1-(Methoxycarbonyl)Methyl-3-Methylimidazolium Bis(Trifluoromethylsulfonyl)Imide: A Commentary

What is 1-(Methoxycarbonyl)Methyl-3-Methylimidazolium Bis(Trifluoromethylsulfonyl)Imide?

Most folks outside the field of advanced chemistry might raise an eyebrow at such a name, but this compound opens plenty of doors where ionic liquids create value. This substance doesn’t look or act like everyday table salt; it bridges the worlds of organic synthesis, electrochemistry, and material development by functioning as one of those rare, low-melting salts that feel at home in both the lab and industrial spheres. The molecular structure, C10H13F6N3O5S2, tells a real story: a cation based on imidazolium frameworks, dressed with a methoxycarbonyl group for extra versatility, paired with a bis(trifluoromethylsulfonyl)imide anion known to show off some of the best stability, both chemically and thermally. As for official tracking, the compound runs under the HS Code 2933299090, which groups it with other heterocyclic compounds containing nitrogen.

Physical Properties and Forms

Forget everyday visuals; this material rarely bothers with the classic “salt” image—grainy white cubes. Depending on storage and temperature, it may show up as off-white solid flakes, fine powder, tiny pearls, or even a viscous, clear-to-pale-colored liquid. Strong, often imperceptible, and remarkably dense, specific gravity lands near 1.42 g/mL at 25°C, which points to a substance more substantial than water or most solvents in the lab. Its crystalline version, when allowed to form, shimmers with a faint waxy look, reminding experienced chemists of the quiet discipline behind these melting-point-tuned ionic liquids. Whether dissolved or neat, it rarely smells and usually stays put in its storage bottle. If tossed in solution, it plays nice; the compound dissolves with ease in polar organic solvents, which paves the way for whole libraries of new reaction chemistry, salts, or electrolytes.

Molecular Structure and Specifications

Looking at diagrams, the imidazolium ring jumps out fast—this is the heart of room-temperature ionic liquids. With a methyl group at the three position and the exotic methoxycarbonylmethyl group tied to the one position, the cation offers both stability and room for further derivatization. The anion’s engineering shines through: bis(trifluoromethylsulfonyl)imide grants low viscosity, broad liquidus, and high chemical resistance. The overall molecular weight stands around 451.35 g/mol, which hints at the solid heft that comes with each liter handled—no wonder researchers often rely on these properties where high-performance counts. Crystal engineers might take advantage of its capacity to hold shape under tough thermal or electrochemical conditions.

Material Category and Applications

Chemists don’t just store this in a drawer for show. As a “raw material,” it moves straight into batteries, especially lithium-ion prototypes aiming for better safety and efficiency. Electroplaters and organic chemists find it ideal as a reaction medium, where the usual volatile smoke of solvents drops off, replaced by quiet, stable progress. The handling experience brings to mind thick, heavy liquids or denser solids than most get used to—always ready for a weighing spoon, never flying away in a draft. Crystals, when unbothered, serve as seeds for further purification work, while a pearl or flake form proves convenient for larger-quantity handling.

Safety, Hazardous Nature, and Chemical Handling

A common question pops up for folks unaccustomed to lengthy chemical names: Is it dangerous? Ionic liquids like this one rarely show flammability or volatility, making them less dramatic than standard organic solvents. Skin contact or inhalation isn’t openly hazardous at small scales, though gloves and goggles never hurt. Long-term exposure lacks the deep study given to table salt or simple alcohols, so anyone in the chemical trades gives the compound solid respect. Used as a raw material, it can’t be labeled completely safe, but it doesn’t fall behind standard laboratory precautions. Environmental and personnel safety teams focus most on disposal, as these molecules carry fluorinated groups that tend to stay put in nature. Nobody truly wants careless dumping or spills, especially as regulatory scrutiny spreads.

Challenges and the Way Forward

One person’s tool can be another’s trial. Expensive to produce at industrial scale, the compound relies on controlled synthesis methods that balance purity, yield, and waste. Factories designing greener batteries, energy storage solutions, or supercapacitors depend on reliable sourcing and transparency about safety. Current rules on chemical imports and exports demand clear labelling under international HS Codes, which keeps tracking tight but challenges logistics. Disposal, too, creates open questions—especially as Europe, the United States, and Asian markets begin to demand full life-cycle accounting for chemicals. Solutions might call for recycling programs, better guidance for research labs moving into pilot production, and more open publication of safety and degradation data.

Supporting Responsible Use with Facts

For anyone dealing closely with such raw materials, attention to property—the density, melting point, solubility, and stability—pays off in risk reduction. Each fact on the product specification sheet isn’t just minor detail: it underpins safer labs and higher-quality manufacturing. A dose of open access to up-to-date research on environmental effects and safe processing helps smart companies and institutions stay clear of regulatory snags while building trust with clients and communities. A few lessons from my own work in chemical storage: mark bottles carefully, always check the material safety data sheet, and never rush to pour anything down a drain, no matter how inert the substance may seem. A little extra care bends the risk curve downward for everyone.

Room for Growth

New entrants in energy storage, advanced catalysis, or circular material development can lean on the adaptability and tested properties of this imidazolium salt. As more manufacturing moves toward clean energy and solvents with lower environmental impact, the value of substances like 1-(Methoxycarbonyl)Methyl-3-Methylimidazolium Bis(Trifluoromethylsulfonyl)Imide rises further. Work remains to be done on recovering, reusing, and safely disposing of fluorinated ionic liquids, but community attention and stronger international rules can push industrial processes in a cleaner, safer, and more sustainable direction.