2-Pyridineacetic Acid Methyl Ester

    • Product Name: 2-Pyridineacetic Acid Methyl Ester
    • Chemical Name (IUPAC): Methyl 2-pyridylacetate
    • CAS No.: 25288-57-1
    • Chemical Formula: C8H9NO2
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    512550

    Cas Number 40056-74-8
    Molecular Formula C8H9NO2
    Molecular Weight 151.17
    Appearance Colorless to pale yellow liquid
    Boiling Point 255-257°C
    Melting Point -
    Density 1.141 g/mL at 25°C
    Purity Typically ≥98%
    Solubility Soluble in most organic solvents
    Refractive Index n20/D 1.516
    Smiles CC(=O)OCc1ccccn1
    Inchi InChI=1S/C8H9NO2/c1-11-8(10)6-7-4-2-3-5-9-7/h2-5H,6H2,1H3
    Synonyms Methyl 2-pyridylacetate

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

    Packing & Storage
    Packing The 2-Pyridineacetic Acid Methyl Ester comes in a 25-gram amber glass bottle, sealed and labeled with product and safety information.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 2-Pyridineacetic Acid Methyl Ester: Typically loaded in 200 kg drums, totaling approximately 80 drums per container.
    Shipping 2-Pyridineacetic Acid Methyl Ester is shipped in tightly sealed containers, compliant with chemical safety regulations. It should be stored and transported in a cool, dry place, away from sources of ignition or incompatible substances. Proper labeling and documentation are required to ensure safe handling during shipping, along with adherence to local and international transport guidelines.
    Storage **2-Pyridineacetic Acid Methyl Ester** should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed when not in use. Store at room temperature, protect from moisture and direct sunlight, and ensure proper labeling to prevent accidental misuse or exposure.
    Shelf Life 2-Pyridineacetic Acid Methyl Ester typically has a shelf life of 2 years when stored in a cool, dry, and dark place.
    Application of 2-Pyridineacetic Acid Methyl Ester

    Purity 98%: 2-Pyridineacetic Acid Methyl Ester with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal byproduct formation.

    Molecular Weight 151.16 g/mol: 2-Pyridineacetic Acid Methyl Ester with a molecular weight of 151.16 g/mol is used in heterocyclic compound synthesis, where accurate molecular mass enables precise stoichiometric calculations.

    Boiling Point 239°C: 2-Pyridineacetic Acid Methyl Ester with a boiling point of 239°C is used in temperature-controlled organic reactions, where thermal stability supports efficient process scale-up.

    Liquid Form: 2-Pyridineacetic Acid Methyl Ester in liquid form is used in continuous-flow chemical processes, where its physical state facilitates streamlined handling and mixing.

    Stability Temperature up to 120°C: 2-Pyridineacetic Acid Methyl Ester stable up to 120°C is used in reaction vessels for esterification, where thermal resistance allows for safe and reliable synthesis.

    Melting Point -10°C: 2-Pyridineacetic Acid Methyl Ester with a melting point of -10°C is used in low-temperature storage systems, where it maintains liquid-phase usability for rapid deployment.

    Density 1.18 g/cm³: 2-Pyridineacetic Acid Methyl Ester with a density of 1.18 g/cm³ is used in compound isolation protocols, where predictable volumetric properties support reproducible separation.

    Refractive Index 1.521: 2-Pyridineacetic Acid Methyl Ester with a refractive index of 1.521 is used in analytical method development, where optical clarity ensures accurate spectroscopic monitoring.

    Solubility in Methanol: 2-Pyridineacetic Acid Methyl Ester soluble in methanol is used in solution-phase synthesis, where miscibility enhances reaction homogeneity.

    Low Water Content <0.5%: 2-Pyridineacetic Acid Methyl Ester with water content below 0.5% is used in moisture-sensitive reactions, where it prevents unwanted hydrolysis and degradation.

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    Certification & Compliance
    More Introduction

    2-Pyridineacetic Acid Methyl Ester: A Closer Look at a Trusted Intermediate

    What Sets 2-Pyridineacetic Acid Methyl Ester Apart

    2-Pyridineacetic acid methyl ester, often called methyl 2-pyridylacetate, packs real value in the world of chemical synthesis. Anyone who has spent time in a research lab or a pharma facility knows how much hinges on the reliability and purity of starting materials, and this compound proves itself over and over again. With the formula C8H9NO2 and a structure featuring the classic pyridine ring fused with an acetic acid methyl ester group, it stands as a go-to building block for medicinal chemistry and agrochemical development.

    In my experience working in academic research and industry collaborations, the success of a project often rests on stable, easily modifiable intermediates like this one. Its appeal partly comes from robust chemical behavior: the ester functional group reacts predictably during transesterification, hydrolysis, or amidation, so researchers can map out multi-step syntheses with more confidence. This kind of reliability isn’t always easy to find, and it can speed up benchwork when deadlines are tight.

    Reliable Specifications to Trust

    Each batch of 2-pyridineacetic acid methyl ester generally arrives as a clear or pale yellow liquid, with a faint odor that’s distinctive but not overwhelming. Standard purity hovers above 98%, which matters more than folks sometimes credit. When working with sensitive catalytic reactions, or developing APIs for eventual drug candidates, small contaminants can sabotage weeks of effort. Using consistently pure material slashes that risk, so workers don’t lose time troubleshooting mysterious outcomes.

    The boiling point, melting point, and solubility aren’t just figures—these numbers shape practical choices in synthetic routes. A boiling range between 115°C and 117°C at reduced pressure makes it practical for distillation and concentration without much decomposition. Beyond the data sheet, handling this compound doesn’t require advanced ventilation or special containment, which stands out compared to other similar intermediates. Still, following standard lab safety protocols makes sense, as it does for any chemical with an aromatic base.

    Why Chemists Keep 2-Pyridineacetic Acid Methyl Ester on Hand

    If you ask a synthetic chemist about their daily work, you’ll hear the same sentiment: having reliable intermediates cuts down on troubleshooting, and lets you focus on the part you actually want to discover. Unlike many other substituted pyridines, this compound handles multiple downstream reactions without fuss. That adaptability turns it into a linchpin for researchers working on both experimental and process-scale synthesis.

    A lot of new therapeutic agents trace their roots back to pyridine-based cores. Drug discovery teams use methyl 2-pyridylacetate to anchor side chains, build heterocyclic frameworks, or introduce new pharmacophores. Its methyl ester group can readily transform into carboxylic acids or amides, which show up in everything from antiviral drugs to novel herbicide precursors. Having spent years observing drug development move from initial hits to preclinical testing, I’ve seen how small bottlenecks in intermediate sourcing can hold back teams, especially in academic or budget-limited settings. Dependable access to this compound shaves months off project timelines.

    Differentiating from Other Pyridine-Based Intermediates

    2-Pyridineacetic acid methyl ester sits apart from other pyridine derivatives in both reactivity and handling ease. Compare it with something like 3-pyridinecarboxylic acid (nicotinic acid) or pyridine-2-carboxaldehyde, and the differences become clear quickly. Nicotinic acid, for instance, offers a carboxylic acid group but doesn’t provide the same flexibility for chain extension and subsequent functionalizations. The methyl ester group, by contrast, brings expanded synthetic possibilities. You can perform selective hydrolysis or amide coupling without losing the pyridine ring, a tough task with unsubstituted analogues.

    I've seen plenty of industrial chemists weigh the pros and cons between methyl esters, ethyl esters, and free acids in route planning. Methyl esters, in my own work and conversations with colleagues, get the nod because of gentler hydrolysis conditions and reliable behavior under both acidic and basic environments. By comparison, ethyl esters resist hydrolysis in some cases, which can gum up scale-up projects where time and yield matter.

    Common Applications: More Than Just Medicine

    While the spotlight often falls on drug design, the value of 2-pyridineacetic acid methyl ester goes well beyond pharmaceutical research. Agrochemical inventors use this compound when developing new pesticides and plant growth regulators. Its structural backbone serves as a launchpad for attaching aliphatic or aromatic groups, and the methyl ester behaves consistently during subsequent modifications. Over the past decade, I’ve watched its usage spread from small crop protection studies to workflow pipelines at major global agrochemical firms.

    The electronics industry also takes interest in such derivatives, especially for the creation of specialty polymers and corrosion inhibitors. Pyridine rings in these materials play a central role in conductivity or resistance properties, and the attached ester group improves processability. My colleagues in applied materials sciences report that switching to methyl esters builds in more leeway for downstream reactions, instead of the rigid limitations set by other functional groups.

    Handling, Storage, and Safety: What Experience Teaches

    Handling this compound doesn’t throw up the usual red flags seen with many pyridine derivatives. Fuming, strong odors, or hazardous decomposition products seldom appear. Still, storing it in amber glass, with tight seals away from light and moisture, helps keep purity intact. From my time working with similar materials, even brief lapses in storage conditions can bring a headache—unexpected impurities, off-odors, harder purification steps. Following good chemical hygiene remains non-negotiable.

    Gloves, goggles, and fume hoods are standard, and I encourage anyone, from the graduate student to experienced process chemist, not to cut corners with these rules. Small accidents—spills, skin exposure, splashes—can happen anywhere. Immediate clean-up and having standard spill kits on hand minimizes risk and protects labmates. Calling attention to everyday safety isn’t busywork; it keeps the flow of good science uninterrupted.

    Opportunities for Synthetic Innovation

    There’s a growing trend to use intermediates like 2-pyridineacetic acid methyl ester as scaffolds for diversity-oriented synthesis projects. Combinatorial chemistry platforms routinely start with this building block because its ester moiety opens doors to dozens of downstream variants. Rapid amide library generation helps researchers hunt for new biological activities or optimize lead compounds. Over a decade on the bench has taught me just how many promising routes stall due to intractable byproducts or uncooperative intermediates. With predictable reactivity, those roadblocks show up less often.

    Targeted catalysis stands as another exciting arena. Metal catalyzed couplings—Suzuki, Heck, or Stille reactions—frequently call on substrates with minimal steric hindrance or predictable electron distribution. This intermediate fits both criteria, avoiding the sluggish rates or unwanted side reactions common with more hindered esters or pyridines with bulky substituents. Teams working on green chemistry protocols or flow chemistry applications report fewer headaches using this compound, since mild operating conditions prevent loss through degradation or unwanted rearrangement.

    Real-World Challenges: Sourcing, Regulation, and Environmental Impact

    Reliable access to specialty chemicals depends on trust in supply chains just as much as technical documentation. Over the past several years, disruptions caused by global events or logistical hurdles have forced many researchers and manufacturers to re-examine their purchasing strategies. Small intermediates like methyl 2-pyridylacetate sometimes fall out of stock when demand spikes unexpectedly or raw material prices rise.

    In practice, working with domestic and international suppliers who certify quality and provide batch-specific analytical data helps avoid wasted time and costly rework. Analytical transparency makes a difference: certificates of analysis, NMR and GC-MS spectra, and details about impurities catch problems before they hit the lab bench. Lapses here can trigger failed reactions, poor yields, or regulatory non-compliance down the road. I've found it pays to vet suppliers not just for price or convenience, but for reliability, traceability, and product stewardship.

    Regulatory compliance, especially in pharmaceuticals, nudges industry users to select compounds with low risk for residual solvents, heavy metals, and allergens. 2-Pyridineacetic acid methyl ester generally scores well here, with manufacturing routes designed to avoid chlorinated solvents or restricted catalysts. Environmentally, the push toward greener processes and biodegradable byproducts asks chemists to remain alert—waste minimization strategies such as closed-loop solvent recovery and micro-scale reactions minimize the footprint of pyridine manufacturing.

    Supporting Sustainability Across the Value Chain

    Reducing environmental impact has moved from aspiration to expectation, particularly in organizations with strong ESG commitments. Synthetic routes that employ 2-pyridineacetic acid methyl ester often allow milder reaction conditions and cut down on hazardous byproducts. For example, ester hydrolysis can proceed under aqueous or enzymatic conditions, sidestepping harsher mineral acids or vast amounts of organic solvents. In the labs where I’ve consulted, these choices prove easier to implement than more headline-grabbing “green chemistry” approaches that require major process redesign.

    Responsible disposal of pyridine-based wastes remains on the radars of both R&D chemists and production engineers. While this ester is less toxic or persistent than some polyaromatic intermediates, strategies such as incineration or advanced oxidation ensure it doesn’t enter local ecosystems. Routine collaboration with waste management experts and regulatory authorities protects community health and helps companies avoid fines and bad press. In my own experience, getting waste disposal right feels like preventive medicine— it seldom wins awards but pays dividends in time saved and risks avoided.

    Looking Forward: Innovation and Adaptation

    Technology and regulation advance quickly, pulling new expectations along for the ride. As automation reshapes chemical R&D, reliable and versatile starting materials like 2-pyridineacetic acid methyl ester matter more than ever. Robotic synthesis platforms, which upend old norms around batch size and timeline, demand intermediates that work predictably across varied conditions. High-throughput screening hinges on reproducibility, and in hundreds of parallel micro-reactions, only the most consistent chemicals earn a place in the platform.

    AI-driven chemistry throws another twist into the mix. Designing new molecules in silico often starts with a small library of interchangeable building blocks. Software tools pick intermediates for virtual evaluations based on cost, availability, and synthetic flexibility. The fact that methyl 2-pyridylacetate continues to hold a place in these inputs speaks loudly; it blends reasonable pricing, steady availability, and broad reactivity—qualities that machine learning tools pick up and pass through the R&D workflow without drama.

    Meeting Future Needs: Suggestions from Field Experience

    Drawing on lessons learned in diverse labs, one way to improve outcomes lies in better communication between suppliers, researchers, and regulatory staff. Transparency around synthetic methods, impurity profiles, and sustainability credentials lets labs make smarter, safer choices. Ongoing investment in greener production tech, such as catalyzed esterifications with low-waste profiles, can lighten environmental burdens and boost resilience during supply interruptions.

    Cross-training chemists in both bench chemistry and environmental management yields more holistic problem-solving abilities. As teams branch into new synthetic applications, combining technical depth with regulatory awareness prevents roadblocks at later stages of development. Peer discussion, user group forums, and cross-organizational workshops encourage best practice sharing, which helps both smaller and larger users get the most out of intermediates like 2-pyridineacetic acid methyl ester.

    Why It Still Matters

    The significance of 2-pyridineacetic acid methyl ester draws from real, lived experience in modern labs and chemical plants. Anyone who has tried to troubleshoot a failed synthesis, or nursed a project through tight deadlines, knows how valuable it is to trust starting materials without hesitation. Consistent quality, reasonable safety, and broad synthetic adaptability turn it from just another catalogue entry into a cornerstone of innovation.

    Advances in drug discovery, agrochemical solutions, and material sciences don’t rest on any one compound, but having reliable intermediates levels the playing field. Whether you’re designing the next antiviral, developing drought-resistant crops, or fine-tuning specialty coatings, products like 2-pyridineacetic acid methyl ester cut through red tape and keep energy on discovery, not troubleshooting. That’s the kind of detail that separates average projects from ones that actually deliver results.

    Practical Proposals for Smoother Workflows

    Adopting centralized inventory management for trusted intermediates keeps teams nimble. In my consulting rounds, labs that log quality reports and share sourcing data spot trends in purity or shelf life before small issues grow into expensive setbacks. Regular staff training reinforces safe handling and prepares workers for the rare curveballs that might arise.

    Supplier partnerships, where researchers provide feedback on reaction outcomes and impurity behaviors, not only improve product offerings but foster mutual trust. It’s a two-way street: feedback loops encourage suppliers to refine their processes while giving labs early warning about shifts in supply or changes in material specs. Transparent collaboration like this feels like professional insurance.

    Finally, carving out space for ongoing professional development—keeping up with regulatory shifts, green chemistry milestones, and new synthetic protocols—pays off when organizations have to shift gears quickly. These investments don’t always grab headlines or win praise outside the lab, but they define whether energy flows into innovation or gets wasted in damage control.

    Conclusion: Building on Proven Foundations

    2-Pyridineacetic acid methyl ester continues to earn its place as a trusted tool for chemists in fields as diverse as hepatitis research, herbicide design, and materials engineering. Each year brings new challenges, but proven, reliable intermediates remain the unsung heroes that keep teams on schedule, error-free, and well-equipped to turn great ideas into functional products.