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Ethanaminium, N-(2-carboxyethyl)-2-hydroxy-N,N-dimethyl-, inner salt, also known as 2-hydroxy-N,N-dimethyl-N-(2-carboxyethyl)ethanaminium, is a complex organic compound with the chemical formula C7H16NO3. It is an inner salt, which means it contains both acidic and basic functional groups that can neutralize each other, resulting in a zwitterion. Ethanaminium, N-(2-carboxyethyl)-2-hydroxy-N,N-dimethyl-, inner salt is derived from the parent compound ethanolamine, with a carboxyethyl group attached to the nitrogen atom and a hydroxyl group on the carbon chain. It is a zwitterionic surfactant, which means it has both cationic and anionic properties, making it useful in various applications such as detergents, emulsifiers, and foaming agents. The compound is also known for its ability to form micelles and has potential applications in drug delivery systems due to its amphiphilic nature.

6249-53-2

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6249-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6249-53-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,4 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6249-53:
(6*6)+(5*2)+(4*4)+(3*9)+(2*5)+(1*3)=102
102 % 10 = 2
So 6249-53-2 is a valid CAS Registry Number.

6249-53-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(N,N-dimethyl-N-(2-hydroxyethyl)ammonio)propionate

1.2 Other means of identification

Product number -
Other names 3-(2-Hydroxyethyldimethylammonio)propionate

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:6249-53-2 SDS

6249-53-2Downstream Products

6249-53-2Relevant academic research and scientific papers

Effect of reactant association on addition of tertiary amines to acrylic acid in aqueous solutions

Malyshev,Shirshin,Kazantsev,Sivokhin,Zhiganov,Kuznetsov

, p. 1629 - 1633 (2006)

The formation of betaines by the reaction of tertairy amines (N,N-dimethyl-N-2-hydroxyethylamine, N,N-dimethylaminoethyl methacrylate, N-methylmorpholine, N,N-dimethylaminopropionitrile, 1,4-diazabicyclo[2.2.2] octane) with acrylic acid in aqueous solutions in a wide concentration range was studied. The concentration effects observed were interpreted taking into account the association of the starting reagents. Nauka/Interperiodica 2006.

Synthesis of carboxy-and sulfobetaines from tertiary amines and unsaturated acids

Kazantsev,Kazakov,Shirshin,Danov

, p. 343 - 349 (2007/10/03)

Reactions of various tertiary amines with 2-propenamido-2-methylpropanesulfonic, 4-propenamido-4-methyl-1, 1-dioxotetrahydrothiophene-3-sulfonic, 2-propenamidoacetic, 6-propenamidohexanoic, and propenoic acids lead to formation of the corresponding zwitte

Hydrolytic stability of N,N-dimethylaminoethyl acrylate

Kazantsev,Shirshin,Danov,Kazakov

, p. 317 - 320 (2007/10/03)

Reasons for different hydrolytic stability of N,N-dimethylaminoethyl acrylate and methacrylate are discussed.

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