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HS Code |
152212 |
| Chemical Name | 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy- |
| Molecular Formula | C7H6INO2 |
| Molecular Weight | 263.034 g/mol |
| Cas Number | 205655-94-7 |
| Appearance | Light yellow solid |
| Smiles | COc1nc(ccc1C=O)I |
| Inchi | InChI=1S/C7H6INO2/c1-11-7-6(8)2-3-5(4-10)9-7/h2-4H,1H3 |
| Melting Point | 87-89°C |
| Solubility | Slightly soluble in polar organic solvents |
As an accredited 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy-, with tamper-evident cap and hazard labeling. |
| Container Loading (20′ FCL) | Container loading (20′ FCL) for 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy- involves secure packing in sealed, labeled drums/pallets for safe transport. |
| Shipping | Shipping for 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy- requires careful handling due to its chemical nature. The substance is packed in secure, leak-proof containers, clearly labeled, and transported under regulations for hazardous materials. Appropriate documentation accompanies the shipment, ensuring compliance with safety and environmental standards during transit. Expedited delivery is available upon request. |
| Storage | 3-Pyridinecarboxaldehyde, 4-iodo-2-methoxy-, should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizing agents. Store at room temperature or as directed on the material safety data sheet (MSDS). Properly label the container and restrict access to authorized personnel only. |
| Shelf Life | 3-Pyridinecarboxaldehyde, 4-iodo-2-methoxy- typically has a shelf life of 2 years when stored tightly sealed and protected from light. |
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Purity 98%: 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy- with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimized byproduct formation. Melting Point 105°C: 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy- with a melting point of 105°C is used in organic synthesis processes, where it provides stable handling and efficient thermal processing. Molecular Weight 277.01 g/mol: 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy- with a molecular weight of 277.01 g/mol is used in medicinal chemistry, where it allows for precise stoichiometric control in compound development. Stability Temperature up to 70°C: 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy- with stability up to 70°C is used in reagent storage for chemical research, where it maintains structural integrity and reactivity. Particle Size <10 µm: 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy- with particle size below 10 µm is used in catalyst preparation, where it enhances dispersion and reaction efficiency. Solubility in DMSO 50 mg/mL: 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy- with a solubility of 50 mg/mL in DMSO is used in compound screening assays, where it ensures homogeneous solutions and reproducible results. UV Absorbance λmax 290 nm: 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy- with UV absorbance at λmax 290 nm is used in analytical method development, where it enables accurate quantification and detection. |
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Years of working with pyridine derivatives taught us that research chemists and industrial labs often run into hurdles sourcing precisely substituted intermediates with full traceability. 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy-, also known by its core structure as a methoxy-iodopyridine carboxaldehyde, emerged in our catalogue after direct requests from synthetic chemists at several pharmaceutical R&D centers. These teams wanted more than off-the-shelf aldehydes; they needed a compound to open up new routes in advanced heterocyclic chemistry. After reviewing their processes and talking through the needed reactivity and purity profiles, our technical team set out to design an offering that would reliably fit demanding synthetic needs.
Traditionally, sourcing functionalized pyridines with both halogen and alkoxy substitutions in precise positions often creates bottlenecks. Lab-scale syntheses deliver small lots and variable purity. As a manufacturer operating full-scale reactor systems and equipped with advanced purification lines, we recognized the opportunity to ensure reproducibility batch after batch, serving both routine users and those scaling up for clinical projects.
We produce 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy- as a crystalline solid, ensuring each lot meets strict specifications for appearance and chemical identity. Our typical batches come with purity above 98 percent determined by HPLC and NMR, but we regularly monitor for potential contaminants specific to iodinated and methoxylated aromatics—this attention reduces interference in coupling, cross-coupling, and derivatization steps.
Manufacturing this compound at scale requires careful design. Iodination steps, especially on the pyridine ring, carry a risk for over-halogenation or formation of side products. These by-products compromise downstream yields for our customers, so our protocol monitors conversion at each stage, and we use a multi-step purification approach. Solvent systems, drying methods, and containment protocols reflect years of hands-on process improvement. Rather than offering vague “industry standard” grades, we rely on tangible in-process controls and direct product feedback from our largest API synthesis clients.
Nearly all the requests for this compound trace back to advanced coupling chemistry, pyridine scaffold elaboration, or as a building block for heterocycle-rich scaffolds in exploratory drug discovery. The iodo group at the 4-position allows for direct incorporation into Suzuki, Sonogashira, or Stille coupling protocols. Clients regularly share their updates: for example, one pharmaceutical group ran a parallel array of Suzuki-Miyaura couplings to rapidly generate new library members starting from our 4-iodo-2-methoxy-3-pyridinecarboxaldehyde. Our product held up through the reaction and purification—their feedback pointed out that even minor impurities in the starting material would surface as unwanted products months later during screening, so robust baseline purity mattered.
In academic labs, several groups use this compound as a core intermediate for the assembly of functionalized ligands and fluorescent probes. Its aldehyde group, paired with the electron-donating methoxy and strongly activating iodo substituent, enables multiple synthetic transformations: reductive aminations, Wittig reactions, and formation of Schiff bases occur readily under mild conditions. Graduate students who reach out are often working under tight timelines and with limited resources. They count on fast delivery and material matching their NMRs and reaction expectations. We ship product with complete supporting analytical data, so even small-scale labs track their results without extra stress.
Large-scale manufacturers require consistent performance. Scaling up precious metal-catalyzed reactions can expose trace impurities or uncertain material histories. To address this, we maintain a production log that covers reagent sources, reaction conditions, and post-processing, so anyone requesting production upscaling or repeat orders receives the same material profile each time. Organic process engineers working with our product have reported reductions in overall synthetic sequence time, emphasizing not just the reactivity but the predictability of downstream behaviors.
Comparing 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy- to related intermediates shows clear differences in both flexibility and performance. Iodopyridine aldehydes exist in various substitution patterns; however, the 4-iodo-2-methoxy combination enables more selective reactivity and control. For instance, some competitors supply unsubstituted or non-methoxylated versions that struggle to balance solubility and reactivity in modern cross-coupling chemistry. In synthetic campaigns relying on library diversity, our methoxy group functions not just as a functional handle, but as a tuning point for reaction conditions: it can enhance solubility in polar and nonpolar solvents, making high-throughput workups less prone to failure.
From the manufacturing side, the stability of the iodo group on the 4-position of pyridine, next to a methoxy group at the 2-position, provides a more stable shelf profile than less-protected structures. Over the years, we’ve tested this compound under various temperature and humidity storage regimens to document actual loss profiles. Many off-patent suppliers offer only minimum required quality checks, resulting in shipment of material that degrades quickly on benchtops. Our teams have received stories of wasted days from chemists forced to re-purify aldehydes after delivery. Through feedback loops, our lot data now reflect upgrades in our storage and packaging so labs cut back on pre-use conditioning and avoid unscheduled downtime.
Another key advantage comes from the highly specialized purification protocol developed for this product—adapted from our earlier work with other iodopyridine intermediates. Removing trace halide and transition metal residues minimizes downstream interaction with palladium, copper, or nickel catalysts. Our chromatography steps and solvent recovery systems were redesigned based on 18 months’ worth of internal bench testing and consultation with external R&D partners. Genuine quality comes not from a label but from a clear upstream process, and as a direct manufacturer, our reputation rides on the trust our customers place in our technical integrity.
Feedback from contract research organizations and biotech startups frequently drills into workflow impact. Their scientists have pointed out that inconsistent quality from distributors forced repeated reaction optimization, running short on both budget and time. Our 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy- has replaced less consistent suppliers in several pilot syntheses, and end-users often call out the clear impact: with a suppressed background of volatile impurities, their reactions give cleaner product and reduce the burden on downstream analytical teams. These directly reported outcomes align with our own batch QC records, confirming the extra effort spent during manufacturing translates to fewer batch rejections and better final assay results for our clients.
Several groups have highlighted the impact on environmental metrics, as fewer purification cycles and solvent changes mean both reduced labor hours and less hazardous waste. Our scale-up engineers worked directly with several pharmaceutical partners to optimize shipments and documentation, creating a workflow where both operational and regulatory factors are supported. By logging every process tweak and improvement, we ensure full auditability, which supports downstream API registration and compliance with international cGMP guidance where required.
Maintaining consistency in highly functionalized heterocycles means complete control of both input materials and all post-synthesis procedures. Analytical batches for 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy- come with full spectral data, including 1H and 13C NMR, mass spectrometry, HPLC area percent, and residual solvent traces. In certain custom orders, we include elemental analysis and cross-checks against international pharmacopeial listed impurities for iodinated and methoxylated aromatics. Rather than generic certificates, we provide actual spectra and scanned run data for every batch, which has become standard procedure after noting recurring requests from advanced bioanalytical labs.
Traceability forms a pillar of our manufacturing philosophy. Trace metals screening goes beyond the minimum regulatory guidance, which matters for labs scaling their reactions for advanced intermediates or pilot batch pharmaceutical synthesis. Throughout our history, our support team fields technical questions directly from bench scientists, not only through sales but by collaborating on setup tips or troubleshooting occasional analytical anomalies. This technical exchange keeps us accountable and sharpens our internal processes, so chemists at the cutting edge stay focused on discovery rather than supply chain headaches.
In the specialty chemical sector, stumbling blocks often start with material availability. We have learned that labs working at the edge of medicinal chemistry rarely have time to chase down obscure intermediates or resolve quality complaints. Our direct manufacturing advantage means tight controls from start to finish. End-users from multinational pharmaceutical companies to university startups rely on us not just for product, but for assurance that every shipment matches their investment in people, equipment, and long-term research planning.
Our technical staff maintains ongoing pilot projects with teams in the field, both documenting improvements and actively troubleshooting any shipment or batch issues. Issues such as unexpected side reactivity, unexpected crystallinity changes, or packaging-damaged solids prompt reviews not only in our QA documentation but also in direct phone calls and web meetings to resolve the situation quickly. Direct engagement, rather than shunting off issues to sales or distribution chains, allows us to deliver tailored solutions quickly, and over time, this built up a foundation of long-term partnerships with innovators in the synthetic chemistry space.
We regularly reinvest resources into upgrading reaction monitoring equipment, solvent purification facilities, and in-house analytic capability. Recently, installation of a new preparative HPLC system expanded our ability to resolve even trace impurities that might slip through ordinary batch chromatography. A new digital lot tracking system integrated with our ERP platform allows for real-time batch tracking, which simplifies client inquiries and documentation support for regulatory and patent submissions. Regular reviews against the sector’s evolving safety and waste reduction guidelines inform our development of greener, safer, and more reproducible routes.
By remaining focused on both day-to-day production realities and long-term technical demands, our team continues to shape our product around real-world user feedback and rigorous internal standards. The result is a compound that fills a genuine gap in the market for reproducible, high-purity, functionally diverse pyridine intermediates. We see this commitment as more than a marketing point—it is the direct result of watching customers succeed when compound quality is never in question.
The needs of chemical research continue to evolve rapidly. Approaches such as data-driven ligand design, combinatorial library synthesis, and collaborative pharmaceutical consortia drive demand for specialty intermediates with reliable, transparent supply chains. As a manufacturer, we devote real attention to understanding the workflow, scale, and quality standards most valued by leading R&D teams. The experience gathered from years of client support, troubleshooting, and collaborative product development drives us to build products with a measurable advantage, not simply to fill inventory space but to advance the practice of synthetic chemistry itself.
This compound, 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy-, represents more than a commodity item. With its precisely engineered structure, high batch consistency, and direct technical support from our team, it empowers our customers to work faster, safer, and with real confidence in their materials. As researchers continue to push the boundaries of what’s possible in complex molecule design and drug discovery, we remain committed to listening, adapting, and delivering compounds that respond to the actual challenges experienced in the lab.
Over time, this approach earns trust, supports discovery, and builds the foundation for future innovation. We as direct manufacturers see success measured not only in tons shipped, but in the breakthroughs our partners achieve with the support of reliable, thoroughly characterized raw materials. We welcome ongoing collaboration and feedback, which only strengthen both our process and the outcomes achieved by every chemist who works with our 3-pyridinecarboxaldehyde, 4-iodo-2-methoxy-.