1-butyl-2,3-dimethylimidazolium profile

## 1-Butyl-2,3-dimethylimidazolium: A Versatile Ionic Liquid

**1-Butyl-2,3-dimethylimidazolium**, often abbreviated as [BMIM][X] where [X] represents the anion, is a type of **ionic liquid** (IL). Ionic liquids are salts with melting points below 100 °C, and are often liquid at room temperature. They are composed of organic cations and various anions.

**Why is [BMIM][X] important for research?**

[BMIM][X] is a fascinating compound with a wide range of applications in various fields due to its unique properties:

**1. Versatile and Tunable Properties:**

* **Ionic liquids** can be designed with specific properties by choosing different cations and anions, leading to diverse applications.
* [BMIM][X] itself can have its properties modified by varying the anion ([X]) which can be a halides, tetrafluoroborate, hexafluorophosphate, or other anions. This allows for fine-tuning of its properties for specific applications.
* **Wide liquid range:** [BMIM][X] often has a wide liquid range, making it suitable for applications requiring high temperatures.

**2. Unique Chemical Properties:**

* **High ionic conductivity:** [BMIM][X] exhibits high ionic conductivity, which is beneficial for applications like batteries and fuel cells.
* **Low vapor pressure:** [BMIM][X] has a very low vapor pressure, making it less volatile than traditional organic solvents, leading to improved safety and reduced environmental impact.
* **High solvating power:** [BMIM][X] can dissolve a wide range of organic and inorganic compounds, making it suitable for various chemical reactions and separations.

**3. Applications in Research:**

* **Catalysis:** [BMIM][X] serves as a solvent and catalyst in organic synthesis, enhancing reaction rates and selectivities.
* **Electrochemistry:** Due to its high ionic conductivity and wide electrochemical window, [BMIM][X] is used as an electrolyte in batteries and fuel cells.
* **Biotechnology:** [BMIM][X] has shown promising applications in biocatalysis, bioseparation, and drug delivery.
* **Materials science:** [BMIM][X] can be used as a template for synthesizing novel nanomaterials with unique properties.
* **Environmental science:** [BMIM][X] is being explored for the removal of pollutants from water and soil.

**Overall, 1-butyl-2,3-dimethylimidazolium is a versatile and promising compound with unique properties that make it important for research in various fields.** Its tunable properties and potential applications in catalysis, electrochemistry, biotechnology, materials science, and environmental science make it a subject of ongoing research and development.

1-butyl-2,3-dimethylimidazolium: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

ID Source	ID
PubMed CID	2734168
CHEMBL ID	3306199
SCHEMBL ID	294424
MeSH ID	M0517735

Synonym
1-butyl-2,3-dimethylimidazol-3-ium
NCGC00248720-04
NCGC00248720-01
NCGC00248720-02
NCGC00248720-03
SCHEMBL294424
108203-89-0
1-butyl-2,3-dimethylimidazolium
DTXSID7048087
CHEMBL3306199
1-butyl-2,3-dimethyl-1h-imidazol-3-ium
1-butyl-2,3-dimethylimidazolium diethyleneglycolmonomethylethersulfate [bdimim] [mdegso4]

Excerpt	Reference	Relevance
" A simplified central composite design (SCCD) was employed to design the concentration distribution of components in binary mixtures to effectively detect the possible toxic interactions between pesticide and IL over the whole concentration range."	( Effect of ionic liquid on the toxicity of pesticide to Vibrio-qinghaiensis sp.-Q67. Liu, HL; Liu, SS; Zhang, J, 2009)	0.35

Timeframe	Studies, This Drug (%)	All Drugs %
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	4 (36.36)	29.6817
2010's	7 (63.64)	24.3611
2020's	0 (0.00)	2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Publication Type	This drug (%)	All Drugs (%)
Trials	0 (0.00%)	5.53%
Reviews	0 (0.00%)	6.00%
Case Studies	0 (0.00%)	4.05%
Observational	0 (0.00%)	0.25%
Other	11 (100.00%)	84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Substance	Relationship Strength	Studies	Classes	Roles
1,2,4-trichlorobenzene 1,2,4-trichlorobenzene : A trichlorobenzene with chloro substituents at positions 1, 2 and 4.	2.11	1	trichlorobenzene
bromide Bromides: Salts of hydrobromic acid, HBr, with the bromine atom in the 1- oxidation state. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)	2.1	1	halide anion; monoatomic bromine
chlorine chloride : A halide anion formed when chlorine picks up an electron to form an an anion.	2.48	2	halide anion; monoatomic chlorine	cofactor; Escherichia coli metabolite; human metabolite
nickel Nickel: A trace element with the atomic symbol Ni, atomic number 28, and atomic weight 58.69. It is a cofactor of the enzyme UREASE.. nickel ion : A nickel atom having a net electric charge.. nickel atom : Chemical element (nickel group element atom) with atomic number 28.	2.1	1	metal allergen; nickel group element atom	epitope; micronutrient
sulfuric acid sulfuric acid : A sulfur oxoacid that consists of two oxo and two hydroxy groups joined covalently to a central sulfur atom.	2.06	1	sulfur oxoacid	catalyst
sulfur dioxide Sulfur Dioxide: A highly toxic, colorless, nonflammable gas. It is used as a pharmaceutical aid and antioxidant. It is also an environmental air pollutant.	2.06	1	sulfur oxide	Escherichia coli metabolite; food bleaching agent; refrigerant
camphor, (+-)-isomer [no description available]	2.03	1	bornane monoterpenoid; cyclic monoterpene ketone	plant metabolite
dichlorvos Dichlorvos: An organophosphorus insecticide that inhibits ACETYLCHOLINESTERASE.. dichlorvos : An alkenyl phosphate that is the 2,2-dichloroethenyl ester of dimethyl phosphate.	2.05	1	alkenyl phosphate; dialkyl phosphate; organochlorine acaricide; organophosphate insecticide	anthelminthic drug; antibacterial agent; antifungal agent; EC 3.1.1.7 (acetylcholinesterase) inhibitor; EC 3.1.1.8 (cholinesterase) inhibitor
furaldehyde Furaldehyde: A heterocyclic compound consisting of a furan where the hydrogen at position 2 is substituted by a formyl group.. furfural : An aldehyde that is furan with the hydrogen at position 2 substituted by a formyl group.	2.06	1	aldehyde; furans	Maillard reaction product; metabolite
ethyl acrylate [no description available]	2.03	1	enoate ester
malondialdehyde Malondialdehyde: The dialdehyde of malonic acid.. malonaldehyde : A dialdehyde that is propane substituted by two oxo groups at the terminal carbon atoms respectively. A biomarker of oxidative damage to lipids caused by smoking, it exists in vivo mainly in the enol form.	2.54	2	dialdehyde	biomarker
semeron [no description available]	2.05	1	1,3,5-triazines
10-camphorsulfonic acid 10-camphorsulfonic acid: solucampher refers to piperazine salt; RN given refers to parent cpd; structure in Negwer. camphorsulfonic acid : A sulfonic acid containing the camphorsulfonate anion.	2.03	1	organosulfonic acid
ruthenium Ruthenium: A hard, brittle, grayish-white rare earth metal with an atomic symbol Ru, atomic number 44, and atomic weight 101.07. It is used as a catalyst and hardener for PLATINUM and PALLADIUM.	2.11	1	iron group element atom; platinum group metal atom
bromine Bromine: A halogen with the atomic symbol Br, atomic number 35, and atomic weight 79.904. It is a volatile reddish-brown liquid that gives off suffocating vapors, is corrosive to the skin, and may cause severe gastroenteritis if ingested.	2.04	1	diatomic bromine
poloxalene Poloxalene: A copolymer of polyethylene and polypropylene ether glycol. It is a non-ionic polyol surface-active agent used medically as a fecal softener and in cattle for prevention of bloat.. pluronic : A triblock copolymer composed of a central hydrophobic chain of poly(propylene oxide) flanked by two hydrophilic chains of poly(ethylene oxide).	2.1	1	epoxide
fluoroboric acid [no description available]	2.11	1	boron fluoride
alkenes [no description available]	2.1	1
5-hydroxymethylfurfural 5-hydroxymethylfurfural: has antisickling activity; HMF is the causative component in honey that affects the presystemic metabolism and pharmacokinetics of GZ in-vivo. 5-hydroxymethylfurfural : A member of the class of furans that is furan which is substituted at positions 2 and 5 by formyl and hydroxymethyl substituents, respectively. Virtually absent from fresh foods, it is naturally generated in sugar-containing foods during storage, and especially by drying or cooking. It is the causative component in honey that affects the presystemic metabolism and pharmacokinetics of GZ in-vivo.	2.06	1	arenecarbaldehyde; furans; primary alcohol	indicator; Maillard reaction product
D-fructopyranose [no description available]	2.06	1	cyclic hemiketal; D-fructose; fructopyranose	sweetening agent
1-butyl-3-methylimidazolium chloride 1-butyl-3-methylimidazolium chloride: structure in first source	2.06	1
1-butyl-3-methylimidazolium 1-butyl-3-methylimidazolium: structure in first source. 1-butyl-3-methylimidazolium : A 1-alkyl-3-methylimidazolium in which the alkyl substituent at C-1 is butyl.	2.03	1	1-alkyl-3-methylimidazolium
1-hexyl-3-methylimidazolium 1-hexyl-3-methylimidazolium: structure in first source. 1-hexyl-3-methylimidazolium : A 1-alkyl-3-methylimidazolium in which the alkyl substituent at C-1 is hexyl.	2.06	1	1-alkyl-3-methylimidazolium
1-butyl-3-methylimidazolium hexafluorophosphate 1-butyl-3-methylimidazolium hexafluorophosphate: structure in first source	2.13	1
buclizine 1-octyl-3-methylimidazolium: structure in first source. 3-methyl-1-octylimidazolium : A 1-alkyl-3-methylimidazolium in which the alkyl substituent at C-1 is octyl.	2.06	1	1-alkyl-3-methylimidazolium
lithium Lithium: An element in the alkali metals family. It has the atomic symbol Li, atomic number 3, and atomic weight [6.938; 6.997]. Salts of lithium are used in treating BIPOLAR DISORDER.	2.06	1	alkali metal atom
1-butyl-3-methylpyridinium 1-butyl-3-methylpyridinium: structure in first source	2.05	1
tellurium Tellurium: An element that is a member of the chalcogen family. It has the atomic symbol Te, atomic number 52, and atomic weight 127.60. It has been used as a coloring agent and in the manufacture of electrical equipment. Exposure may cause nausea, vomiting, and CNS depression.	2.1	1	chalcogen; metalloid atom
mocetinostat mocetinostat: undergoing phase II clinical trials for treatment of cancer. mocetinostat : A benzamide obtained by formal condensation of the carboxy group of 4-({[4-(pyridin-3-yl)pyrimidin-2-yl]amino}methyl)benzoic acid with one of the amino groups of benzene-1,2-diamine. It is an orally active and isotype-selective HDAC inhibitor which exhibits antitumour activity (IC50 = 0.15, 0.29, 1.66 and 0.59 muM for HDAC1, HDAC2, HDAC3 and HDAC11).	2.13	1	aminopyrimidine; benzamides; pyridines; secondary amino compound; secondary carboxamide; substituted aniline	antineoplastic agent; apoptosis inducer; autophagy inducer; cardioprotective agent; EC 3.5.1.98 (histone deacetylase) inhibitor; hepatotoxic agent
chlorophyll a Chlorophyll: Porphyrin derivatives containing magnesium that act to convert light energy in photosynthetic organisms.. chlorophyll : A family of magnesium porphyrins, defined by the presence of a fifth ring beyond the four pyrrole-like rings. The rings can have various side chains which usually include a long phytol chain.	2.13	1	chlorophyll; methyl ester	cofactor

1-butyl-2,3-dimethylimidazolium

Description

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Synonyms (12)

Research Excerpts

Toxicity

Research

Studies (11)

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Research Demand Index: 17.38

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