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2-Bromo-Isonicotinic Acid Methyl Ester

    • Product Name 2-Bromo-Isonicotinic Acid Methyl Ester
    • Alias 2-Bromo-4-pyridinecarboxylic acid methyl ester
    • Einecs 847-620-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    540767

    Product Name 2-Bromo-Isonicotinic Acid Methyl Ester
    Cas Number 50890-83-0
    Molecular Formula C7H6BrNO2
    Molecular Weight 216.03
    Appearance White to off-white solid
    Melting Point 53-56°C
    Purity Typically >98%
    Smiles COC(=O)C1=NC=CC(Br)=C1
    Synonyms Methyl 2-bromoisonicotinate
    Storage Temperature 2-8°C (Refrigerated)
    Solubility Soluble in organic solvents such as DMSO and methanol

    As an accredited 2-Bromo-Isonicotinic Acid Methyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 5g amber glass bottle with a tight-sealed cap, featuring a printed label indicating "2-Bromo-Isonicotinic Acid Methyl Ester."
    Shipping 2-Bromo-Isonicotinic Acid Methyl Ester is securely packaged in sealed containers to prevent contamination and degradation. Shipping complies with relevant chemical transport regulations, ensuring temperature-controlled or dry conditions as necessary. All shipments include proper labeling, documentation, and safety data sheets (SDS) for safe handling during transit and upon receipt.
    Storage 2-Bromo-Isonicotinic Acid Methyl Ester should be stored in a tightly sealed container, away from moisture and light, in a cool, dry, and well-ventilated area. Keep it at room temperature or as specified by the manufacturer. Ensure storage location is free from incompatible substances and ignition sources. Properly label the container and restrict access to trained personnel only.
    Application of 2-Bromo-Isonicotinic Acid Methyl Ester

    Applications of 2-Bromo-Isonicotinic Acid Methyl Ester in Industrial Manufacturing

    Our high-purity 2-Bromo-Isonicotinic Acid Methyl Ester supports advanced synthesis for key downstream industries. The following applications reflect established, real-world use cases where this intermediate plays a specialized role in regulated manufacturing environments, underlining quality and traceability expectations.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical manufacturers utilize this compound as a building block for the synthesis of pyridine-based active pharmaceutical ingredients (APIs). Its functionalized pyridine ring enables controlled halogenation and methyl ester formation in multi-step production routes of advanced drug molecules. Downstream facilities require precise quantities and robust process controls when incorporating brominated pyridine esters at defined steps to ensure consistent batch-to-batch reproducibility and regulatory conformity for market authorization.

    Industry compliance standards

    • Good Manufacturing Practice (GMP) as per ICH Q7 and EU GMP Annex 1
    • U.S. FDA 21 CFR Part 211
    • European Pharmacopoeia (Ph. Eur.) and United States Pharmacopeia (USP) standards
    • REACH Registration for chemical intermediates

    Typical usage ratio

    • Ranges from 0.5 molar equivalents to 1.2 molar equivalents relative to the target core structure depending on synthetic route; exact proportions specified by reaction scheme and scale.

    Downstream process integration

    • Introduced during scaffold functionalization or intermediate step, typically after initial pyridine protection phases and before final API crystallization or purification.

    Final product types

    • Pyridine-derivative APIs for anti-tubercular, anti-viral, or oncology therapies
    • High-value pharmaceutical intermediates for global generic production

    2. Agrochemical Intermediate Manufacturing

    This methyl ester derivative serves as an essential intermediate in producing selective herbicides and insecticides. Agrochemical synthesis plants leverage its bromopyridine moiety for iterative coupling, introducing pesticide-relevant functional groups through nucleophilic substitution reactions. Manufacturers need accurate metering and contaminant-free supply to conform with agrochemical pre-registration requirements and batch reproducibility for large-scale, field-tested formulations.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Substances
    • ISO 9001:2015 Quality Management System
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • REACH compliance for industrial intermediates

    Typical usage ratio

    • 0.9–1.1 mol equivalents depending on the final pesticide backbone; slight adjustments are made per downstream target molecule complexity.

    Downstream process integration

    • Fed as a coupling partner after pyridine scaffold setup, typically during halogen-exchange or esterification pre-final formulation blending.

    Final product types

    • Brominated herbicide active ingredients
    • Precursor intermediates for systemically absorbed insecticides

    3. Specialty Chemical Synthesis for Dye and Pigment Intermediates

    Producers of specialty dyes and pigment intermediates employ this methyl ester as a base unit for constructing colorant molecules designed for high-performance plastics, textiles, and printing inks. Its halogen functionality enables downstream coupling techniques, particularly Suzuki and Buchwald-Hartwig cross-coupling, driving the installation of chromophoric groups. Supply chains demand consistent purity and robust documentation to satisfy global chemical management regulations.

    Industry compliance standards

    • ISO 14001 Environmental Management Certification
    • EN 71-3 (Safety of Toys – Migration of certain elements) for pigment use
    • Registration and documentation under REACH and global GHS
    • Product Safety Assessment for import/export (SDS/HS documents)

    Typical usage ratio

    • 1.0–1.5 mol equivalents based on the dye core scaffold’s targeted structure; proportional modifications for different chromophore synthesis.

    Downstream process integration

    • Processed post-initial aromatic amination and prior to coupling with azo or anthraquinone functional units during pigment molecule formation.

    Final product types

    • Intermediate dyes for high-heat-resistant polymers
    • Halogenated pigment precursors for digital and offset printing inks

    4. Material Sciences: Organic Electronic Component Precursors

    In the advanced material sector, this compound plays a pivotal role as a nucleating agent precursor for synthesizing organic semiconducting materials. Research-grade and manufacturing-grade facilities employ it for fabricating electronic component precursors demanding tightly controlled halogen substitution, enabling the creation of pyridine-modified polymers for organic light-emitting diodes (OLEDs) and organic photovoltaic devices. Stringent analytical QC and traceability systems govern each batch intended for integration in high-performance materials.

    Industry compliance standards

    • ISO 9001:2015 for manufacturing process and quality management
    • IEC 62321:2017 for determination of certain hazardous substances in electrical and electronic equipment
    • RoHS Directive (2011/65/EU) for electronic substrate input chemicals
    • Supply chain audits for conflict minerals and sustainability standards

    Typical usage ratio

    • 0.8–1.3 molar proportions depending on the complexity of the target organic electronic structure; adapted per polymerization or conjugation efficiency requirements.

    Downstream process integration

    • Added during the formation of monomer or oligomer units, prior to vacuum deposition or casting of the organic material layer for device assembly.

    Final product types

    • Precursor compounds for OLED display components
    • Pyridine-containing building blocks for flexible photovoltaic modules
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    Certification & Compliance
    More Introduction

    2-Bromo-Isonicotinic Acid Methyl Ester: Product Overview and Industry Perspective

    Direct from Manufacturer: Consistent Quality, Reliable Experience

    In our chemical manufacturing operations, we have been working with niche pyridine derivatives for decades. 2-Bromo-Isonicotinic Acid Methyl Ester stands out among our portfolio due to its precise reactivity profile and versatility in downstream synthesis. We produce this compound to strict internal standards, maintaining close control over batch consistency, physical appearance, and purity thresholds that meet longtime customer feedback and laboratory trends. Our experience comes from not just designing processes around theory, but from hearing about real-world challenges in pharmaceutical, agrochemical, and material science labs—and then addressing them in our plant processes.

    Model and Physical Parameters: Detail Matters

    The compound’s systematic designation as 2-bromo-4-pyridinecarboxylic acid methyl ester reflects its core chemistry. In our typical batches, you’ll find methyl 2-bromoisonicotinate appearing as a fine off-white to pale yellow crystalline powder. The melting point falls within a tightly controlled range, which we monitor alongside GC and NMR analysis to ensure low levels of impurities and isomeric byproducts. Customers often mention a preference for our robust analytical support—a result of decades developing tailored purification and crystallization workflows in our production line.

    We emphasize actual measurements, not just catalog promises: every order ships with reflective spectroscopy data and a batch-specific certificate of analysis. Moisture content rests below industry-accepted limits, as determined by Karl Fischer titration, preventing hydrolysis during extended storage. Odor and solubility characteristics are described precisely so end users can plan process integration without guesswork. Over time, we have minimized batch variability—with HPLC values tracking above the 99% mark in most lots—precisely because researchers and process engineers have shared the impact that even minor inconsistencies can pose when scaling up.

    Where 2-Bromo-Isonicotinic Acid Methyl Ester Works Best

    This compound sees steady demand for constructing complex scaffolds in medicinal chemistry due to the unique placement of both bromine and methyl ester groups on a pyridine ring. Our clients rely on the ability of the ester group to serve as a convenient handle for further transformations, such as hydrolysis or amidation, while the ortho-bromo substituent enables selective cross-coupling or direct arylation reactions. Academic and commercial labs confirm that this particular isomer often solves selectivity issues that arise with alternative halopyridine derivatives. Early in our business, process chemists pointed out that using para- or meta-bromo isomers would introduce significant purification headaches—feedback that helped us fine-tune our chlorination and bromination conditions to focus on the 2-isomer.

    By controlling our starting materials and reaction temperatures, we consistently achieve the desired regioselectivity demanded by process development chemists. Researchers conducting SAR studies (structure-activity-relationship) find that the electron distribution across this isomer makes certain pharmaceutical intermediates more accessible, whereas similar products create bottlenecks or introduce undesired by-products. Our work directly with scaled-up batches for pilot plants and kilo-labs illustrates how our consistency brings real savings in both turnaround and total cost of synthesis.

    How We Approach Purity and Reliability

    Years in manufacturing have shown that purity rarely comes down purely to final crystallization or filtration steps; it starts with material selection and equipment hygiene at every stage. Our plant runs dedicated lines for pyridine derivatives, with solvent recovery processes that avoid cross-contamination. Distillation columns handle only closely related compounds. Several pharmaceutical partners have commented that our 2-Bromo-Isonicotinic Acid Methyl Ester maintains higher batch-to-batch reproducibility than imports from secondary traders or those who juggle unrelated chemistries on shared equipment.

    In our own hands, we see how impurities, even at low parts-per-thousand, can complicate later-stage reactions, lower catalyst efficiency, or trigger unexpected side reactions in scale-up. Each batch receives a full impurity profile. The methyl ester group presents some hydrolysis risk under ambient humidity—so we pay particular attention to vacuum-sealing and moisture-barrier packaging, based on several cases where subpar packaging caused customer frustration and unnecessary downtime. These points have driven many standard operating procedures that we follow rigidly today.

    Why Users Choose 2-Bromo-Isonicotinic Acid Methyl Ester Over Alternatives

    Not all halogenated isonicotinic esters behave the same. Chemists frequently explain to us that 2-chloro analogues react differently under Pd-catalyzed Suzuki or Buchwald–Hartwig coupling, sometimes requiring higher loading of catalyst or leading to harsher reaction conditions. Our 2-bromo version enables milder and more efficient couplings. In our own internal R&D, we’ve run side-by-side campaigns using bromide, chloride, and iodide analogues; we saw improved yields and fewer purification problems with the bromo derivative under a range of ligand-catalyst systems. The consistent story from end users: this translates into fewer headaches, shorter timelines, and easier work-up during process scale-up.

    On another note, the placement of the bromine adjacent to the ring nitrogen (the “2” position) introduces an electron-withdrawing effect that can stabilize certain intermediates better than other isomers. Our technical support teams regularly field questions about comparative reactivity and have collated customer case studies where switching isomers has unlocked access to new chemical space or sharper biological activity.

    Production Process—Decisions Based on Real-World Feedback

    Scaling up synthesis of 2-Bromo-Isonicotinic Acid Methyl Ester means listening to users and learning from actual plant conditions. Compared to contract manufacturers, our process optimization goes deeper than just cutting costs. Early years saw bottlenecks due to excessive halogenation byproducts, slow reaction rates, and recovery syndromes; these problems mattered to our end customers, who needed scheduled delivery for multistep synthesis. After conversations with users facing frequent unplanned downtime, we adjusted our reaction campaigns—focusing on temperature ramping profiles, agitation speeds, and bromine addition rates tailored for our reactors.

    Process monitoring tracks real-time reaction progress via in-line spectroscopic methods. We fine-tune post-reaction crystallization based on feedback from customer trials, helping us refine solvent mixes and temperatures to push purity even higher. The solvent management crew keeps a running log of solvent purity and usage, learning from a few early incidents where improper flush sequences cost time and introduced off-specification color to the final crystals. By working closely with chemists inside and outside the company, we have a clear understanding of which process tweaks bring results on the lab bench and at scale.

    Packaging and Transportation—Less Room for Surprises

    Where shipping specialty organics is concerned, nothing replaces firsthand experience in witnessing the pitfalls of moisture intrusion, packaging stress, or even subtle shifts in temperature during storage and transport. Our shipping protocols grew out of several years of trial and error, direct conversations with users, and follow-ups investigating packaging failures elsewhere in the industry. We select multilayer moisture barrier bags and rigid HDPE outer drums for large shipments, and smaller glass containers for lab-scale needs.

    We log and track all batches with full traceability for raw materials and packaging components, so any user able to reference a lot number gets a detailed record back to the source, as this has often resolved questions about unexpected behavior in synthesis. Experience proves that thoughtful packaging avoids unnecessary delays and upsets, particularly when compounds face long ocean transit or sit at a warehouse over a wet season. Our staff are formally trained in handling hazardous secondary components and maintain a zero-tolerance policy on reusing packaging across product lines, a policy traced back to lessons learned from early product launches.

    Technical Support—Built Around User Experience

    We offer practical support that reflects our own hands-on work with 2-Bromo-Isonicotinic Acid Methyl Ester, rather than generic call center advice. Our technical staff draws from years of lab, process, and plant operation, so we answer queries using language and reasoning familiar to synthetic chemists, process technicians, and purchasing managers alike. Most questions concern fine points: solubility in specific solvents, recrystallization approaches, or impurities encountered after downstream transformations. We resolve these issues by referencing actual lab-scale retrospectives and data, not just templated FAQ responses.

    Having run the synthesis from grams to hundreds of kilograms, we understand the cumulative effects of temperature, humidity, and solvent selection on both reaction and storage stability—all critical when users must plan inventory for longer periods. We field user feedback promptly and log technical concerns into future staff training. More than half the process improvements in our current plant adopted suggestions rooted in recurring questions, which our management views as critical for continued progress.

    Comparisons to Other Pyridine-Derived Esters and Halides

    Many customers come to us after working with related halogenated isonicotinic esters or other substituted pyridines, and their feedback informs our product focus. Where methyl 4-bromonicotinate or 3-bromopyridine-4-carboxylate are concerned, practical experience reveals unique trade-offs in terms of reaction yields and workup complexity. Scouting reports from pharmaceutical process chemists pinpoint that alternative position (3,4, or 5) bromo-isomers rarely match the regioselectivity and reactivity profile delivered by the 2-bromo isomer.

    In Suzuki-Miyaura couplings and other arylations, users report that the 2-bromo group provides an optimal balance—more reactive than the 2-chloro but less problematic than the 2-iodo, which carries higher costs and greater liability in large-scale handling. The methyl ester also resists saponification under common laboratory conditions better than analogous ethyl or propyl esters, offering wider flexibility in later-stage transformations. In actual process runs performed for pilot clients, our 2-Bromo-Isonicotinic Acid Methyl Ester returned better repeatability and higher isolated yields over multi-batch synthesis, which our clients attributed to the interplay between ring electronics and sterics specific to this structural arrangement.

    From a physical handling perspective, our product generally avoids heavy odors or dusting issues that can occur with some isomeric or larger alkyl esters. It flows cleanly into reactors and resists agglomeration in storage, an advantage for operators handling larger batch charges. Close monitoring of particle size and moisture has paid dividends in user satisfaction, reflected in fewer field complaints and repeat orders.

    Scale-up Case Studies: Factory Floor Insights

    Some of our most instructive moments have come from seeing how our compound behaves not just in the 5-liter glass flasks of R&D, but in industrial reactors ranging from 50 up to 1,500 liters. We learned, for example, that slightly slower addition of bromine and careful monitoring of the in-process temperature ramp avoids both over-bromination and runaway exotherms—a lesson first made clear when a customer scaled up and experienced inconsistent product color and byproduct formation, which we later traced back to uncontrolled heat accumulation.

    Process analytical chemistry equipment on-site allows us to follow reaction progress in real time, not just with classic TLC or sampling, but with in-line FTIR and automated GC. These investments emerged after firsthand exposure to batch delays and off-spec outcomes. Our practitioners understand that translating chemistry from the bench to the plant is never just a matter of multiplying quantities; it takes a willingness to isolate and correct issues before they turn into shipment delays or rejected lots down the line.

    Pilot Trials, Troubleshooting, and Lessons Shared

    We encourage customers to conduct pilot trials using our product, and we actively collect their technical feedback. For example, materials scientists using 2-Bromo-Isonicotinic Acid Methyl Ester in the preparation of functionalized ligands reported small but significant influences on crystallization and dopant incorporation—feedback which we translated into slight tweaks in drying conditions to preserve optimal particle morphology. In another case, a process team scaling the synthesis of an agrochemical active noticed seasonal variation in product moisture due to local humidity; this prompted us to review warehouse and container protocols in our supply chain to stabilize conditions.

    We see the compound’s footprint far beyond the main pharmaceutical and agrochemical sectors. Customers synthesizing advanced OLED materials have pointed to the product’s clean spectral signature as critical for minimizing downstream purification, where minor ring-substituted byproducts would otherwise impair electronic performance. This insight backed up our own findings that maintaining a low-impurity process not only meets but also anticipates rapidly evolving specifications from leading labs worldwide.

    Industry Impact: Factual Real-World Value

    Based on years of order data, plant floor experience, and user engagement, our take on 2-Bromo-Isonicotinic Acid Methyl Ester is rooted in actual performance, not just catalog listings. This compound’s reactivity makes it indispensable for targeted N-arylation and amidation protocols. Consistently tight control over moisture, particle size, and purity reduces the need for pre-use purification, which saves our clients time, solvent costs, and labor. These practical benefits, voiced by customers who must hit timelines and quality milestones, have shaped our manufacturing so it stays relevant across new applications in both routine and high-end research settings.

    We pay close attention to customer trends, storage realities, and future regulatory considerations. The global market has grown more choosy—auditors look at everything from trace impurities to batch documentation. Our ongoing investments in traceability, staff training, and non-stop QC are direct responses to feedback. The end result: users accessing our material benefit from a transparent and technically supported source, avoiding surprises and benefiting from years of accumulated knowledge. Our management believes these principles matter for both routine orders and the most challenging, cutting-edge applications yet to emerge.

    Commitment to Progress

    We stand by our belief that attentive, real-world practice brings more value to the end user than generic market positioning. By focusing on direct plant feedback, evolving synthesis methods, and genuine collaboration, we keep our product standards aligned with what chemists, engineers, and factory operators encounter in daily work. If you seek a consistent, thoroughly supported source for 2-Bromo-Isonicotinic Acid Methyl Ester, our record, experience, and customer-driven adjustments over time offer a pathway to smooth integration into any ambitious or routine chemical synthesis program.