Online Database of Chemicals from Around the World

1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide
[CAS# 174899-83-3]

List of Suppliers
Leap Chem Co., Ltd. China Inquire  
+86 (852) 3060-6658
market19@leapchem.com
QQ chat
Chemical manufacturer since 2006
chemBlink standard supplier since 2015
Shanghai Yuanye Bio-Technology Co., Ltd. China Inquire  
+86 (21) 6184-5781
+86 13585604150
shyysw053@163.com
QQ chat
Chemical manufacturer since 2009
chemBlink standard supplier since 2016
Monils Chemical Engineering Science & Technology (shanghai) Co., Ltd. China Inquire  
+86 (21) 3822-8895
heqing@ilschem.cn
QQ chat
Chemical manufacturer since 2014
chemBlink standard supplier since 2019
Zhejiang Arts & Crafts Imp & Exp.co., Ltd. China Inquire  
+86 571 87238903
jocelynpan@zjarts.com
Chemical distributor since 1992
chemBlink standard supplier since 2024
IOLITEC Ionic Liquids Technologies, Inc. USA Inquire  
+1 (205) 348-2831
info@iolitec-usa.com
Chemical manufacturer since 2002
Kishida Chemical Co., Ltd. Japan Inquire  
+81 (6) 6946-8061
shiyaku@kishida.co.jp
Chemical manufacturer
Santa Cruz Biotechnology, Inc. USA Inquire  
+1 (831) 457-3800
scbt@scbt.com
Chemical manufacturer
abcr GmbH Germany Inquire  
+49 (721) 950-610
info@abcr.de
Chemical manufacturer
Complete supplier list of 1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide
Identification
Classification Chemical reagent >> Organic reagent >> Ionic liquid
Name 1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide
Synonyms bis(trifluoromethylsulfonyl)azanide;1-butyl-3-methylimidazol-3-ium
Molecular Structure CAS # 174899-83-3, 1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, bis(trifluoromethylsulfonyl)azanide,1-butyl-3-methylimidazol-3-ium
Molecular Formula C10H15F6N3O4S2
Molecular Weight 419.36
CAS Registry Number 174899-83-3
EC Number 605-742-4
SMILES CCCCN1C=C[N+](=C1)C.C(F)(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F
Properties
Refractive index 1.428
Flash point >200 ºC
Safety Data
Hazard Symbols symbol symbol symbol symbol   GHS05;GHS06;GHS08;GHS09 Danger    Details
Hazard Statements H301+H311-H301-H311-H314-H373-H411    Details
Precautionary Statements P260-P262-P264-P270-P273-P280-P301+P316-P301+P330+P331-P302+P352-P302+P361+P354-P304+P340-P305+P354+P338-P316-P319-P321-P330-P361+P364-P363-P391-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.3H301
Skin corrosionSkin Corr.1BH314
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Acute toxicityAcute Tox.3H311
Specific target organ toxicity - repeated exposureSTOT RE2H373
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Transport Information UN 2922
SDS Available
up Discovory and Applicatios
1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (BMIM TFSI) is a well-known ionic liquid with the molecular formula C9H11F6N3O4S2. It is highly regarded for its excellent properties and is highly valued in a variety of scientific and industrial applications.

BMIM TFSI originates from the broader field of ionic liquids, which has received widespread attention since the late 20th century. Researchers sought solvents with enhanced performance characteristics compared to traditional organic solvents, such as low volatility, high thermal stability, and a wide electrochemical window. BMIM TFSI was developed to meet these needs by combining the 1-butyl-3-methylimidazolium cation with the bis(trifluoromethylsulfonyl)imide anion. 1-Butyl-3-methylimidazolium chloride (BMIM Cl) reacts with lithium bis(trifluoromethylsulfonyl)imide (LiTFSI) to produce BMIM TFSI and a byproduct lithium chloride (LiCl) precipitate. 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 TFSI is widely used in electrochemical applications due to its high ionic conductivity and wide electrochemical stability window. It can be used as an electrolyte in a variety of energy storage devices, including lithium-ion batteries, supercapacitors, and fuel cells. Its low viscosity and thermal stability improve the efficiency and performance of these devices, making it a key component in advanced energy technologies.

As a green solvent, BMIM TFSI has significant advantages over traditional organic solvents. It is non-volatile and environmentally friendly, reducing the risks associated with traditional solvents. BMIM TFSI is used in organic synthesis and extraction processes to improve reaction efficiency and selectivity while minimizing environmental impact.

In catalysis, BMIM TFSI can be used as both a solvent and a catalyst. It is able to dissolve a wide range of organic and inorganic compounds, becoming a versatile medium for catalytic reactions. BMIM TFSI is used in homogeneous and heterogeneous catalysis to improve reaction rates, yields, and selectivity. Its use helps achieve more sustainable and efficient chemical synthesis.

BMIM TFSI is very effective in separation processes, including liquid-liquid extraction and gas absorption. Its unique solvation properties enable the selective extraction and separation of specific compounds from a mixture. This application is valuable in drug purification, metal extraction, and separation of organic compounds to improve process efficiency and selectivity.

In materials science, BMIM TFSI is used to synthesize and modify materials with customized properties. It plays a role in the preparation of nanoparticles, polymers, and other advanced materials. BMIM TFSI can act as a template or stabilizer during the synthesis of nanomaterials, affecting their size, shape, and stability, thereby developing new materials with special properties.
Market Analysis Reports
List of Reports Available for 1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide
Related Products
2-Butyl-5-[methanesulfonamido]benzofuran  7-Butyl-6-(4-methoxyphenyl)-5H-pyrrolo[2,3-b]pyrazine  4-Butyl-2-methylaniline  alpha-Butyl-N-methylbenzylamine  Butyl 2-methylbutyrate  trans-5-Butyl-2-methyl-1,3-dioxane  4-Butyl-1-methyl-2,5-dioxo-4-imidazolidinecarboxaldehyde  Butyl methyl ether  1-Butyl-2-methyl-1H-imidazole  3-Butyl-1-methylimidazolium acetate  1-Butyl-3-methylimidazolium bromide  1-Butyl-3-methylimidazolium chloride  1-Butyl-3-methylimidazolium dibutyl phosphate  1-Butyl-3-methylimidazolium dicyanamide  3-Butyl-1-methyl-1H-imidazol-3-ium di4-methylbenzenesulfonate  1-Butyl-3-methyl-1H-imidazolium heptachlorodialuminate  1-Butyl-3-methylimidazolium hexafluorophosphate  1-Butyl-3-methyl-1H-imidazolium hydrogen sulfate  1-Butyl-3-methylimidazolium iodide  1-Butyl-3-methylimidazolium mesylate