Products

1,3-Dimethyl-2-Imidazolidinone

    • Product Name: 1,3-Dimethyl-2-Imidazolidinone
    • Alias: DMI
    • Einecs: 210-199-3
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: sales3@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    846450

    Chemical Name 1,3-Dimethyl-2-Imidazolidinone
    Cas Number 80-73-9
    Molecular Formula C5H10N2O
    Molecular Weight 114.15 g/mol
    Appearance Colorless liquid
    Boiling Point 225-226°C
    Melting Point 7-9°C
    Density 1.034 g/cm³ at 25°C
    Solubility In Water Miscible
    Flash Point 123°C
    Refractive Index 1.454 at 20°C

    As an accredited 1,3-Dimethyl-2-Imidazolidinone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g of 1,3-Dimethyl-2-Imidazolidinone is packaged in a sealed amber glass bottle with a tamper-evident screw cap.
    Shipping **1,3-Dimethyl-2-Imidazolidinone** (DMI) should be shipped in tightly sealed containers made of compatible materials. Store and transport in a cool, dry, and well-ventilated area away from heat, sparks, and incompatible substances. Ensure all packaging is clearly labeled according to relevant regulations. Handle with care to prevent leaks or spills.
    Storage 1,3-Dimethyl-2-imidazolidinone (DMI) should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from heat, sparks, and open flames. Keep it away from incompatible materials such as strong oxidizers and acids. Store at room temperature and protect from moisture. Ensure containers are properly labeled and follow all relevant safety regulations.
    Application of 1,3-Dimethyl-2-Imidazolidinone

    Purity 99%: 1,3-Dimethyl-2-Imidazolidinone with purity 99% is used in pharmaceutical synthesis processes, where it ensures high reaction yield and minimal impurities.

    Boiling Point 225°C: 1,3-Dimethyl-2-Imidazolidinone with boiling point 225°C is used in high-temperature polymerizations, where it maintains solvent integrity and prevents decomposition.

    Low Water Content: 1,3-Dimethyl-2-Imidazolidinone with low water content is used in lithium battery electrolyte formulations, where it enhances ionic conductivity and stability.

    Molecular Weight 114.15 g/mol: 1,3-Dimethyl-2-Imidazolidinone with molecular weight 114.15 g/mol is used in agrochemical formulations, where it improves solubility of active ingredients.

    Melting Point 7°C: 1,3-Dimethyl-2-Imidazolidinone with melting point 7°C is used in peptide synthesis, where it facilitates efficient coupling reactions at room temperature.

    Stability Temperature 150°C: 1,3-Dimethyl-2-Imidazolidinone with stability up to 150°C is used in specialty coatings manufacturing, where it prevents thermal degradation of additives.

    Viscosity 1.3 mPa·s: 1,3-Dimethyl-2-Imidazolidinone with viscosity 1.3 mPa·s is used in ink formulation, where it enables smooth flow and consistent print quality.

    Low Residual Amines: 1,3-Dimethyl-2-Imidazolidinone with low residual amines is used in electronics cleaning applications, where it reduces surface contamination and improves device reliability.

    Optical Clarity: 1,3-Dimethyl-2-Imidazolidinone with high optical clarity is used in optical fiber coating processes, where it ensures minimal light scattering and high transmission efficiency.

    Low Volatility: 1,3-Dimethyl-2-Imidazolidinone with low volatility is used in separation science as an HPLC solvent, where it minimizes solvent loss and maintains consistent elution profiles.

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    Certification & Compliance
    More Introduction

    1,3-Dimethyl-2-Imidazolidinone: A Closer Look at a Unique Solvent

    Understanding 1,3-Dimethyl-2-Imidazolidinone

    1,3-Dimethyl-2-Imidazolidinone, or DMI for short, doesn’t usually show up in household conversations, yet those who spend their days at the bench or in industrial labs know this chemical as a bit of a workhorse. With its clear, nearly odorless character and high boiling point, people in chemical processing, pharmaceuticals, electronics, and plastics have come to rely on DMI for a set of properties that aren’t easy to find packed into one molecule.

    It isn’t just about what DMI is. It’s about why it has become the solvent of choice for many tough jobs. In synthesis, certain reactions need a strong, polar environment to really get going, and DMI steps up where others fail. As someone who’s tackled finicky nucleophilic reactions, I’ve watched DMI dissolve substrates that sat stubbornly undissolved in DMF or NMP. This chemical’s ability to break down barriers comes from its structure: the imidazolidinone ring brings stability, while the methyl groups change the way the solvent interacts with water and organics alike. The result is a liquid that supports efficient mixing of substances that don’t usually play well together.

    Molecular Structure and Why It Matters

    The model for DMI is simple in concept but powerful in effect. Two methyl groups sit on the ring opposite the carbonyl, shaping a molecule that resists side reactions and remains inert even under tough conditions. That means when you need to make highly substituted amides, or dig into heterocyclic chemistry, DMI doesn’t interfere—it just creates a supportive environment. Its chemical formula sits at C5H10N2O, and it melts close to 8°C but boils far above water at around 225°C. That kind of thermal range opens up possibilities where lower-boiling solvents would simply evaporate away.

    In my own work, DMI’s true strength lies in reactions run at high temperature or in situations where you just can’t have a reactive, finicky solvent. During a complex amide coupling, shifting from DMF to DMI allowed for higher yields and easier work-up. That’s not just luck—it’s grounded in solid chemical principles. Its high polarity and aprotic nature make it a partner for both polar and nonpolar reagents, so folks in the field get the most out of every gram of starting material.

    Specifications: Making Use of DMI’s Properties

    Pure DMI, used in research or manufacturing, looks like a colorless liquid. It will freeze in a cold room, but at standard lab bench temperatures it stays fluid. The density, roughly 1.03 g/cm³, clues you in that you’re not just handling water. Its high dielectric constant means it shines in situations demanding strong solvation of ionic species.

    Not every solvent can handle aggressive chemicals without breaking down or causing reactions you didn’t plan for. From my time formulating coatings for microelectronics, I’ve seen how DMI holds up against acids, bases, and oxidants. This is not a luxury—it’s essential for precise control in thin-film deposition, lithium battery electrolytes, and semiconductor processing. Its ability to wash away polar residues or facilitate uniform coatings across surfaces sets it apart from old standbys like acetone or acetonitrile.

    Industrial and Laboratory Uses

    People tend to appreciate DMI most in roles where traditional solvents start to show cracks. For example, during the manufacture of pharmaceuticals, scalable processes have to minimize impurities and maximize yield. DMI fits neatly because it rarely gives side products, and its low toxicity by comparison to DMF and NMP can have real cost-cutting and regulatory relief benefits. In NMR spectroscopy and other analytical protocols, its transparency at wide frequencies makes it suitable for a variety of nuclei, helping researchers gather information without background interference.

    In the plastics industry, DMI dissolves polymers that defeat solvents like toluene or chloroform. Polyimide and polyacrylonitrile, used in high-performance fibers and membranes, need careful handling. Switching to DMI provides better fiber spinning and more consistent membrane porosity. These aren’t just academic details. They matter in industries building lighter airplanes, more reliable medical devices, or water purification membranes with tighter controls on molecular passage.

    Comparing DMI With Other Solvents

    At first glance, DMI sits in the same basket as DMF (N,N-Dimethylformamide) and NMP (N-Methyl-2-pyrrolidone). All three dissolve many salts, organic reagents, and resins. But the practical experience has made their differences clear. Both DMF and NMP have well-documented toxicity and regulatory challenges. In European and North American settings, this gets sharper as environmental law tightens. DMI’s lower toxicity and less troubling health profile give it an edge in long-term applications and for workers' safety.

    Solubility is another point worth highlighting. DMI manages to dissolve a wider spectrum of compounds, particularly those with a stubbornly hydrophobic backbone, thanks to its polar structure that isn’t as easily disrupted. In reactions sensitive to trace water, DMI holds less inherent moisture and is easier to dry. As all who have fought to keep water out of a reaction mix know, this small detail can save an entire batch and prevent expensive troubleshooting. It stands up to heat, doesn’t give off the fishy smell that DMF fans out, and doesn’t leave behind difficult-to-remove residues.

    Health and Environmental Considerations

    Years working with multiple solvents train you to give a sharp look to both health data sheets and environmental impact. DMI comes out better than many competitors, especially DMF and NMP, neither of which would pass the stricter toxicology benchmarks moving steadily into law. Studies have placed DMI in a lower hazard tier for chronic health effects and air emissions.

    Wastewater from DMI processes can be managed through standard organic solvent treatments, reducing the need for complex remediation. Less risk to workers and the surrounding neighborhood makes it attractive for operations scaling up in populated areas. That doesn’t mean it’s without risk—no one should treat a potent solvent carelessly. Gloves, goggles, fume hoods, and responsible waste handling stay critical. Still, the balance between performance and safety moves closer to center with DMI than with older choices.

    Stories from the Field: Where DMI Makes a Difference

    During a project designing lithium-ion battery electrolytes, our group hit a wall with cycling stability. Early runs with ether-based mixtures degraded rapidly under load. Inserting DMI as a co-solvent boosted overall conductivity and prolonged battery life through relentless charge-discharge cycles. It wasn’t a silver bullet, but the improvement brought our project out of the pilot stage. In another example, a formulary for photoresist development in microchip fabrication swapped out NMP for DMI, drastically reducing worker exposure incidents and simplifying permitting with local regulators.

    Colleagues share similar stories from pharmaceutical scale-up reactors. Reactions that ran sluggishly or turned out low-grade product with standard solvents got a second wind after switching to DMI. Yields increased, clean-up steps shrank, and fixed costs dropped as the need for elaborate monitoring and waste-handling scaled back. Not every problem boils down to solvent switch, but in experience, the right solvent opens doors.

    Navigating Challenges with DMI

    No one chemical solves all the problems. DMI does have a higher purchase price compared with legacy solvents, and some companies hesitate at the sticker. For smaller laboratories, or production units tied to tight budgets, convincing decision-makers that long-term savings outweigh initial investment takes evidence and advocacy.

    Further, legislative changes could someday target DMI itself, just as regulators have moved against DMF and NMP in light of emerging toxicity data. Ongoing monitoring and environmental impact research matter to stay ahead of the rules. Entering new markets—especially exports to countries with tighter chemical import laws—may require additional paperwork or safety certifications. DMI still requires careful handling and full compliance with industrial hygiene standards.

    Having a solvent with a high boiling point sometimes becomes its own challenge. Distillation for recovery takes significant energy, and some users note higher costs for solvent recycling. Advanced distillation columns and process intensification may offset this, but it’s a factor anybody managing an industrial plant needs to keep on the table. Add to this the need for robust transportation and storage, particularly in high-volume operations challenged by seasonal temperature swings—DMI’s freezing point isn’t an afterthought.

    Opportunities: Improving Industry Practices

    DMI’s increasing popularity serves as a prompt for the wider industry. Companies developing new synthetic routes or scaling up production have a rare chance to design solvent recycling or substitution into the beginning of their work, rather than retrofitting solutions after problems arise. I’ve watched several firms use DMI as a springboard to invest in closed-loop solvent recovery, benefiting the bottom line and stepping up environmental care. Integrating energy recovery from distillation and catalysis optimization reduces both solvent loss and utility costs.

    There’s also strong momentum behind research on greener solvent blends. Universities and innovation labs keep pushing for binary or ternary solvent systems that pair DMI with bio-based solvents, aiming for the best of all worlds: strong solvation, reduced toxicity, and enhanced biodegradability. Some alternatives appear promising for select reactions, using DMI at lower total loadings by matching it to a supporting cast of less impactful co-solvents. This kind of research turns theory into concrete solutions over time.

    Future Outlook: Keeping Perspective

    Looking ahead, the real test comes not just in performance but in how DMI fits into a world waking up to safer, more sustainable chemicals. Global manufacturers now factor in greenhouse gas emissions, cradle-to-grave environmental impact, and workplace safety in their chemical choices. DMI stands as a solid answer for today’s demands. If new evidence shows risks or environmental drawbacks, the scientific community’s responsibility is to adapt fast.

    Technological progress in chemical engineering often runs into social and ecological boundaries. Workers and communities hold a bigger stake in chemical decisions than ever before. DMI’s path from niche solvent to industrial staple has leaned on its adaptability, and the future will likely see it as part of more intricate, carefully managed systems. For companies still relying on DMF, NMP, or other high-risk solvents, the clock ticks toward change. Costs in health, compliance, and reputation stack up over time.

    Getting the Most from DMI

    Successful adoption of DMI rests not just on knowing its technical edge, but on designing protocols that leverage that edge while raising safety standards. In one team, a regular review of all solvent-based processes every fiscal quarter made switching more than just a response to problems—it became a standard part of continuous improvement. Documenting small but measurable gains in worker satisfaction, waste processing, and reaction yields help build a concrete case for expanding use.

    Sharing best practices with industry networks—through conferences, open-access journals, or professional societies—spreads understanding and builds up a collective resource for future challenges. Groups creating open benchmarking data make it easier for others to weigh their own solvent choices against current evidence. Well-run operations don’t exist in isolation; the lessons learned during DMI integration today shape opportunities for safer, smarter chemistry tomorrow.

    Conclusion: The Ongoing Role of DMI

    Countless breakthroughs depend not just on brilliance or luck, but on picking the right tools—often down to the solvent in the flask. 1,3-Dimethyl-2-Imidazolidinone doesn’t promise an easy fix for every sticky situation, but in the right context, it delivers reliability, safety improvements, and technical performance that count in practice as much as on paper. Scientists, engineers, and managers making these calls rely as much on shared testimony and lived experience as on manufacturer data sheets.

    Our journey with DMI continues to inform how the next generation of chemicals will be evaluated, regulated, and improved. If there’s one takeaway, it’s that outcomes improve the more voices and perspectives get included in the conversation. DMI, for now, gives the industry a powerful option—a reminder that, done thoughtfully, the choice of solvent shapes innovation, workplace safety, and environmental responsibility in ways not always obvious on the surface.

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