Triethanolamine hydriodide

Base Information

• Chemical Name: Triethanolamine hydriodide
• CAS No.: 7601-53-8
• Molecular Formula: C6H16INO3
• Molecular Weight: 277.102
• European Community (EC) Number: 231-508-2
• UNII: DT98IT03JK
• DSSTox Substance ID: DTXSID60226921
• Wikidata: Q27276587
• RXCUI: 1942478
• Mol file: 7601-53-8.mol

Synonyms:Triethanolamine hydriodide;7601-53-8;TEA-HYDROIODIDE;UNII-DT98IT03JK;EINECS 231-508-2;DT98IT03JK;2,2',2''-Nitrilotrisethanol hydroiodide;TRIETHANOLAMINE HYDROIODIDE;2-[bis(2-hydroxyethyl)amino]ethanol;hydroiodide;Ethanol, 2,2',2''-nitrilotri-, hydriodide;Ethanol, 2,2',2''-nitrilotris-, hydriodide;2-[bis(2-hydroxyethyl)amino]ethanol,hydroiodide;IODERMOL;IODOTRAT;triethanolammonium iodide;C6H15NO3.HI;SCHEMBL378914;Ethanol,2,2',2''-nitrilotris-, hydriodide (9CI);TEA-HYDROIODIDE [INCI];DTXSID60226921;C6-H15-N-O3.H-I;2,2',2''-nitrilotriethanol hydroiodide;TRIETHANOLAMMONIUM IODIDE [WHO-DD];FT-0636532;2, 2', 2''- nitrilotrisethanol hydroiodide;Ethanol,2,2',2''-nitrilotris-,hydriodide(9ci);Q27276587;ETHANOL, 2,2',2''-NITRILOTRIS-, HYDRIODIDE (1:1)

Chemical Property of Triethanolamine hydriodide

Chemical Property:

• Appearance/Colour: white crystalline powder
• Vapor Pressure: 8.38E-06mmHg at 25°C
• Melting Point: 168 °C
• Boiling Point: 335.4 °C at 760 mmHg
• Flash Point: 185 °C
• PSA: 63.93000
• LogP: -0.73650
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 6
• Exact Mass: 277.01749
• Heavy Atom Count: 11
• Complexity: 55.7

Purity/Quality:

99%, ^*data from raw suppliers

TRIETHANOLAMINE HYDROIODIDE 99.00% ^*data from reagent suppliers

Safty Information:

• Safety Statements: S24/25:Avoid contact with skin and eyes.

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(CO)N(CCO)CCO.I

Technology Process of Triethanolamine hydriodide

There total 5 articles about Triethanolamine hydriodide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 87.0%

1-(iodomethyl)silatrane (52741-69-2) + monophenylthiourea (103-85-5) → tris(2-hydroxyethyl)amine hydroiodide (7601-53-8)

Guidance literature:

In butan-1-ol; for 12h; Heating;

DOI:10.1023/B:RUGC.0000031856.58701.2c

Reference yield: 83.0%

C11H18N2O3SSi*HI + triethanolamine (102-71-6,64114-46-1) → 1-phenyl-2-(2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undec-1-ylmethyl)-isothiourea; hydriodide + tris(2-hydroxyethyl)amine hydroiodide (7601-53-8)

Guidance literature:

In chloroform;

DOI:10.1023/B:RUGC.0000031856.58701.2c

Reference yield: 13.0%

allyl iodid (556-56-9) + germatrane (67453-19-4) → 1-iodogermatrane (70559-36-3) + allylgermatrane (84664-63-1) + tris(2-hydroxyethyl)amine hydroiodide (7601-53-8)

Guidance literature:

In benzene; under dry N2; mixt. boiled for 35 min; cooled; triethanolamine hydriodide isolated; a mixt. pptd. by evapn. of filtrat;e; recrystd. from hexane and allylgermatrane isolated;

upstream raw materials:

triethanolamine

1-(iodomethyl)silatrane

monophenylthiourea

1-(chloromethyl)silatrane

Refernces

• 1、 -. "PROCESS FOR THE PREPARATION OF ALKYLENE CARBONATE". Page/Page column 5. . Retrieved 2008/06/13.