1-Ethyl-2,3-Dimethylimidazolium Bis(Fluorosulfonyl)Imide: Description and Insight

What is 1-Ethyl-2,3-Dimethylimidazolium Bis(Fluorosulfonyl)Imide?

1-Ethyl-2,3-dimethylimidazolium bis(fluorosulfonyl)imide, with a molecular formula of C7H13F2N3O4S2, stands out among ionic liquids for its distinctive structure and performance. Its chemical structure includes an imidazolium ring substituted with ethyl and two methyl groups, paired with the robust bis(fluorosulfonyl)imide anion. This structure is not just for show—chemists care about it because it shapes the ionic liquid’s behavior, particularly its thermal stability and conductivity. With a molecular weight around 341.32 g/mol, every batch comes with a sense of gravitas not often found in everyday laboratory chemicals. The way the cation and anion combine shapes everything from its melting point to its resistance to oxidative breakdown.

Properties and Specifications

Chemists working in labs or industries specializing in electronics, energy storage, or advanced material design expect certain things from this material. It tends to appear transparent or faintly yellow, with densities near 1.5 g/cm³ depending on purity and temperature, usually presenting as a clear liquid at room temperature but sometimes forming crystalline solids or flakes under cooler storage conditions. Some suppliers deliver it in powder, pearl, or even solution forms, recognizing that different projects demand different approaches. Its low volatility means lower risk for inhalation, but it resists water so well that simple cleanup jobs can get complicated—try washing it away with water, and it’ll just slide off, reminding you that this isn’t your average table salt.

Chemical Structure and Molecular Detail

The imidazolium core, functionalized by the ethyl group at the N1 position and methyl groups at C2 and C3, doesn’t just look good on paper. Adding the bis(fluorosulfonyl)imide anion, a tried-and-tested workhorse in electrochemistry, gives a material tuned for ionic mobility and impressive electrochemical windows. It takes real-world handling—pale solid forms become soft crystals or even a clear liquid when warmed up. In the lab, dense texture and high viscosity in colder environments stand out. Experienced users pay attention to its reactivity with moisture and its chemical resilience. The formula gives it flexibility in several synthetic and industrial reactions, where molecular stability counts for more than fleeting appearances.

Physical Forms: Liquid, Solid, Powder, and More

You don’t get the same thing every time you order this chemical. Sometimes it comes as a thick, viscous liquid—almost syrupy in behavior—sometimes as fine crystalline flakes or even chunky pearls that rattle in their vial. These variations are not just appearances; each physical state hints at purity, handling requirements, and potential for contamination. Powders might be easier to measure, but the pearls and liquids pour more cleanly. Some researchers need the crystalline form for solid-state studies, especially when investigating phase transitions or conductivity in lithium battery electrolytes. In terms of volume, laboratories measure it in liters for solution work, while grams or kilograms suit those using it as a raw material. Whatever the form, expect that distinctive weight in the hand and resistance to evaporation.

Material Uses and Handling

This isn’t your friendliest household chemical. Industries prefer it for performance—not for safety. It features heavily in battery electrolytes, supercapacitors, and advanced lubricants because it stands up under harsh conditions and doesn’t combust easily. Raw materials like this are often the unsung backup singers in big tech projects—quietly ensuring that electric cars work through winters and electronics survive long summers. On the job, precautions matter: researchers handle it with gloves, always away from water or strong acids, since reactions can form hazardous byproducts. Storage means sealed, moisture-free bottles in cool rooms, reminding users that these materials never quite forgive sloppiness with lids or temperature logs.

Safety, Hazards, and Regulatory Details

Despite its robust uses, this chemical requires respect. Exposure can irritate skin or eyes, especially during accidental spills, and inhalation of vapors—though rare thanks to low volatility—raises health questions under poorly ventilated conditions. The bis(fluorosulfonyl)imide component introduces risks associated with fluorinated chemicals; decomposition in fire or with acids may yield toxic gases. Proper disposal matters, too; dumping it down a sink would never fly under good laboratory practices. Safety Data Sheets urge regular protective practices, including eye protection, gloves, and fume hoods during transfers or longer syntheses. On the shipping end, the HS code tags it under specialized organosulfur compounds, not typical commercial chemicals—so every country’s customs process takes a closer look at what’s in the barrel or drum.

Applications and Real-World Importance

Most people outside the lab don’t realize how important new ionic liquids are for the devices they use every day. From rechargeable phones to grid-scale batteries, 1-ethyl-2,3-dimethylimidazolium bis(fluorosulfonyl)imide shapes the reliability, efficiency, and safety of energy storage. Scientists who remember the agony of solvent evaporation or the unreliability of old-school salts appreciate how this material lasts longer and avoids the pitfalls of flammable or volatile electrolytes. Still, there’s always work to do controlling costs and lowering the toxicity profile—most large-scale applications will only take off once recyclability and molecular modifications deal with environmental fallout and occupational hazards. Open conversations among researchers, manufacturers, and policymakers help steer development toward safer, greener versions while still letting the chemistry shine in the fields where it makes the most difference.