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

2717-15-9

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2717-15-9 Usage

Uses

TEA-oleate is a mild emulsifier and surfactant.

Check Digit Verification of cas no

The CAS Registry Mumber 2717-15-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,1 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2717-15:
(6*2)+(5*7)+(4*1)+(3*7)+(2*1)+(1*5)=79
79 % 10 = 9
So 2717-15-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H34O2.C6H15NO3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20;8-4-1-7(2-5-9)3-6-10/h9-10H,2-8,11-17H2,1H3,(H,19,20);8-10H,1-6H2/b10-9+;

2717-15-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name TRIETHANOLAMINE OLEATE

1.2 Other means of identification

Product number -
Other names tea-oleate

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:2717-15-9 SDS

2717-15-9Synthetic route

triethanolamine
102-71-6

triethanolamine

cis-Octadecenoic acid
112-80-1

cis-Octadecenoic acid

oleic acid triethanolamine salt
2717-15-9

oleic acid triethanolamine salt

Conditions
ConditionsYield
for 1h; Inert atmosphere;

2717-15-9Downstream Products

2717-15-9Relevant academic research and scientific papers

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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