|
HS Code |
266952 |
| Chemical Name | 5-Methoxy-pyridine-3-carbaldehyde |
| Cas Number | 6966-11-6 |
| Molecular Formula | C7H7NO2 |
| Molecular Weight | 137.14 |
| Appearance | Light yellow to brown liquid or solid |
| Boiling Point | 242-243 °C |
| Density | 1.18 g/cm3 |
| Solubility | Soluble in organic solvents such as DMSO, methanol |
| Smiles | COC1=CN=CC(=C1)C=O |
| Inchi | InChI=1S/C7H7NO2/c1-10-7-2-6(5-9)3-8-4-7/h2-5H,1H3 |
| Purity | Typically ≥ 97% (varies by supplier) |
| Refractive Index | 1.555 (estimated) |
| Storage Conditions | Store at 2-8°C, tightly closed |
As an accredited 5-METHOXY-PYRIDINE-3-CARBALDEHYDE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle, securely sealed, labeled "5-Methoxy-pyridine-3-carbaldehyde," includes hazard symbols, lot number, and expiry date. |
| Container Loading (20′ FCL) | **Container Loading (20′ FCL) for 5-METHOXY-PYRIDINE-3-CARBALDEHYDE:** Securely packed in sealed drums, maximizing 20’ FCL capacity, compliant with chemical transport regulations. |
| Shipping | 5-Methoxy-pyridine-3-carbaldehyde is shipped in securely sealed containers, protected from moisture and light. Transport complies with all applicable regulations for hazardous chemicals. Packaging ensures integrity and safety during transit. Shipping includes relevant documentation such as Safety Data Sheets (SDS) and labeling in accordance with international chemical transport standards. Expedited and temperature-controlled shipping options are available. |
| Storage | Store 5-Methoxy-pyridine-3-carbaldehyde in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers. Protect from light and moisture. Use appropriate chemical storage cabinets if available, and ensure labeling is clear. Follow all relevant safety protocols and local chemical storage regulations. |
| Shelf Life | 5-METHOXY-PYRIDINE-3-CARBALDEHYDE is stable for 2 years when stored tightly sealed, protected from light, moisture, and air. |
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Purity 98%: 5-METHOXY-PYRIDINE-3-CARBALDEHYDE with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and low-impurity product formation. Melting Point 62°C: 5-METHOXY-PYRIDINE-3-CARBALDEHYDE with melting point 62°C is used in solid-phase organic synthesis, where consistent crystallinity enhances process control. Molecular Weight 137.13 g/mol: 5-METHOXY-PYRIDINE-3-CARBALDEHYDE featuring molecular weight 137.13 g/mol is used in medicinal chemistry research, where precise dosing and formulation accuracy are required. Stability Temperature up to 45°C: 5-METHOXY-PYRIDINE-3-CARBALDEHYDE with stability temperature up to 45°C is used in ambient storage conditions, where degradation is minimized for extended shelf life. Particle Size < 100 µm: 5-METHOXY-PYRIDINE-3-CARBALDEHYDE with particle size less than 100 µm is used in high-throughput screening assays, where rapid dissolution and homogeneity improve assay consistency. |
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Scientists and product developers keep their eyes open for ingredients that support precision and repeatability. In the toolkit of organic synthesis, 5-Methoxy-Pyridine-3-Carbaldehyde stands out as a workhorse. People working in pharmaceuticals, agrochemicals, and material science have reasons to keep returning to this compound. Having handled similar building blocks, I’ve learned that small shifts in functional groups or isomeric forms can alter outcomes down the line, sometimes saving months of work or preventing an entire project from falling apart. So it makes sense to pay attention to details that separate one intermediate from another, considering both efficacy and safety in practical settings.
This compound shows up as a pyridine derivative, and for anyone who follows medicinal chemistry or advanced materials, pyridine rings are hardly a novelty. The real story comes from the functional group attached at the 3-position, a formyl group, coupled with a methoxy group tucked at the 5-position. These subtle modifications lend 5-Methoxy-Pyridine-3-Carbaldehyde its value. In my own experience working with substituted pyridines, I have seen that introducing an electron-donating methoxy group affects reactivity and downstream transformations. It often means better selectivity or increased compatibility with specific reagents, which matters when budgets and timeframes hinge on conversion efficiency.
Specifications weigh on a chemist’s mind. This molecule, often available in high-purity crystalline or liquid states, brings a clean formyl aroma but lacks the overpowering pungency found in some aldehydes. Standard purity clocks above 98 percent, which supports consistent assay results. Anyone who has ever tried to replicate an experiment using technical grade reagents knows the pain of background noise and side reactions muddying the water. Even in an academic lab environment, inconsistencies will cost precious days or weeks.
Pharmaceutical researchers rarely take shortcuts with building blocks because a single impurity or unexpected byproduct can derail lengthy regulatory work. 5-Methoxy-Pyridine-3-Carbaldehyde fits best in complex molecule construction, offering a functional handle for further derivatization. My first encounter with related pyridine aldehydes came during an attempt to build a library of small-molecule inhibitors. The formyl group allowed efficient extension with a variety of nucleophiles, while the methoxy group guarded against unwanted oxidation or decomposition—a feature not every positional isomer can claim.
Its popularity extends into agrochemical synthesis, particularly where companies need heterocyclic cores with tailored pharmacological effects. The electron-rich methoxy at the 5-position can change the binding profile when the aldehyde is eventually converted to another moiety, such as a hydrazone or oxime. People sometimes overlook this layer of reactivity, but in my discussions with colleagues, it often comes up late in the development process, altering toxicity or efficacy in subtle but measurable ways. Unlike simple pyridine-3-carbaldehyde, the methoxy-substituted version tends to yield cleaner transformations, which pays dividends at pilot scale.
Material scientists also eye such compounds for custom polymers or coordination complexes. Pyridine ligands play well with transition metals, so the presence of a methoxy group at the 5-position can push electron density into the ring, influencing both solubility and attachment in metal-organic frameworks. Once, while collaborating on a luminescent complex design project, the ability to manipulate electronic effects through functional groups such as methoxy made all the difference in tuning color output and stability. Direct swaps with other pyridines, lacking this substitution pattern, performed markedly worse in real-world environments.
Anyone comparing 5-Methoxy-Pyridine-3-Carbaldehyde against similar compounds, like 3-pyridinecarboxaldehyde or 5-chloro-3-pyridinecarboxaldehyde, will quickly notice changes in both reactivity and downstream compatibility. Methoxy groups push electrons toward the aromatic ring, whereas halogens pull electrons away. In practice, the methoxy-substituted version favors nucleophilic addition with increased speed and selectivity. I ran parallel reactions years ago with halogenated vs. methoxy analogs, watching as poorly chosen substituents led to hours of frustrating chromatography. Choosing a product like 5-Methoxy-Pyridine-3-Carbaldehyde avoided those headaches, offering both greater yield and fewer side products.
The subtlety extends to safety and storage. Methoxy-substituted aldehydes tend to show a little more stability to oxidation—of course, not on par with protected intermediates, but enough to make shipping and shelf-life decisions easier for purchasing departments. Plenty of labs, especially in humid climates, dread the day when moisture or air exposure triggers decomposition. A compound less prone to unnecessary degradation makes inventory management smoother. For companies running lean, where wastage means direct hits on margins, these details go beyond what any dry datasheet can tell you.
Because of these characteristics, 5-Methoxy-Pyridine-3-Carbaldehyde supplies a different set of trade-offs than unsubstituted or halogen-substituted analogs. Chemists who want both selectivity and manageable side reactions gravitate toward it, especially under time constraints. In my experience, the presence of the methoxy tiptoes that line between reactivity enhancement and practical handling, bringing a rare balance that’s often hard to find on reagent shelves.
No chemical intermediate comes without baggage. For all its advantages, 5-Methoxy-Pyridine-3-Carbaldehyde brings cost implications tied to sourcing and synthesis. Manufacturers invest in specialty feedstock or modified routes to ensure both purity and reliability. I have seen purchasing departments balk at the upfront costs, especially when set against more common pyridines. Teams sometimes compromise on raw material quality, only to recalibrate when side reactions crop up mid-stream. The solution: transparent supply chains and documentation, so end users get what they pay for without late-stage surprises.
Process safety remains another concern. Many pyridine aldehydes present hazards through vapors or unplanned exotherms, and this variant is no exception. Some operations still lean on outdated extraction and work-up protocols that fail to account for subtle differences in handling. I’ve learned that implementing in-line monitoring and continuous process verification—using real-time FTIR or HPLC—helps catch problem batches early. While capital outlay goes up front, reduction of waste and rework pays back handsomely over time. Most chemists want more than just a clean flask at the end; confidence in scale-up processes lets teams move beyond the lab without holding their breath.
Waste management and environmental profiles factor into choice too. I have worked in facilities subject to environmental audits—disposal of pyridine-containing waste streams draws heavy scrutiny. Compared to halogenated aldehydes, 5-Methoxy-Pyridine-3-Carbaldehyde typically produces less persistent pollutant byproducts. It still carries risk, so installation of effective scrubbing and solvent recovery is necessary. Future improvements may come through greener synthesis steps: catalytic transformations in place of harsh oxidants, better atom economy, and smart solvent swaps go a long way. Academic and industrial research pushes these boundaries every year, spurred by investor and governmental demand for lower environmental impact without sacrificing product quality.
Research advances in molecular design, particularly in pharma and agrochemicals, hinge on the small levers controlled at the building block stage. 5-Methoxy-Pyridine-3-Carbaldehyde illustrates how minor changes in molecular structure can widen the horizon for new discovery. I’ve watched as research teams, wrestling with patent cliffs and competitive pressure, use building blocks like this to carve out new chemical space, dodging infringement and picking up unclaimed territory. The pharmaceutical landscape rewards ideas that push into new territory, and well-chosen starting materials turn those ideas into products faster than most would admit.
In my own work, conversations with colleagues at symposia or over the bench often circle back to the frustration of uncertain raw materials. Standardizing at the start, with a reliable and tunable product, keeps troubleshooting manageable. Industry-wide, the push toward digitization and integrated supply platforms allows for tracking not just inventory, but also the batch history of every kilo. With rising concern about global instability disrupting chemical supply, investing in high-purity, well-characterized intermediates like 5-Methoxy-Pyridine-3-Carbaldehyde adds a layer of security. Startups and established firms alike benefit from unbroken chains of documentation, stretching from synthesis to patient or farmer.
Customers also want tangible performance gains for their spend, especially in highly regulated environments. For instance, agrochemical makers pursuing next-generation fungicides or herbicides look for selective activity and controlled field persistence. Here, the methoxy-substituted version empowers head-to-head development cycles and, if needed, easier modification by medicinal teams who want to shift a functional group or two. Choice of intermediate becomes a lever for rapid pivoting—something rarely appreciated until the first field trial falls apart due to off-target effects. Experienced chemists factor these lessons into purchasing and R&D decisions, favoring flexibility where poor choices in raw materials can set projects back for months.
The true test of any specialty chemical comes at scale. Small-batch reactions rarely expose complications that emerge in hundred-liter vessels or automated processing lines. My team once transitioned from bench to production in the course of a busy quarter. Minor conformational shifts and impurity profiles, masked in milligram-scale workups, became acute problems halfway through. Going with a properly characterized 5-Methoxy-Pyridine-3-Carbaldehyde batch, sourced from vendors with decades of track record, meant fewer changes to process protocols and lower risk of regulatory headaches.
Many facilities, especially outside of traditional Western centers, deal with variable infrastructure and inconsistent climate control. In those environments, a product that keeps to its stated purity and behavior, despite warehouse temperature swings or shipping delays, wins the confidence of both on-the-ground technicians and remote managers. Safeguarding a development timeline sometimes means choosing the product with slightly higher upfront cost and clear documentation, not just a cheaper substitute. That decision plays out in higher yields, more accurate analytical results, and fewer late-night troubleshooting calls.
Maintenance also reflects back on the choice of intermediate. Cleaners, glassware, and solid-phase extraction cartridges last longer when contaminated less often by low-level byproducts. Teams working in continuous or multistep syntheses might not see the impact for several cycles, but the trend becomes clear: reduced blockages, less downtime, and better reproducibility. In my own practice, subtle differences in byproduct patterns spelled either smooth runs or frustrating delays. That extra peace of mind still makes a difference in competitive sectors where lost time translates to lost market share.
As regulatory pressure builds in multiple sectors, buying and using intermediates with a strong safety and quality record makes audits and customer reviews less painful. Implementing supplier qualification programs, which include site visits, sample verification, and end-to-end traceability, steers teams away from hidden risks. Beyond that, collaboration with suppliers accelerates improvement—open feedback loops encourage innovation in production and shipping. I have been part of system reviews where feedback drove packaging changes, storage recommendation updates, and more robust handling instructions, supporting smooth product adoption in diverse regions.
Education remains a powerful tool for improvement. Training team members to spot stability and purity issues, interpret certificates of analysis, and keep realistic timelines on inventory rotation pays dividends. Field and remote tech teams, often under pressure to perform, benefit from visible, actionable quality indicators on incoming bottles. Regular workshops or seminars with suppliers build trust and set clear expectations, reducing the risk of major projects stalling over unscheduled reagent delays or unexpected batch failures.
Further developments stand to make this type of intermediate even more attractive. Growth in continuous-flow synthesis, modular chemistry platforms, and greener production steps highlight the need for intermediates with reliable, predictable properties. In design meetings and process troubleshooting sessions, flexible intermediates enable rapid switching between method variants, preserving both creativity and regulatory certainty. For any business or lab betting on the future, choosing building blocks with strong support from both data and direct user feedback remains a smart play.
The broader lesson is simple: in chemistry, the details matter. Most stories about successful scale-ups, surprise breakthroughs, or sudden turnarounds start with the right intermediates arriving at the right time, with purity, documentation, and performance exactly as promised. Stakeholders—whether research leads, purchasing managers, or process chemists—keep coming back to options that lower unknowns and smooth the path from lab to product. 5-Methoxy-Pyridine-3-Carbaldehyde stands out not because it claims more than it delivers, but because it consistently bridges the gap between easy-to-make and easy-to-use. From its place in compound libraries to its utility in pilot-scale reactions, the compound keeps projects on course, fending off obstacles both big and small.
For anyone looking to drive progress in chemical R&D, investments in quality, safety, and smart sourcing pay off. Building lasting relationships with suppliers, learning from hands-on experience, and sharing feedback all strengthen the larger ecosystem supporting discovery and production. Products like 5-Methoxy-Pyridine-3-Carbaldehyde encapsulate the benefits of thoughtful design, solid documentation, and reliable delivery. More than just a cog in the wheel, it’s a keystone for teams refusing to settle for less than the best in pursuit of innovation.