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HS Code |
371285 |
| Chemical Name | 1-Ethoxymethyl-2-Iodoimidazole |
| Molecular Formula | C6H9IN2O |
| Molecular Weight | 252.05 g/mol |
| Cas Number | 147260-97-1 |
| Appearance | White to off-white solid |
| Purity | Typically >98% |
| Solubility | Soluble in common organic solvents (e.g., DMSO, DMF) |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
| Smiles | CCOCOc1ncc(n1)I |
| Inchi | InChI=1S/C6H9IN2O/c1-2-10-4-9-3-5(7)8-6-9/h3,6H,2,4H2,1H3 |
| Synonyms | 2-Iodo-1-(ethoxymethyl)-1H-imidazole |
As an accredited 1-Ethoxymethyl-2-Iodoimidazole 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 1-Ethoxymethyl-2-Iodoimidazole, sealed with a screw cap, labeled with hazard and identification information. |
| Shipping | 1-Ethoxymethyl-2-iodoimidazole is shipped in tightly sealed, chemically resistant containers to prevent contamination and moisture exposure. The package is clearly labeled with hazard and handling information. It is shipped according to relevant local and international regulations for hazardous chemicals, ensuring temperature and light stability during transit. |
| Storage | 1-Ethoxymethyl-2-Iodoimidazole should be stored in a tightly sealed container, away from light, heat sources, and moisture, in a cool, dry, and well-ventilated area. Store separately from incompatible substances, especially strong oxidizers. Clearly label the container and ensure access is restricted to trained personnel. Follow all relevant institutional and chemical safety protocols for handling and storage. |
Applications of 1-Ethoxymethyl-2-Iodoimidazole in Industrial Manufacturing1-Ethoxymethyl-2-Iodoimidazole serves as a specialized intermediate in select industrial value chains requiring precise iodoimidazole functionality. The following scenarios detail its proven integration into established downstream manufacturing processes, drawing on our direct application expertise and customer data from global regulatory-compliant production sites. 1. Active Pharmaceutical Ingredient (API) Synthesis for Antifungal CompoundsOur material functions as a critical building block for pharmaceutical manufacturers synthesizing advanced imidazole-based antifungal agents. Its stable iodo and ethoxymethyl groups facilitate late-stage substitution reactions, directly impacting the yield and purity of the active compound. Chemists incorporate it during the penultimate or final steps to ensure precise modification, taking into consideration not only reaction kinetics but batch traceability under regulated environments. Process Chemists rely on its batch-to-batch consistency to manage critical quality attributes essential for FDA submission dossiers and EU market registrations. Industry compliance standards
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2. Specialty Polymerization Catalyst ManufacturingIn advanced polymer production, particularly for engineering thermoplastics requiring polar functionality, compounders apply this material as a functionalized imidazole catalyst. Its ethoxymethyl moiety allows fine-tuning of catalyst activity, benefiting processes where conventional imidazole derivatives lack the required initiation efficiency. We directly supply polymerization facilities where safety, purity and reproducibility are mandatory under recognized technical standards. Industry compliance standards
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3. Electronic Grade Crosslinking Agent for Photoresist ManufacturingFabricators of semiconductor photoresists and novel imaging resins depend on this compound for its highly reactive iodoimidazole core, improving crosslinking density and pattern transfer sharpness. Its chemical stability and purity help meet the stringent criteria set by microelectronics cleanroom processes. Our electronic-grade production systems supply leading resist makers with lot-specific QA, facilitating their own traceability for process audits under ISO and SEMI regulations. Industry compliance standards
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4. Intermediate for High-Purity Agrochemical SynthesisAgrochemical manufacturers use this compound as a selective halogenating and functionalizing agent during synthesis of imidazole-based crop protection molecules. Its predictable reactivity supports formation of active ingredients with improved field stability, residue profiles, and environmental safety. We deliver material directly into GMP and GLP-compliant synthesis lines for customers supplying the food production chain globally. Industry compliance standards
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Producing 1-Ethoxymethyl-2-Iodoimidazole in our facility calls for more than routine technique, a point that’s probably lost on those who work outside the lab or cleanroom. This compound doesn't forgive carelessness, and its nuances show just how much the consistency in raw materials, thorough process control, and well-maintained equipment decide the outcome. Over years of scaling up production batches, feedback from end-users—research chemists and development teams—has shown consistent praise for both purity and batch reproducibility. We get requests from small molecule discovery labs and custom synthesis departments that value high-precision iodinated imidazoles, and for good reason. The subtlety of the iodine substituent at the 2-position, combined with an ethoxymethyl group at the 1-position, introduces chemical behavior quite different from both unsubstituted analogues or those with halogenation at different sites.
A big topic in fine chemical manufacture circles centers on the quality of reagents sourced directly from the manufacturer. Pure 1-Ethoxymethyl-2-Iodoimidazole needs rigorous control during the substitution step and careful purification after the reaction. Quality at this stage translates to fewer byproducts and impurities, letting customers skip repeat extractions or column runs on their end. Over the decades, improvements in reactor design, solvent handling, and in-line monitoring have advanced far beyond what the industry followed even ten years ago. Today, we apply real-time NMR and chromatography to confirm minimal isomeric contamination and batch-to-batch consistency.
From experience, we know that producers face hurdles maintaining this level of consistency when scaling for pilot or kilogram quantities. Some suppliers push for volume before optimizing for quality, which often shows up plainly on end-user chromatograms. We caught on early that a robust workflow, controlled temperature profiles, and timely intervention make all the difference for compounds like this one. Our customers, especially those in pharma synthesis or materials research, relay that well-characterized, predictable building blocks save them project time, reduce troubleshooting headaches, and limit failed syntheses downstream.
We have found that the unique combination of an ethoxymethyl and iodine group creates reactivity that customers use for everything from selective cross-coupling to protecting group strategies and nucleoside analog development. Our in-house specs reflect direct requests from these sectors: purity above 98 percent by HPLC, minimal water content, and trace heavy metals below stringent thresholds. Recrystallization and vacuum drying protocols take precedence for every batch that leaves our site.
Providing a well-documented product isn’t just about satisfying paperwork. Raw NMR analysis, batch COAs, and, if needed, mass spectrometry profiles come baked into the order process. Research groups use this for their own records, reproducibility checks, or transfer to regulatory filings. For example, polymer researchers and antiviral compound developers depend on quick access to structural confirmation and impurity profiles as they move from bench to pilot scale.
Most orders for 1-Ethoxymethyl-2-Iodoimidazole head to research organizations and specialty synthesis groups engaged in novel heterocycle construction, small-molecule drug discovery, or in some cases, development of advanced organic materials. The electron-donating ethoxymethyl group on N1, paired with the iodine at C2, creates a chemical handle that supports further functionalization through cross-coupling or nucleophilic substitution. We’ve watched teams integrate this structure into nucleoside analogs, modified biomolecules, and organic light-emitting diode precursors.
Feedback from medicinal chemistry customers reveals that this reagent often streamlines late-stage diversification. Conventional iodoimidazole analogs sometimes create regioselectivity headaches; the unique substitution pattern here eases the design of synthetic routes, especially in heterocycle libraries or fragments for kinase inhibitors. Another group working with radiolabels tested the suitability of our batches for radioiodination, and the consistent purity and robust physical profile of the product prevented unwanted side reactions.
Tech transfer feedback matters to us. Researchers running multi-step syntheses have provided batch reports confirming less chromatography required post-coupling, and no surprise NMR peaks associated with under-characterized starting points. Reducing uncertainty at this stage means fewer wasted runs, and time out of the hood is often the best evidence a product like this solves real everyday problems in the lab.
Early on, academic and commercial groups made their own iodinated imidazoles in lab-scale quantities. Yields often disappointed, side reactions multiplied, and batch reproducibility suffered. Differentiation comes sharply into focus if you stack 1-Ethoxymethyl-2-Iodoimidazole against simpler analogues like 2-iodoimidazole or 1-alkylated isomers. The ethoxymethyl moiety not only boosts solubility in common organic media, but it also provides a protecting group strategy pivotal for downstream chemistry.
Unlike conventional 2-iodoimidazole, the ethoxymethyl group increases reaction site selectivity, and researchers synthesize more complex molecules without facing breakdown or over-alkylation. We’ve gotten requests to prepare side-by-side samples so customers can benchmark performance in SNAr reactions, metal-catalyzed transformations, or Suzuki-Miyaura couplings. These collaborative tests show that the unique substitution pattern in 1-Ethoxymethyl-2-Iodoimidazole confers improved yields and better control over side reactions. It’s also evident during reaction workup; less emulsion formation and faster phase separation both matter in the kind of intensive workflow that defines modern synthetic chemistry.
Manufacturing provides a close-up view of recurring pitfalls in specialty chemical synthesis. In contrast to traders or distributors, we answer for every irregularity, every off-spec vial, every batch that lands customer complaints in our inbox. No third-party handler intervenes—our process, accountable from raw material acceptance to final release, decides the quality you get.
Responsiveness traces back to production people—those who run shifts, watch reactions, and make real calls on whether a batch passes or fails. We don’t outsource cleaning validation or maintenance; our technical crew trains in-house, and most of them cross-train on analytics, downstream processing, and QC. Batch records tell a story, but so do the habits written in the routines of seasoned operators. This attention to detail shapes each gram shipped, building trust for repeat customers. If a researcher hits an unexpected impurity or sees an off-color sample, their contact reaches the same technicians who handled their batch.
We have learned to prioritize lot-to-lot traceability. For pharmaceutical teams who rely on these materials for IND or NDA filings, a misplaced or incomplete document can derail months of work. Our internal culture keeps digital as well as old-school paper records, letting us chase issues back to the root faster. On more than one occasion, this practice identified a supplier-level inconsistency in one solvent or iodination reagent, flagging a nonconformity before it entered critical product lines.
Working directly from the manufacturing side reveals that the industry’s push for transparency isn’t some distant regulatory demand but a real shifting of customer expectation. Large-scale research teams pressure their suppliers for chain-of-custody records, process validation data, and open access to safety information. We meet those requests, not because regulations require us to, but because open communication earns customer loyalty and real project success.
Today’s chemical buyers—especially in the biotech, materials, or university sectors—don’t just want a reagent; they want assurance that their critical path isn’t at the mercy of invisible middle layers. Orders placed directly with us connect labs and development teams to daily process logs, in-situ analytic snapshots, and direct answers rather than vague technical bulletins.
On our end, this approach sets a higher bar for internal oversight but ultimately cuts down issue resolution time. Open reporting and streamlined document sharing aren’t abstract industry trends—they’re a necessity born from the rising value placed on experimental reproducibility, safety, and regulatory compliance.
From years of feedback—especially with newer graduate students or startup teams—we've seen the hazard management gaps that can happen when compounds like 1-Ethoxymethyl-2-Iodoimidazole change hands outside direct manufacturer support. Specialty reagents with heavy halogen content call for smart storage, use in an appropriate environment, and clear situational awareness. Our technical data sheets go out with every lot, and pre-shipment consults clarify these handling requirements, including compatibility with common solvents, light, and thermal limits.
Some years back, a customer relayed a thermal runaway event traced to improper charge order and unventilated setup. Instead of brushing off the risk, we augmented our lot packaging and updated storage warnings to highlight possible exothermic hazards in larger-scale processes. Every new process tweak, every revised warning, pulls from real lab history—accidents, after all, don't forgive ignorance, and chemical safety can't just rely on generic SDSs.
Education extends beyond paperwork. We provide walkthroughs on safe handling, contamination avoidance, and emergency planning for labs ramping up from milligram to multi-gram scales. Our field experience with technical teams showed that site visits and hands-on troubleshooting save time and prevent material loss. Users benefit most from quick, clear lines back to our chemists.
Chemical manufacturing, especially for custom imidazole derivatives, never freezes in place. Modernization brings automation to transfer lines, in-line real-time analytics, and smarter cleaning regimes. We invested in multi-stage scrubbers to address both operator safety and environmental compliance—decades back, this would have counted as an optional expense. Now, it’s just part of responsible stewardship, and it also reassures our customers that product quality won’t be compromised by uncontrolled environmental variables.
Upgrading detection methods, from old single-channel GC to fast multidimensional HPLC and NMR, makes live data more available. These upgrades tighten specifications for controlling side products like unreacted starting materials or unwanted byproducts, which make a critical difference for high-stakes research. We’ve watched customer projects avoid months of analytical downtime because our batch releases contain exhaustive impurity data. Tech transfer processes, scale-up protocols, and publication standards all flow more smoothly when every source material enters the pipeline clearly labeled, tested, and properly documented.
Direct dialogue with customers—whether by phone or at the bench—remains central to how we refine our manufacturing protocols. No feedback loop operates outside our process; modifications to purification, drying, or packaging always come after real-world trials and recurring questions. For example, one research team using our 1-Ethoxymethyl-2-Iodoimidazole for radiolabeling found that a minor solvent residue altered their labeling efficiency. Armed with their data, we adjusted our solvent switch strategy, and batches since have stayed residue-free to their specifications.
Laboratory scientists value open lines with chemical producers not just for replacement claims or documentation but to troubleshoot their method development steps. Being able to offer alternatives—different particle sizes, modified drying, or improved sealing—makes a difference not just for one customer but in refining our baseline processes for all. In many cases, those improvements become permanent upgrades to our overall manufacturing workflow.
Modern manufacturing pays closer attention to solvent recycling, energy usage during thermal processes, and safe neutralization of byproducts. Plant operations built for small to medium scales allow us to pivot more quickly to new green chemistry approaches. Solvent recovery units and closed-loop nitrogen purging not only save on cost but reduce the overall environmental footprint of high-value products like 1-Ethoxymethyl-2-Iodoimidazole.
We keep close watch over each element of our supply streams as raw material price volatility and regulatory landscapes can affect pricing and availability. When shortages arise, customers appreciate timely updates—our operations keep a flexible stock model and try to forecast enough inventory to avoid back orders or unpleasant surprises for project timelines.
We also encourage labs to plan disposal ahead of use, taking advantage of our updated disposal protocols and supporting recommendations for safe, compliant handling of both spent reagent and process byproducts.
Anyone who has run a demanding synthesis knows the pain of failed reactions due to under-characterized or inconsistent starting materials. When you work directly with a chemical manufacturer, every batch of 1-Ethoxymethyl-2-Iodoimidazole reflects stringent process control, customer-driven improvements, and a commitment to clear communication at every step. Years of direct dialogue with development teams and research scientists have refined our operations, eliminated avoidable defects, and delivered a reagent that serves the demanding needs of today’s advanced chemical R&D.
Choosing the right source for 1-Ethoxymethyl-2-Iodoimidazole isn’t a minor purchasing decision; it shapes the success of your research pipeline, protects investment in project timelines, and builds confidence among regulatory reviewers and collaborators. Every day, this compound leaves our facility, shaped by decades of hands-on experience, ready to help you push the boundaries of discovery and innovation.