21054-72-8 Usage
Uses
Used in Cleaning and Detergent Industry:
1-Dodecyl-2-methyl-3-benzylimidazolium chloride is used as a surfactant for its ability to reduce the surface tension of water, facilitating the cleaning process and enhancing the solubility of hydrophobic substances in water.
Used in Emulsification:
1-Dodecyl-2-methyl-3-benzylimidazolium chloride is used as an emulsifier to stabilize mixtures of immiscible liquids, such as oil and water, by reducing the interfacial tension between the two phases.
Used in Corrosion Inhibition:
1-Dodecyl-2-methyl-3-benzylimidazolium chloride is used as a corrosion inhibitor to protect metal surfaces from degradation and corrosion, particularly in industrial settings where metal components are exposed to harsh environments.
Used in Disinfectant Products:
1-Dodecyl-2-methyl-3-benzylimidazolium chloride is used as an antimicrobial agent in disinfectant products due to its ability to disrupt the cell membranes of microorganisms, effectively killing or inhibiting their growth.
Used in Chemical Industry:
1-Dodecyl-2-methyl-3-benzylimidazolium chloride is used as a versatile compound in the chemical industry for its multiple potential applications, including as a surfactant, emulsifier, detergent, corrosion inhibitor, and antimicrobial agent, making it a valuable asset in various chemical processes and formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 21054-72-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,5 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21054-72:
(7*2)+(6*1)+(5*0)+(4*5)+(3*4)+(2*7)+(1*2)=68
68 % 10 = 8
So 21054-72-8 is a valid CAS Registry Number.
InChI:InChI=1/C23H38N2.ClH/c1-3-4-5-6-7-8-9-10-11-15-18-24-19-20-25(22(24)2)21-23-16-13-12-14-17-23;/h12-14,16-17,19-20,22H,3-11,15,18,21H2,1-2H3;1H
21054-72-8Relevant articles and documents
Highly alkaline stable N1-alkyl substituted 2-methylimidazolium functionalized alkaline anion exchange membranes
Yang, Congrong,Wang, Suli,Ma, Wenjia,Jiang, Luhua,Sun, Gongquan
, p. 8559 - 8565 (2015/04/22)
Steric hindrance and hyperconjugative effects, introduced at the N1 position of 2-methylimidazolium, greatly enhance the alkaline stability of the 2-methylimidazolium functional group. 2-Methylimidazolium small molecule compounds with N1-substituents (but