|
HS Code |
127381 |
| Chemical Name | Methyl 2-pyridineacetate |
| Molecular Formula | C8H9NO2 |
| Molar Mass | 151.16 g/mol |
| Cas Number | 2446-32-6 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 247-249°C |
| Density | 1.129 g/cm3 |
| Smiles | COC(=O)CC1=CC=CC=N1 |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents |
As an accredited Methyl 2-pyridineacetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Methyl 2-pyridineacetate is supplied in a 100g amber glass bottle with a secure screw cap and tamper-evident seal. |
| Container Loading (20′ FCL) | Methyl 2-pyridineacetate is typically loaded in 20′ FCL using sealed HDPE drums or IBC tanks, complying with chemical safety regulations. |
| Shipping | Methyl 2-pyridineacetate should be shipped in tightly sealed containers, protected from light and moisture. Handle with care, avoiding exposure to heat and incompatible substances. Label according to local regulations for chemicals. Ensure transport vehicles are well-ventilated and equipped to manage minor leaks or spills, and keep away from food and drink items. |
| Storage | Methyl 2-pyridineacetate should be stored in a cool, dry, well-ventilated area, away from heat sources and direct sunlight. Keep the container tightly closed and properly labeled. Store separately from strong acids, bases, and oxidizing agents. Use appropriate chemical storage cabinets, preferably those dedicated to organic chemicals, to ensure safety and minimize contamination risk. |
| Shelf Life | Methyl 2-pyridineacetate typically has a shelf life of 2-3 years when stored tightly sealed in a cool, dry place. |
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Purity 98%: Methyl 2-pyridineacetate with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield of target compounds. Molecular weight 151.16 g/mol: Methyl 2-pyridineacetate with molecular weight 151.16 g/mol is used in agrochemical development, where accurate formulation of active agents is achieved. Boiling point 242°C: Methyl 2-pyridineacetate with boiling point 242°C is used in high-temperature organic reactions, where thermal stability facilitates safer process control. Density 1.15 g/cm³: Methyl 2-pyridineacetate with density 1.15 g/cm³ is used in material science research, where consistent compound dispersion is maintained. Stability temperature 200°C: Methyl 2-pyridineacetate with stability temperature 200°C is used in catalyst preparation, where decomposition is minimized under process conditions. Melting point -5°C: Methyl 2-pyridineacetate with melting point -5°C is used in liquid-phase synthesis, where ease of handling at ambient temperatures is achieved. Refractive index 1.500: Methyl 2-pyridineacetate with refractive index 1.500 is used in analytical chemistry applications, where precise detection and quantification are improved. Water content ≤0.3%: Methyl 2-pyridineacetate with water content ≤0.3% is used in moisture-sensitive syntheses, where product integrity is preserved. Acidity as pyridine ≤0.05%: Methyl 2-pyridineacetate with acidity as pyridine ≤0.05% is used in fine chemical production, where unwanted side reactions are suppressed. Residual solvent ≤0.1%: Methyl 2-pyridineacetate with residual solvent ≤0.1% is used in flavor and fragrance development, where regulatory compliance is ensured. |
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Few chemicals pop up as frequently in organic synthesis work as Methyl 2-pyridineacetate. I first encountered it back in graduate school, during some long afternoons in the hood, and noticed right away how much chemists came to rely on this building block. Rather than being an exotic specialty chemical, it fills a role that bridges fundamental research and practical applications—an asset you’d want at hand whether your work involves making pharmaceuticals or mapping out new reaction pathways.
The structure of Methyl 2-pyridineacetate might look plain compared to extended ring systems or heavily protected intermediates, but its design packs in versatility. With a pyridine ring and an ester side chain, the compound brings options for both nucleophilic and electrophilic modification. Most folks in the lab recognize it quickly for its light, almost sweet odor and liquid state at room temperature, both signals of easy handling.
In everyday lab use, the model known as C8H9NO2—for its molecular formula—offers a clear, colorless appearance and typical weight that make it straightforward to measure, pipette, and store. I have measured out more than a few grams without worrying about odd viscosities or unstable reactions. Unlike some analogues, it resists absorbing water from the air and stays stable on the shelf if you screw the cap on tight. Specifications tend to run about 99% minimum purity, which is the threshold most synthetic protocols expect.
Much of my work related to this ester revolved around basic organic synthesis. It serves as a starting point or intermediate in many reactions that go on to create flavors, fragrances, pharmaceuticals, or agrochemicals. Companies value its ability to take part in straightforward transesterification and amidation reactions due to its accessible ester group. The functional handle on the pyridine ring means it sits at a sweet spot for further transformations—a fact that synthetic chemists take advantage of, especially if the aim is to create substituted pyridines or more complicated heterocyclic structures.
Pharmaceuticals often trace their origins back to simple, reliable intermediates, and Methyl 2-pyridineacetate delivers just that. In one project, our lab group worked on inhibitors that targeted enzyme pathways, and using this ester as a precursor meant we could change the N-substitution pattern on the ring with relative ease. Its ability to respond predictably to reducing agents or Grignard reagents, for instance, reduces surprises at the bench. This saves time and budget. Unlike less stable analogs, which sometimes left us with decomposition messes or inconsistent yields, this compound proved steady.
Methyl 2-pyridineacetate often gets compared with methyl nicotinate or ethyl 2-pyridineacetate—close chemical cousins. The small shift from methyl to ethyl substituent can sound like hair-splitting, but that shift has practical effects. The methyl ester hydrolyzes a bit more easily under basic conditions, for example, so if you’re aiming for downstream reactions where speed matters, methyl can offer an edge. That also makes it more suitable for quick derivatization or for synthesis environments where time is in short supply.
On the other hand, heavier or more complex esters sometimes increase boiling points or introduce solubility hassles. Methyl 2-pyridineacetate strikes a balance: it keeps the process manageable for both scale-up and fine-tuning in the lab. I’ve found it dissolves easily in common organic solvents; this cuts down on prep work and lets you focus on the chemistry rather than wrestling with dissolving stubborn solids.
Unlike pyridineacetic acid itself, the methylated form delivers more stability during storage and use. No one enjoys opening a bottle only to find a crust of degraded acid at the bottom—a problem methyl esters can prevent. Folks running industrial reactors or pilot lines know the value of reliable reagents; downtime from material uncertainty gets expensive fast.
Over the years, I watched more than a few projects stall because a key reagent produced inconsistent results. Purity and consistency sound basic, but they directly affect yield, scalability, and regulatory acceptance. It’s no secret that even minor impurities in starting materials can derail drug approval or FDA submission, so batches of Methyl 2-pyridineacetate with verified certificates of analysis make a difference. In field settings, especially contract research organizations, having a trusted source for well-characterized intermediates trims risk and makes collaboration smoother.
I’ve also met chemists who push materials harder than their guidelines, running them through extremes of heat or pH, so seeing Methyl 2-pyridineacetate turn up unchanged means less troubleshooting. This becomes a quiet success factor: reactions run smoother, with less batch-to-batch guesswork, letting teams focus on innovation rather than spending hours solving supply issues.
Even with the upsides, no chemical sits without challenges. A recurring issue for folks purchasing bulk or kilo-lab quantities centers on solvent residues or minor byproducts from synthesis. While purity of commercial samples averages high, storage and transport conditions sometimes nudge levels of unknowns upward. Tightening controls from supplier to shipping matters a lot, especially in regulated industries.
One step forward lies in shared testing protocols. When both supplier and end user agree on the methods for checking purity—like using advanced HPLC techniques or better NMR protocols—misunderstandings shrink. Some companies have shifted towards more open data sheets, listing not just purity, but also impurity fingerprints and recommended storage conditions. This helps bench chemists plan for unexpected phenomena before they happen.
Sustainability has also become a mark of responsible sourcing. Over the past few years, some manufacturers began switching to greener synthetic pathways, cutting down on waste solvents or energy use. I’ve noticed a small but growing demand from labs and companies looking to buy only from those who build circularity or recyclability into their processes. Folks in procurement and EHS will recognize the push; those reputational and operational benefits stack up long-term.
Among esters and pyridine derivatives, Methyl 2-pyridineacetate earns a reputation as straightforward and manageable under most standard protocols. Like any aromatic ester, reasonable care in storage and handling applies. In practical lab settings, I’ve sometimes seen colleagues treat it with respect similar to that owed to midweight organics—good ventilation, gloves, and thoughtful waste disposal.
One factor in its favor: it lacks the high volatility or strong, persistent odor found with some other pyridine esters, which lets both research and production teams worry less about air quality or undue staff exposure. The main hazards get tied to ingestion, skin contact, or inhalation at high concentrations, but adherence to routine chemical hygiene practices addresses these. Frequent users do well to store it in tightly sealed glass or HDPE containers, away from acids and oxidizers.
Decision-making in research and chemical manufacturing involves weighing reliability, performance, and suitability for the task at hand. From my bench experience, Methyl 2-pyridineacetate consistently delivers, whether working up a new molecule or scaling production. Its chemical stability, clear reactivity profile, and handling ease have earned it a place in toolkits across fields from pharmaceuticals to specialty chemical development.
As industries and labs place bigger bets on efficiency and reproducible outcomes, familiar compounds like this methyl ester serve as quiet enablers. They let researchers shift focus from troubleshooting raw materials to the real work of creativity and innovation. Where supply chains, regulatory pressures, or sustainability mandates come into play, companies can lean on proven materials that already meet tight standards.
Looking ahead, the story of Methyl 2-pyridineacetate mirrors broader trends toward precision, transparency, and shared knowledge between producers and users. As methods improve and the focus sharpens on greener or more efficient practices, this reliable intermediate seems set to underpin future advances across several sectors. Strategic use of this compound not only speeds time to market but creates less friction from lab bench to product launch—a benefit every chemist and company can appreciate.
Reliable commentary and facts on Methyl 2-pyridineacetate often trace back to peer-reviewed organic chemistry texts, as well as technical documentation published by leading research suppliers. For chemical safety, the National Institutes of Health, Sigma-Aldrich’s technical bulletins, and the Royal Society of Chemistry’s journal archives offer trustworthy perspectives. Keeping pace with improvements means reading updates from environmental organizations, professional societies, and regulatory bodies—where the conversation broadens from simple usage to bigger questions about transparency, supply chain security, and environmental impact.