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1 decyl 3 methylimidazolium chloride

Manufactured by Merck Group
Sourced in Belgium, Switzerland

1-decyl-3-methylimidazolium chloride is a chemical compound used in various laboratory applications. It is an ionic liquid with a well-defined structure and physical properties. The core function of this product is to serve as a solvent, reagent, or additive in research and development activities, where its unique characteristics may be leveraged to achieve specific experimental objectives.

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3 protocols using 1 decyl 3 methylimidazolium chloride

1

Preparation of Lipid Bilayer Membranes

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DMPC was purchased from Avanti Polar Lipids (Alabaster, AL). 1-butyl-3-methylimidazolium chloride [C4mim]Cl, assay ≥ 98%, 1-octyl-3-methylimidazolium chloride [C8mim]Cl, assay ≥ 97%, 1-decyl-3-methylimidazolium chloride [C10mim]Cl, assay 96%, 1-Butyl-3-methylimidazolium tetrafluoroborate [C4mim][BF4], assay ≥ 97%, 1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide [C4mim][Tf2N], assay ≥98%, were purchased from Sigma-Aldrich (Diegem, Belgium). A schematic of the chemicals used is given in Fig 1. A list including the CACs of the ionic liquids used can be found in S1 Table). Spectroscopic grade chloroform assay 99.3% (stabilized with about 0.6% ethanol) was obtained from Analar (Normapur). HEPES buffer (pH 7.4) consisting of 10 mM HEPES from Fisher Scientific (assay 99%) and 150 mM NaCl-from Sigma-Aldrich (assay ≥ 99.5%) was used for hydration of the dried lipids. The quantities of lipids to reach the desired mixture concentrations were determined gravimetrically using a Sartorius balance yielding a maximal mole fraction uncertainty of ± 0.002.
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2

Screening Kinase Inhibitor Library

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A collection of 80 kinase inhibitors (Tocriscreen kinase inhibitor Toolbox) was purchased from Tocris Bio-Techne AG (Zug, Switzerland). All kinase inhibitors were provided in DMSO at a concentration of 10 mM and stored in aliquots at −20 °C. The compounds 1-dodecyl-3-methylimidazolium iodide, 1-decyl-3-methylimidazolium chloride, 1,3-didecyl-2-methylimidazolium chloride, 1-hexyl-3-methylimidazolium iodide, 1-benzyl-3-methylimidazolium chloride, cycloheximide, rapamycin, chloroquine, brefeldin A, bafilomycin A1, and mifepristone were all purchased from Sigma-Aldrich (Buchs, Switzerland).
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3

Synthesis of Ionic Liquid-Based Compounds

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Didodecyldimethylammonium chloride (DDAB, >98%) was purchased from TCI Chemicals. 1-decyl-3methyl imidazolium chloride ([C10mim]Cl, 96%), iron (III) trichloride (99.99%) and holmium chloride hexahydrate (99.9%), were purchased from Sigma Aldrich and used without further purification. Didodecyldimethylammonium tetrachloroferrate (DDAF) was synthesized according to literature [19] by stirring didodecyldimethylammonium chloride with an equimolar amount of iron (III) chloride in methanol overnight. The solvent was removed under reduced pressure and the residue dried in vacuo at 80 °C overnight. 1-decyl-3-methyl imidazolium tetrachloroholminate ([C10mim][HoCl4]) was also synthesized according to literature [14] , whereby 1 eq. of metal chloride was added to a methanolic solution of [C10mim]Cl and stirred overnight at room temperature, then dehydrated in vacuo at 80 °C for 48 hours. The resulting product is a putty-like substance.
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