• Triethanolamine

Triethanolamine

  • CasNo:102-71-6
  • Purity:99%

Product Details;

CasNo: 102-71-6

Molecular Formula: C6H15NO3

Appearance: Clear, amber viscous liquid

Buy Reliable Quality Wholesale 102-71-6 with Cheapest Price

  • Molecular Formula:C6H15NO3
  • Molecular Weight:149.19
  • Appearance/Colour:Clear, amber viscous liquid 
  • Vapor Pressure:0.01 mm Hg ( 20 °C) 
  • Melting Point:21 °C 
  • Refractive Index:n20/D 1.485(lit.)  
  • Boiling Point:335.4 °C at 760 mmHg 
  • PKA:7.8(at 25℃) 
  • Flash Point:185 °C 
  • PSA:63.93000 
  • Density:1.171 g/cm3 
  • LogP:-1.73470 

Triethanolamine(Cas 102-71-6) Usage

General description

Triethanolamine is a hygroscopic liquid with a weak ammoniacal odor, ranging in color from colorless to pale yellow. It may turn brown upon exposure to air and light, and at lower temperatures, it can form colorless or pale yellow cubic crystals. With a melting point of 21.2°C, a boiling point of 360°C, a flash point of 193°C, a relative density (d420) of 1.1242, and a refractive index (nD20) of 1.4852, triethanolamine is a versatile compound. It is miscible with water, ethanol, and acetone, while being slightly soluble in ether, benzene, and carbon tetrachloride.

Uses

Triethanolamine exhibits strong alkalinity, allowing it to function as a base by accepting protons, making it suitable for condensation reactions. In the cement industry, triethanolamine serves as an early strength agent. It accelerates the hydration process of cement in concrete, enhancing early strength, increasing concrete density, and providing anti-permeability and antifreeze properties. In pharmaceutical formulations, triethanolamine is utilized in emulsions and as an alkylating agent. It finds application in various pharmaceutical products, including topical preparations, injectable solutions, topical analgesics, and sunscreens.

Production Methods

Triethanolamine is prepared commercially by the ammonolysis of ethylene oxide. The reaction yields a mixture of monoethanolamine, diethanolamine, and triethanolamine, which are separated to obtain the pure products.

Definition

ChEBI: A tertiary amino compound that is ammonia in which each of the hydrogens is substituted by a 2-hydroxyethyl group.

Brand name

Mobisyl [as salicylate] (Ascher);Sabrilex.

Shipping

UN2491 Ethanol amine or Ethanolamine solutions, Hazard class: 8; Labels: 8-Corrosive material.

Waste Disposal

Controlled incineration; incinerator equipped with a scrubber or thermal unit to reduce nitrogen oxides emissions

InChI:InChI=1/C6H15NO3/c8-4-1-7(2-5-9)3-6-10/h8-10H,1-6H2

102-71-6 Relevant articles

Hydration of cement — role of triethanolamine

V.S Ramachandran

, Cement and Concrete Research Volume 6, Issue 5, September 1976, Pages 623-631

Triethanolamine (TEA) accelerated the hydration of 3CaO.Al2O3 and 3CaO.Al2O3-CaSO4.2H2O systems and extended the induction period of the hydration of 3CaO.SiO2. In portland cement paste TEA decreased the strength at all ages and setting characteristics were drastically altered, especially at higher TEA contents.

AFFINITIES OF CROWN ETHERS, GLYMES, AND POLYAMINES FOR ALKALI PICRATES IN TOLUENE. APPLICATION OF POLYMER-SUPPORTED LINEAR POLYETHERS.

Xu,Smid

, p. 3790 - 3796 (1984)

This work reports the measurements of K ...

Structures of monoethanolamine (MEAM), diethanolamine (DEAM) and triethanolamine (TEAM)

D. Mootz, D. Brodalla and M. Wiebcke

, Acta Cryst. (1989). C45, 754-757

(IUCr) Structures of monoethanolamine (MEAM), diethanolamine (DEAM) and triethanolamine (TEAM) … 756 MONOETHANOLAMINE, DIETHANOLAMINE AND TRIETHANOLAMINE...

Organoboranes. LI. Convenient procedures for the recovery of pinanediol in asymmetric synthesis via one-carbon homologation of boronic esters

Brown, Herbert C.,Rangaishenvi, Milind V.

, p. 15 - 30 (1988)

Matteson's asymmetric synthesis via a on...

102-71-6 Process route

propylene glycol
57-55-6,63625-56-9

propylene glycol

triethanolamine
102-71-6,64114-46-1

triethanolamine

Conditions
Conditions Yield
 
 
1-methylsilatrane
2288-13-3

1-methylsilatrane

triethanolamine
102-71-6,64114-46-1

triethanolamine

methylsilanetriol
2445-53-6

methylsilanetriol

Conditions
Conditions Yield
With disodium hydrogenphosphate; potassium dihydrogenphosphate; at 40 - 70 ℃; Kinetics; Thermodynamic data; Mechanism; hydrolysis in neutral medium;
 

102-71-6 Upstream products

  • 75-21-8
    75-21-8

    oxirane

  • 141-43-5
    141-43-5

    ethanolamine

  • 555-77-1
    555-77-1

    tris-(2-chloro-ethyl)-amine

  • 7529-23-9
    7529-23-9

    tris(2-hydroxyethyl)amine-N-oxide

102-71-6 Downstream products

  • 104095-80-9
    104095-80-9

    tris-[2-(4-nitro-benzoyloxy)-ethyl]-amine

  • 141-46-8
    141-46-8

    Glycolaldehyde

  • 111-42-2
    111-42-2

    2,2'-iminobis[ethanol]

  • 3002-18-4
    3002-18-4

    tris-(2-acetoxy-ethyl)-amine

Inquiry

Name:
*CompanyName:
*Email:
*Requirements:
*Code:
Submit