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TRIETHANOLAMINE STEARATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

4568-28-9

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4568-28-9 Usage

General Description

Brown waxy solid. pH of 5% aqueous dispersion at 77° F: 8.8-9.2.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Basic salt of an amine. Aqueous solutions contain moderate concentrations of hydroxide ions and have pH's greater than 7.0. They react as bases to neutralize acids. These neutralizations generate heat, but less or far less than is generated by neutralization of the bases in reactivity group 10 (Bases) and the neutralization of amines. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible.

Fire Hazard

Flash point data for TRIETHANOLAMINE STEARATE are not available, but TRIETHANOLAMINE STEARATE is probably combustible.

Check Digit Verification of cas no

The CAS Registry Mumber 4568-28-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,6 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4568-28:
(6*4)+(5*5)+(4*6)+(3*8)+(2*2)+(1*8)=109
109 % 10 = 9
So 4568-28-9 is a valid CAS Registry Number.

4568-28-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name octadecanoate,tris(2-hydroxyethyl)azanium

1.2 Other means of identification

Product number -
Other names EINECS 224-945-5

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:4568-28-9 SDS

4568-28-9Downstream Products

4568-28-9Relevant articles and documents

Characterising the phase behaviour of stearic acid and its triethanolamine soap and acid-soap by infrared spectroscopy

Pudney, Paul D. A.,Mutch, Kevin J.,Zhu, Shiping

, p. 5010 - 5018 (2009)

The behaviour of stearic acid neutralised by triethanolamine to form soap and its acid-soap has been examined by infrared spectroscopy. It was found that not only could the neutralisation behaviour be characterised, but the thermotropic behaviour could also be followed. The neutralisation confirmed the formation of a fixed stoichiometeric ratio, 2:1, acid-soap. When following the thermotropic behaviour the break up of the acid-soap could be followed along with various disordering and melting transitions of the alkyl chain tail. This allowed all the thermal transitions that have been observed to be characterised in terms of the type of molecular rearrangement that was occurring and also the transition temperature at which they occurred. This allowed the binary phase diagram to be plotted and understood for this system. This is the first time IR has been used to measure a whole phase diagram of this type. The nature of the acid-soap complex itself was also characterised, with very short hydrogen bonds being present as well as a free, non-hydrogen bonded, hydroxyl group. the Owner Societies 2009.

Phase Behavior and Physical Properties of New Biobased Ionic Liquid Crystals

Toledo Hijo, Ariel A. C.,Maximo, Guilherme J.,Costa, Mariana C.,Cunha, Rosiane L.,Pereira, Jorge F. B.,Kurnia, Kiki A.,Batista, Eduardo A. C.,Meirelles, Antonio J. A.

, p. 3177 - 3189 (2017/06/07)

Protic ionic liquids (PILs) have emerged as promising compounds and attracted the interest of the industry and the academy community, due to their easy preparation and unique properties. In the context of green chemistry, the use of biocompounds, such as fatty acids, for their synthesis could disclose a possible alternative way to produce ILs with a low or nontoxic effect and, consequently, expanding their applicability in biobased processes or in the development of bioproducts. This work addressed efforts to a better comprehension of the complex solid-[liquid crystal]-liquid thermodynamic equilibrium of 20 new PILs synthesized by using fatty acids commonly found in vegetable oils, as well as their rheological profile and self-assembling ability. The work revealed that their phase equilibrium and physical properties are significantly impacted by the structure of the ions used for their synthesis. The use of unsaturated fatty acids and bis(2-hydroxyethyl)ammonium for the synthesis of these biobased ILs led to a drastic decreasing of their melting temperatures. Also, the longest alkyl chain fatty acids promoted higher self-assembling and more stable mesophases. Besides their sustainable appeal, the marked high viscosity, non-Newtonian profile, and very low critical micellar concentration values of the PIL crystals here disclosed make them interesting renewable compounds with potential applications as emulsifiers, stabilizers, thickeners, or biolubricants.

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