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1-butyl-1-ethylpiperidinium is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23624-40-0

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23624-40-0 Usage

Chemical composition

1-butyl-1-ethylpiperidinium consists of a piperidinium cation with one butyl and one ethyl substituent.

Usage

It is often used as a component in ionic liquid mixtures for various applications, such as a solvent and a catalyst in organic synthesis.

Alternative solvent potential

1-butyl-1-ethylpiperidinium has been studied as an alternative to traditional solvents due to its low volatility, high thermal stability, and ability to dissolve a wide range of chemicals.

Industrial applications

It has shown promise in applications such as gas separation, electrochemical devices, and bio-catalysis.

Interest in research and industry

1-butyl-1-ethylpiperidinium has garnered interest for its unique properties and potential for use in various industrial and research settings.

Check Digit Verification of cas no

The CAS Registry Mumber 23624-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,6,2 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 23624-40:
(7*2)+(6*3)+(5*6)+(4*2)+(3*4)+(2*4)+(1*0)=90
90 % 10 = 0
So 23624-40-0 is a valid CAS Registry Number.

23624-40-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-butyl-1-ethylpiperidin-1-ium,bromide

1.2 Other means of identification

Product number -
Other names 1-Aethyl-1-n-butylpiperidiniumbromid

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:23624-40-0 SDS

23624-40-0Downstream Products

23624-40-0Relevant academic research and scientific papers

Diagnosing the plasma formed during acoustic cavitation in [BEPip][NTf2] ionic liquid

Pflieger, Rachel,Lejeune, Manuel,Noel, Cédric,Belmonte, Thierry,Nikitenko, Sergey I.,Draye, Micheline

, p. 1183 - 1189 (2019)

Sonoluminescence (SL) spectra of a very dry [BEPip][NTf2] ionic liquid were measured in the first minutes of sonication under Ar. The intense sonoluminescence allowed us to monitor the time-evolution of the SL spectra. Several molecular emissions were observed. Rovibronic temperatures of C2 and CN were determined giving vibrational temperatures of 5800 ± 500 K and 6000 ± 500 K and rotational temperatures (i.e. translational or gas temperatures) of 4000 ± 500 K. These temperatures stay remarkably constant during the sonolysis, while SL spectra undergo strong changes that illustrate the very fast evolution of the plasma during the first minutes of sonication. The expected strong decrease in the plasma electron energy also reflects in the evolution of the populations of CH electronically excited states. The physical meaning of temperatures derived from molecular emissions in SL spectra is discussed.

Surface characterization of 1-butyl-1-ethylpiperidinium bromide by inverse gas chromatography

Papadopoulou, Stella K.,Papaiconomou, Nicolas,Baup, Stéphane,Iojoiu, Cristina,Svecova, Lenka,Thivel, Pierre-Xavier

, (2019)

This work addresses the surface characterization of an organic salt based on a piperidinium cation and a halide anion, similar to a first generation ionic liquid, using the Inverse Gas Chromatography (IGC)technique. IGC was employed in order to assess the dispersive surface energy and the acid/base character of 1-butyl-1-ethylpiperidinium bromide, [C2C4PIP]Br at a temperature range (313.15–343.15 K)well below its melting point, where the retention mechanism is governed by the surface adsorption of the probes. This type of characterization was possible due to the high melting point of [C2C4PIP]Br, namely 413.15 K. The dispersive component of the surface energy was estimated with the aid of the Schultz method and the Dorris-Gray method. Results obtained using the first method were higher than the ones obtained by the latter. The discrepancy between the two methods was found to increase with the increase of temperature. The acid/base characterization was implemented by using the Flour and Papirer approach as well as the Brookman and Sawyer method. The acidity and basicity constants of the surface of [C2C4PIP]Br revealed that it is amphoteric with a predominantly basic character.

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