|
HS Code |
464113 |
| Iupac Name | methyl 2-methoxynicotinate |
| Molecular Formula | C8H9NO3 |
| Molecular Weight | 167.16 g/mol |
| Cas Number | 7369-54-4 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 263-264 °C |
| Density | 1.17 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 138 °C |
| Smiles | COC(=O)c1cccnc1OC |
| Refractive Index | 1.516 |
| Pubchem Cid | 39604 |
As an accredited 3-Pyridinecarboxylic acid, 2-methoxy-, methyl ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The product is packaged in a 25-gram amber glass bottle with a secure screw cap, labeled with product details and safety information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 14 metric tons packed in 200 kg HDPE drums, safely secured for international chemical shipment. |
| Shipping | The chemical **3-Pyridinecarboxylic acid, 2-methoxy-, methyl ester** should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It must comply with local and international regulations, using appropriate labeling and safety documentation. Handle with care to prevent leakage or spillage during transit. Store at recommended temperatures. |
| Storage | **Storage Description for 3-Pyridinecarboxylic acid, 2-methoxy-, methyl ester:** Store in a tightly closed container in a cool, dry, and well-ventilated area away from heat, sparks, and open flame. Keep away from incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Ensure proper labeling and avoid prolonged exposure to air to prevent degradation or contamination. |
| Shelf Life | Shelf life of 3-Pyridinecarboxylic acid, 2-methoxy-, methyl ester is typically 2-3 years if stored airtight, cool, and dry. |
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Purity 99%: 3-Pyridinecarboxylic acid, 2-methoxy-, methyl ester with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced impurities in the final product. Melting point 72°C: 3-Pyridinecarboxylic acid, 2-methoxy-, methyl ester with a melting point of 72°C is used in fine chemical manufacturing, where stable solid-state storage and handling are promoted. Molecular weight 165.16 g/mol: 3-Pyridinecarboxylic acid, 2-methoxy-, methyl ester with a molecular weight of 165.16 g/mol is used in agrochemical formulation, where precise dosing and formulation design are facilitated. Stability temperature 120°C: 3-Pyridinecarboxylic acid, 2-methoxy-, methyl ester with a stability temperature of 120°C is used in high-temperature reaction processes, where thermal degradation is minimized. Moisture content <0.2%: 3-Pyridinecarboxylic acid, 2-methoxy-, methyl ester with moisture content below 0.2% is used in dry formulation protocols, where product stability and shelf-life are extended. Viscosity 1.25 mPa·s: 3-Pyridinecarboxylic acid, 2-methoxy-, methyl ester with a viscosity of 1.25 mPa·s is used in automated liquid handling systems, where accurate and consistent dispensing is achieved. |
Competitive 3-Pyridinecarboxylic acid, 2-methoxy-, methyl ester prices that fit your budget—flexible terms and customized quotes for every order.
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Producing 3-pyridinecarboxylic acid, 2-methoxy-, methyl ester—often called methyl 2-methoxynicotinate around the plant—takes precision, know-how, and a grounded understanding of organic chemistry’s finer points. Our chemists blend practical experience with theoretical expertise because this compound doesn’t tolerate shortcuts. We have spent years refining our procedures, troubleshooting issues unique to this family of pyridine derivatives, and developing reliable ways to achieve consistent quality in every batch.
Unlike third-party sellers who might not see the inside of a reactor or the tang of raw solvents, those of us at the production line gauge product by hands-on knowledge. We have handled its faintly floral odor on a Friday night shift, monitored traces of starting material via our own chromatography work, and overhauled our glassware processes to stop cross-contaminations. Coming face-to-face with production hurdles, we know that the little details define the actual product rather than just its purity numbers.
Methyl 2-methoxynicotinate sits at a confluence of pharmacological, agricultural, and material chemistry interests. From our perspective as those who manufacture it, one key distinguishing feature is its methoxyl group at the 2-position, which nudges the reactivity of the pyridine ring differently compared to its unsubstituted or halogenated cousins. When we talk to colleagues in pharmaceutical R&D, they ask about this—some intermediates simply cannot be swapped out without losing the performance edge.
In our real-world experience, this ester provides a handle for ester hydrolysis, transesterification, or further substitution, suiting it for various downstream syntheses. We support projects developing new APIs and pesticide actives, with clients valuing its clean reactivity profile and relatively mild conditions for conversion. Subtle differences in electronic distribution across the aromatic ring dictate whether a building block behaves as expected in multi-step synthesis. Those small tweaks save both time and budget during scale-up phases, and we have seen cost savings come straight from choosing this structure over less predictable analogs.
Our journey starts with sourcing solid precursors. We have learned to demand detailed certificates of analysis from our raw material providers, checking for common contaminants like residual oxidants. Any slip at this step adds hidden costs later: fouled columns, lost product, or—worse—off-odors that signal deeper process problems.
Several years back, during an unusually damp summer, we faced issues with humidity creeping into our methylation step. Residual water skewed our yields and forced us to look at drier storage solutions for our methoxylating agents. Engineers and operators collaborated on airflow redesign and the problem retreated, but not before the experience reminded everyone in the plant that you cannot wish away environmental influences. Small climate shifts inside a facility can ripple right through product quality—something all the textbook chemistry leaves out.
Once we resolved those humidity concerns, we paid close attention to reaction timing, temperature, and, crucially, the cleanup phase. The regular purity you see on a chromatogram doesn’t come from luck: it comes from methodical solvent washes, careful control of distillation rates, and—occasionally—restarting an entire batch when minor issues emerge. We do not release product for downstream use unless every sample meets our lab’s real-world criteria, which always run tighter than any catalogue minimums.
Technical data doesn’t exist in a vacuum. Each batch goes under the microscope—high-performance liquid chromatography and mass spec results inform not just whether we’ve met a spec, but also where microscopic adjustments might deliver even tighter consistency. Over time, we have shifted from aiming for “above 98%” to “how close can we get this to 100% without creating unneeded waste or cost?”
One lesson: demanding both colorless and odor-free output means obsessing over each stage of purification. We have tried short-path distillation, flash chromatography, and even zone refining by request. Some customers—especially those preparing high-value intermediates—insist on a tighter boiling range or lower residual solvent levels. Feedback from trusted partners has prompted us more than once to revisit old assumptions about acceptable trace impurities, especially if those could interfere with scale-up or specific analytical methods.
To pick an example, one of our regular clients working in fine fragrance chemistry needed assurance regarding even trace pyridine contaminants. We fine-tuned our purification protocol and now include additional analytical steps in their released COAs. This process of continual improvement is something we see as part of our job, not an above-and-beyond extra.
It’s easy for non-specialists to lump all methyl ester derivatives of pyridinecarboxylic acid together. From a process chemistry standpoint, we argue against that: the position and identity of each group on the ring shape everything from solubility to reaction kinetics. The 2-methoxy substitution, for example, tends to lower melting point and can increase solubility in organic solvents, making our product easier to handle during multi-step synthesis, compared to 3- or 4-methoxy analogues. Workers on our team regularly compare shades and textures, identifying outliers by the naked eye before an analyst confirms the difference instrumentally.
Perhaps more importantly to advanced customers, the 2-methoxy configuration sets up different reactivity at the nitrogen of the ring—a subtlety only visible through repeated hands-on runs and a historical understanding of how alternative esters act in real workflows. As one of the few chemical manufacturers with years of comparative production experience, we can say with confidence that this specific structure reduces some types of byproduct formation common with other esters. R&D teams who need reliable conversion pathways often call us up to discuss those quirks.
From a formulation viewpoint, the methyl ester group impacts volatility and shelf stability. Over the past decade, the feedback we’ve gathered from agricultural chemistry applications suggests this compound holds up better in some UV-exposed environments than nicotinic derivatives without methoxy protection. We continually test samples under stress to challenge and confirm these features in the products we deliver.
Years of direct user feedback inform our approach, and those conversations have made us rethink more than once how we batch, pack, and ship methyl 2-methoxynicotinate. In one memorable case, a regular client in pharmaceutical manufacturing identified microscopic solids present after transportation on a humid day. Our internal investigation traced those back to packaging liner compatibility. We’ve since moved to a higher-grade material that resists absorption and maintains integrity through varying temperatures and humidity. That shift didn’t come from a datasheet demand; it came from putting ourselves in the shoes of the chemists who open the drum at the other end.
Customers ask pointed questions—sometimes more insightful than those we run through our QC lab. One R&D partner found a trace of a byproduct during a scale-up that didn’t register in our release analytics. Working together, we identified both the cause (a subtle tweak in our reaction solvent) and a fix. Now, we draw samples from different points in the batch, not just the finished drum—slowing production a bit, but catching subtle variations earlier.
That ongoing dialogue builds trust and helps us innovate. We routinely swap technical notes with our users, learning as much from their findings as they do from our process details. If a new regulatory standard emerges, we work collaboratively to understand what changes the end customer might face, rather than waiting for a recall to force our hand.
This compound’s most noticeable demand, from where we stand, comes from intermediate use in API development. Some very modern actives build up from simple starting materials that tolerate functionalization, and here the methoxy and methyl ester groups play pivotal roles. We have supplied batches for both multinational innovators and nimble startups; each finds slightly different uses, but those with deep experience consistently value consistent purity and compatibility with standard coupling agents.
Chemists exploring agricultural innovation also draw on its mild reactivity. We’ve heard from users who deploy it in synthesizing new generations of crop protection agents, where the 2-methoxy substitution blocks unwanted photodegradation and supports field longevity. Decades of iterative product release, driven by evolving field requirements, have moved us toward formulations that anticipate these real-world exposures.
A final group, the material scientists, have occasionally approached us about resin modification, UV stabilizer design, or specialty coatings. Though demand there ebbs and flows, any application that values stability alongside clean transformation will see the reason for this molecule’s enduring role.
We have picked up some distinctly practical wisdom about shipping and storing this compound. It resists bulk caking but demands dry, sealed containers because trace water will eventually hydrolyze the ester, defeating its purpose as a stable intermediate. Our storage team favors cool conditions, strong vapor barriers, and careful rotational handling, so none of the drums spend long periods exposed. These practices come directly from lessons learned handling tonnage, not just kilogram-scale pilot runs.
We worked out long ago to avoid unnecessary repackaging at the customer end. Each new transfer increases contamination risk, so we support shipments in custom sizes whenever possible. We guide clients on best transfer practices learned from our own filling and decanting routines—knowledge that cuts down on wasted hours and frustrating product loss.
Transportation challenges pop up especially during hot or humid spells or long-distance shipping in summer. We check for container condensation, and staff have learned by trial and error how to precondition shipments if a long southern transit route is forecasted. Direct experience tells you exactly how much time you really get before condensation starts becoming a problem, and the best preventive measures rarely turn up in a packaging spec.
Direct collaboration means something very practical to us. We don’t view customers as detached recipients but as colleagues facing the same pressure to improve process, lower costs, and adapt to new research. We have set up one-on-one technical calls to address issues ranging from scale-up thresholds to residue monitoring, and in each conversation, we aim for candid, fact-based advice—not generic platitudes.
Sometimes, teams face regulatory shifts impacting solvent selection or residual thresholds. Our approach is to test new methods ourselves and then advise with case data, not abstract promises. Once, a client preparing to audit for a new API registration needed assurance regarding trace N-oxides. Instead of sending a generic compliance certificate, our in-house experts ran additional analyses and shared spectra and batch records. We would rather work through specifics than lean on vague guarantees.
Our internal troubleshooting isn’t limited to the four walls of our plant. We routinely visit client sites, seeing for ourselves where bottlenecks arise or why certain product presentations fail under real workload. This boots-on-the-ground attitude—forged by necessity, strengthened by years of getting results—keeps us nimble and able to innovate as demands shift.
The market rarely sits still, and our production strategy has adjusted with each new decade. Where quality once meant satisfying a local customer, today we answer to clients working toward global regulatory files and sustainability standards. We actively monitor for new guidance from industry authorities, asking how such shifts ripple down to our preferred solvents, intermediates, and test metrics.
More recently, sustainability has become a constant driver. Some clients request environmental impact data on batches, tracking waste generation or the proportion of renewable feedstocks. We now work with partners seeking greener solvents and lower carbon footprints, and we have invested in recycling streams to ensure our process doesn’t just meet traditional specs but reflects environmental leadership. We share these details—not because marketing demands transparency, but because our technical user base expects it.
Continuous process improvement stems from keeping both ears open. We listen to line operators who notice subtle reaction changes and veteran QC staff who suggest new analytical markers. Each process review considers these frontline insights, letting actual practice guide policy.
Talking simply about “specs” misses the practical reality of working with 3-pyridinecarboxylic acid, 2-methoxy-, methyl ester. From our vantage point, the real value lies in a well-tuned production process, extensive troubleshooting history, and long conversations with users addressing real production concerns. We guarantee each batch reflects not just technical standards, but also the accumulated wisdom of operators who have solved problems, managed mishaps, and driven improvement through concrete experience. The result: a product that does more than just fill a niche. It answers to chemists, engineers, and scientists demanding the true value only hands-on manufacturers deliver.