|
HS Code |
842037 |
| Cas Number | 100-54-9 |
| Iupac Name | methyl pyridine-2-carboxylate |
| Molecular Formula | C7H7NO2 |
| Molecular Weight | 137.14 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 222°C |
| Melting Point | -13°C |
| Density | 1.16 g/cm3 |
| Solubility In Water | Slightly soluble |
| Refractive Index | 1.527 |
| Smiles | COC(=O)C1=CC=CC=N1 |
| Synonyms | Methyl picolinate |
| Flash Point | 88°C |
| Pubchem Cid | 11998 |
| Odor | Characteristic |
As an accredited methyl 2-pyridinecarboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g amber glass bottle with a secure screw cap, labeled "Methyl 2-pyridinecarboxylate" and hazard information clearly displayed. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 80 drums, each 200 kg, totaling 16,000 kg methyl 2-pyridinecarboxylate, securely packed for transport. |
| Shipping | Methyl 2-pyridinecarboxylate is shipped in tightly sealed containers made of compatible materials, protected from moisture, heat, and direct sunlight. During transit, it should be handled as a chemical reagent, following standard safety protocols and local regulations. Appropriate hazard labeling and documentation must accompany the shipment to ensure safe and compliant delivery. |
| Storage | Methyl 2-pyridinecarboxylate should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Proper labeling and secondary containment are recommended to prevent spills and accidental exposure. Store at room temperature and keep container upright to avoid leaks. |
| Shelf Life | Methyl 2-pyridinecarboxylate typically has a shelf life of 2-3 years when stored in tightly sealed containers at room temperature. |
|
Purity 99%: Methyl 2-pyridinecarboxylate 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high-yield and low-impurity product formation. Boiling Point 238°C: Methyl 2-pyridinecarboxylate with a boiling point of 238°C is used in high-temperature reaction processes, where it provides thermal stability and minimizes decomposition. Molecular Weight 137.14 g/mol: Methyl 2-pyridinecarboxylate with a molecular weight of 137.14 g/mol is used in agrochemical formulation, where it enables precise stoichiometric calculations for consistent batch quality. Density 1.17 g/cm³: Methyl 2-pyridinecarboxylate with a density of 1.17 g/cm³ is employed in liquid-phase catalytic reactions, where it promotes uniform reactant dispersion and homogeneous mixing. Melting Point -12°C: Methyl 2-pyridinecarboxylate with a melting point of -12°C is used in low-temperature storage applications, where it maintains its liquid state and guarantees process fluidity. Stability (ambient light): Methyl 2-pyridinecarboxylate stable under ambient light is used in laboratory reagent storage, where it avoids photodegradation and prolongs shelf life. Solubility in methanol: Methyl 2-pyridinecarboxylate with high solubility in methanol is used in analytical chemistry, where it facilitates rapid sample preparation and accurate assay results. Water content ≤0.2%: Methyl 2-pyridinecarboxylate with water content less than or equal to 0.2% is used in moisture-sensitive synthesis, where it reduces unwanted side reactions and improves product integrity. |
Competitive methyl 2-pyridinecarboxylate 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@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
People who have spent time in a chemistry lab or worked with pharmaceuticals might recognize methyl 2-pyridinecarboxylate. This compound, often found under the abbreviation M2PC, showcases a simple molecular structure, yet it supports a range of applications that stretch from drug development to advanced material research. My own journey with M2PC started in a university lab, tracking yields for organic syntheses. Back then, the scent of pyridine derivatives never left the air for long, and every researcher carried an opinion about which compound handled best on the bench. Methyl 2-pyridinecarboxylate stood out as both reliable and versatile, never as volatile as some cousins in the pyridine family. Rather than focusing on density charts and boiling points, real utility often comes from how straightforward a chemical feels to work with and how much potential it unlocks in day-to-day projects.
Unlike methyl nicotinate or ethyl 2-pyridinecarboxylate, this compound offers a middle ground: a methyl ester with a six-membered ring, providing moderate reactivity while balancing stability during storage. Chemists appreciate this for batch reactions that demand patience—few surprises, fewer spills. It dissolves easily in most common organic solvents but resists breaking down, so it keeps its form until the experimenter wants it to change. Through my hands-on experience, pre-weighing and transfer are simple thanks to a manageable melting point. Compared with bulkier esters, M2PC takes less energy to heat or stir, making it a smart choice for small and medium-scale syntheses.
One point worth talking about is its distinct chemical footprint. The methyl group on the carboxylate brings just enough hydrophobicity, which helps in extractions and purification. Meanwhile, the pyridine ring anchors the molecule, resisting unwanted side-reactions even in tough conditions—a factor that often determines whether a lab chooses one reagent over another. Pharmaceutically, the molecule doesn’t crowd out receptor sites like some larger esters might. In my own experience with bioactive compound synthesis, M2PC regularly played a supporting role, giving structure without overshadowing the main pharmacophore.
Take a walk through academic labs, you’ll see it lining the back shelves, ready for esterification, alkylation, or coupling reactions. Research groups trying to build up heterocyclic frameworks or modify aromatic rings often use M2PC as a starting material. It turns out that the methyl ester group comes off with the right reagents, so you’re left with a carboxylic acid ripe for further manipulation. People who design ligands for catalysis or metal chelation count on that pyridine ring to stabilize metal centers.
Outside of synthesis, methyl 2-pyridinecarboxylate shows up in the pharmaceutical world more often than many realize. Whether it’s serving as a building block for anti-inflammatory drugs or acting as a precursor in a multi-step route, its reliability makes it a staple. I’ve spoken to chemists in process development who chuckle about how everyone’s tried to skip steps by using a bulkier ester or a different pyridyl isomer, only to come back to M2PC for its superior balance of activity and manageability. It doesn’t gum up reactions or deliver unpredictable byproducts, smoothing the path for approval and scale-up.
Everyone in chemistry knows that what’s on paper doesn’t always match what happens at the bench, so the real-world specs become a kind of folklore. Methyl 2-pyridinecarboxylate usually comes as a clear to pale yellow liquid, with a slight aromatic odor. It resists discoloration during storage better than most light-sensitive reagents. With a melting point comfortably below room temperature, solidification rarely poses problems. Most batches meet or exceed the 98% purity mark, which handles the majority of research-to-production environments. Impurities mostly show up as aromatic byproducts, easy to spot and separate.
You won’t find much excitement around the water solubility of M2PC—it’s modest in that area. Toss it into an organic phase, though, and you get quick dispersion and a predictable response to standard solvents like dichloromethane or ethyl acetate. Synthetic chemists who want to get on with their work appreciate this predictability, since rogue dissolutions and inconsistent phase separations eat up time. Even after years working with it, I rarely encounter surprises when scaling from grams to kilograms, a testament to the reliability that matters in both research and manufacturing.
Every seasoned chemist trades notes about unpleasant smells and reactivity quirks. Some worry about pyridine esters bringing unwelcome odors into small labs, but I’ve found M2PC to be less pungent than many related compounds. If you’ve ever spilled butyl pyridinecarboxylate, you’ll know the difference. Shelf life hardly raises concerns—as long as the bottle stays sealed and out of direct sun, the compound keeps its properties. Storage under an inert atmosphere isn’t necessary for general use. Still, those working in environments where every impurity counts—high-throughput screening, for example—should source material from reliable suppliers who offer analytical backup. There’s an old saying that the most expensive part of any reaction is the one you have to redo because some contaminant crept in. M2PC, thankfully, stays steady with standard procedures.
Environmental questions occasionally come up, especially now that labs must answer for every bottle on the waste log. Compared to more volatile or bioaccumulative pyridine derivatives, M2PC’s relatively low vapor pressure and straight degradation pathways make it easier to handle in terms of safety and disposal. I’ve gone through waste audits where it passed scrutiny without issue—a relief, given how regulators scrutinize nitrogen-containing chemicals.
Working with methyl 2-pyridinecarboxylate follows the usual rules: gloves, goggles, and respect for the material. Though not infamous for toxicity, any pyridine derivative deserves attention, since repeated exposure can add up over a long career. Good ventilation solves most nuisance odor problems, and basic spill control procedures keep the lab clean. For teams handling large volumes, extra care ensures that methyl esters don’t hydrolyze to acids—something that can spoil a whole batch if unnoticed. Using a lab notebook to track opening dates and storage conditions helps, especially when multiple people share reagents. Everyone remembers the day a bottle went off after months of back-and-forth across research groups.
One point that often goes unspoken is the importance of supplier choice. The difference between a routine reaction and a cleanup headache can trace back to source purity. I’ve worked through my share of batches with slight contamination—enough to compromise yields or introduce color changes in products. Sticking to tested vendors and keeping batch records makes troubleshooting much easier. Trust plays a role here—chemistry is still a people business, even when talking molecules and reactions.
Researchers and process chemists often feel pressure to innovate without reinventing the wheel. Methyl 2-pyridinecarboxylate reduces steps in many synthetic sequences. In medicinal chemistry, the presence of a methyl ester makes further derivatization easy, unlocking skeletal diversification that grows lead compound libraries. In my own projects, the time saved moving from carboxylate-protected to deprotected intermediates made all the difference, especially up against funding deadlines. Scale-up teams often talk about the “click” moment, when a reagent transitions from being niche to “workhorse.” For my group, that moment came when M2PC survived two process redesigns without getting swapped out—a small testament to its place in chemical development.
Facilities that emphasize green chemistry and cost-effectiveness like how M2PC can be handled with modest equipment. Its boiling point allows for simple solvent exchanges, limiting the need for high-vacuum lines or expensive glassware. I recall a pilot batch that leveraged this property, allowing for quick phase switches without solvent waste. No complex distillation columns—just smart chemistry, routine work, and reliable results.
Laboratories and process plants face a dizzying selection of pyridinecarboxylate esters. Ethyl and butyl versions compete in the catalog shelves, but their increased steric hindrance or volatility create extra hurdles. The methyl ester hits a sweet spot—not too light for runaway evaporation, not so bulky it hinders reactivity. It offers a subtler odor, which matters in open-plan labs where air quality carries weight for comfort and safety.
People sometimes assume all pyridine esters behave the same. Experience says otherwise. Take methyl nicotinate, for example. It’s structurally similar, but the nitrogen’s position on the ring alters both reactivity and scent in side reactions. When fine-tuning conditions for ligand synthesis, these small differences steer results more than textbooks suggest. My time working in combinatorial chemistry showed how one failed sequence can come down to the wrong starting ester—details that don’t make the procurement sheet, but show up in actual results.
In specialty synthesis—like active pharmaceutical intermediates or specialty dyes—the specific balance of reactivity, odor, and stability that M2PC offers turns out to be more than a footnote. Formulators lean on it when unwanted side products from other esters threaten batch purity. For me, that’s what builds long-term trust in a reagent: it works quietly and well, with few surprises, letting the chemist focus on the real challenge—innovation, not troubleshooting.
Any chemical brings a set of headaches if it’s misunderstood. M2PC is no exception. The main worries circle around purity, safe handling, and consistent performance at scale. For purity, choosing suppliers who offer full spectral data and batch-specific certificates helps. Some labs invest in extra in-house QC, but I’ve found most issues disappear by vetting the supply chain and requesting reference standards.
Safe handling issues rarely demand extra protocols beyond standard PPE and fume hoods, but training staff and reviewing procedures periodically keep skills sharp. For facilities processing large quantities, installing local sensors for vapor detection adds peace of mind—plus, it cushions against regulatory challenges.
Performance on scale-up sometimes exposes unexpected reaction slowdowns or emulsions. Batch record-keeping—detailing every solvent source, ambient humidity, and exact weights—often solves these puzzles. One colleague kept a shared troubleshooting log, cataloging small errors that saved hours and averted repeat mistakes. Building that kind of team memory might seem boring, but it’s how experienced labs thrive.
Trends in chemical manufacturing and research continue to lean toward complexity—bigger molecules, tighter controls, greener processes. Through it all, workhorse reagents like methyl 2-pyridinecarboxylate keep finding new niches. Startups exploring sustainable pesticides, med chem teams hunting drug targets, and electronics firms prototyping sensors all make use of the compound. It’s less glamorous than flashy catalysts but holds a role as trusted support. The real-world virtue lies in its ability to step into different projects and keep pace with increasing demands for reliability and environmental stewardship. My own hope is that open discussion about sourcing, best practices, and bench experience helps keep reagents like this accessible to all who need them.
So, when colleagues ask what makes methyl 2-pyridinecarboxylate worth stocking, I point to the track record. Decades of lab use, successful scale-ups, and straightforward handling set it apart. In science, as in most fields, it’s the consistent performers who become most valued.