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HS Code |
908782 |
| Compound Name | 4,5-Diiodo-2-Methyl-1H-Imidazole |
| Molecular Formula | C4H4I2N2 |
| Molecular Weight | 345.90 g/mol |
| Cas Number | 16250-76-1 |
| Appearance | White to Off-white solid |
| Melting Point | 220-225°C |
| Synonyms | 2-Methyl-4,5-diiodoimidazole |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically >97% |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Smiles | Cc1[nH]c(I)n1I |
| Inchi | InChI=1S/C4H4I2N2/c1-2-7-3(5)4(6)8-2/h1H3,(H,7,8) |
As an accredited 4,5-Diiodo-2-Methyl-1H-Imidazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, sealed with a screw cap, labeled; contains 5 grams of 4,5-Diiodo-2-Methyl-1H-Imidazole, for laboratory use. |
| Shipping | 4,5-Diiodo-2-Methyl-1H-Imidazole is shipped in securely sealed, chemical-resistant containers to prevent moisture and contamination. The package is labeled according to regulatory guidelines, indicating hazardous material if applicable. It is transported under controlled temperature and handled by authorized personnel, ensuring safety and compliance with chemical shipping regulations. |
| Storage | 4,5-Diiodo-2-Methyl-1H-Imidazole should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, preferably in a chemical storage cabinet designated for hazardous materials. Ensure that appropriate labeling and safety precautions are followed at all times. |
Applications of 4,5-Diiodo-2-Methyl-1H-Imidazole in Industrial ManufacturingAs a direct manufacturer, we supply high-purity 4,5-Diiodo-2-Methyl-1H-Imidazole that serves as a critical intermediate for specialty synthesis in chemical, pharmaceutical, and electronics sectors. Our material supports downstream formulation and process innovation where selectivity, iodination, and imidazole motifs are core requirements. 1. Active Pharmaceutical Ingredient (API) Intermediate for Antifungal AgentsOur product is a strategic intermediate in the multistep synthesis of certain triazole-based antifungal APIs. Its iodo groups and methylated imidazole ring facilitate regioselective coupling, allowing customers to achieve precise molecular structures during API assembly. Strict impurity and trace metal limits are maintained to support regulatory filings, and usage ratios adjust based on specific route optimization. Our technical support extends to customers’ QC, batch record, and process validation tasks. Industry compliance standards
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2. Functional Material Intermediate for Organic Electronic ComponentsThis imidazole derivative is used in custom synthesis pathways for organic semiconductors and charge transport materials in the electronics sector. Its diiodo positions allow selective cross-coupling (such as Suzuki or Buchwald–Hartwig routes), ensuring desired electronic properties in final polymer structures. Batch purity, dryness, and lot consistency are rigorously controlled for reproducible device characteristics. Industry compliance standards
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3. AgI Complex Synthesis for Radiopaque Medical Imaging Reagents4,5-Diiodo-2-Methyl-1H-Imidazole provides a robust iodination source and ligand in the preparation of silver-iodine complexes for contrast agents used in medical imaging. Through direct ligand exchange and precise stoichiometry, manufacturers achieve high-contrast radiodense compounds for X-ray and CT contrast. We offer documented batch traceability and process validation data for regulated use. Industry compliance standards
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4. Building Block in Agrochemical Synthesis—Azole Fungicide DevelopmentFormulators use 4,5-Diiodo-2-Methyl-1H-Imidazole as a core starting material in the custom synthesis of methylated and halogenated azole fungicides. The compound enables specific C-N and C-C bond formation steps, allowing downstream chemists to fine-tune fungicidal specificity and safety margin. Customers select grade and purity based on target registration dossiers and environmental profile requirements. Industry compliance standards
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5. Precursor in Heterocyclic Dye Manufacture for Analytical ReagentsThe imidazole derivative acts as a selective precursor in the synthesis of heterocyclic dyes for chromatographic and titrimetric analytical reagents. Its distinct electron-rich structure is used to tailor chromophore resonance, yielding dyes with sharp spectral features for UV/Vis detection. Manufacturers deploy IR, HPLC, and trace metal QC to guarantee quality for laboratory and industrial reagent kits. Industry compliance standards
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Working in chemical synthesis every day, certain molecules earn a reputation on the production line. 4,5-Diiodo-2-Methyl-1H-Imidazole is one of those compounds that reminds us why precise control and deep process knowledge matter. Each batch moving through our facility tells a story of hands-on technique, vigilance, and cooperation between chemists and operators. With a chemical formula of C4H4I2N2 and a consistent appearance as off-white to pale yellow crystals, this compound stands out for more than just its structure—the value comes from what it allows researchers and manufacturers to achieve.
It’s easy to look at halogenated imidazoles and lump them together. On the manufacturing floor, minor shifts in substitution change everything. The placement of iodine atoms at the 4 and 5 positions on the imidazole ring grants this molecule a versatility and reactivity profile different from mono-substituted or non-substituted analogues. The methyl group at position two does more than fill space. In reactions where stability under heat or challenging conditions matters, that methyl group has a direct influence over the way the molecule behaves, especially during coupling reactions or when exposed to strong bases during process scale-up.
Competitors sometimes market similar diiodo imidazoles, but alterations at even one position, or use of different halogens, can greatly affect both synthetic intermediates and finished fine chemicals. Our long-running relationship with this product underscores how crucial those molecular details turn out to be in real-world processes.
People often think of specialty intermediates as simple to crank out. Our operators know otherwise. Each batch of 4,5-Diiodo-2-Methyl-1H-Imidazole begins with raw materials that require close inspection. Even trace impurities show up later as problems—unexpected colors, poor yields, or inconsistent crystallization. Holding strict raw input specifications keeps each lot on spec. No two runs look entirely the same, so every step—from reaction charge to isolation—calls for close measurement and oversight from experienced hands.
One key to success with this compound is its sensitivity during halogenation. Iodine’s tendency to participate in side reactions means there’s no room for error with oxidants or temperature control. Once, in scaling up for a pharmaceutical customer, we caught an anomalous exotherm that depleted our iodine source faster than predicted. Immediate manual quenching kept the batch within limits. It comes down to knowing how the reaction “feels”—something you can’t capture in software or datasheets.
Purification and drying demand patience and the right tools. We do not rely on batch-to-batch luck or fleeting shortcuts. Each lot ends up passing through crystallization and vacuum drying until it passes our inspection for purity, melting point, and coloration. These are not box-ticking exercises but habits built from real experience—habits that prevent contamination of downstream products and safeguard partnerships with customers who count on each detail.
The most rewarding part comes when we see what customers can do with it. 4,5-Diiodo-2-Methyl-1H-Imidazole draws steady demand from research and industrial customers who value reliability and traceable origins. Research chemists value its role as a building block in the creation of bioactive molecules and functionalized pharmaceuticals. For anyone working with cross-coupling reactions—Suzuki, Sonogashira, Stille or Ullmann variations—this compound’s diiodo profile gives them more handles, so to speak, for diverse transformations. They can selectively substitute at either halogen site or both, expanding their synthetic options for heterocyclic targets.
Beyond fine chemicals and drug intermediates, there’s specialty dye and pigment synthesis. The dual iodine groups open unique synthetic routes. One technical customer in the agrochemical sector turned to us because their previous sources offered only mono-iodo analogues, which resulted in poor yields for their catalytic applications. Consistent access to this structure allowed their project to scale, confirming the importance of getting the right molecular features from the beginning.
Every molecule leaving our line is a testament to our belief in traceability and strict quality controls. We invest in full-spectrum analytical checks: HPLC, NMR, and elemental analysis ensure the claimed iodine content matches reality. Consistency of batch-to-batch melting point, color, and impurity profile matters for those running tightly validated synthetic routes. Differentiators emerge when the product works exactly as expected—a point not lost on anyone who’s lost time or reputation chasing after a contaminated intermediate from a generic source.
Over the years, we’ve documented every deviation, every outlier. That in itself benefited process control. In one case, environmental humidity on a rainy day created minor but persistent changes in drying behavior, making the product cake instead of free-flowing crystals. Adjusting the drying cycle, and not being satisfied with “good enough,” allowed us to restore delivery of batches that poured smoothly and stored longer without caking.
Our long-term buyers do not want vague promises. They ask detailed questions: How is the residual solvent content managed? What cleaning protocols prevent cross-contamination with other halogenated intermediates? These are not just compliance checkboxes but agreements of trust. We invite audits and supply comprehensive certificates of analysis that include real numbers and supporting data, not boilerplate claims. Trust builds on the repeated delivery of a product that matches not only the agreed specifications but the expectations developed through honest interaction.
In the face of regulatory change—such as evolving restrictions on certain iodine precursors—we adapt our syntheses, report all relevant changes, and revalidate every new process. Costs sometimes rise. Still, the alternative—compromising on process or purging transparency—never enters the conversation here.
Cost comparisons in specialty intermediates miss some essential truths. Customers who come to us after trying lower-cost options report a consistent pattern: losses from wasted batches, analytical headaches, and schedule overruns that quickly swallow any upfront savings. Our facility’s record of consistent quality stems from investments in validated control, not in cutting corners. We run ongoing training for our team on changes in analytical equipment, waste handling, and regulatory documentation so the standard never slips.
Working directly with downstream formulators, we gather feedback on long-term storage behavior and reactivity downstream. It’s routine for us to supply detailed guidance on handling, packaging, and shelf life, because we have tracked every mode by which this compound can degrade or react. In one notable project, shipping delays during a hot summer posed a stability challenge. Because we had studied the compound’s thermal profile, we promptly recommended a revised packaging format and included real-data-based guidance in the COA. The customer’s process ran as planned, avoiding delays or red tape.
Responsible chemical manufacturing goes beyond the spreadsheet. Iodinated intermediates, especially diiodo types, require controlled handling for safety and environmental compliance. Our internal processes, developed through direct engagement with waste authorities and practical hazard analyses, reduce emissions and prevent reagent loss. We recycle solvents wherever possible and engage in continuous method upgrades to cut down on hazardous waste.
Transporting and storing 4,5-Diiodo-2-Methyl-1H-Imidazole requires secondary containment, up-to-date hazard labeling, and transport documentation developed through careful reading of actual requirements—not guesswork. Training workers on real risks instead of generic warnings keeps every shift safe. We log every near-miss and circulate that knowledge, shrinking the space for preventable errors.
Trusted relationships grow not from single transactions but from an ongoing exchange of information. We make a practice of transparent communication, whether sharing batch data ahead of orders or responding rapidly to changes in customer needs. Many of our long-term clients started with a single project and have grown alongside us as their own requirements evolved. We have run technical trials jointly, inviting feedback and redesigning isolation steps to better align with the downstream purification needs of our partners.
Sometimes requirements shift unexpectedly. One research user needed finer particle size for rapid dissolution in a continuous processing setting. Instead of off-the-shelf answers, our process team ran a quick series of mill trials and delivered test samples for direct evaluation. Feedback from their side provided valuable insight into the physical properties that matter—not just in the lab but in full-scale manufacturing—and the lessons filtered back into our main production lines. The guiding principle remains: listen, experiment, adjust, and confirm through real-world use.
Every new insight in imidazole chemistry, every method improvement, has a direct and lasting impact on how we produce 4,5-Diiodo-2-Methyl-1H-Imidazole. Collaborations with academic labs, direct investment in small-scale studies, and persistent monitoring of patent literature help us keep the process on the cutting edge. Recent trends in chem-catalyzed direct amination, for instance, have prompted additional lookbacks at our purity needs and led to stricter control of inorganic by-products.
Our R&D team maintains an open-door policy with both in-house and external project teams. Whether it concerns improving handling for end users or modifying crystal habit for easier downstream blending, we see the work as unfinished and always in need of refinement. That attitude keeps us nimble in facing evolving market needs or changing regulatory environments.
A specialty intermediate such as 4,5-Diiodo-2-Methyl-1H-Imidazole represents far more than its chemical formula. For every successful molecule, there are hands-on stories—midnight rechecks of cooling profiles, recalculations when a new supplier brings a slightly different grade of a starting amine, and cautious optimism when the NMR spectrum is read for the final time on each lot.
The people developing therapies, specialty materials, or new agrochemical compounds depend on intermediates with data they can trust, origins they can trace, and suppliers committed to partnership rather than faceless transactions. That’s what guides us in producing every gram, every batch, and every order—the conviction that chemistry is a relationship between those who make and those who create.
Markets and techniques will continue to shift. Customers may demand ever greater reactivity, higher purity, or new supply formats. What won’t change is our hands-on commitment to managing each process step and solving emerging challenges in real time, not on paper. Our track record with 4,5-Diiodo-2-Methyl-1H-Imidazole brings new inquiries all the time—not because the name is familiar, but because our approach to its manufacture and supply stands for trust, transparency, and grit built across years of trial, learning, and honest hard work on the floor.