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N-[2-[(2-aminoethyl)amino]ethyl]stearamide is a complex organic compound with the chemical formula C24H50N2O. It is a derivative of stearamide, which is a fatty acid amide. N-[2-[(2-aminoethyl)amino]ethyl]stearamide is characterized by the presence of a stearamide group (a long-chain fatty acid amide) and a triamine (3-aminopropylaminoethylamine) moiety. The structure features a stearamide backbone with an amide linkage to a 2-aminoethyl group, which is further connected to another 2-aminoethyl group, forming a branched chain. N-[2-[(2-aminoethyl)amino]ethyl]stearamide is of interest in various chemical and industrial applications, such as in the synthesis of surfactants, emulsifiers, and other specialty chemicals, due to its unique structure and properties.

3574-73-0

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3574-73-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3574-73-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,7 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3574-73:
(6*3)+(5*5)+(4*7)+(3*4)+(2*7)+(1*3)=100
100 % 10 = 0
So 3574-73-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H47N3O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-22(26)25-21-20-24-19-18-23/h24H,2-21,23H2,1H3,(H,25,26)

3574-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2-(2-aminoethylamino)ethyl]octadecanamide

1.2 Other means of identification

Product number -
Other names Stearic acid,diethylenetriamine monoamide

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:3574-73-0 SDS

3574-73-0Relevant academic research and scientific papers

Some imidazoline derivatives as corrosion inhibitors

Aiad, Ismail Abdelrhman,Hafiz,El-Awady,Habib

experimental part, p. 247 - 254 (2011/12/02)

In this study, cationic surfactants having different alkyl chain lengths were prepared by amidation of lauric, myristic, palmitic, stearic, oleic acids with diethylene triamine. The products were quaternized using chlo-roacetic acid. The chemical structure of the prepared compounds was elucidated using different spectroscopic techniques. The critical micelle concentration (CMC) and the free energy of the micellization and adsorption of these compounds were determined by surface tension and conductivity measurements. The products were evaluated as surface-active agents as well as corrosion inhibitors for steel alloy in 1 M hydrochloric and sulfuric acid, the results indicate that these materials have a high efficiency as corrosion inhibitors and as surface active agents. These results were correlated with the chemical structure of the prepared compounds. AOCS 2009.

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