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1,3-Dihydro-4-Methyl-2H-Imidazol-2-One

    • Product Name 1,3-Dihydro-4-Methyl-2H-Imidazol-2-One
    • Alias 4-Methyl-2-imidazolone
    • Einecs 219-012-2
    • 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

    705544

    Cas Number 616-47-7
    Molecular Formula C4H8N2O
    Molecular Weight 100.12 g/mol
    Iupac Name 4-methyl-1,3-dihydro-2H-imidazol-2-one
    Appearance White to off-white solid
    Melting Point 155-158 °C
    Solubility In Water Soluble
    Density 1.176 g/cm3 (calculated)
    Smiles CC1CNC(=O)N1
    Pubchem Cid 12215
    Synonyms 4-Methylimidazolidin-2-one

    As an accredited 1,3-Dihydro-4-Methyl-2H-Imidazol-2-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100 grams, labeled with chemical name, hazard warnings, CAS number, and supplier logo. Tamper-evident seal included.
    Shipping 1,3-Dihydro-4-Methyl-2H-Imidazol-2-One is typically shipped in sealed, labeled containers to prevent contamination and degradation. It should be transported in compliance with relevant chemical regulations, kept away from incompatible substances, and stored in a cool, dry place. Ensure proper documentation and safety measures during handling and transit.
    Storage 1,3-Dihydro-4-Methyl-2H-Imidazol-2-One should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture, heat, and direct sunlight. Use appropriate chemical storage cabinets, and ensure the area is clearly labeled. Handle using proper personal protective equipment to avoid exposure.
    Application of 1,3-Dihydro-4-Methyl-2H-Imidazol-2-One

    Applications of 1,3-Dihydro-4-Methyl-2H-Imidazol-2-One in Industrial Manufacturing

    As a chemical raw material manufacturer, we supply high-purity 1,3-dihydro-4-methyl-2H-imidazol-2-one for critical roles in several industrial downstream sectors. The material finds established applications in pharmaceutical synthesis, photographic chemicals, polymer intermediates, agrochemical formulations, and specialty cosmetic ingredients. Below, we detail the specific compliance context, dosage guidance, integration steps, and finished product examples unique to each segment.

    1. Pharmaceutical Intermediate for Thiazolidinedione Synthesis

    In the pharmaceutical sector, 1,3-dihydro-4-methyl-2H-imidazol-2-one serves as a key building block for thiazolidinediones, a class of antidiabetic agents. The material enters multi-stage organic syntheses involving condensation and heterocyclization, requiring strict process controls. Its purity profile and residual solvent levels impact both API yield and regulatory compliance for global markets.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredient Manufacturing
    • USP General Chapters <232>, <233> for elemental impurities
    • EDQM CEP certification for European finished drugs
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • Mol ratios: 1.0 eq per target thiazolidinedione core (typically 0.98–1.10 equivalents, adjusted for route efficiency and batch scale)

    Downstream process integration

    • Charged during early condensation with aldehydes or ketones in a sealed reactor
    • Follows strict in-process QC for residual moisture and purity
    • Intermediate undergoes further transformation before final API crystallization

    Final product types

    • Glitazone antidiabetic agents (Pioglitazone, Rosiglitazone intermediates)
    • Related thiazolidinedione derivatives for preclinical research

    2. Photographic Chemical Synthesis (Developing Agent Precursor)

    Within the photographic industry, 1,3-dihydro-4-methyl-2H-imidazol-2-one is used during the synthesis of complexing agents and reduction boosters for developer solutions. Manufacturers incorporate it for selective imidazolone ring applications, which can influence image densities and development speed in both black-and-white and color film processing. Quality parameters such as trace metal content and residual solvent impurities are monitored due to direct product interaction with sensitive film materials.

    Industry compliance standards

    • ISO 18901: Imaging materials — Processed silver-gelatin type black-and-white films
    • IEC 62321-6:2015 for hazardous substance analysis in electro-photographic products
    • Manufacturer-specific QC on photochemical precursors

    Typical usage ratio

    • Dosage: 0.5–2.2% by weight in concentrate developer formulations; optimization based on desired reduction potential and grain structure

    Downstream process integration

    • Dissolved in solvent blend at controlled temperature, prior to the addition of core developer salts
    • Precursor monitored for full dissolution and lack of particulates
    • Supports further functionalization for advanced developer types

    Final product types

    • Black-and-white film and paper developers
    • Color negative bath additives (auxiliary agents)
    • Specialty high-contrast imaging chemicals

    3. Polymerization Intermediate for Specialty Polyamides

    Specialty polymer manufacturers use this raw material as a block unit in the production of imidazolone-functionalized polyamides. It enables incorporation of nitrogen-bearing heterocycles, which confer unique mechanical properties and increased chemical resistance in engineering plastics. Raw material quality, including low monomeric residue and narrow molecular weight distribution, ensures target performance in high-spec downstream applications.

    Industry compliance standards

    • ISO 9001:2015 for polymer production quality management
    • FDA 21 CFR 177.1500 for plastics used in food-contact articles (where applicable)
    • REACH registration for raw monomers and intermediates in Europe

    Typical usage ratio

    • 5–20 mol% incorporation relative to co-monomer feed; actual ratio adjusted for targeted material properties (tensile strength, thermal stability)

    Downstream process integration

    • Blended into polyamide synthesis reactor with diamines and diacids
    • Charged under nitrogen to minimize oxidation during polymer growth
    • Quality verified by NMR and GPC prior to extrusion or pelletizing

    Final product types

    • High-performance polyamides for automotive and electronics parts
    • Specialty fibers for industrial filtration and textile reinforcement

    4. Agrochemical Intermediate in Heterocyclic Fungicide Synthesis

    Agrochemical producers employ this compound in the synthesis of imidazolone-based fungicides and plant growth regulators. Its reactivity profile makes it suitable for coupling with a variety of aromatic and aliphatic precursors under controlled conditions. The production environment follows robust crop protection safety protocols, with trace analysis for persistent organic pollutants and regulatory pesticide standards.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials
    • ISO 9001:2015 for agrochemical production
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • US EPA 40 CFR Part 180 for residue tolerance on food crops

    Typical usage ratio

    • 0.7–1.5 eq per fungicide active intermediate; adaptation based on specific crop targets and synthetic yield

    Downstream process integration

    • Enters condensation or cyclization step in multi-stage synthesis
    • Material purity supports selectivity and minimizes byproduct formation
    • Intermediate proceeds to formulation after hydrolysis and purification

    Final product types

    • Imidazolone-based fungicide actives
    • Precursor substances for plant growth regulators

    5. Cosmetic Intermediate for Hair Dye and Colorant Formulation

    In personal care manufacturing, formulators use this material during the synthesis of advanced oxidative hair dye colorants. The heterocyclic structure participates in the formation of chromophore precursors, impacting shade brightness and colorfastness. Cosmetic compliance requirements and batch traceability necessitate low residual amine and free impurity content, especially for Europe and North American markets.

    Industry compliance standards

    • EU Regulation (EC) No 1223/2009 for cosmetic product safety
    • Cosmetic Ingredient Review (CIR) assessment
    • Japanese Standards of Quasi-drug Ingredients (JSQI) for hair dye raw materials

    Typical usage ratio

    • 0.3–1.8% in oxidative dye precursor charge; proportion modulated according to desired shade intensity and stability

    Downstream process integration

    • Added to dye precursor reaction with selected aromatic amines
    • Monitored for full conversion using in-process HPLC
    • Reaction mass filtered and neutralized prior to downstream blending

    Final product types

    • Permanent and semi-permanent hair dyes
    • Specialty color enhancer additives for salon use
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    Certification & Compliance
    More Introduction

    1,3-Dihydro-4-Methyl-2H-Imidazol-2-One: A Closer Look at a Key Intermediate

    Decades of hands-on experience with heterocycles have taught our team that details matter—small substitutions and process techniques can set one compound apart from another, even in a family as well-studied as imidazolones. Among the imidazolones we manufacture, 1,3-Dihydro-4-Methyl-2H-Imidazol-2-One holds a distinct position for several reasons that have proven themselves on both the production floor and in our partners’ final applications.

    Understanding the Compound

    1,3-Dihydro-4-Methyl-2H-Imidazol-2-One steps away from the generic imidazolone structure by carrying a methyl group at the 4-position of the ring. This change might look modest from the outside, yet it alters more than just its chemistry textbooks listing. Over years of practical synthesis, we have found that this particular substitution influences both reactivity and stability in downstream reactions, opening up new possibilities for custom synthesis requests where other imidazolones fall short.

    Our team produces this material in several grades, suitable for both research-scale and commercial batch runs. We follow strict process control from starting material to final purification, ensuring the reproducibility crucial for advanced development programs. The process control also affects physical characteristics: consistent particle morphology aids in subsequent handling, and absence of colored impurities speaks to careful distillation and drying routines. Our standard offering maintains purity levels above 98%, but we support custom purification schemes for highly sensitive applications where byproducts from ring construction, including possible trace secondary amines, must be definitively excluded.

    Where the Methyl Group Makes a Difference

    Through hundreds of syntheses and analytical runs, the 4-methyl modification has shown two key effects. For one, it shields the ring system slightly from nucleophilic attack, which becomes important for chemists designing stepwise assembly of pharmaceuticals, specialty chemicals, or polymer additives. In some oxidation states or amidation schemes, this added persistence under various conditions allows for higher process yields without excessive overreaction or ring opening. Our direct customers often remark that upstream imidazolone intermediates without this group require extra care during scale-up, including additional inerting, slower feed rates, or stabilizers—steps that can be side-stepped here. On the other hand, the methylation tweaks both boiling point and solubility. Our product dissolves easily in a range of polar aprotic solvents, which aids purification and end-use formulation. Some clients find it permits cleaner isolation of desired products downstream, whether incorporating this intermediate into APIs or complex monomers.

    Applications and Real-World Value

    Over the years, we have shipped 1,3-Dihydro-4-Methyl-2H-Imidazol-2-One to a wide range of development labs and full-scale plants. In pharmaceutical synthesis, it appears in routes to beta-lactam scaffolds and in certain enzyme inhibitor programs. In textile chemistry, it helps build reactive dye structures known for superior wash resistance and shade control. In agrochemical development, it can serve as a building block for cyclic ureas and related functionalities found in crop protection agents. Some research customers also use it as a ligand precursor for coordination compounds or catalytic materials, capitalizing on the ring’s nitrogen atoms to chelate metals. As experienced chemical producers, we keep a close eye on consistency between batches—a crucial factor when the performance in a catalyst or a dye relies on nothing more than molecular structure and purity. Our long-term customers know that process reproducibility translates directly to repeatable results in their own labs and plants.

    Unlike some generic imidazolones, this molecule exhibits a distinctive melting range, allowing for separation methods that avoid extremes of temperature or solvent polarity. That’s a subtle benefit but can mean the difference between a workable and an unworkable isolation protocol, especially at kilo scales. Drawing on years of customer feedback, we have tweaked crystallization solvents, drying protocols, and even packing particle size, knowing these small changes can affect everything from filter speed to downstream blending.

    Why Direct Production Matters

    There’s a lot said about supply chain transparency these days, but nothing beats direct control over synthesis. We design our route from simple glycine derivatives, running ring closure reactions under controlled conditions to minimize byproduct formation. Using our own raw materials gives insight into trace impurity profiles and ensures we can preemptively address potential cross-contamination from related amines or aldehydes. It also allows us to scale cleanly from pilot up to commercial quantities without risking variations in performance.

    Having our own plant means we can collect and analyze every fraction, whether distillate, cake, or side-product, and adapt rapidly when faced with process deviations. If a customer requires changes—such as retained solvent, tighter particle control, or alternate packaging—we integrate these at the source, saving weeks of delay by sidestepping the indirect communication common when only working through traders or brokers. Feedback from one customer improves process parameters for the next, a cycle that drives incremental gains in both purity and operational safety.

    Comparing with Related Imidazolone Products

    In routine work, questions often come up about the differences between 1,3-Dihydro-4-Methyl-2H-Imidazol-2-One and its less-substituted or differently-substituted siblings. Even though structural analogues such as the unsubstituted 2H-imidazol-2-one or other alkyl-substituted versions might all appear as fine powders or crystalline masses, small variances dictate their reactivity, solubility, and stability. Our hands-on process knowledge and dedicated analytical staff help match each grade to its intended use. For instance, the parent 2H-imidazol-2-one shows higher baseline reactivity and broader solubility, making it suitable for routes where subsequent modifications target the ring itself. Yet that same reactivity can cause it to degrade earlier under strong bases or oxidants—something process chemists tackle daily.

    The methyl analog we offer here provides a balance between persistence and reactivity. Our clients confirm that, during scale-up, the product’s single-point substitution gives better tolerance of temperature swings and chemical exposure, which saves on utility costs, reduces solvent changes, and simply keeps the operation running smoothly. Some alternative routes or suppliers trim costs by relaxing specs, but we have found that fine-targeted specifications, from water content to trace residuals, have saved downstream users time and resources—especially where a failed reaction run would mean days or weeks lost for a batch restart.

    Handling and shelf-life also differ meaningfully. While some imidazolone derivatives degrade in inconsistent temperature and humidity, our batch stability testing across real field conditions has demonstrated that careful sealing and low residual solvent extend shelf life. For specialty chemical producers, this means lower storage losses, reduced disposal costs, and more reliable warehousing. In our experience, the seemingly minor excess costs of slightly improved packing and in-house blending pale next to the expenses and logistical headaches of product recalls or delayed formulations.

    Production Realities and Process Know-How

    Not every batch is identical, nor is every reaction straightforward. Process upsets can spell disaster for product consistency and regulatory reliability; our production engineers have learned to watch the small details, like adjusting agitation rates or switching the quench sequence to limit foam or emulsions. Each cycle offers a chance to learn something new: the effect of humidity on solidification, or the consequences of overfiltration leading to product loss. These are the hard-won process insights that only accrue through direct manufacturing experience.

    Raw material markets for our input chemicals can fluctuate, as seen in recent years. We address this reality by holding strategic buffers of critical precursors and working closely with upstream partners for quality guarantees. Over the long haul, this approach keeps lead times within customer expectations, even when utility costs or energy crises suddenly strike the broader supply chain. Throughout it all, direct access to plant data—reaction time, pressure records, impurity fingerprints—lets us make fact-based adjustments that maintain product quality from batch to batch and year to year.

    Analytical support also matters: in our labs, every batch receives full identity and purity confirmation using both spectroscopy and chromatography. If a client requires coherence with their own in-house test methods, we work with their teams to validate transfer protocols or parallel method development. This collaborative, hands-on approach helps prevent costly missteps during regulatory filing or customer approval processes. Because many of our customers run development projects with rigid milestones, process security from direct and traceable supply is non-negotiable.

    Meeting Evolving Application Needs

    Industries move fast, and end uses for 1,3-Dihydro-4-Methyl-2H-Imidazol-2-One continue to expand. Our research partners have published on new applications ranging from cross-linked resins to advanced sensors and fine-tuned polymer networks. For each emerging use, application-specific demands surface—tighter color control for dyes, smaller particle size for inkjet systems, or higher assay standards for electronic chemical precursors. As a manufacturer, we invest not only in capacity but also in process upgrades and technical support that anticipate rather than react to these evolving expectations.

    We’ve witnessed the pitfalls of chasing only large volume sales; our selective approach means fewer grade variations but greater control. Custom synthesis projects come with their challenges, but nothing beats hands-on engagement in working out the quirks of a new crystallization or downstream purification method. By keeping our core process stable, it becomes much simpler to extend parameters for specialty work—whether that means isolating a metastable polymorph for a pilot project or packaging ultra-dry product for a sensitive solid-state synthesis.

    What stands out after dozens of these collaborations is that robust, transparent communication between manufacturer and user yields the most reliable and cost-effective outcomes. We regularly schedule plant tours, quarterly data reviews, and roundtable testing sessions. This feedback loop often uncovers overlooked needs—maybe a new purity marker that signals potential degradation, or an adjustment in physical form that improves all downstream handling. Our practitioners on the shop floor and analytical teams in the lab keep the learning curve steep and ensure current best practices flow directly back into our process controls.

    Looking Ahead: Risks, Solutions, and Opportunities

    Even as demand for specialty building blocks like 1,3-Dihydro-4-Methyl-2H-Imidazol-2-One grows, industry faces pressures—regulatory change, pressure for greener manufacturing, and intricacies of maintaining consistent output across global supply chains. Our commitment means regular investments in emission controls, solvent recycling facilities, and closed-vent reaction systems. Beyond compliance, these upgrades reduce variable costs over the product’s lifetime and help clients meet their own sustainability mandates. The path isn’t always easy, but adaptation pays dividends in operational resilience.

    One challenge that continues to surface involves balancing inventory risk with customer flexibility. Procurement timelines can shift unexpectedly, with surges or lulls making forecasting difficult. To address this, we keep a flexible production schedule, run smaller campaign lots, and coordinate drop-shipping for international clients. Feedback from end-users has shown that the ability to ship product tailored to evolving application grades or package sizes can be just as decisive as a sharp price point or paperwork turnaround.

    Constant customer engagement also brings opportunities. As new research identifies uses for our methylated imidazolone in fields as diverse as biomedical diagnostics, polymer composites, or battery technology, our technical staff tracks emerging synthesis methods and downstream effects. Organic electronics, for example, have pushed us to refine our isolation protocols and particle distribution characteristics, while new environmental requirements ensure that our effluent streams meet both local and international standards.

    Trust Built From the Ground Up

    Having led a vertically integrated production site for many years, we know that a product like 1,3-Dihydro-4-Methyl-2H-Imidazol-2-One is more than just a chemical compound. Behind every specification sheet lies the cumulative experience of hundreds of small process decisions: how fast to cool the reactor, the best filter to use for a particular batch, when to switch a solvent to protect both yield and purity. Our continued success depends on attention to those specifics and a willingness to adapt them as customer needs change.

    Ultimately, reliability is what matters most. For partners scaling up new pharmaceutical payloads, dye formulations, or specialty chemical synthesis, knowing where every molecule comes from—and how the next batch will compare—brings peace of mind and lets them focus on innovation. Through direct production, strong analytical capability, and persistent two-way communication, we aim to offer more than just a chemical intermediate. Our goal is to deliver assurance, technical insight, and a shared commitment to advancing new applications.

    For any development team that depends on consistency, technical problem-solving, and real-world adaptability, 1,3-Dihydro-4-Methyl-2H-Imidazol-2-One offers not just a molecular solution, but a direct bridge between laboratory imagination and manufacturable reality.