|
HS Code |
903943 |
| Chemical Name | 3-Pyridinecarboxaldehyde, 2-methoxy- |
| Cas Number | 14462-28-9 |
| Molecular Formula | C7H7NO2 |
| Molecular Weight | 137.14 |
| Iupac Name | 2-methoxypyridine-3-carbaldehyde |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 222-224 °C |
| Density | 1.16 g/cm3 |
| Solubility In Water | Slightly soluble |
| Smiles | COC1=NC=CC(=C1)C=O |
| Inchi | InChI=1S/C7H7NO2/c1-10-7-6(5-9)3-2-4-8-7/h2-5,9H,1H3 |
| Storage Temperature | Store at 2-8°C |
| Synonyms | 2-Methoxy-3-formylpyridine |
| Refractive Index | 1.545 |
As an accredited 3-Pyridinecarboxaldehyde, 2-methoxy- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100-gram amber glass bottle labeled "3-Pyridinecarboxaldehyde, 2-methoxy-" with hazard symbols, lot number, and manufacturer's information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 3-Pyridinecarboxaldehyde, 2-methoxy-: 160 drums (200 kg each), totaling 32 metric tons (net). |
| Shipping | 3-Pyridinecarboxaldehyde, 2-methoxy- is typically shipped in tightly sealed containers under ambient conditions. It should be protected from light, moisture, and incompatible substances. Standard chemical shipping regulations apply, including proper labeling and documentation. Handle with care during transport to prevent leakage or contamination. Shipping may require adherence to specific hazardous materials guidelines. |
| Storage | 3-Pyridinecarboxaldehyde, 2-methoxy- 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 oxidizing agents. Protect the chemical from light and moisture. Use appropriate safety measures to avoid inhalation, ingestion, or skin contact. Store according to local regulations and manufacturer's instructions. |
| Shelf Life | 3-Pyridinecarboxaldehyde, 2-methoxy- typically has a shelf life of 2 years if stored tightly sealed, cool, and protected from light. |
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Purity 98%: 3-Pyridinecarboxaldehyde, 2-methoxy- with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high product yield and reduced impurities. Melting Point 38°C: 3-Pyridinecarboxaldehyde, 2-methoxy- with a melting point of 38°C is used in fine chemical manufacturing, where it allows consistent handling and reactivity under controlled conditions. Molecular Weight 137.14 g/mol: 3-Pyridinecarboxaldehyde, 2-methoxy- with a molecular weight of 137.14 g/mol is used in heterocyclic compound development, where it provides precise molecular incorporation and predictable reaction outcomes. Stability Temperature up to 120°C: 3-Pyridinecarboxaldehyde, 2-methoxy- stable up to 120°C is used in high-temperature reaction protocols, where it maintains structural integrity and reliable performance. Low Water Content (<0.5%): 3-Pyridinecarboxaldehyde, 2-methoxy- with water content below 0.5% is used in moisture-sensitive synthesis, where it prevents unwanted side reactions and ensures reaction accuracy. |
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On the production floor, we see the evolution of chemicals like 3-Pyridinecarboxaldehyde, 2-methoxy- from raw starting materials to the neatly labeled drum ready for shipment. Years of refining methods, dealing with different batches, and responding to variable market demands have shaped the way we approach the manufacture and delivery of this aldehyde. As working chemists and chemical engineers, we know that 2-methoxy-3-pyridinecarboxaldehyde stands out from generic pyridine derivatives. Its unique structure—a methoxy group on the 2-position of the pyridine ring, coupled with an aldehyde at the 3-position—brings novel reactivity and value.
Manufacturing this compound requires vigilance at every step. We opt for high-purity starting materials to sidestep avoidable byproducts, and we’ve honed both oxidative and substitution routes that curb impurity profiles. Typical purity for our output usually sits above 98% by GC or HPLC, a threshold that prevents headaches downstream for both research and industrial users. We avoid simply filling every batch to theoretical capacity, instead focusing on well-controlled distillation and attentive monitoring of color and odor. Piperidine- or other amine-related impurities can complicate downstream reactions, so we implement in-process controls to suppress their formation.
Handling requests for specialized grades—for instance, low-water variants or analytical reference standards—illustrates the diversity of real-world applications. Bulk customers sometimes ask for larger packing sizes, but most research and production teams value secure, detailed packaging and batch test sheets. Transparency builds trust; every drum or bottle leaves our facility with a conclusive analysis and provenance. From weighing to sealing, our operators treat each batch as something that could end up in a high-stakes synthesis.
Traditional pyridine derivatives serve as backbones in plenty of synthetic schemes, but adding a methoxy group changes the landscape. Analytical chemists notice greater stability compared to non-alkoxy analogs under typical bench-top storage. For synthetic organic chemists, that 2-methoxy group alters electron density, guiding reactivity in cross-couplings, reductive amination, and heterocycle construction.
From our interactions with end-users, the pharmaceutical sector often leads demand. Medicinal chemists have found this compound can readily serve as a building block for molecules targeting neurological, infectious, or metabolic pathways—especially when seeking improved bioavailability or metabolic stability by manipulating ring electronics. The methoxy group helps shift distribution, solubility, and pharmacologic interactions relative to unsubstituted or methyl-substituted pyridinecarboxaldehydes.
In material science, laboratories chase new optoelectronic or coordination materials and favor this compound for assembling ligands with fine-tuned donor-acceptor properties. Our experience shows that polymer researchers sometimes select this aldehyde derivative to achieve chain-linking patterns that improvise conductivity or alter degradation profiles. Applications in flavors or agrochemical intermediates aren’t as common, but we’ve fielded inquiries. We keep channels open; sometimes an industrial direction surprises even us.
We’ve produced a long roster of pyridinecarboxaldehydes, from the parent 3-formylpyridine to chloro- or methyl-substituted analogues. Adding a methoxy group at the 2-position doesn’t just tune the molecule’s reactivity; it alters its handling and potential hazards. Methoxy groups are electron-donating, shifting both chemical behavior and workplace characteristics. As a liquid at room temperature (depending on purity grade), this compound avoids the sticky solidification issues that can challenge handling of similar aldehydes in colder climates.
Whereas the parent 3-pyridinecarboxaldehyde gives chemists a reactive handle for condensation or nucleophilic addition, the methoxy derivative offers a more predictable selectivity in the same reactions. Quaternization, nucleophilic aromatic substitution, and cross-coupling protocols accept this compound with fewer side products. We’ve analyzed batch performance in Suzuki and Heck reactions and found cleaner product streams versus the unsubstituted version. This saves time on purification later, and users appreciate that kind of operational reliability.
Hydrolysis sensitivity—an issue in some pyridine derivatives—decreases with the presence of the methoxy group, at least within the pH range seen in most lab operations. We note fewer complaints about resin fouling and filter clogging during customer trials. The compound’s smell is another distinguishing trait: some pyridinecarboxaldehydes carry strong, lingering odors, enough to bring complaints from process technicians. The 2-methoxy analog is less pungent, making routine handling easier, though good ventilation remains important.
We also notice packaging adaptations. The chemical’s volatility falls between classic aldehydes and heavier pyridines. Our engineers designed tight-seal containers that retain quality during extended transit, even in humid conditions. Some clients with sensitive storage requirements need nitrogen-flushed glass; others in bulk ask for corrosion-resistant drums. We’ve made those investments based on years of feedback from real production lines—not paperwork guesses.
Unlike intermediaries who shuffle inventory, our line chemists know that one failed intermediate can halt a project for a week. Retests of archived batches show stable purity after six months at ambient temperatures, with only minor shifts in the trace impurity fingerprint—most often related to vendor variation in precursor supplies. This keeps users’ method validation straightforward, a detail our analytical clients appreciate.
Spectral analysis in our onsite lab routinely gives sharp NMR and mass spectral signals—chemists prefer not to waste time untangling messy spectra. We’ve noticed the 2-methoxy variant’s aldehyde proton appears slightly upfield compared to its methyl sibling, a subtle signal that groups working on structure-activity relationships find useful when prospecting new analogs.
Several customers have returned with feedback after multiple production cycles. Reduced purification steps, fewer solvent changes, and improved yield consistency pop up regularly in their commentary. For us, lower solvent usage—especially in post-processing—means a smaller environmental footprint. It’s one way we keep our sustainable chemistry goals in check amidst growing pressure from regulatory agencies and brand owners alike.
Manufacturing 3-pyridinecarboxaldehyde, 2-methoxy-, like many specialized aromatic aldehydes, throws up challenges you rarely read in textbooks. Achieving high isomeric purity starts with careful temperature profile management during methylation and oxidation. Too much heat and we risk over-oxidation or byproduct formation; our operators monitor exotherms with in-line sensors, tweaking jacketed vessel flows by hand if output color shifts.
Methoxy migration byproducts can form under uncontrolled pH, especially in continuous operations configured for higher yields. We developed modular pH adjustment steps and longer quiescent settling periods to thin out side streams before isolation. Waste management also needs tight tracking. Down-the-drain disposal is a thing of the past for us. Condensed side streams reach an in-house treatment system set up for aromatic aldehydes, reducing overall permits paperwork for customers and ourselves.
Aldehyde functional groups bring reactivity, but they also create shelf-stability demands. Quality audits mean cycling samples through freeze-thaw and accelerated aging conditions. Our longtime customers often remind us that a few grams of degraded intermediate in a pharmaceutically relevant route can add weeks of rework. So we measure, then share, stability as a matter of routine, not checkbox compliance.
Only by talking to users do we learn what makes a chemical valuable in the field. With this compound, material compatibility cropped up early. Glass is fine, but some early customers saw label adhesion issues with plastic vials; we tweaked surface preparation to keep barcodes readable and safe from solvent attack. Drip-free dispensing nozzles cut waste in high-throughput facilities—another small but appreciated adjustment.
A government research group once requested a batch with isotopic labeling on both methoxy and aldehyde carbons. Our team handled precursor synthesis in-house, then coordinated two shifts to ensure no cross-contamination. It stretched our analytical resources, but the relationship grew stronger as a result. Special requests teach us more about our process at every turn, and add depth to our troubleshooting database for future challenges.
As production volumes grew, we invested in improved air handling and containment. This doesn’t just tick off compliance—they keep process operators safer and limit batch-to-batch fragrance variance. Reliable conditions unlock better yields, but more important, they support consistency for customers scaling pilot batches to plant quantities.
Experience counts for more than technical datasheets can reveal. Our development chemists have learned the nuances of each reaction—color cues during work-up, subtle temperature bumps that might signal starting material exhaustion. Problems like “trailing arms” in distillation, local clustering of trace water in drums, or even the slow degradation of container seals all cropped up and got solved by teams with real-time, hands-on knowledge.
On the broader scale, safety and sustainability considerations inform our every production decision. A few years back, we observed a runoff spike containing traces of aromatic aldehydes after an unpredicted shift in effluent pH. We quickly updated floor protocols, adding extra holding tanks and alarms. Our team tracks solvent reclamation rates batch-by-batch, and we’ve made real reductions in emissions—evidence that learning from experience improves the entire delivery chain.
Working closely with users lets us anticipate changes in demand, whether from shifts in agricultural chemical R&D or oncology drug discovery efforts. We’ve watched the ebb and flow of pyridine derivative use in academic versus pharma settings, and tailored our documentation and batch scales accordingly. Being woven into the process as manufacturer, not through endless intermediaries, means we adapt quickly. If a rare impurity pops up or a storage requirement shifts, we answer with more than speculation—we test, revise, and implement based on hands-on data.
Producing this aldehyde derivative goes far beyond delivering a bottle with a correct label. From our vantage point, each improvement in purity, packaging, and supply flow saves time and resources down the line for chemists and technicians. Experience means noticing trends fast: a batch that looks fine on paper, for instance, but triggers clouding in a customer’s formulation for the first time. We rerun analysis to identify microimpurities and reach out to the affected parties, factoring their input into the next campaign.
We think the next chapter will focus even more on traceability and process transparency. Chemists working in intellectual property-sensitive environments want clear, irrefutable batch records and provenance—not just promises or distributor talk. We ship with full documentation and back up every claim with a willingness to share method details (within the boundary of legal IP, of course). This approach builds trust, especially as regulatory scrutiny rises across chemical sectors globally.
Lab automation, batch size flexibility, and digital traceability are becoming core to our operations. Standardized production methods allow for scale-up without surprising property shifts. We see more requests for fully digital CoA (Certificate of Analysis) tracking, integrated with customer LIMS (Laboratory Information Management Systems). Meeting these needs keeps us focused on accuracy and reproducibility.
As a manufacturer, each connection with an end-user adds to our own knowledge. Sometimes a university research team pushes us to rethink a purification method; sometimes a pharmaceutical partner highlights a new use, feeding our own process improvements. We remain deeply interested in their real-world experiences—not just satisfaction scores, but operational feedback that guides us to a more robust, valuable product.
From our hands-on experience, 3-pyridinecarboxaldehyde, 2-methoxy- fulfills roles its analogues can’t match, consistently supporting breakthroughs in pharmaceutical, materials, and analytical research. Ongoing collaboration with researchers keeps us focused on practical improvements, and our drive to maintain high purity, reliable delivery, and responsive support ensures this product keeps meeting the evolving needs of scientists worldwide.