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Usage

Uses

Used in Catalysis:
3-Dodecyl-1-methyl-1H-imidazolium nitrate is utilized as a catalyst in various chemical reactions due to its ability to facilitate and enhance the reaction rates, making it a valuable component in the field of catalysis.
Used in Extraction Processes:
In the realm of extraction processes, 3-Dodecyl-1-methyl-1H-imidazolium nitrate serves as an efficient extractant, leveraging its unique solvation properties to selectively separate and concentrate target compounds from complex mixtures.
Used as a Lubricant Additive:
3-Dodecyl-1-methyl-1H-imidazolium nitrate is employed as a lubricant additive to improve the performance characteristics of lubricants. Its incorporation can enhance the thermal stability, reduce friction, and improve the overall efficiency of the lubricant, making it suitable for use in various mechanical applications.
Used in Chemical Synthesis:
3-Dodecyl-1-methyl-1H-imidazolium nitrate is used as a reagent in chemical synthesis, where its unique structure can participate in a variety of organic reactions, contributing to the formation of desired products with high selectivity and yield.
Used in the Pharmaceutical Industry:
In the pharmaceutical sector, 3-Dodecyl-1-methyl-1H-imidazolium nitrate is used as a solubility enhancer for poorly water-soluble drugs, improving their bioavailability and therapeutic efficacy.
Used in the Energy Industry:
3-Dodecyl-1-methyl-1H-imidazolium nitrate is applied in the energy industry, particularly in processes related to the extraction and purification of valuable compounds from natural resources, such as oil and gas.
Each application of 3-Dodecyl-1-methyl-1H-imidazolium nitrate leverages its distinct chemical properties, making it a multifunctional compound with broad industrial relevance.

Upstream product

• 892449-24-0 1-dodecyl-3-methylimidazolium hydroxide 
• 112-53-8 1-dodecyl alcohol 
• 616-47-7 1-methyl-1H-imidazole 
• 13277-59-3 Dodecylnitrat 

Relevant academic research and scientific papers

Activation of hydrogen peroxide by the nitrate anion in micellar media

We present the activation of hydrogen peroxide by micellar imidazolium nitratesviaH-bond formation in water, as shown by vibrational spectroscopy and supported by DFT calculations. Mechanistic insight into the interactions of the surfactant cation, the nitrate anion and H2O2is given. The micelles solubilise and epoxidise cyclooctene in the aqueous phase.

Stable gasoil/sunflower oil fuel microemulsions prepared by using methylimidazolium based ionic liquids as surfactant

The fuel microemulsions of water in a 4:1 (v:v) blend of gasoil and sunflower oil (respectively) by using of 1-dodecyl-3-methylimidazolium nitrate ([C12mim][NO3]) and 1-butyl-3-methyl imidazolium nitrate ([Bmim][NO3]) ionic liquids as surfactant and 1-butanol as co-surfactant. Also, the performance of 50:50 wt% blend of the mentioned ionic liquids with Span 80 as surfactant was evaluated in this work. The comparison of the phase diagrams of the samples has revealed a larger single phase region for samples prepared with ionic liquids than the conventional Span 80 surfactant or their blends with Span 80. The dynamic viscosity, and density of two samples with high oily phase content was measured according to the standards showing very close values to the net diesel fuel. DLS analysis indicated a water droplets of 9 nm (up to 70%) for [Bmim][NO3], 3–6 nm (up to 64–82%) for [C12mim][NO3], and 331 nm (up to 53%) for systems prepared by Span 80. Meanwhile, a very narrow size distribution was observed for the samples prepared by ionic liquids. No phase separation has been observed for the prepared samples over 6 months on the shelf.

Silver-free synthesis of nitrate-containing room-temperature ionic liquids

Nitrate-containing 1-alkyl-3-methylimidazolium ionic liquids, [C n-mim]NO3, where n = 4, 6, 8, 12, are synthesized in one step by reacting 1-methylimidazole with alkyl nitrates under various conditions without using AgNO3 and 1-alkyl-3-methylimidazolium halides.