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411222-01-0

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411222-01-0 Usage

Chemical Properties

White cystalline solid

Check Digit Verification of cas no

The CAS Registry Mumber 411222-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,1,2,2 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 411222-01:
(8*4)+(7*1)+(6*1)+(5*2)+(4*2)+(3*2)+(2*0)+(1*1)=70
70 % 10 = 0
So 411222-01-0 is a valid CAS Registry Number.

411222-01-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Hexyl-2,3-Dimethylimidazolium Bromide

1.2 Other means of identification

Product number -
Other names 1-hexyl-2,3-dimethylimidazol-3-ium,bromide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:411222-01-0 SDS

411222-01-0Downstream Products

411222-01-0Relevant articles and documents

The Viscosity and Density of Ionic Liquid + Tetraglyme Mixtures and the Effect of Tetraglyme on CO2 Solubility

Fillion, Joseph J.,Bennett, Joshua Edward,Brennecke, Joan F.

, p. 608 - 622 (2017)

We show that the addition of tetraglyme (TG), which is a low viscosity liquid with relatively low vapor pressure, is effective in reducing the viscosity of ionic liquids (ILs). In particular, we measure the viscosities of mixtures of 18 ionic liquids with tetraglyme at temperatures between 278.15 and 323.15 K, with a focus on mixtures that are primarily ionic liquid. Thirteen of the ionic liquids contain aprotic heterocyclic anions (AHA ILs) paired with tetra-alkylphosphonium and imidazolium cations, which we have developed for cofluid vapor compression refrigeration and postcombustion CO2 capture applications. Three bis(trifluoromethylsulfonyl)amide ([Tf2N]-) ionic liquids are included for comparison, as well as trihexyltetradecylphosphonium acetate and trihexyltetradecylphosphonium dicyanamide ([P66614][acetate] and [P66614][DCA]). In addition, we present the densities of trihexyltetradecylphosphonium 1,2,3-triazolide ([P66614][3-Triz]) + tetraglyme mixtures at temperatures between 283.15 and 353.15 K. Finally, we show that the solubility of CO2 in mixtures of [P66614][3-Triz] + 30 mol % tetraglyme and trihexyltetradecylphosphonium 1,2,4-triazolide ([P66614][4-Triz]) + 30 mol % tetraglyme at 313.15, 333.5, and 353.6 K and pressures to 34 bar can be represented reasonably well by a mole fraction weighted sum of the solubilities (on a mole ratio basis) in the two pure components. (Figure Presented).

Ionic liquids promote PCR amplification of DNA

Shi, Yugang,Liu, Yen-Liang,Lai, Peng-Yeh,Tseng, Ming-Chung,Tseng, Min-Jen,Li, Yudong,Chu, Yen-Ho

supporting information; experimental part, p. 5325 - 5327 (2012/06/30)

A bicyclic imidazolium ionic liquid (4d), [b-4C-im][Br], was found to be highly effective not only for promoting PCR of GC-rich DNA by minimizing non-specific amplification, but also for facilitating PCR of normal-GC DNA under mild conditions.

High-pressure phase behavior of carbon dioxide with imidazolium-based ionic liquids

Aki, Sudhir N. V. K.,Mellein, Berlyn R.,Saurer, Eric M.,Brennecke, Joan F.

, p. 20355 - 20365 (2008/01/27)

Previously we have shown that supercritical carbon dioxide can be used to extract organics from ionic liquids (ILs). Subsequently, ionic liquids/carbon dioxide biphasic solutions have been used for a variety of homogeneously catalyzed reactions. Therefore, an understanding of the phase behavior of carbon dioxide with ionic liquids is needed to design extraction and reaction processes necessary for these applications. We present measurements of the solubility of carbon dioxide in 10 different imidazolium-based ionic liquids at 25, 40, and 60?°C and pressures to 150 bar. As expected, the solubility increases with increasing pressure and decreases with increasing temperature for all the ILs investigated. To investigate the influence of the anion, seven of the ILs studied have 1-butyl-3-methylimidazolium ([bmim]) as the cation. The anions are dicyanamide ([DCA]), nitrate ([NO3]), tetrafluoroborate ([BF4]), hexafluorophosphate ([PF6]), trifuoromethanesulfonate ([TfO]), bis(trifluoromethylsulfonyl)imide ([Tf 2N]), and tris(trifluoromethylsulfonyl)methide ([methide]). The other ILs considered in the study, chosen to investigate the influence of varying number and length of alkyl chains on the cation, include 1-hexyl-3- methylimidazolium bis(trifluoromethylsulfonyl)imide ([hmim][Tf2N]), 2,3-dimethyl-1-hexylimidazolium bis(trifluoromethylsulfonyl)imide ([hmmim][Tf2N]), and 1-octyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([omim][Tf2N]). Results show that the solubility of carbon dioxide is strongly dependent on the choice of anion. In particular, CO2 solubility is greater in ILs with anions, such as [Tf2N] and [methide], which contain fluoroalkyl groups. Also, we observe that an increase in the alkyl chain length on the cation increases the CO2 solubility marginally.

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