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2-Methoxy-N,N,N-trimethylethanaminium, also known as 2-methoxy-N,N,N-trimethylethanaminium chloride or methyltrioctylammonium chloride, is a quaternary ammonium compound with the chemical formula C11H26ClNO. It is a colorless, viscous liquid that is soluble in water and organic solvents. 2-methoxy-N,N,N-trimethylethanaminium is widely used as a phase-transfer catalyst in organic synthesis, a surfactant in various applications, and as a biocide in industrial processes. It is also employed in the production of certain pharmaceuticals and agrochemicals. Due to its cationic nature, it exhibits antimicrobial properties, making it in useful disinfectant formulations. The compound is generally considered to be stable and non-flammable, but it should be handled with care due to its potential irritant and toxic properties.

6340-44-9

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6340-44-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6340-44-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6340-44:
(6*6)+(5*3)+(4*4)+(3*0)+(2*4)+(1*4)=79
79 % 10 = 9
So 6340-44-9 is a valid CAS Registry Number.

6340-44-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxyethyl(trimethyl)azanium,chloride

1.2 Other means of identification

Product number -
Other names Choline methyl ether chloride

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:6340-44-9 SDS

6340-44-9Downstream Products

6340-44-9Relevant academic research and scientific papers

The application of novel hydrophobic ionic liquids to the extraction of uranium(vi) from nitric acid medium and a determination of the uranyl complexes formed

Bell, Thomas James,Ikeda, Yasuhisa

experimental part, p. 10125 - 10130 (2011/12/04)

Novel ammonium based hydrophobic ionic liquids (ILs) have been synthesised and characterised, and their use in the liquid-liquid extraction of uranium(vi) from an aqueous nitric acid solution using tri-n-butyl phosphate (TBP), studied. On varying the nitr

The importance of molecular parameters of quaternary ammonium salts in their antigibberellin (retardant) activity

Gafurov,Grigor'ev,Proshin,Chistyakov,Martynov,Zefirov

, p. 592 - 598 (2007/10/03)

The importance of six theoretically calculated molecular parameters in the antigibberellin (retardant) activity of quaternary ammonium salts is studied using a regression analysis. A bioassay system based on cell culture of fungus Gibberella fujikuroi is used to determine the activity. In the case of N,N,N-trimethyl-N-(2-hydroxyethyl)ammonium chloride (choline) and N,N,N-triethyl-N-(2-hydroxyethyl)ammonium chloride (N,N,N-triethylcholine) derivatives with linear structure, the polarizability, proton acceptor activity, and lipophilicity of these compounds exert the largest effect on the antigibberellin activity. The antigibberellin activity of more sterically hindered N,N-dialkylpiperidinium salts was mainly defined by the steric parameter, while the polarizability, proton acceptor activity, and (through them) lipophilicity exert a lesser effect. Other parameters are of minor importance for the three groups of compounds studied.

Thiomolybdate analogues and uses thereof

-

, (2008/06/13)

The current invention provides novel thiomolybdate derivatives, methods of making novel thiomolybdate derivatives, pharmaceutical compositions of novel thiomolybdate derivatives, methods of using novel thiomolybdate derivatives to treat diseases associated with aberrant vascularization and methods of using pharmaceutical compositions of thiomolybdate derivatives to treat diseases associated with aberrant vascularization.

Thiomolybdate analogues and uses thereof

-

, (2008/06/13)

The current invention provides novel thiomolybdate derivatives, methods of making novel thiomolybdate derivatives, pharmaceutical compositions of novel thiomolybdate derivatives, methods of using novel thiomolybdate derivatives to treat diseases associated with aberrant vascularization, copper metabolism disorders, neurodegenerative disorders, obesity or NF-κB dysregulation and methods of using pharmaceutical compositions of thiomolybdate derivatives to treat diseases associated with aberrant vascularization, copper metabolism disorders, neurodegenerative disorders, obesity or NF-κB dysregulation.

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