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Nitrilotriethylene trilaurate, also known as N,N-bis(2-hydroxyethyl)-N'-(2-hydroxyethyl)-N'-dodecyl-1,2-ethanediamine trilaurate, is a complex organic compound with the chemical formula C42H81N3O6. It is a type of nonionic surfactant, which is widely used in various industries such as cosmetics, pharmaceuticals, and lubricants due to its emulsifying, wetting, and dispersing properties. The compound is derived from the reaction of nitrilotriacetic acid (NTA) with lauric acid, resulting in a molecule that has three laurate chains attached to the nitrogen atoms of the nitrilotriacetic structure. This unique structure allows it to form stable emulsions and dispersions, making it a valuable ingredient in formulations that require these properties.

3002-20-8

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3002-20-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3002-20-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,0 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3002-20:
(6*3)+(5*0)+(4*0)+(3*2)+(2*2)+(1*0)=28
28 % 10 = 8
So 3002-20-8 is a valid CAS Registry Number.
InChI:InChI=1/C42H81NO6/c1-4-7-10-13-16-19-22-25-28-31-40(44)47-37-34-43(35-38-48-41(45)32-29-26-23-20-17-14-11-8-5-2)36-39-49-42(46)33-30-27-24-21-18-15-12-9-6-3/h4-39H2,1-3H3

3002-20-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[bis(2-dodecanoyloxyethyl)amino]ethyl dodecanoate

1.2 Other means of identification

Product number -
Other names nitrilotriethane-2,1-diyl tridodecanoate

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:3002-20-8 SDS

3002-20-8Downstream Products

3002-20-8Relevant academic research and scientific papers

Synthesis, surface properties, and biological activity of some cationic surfactant complexes

Adawy, Ahmed I.,Abbas, Mohammed A.,Zakaria, Khaled

, p. 77 - 89 (2021/07/02)

Various surfactants were designed in this analysis by esterification of triethanol amine with dodecanoic acid then quaternized through benzyl bromide then complexed with hydrated cobalt chloride to produce metallocationic surfactants. Characterization of

Bilayer Membranes of Triple-Chain Ammonium Amphiphiles

Kunitake, Toyoki,Kimizuka, Nobuo,Higashi, Nobuyuki,Nakashima, Naotoshi

, p. 1978 - 1983 (2007/10/02)

Ten ammonium amphiphiles which possess three long-chain alkyl tails (C12 or C16) were prepared.They form clear aqueous dispersions upon sonication.Electron microscopy and light scattering experiments indicated the formation of huge bilayer aggregates except for one case.These bilayers undergo the characteristic crystal-to-liquid crystal-phase transition, as confirmed by differential scanning calorimetry (DSC) and by fluorescence depolarization of a diphenylhexatriene probe.Riboflavin, a water-soluble fluorescent probe, was shown to be trapped in bilayer vesicles of some triple-chain amphiphiles.Mixing of these bilayers with those of single-chain and double-chain amphiphiles was examined by DSC and by absorption spectroscopy.Together with our previous results, the present study establishes that the bilayer formation is a general phenomenon that is observable for a wide variety of synthetic amphiphiles.

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