54384-48-4

Basic information

• Product Name: 2,2',2''-[nitrilotris(ethane-2,1-diyloxy)trisethanol
• Synonyms: 2,2',2''-[nitrilotris(ethane-2,1-diyloxy)trisethanol;Triethanolamin-tris-glykolether;2,2',2''-[nitrilotris(2,1-ethanediyloxy)]tris-Ethanol;2,2',2''-[Nitrilotris(2,1-ethanediyloxy)]triethanol;Einecs 259-136-6;Ethanol, 2,2',2''-(nitrilotris(2,1-ethanediyloxy))tris-;2,2',2''-((nitrilotris(ethane-2,1-diyl))tris(oxy))triethanol;2,2',2''-((Nitrilotris(ethane-2,1-diyl))tris(oxy))tris(ethan-1-ol)
• CAS NO: 54384-48-4
• Molecular Formula: C₁₂H₂₇NO₆
• Molecular Weight: 281.3459
• EINECS: 259-136-6
• Mol File: 54384-48-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 174-176 °C(Press: 0.004 Torr)
• Appearance: /
• Density: 1.146±0.06 g/cm3(Predicted)
• PKA: 13.92±0.10(Predicted)
• CAS DataBase Reference: 2,2',2''-[nitrilotris(ethane-2,1-diyloxy)trisethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2',2''-[nitrilotris(ethane-2,1-diyloxy)trisethanol(54384-48-4)
• EPA Substance Registry System: 2,2',2''-[nitrilotris(ethane-2,1-diyloxy)trisethanol(54384-48-4)

Safety Data

• Hazardous Substances Data: 54384-48-4(Hazardous Substances Data)

Usage

Structure

A triethanolamine derivative with three ethoxy groups connected to the central nitrogen atom, and each ethoxy group is further linked to an ethane moiety.

Industrial and Consumer Applications

Widely used in various industries and consumer products.

Primary Use

As an emulsifying agent in cosmetics and personal care products.

Secondary Use

A pH adjuster and stabilizer in pharmaceuticals and topical medications.

Other Uses

Corrosion inhibitor in metalworking fluids and as a surfactant in cleaning products.

Solubility

Known for its ability to enhance the solubility of various substances.

Safety

Mild and non-irritating properties, making it a valuable chemical in many industries.

Upstream product

• 75-21-8 oxirane 
• 111-41-1 2-(2-Aminoethylamino)ethanol 
• 628-89-7 2-(2-Chloroethoxy)ethanol 
• 929-06-6 2-(2-Aminoethoxy)ethanol 

Relevant articles and documents

A halogen-bonding-based heteroditopic receptor for alkali metal halides

A new heteroditopic receptor for alkali metal halides has been designed and synthesized. It is comprised of a well-established motif for cation binding and a motif for halogen-bonding-based anion recognition processes. The single-crystal X-ray structure of the complex between the heteroditopic receptor and sodium iodide is reported. Thanks to the cooperativity of metal coordination and the strong I-...I halogen bonding, the ion pair is fully separated. The boosting effect of the binding of the anion through halogen bonding on the coordination of the cation by the receptor has been proved also in solution by NMR experiments. The selectivity of the new heterotopic receptor toward different alkali metal halides has been tested by ESI mass experiments. Copyright

SYNTHESIS AND CHARACTERIZATION OF A NEW MACROBICYCLIC (CRYPTAND) SIDEROPHORE CONTAINING THREE ENDOCYCLIC HYDROXAMATE DONOR GROUPS

The first trishydroxamate cryptand ligand was synthesized by tripodal coupling of a tris acid chloride and a tris O-benzylhydroxylamine.The spectrophotometric properties of its Fe(III) complex were investigated and compared with those of desferriferrioxamine B.Its 1:1 Ga(III) complex was also prepared and characterized.