|
HS Code |
279245 |
| Iupac Name | methyl pyridine-4-carboxylate |
| Cas Number | 100-09-4 |
| Molecular Formula | C7H7NO2 |
| Molar Mass | 137.14 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 258-260 °C |
| Melting Point | 19-22 °C |
| Density | 1.193 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 117 °C |
| Smiles | COC(=O)C1=CC=NC=C1 |
| Pubchem Cid | 76729 |
| Refractive Index | 1.532 |
As an accredited methyl pyridine-4-carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g amber glass bottle of methyl pyridine-4-carboxylate, securely sealed with a screw cap and labeled with hazard warnings. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Methyl pyridine-4-carboxylate packed securely in 200 kg HDPE drums, 80 drums per container, total net weight 16 MT. |
| Shipping | Methyl pyridine-4-carboxylate should be shipped in a tightly sealed, chemical-resistant container, protected from light and moisture. It must be labeled according to chemical regulations and handled as a hazardous material, with documentation and transport in compliance with local, national, and international regulations, such as IATA, IMDG, or DOT guidelines. |
| Storage | Methyl pyridine-4-carboxylate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect the chemical from moisture and direct sunlight. Store at room temperature, and ensure proper labeling to prevent accidental misuse or exposure. Follow all relevant safety and regulatory guidelines. |
| Shelf Life | Methyl pyridine-4-carboxylate typically has a shelf life of 2-3 years when stored in a cool, dry, and airtight container. |
|
Purity 99%: Methyl pyridine-4-carboxylate with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and minimal impurities. Molecular Weight 137.14 g/mol: Methyl pyridine-4-carboxylate at molecular weight 137.14 g/mol is used in agrochemical formulations, where it enables precise stoichiometric calculations for batch reactions. Melting Point 72°C: Methyl pyridine-4-carboxylate with melting point 72°C is used in solid-state catalyst preparations, where it allows controlled thermal processing for uniform mixing. Stability Temperature 120°C: Methyl pyridine-4-carboxylate with stability temperature 120°C is used in high-temperature organic synthesis, where it maintains chemical integrity during extended heating cycles. Viscosity Grade Low: Methyl pyridine-4-carboxylate of low viscosity grade is used in resin manufacturing, where it facilitates smooth blending and homogeneous dispersion of additives. Particle Size < 50 micron: Methyl pyridine-4-carboxylate with particle size less than 50 micron is used in powder coating formulations, where it ensures excellent surface coverage and consistent film thickness. |
Competitive methyl pyridine-4-carboxylate 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!
Ask anyone who works in a chemical lab what matters most, and they’ll likely tell you it’s the integrity of their raw materials. In my experience, the difference between a forgettable experiment and a meaningful breakthrough often comes down to the quality and consistency of a single compound. Take methyl pyridine-4-carboxylate, for example. Sitting quietly in amber bottles on workbenches across the pharmaceutical and fine chemical industries, this molecule—sometimes called methyl isonicotinate—carries more significance than it usually gets credit for.
Official descriptions call methyl pyridine-4-carboxylate a pale yellow liquid or solid, depending on the environment, with a chemical formula of C7H7NO2. Its structure shows a methyl ester hooked to a nitrogen-containing aromatic ring, a configuration that’s surprisingly adaptable in synthetic chemistry. What’s striking about this molecule isn’t just its appearance or textbook designation, but its balance of reactivity and manageability. In labs where every minute and every step counts, predictability becomes more than a convenience—it becomes the peace of mind that work won’t derail, batch after batch.
One of the most common uses for methyl pyridine-4-carboxylate comes in the early stages of active pharmaceutical ingredient (API) development. Chemists who’ve spent late nights wrestling with complex reaction schemes know that this ester forms the backbone of key intermediates for drugs targeting everything from tuberculosis to inflammatory diseases. The methyl group provides a controlled entry point for later modifications, making the molecule a go-to choice for transformations where selectivity matters.
In agrochemical research circles, it shows up in discussions of new crop protection molecules. Its presence in these settings isn’t just a coincidence. Experienced formulators lean on the molecule’s predictable melting point (usually hovering near 50°C) and moderate solubility in common organic solvents. In a field where reproducibility across manufacturing facilities on separate continents makes or breaks a product line, methyl pyridine-4-carboxylate offers reliability few other esters can match.
Most suppliers offer methyl pyridine-4-carboxylate with purity levels above 98%, often confirmed by HPLC or GC analysis. Skeptics might ask whether that last percent really matters. From personal experience, it does. That trace impurity lurking in a less-refined sample has a way of complicating downstream reactions or clouding test results. I remember a failed batch of pyridine-based ligands during a project years back—it turned out a low-level chloride impurity from the precursor ester was the culprit, costing a week’s worth of work. Consistent high purity translates into fewer headaches, which is something every bench chemist values more than any certificate of analysis can capture.
Boiling at about 260°C and dissolving well in both dichloromethane and ethanol, the compound brings flexibility to labs juggling a range of solvent systems. Compared to some pyridine carboxylate relatives, such as methyl 2-pyridinecarboxylate or methyl 3-pyridinecarboxylate, the 4-position ester displays a notable difference in reactivity toward nucleophiles. For researchers tinkering with novel synthetic routes, this opens doors not just in forming simple amides or acids, but in creating more elaborate bi-heterocyclic frameworks where position matters just as much as purity.
My first introduction to methyl pyridine-4-carboxylate happened while working in a drug discovery program for central nervous system agents. We found that swapping a carboxylate at the 4-position with a bulkier ester often improved brain penetration without significantly altering toxicity. That one tweak, made practical by the commercial availability of high-grade methyl pyridine-4-carboxylate, allowed us to leapfrog several bottlenecks in our lead optimization campaign. This is why it has become a mainstay in libraries where small molecular changes can mean the difference between a dead end and a clinical candidate.
The world of pyridine carboxylates doesn’t lack variety. Each isomer brings a distinct chemical personality to the table, but methyl pyridine-4-carboxylate distinguishes itself through both its relative stability and its controlled reactivity. Try working with methyl 2-pyridinecarboxylate, for instance, and you’ll see how the positioning of the carboxyl group changes electronic properties, shifting reaction outcomes. In side-by-side trial syntheses, I’ve seen methyl pyridine-4-carboxylate consistently deliver higher yields and fewer byproducts in cross-coupling reactions, a detail that matters for anyone scaling chemistry beyond milligram batches.
Where methyl 3-pyridinecarboxylate often brings challenges during ester hydrolysis due to tautomer formation, the 4-isomer sidesteps many of these. That difference makes for easier purification and less frustration cleaning up reaction mixtures. Not every product can claim to quietly remove hurdles that cost time and money, but manufacturers and researchers depending on reproducible process chemistry take note of these kinds of details.
That said, no chemical comes without headaches. Recent supply chain disruptions have highlighted the fragile nature of sourcing fine chemicals, and methyl pyridine-4-carboxylate is no exception. Fluctuations in global pyridine markets trickle down, leading to pricing volatility and occasional delays in shipments. I recall a period where a spike in demand for vitamin B3, made from a related pyridine derivative, sucked much of the raw material from specialty chemicals markets. Research timelines don’t pause for shortages, so the importance of maintaining multiple supply partners becomes clear very quickly.
On the manufacturing side, careful attention to handling is key. Pyridine derivatives, particularly esters, can degrade if exposed to light and air for extended periods. Labs working without proper storage often report shifts in color or a faint amine odor—signs that the material’s decomposing, even if only subtly. I learned early to insist on fresh batches for sensitive projects, which meant building solid relationships with trusted suppliers who understood these nuances.
Handling organic chemicals comes with responsibilities that reach beyond the benchtop. Pyridine esters aren’t typically classified as highly hazardous, but spills can lead to respiratory irritation, and disposal requires more than a casual toss in the waste bin. Labs that take environmental stewardship seriously invest in closed-system handling, solvent recycling, and proper neutralization or incineration protocols. From what I’ve witnessed, those steps not only protect colleagues but also keep regulators satisfied and research free from unnecessary scrutiny.
Skeptics might argue that these are just standard precautions, yet the difference these practices make when dealing with kilograms (as opposed to grams) of reagent shows up quickly. There’s an old saying in the chemical industry: you don’t respect a reagent until you’ve had to clean up a spill at 2 a.m. I don’t recommend learning the hard way, but those who do often become the strongest advocates for safety and thoughtful materials stewardship.
Researchers love to find new applications for established compounds. Recent publications in scientific literature suggest that methyl pyridine-4-carboxylate now finds a role in catalyst development, polymer chemistry, and as a component in advanced dyes. These aren’t just hobby projects. The molecule’s unique ability to transmit electronic effects through its aromatic ring gives it value in creating tunable polymers with controlled charge transport properties. Colleagues in material science have reported that tweaks to the ester side chain enable fine control of polymer flexibility—something that once required far more complicated synthetic maneuvers.
Green chemistry efforts, too, have started to circle around methyl pyridine-4-carboxylate. Choosing benign starting materials with easy downstream degradation profiles becomes crucial in a world that scrutinizes carbon footprints. Not many esters made it through initial screens for environmental acceptability and performance in the medical device sector, but methyl pyridine-4-carboxylate proved surprisingly suitable by breaking down into less persistent byproducts under standard conditions. Environmental scientists still debate the best disposal technologies, but the molecule’s trajectory appears promising compared to more stubborn aromatic compounds.
Of course, perfection remains elusive. Efforts to lower production costs without sacrificing purity still keep process engineers awake at night. Solvent-intensive steps in current synthesis protocols generate waste that both companies and researchers would rather avoid. Collaborative shifts toward greener, more atom-efficient routes can benefit everyone from the largest manufacturers to the smallest startups. Investment in process intensification—think flow chemistry and in-line purification—is slowly changing the landscape, but meaningful progress requires leadership from both buyers and sellers in the supply chain.
I’ve seen firsthand how partnerships with academic research groups can drive innovation on this front. Incentives for process optimization and recycling not only reduce costs but build goodwill between buyers and producers. The most successful supply agreements often come from relationships where both sides share a commitment to improving quality and reducing environmental impact, even if it means navigating a few initial bumps in the process.
If the past few years have taught the chemical community anything, it’s the value of visibility across the supply chain. Knowing where a sample of methyl pyridine-4-carboxylate comes from—and how closely it’s tracked throughout its journey—means more than ever as regulations tighten around pharmaceutical precursors and environmentally sensitive materials. Buyers now routinely request batch-level documentation, shipping histories, and even third-party purity profi results. This is less about red tape and more about building confidence that what arrives in the bottle matches what’s promised on the label.
The biggest suppliers use digital tracking tools as standard practice, allowing chemists to trace a compound’s history back to the original manufacturing lot. Having tried both tracked and non-tracked sourcing in my own projects, the difference in convenience and peace of mind is stark. Should something go wrong, these systems allow for rapid recalls and targeted troubleshooting, reducing disruption instead of amplifying it. Laboratories planning to scale their research or production owe it to their teams—and their clients—to push for this kind of robust documentation.
Most buyers look for quality certificates as a bare minimum. From experience, what matters even more is the culture of the producer. Organizations that embrace continuous improvement—refining their purification steps, investing in better analytical equipment, and pursuing feedback from end users—tend to become the most reliable partners over time. The best batches of methyl pyridine-4-carboxylate I’ve used came not from faceless conglomerates but from small to mid-sized operations with a reputation for listening and adapting.
This culture of responsiveness shows up in the details—labeling that doesn’t peel off in cold rooms, packaging that keeps out moisture, and customer support that responds to technical questions with specific, practical advice. In industries where new questions surface with each experiment, this kind of support becomes invaluable. The difference between a successful week and a project setback sometimes traces back to a five-minute phone call with a technical expert.
Researchers and procurement officers have more power than they think. Choosing a supplier who invests in quality and cares about traceability impacts more than just that one purchase. By favoring transparent partners, buyers signal to the entire industry that deeper accountability and better customer service matter. Taking the time for occasional audits, providing feedback on product performance, and staying active in industry networks can all help drive standards higher.
On the technical side, sharing application notes, troubleshooting tips, and successful reaction conditions with colleagues and suppliers feeds a culture of collaboration. In one lab I worked with, we started an internal “compound of the month” bulletin. Early on, methyl pyridine-4-carboxylate earned a feature not only for its reliability but for the new cross-coupling strategy it enabled—a strategy that later saved considerable development time across our portfolio.
Looking back over years spent at the intersection of chemistry and real-world needs, it’s easy to take certain materials for granted—until their value becomes impossible to ignore. Methyl pyridine-4-carboxylate’s place in the toolkit of drug discovery, agrochemicals, and advanced materials science reflects both its robust chemical attributes and the commitment of those who work to keep its supply timely and dependable.
Its journey from niche synthetic intermediate to staple reagent says as much about market trends as it does about shifting expectations for transparency and quality. For those charting unexplored territory in molecular design or grappling with the nuts and bolts of scalable synthesis, products like methyl pyridine-4-carboxylate don’t just fill a need—they enable new directions entirely. In an era where every material’s impact gets parsed for performance, sustainability, and trustworthiness, this compound has quietly emerged as a reliable partner for those committed to making safe and groundbreaking progress in the chemical sciences.