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4-Iodo-1-Methyl-1H-Imidazole-5-Carboxaldehyde

    • Product Name 4-Iodo-1-Methyl-1H-Imidazole-5-Carboxaldehyde
    • Alias 4-Iodo-5-formyl-1-methylimidazole
    • Einecs 852-771-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    692142

    Chemicalname 4-Iodo-1-Methyl-1H-Imidazole-5-Carboxaldehyde
    Casnumber 1159818-35-1
    Molecularformula C5H5IN2O
    Molecularweight 236.02
    Appearance Off-white to light yellow solid
    Purity Typically ≥98%
    Solubility Soluble in DMSO, methanol, and ethanol
    Smiles Cn1cnc(C=O)c1I
    Inchi InChI=1S/C5H5IN2O/c1-8-2-7-4(6)5(8)3-9/h2-3H,1H3
    Storagetemperature 2-8°C
    Synonyms 1-Methyl-4-iodo-1H-imidazole-5-carboxaldehyde

    As an accredited 4-Iodo-1-Methyl-1H-Imidazole-5-Carboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with tamper-evident cap, labeled “4-Iodo-1-Methyl-1H-Imidazole-5-Carboxaldehyde, 5 grams, for laboratory use only.”
    Shipping 4-Iodo-1-Methyl-1H-Imidazole-5-Carboxaldehyde is shipped in tightly sealed containers, protected from light and moisture. It is packed according to regulatory guidelines for hazardous chemicals and includes proper labeling and documentation. Transport is handled by certified carriers, ensuring compliance with safety and environmental regulations for chemical substances.
    Storage Store 4-Iodo-1-Methyl-1H-Imidazole-5-Carboxaldehyde in a tightly sealed container, protected from light and moisture, at 2-8 °C (refrigerator). Keep it in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Handle under an inert atmosphere if possible, and avoid prolonged exposure to air. Ensure all storage complies with local safety regulations.
    Application of 4-Iodo-1-Methyl-1H-Imidazole-5-Carboxaldehyde

    Applications of 4-Iodo-1-Methyl-1H-Imidazole-5-Carboxaldehyde in Industrial Manufacturing

    As the primary manufacturer, we process and supply 4-Iodo-1-Methyl-1H-Imidazole-5-Carboxaldehyde to serve advanced sectors from pharmaceutical intermediates to agrochemical synthesis. We focus on high-purity material to support specialized downstream transformations while meeting the distinct chemical and regulatory requirements of each target sector.

    1. Pharmaceutical Active Ingredient Synthesis

    This compound serves as a key intermediate in the preparation of selective kinase inhibitors and investigational cancer therapeutics. Customers deploy it in structurally complex imidazole-core drugs, particularly where precise halogen placement enhances receptor selectivity. Its carboxaldehyde group supports conjugation in multi-step organic synthesis, demanding strict process controls and documented traceability. Our material supports scale-up from method development to cGMP API manufacturing.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 US cGMP regulations
    • European Pharmacopoeia Monographs (where applicable for intermediates)
    • FDA/EMA route-specific impurity guidelines

    Typical usage ratio

    • Applied at 0.1–0.3 molar equivalents per final API batch, adjusted according to synthetic route optimization and physicochemical compatibility

    Downstream process integration

    • Enters in the early condensation or cyclization stages for constructing imidazole frameworks within small molecule synthesis

    Final product types

    • Small-molecule kinase inhibitors
    • Anti-cancer drug candidates
    • Imidazole-based targeted therapeutics
    • Reference standards for pharmaceutical R&D

    2. Agrochemical Intermediate Production

    Major agrochemical formulators use our imidazole aldehyde within the segmented synthesis chain for plant growth regulators and systemic fungicides. Its iodine content is critical for downstream halogen-exchange and derivatization steps that benefit compound stability in crop protection applications. We maintain full batch documentation, aligned with supplier audits required by global agricultural majors.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for chemical production
    • FAO/WHO International Code of Conduct on Pesticide Management
    • REACH registration for EU import and usage
    • China National Standard GB 2763 (MRL guidelines for agrochemical residues, where applicable)

    Typical usage ratio

    • Charged at 0.05–0.15 molar equivalents relative to main synthetic substrate, tailored to desired activity spectrum and local formulation preferences

    Downstream process integration

    • Added during the functionalization phase of imidazole-derived pesticide active ingredient synthesis, after initial ring assembly and prior to halogen substitution

    Final product types

    • Systemic fungicides (e.g., imidazole-based actives)
    • Plant growth regulating agents
    • Intermediate compounds for seed treatment formulations
    • Herbicide research intermediates

    3. Fine Chemical Research and Development

    Leading fine chemical firms and contract researchers source 4-Iodo-1-Methyl-1H-Imidazole-5-Carboxaldehyde for probe molecule libraries, radiolabeling programs, and combinatorial screening. Its dual reactive sites make it invaluable in structure-activity relationship (SAR) studies. We guarantee analytical documentation and customizable batch sizing to facilitate precise R&D protocols and technical transfer processes.

    Industry compliance standards

    • ISO/IEC 17025:2017 (analytical laboratory qualification for supporting method validation)
    • Standard industrial chemical hygiene programs (OSHA 29 CFR 1910.1450)
    • GLP (Good Laboratory Practice) for non-clinical research uses
    • Chemical tracking under applicable CWC or export controls (if relevant)

    Typical usage ratio

    • 1–20 mmol scale depending on scope of parallel synthesis and research concept; flexible based on high-throughput screening parameters

    Downstream process integration

    • Utilized in pivotal derivatization, isotopic labeling, or fragment linkage steps within test-molecule generation or probe compound assembly

    Final product types

    • SAR probe molecules
    • Radiolabeled research chemicals
    • Combinatorial library elements
    • Fragment-linked screening compounds

    4. Electronic Chemicals for Advanced Material Fabrication

    Companies in organic semiconductor and dielectric material industries incorporate the imidazole aldehyde as a building block for heterocyclic surface modifiers and functionalized thin-film precursors. The controlled introduction of iodine into organic substrates can enhance electronic conductivity or reactivity for subsequent functionalization. We assure electronic-grade purity and full lot traceability serving global electronics manufacture.

    Industry compliance standards

    • SEMI C3-0709: Specifications for High Purity Materials in Microelectronics
    • RoHS Directive 2011/65/EU compliance
    • Required internal electrochemical quality standards
    • ISO 14001:2015 for environmental management in electronics production

    Typical usage ratio

    • 0.5–5% w/w as a functional additive, with optimization based on intended surface energy, conductivity, or layer uniformity

    Downstream process integration

    • Integrated during the precursor solution mixing in organic thin-film transistor and dielectric layer production, before deposition or polymerization

    Final product types

    • Functionalized dielectric coatings
    • Organic semiconducting films
    • Advanced heterocycle-based sensor materials
    • Surface treatment reagents for microelectronics

    5. Specialty Dye and Pigment Synthesis

    Manufacturers of specialty dyes utilize this compound in the design of halogenated imidazole chromophores for optical and photoactive pigment systems. The aldehyde group enables various condensation and coupling strategies for building extended conjugated structures, providing targeted absorbance spectra. Our controlled particle size and purity measures support direct integration into high-value pigment manufacturing workflows.

    Industry compliance standards

    • Oeko-Tex Standard 100 (textile applications)
    • EN 71-3:2019 (Safety of Toys – migration of certain elements for pigment-containing toys)
    • ISO 1248:2006 (Pigments – general test methods)
    • REACH Annex XVII (restrictions on uses of certain hazardous substances)

    Typical usage ratio

    • 3–10% of batch formulation, determined by target chromophore yield and desired color properties

    Downstream process integration

    • Employed in condensation or oxidative coupling steps after primary dye skeleton assembly; functions as a halogen source and functional group handle for further modifications

    Final product types

    • Photoactive dyes for imaging
    • Halogenated pigment dispersions
    • UV-absorbing textile colorants
    • Specialized inks for security printing
    Free Quote

    Competitive 4-Iodo-1-Methyl-1H-Imidazole-5-Carboxaldehyde prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    4-Iodo-1-Methyl-1H-Imidazole-5-Carboxaldehyde: Pushing the Boundaries in Imidazole Chemistry

    Introducing Our Imidazole Aldehyde Molecule

    In the fine chemicals field, 4-Iodo-1-Methyl-1H-Imidazole-5-Carboxaldehyde stands out for its purpose and reliability. We have synthesized this compound for nearly a decade, tuning our process to deliver consistently pure and stable material suited for major pharmaceutical and research applications. This imidazole derivative, carrying both an iodo and aldehyde group on a methylated imidazole ring, enables reaction pathways impossible or highly inefficient with simpler or non-iodinated analogs. Through years of iterative process improvements, we have shaped each batch to satisfy demanding specifications set by both global innovators and domestic partners.

    Our Approach to Manufacturing

    We have viewed every production run as an opportunity to learn and adapt. Strict feedstock sourcing, fine control over oxidation and substitution steps, and robust purification all help us reduce impurities, particularly those often persistent in standard runs elsewhere—residual methylimidazole precursors, dialdehydes, halide exchange by-products. Chromatographic fingerprinting tests for batches to confirm low single-digit ppm levels of these impurities. Routine QC methods are based on NMR, HPLC, and elemental analysis so that users spend less time troubleshooting and more time advancing their work.

    We produce this compound in kilogram lots, with efficient scaling tools drawn from both lab and plant experience. Our reactors are designed for exothermic halogenations and can handle the thermal, corrosive, and environmental challenge that iodine chemistry brings. Methylation and aldehyde installation require precise timing, temperature, and feed rate, and our operators have hands-on experience with these variables. This fine control gives us an edge when purity and batch repeatability make a difference in downstream results.

    Model and Specifications

    The standardized model we offer has a molecular formula of C5H5IN2O. The iodo function on the 4-position, methyl group on the 1-nitrogen, and aldehyde group on the 5-position differentiate it from most naturally occurring imidazole derivatives. In practical use, the compound appears as an off-white solid, sometimes with a faint yellow tinge if trace iodine is present. Melting point and spectroscopic data match literature and in-house reference lots. Our batches retain a purity exceeding 98 percent by HPLC area normalization, with typical water content below 0.5 percent determined by Karl Fischer titration.

    To help users focus on core research, we include detailed batch-level chromatograms and NMR spectra with each shipment. Analytical support—such as confirmation testing for residue solvents or critical elements—backs up the material’s fit for downstream synthesis, including heterocycle transformation, metal-catalyzed couplings, or fragment-based library construction. Documentation aligns with regulatory requirements that major customers request, but we also provide practical tips drawn from daily plant life, such as dissolving protocols and storage stability.

    Real-World Applications

    Few building blocks offer as much synthetic latitude as this iodo-imidazole-aldehyde. Chemists value the compound for introducing both carbon-iodine and carbonyl moieties onto their molecular scaffolds. The iodo function grants access to a spectrum of palladium- or copper-catalyzed couplings—Suzuki, Sonogashira, Buchwald–Hartwig among them—building routes for N-heterocycle-based drugs, MRI contrast agents, or material science probes. We have kept close ties with research partners who report on both classic and non-classical uses, from spirocyclic library synthesis to N-heterocyclic carbene formation.

    The aldehyde group at the 5-position is a reliable linchpin for further elaboration. Reductive amination, borohydride reduction, and Wittig olefination all benefit from the robustness of the imidazole ring and the compatibility with mild or strong reagents. Scientists—academic and commercial—report that the unique reactivity profile lets them generate libraries unlikely to be assembled by less functionalized analogs. The methylation on the N1 nitrogen delivers improved solubility, enabling straightforward handling in polar and non-polar media, which can streamline purification and analysis workflows.

    Over the years, we’ve seen this compound feature in patent filings, early drug candidate syntheses, asymmetric catalysis studies, and even labeled as a tracer in mechanistic investigations. Each context relies on the distinct attributes this molecule brings—attributes not easily mimicked or replaced in organic chemistry's toolkit. By keeping communication open with innovators, we continue to deepen our understanding of how real users apply the material and what improvements matter most on the lab bench or in scale-up.

    What Sets It Apart From Other Imidazole Derivatives

    Researchers familiar with functionalized imidazoles recognize the rarity of high-purity 4-iodo-1-methyl-1H-imidazole-5-carboxaldehyde. The co-presence of iodine and aldehyde groups presents specific technical hurdles in synthesis and purification. Many commercially listed imidazole compounds lack the orthogonality needed for dual-functionality—either missing the iodo substituent or bearing it in less reactive or more sterically hindered positions. Generic methylimidazole or carboxaldehyde-substituted imidazoles rarely enable the fine-tuned cross-coupling or further transformations that this arrangement offers.

    Our technical dialogue with chemists reveals that many prior attempts to source similar double-functionalized imidazoles ended in low yield or inconsistent batch profiles. The combination of a pure iodo group—resistant to exchange or dehalogenation under storage and vigorous reactions—and a stable, analytically-confirmed aldehyde function reduces the risk of side impurities that can compromise tracers, coupling yields, or bioactivity screens. Our in-process analytics catch minor degradation markers before any flakes or powder leave the plant. This direct feedback loop gives our teams insights they apply in each cycle, ensuring small differences do not add up to bigger hurdles for our customers.

    Shelf stability and storage troubles have long challenged users of iodo-containing building blocks, due to both volatility of free iodine and the potential decomposition of aldehyde moieties under light, oxygen, or residual acid. With this product, we addressed those constraints by integrating solid-phase adsorption and double vacuum packaging as standard practice. Each lot undergoes thermal and photostability testing before release. These adjustments did not arise from abstract theory but from direct feedback from bulk and project customers who experienced sporadic loss of activity or darkening in older lots from less rigorous suppliers.

    Environmental and Safety Values in Production

    Handling iodine and methylating agents in a safe, responsible way has shaped the investments we make in waste management and operator protection. Historical practices across the industry often left questions about the handling of organoiodine waste, solvent emissions, or exposure during high-energy steps. By learning from earlier missteps—inside and outside the company—we recalibrated our waste capture and solvent recovery procedures, moving towards closed systems and real-time gas monitoring, long before these changes became industry norms.

    For our operators and customers alike, purity and safety are intertwined. Impurities—such as methyl iodide, ammonia, or polymeric by-products—threaten both downstream reactions and worker safety during matter transfer or new batch production. We invest energy into routine operator training and knowledge-sharing so that every technician understands why precautions matter, even when the highest yield sits just around the corner. Our QA review cycle includes not only document compliance but live plant walk-throughs and follow-up discussion sessions.

    Customer-facing safety documents and procedures aim for practical clarity. Over the years, reports of accidental skin exposure or spills have dropped thanks to simple improvements—grounding funnels, splash screens, dedicated weighing booths—developed from firsthand feedback and near-miss analyses. These details may not feature in product specifications, but real users cite them as factors in choosing a manufacturing partner that aims for more than just regulatory minimums.

    Listening to Researchers and Innovators

    Material development does not occur in a vacuum—or only inside the boundaries of a plant. We have kept our doors open to university labs, pharmaceutical groups, specialty chemical researchers, and start-ups, welcoming both feedback and criticism. In some cases, customers share spectral results when they detect unexpected peaks or performance changes. In those moments, we work to reconstruct synthetic routes, check for shipping exposures, or revisit raw material sources—sometimes even pulling lots from future shipment and rerunning assays for assurance.

    Our technical service team sees its work as ongoing. The route to improvement is rarely straight; lab-to-plant scale-up delivers surprises. Six years ago, a partner flagged a series of unsuccessful cross-couplings in their library preparation, tracing the cause to persistent trace impurities from incoming lots. This finding spurred revisions in both purification and in-line controls, which now benefit every new customer. We remain in close touch with customers who are fine-tuning automation platforms for compound library expansion; they report time savings and fewer failed couplings after transitioning to our material.

    Synthetic chemists, especially in early-stage settings, often run short on human and technical resources. We prepare practical notes on solubility in DMSO, DMF, ethanol, or aqueous-organic systems, as well as guidance for aliquoting and long-term storage. These notes build on not only internal testing but fielding calls and emails from users who encountered clumping, instability, or dissolution lags with less refined lots sourced elsewhere. Over time, this feedback culture has fostered incremental improvements in our process and packaging, strengthening the working relationship between manufacturing and research stakeholders.

    Supporting Innovation Through Consistency

    Significant breakthroughs in chemical science depend on reliable building blocks, and experience has shown us how even small batch-to-batch changes can disrupt innovative work. Inconsistencies in crystal form, particle size, or minor impurity levels can mean failed reactions or misleading results. In the early years, few suppliers could deliver this iodo-imidazole-aldehyde with repeatable quality, spawning frustration and costly workarounds for researchers. We have invested in analytical and production infrastructure that reflects real-world needs, not just internal standards.

    Through our partnerships, the requests we receive often touch on specialty packaging, supply flexibility, or documentation alignment. Rather than standardizing in isolation, we solicit routine check-ins and review survey feedback. Customers facing tight project windows or scale-out challenges rely on us to not only ship material but to diagnose issues collaboratively. The lessons learned serve beyond marketing; they guide us on whether to reformulate, retest, or revise a protocol to suit emerging applications—whether in nucleoside modification, probe development, or late-stage drug synthesis.

    Addressing Supply Chain Resilience and Transparency

    Fluctuations in raw material supply, particularly iodine and specialty precursors, test a manufacturer’s resilience. During periods of restricted iodine exports or logistic backlogs, we have responded by broadening supplier bases, investing in buffer inventory, and even refining recycling processes to get more from less. Our quality oversight begins with incoming goods—testing for both chemical and physical properties long before synthesis starts. Sometimes this means turning down lower-cost or higher-risk starting materials, even when markets are tight, so that finished product quality does not suffer.

    We hear from users that transparency in origin, testing, and storage matters just as much as yield or price, especially in regulated markets. Over time, we have evolved our traceability protocols to link each lot back to source and method, storing digital and paper records securely for audits and customer reassurance. News of environmental incidents, regulatory tightening, or fraud in the specialty chemicals trade reinforce the value of verifiable provenance and consistent process control. In our view, trust is built batch by batch, with every problem faced openly rather than buried for convenience.

    Practical Solutions to Common Challenges

    Synthetic chemists working with this imidazole derivative commonly report three main challenges: prolonged dissolution, degradation under light or air, and avoidance of stubborn color or impurity traces. Each of these pinpoints real-world performance, not just on-paper metrics. Based on years of operational dialogue and follow-up testing, we routinely offer dissolution guidance keyed to volume, solvent choice, agitation, and temperature. Storage protocols have shifted—not just labeling for dark, cool conditions, but including double-sealed packaging and short-term transport safeguards.

    Color and impurity variability trace back not only to synthetic pathway but also to container materials, residual solvent from purification, or atmospheric exposure. We have minimized these through in-process sampling, choice of packaging, and staff education on best transfer practices. Should end users find unexplained variability, our open-door technical support investigates shipment records, plant logs, and batch analytics together with their lab teams to pinpoint root causes.

    Building on a Foundation of Expertise

    Our history as a direct manufacturer—not a trader or reseller—anchors our deep engagement with users. Having managed all phases of production from raw material intake to final packing, we have witnessed both the incremental headaches and the “aha” solutions that transform a challenging chemistry into a reliable workhorse. Quality in this field means more than just analytical numbers; it requires sustained attention at every touchpoint—operations, relationships, learning from error, and implementing process tweaks that remain invisible but crucial for success in application.

    Commitment to transparency, responsiveness, and technical rigor guides our work with 4-Iodo-1-Methyl-1H-Imidazole-5-Carboxaldehyde. Projects rise or fall on small differences—trace impurities, shipment stability, or documentation gaps—and every improvement springs from our readiness to listen and adapt. With each lot shipped, we take pride not only in the chemistry but in supporting a broader network of inquiry and discovery, where details and relationships matter as much as—if not more than—quantitative performance.