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HS Code |
477647 |
| Product Name | 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde |
| Cas Number | 886373-28-4 |
| Molecular Formula | C7H6INO2 |
| Molecular Weight | 263.03 g/mol |
| Appearance | Light yellow to brown solid |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
| Purity | Typically >98% |
| Smiles | COC1=NC=C(C(=O)C=O)C(=C1)I |
| Inchi | InChI=1S/C7H6INO2/c1-11-7-5(8)2-4(3-10)6(9)12-7/h2-3H,1H3 |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Synonyms | 4-Iodo-2-methoxy-nicotinaldehyde |
As an accredited 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A tightly sealed amber glass bottle containing 10 grams of 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde, clearly labeled with hazard and product information. |
| Container Loading (20′ FCL) | Container loading (20′ FCL) for 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde ensures secure, moisture-free packing of 200–400 drums or bags. |
| Shipping | The chemical 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde is shipped in tightly sealed containers, protected from light and moisture. Packaging complies with regulations for hazardous materials. It is transported at ambient temperature with clear labeling to ensure safe handling and delivery. All relevant documentation and safety data sheets accompany the shipment. |
| Storage | 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally in a designated chemical storage cabinet. Avoid exposure to incompatible substances such as strong oxidizers. Properly label the container and follow all applicable safety and handling guidelines for hazardous chemicals. |
| Shelf Life | Shelf life of 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde: Stable for at least 2 years when stored in a cool, dry place. |
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Purity 98%: 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and selectivity. Melting Point 105°C: 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde (melting point 105°C) is used in medicinal chemistry research, where it provides stable solid-state handling. Molecular Weight 277.03 g/mol: 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde with a molecular weight of 277.03 g/mol is used in heterocyclic compound development, where accurate stoichiometric calculations are required. Particle Size < 20 µm: 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde with particle size < 20 µm is used in fine chemical formulation, where rapid dissolution and homogeneous mixing are achieved. Stability Temperature up to 40°C: 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde with stability up to 40°C is used in long-term reagent storage, where it maintains structural integrity and purity. |
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In the years spent refining pyridine derivatives for pharmaceutical and chemical manufacture, few products strike the right balance of versatility and reliability like 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde. Within our production facilities, we know how even minute batch-to-batch variability can impact complex molecule synthesis downstream. This intermediate’s unique structure, featuring an iodine atom at the 4-position alongside the methoxy and formyl functional groups, brings forward several advantages for chemists seeking selective reactivity with a focus on high-purity end products.
Unlike more commoditized aldehyde intermediates, this compound presents clear benefits for directed coupling reactions, especially when working with cross-coupling or substitution strategies in the advancement of pharmaceutical candidates. The role of the iodine atom deserves special mention. Iodinated pyridines typically lend themselves to smoother halogen-metal exchange, Suzuki-Miyaura couplings, and other palladium- or copper-catalyzed transformations, often under milder conditions or with improved yields compared to bromo or chloro analogues. Our customers repeatedly report how cleaner downstream extractions and reduced byproducts help ease development burdens, saving not just time, but significant cost.
The molecular formula C7H6INO2 and the distinct arrangement of functional groups set this aldehyde apart. Over the years, we have seen research teams using standard 2-methoxy-3-pyridinecarboxaldehyde variants struggle with late-stage iodination and protecting-group puzzles. Pre-installing the iodine on the aromatic core translates into a more reliable toolbox for those developing kinase inhibitors, agrochemical leads, or diagnostic probes.
During scale-up, impurity profiles turn into a leading concern. We choose to control each lot’s output through high-precision crystallization and analytical verification by NMR, HPLC, and mass spectrometry. Our in-house protocols sidestep the contamination with regioisomeric byproducts, such as 5-iodo or 6-iodo derivatives, which can complicate final purification and affect assay development. Direct feedback from production chemists allows regular reviews and adjustments at each manufacturing step, so the product aligns with demanding research and synthesis specifications.
Many labs approach us after navigating unreliable supply chains for comparable aldehyde intermediates. Years prior, options for 4-iodinated pyridinecarboxaldehydes were narrow and the available grades were inconsistent. Our own production challenges reinforced the importance of solvent selection and temperature control during iodination, and maintaining strict limits for water content to prevent side reactions during subsequent synthetic steps.
We routinely supply research institutes and industrial partners who require gram-to-kilogram quantities of 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde. In their hands, the product’s stability and ease of handling matter. Moisture sensitivity and aromatic degradation threaten product shelf-life in lower-grade material, so our drying and packaging step receives as much attention as synthesis itself. Chemists comment on smoother filtration, less fouling during work-up, and better recovery after coupling reactions due to our focus on minimizing oxidative and hydrolytic impurities.
Some might weigh the cost or accessibility of 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde against more basic carboxaldehyde variants, or against compounds constructed on 3-iodopyridine or 2-iodopyridine scaffolds. Across projects, the direct placement of the iodine atom at C4 and the electron-donating methoxy group at C2 shortens overall synthetic sequences, facilitating downstream functionalizations with less risk of over-oxidation or undesired rearrangements.
Bromide and chloride analogues still find their way into some discovery programs. Yet, feedback from process chemists tells us that iodide leavings produce less hazardous inorganic waste streams and open new possibilities with less stringent reaction temperatures. This can offer a practical advantage for scale-up, especially as energy and environmental controls take priority worldwide. The lower toxicity profile compared to certain other aryl halides gives EHS teams fewer difficulties during approval and handling stages, lowering total project cost and regulatory burden.
Manufacturers focused on active pharmaceutical ingredient (API) synthesis prize this compound for its role in constructing heterocyclic cores within kinase inhibitors and antivirals. More recent years have brought requests from agricultural chemistry engineers and those designing high-sensitivity fluorophore dyes, especially initiators that require site-specific halogenation.
The aldehyde group remains a prime entry point for reductive amination, Wittig extensions, and further oxidation to acids or nitriles. In factory settings, our chemists run direct scale-up trials to check reactivity for customer-specific transformations. Those who have attempted in-situ generation of the iodinated core often see far worse yields, greater impurity load, and larger waste volumes than by starting from our isolated product.
Nothing disrupts production like finding material drifted beyond agreed purity, especially when legacy or imported supply lots linger in the warehouse. Industry partners judge each manufacturing batch by more than just its certificate of analysis—actual trial results weigh most heavily. In our case, we trace every drum and archive batch samples so we can react quickly to any post-delivery reactivity issues.
Proper packaging ranks highly in reliability. Poor sealing invites moisture and decomposition, clouding solutions and inviting doubts about reproducibility. Our customers store the aldehyde under inert conditions and confirm that opening one of our containers months after receipt provides the same free-flowing crystalline product as on day one. Inspection by thin-layer chromatography, as well as matching melting points and spectral data, affirms confidence batch to batch.
Dialogue between our R&D chemists and clients’ technical teams has always advanced our formulations. Input from partners guides our process adjustments, whether to minimize certain trace metals or reduce reliance on hazardous solvents. This approach, backed by routine audits and re-qualification runs, ensures we can scale with scientific demand and regulatory scrutiny.
Handling the material directly, our chemists find the solid dissolves cleanly in DMF, DMSO, or standard ether blends. In multi-step syntheses where reduced handling time makes a difference, ready solubility with minimal insoluble residue helps speed up runs. Stability during workup and purification, especially avoiding polymerization or isomerization, stays high on our verification checklist, drawing on production chemists’ real-shift experience rather than just numbers in a report.
Demand for iodine-containing building blocks continues to grow as researchers explore halogen effects on biological activity and materials performance. The unique mix of electron-rich methoxy and electrophilic formyl groups on the pyridine ring provides a foundation for exploring functionalization strategies that remain inaccessible using other intermediates.
Specialty chemicals markets keep evolving, but certain reactions anchor themselves on established, reliable intermediates. By producing 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde consistently at scale, we supply large formulators, pilot plant teams, and bench-level researchers with material that fits into both established and newly-emerging synthetic strategies.
The synthesis of this compound involves careful balance between yield optimization and operator safety. During the halogenation step, strict in-house controls mitigate iodine vapor exposure, and well-designed fume extraction ensures worker safety and compliance with local regulatory bodies. Final product isolation proceeds under nitrogen to preserve product quality and extend shelf-life.
One insight we share with partners is the positive effect of early engagement during process development. Collaborating before finalizing a compound’s route allows joint troubleshooting of reactive impurities, transport bottlenecks, and purification hurdles. This spirit of knowledge-sharing draws on lessons from our own failed pilot runs, helping downstream users avoid hours of wasted lab work.
Analytical rigor holds a central place in our operational philosophy. Each batch of 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde undergoes full spectral analysis alongside purity checks using chromatographic methods. For our customers in regulated industries, this depth of data speeds up documentation processing for regulatory filings and quality assurance reviews.
We meet not only standard minimums for purity, but also customer-specific demands for residual solvents, moisture levels, and trace metal content. Past collaborations have pushed us to develop specialty processes for ultra-low-metal grades, particularly for use in catalytic hydrogenation or light-sensitive synthetic steps.
To keep supply chains resilient, we pack 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde in moisture-barrier drums with tamper-evident seals. This allows confident storage in a range of climates, and batch-specific tracking gives downstream chemists confidence in source and quality. During the pandemic years, such reliability prevented gaps in production for partner companies racing to develop new entities and generic medicines.
Our logistics partners receive advance product handling instructions, and on rare occasions of transport-related queries, our technical team responds promptly to resolve documentation or labelling issues. The goal remains to safeguard product quality from plant to user, minimizing risk of cross-contamination or delays.
Nothing replaces real-user commentary. Many technical modifications in our process have grown directly from partner feedback describing specific impurities, solubility needs, or unique workflow constraints. Active, honest dialogue with chemists, engineers, and technical buyers remains the backbone of our service model.
A recent example involved a mid-sized pharmaceutical team troubleshooting a bottleneck from a supplier shift. Quick analytical documentation and sample retesting on our end allowed them to proceed without production delays or costly work-arounds, reinforcing their decision to establish long-term agreements with our operation.
Chemical manufacturing doesn’t stand still, and neither can approaches to reliable intermediate supply. As more fields recognize the nuanced reactivity and selectivity available through iodinated pyridine rings, we see a growing shift towards materials like 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde for their direct applicability and time-saving qualities.
Ongoing collaboration and transparency anchor our engagement with customers at every stage—from pre-clinical synthesis through market-scale manufacturing. The emphasis on hands-on feedback, rapid technical response, and ongoing verification ensures that our reputation rests on more than just standard specifications, but on firm experience borne of real-world industrial practice.
Manufacturing advances depend on reliable, characterizable building blocks. Our experience producing 4-Iodo-2-methoxy-3-pyridinecarboxaldehyde reinforces the importance of direct feedback, continuous improvement, and absolute attention to technical detail. Reliable supply of such intermediates empowers discovery, shortens project timelines, and reduces waste at every stage. In this way, careful manufacturing not only serves customers’ science—but also strengthens the foundations of progress across the chemical industry.