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1-Methyl-1H-Imidazole-5-Carboxaldehyde

    • Product Name 1-Methyl-1H-Imidazole-5-Carboxaldehyde
    • Alias 1-Methylimidazole-5-carboxaldehyde
    • Einecs 685-427-8
    • 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

    172526

    Chemicalname 1-Methyl-1H-Imidazole-5-Carboxaldehyde
    Casnumber 223781-28-8
    Molecularformula C5H6N2O
    Molecularweight 110.12
    Appearance Light yellow to yellow powder
    Meltingpoint 74-78°C
    Solubility Soluble in polar solvents such as DMSO and methanol
    Purity Typically ≥98%
    Smiles Cn1cncc1C=O
    Inchi InChI=1S/C5H6N2O/c1-7-3-6-2-5(7)4-8/h2-4H,1H3
    Synonyms 1-Methylimidazole-5-carbaldehyde
    Storageconditions Store at 2-8°C, protected from light and moisture

    As an accredited 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 containing 25 grams of 1-Methyl-1H-Imidazole-5-Carboxaldehyde, tightly sealed, with hazard and identification labeling.
    Shipping 1-Methyl-1H-Imidazole-5-Carboxaldehyde is shipped in tightly sealed containers, protected from moisture and light. It should be handled by trained personnel, following all regulatory guidelines for chemical transport. Ensure the material is properly labeled and packaged to prevent leaks or spills during transit. Shipping is usually via ground or air, depending on regulations.
    Storage 1-Methyl-1H-Imidazole-5-carboxaldehyde should be stored in a tightly sealed container, away from light, moisture, and incompatible materials such as strong oxidizers. Keep it in a cool, dry, well-ventilated area, preferably in a chemical storage cabinet. Properly label the container and avoid exposure to heat or direct sunlight. Always follow local regulations and safety procedures when handling and storing this compound.
    Application of 1-Methyl-1H-Imidazole-5-Carboxaldehyde

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

    1-Methyl-1H-imidazole-5-carboxaldehyde serves as a specialized intermediate relied upon by manufacturers in several technology-driven sectors. Our direct supply ensures traceability for regulated supply chains and accurate integration into certified downstream production environments. Below we outline established industrial application scenarios, detailing the compliance standards, additive ratios, process entry points, and precise categories of final products into which this molecule is incorporated.

    1. Active Pharmaceutical Ingredient (API) Intermediates

    Pharmaceutical synthesis chains often utilize this compound during the preparation of certain heterocyclic API intermediates where strict impurity profiles and traceability are crucial. Manufacturers rely on certified quality and high-purity lot release when integrating it into building blocks such as highly functionalized imidazole core molecules. Adaptability to batch synthesis under GMP protocols supports its role in recipes for oncology, anti-infective, or central nervous system (CNS) candidate molecules.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II API regulations
    • 21 CFR Part 211 cGMP (FDA)
    • USP/EP monographs for final APIs, traceability in DMF submissions

    Typical usage ratio

    • Usually 0.5–3 molar equivalents as a key intermediate in multi-step synthesis; exact amount tailored to route optimization and yield balancing.

    Downstream process integration

    • Introduced at the cyclization or formylation step of heterocyclic compound assembly; dissolved in solvent phase before coupling, frequently purified in situ via chromatography or crystallization before proceeding to the next synthetic transformation.

    Final product types

    • Intermediates for imidazole-derived APIs including antifungal, anti-arrhythmic, or neurological drug substances
    • Fine chemicals prepared for further contract manufacturing in regulated pharma pipelines

    2. Advanced Agrochemical Intermediate Synthesis

    Crop protection actives with imidazole scaffolds depend on tightly controlled intermediates during their synthetic routes. Using this molecule, downstream plants streamline the formylation of functional aromatic rings, enhancing selectivity in heterocycle assembly for fungicide and insecticide formulations. Agrochemical technical-grade production plants implement this raw material for the development of both active ingredient precursors and several formulation side chains.

    Industry compliance standards

    • FAO/WHO agrochemical specification guidelines
    • OECD Principles of GLP for test item production
    • ISO 9001:2015 (process quality assurance in agrochemical plants)
    • REACH Registration (applicable for import to EU market)

    Typical usage ratio

    • Typical addition 2–5% w/w in intermediate synthesis steps; adjusted according to target molecule and reaction stoichiometry.

    Downstream process integration

    • Fed into closed reactors at the imidazole ring formylation or N-methyl functionalization stage; typically followed by purification and condensation with other heterocycles before formulation into technical concentrate.

    Final product types

    • Advanced intermediates for strobilurin and triazole-class fungicides
    • Precursors for imidazole-based insecticides
    • Herbicide technical actives containing imidazole frameworks

    3. Electronic Chemicals for Functional Material Synthesis

    This fine chemical increasingly finds use within the electronics industry as a precursor for the synthesis of conductive imidazole-based resins and advanced functional polymers. Manufacturers leverage the aldehyde functionality for selective crosslinking and backbone modification, targeting improved charge transfer and thermal stability needed in printed circuit boards and flexible electronics. For such applications, consistent purity and ultra-low metal content provide value in downstream production and contamination-sensitive processing.

    Industry compliance standards

    • IPC-4101/126 (laminate and prepreg base material specifications)
    • RoHS Directive 2011/65/EU (restriction of hazardous substances in electronics)
    • ISO 14001 (environmental management with respect to chemical use)

    Typical usage ratio

    • Ranging from 1–8% weight of resin precursor batch, adjusted for target polymer network density and end-performance requirements.

    Downstream process integration

    • Integrated into pre-polymerization mix during resin synthesis to introduce imidazole functionality; reacted via controlled heating and catalyst systems, with post-cure crosslinking step before final shaping or film casting.

    Final product types

    • High-performance imidazole-epoxy resins for multilayer printed circuit boards
    • Compounds used in electronic adhesives with enhanced dielectric properties
    • Conductive polymer coatings for flexible devices and sensors

    4. Specialty Dye and Pigment Intermediate Production

    Industrial dye and pigment suppliers employ this compound as a targeted formyl source in the construction of imidazole-based chromophores. Its structural features promote controlled functionalization during the assembly of colorant molecules, providing enhanced color fastness and improved solubility in end-use textile and inkjet formulations. Controlled batch integration supports tight shade reproducibility in downstream processing.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (textile dye chemical input standards)
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) guidance
    • ISO 9001:2015 QC in synthetic dye production

    Typical usage ratio

    • Inserted at 1–7 mol% of chromophore assembly mixture; dosage guided by chromogenic group density and purity specifications of the colorant.

    Downstream process integration

    • Added during initial aromatic aldehyde condensation steps; processed via multi-stage reactions and purified by recrystallization or solvent extraction prior to formulation or application testing.

    Final product types

    • Textile reactive dyes based on imidazole chromophores
    • Specialty pigments for digital inkjet printing
    • High-stability industrial colorants for coatings and plastics
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    Certification & Compliance
    More Introduction

    1-Methyl-1H-Imidazole-5-Carboxaldehyde – An Everyday Essential in Modern Synthesis

    Redefining Specialty Chemical Building Blocks

    Over the last decade, research labs and industrial producers have challenged chemical manufacturers to keep up with fast-changing trends in active pharmaceutical ingredients, specialty monomers, and custom solutions. Having worked shoulder-to-shoulder with R&D teams across continents, we notice one recurring theme: success often starts with the careful choice of building blocks. 1-Methyl-1H-imidazole-5-carboxaldehyde stands out for chemists seeking reliability and consistency in their synthetic work.

    Our Insights on Production

    We manufacture 1-methyl-1H-imidazole-5-carboxaldehyde from raw precursors using an optimized process involving controlled formylation of methylimidazole. This technology allows us to deliver precise batches with a strictly monitored methyl substitution at the 1-position and targeted aldehyde group at the 5-position. Years of running these reactions taught us that many downstream reactions—condensations, coupling, or even functional group modifications—depend on having the exact substitution pattern in place, with minimal isomer or over-reaction impurities. Our own teams have run thousands of kilo-scale reactions, watching for subtle changes in parameters that could affect purity or yield. We take extra care in drying protocols and solvent controls, practices informed not by theory, but by endless hours in the plant. Each detail in the process matters more than any abstract assurance of quality.

    Specifications – Our Approach to Purity

    On our shop floor, purity isn’t just a marketing line—it is something you can see, smell, and measure. Each lot of our 1-methyl-1H-imidazole-5-carboxaldehyde is brought to a minimum purity of 98%, as determined by HPLC and NMR. Our team performs rigorous checks for water, common byproducts, and trace solvents before any liter leaves our facility. Over time, we have collected feedback from analytical departments that found even tiny levels of non-specific aldehydes or unreacted starting material could undermine their target reactions. Thus material from our reactors reaches the glassware of scientists in a state fit for sensitive transformations: light yellow crystals with low water content, minimal color change on standing, and reliable retention times across batches. We’ve avoided the temptation to push for marginal cost savings that compromise these traits, having received a few horror stories from clients who tried alternate suppliers.

    Performance in Application – Learning by Experience

    We are often asked why chemists keep coming back to this particular aldehyde. Our take comes straight from seeing its use in house: 1-methyl-1H-imidazole-5-carboxaldehyde enables smooth formation of imine and hydrazone linkages. It sneaks its way into nucleoside analogues, custom heterocyclic scaffolds, and drug candidates, particularly in settings where regioselectivity can’t be left to chance. Its unique methyl group at position-1 gives rise to a chemical behavior that our customers value: increased resistance to oxidative ring cleavage and higher solubility in many polar organic solvents. In contrast, the unsubstituted 1H-imidazole-5-carboxaldehyde or the 2-substituted analogues often fall short, either due to instability or low melting points, leading to headaches during isolation or handling.

    Customers who synthesize advanced intermediates often call us after trying carboxaldehydes from generic sources. We hear about aldehyde batches that arrive packed with moisture, unstable isomers, or off-odors. Working closely with formulators who build new ligands for catalysis, we have seen how even tiny inconsistencies in ring substitution affect subsequent metalation or cross-coupling. Robust, methyl-protected imidazole rings cut these variables down to almost nothing. To top it off, with our process, each specification is confirmed batch to batch, sparing chemists any unpleasant surprises during scale-up.

    Differentiation in Synthetic Strategy

    Many commercial imidazole-5-carboxaldehydes can seem interchangeable on paper. In our day-to-day reality, small differences ripple out. Introducing the methyl group at position-1 helps block unwanted side reactions at the nitrogen, allows more controlled condensation with nucleophiles, and shifts electron density across the ring. Colleagues focused on medicinal chemistry appreciate the way this N-alkylation shields unwanted metabolic pathways in biological testing. If your route calls for a building block that holds up in harsh conditions or in water-sensitive domains, this material is far from generic.

    We have watched teams attempt to substitute the unprotected imidazole parent, chasing lower purchase prices, only to deal with reactivity that derails scale-up. More than once, projects stalled due to unexpected byproduct loads or ambiguous NMR traces. Through years spent troubleshooting alongside clients, a repeated outcome emerges: when the methyl group is missing or misplaced, even minor, the cost of failed syntheses and lost time wipes out any imagined savings. We keep these lessons front and center, documenting each performance characteristic batch-by-batch, offering real references instead of just a generic datasheet.

    Safety by Design, Not by Accident

    Handling sensitive aldehydes comes with its own set of challenges—stability, airborne emissions, and the tendency toward rapid resinification in the presence of trace moisture or acids. Our plant crews have learned to turn these risks into recurring best practices. We store finished product under nitrogen, select containers proven to withstand long storage, and run shelf-life tests to validate our claims. Our QA team tracks stability with ongoing analytics, so every gram delivered matches the sample we sent for evaluation, even after months in transit. End-users notice the difference: less discoloration, fewer stability complaints, and no need to scramble for last-minute purification.

    These little tweaks—tight moisture control, sealed drums, stored away from air—sound simple, but anyone who has ever walked through a plant after a spill or spoiled batch knows why these steps matter. Customer after customer gives the feedback: our 1-methyl-1H-imidazole-5-carboxaldehyde keeps well on the shelf, sparing scientists from scrambling for backup when a deadline approaches. Our lab has made its share of mistakes in the past; through those, we built a system that tackles these issues head-on.

    Consistent Support for Specialty Synthesis

    Beyond pharmaceuticals, 1-methyl-1H-imidazole-5-carboxaldehyde draws interest from pigment designers, material scientists, and agrochemical innovators. The chemistry community often experiments with imidazole derivatives for developing corrosion inhibitors, antistatic agents, or even as specialty ligands in coordination chemistry. Projects from across the world call for a compound that won’t throw off their controls or behave differently when scaled—from milligrams to multi-kilograms. Our process locks down not just the substitution pattern but also the impurity profile. We document the presence of trace impurities and residual solvents, providing transparency that supports regulatory filings and academic publication.

    Material scientists at advanced coatings labs explained how poorly purified derivatives once created trouble with batch reproducibility and physical film properties. They noted improvements in curing and end-use stability since switching over to lots produced under our strict guidelines. When you can count on a building block to act the same across hundreds of syntheses, you save much more than just time—you protect the integrity of your research.

    Learning from Customer Challenges

    Maintaining a dialogue with end-users has reshaped our approach. We regularly receive feedback on reaction timelines, process bottlenecks, and downstream challenges. An example: a custom synthesis group working on fluorescent probes found that switching to “cheaper” imidazole aldehydes from generic suppliers led to detectable background signals in their final analytical work. Upon switching back to our batches, they found background fluorescence nearly disappeared, allowing credible data generation again. These sorts of lessons push us to never let up on batch documentation or supply chain controls.

    For producers scaling up to GMP or full commercial status, the stakes climb further. Our teams provide transparent batch histories and archived analytical data, helping customers satisfy regulatory questions and batch-release protocols. Several multinationals shared how audits run more smoothly when product data and impurity records trace back to producer-level documentation, not just a secondary warehouse or reseller.

    Environmental Insights and Process Responsibility

    Operating as a direct manufacturer means facing the impacts of solvent management, emissions, and byproduct disposal head-on. We designed our plant to minimize waste generation, filtering and reclaiming solvents wherever possible. Our formylation chemistry operates at moderate temperatures, limiting energy consumption compared to older high-temperature routes. We review waste output batch by batch and continuously invest in recovery systems aimed at reducing both emissions and hazardous waste shipments. These investments are more than box-checking; every kilogram saved from landfill or incinerator makes the job easier for those in compliance and planning. Clients with strict ESG targets increasingly ask for this information, looking for chemical partners accountable throughout the lifecycle.

    We source raw materials from long-standing partners, track raw batch certification, and document every adjustment made to the process. Our teams know there’s no shortcut around careful batch disposition and transparent yields. Environmental stewardship looks different up close—we see opportunities to improve water consumption and optimize batch scheduling for lower peak loads. Over the years, we invested in continuous training for our technician teams, prioritizing both safety and reduced resource consumption. That commitment translates into every liter we produce.

    Supporting Innovative Chemistry

    Many of our product’s applications didn’t exist only five years ago. Scientists in DNA-encoded library construction, metal-organic framework synthesis, and targeted drug discovery have each written us, describing new uses for 1-methyl-1H-imidazole-5-carboxaldehyde. In these cases, the compound’s careful methylation and pure aldehyde function create new possibilities—building blocks for complex architectures, not prone to rearrangement or unwanted polymerization.

    In complex multistep syntheses, each intermediate has to stand up to diverse reagents, reaction conditions, and purification protocols. Our experience watching scaled reactions in pilot plants reminded us that even tiny quality slips magnify as batches scale from test tube to reactor. Our staff supports customers with technical documentation, suggesting optimal storage, handling, and protocols tuned to their exact process. Collecting this feedback, we improved labeling, humidity-resistant packaging, and even introduced batch-specific technical summaries, tailored to the way chemists actually work in labs and plants.

    Why It Makes a Difference

    For many synthetic chemists, the project begins with a seemingly simple step—choose an aldehyde, weigh it, add it to the flask. In practice, that initial choice sets off a cascade of downstream results. Having observed both successful and failed reactions firsthand across countless projects, we understand why our end-users keep returning to this product line. Their trust validates our investment in real-world quality and partnership.

    Pharmaceutical project leads point to this product as a rare example of a building block that bridges early discovery and advanced API development. They rely on its clear NMR spectra, single-peak HPLC traces, and robust shelf life. QC managers from Asia to Europe have contacted our team to ask for new documentation or support in ever-changing compliance climates—and we have the records ready, built up over years of meticulous logging.

    Academic teams share the pressure of publication deadlines and funding cycles with us, seeking a supplier who doesn’t just drop off a package and leave. We’ve worked behind the scenes, troubleshooting a synthesis gone awry or solving a purification snag, knowing that each challenge solved together strengthens our own process. New routes for custom ligands, functionalized polymers, or imaging probes have come out of those collaborations.

    Value Built on Experience, Not Hype

    Too often, chemical procurement looks like a race to the bottom—a chase for the lowest cost without considering what gets lost along the way. Years of resolving real-world issues taught us how minor details in synthesis, packaging, or documentation become major determinants of productivity, reproducibility, and good science.

    We maintain close ties with both innovators and process engineers. Over time, end-users’ evolving needs have shaped our approach just as much as what goes into the reactor. Whether it’s trialing smaller pack sizes for startups or investing in stability studies for large pharmaceutical customers, the underlying theme remains the same: deliver what chemists truly use, not just what’s listed in the catalog.

    The Path Forward — Listening, Learning, Delivering

    Every kilo of 1-methyl-1H-imidazole-5-carboxaldehyde reflects years of refining process and support. It symbolizes long hours fixing process hiccups, redoing test batches, and analyzing where things could have gone wrong. These experiences keep us grounded in the demands of real chemistry. Looking ahead, we see opportunities to further shrink impurity loads, optimize waste streams, and listen to the chemists who find new uses for imidazole derivatives each year. Tomorrow’s innovations come from today’s diligence. Chemistry may start with molecules, but success comes from commitment to every step in the journey—from our reactor to your results.