|
HS Code |
875876 |
| Chemical Name | methyl 2-acetylpyridine-4-carboxylate |
| Molecular Formula | C10H9NO3 |
| Molecular Weight | 191.18 g/mol |
| Cas Number | 88599-43-9 |
| Appearance | Yellow solid |
| Melting Point | 78-82°C |
| Solubility | Soluble in organic solvents such as methanol and dichloromethane |
| Smiles | COC(=O)c1ccnc(C(=O)C)c1 |
| Inchi | InChI=1S/C10H9NO3/c1-7(12)8-6-9(10(13)14-2)4-5-11-8/h4-6H,1-2H3 |
| Purity | Typically >97% |
| Storage Conditions | Store in a cool, dry place, away from light |
As an accredited methyl 2-acetylpyridine-4-carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The product is supplied in a 5-gram amber glass bottle with a screw cap, labeled with chemical name, quantity, and hazard warnings. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packed methyl 2-acetylpyridine-4-carboxylate in sealed drums or bags, ensuring stability and compliance. |
| Shipping | Methyl 2-acetylpyridine-4-carboxylate is shipped as a chemical reagent in tightly sealed, chemical-resistant containers, protected from moisture, heat, and direct sunlight. It must be labeled according to hazardous material regulations and transported with proper documentation, following safety guidelines to prevent spills or exposure during transit. Handle with appropriate personal protective equipment (PPE). |
| Storage | Methyl 2-acetylpyridine-4-carboxylate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat sources, direct sunlight, and incompatible substances such as strong oxidizers. Store at room temperature and shield from moisture. Proper labeling and secondary containment are recommended to prevent accidental exposure or spills. Handle following standard chemical hygiene protocols. |
| Shelf Life | Methyl 2-acetylpyridine-4-carboxylate typically has a shelf life of 2 years when stored in a cool, dry, and dark place. |
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Purity 99%: methyl 2-acetylpyridine-4-carboxylate with a purity of 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Molecular weight 193.19 g/mol: methyl 2-acetylpyridine-4-carboxylate with a molecular weight of 193.19 g/mol is used in agrochemical research formulations, where precise dosage calculations enhance process reproducibility. Melting point 83-85°C: methyl 2-acetylpyridine-4-carboxylate with a melting point of 83-85°C is used in solid-state drug development studies, where controlled crystallization supports formulation stability. Particle size <50 μm: methyl 2-acetylpyridine-4-carboxylate with particle size below 50 μm is used in catalyst support applications, where increased surface area improves catalytic efficiency. Stability temperature up to 120°C: methyl 2-acetylpyridine-4-carboxylate with stability temperature up to 120°C is used in high-temperature reaction processes, where thermal resistance maintains compound integrity. Water content <0.5%: methyl 2-acetylpyridine-4-carboxylate with water content less than 0.5% is used in moisture-sensitive synthesis, where minimal hydrolysis risk preserves final product quality. |
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For years, we have watched the landscape of pyridine derivatives shift and expand as researchers push for higher efficiency and selectivity in chemical synthesis. Methyl 2-acetylpyridine-4-carboxylate exemplifies one area where attention to detail, process control, and purity level genuinely impact end-user success. Working daily with this compound, our teams observe recurring themes and challenges across both custom research and industrial-scale projects. There is no secret formula—success comes through diligent handling, practical adjustments based on reaction specifics, and a deep understanding of what makes this molecule unique.
Chemists often ask what makes methyl 2-acetylpyridine-4-carboxylate truly different from other pyridine carboxylates or related intermediates. Our answer always returns to the combination of its acetyl group at the 2-position and the ester at the 4-position. These features open flexibility for subsequent synthetic steps, crucial for constructing larger heterocyclic scaffolds or introducing more functional groups in pharmaceutical development. Unlike its close relatives such as methyl nicotinate or 2-acetylpyridine, our compound’s functional layout enables specific condensation, acylation, and cross-coupling reactions while also supporting diverse protecting group strategies. We regularly field requests from customers needing batch modifications to suit custom reaction conditions, and we respond by drawing on firsthand trials—not just lab theory.
Each batch runs through rigorously controlled processes, honing in on purity, moisture content, and consistency in melting point and spectral signature. Chemistry at this level leaves little room for error. Through years refining our technique, our standard model for methyl 2-acetylpyridine-4-carboxylate centers around solid-phase batch manufacture, secure glassware, and immediate protection from airborne contaminants and excess heat. The workhorse remains a carefully dialed-in esterification-acetylation pathway, fine-tuned with effective catalysts and purification routines. Years ago, production held risks of byproduct accumulation and color impurities—our current processes almost entirely eliminate those problems.
We keep residual water carefully below 0.5%, as higher levels bring real headaches during scale-up or subsequent use. NMR and HPLC checks routinely peg purity above 98%—sometimes pushing close to 99.5%, depending on application needs. These benchmarks stem from talking directly to technical managers frustrated with blocked reactions due to trace aldehyde or acid impurities, or sticky filtration steps that slow down timelines. Each parameter in our specification sheet answers a pain point we've seen on the ground, often through much trial and error.
Day by day, requests arrive from university groups chasing novel kinase inhibitors, from pharmaceutical scale-up teams, and from flavor and fragrance specialists searching for both specificity and reactivity. The distinguishing flexibility of methyl 2-acetylpyridine-4-carboxylate lies in the ease of further functionalization. The pyridine ring, unconstrained by steric encumbrance at the meta and para positions, enables nucleophilic substitutions, Suzuki couplings, or condensation reactions leading to more complex nitrogen heterocycles. The acetyl side group influences tautomer stability and intermediate reactivity, allowing chemists to build up to larger molecules or ring systems without excess byproduct formation.
Several clients pivoted to this compound when making intermediates for anti-infective agents, drawn by how well the 4-carboxylic ester fends off hydrolysis under moderately basic conditions. Where methyl nicotinate breaks down more rapidly in methanolic ammonia, methyl 2-acetylpyridine-4-carboxylate holds up and delivers cleaner yields—again, a difference that only shows after repeated trial. We have documented dozens of instances where teams reduced reaction time by up to 30% and increased selectivity for downstream reactions simply by switching to our methyl 2-acetylpyridine-4-carboxylate.
Nothing about commercial synthesis of pyridine esters happens on autopilot. Tiny fluctuations in temperature, solvent choice, or purity of starting materials quickly show up as impurities, altered crystallization, or color problems. Our production staff have spent years fine-tuning parameters, including slow temperature ramps and highly efficient stirring to avoid localized overreactions. Several batches in the early years suffered from undetectable polymerization or partial hydrolysis, which took persistent root cause analysis to resolve. These lessons translate directly to end-user trust—we remember being on the receiving end of residues that couldn't be traced, and we've taken every step to eliminate those headaches for our customers.
Over the years, we invested in real-time analytics to track and correct solvent traces, and we collaborated with research chemists to pinpoint which GC and HPLC peaks matter for actual performance. End-users—particularly API manufacturers—lean on these details to decide whether a raw material will create regulatory headaches or rework. From our side, every adjustment we make to the process—swapping a drying agent, changing the time curve of acetylation, or even shifting the storage protocol—flows directly from customer bottlenecks or reports from the lab floor.
More than once, we've run side-by-side tests comparing methyl 2-acetylpyridine-4-carboxylate with methyl 2-pyridinecarboxylate, 2-acetylpyridine, and the widely used methyl 4-pyridinecarboxylate. For certain Suzuki and Heck couplings, methyl 2-acetylpyridine-4-carboxylate shows superior performance—likely due to the combined electron-withdrawing effect driving cleaner selectivity and lowering side-reaction rate. From a handling perspective, the crystalline form of this compound ensures smoother weighing, faster dissolution in methanol or ethyl acetate, and less contamination during transfer compared to oils or difficult solids.
Other pyridine esters, such as methyl nicotinate, appeal for less cost but deliver more surprises downstream—instability under standard alkaline hydrolysis, mixed product streams, or loss of yield during condensation. More than one customer has switched over permanently after trying a kilogram trial batch, citing greater reproducibility and reaction confidence. Raw material choice sets the tone for the entire synthesis sequence. Cutting corners at this stage typically causes more troubleshooting and analysis in later steps—something we've seen from both sides of the supply chain.
Pharmaceutical research remains the area where the features of methyl 2-acetylpyridine-4-carboxylate shine brightest. Its unique balance between functional stability and reactivity has unlocked new structure-activity relationship studies in enzyme inhibitor projects, where minor changes at the 2- and 4-positions spell the difference between a dead end and a lead compound. Medicinal chemists report that it tolerates a wide range of catalytic conditions, whether they’re running palladium coupling or attempting late-stage acylations. Our teams work closely with project chemists to ensure batch-to-batch repeatability, with each delivery reflecting the practical lessons we've learned through hands-on experience.
In agrochemical synthesis, the presence of both the electron-withdrawing carboxylate and the acetyl group has made it possible for researchers to build new herbicide and plant-growth regulator scaffolds at a faster pace, with less intermediate loss. Some of our bulk customers report using methyl 2-acetylpyridine-4-carboxylate to introduce differentiable markers in combinatorial libraries, leveraging its resistance to hydrolysis for high-throughput screening processes. This resistance, not found in methyl nicotinate or 2-pyridinecarboxylate, prevents analytical drift and supports reproducible activity screening across thousands of samples.
Over in the flavor and fragrance industry, smaller amounts of this compound serve both as core intermediates and tailored modifiers, giving rise to novel notes or enhancing stability in challenging matrices. The ester group promises lower volatility, reducing losses in batch processing, and the acetyl feature brings distinct aromatic contributions not easily achieved through relatives lacking the dual substitution pattern. Unlike many laboratory-scale products, our industrial lots go through dual-stage drying and secondary impurity filtering, cutting down on trace off-odors or colorants that might otherwise render a batch unsuitable for sensitive applications.
Working directly in chemical manufacture, we don’t just look at numbers on a specification sheet—we factor in shelf life, resistance to both acid and base, and the way this compound behaves in real industrial settings. Our best batches show no significant degradation after six months at ambient temperature when sealed under nitrogen, a testament to both process rigor and careful downstream handling. Customers hoping to store bulk product or ship it to facilities across different climates rely on this resilience to avoid loss and unnecessary waste. The ester linkage holds up well during standard shipping, resisting hydrolytic breakdown, and the solid form discourages caking or bridging that could lead to weighing errors or unsafe dust.
We receive regular feedback about how minor impurities in competing products force end-users to perform complicated in-house purification, extending project timelines and increasing solvent use. Our operation puts testing at the heart of every production run, with full transparency provided to buyers seeking detailed impurity profiling. Requests for residual solvent content or trace-metal analysis receive fast and complete documentation, providing peace of mind both for regulatory needs and everyday lab work. Our approach reflects real conversations with end customers facing rigid compliance requirements—especially those in regulated industries where raw material quality links directly to product release or approval timelines.
One core strength we’ve developed comes from scaling this product line for different end markets—gram-scale research, multi-kilogram industrial synthesis, and intermediate scales for custom projects. Not all synthetic chemistry tolerates scale-up, but the robust pathway we engineered for methyl 2-acetylpyridine-4-carboxylate translates well from lab glassware to reactor vessels without changes in impurity profile. Our production supervisors keep close tabs on each shift in mixing, temperature hold, and extraction to ensure that performance remains steady regardless of batch size. Even on tight deadlines, our repeat trials record the real problems labs run into: unexpected emulsions, crystallization lags, or complications with glassware carryover.
By tailoring purification, drying, and quality checks to the exact nature of each batch, we help labs transition smoothly from concept to scale-up, often troubleshooting side by side with their chemists. We don’t prescribe cookie-cutter solutions. Instead, process data and customer feedback push each refinement. One pharmaceutical customer tracing a troublesome NMR peak to a minor solvent recently shared how the change in our drying protocol solved both an analytical and regulatory issue overnight. These stories shape how we craft each lot and how we advise technical teams planning synthetic sequences or validation studies.
Every day on the manufacturing floor brings safety into stark focus. Handling methyl 2-acetylpyridine-4-carboxylate presents challenges familiar to anyone managing aromatic esters—dust management, prevention of cross-contamination, and containment of process vapors. We have invested heavily in enclosure upgrades, more responsive spill controls, and automated weighing lines, not just for regulatory compliance but to protect our team and downstream users. Chemists receiving our batches know this firsthand—the absence of residual dust clinging to containers, the consistent color, and the predictable flow reflect our experience battling real-life handling issues.
The same vigilance flows into transportation, where strict packaging and real-time tracking reduce the likelihood of exposure or contamination during cross-border shipping. For many of our largest customers, buying direct from a manufacturer means having a partner ready to respond with replacement or troubleshooting advice at hours when distributors might not pick up the phone. We use our own near-miss reports, field audits, and customer follow-up to drive incremental improvements, shaping both safety culture and material quality far beyond what a trader or repacker can guarantee.
Whether a buyer plans to use methyl 2-acetylpyridine-4-carboxylate for a single synthesis or a long-term pipeline, our goal remains consistent: support practical, safe, and robust use. We share technical bulletins, tips for optimal storage, and even hard-earned troubleshooting strategies. Many times, our experience with production upsets or customer feedback about reaction bottlenecks leads to lasting improvements and new process controls. No intermediate exists in a vacuum—its true value comes from the usability, reproducibility, and problem-solving history it brings to the table.
Chemistry thrives on shared insights and on-the-ground learning. Through fielding repeated questions about stability, impurity removal, or tailored specification, we have built a knowledge base that helps not just seasoned researchers but also those encountering methyl 2-acetylpyridine-4-carboxylate for the first time. The focus never drifts from real-world use: reliable delivery when deadlines loom, transparency for all analytical metrics, and willingness to evolve according to project demands.
We have seen trends come and go—a rush toward lower cost entrants, fleeting interest in one-off exotic esters. Yet, time and again, customers return seeking substance: batches that behave as promised, technical support rooted in production experience, and adaptation without cutting corners. In the broader context of pyridine intermediates, the reputation of methyl 2-acetylpyridine-4-carboxylate has been built not just by its novelty or chemical layout, but by the consistent, incremental improvements made by those who manufacture and use it. That legacy gets written every day on our production floor and in the results our customers achieve.
For anyone planning a project requiring both versatility and stability, our experience with this compound shows how close attention transforms everyday challenges into lasting advantages. The best chemical solutions do not emerge overnight but through years of iteration, direct feedback, and a commitment to both product and people. We continue to evolve our approach, understanding that methyl 2-acetylpyridine-4-carboxylate stands as more than a line on a catalog—it represents a manufacturer’s daily investment in quality, reliability, and shared chemical progress.