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1-Butyl-3-methylimidazolium nitrate
[CAS# 179075-88-8]

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Identification
Classification Chemical reagent >> Organic reagent >> Ionic liquid
Name 1-Butyl-3-methylimidazolium nitrate
Molecular Structure CAS # 179075-88-8, 1-Butyl-3-methylimidazolium nitrate
Molecular Formula C8H15N3O3
Molecular Weight 201.22
CAS Registry Number 179075-88-8
EC Number 629-008-8
SMILES CCCCN1C=C[N+](=C1)C.[N+](=O)([O-])[O-]
Safety Data
Hazard Symbols symbol symbol   GHS03;GHS07 Danger    Details
Hazard Statements H272-H315-H319-H335    Details
Precautionary Statements P210-P220-P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P370+P378-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Oxidising solidsOx. Sol.2H272
Specific target organ toxicity - single exposureSTOT SE3H335
Oxidising liquidsOx. Liq.2H272
Transport Information UN 1479
SDS Available
up Discovory and Applicatios
1-Butyl-3-methylimidazolium nitrate (BMIM NO₃) is a well-known ionic liquid with the chemical formula C₉H₁₁N₃O₃. This compound belongs to the broader class of ionic liquids, which have attracted attention for their unique properties and wide applications in various scientific and industrial fields.

The development of BMIM NO₃ stems from the growing interest in ionic liquids, which began in the late 20th century. Researchers sought to create solvents with favorable properties such as low volatility, high thermal stability, and high ionic conductivity. The synthesis of BMIM NO₃ was designed to take advantage of these properties by combining the 1-butyl-3-methylimidazolium cation with the nitrate anion. The synthesis involves the reaction of 1-butyl-3-methylimidazolium chloride (BMIM Cl) with sodium nitrate (NaNO₃), in which BMIM Cl reacts with NaNO₃ to form BMIM NO₃ and NaCl. The process is usually carried out in a suitable solvent or directly in the ionic liquid phase, followed by purification to separate the ionic liquid.

BMIM NO₃ is used in electrochemical applications due to its good ionic conductivity and stability. It can be used as an electrolyte in a variety of energy storage and conversion devices, including batteries and supercapacitors. Its low viscosity and high thermal stability improve the performance and efficiency of these devices, making it a valuable component in the field of energy technology.

As a green solvent, BMIM NO₃ provides an environmentally friendly alternative to traditional organic solvents. It is non-volatile and recyclable, thus reducing the environmental impact of chemical processes. BMIM NO₃ is used in organic synthesis and extraction processes to improve reaction efficiency and selectivity while minimizing waste.

In catalysis, BMIM NO₃ can be used as both a solvent and a co-catalyst. Its ability to dissolve a wide range of organic and inorganic compounds makes it a versatile medium for catalytic reactions. BMIM NO₃ is used in a variety of catalytic processes, both homogeneous and heterogeneous, to increase reaction rates and yields.

BMIM NO₃ is very effective in separation processes, such as liquid-liquid extraction and ion exchange. Its unique solvation properties allow for the selective extraction and separation of specific compounds from mixtures. This application is particularly useful in drug purification and the recovery of valuable metals from ores.

In materials science, BMIM NO₃ is used to synthesize and modify materials with tailored properties. It plays a role in the preparation of nanoparticles and advanced polymers. BMIM NO₃ can act as a solvent or stabilizer during the synthesis of nanomaterials, affecting their size, shape, and stability.

References

2023. Tutorial for thermal analysis of ionic liquids. Journal of Thermal Analysis and Calorimetry.
DOI: 10.1007/s10973-023-12439-z

2020. Applications of Ionic Liquids in Chemical Reactions. Nanotechnology-Based Industrial Applications of Ionic Liquids.
DOI: 10.1007/978-3-030-44995-7_15

2021. Structural and Conformational Analysis of 1-Butyl-3-methylimidazolium Nitrate. Journal of Chemical Crystallography.
DOI: 10.1007/s10870-021-00899-w
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