Ethyl 2-bromopyridine-4-carboxylate" and safety information.
    Container Loading (20′ FCL) Container loading (20′ FCL): 12 MT packed in 25kg fiber drums, palletized, with inner PE bags—suitable for safe, bulk shipment.
    Shipping Ethyl 2-bromopyridine-4-carboxylate should be shipped in tightly sealed containers, protected from moisture and light. Ensure packaging materials are compatible to prevent leakage. Ship in compliance with local and international regulations for hazardous materials, including appropriate labeling and documentation. Handle with care to prevent spills or exposure during transport.
    Storage Store ethyl 2-bromopyridine-4-carboxylate in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers and bases. Keep it at room temperature, protected from moisture. Ensure all containers are clearly labeled and handled using standard laboratory safety procedures to prevent accidental exposure or contamination.
    Shelf Life Shelf life: Ethyl 2-bromopyridine-4-carboxylate is stable for at least 2 years when stored tightly sealed, protected from light, and moisture.
    Application of ethyl 2-bromopyridine-4-carboxylate

    Purity 98%: Ethyl 2-bromopyridine-4-carboxylate with 98% purity is used in pharmaceutical intermediate synthesis, where high chemical purity ensures minimal byproduct formation.

    Molecular weight 244.05 g/mol: Ethyl 2-bromopyridine-4-carboxylate at 244.05 g/mol is used in agrochemical development, where accurate molecular weight allows precise dosage calculation.

    Melting point 62–65°C: Ethyl 2-bromopyridine-4-carboxylate with a melting point of 62–65°C is used in organic synthesis processes, where controlled melting enhances process reproducibility.

    Stability temperature up to 80°C: Ethyl 2-bromopyridine-4-carboxylate stable up to 80°C is used in high-temperature catalytic reactions, where thermal stability improves product reliability.

    Low moisture content <0.5%: Ethyl 2-bromopyridine-4-carboxylate with moisture content below 0.5% is used in moisture-sensitive coupling reactions, where low water content prevents unwanted hydrolysis.

    Fine particle size <75 μm: Ethyl 2-bromopyridine-4-carboxylate with particle size under 75 μm is used in formulation of solid dosage forms, where fine granularity promotes homogeneous mixing.

    Assay ≥99%: Ethyl 2-bromopyridine-4-carboxylate with assay ≥99% is used in custom chemical manufacturing, where high assay level ensures target compound yield.

    UV absorbance at 330 nm: Ethyl 2-bromopyridine-4-carboxylate showing UV absorbance at 330 nm is used in analytical calibration standards, where distinct spectral properties facilitate accurate quantification.

    Free Quote

    Competitive ethyl 2-bromopyridine-4-carboxylate prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@bouling-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@bouling-chem.com

    Get Free Quote of Nantong Acetic Acid Chemical Co., Ltd.

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Ethyl 2-Bromopyridine-4-Carboxylate: A Closer Look from the Manufacturer’s View

    Understanding the Product Behind the Label

    Years spent in the lab and on the production floor teach more than any textbook can offer. You handle raw materials. You listen to chemists explaining what failed at the pilot scale and why one batch turns out right while another falls short. Over time, you develop more respect for every molecule that crosses your path. Ethyl 2-bromopyridine-4-carboxylate carries its own quirks and strengths, honed through both research and real-world application.

    This compound, found in niche but vital transformations, isn’t just another brominated pyridine on a product list. The industry recognizes it not because of slick marketing but because of how it fits into synthetic routes that matter. From agrochemical intermediates to diverse heterocyclic manipulations, it proves its worth daily in the hands of researchers and process chemists looking for reliability.

    Model and Authentic Characteristics of Ethyl 2-Bromopyridine-4-Carboxylate

    Our focus stays fixed on two core principles: purity is non-negotiable, and repeatability keeps projects running. Samples pulled from each lot—we test these beyond standard practice. NMR and GC-MS analyses establish purity, spotlighting the absence of unwanted isomers or contaminants that would trip up downstream chemistry. We monitor the melting range, trace water content, even the faintest deviations in color or odor, because seasoned bench workers know: one off-note in a reagent breeds days of troubleshooting.

    This chemical does not masquerade as a multipurpose commodity. It commands attention exactly because it has a defined role. At room temperature, it presents as a lightly colored solid—sometimes with a faintly yellow hue, a natural aspect of stored brominated pyridines, not an indicator of spoilage. The ester group remains vulnerable to hydrolysis, so packaging resists moisture and light, preventing subtle shifts over weeks on a shelf.

    Production Realities and Hard-Learned Lessons

    Bromination of pyridines can lead operators down a dangerous path. When people buy from bulk traders who don’t control production, they risk getting run-to-run shifts in regioisomer content or trace byproducts from incomplete reactions. Even tiny amounts of 3- or 5-bromo impurities degrade performance or, worse, lead to regulatory headaches if left unnoticed. Direct control of our synthesis makes a difference—tank temperatures climb too fast, and you get red-brown decomposed tar; too slow, and conversion suffers. Every lot speaks to the rhythm of careful chemistry, not simply theoretical yields.

    Our reactors carry baffles and efficient cooling because the pyridine ring resists consultation. Without this, runaway exotherms sneak up fast once you introduce brominating agents. Operators wear scars from the learning curve, but through trial, we established a cleaning protocol and flow control that keeps product throughput high and downstream repurification minimal.

    Functional Uses: Where This Compound Earns Its Keep

    No marketing spin needed—those in API and agrochemical synthesis know their steps hinge on reliable building blocks. Ethyl 2-bromopyridine-4-carboxylate takes a seat at key positions in cross-coupling reactions, often Suzuki and Stille types, forming structural frameworks or supplying a handle for further functionalization. Chemists using it aren’t just idly substituting reagents; they select it based on electronic positioning and the ease with which the ester survives reaction conditions that would ruin free carboxylic acids.

    The versatility of this compound stems from its robust reactivity at the 2-position bromide, which will readily undergo palladium-catalyzed coupling with boronic acids or stannanes. Teams synthesizing novel pharmaceuticals or screening agrochemical candidates count on it, especially when other leaving groups underperform or when regioselectivity drives success. The 4-carboxylate acts as both a protecting group and a springboard for further transformations, from hydrolysis to amidation, without the process headaches that plague analogues bearing differently positioned esters.

    Stark Differences from Other Pyridines in the Catalog

    Experience builds a deep appreciation for why subtle changes on the pyridine ring yield major practical differences. An investigator might reach for 2-bromopyridine or its 3- and 4-bromo siblings as starting points—yet each one dances to its own set of rules. Through hands-on scaling, we assert this: the 4-carboxylate modification makes or breaks outcomes during coupling and derivatization.

    Pure 2-bromopyridine lacks the directing power the carboxylate brings. Downstream transformations run with fewer byproducts when using the ethyl ester because it resists harsh bases better than methyl or tert-butyl substitutes. We watched researchers try to swap it with 2-bromopyridine-3-carboxylate; results lagged, separation turned costly, yields lower, purity subpar. The 4-position carboxylate avoids those issues—and, more importantly, opens up routes toward libraries of substituted pyridines that medicine and crop science demand.

    Bulk producers sometimes dismiss subtleties. Our own records and customer feedback say otherwise—each lot released with higher than 99% purity leads to fewer reworks, cleaner downstream analytics, and less need for labor-intensive purification. Besides, not every bromopyridine is made the same way; our in-house process avoids cross-contamination that happens in multi-use plants. Having direct oversight from raw bromine to finished ester now seems essential, not optional.

    Why Purity and Origin Tracking Matter

    Plant process expansion brought into focus why every step is scrutinized. Shipments from competitors, sometimes relabeled or sourced third-hand, resulted in client complaints about failed reactions or mystery peaks on analysis reports. We started archiving reference spectra for every lot, which let us resolve disputes and, more importantly, adapt synthesis parameters in real-time if flaws appeared.

    Batch numbers aren’t just for show—they connect the actual origin back to our reactors and raw-input logs. Our investment in analytic equipment was driver by need, not marketing: high-performance liquid chromatography picks up trace acids or unreduced byproducts missed elsewhere. As a result, we can pinpoint cause at the source, saving users time and money. Several academic groups and process developers later documented increased throughput on downstream steps simply by choosing consistent material.

    In the past, some tried to push low-cost alternatives, citing price rather than performance. Eventually, yield losses, hard-to-separate impurities, or inconsistent reactivity catch up to projects and make buyers rethink their choices. Traceability, analytical rigor, and openness about synthesis protocols all build trust—something only hands-on makers can offer.

    Real-World Bottlenecks and Solutions Adopted in Practice

    Handling and storage for ethyl 2-bromopyridine-4-carboxylate brought early surprises. Moisture pickup and light exposure nudged the ester group toward hydrolysis, increasing acidity and muddying NMR peaks. Our practical solution remains simple yet effective—use of low-permeability containers, desiccant packs, laminated foil, and immediate nitrogen flush before sealing every drum.

    Logistics posed a new challenge. Ambient temperature swings during transport led to clumping or caking in the past. We responded by shifting to temperature-controlled warehousing wherever feasible, reducing product returns linked to handling issues. The lesson was clear: no shortcut beats stable storage and prompt shipping from point of origin to end user.

    Operators in customer pilot plants flagged odor buildup during large-scale handling. Feedback led us to refine our ventilation and secondary containment systems, cutting down on airborne residues. Sharing these insights even aided several clients in troubleshooting their own operational headaches—a win that only direct manufacturers can deliver.

    Notes from Downstream Users: Feedback That Drives Improvement

    An R&D manager in a pharmaceutical client’s lab once described how switching to our material dropped their reaction failure rate by a third over the course of a project. Another, from the agrochemical sector, pointed out cleaner mass spectral data for key synthons. Only a direct relationship between user and manufacturer brings these results to light—spotting repeat requests for new pack sizes, identifying pain points in delivery, and then responding with action instead of vague promises.

    What outsiders often miss: adaptation cycles matter more than stubborn adherence to routine. When users need a change—an alternate solvent for dissolution, or enrichment above 99.5% for a regulatory submission—we work backward to reconfigure conditions at the source, not through tweaking a generic grade. These field-driven upgrades go into new standard processes, because every win for an end user, sooner or later, translates to a better product line for everyone relying on predictable chemistry.

    Environmental Stewardship and Safe Handling: Manufacturer’s Commitment

    Operating reactors that generate byproducts and waste puts responsibility squarely on our shoulders. Regulations on brominated organics tighten every year, and simply “meeting the standard” seems shortsighted. Instead, we invest in solvent recycling, smart vent scrubbing, and reagent recovery. The waste stream from each run is minimized, monitored, and logged for long-term impact assessments.

    Shipping remains a regulated activity. Full transparency with documentation—not just a paper exercise—lets receiving facilities prep containment and PPE based on accurate information. It’s the difference between safe use and a near-miss incident. Transporting this product by sea or air takes more planning, but the reward comes in years without an incident, fines, or product recalls. These are standards built from direct experience, not distant theorizing.

    Future Pathways and the Value of Direct Manufacture

    In the future, chemists will push for even higher selectivity, cleaner routes, and more precise building blocks. Our experience tells us industry can’t pivot with agility on generic stocks; only controlled, in-house production lets teams rapidly optimize output for evolving needs. Variants—think isopropyl esters, novel labeling, or different bromine positioning—get vetted at gram scale in our own labs before they ever reach the customer bench.

    R&D teams have unique requests: scale-up to meet pilot trial deadlines, tweaks for regulatory registration, documentation with comprehensive spectra, or custom formulation for lab automation. Providing each of these means keeping expertise close—not relying on a chain of intermediaries who never see the inside of a reactor or understand the outcome of a subtle shift in catalyst loading.

    The chemistry behind ethyl 2-bromopyridine-4-carboxylate doesn’t exist in isolation. It sits in a matrix of relationships—chemist to operator, operator to analyst, analyst to end user. This dialogue informs continuous improvement far better than distant trading. Above all, it reminds us that pride in manufacture is more than just supply; it’s a daily commitment to better chemistry, cleaner results, and shared progress for everyone who reaches for a bottle in a lab or a drum in a warehouse.

    Summary: Standing out by Learning from Every Batch

    Long experience in the chemical industry steers us away from shortcuts. Every batch of ethyl 2-bromopyridine-4-carboxylate reflects the sum of years of troubleshooting, operator ingenuity, R&D partnership, and investment in analysis. The real value flows from tight process control, direct quality management, traceability, and honest feedback from those who use the material in real applications. That’s what separates a true manufacturer’s product from anything pulled from a generic stock list.

    In an era where “good enough” rarely is, we hold to the idea that every molecule counts—because the chemists relying on our work know the difference. From the start of synthesis to delivery at the bench, ethyl 2-bromopyridine-4-carboxylate demonstrates what industry expertise and direct involvement truly achieve.