112400-86-9

Usage

Chemical Properties

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InChI:InChI=1/C10H16N.ClH/c1-3-4-7-11-8-5-10(2)6-9-11;/h5-6,8-9H,3-4,7H2,1-2H3;1H/q+1;/p-1

Upstream product

• 108-89-4 picoline 
• 109-69-3 n-Butyl chloride 

Downstream Products

• 74-87-3 methylene chloride 
• 882172-79-4 1-butyl-4-methylpyridinium trifluoromethylsulfonate 
• 343952-33-0 4-methyl-N-butylpyridinium tetrafluoroborate 
• 1310824-61-3 1-butyl-4-[2-(4-dimethylaminophenyl)ethenyl]pyridinium chloride 
• 64-18-6 formic acid 
• 141-82-2 malonic acid 
• 144-62-7 oxalic acid 
• 64-19-7 acetic acid 
• 110-17-8 (2E)-but-2-enedioic acid 

Relevant academic research and scientific papers

Effects of halide anions to absorb SO2 in ionic liquids

Ionic liquids with halide anions were prepared and the dependency of halide anions on the SO2 solubility of ILs was investigated. The study shows that the SO2 solubility of ionic liquids lies in the range 1.91 ～ 2.22 SO2/ILs mol ratio. SO2 solubility in ionic liquids with varying halide anions follows the order Br > Cl > I. Theoretical investigation was also conducted at the B3LYP level using the Gaussian 03 program. From the theoretical consideration of the interaction between SO2 and [EMIm]X (where X = Cl, Br, and I), it has been proposed that primary interaction of halide occurs with C2-H of the imidazolium and S of SO2. Experimental results further shows that the absorption and desorption process of SO2 in ILs was reversible by the three cycles of the absorption at 50 °C and desorption at 140 °C. The reversibility of SO2 absorption was confirmed by FT-IR studies.

Densities and viscosities of imidazolium and pyridinium chloroaluminate ionic liquids

The chloroaluminate ionic liquids are used in various types of reactions. However, due to their particular vulnerability on water, their physical properties have not been previously investigated very extensively. The densities and viscosities of series imidazolium and pyridinium chloroaluminate ionic liquids having alkyl (butyl, hexyl, octyl) or aralkyl (benzyl, ethylphenyl) chain at the cation, various effective molar fraction of AlCl3 (χAlCl3 = 0.5, 0.65, 0.7), as well as they mixture and mixture with common organic solvents (hexane, toluene) were measured at the temperature range 293.15-343.15 K (20-70 °C). Densities, and particularly viscosities decrease with the increase of temperature. The density decreases with the increase of the length of the alkyl chain. The type of cation also influences the density, however, the order is different than for non-haloaluminate ionic liquids and depends on the alkyl chain length. Viscosity increases with increasing alkyl chain length, but it is not a linear trend. The ionic liquid with meta position of the alkyl chain is considerably more dense and more viscous than para isomer. The presence of aromatic phenyl ring at the side chain of the cation increases both density and viscosity. Higher effective molar fraction of AlCl3 increases density and decreases viscosity, however, for the imidazolium ionic liquid the change of viscosity diminishes at higher temperatures. Organic solvents decrease both density and viscosity of the ionic liquids, but aliphatic hexane imposes much smaller effect than aromatic toluene. The mixture of two ionic liquids has density and viscosity between those for constituents. This extends the application of the aralkyl ionic liquids over temperatures, in which they are in solid state.

Organic salt conditioner, organic salt-containing composition, and uses thereof

The present invention relates to the use of, and a composition containing, at least one non-polymeric organic salt with a melting point of less than 60° C. These organic salts may be imidazolium, pyrazolium, pyridinium, pyrimidinium or tetraalkylphosphonium salts. The inventinon composition may be used for washing (cleaning) and/or conditioning keratin materials, and especially the hair.