26323-02-4

Basic information

• Product Name: Bis(dodecyltrimethylammonium) sulfate
• Synonyms: BIS(DODECYLTRIMETHYLAMMONIUM) SULFATE;N,N,N-Trimethyl-1-dodecanaminium sulfate (2:1)
• CAS NO: 26323-02-4
• Molecular Formula: C30H68N2O4S
• Molecular Weight: 552.94
• Mol File: 26323-02-4.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Bis(dodecyltrimethylammonium) sulfate(CAS DataBase Reference)
• NIST Chemistry Reference: Bis(dodecyltrimethylammonium) sulfate(26323-02-4)
• EPA Substance Registry System: Bis(dodecyltrimethylammonium) sulfate(26323-02-4)

Safety Data

• Hazardous Substances Data: 26323-02-4(Hazardous Substances Data)

Usage

General Description

Bis(dodecyltrimethylammonium) sulfate is a chemical compound that belongs to the class of quaternary ammonium compounds. It is a surfactant and cationic detergent, commonly used in industrial and household cleaning products. Bis(dodecyltrimethylammonium) sulfate is composed of a sulfate anion and two dodecyltrimethylammonium cations, making it highly effective in reducing surface tension and improving the wetting and spreading properties of liquids. It is also used as an emulsifier, stabilizer, and antimicrobial agent in various applications. However, it is important to handle this chemical with caution due to its potential toxicity and environmental impact.

InChI:InChI=1/2C15H34N.H2O4S/c2*1-5-6-7-8-9-10-11-12-13-14-15-16(2,3)4;1-5(2,3)4/h2*5-15H2,1-4H3;(H2,1,2,3,4)/q2*+1;/p-2

Upstream product

• 616-38-6 carbonic acid dimethyl ester 
• 124-22-1 n-Dodecylamine 
• 77-78-1 dimethyl sulfate 

Relevant articles and documents

Synthesis and evaluation of the antimicrobial activity of Dodecyl trimethyl ammonium and N-(N, N-Dimethylamino) propyl glucosylamine

In this study Dodecyl trimethyl ammonium sulphate (DTA) was obtained through quaternization reaction between dodecylamine and dimethyl sulfate (yield: 51.5%) while Dimethylamino propyl glucosylamine (DAPGA) was successively synthesized from D-glucose and 3-Dimethylamino propylamine (yield: 93.6%). Both compounds were analyzed through NMR spectroscopy. Evaluation of their biological activity against Salmonella Typhimurium, Staphylococcus aureus and Fusarium oxysporum cubens indicated that at a concentration greater than 0.001 10- 4 mole mL -1, DTA significantly inhibited growth of Salmonella Typhimurium and Staphylococcus aureus while DAPGA was not effective. Furthermore, these two compounds showed a pronounced antifungal activity against a toxicogen fungal, Fusarium oxysporum cubens.

The synthesis of quaternary ammonium salts from ammonium salts and dialkyl carbonate

Quaternary ammonium salts were synthesized from ammonium salts and dialkyl carbonates over an ionic liquid catalyst 1-ethyl-3-methylimidazolium bromide. The Royal Society of Chemistry 2006.