Online Database of Chemicals from Around the World

1-Butyl-3-methylimidazolium tetrafluoroborate
[CAS# 174501-65-6]

List of Suppliers
Shanghai Chengjie Chemical Co., Ltd. China Inquire  
+86 (21) 6489-6788
shyfhx@aliyun.com
Chemical manufacturer
chemBlink standard supplier since 2007
Simagchem Corporation China Inquire  
+86 13806087780
sale@simagchem.com
Chemical manufacturer since 2002
chemBlink standard supplier since 2008
Nanjing MSN Chemical Co., Ltd. China Inquire  
+86 (25) 5701-5632
+86 18013328036
info@msnchem.com
Skype Chat
QQ chat
Chemical manufacturer since 2013
chemBlink standard supplier since 2008
HBCChem, Inc. USA Inquire  
+1 (510) 219-6317
sales@hbcchem-inc.com
Chemical manufacturer
chemBlink standard supplier since 2008
Hefei TNJ Chemical Industry Co., Ltd. China Inquire  
+86 (551) 6541-8684
sales@tnjchem.com
Chemical manufacturer since 2001
chemBlink standard supplier since 2010
Wuhu Huaren Science and Technology Co., Ltd. China Inquire  
+86 (553) 584-2013
wuhuhuaren@163.com
Chemical manufacturer since 2006
chemBlink standard supplier since 2010
BOC Sciences USA Inquire  
+1 (631) 485-4226
info@bocsci.com
Chemical manufacturer
chemBlink standard supplier since 2010
Intatrade Chemicals GmbH Germany Inquire  
+49 (3493) 605-465
sales@intatrade.de
Chemical distributor
chemBlink standard supplier since 2011
Complete supplier list of 1-Butyl-3-methylimidazolium tetrafluoroborate
Identification
Classification Chemical reagent >> Organic reagent >> Ionic liquid
Name 1-Butyl-3-methylimidazolium tetrafluoroborate
Molecular Structure CAS # 174501-65-6, 1-Butyl-3-methylimidazolium tetrafluoroborate
Molecular Formula C8H15N2.BF4
Molecular Weight 226.02
CAS Registry Number 174501-65-6
EC Number 638-831-1
SMILES [B-](F)(F)(F)F.CCCCN1C=C[N+](=C1)C
Properties
Density 1.2077
Melting point -71 ºC
Refractive index 1.52
Flash point 288 ºC
Safety Data
Hazard Symbols symbol symbol symbol   GHS06;GHS07;GHS09 Danger    Details
Hazard Statements H301-H315-H319-H335-H411    Details
Precautionary Statements P261-P264-P264+P265-P270-P271-P273-P280-P301+P316-P302+P352-P304+P340-P305+P351+P338-P319-P321-P330-P332+P317-P337+P317-P362+P364-P391-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Acute toxicityAcute Tox.3H301
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Specific target organ toxicity - single exposureSTOT SE3H335
Acute toxicityAcute Tox.4H302
Skin corrosionSkin Corr.1CH314
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Serious eye damageEye Dam.1H318
SDS Available
up Discovory and Applicatios
1-Butyl-3-methylimidazolium tetrafluoroborate (BMIM BF4) is a versatile ionic liquid with the molecular formula C8H15BF4N2. As a member of the imidazolyl ionic liquid family, BMIM BF4 has attracted great interest due to its unique properties and wide applications in various fields.

The development of BMIM BF4 is part of the extensive research on ionic liquids that began in the mid-20th century. Researchers were looking for alternatives to traditional organic solvents that could offer advantages such as low volatility, non-flammability, and high thermal stability. The synthesis of BMIM BF4 involves a direct reaction between 1-butyl-3-methylimidazolium chloride (BMIM Cl) and sodium tetrafluoroborate (NaBF4). In this process, BMIM Cl reacts with NaBF4 to produce BMIM BF4 and sodium chloride (NaCl) as a byproduct. The resulting BMIM BF4 is then purified to obtain a high-purity ionic liquid.

The most notable application of BMIM BF4 is as a green solvent. Traditional organic solvents are often volatile and toxic, posing risks to the environment and health. In contrast, BMIM BF4 is non-volatile and recyclable, making it an environmentally friendly alternative. It is widely used in organic synthesis to dissolve a wide range of compounds and promote cleaner, more efficient reactions. Its ability to stabilize transition states and intermediates makes it valuable in catalysis.

BMIM BF4 is highly regarded in electrochemical applications for its excellent ionic conductivity and electrochemical stability. It can be used as an electrolyte in batteries, fuel cells, and supercapacitors, helping to improve the efficiency and lifetime of these devices. Its wide electrochemical window and low viscosity make it ideal for the development of advanced energy storage and conversion systems.

In the field of catalysis, BMIM BF4 can be used as both a solvent and a co-catalyst. It can dissolve a wide range of catalytic species and promote homogeneous catalysis. Its role in improving reaction rates, selectivity, and yields makes it an essential component in a variety of catalytic processes, including hydrogenations, oxidations, and polymerizations.

BMIM BF4 is used in extraction and separation processes for its ability to selectively dissolve and separate different compounds. It is used in liquid-liquid extraction to extract valuable components from mixtures, such as bioactive compounds from plant materials or metals from ores. Its low volatility and recyclability enhance the sustainability of these processes.

In materials science, BMIM BF4 is used to synthesize and modify materials with specific properties. It plays a role in the preparation of nanoparticles, polymers and other advanced materials. BMIM BF4 can act as a template or stabilizer during the synthesis of nanomaterials, affecting their size, shape and stability. This application leads to the development of new materials tailored for various technological applications.
Market Analysis Reports
List of Reports Available for 1-Butyl-3-methylimidazolium tetrafluoroborate
Related Products
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  1-Butyl-3-methylimidazolium 1-octyl sulfate  1-Butyl-3-methylimidazolium tetrachloroferrate  1-Butyl-3-methylimidazolium thiocyanate  1-Butyl-3-methylimidazolium tosylate  3-Butyl-1-methylimidazolium trifluoroacetate  1-Butyl-3-methylimidazolium trifluoromethansulfonate  1-Butyl-3-methylimidazolium trifluoro(trifluoromethyl)borate  1-Butyl-2-methylindole  Butyl 3-methyl-2-(2R,3S)-oxiranecarboxylate  N-(4-Butyl-2-methylphenyl)acetamide  5-Butyl-3-(4-methylphenyl)-1,2,4-oxadiazole  1-Butyl-1-methylpiperidinium bis(trifluoromethylsulfonyl)imide