|Preferred IUPAC name
3D model (JSmol)
|Molar mass||149.19 g·mol−1|
|Density||1.124 g mL−1|
|Melting point||21.60 °C; 70.88 °F; 294.75 K|
|Boiling point||335.40 °C; 635.72 °F; 608.55 K|
|Vapor pressure||1 Pa (at 20 °C)|
|UV-vis (λmax)||280 nm|
Refractive index (nD)
Heat capacity (C)
|389 J K−1 mol−1|
Std enthalpy of
|−665.7 – −662.7 kJ mol−1|
Std enthalpy of
|−3.8421 – −3.8391 MJ mol−1|
|Safety data sheet||hazard.com|
|GHS signal word||WARNING|
|Flash point||179 °C (354 °F; 452 K)|
|325 °C (617 °F; 598 K)|
|Lethal dose or concentration (LD, LC):|
LD50 (median dose)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Triethanolamine aka Trolamine (abbr. as TEOA to distinguish it from TEA which is for triethylamine) is a viscous organic compound that is both a tertiary amine and a triol. A triol is a molecule with three alcohol groups. Triethanolamine is a strong base. Approximately 150,000 tonnes were produced in 1999. It is a colourless compound although samples may appear yellow because of impurities.
- 1 Production
- 2 Applications
- 3 Safety and regulation
- 4 See also
- 5 References
Triethanolamine is produced from the reaction of ethylene oxide with aqueous ammonia, also produced are ethanolamine and diethanolamine. The ratio of the products can be controlled by changing the stoichiometry of the reactants.
Triethanolamine is used primarily in making surfactants, such as for emulsifier. It is a common ingredient in formulations used for both industrial and consumer products. The triethanolamine neutralizes fatty acids, adjusts and buffers the pH, and solubilizes oils and other ingredients that are not completely soluble in water. Triethanolammonium salts in some cases are more soluble than salts of alkali metals that might be used otherwise, and results in less alkaline products than would from using alkali metal hydroxides to form the salt. Some common products in which triethanolamine is found are sunscreen lotions, liquid laundry detergents, dishwashing liquids, general cleaners, hand sanitizers, polishes, metalworking fluids, paints, shaving cream and printing inks.
Triethanolamine is also used as organic additive (0.1 wt%) in the grinding of cement clinker. It facilitates the grinding process by preventing agglomeration and coating of the powder at the surface of balls and mill wall.
Cosmetics and medicine
Various ear diseases and infections are treated with eardrops containing triethanolamine polypeptide oleate-condensate, such as Cerumenex in the United States. In pharmaceutics, triethanolamine is the active ingredient of some eardrops used to treat impacted earwax. It also serves as a pH balancer in many different cosmetic products, ranging from cleansing creams and milks, skin lotions, eye gels, moisturizers, shampoos, shaving foams, and so on. TEOA is a fairly strong base: a 1% solution has a pH of approximately 10, whereas the pH of skin is less than pH 7, approximately 5.5−6.0. Cleansing milk–cream emulsions based on TEOA are particularly good at removing makeup.
In the laboratory and in amateur photography
Another common use of TEOA is as a complexing agent for aluminium ions in aqueous solutions. This reaction is often used to mask such ions before complexometric titrations with another chelating agent such as EDTA. TEOA has also been used in photographic (silver halide) processing. It has been promoted as a useful alkali by amateur photographers.
TEOA is used to provide a sensitivity boost to silver-halide-based holograms, and also as a swelling agent to color shift holograms. It is possible to get the sensitivity boost without color shift by rinsing out the TEA before squeegee and drying.
In electroless plating
TEOA is now commonly and very effectively used as a complexing agent in electroless plating.
In ultrasonic testing
2-3% in water TEOA is used as an corrosion inhibitor (anti-rust) agent in immersion ultrasonic testing.
Safety and regulation
A 1996 study found that triethanolamine (TEOA) occasionally causes contact allergy. A 2001 study found TEOA in a sunscreen caused an allergic contact dermatitis. A 2007 study found TEOA in ear drops caused a contact allergy. Systemic and respiratory tract (RT) toxicity was analyzed for 28 days in a nose specific inhalation 2008 study in Wistar rats; TEOA seems to be less potent in regard to systemic toxicity and RT irritancy than diethanolamine (DEA). Exposure to TEOA resulted in focal inflammation, starting in single male animals from 20 mg/m3 concentrations.
A 2009 study stated that patch test reactions reveal a slight irritant potential instead of a true allergic response in several cases, and also indicated the risk of skin sensitization to TEOA seems to be very low.
Reports indicated that TEOA causes an increased incidence of tumor growth in the liver in female B6C3F1 mice, but not in male mice or in Fischer 344 rats. A 2004 study concluded "TEOA may cause liver tumors in mice via a choline-depletion mode of action and that this effect is likely caused by the inhibition of choline uptake by cells."
A 2009 study found that TEOA has potential acute, sub-chronic and chronic toxicity properties in respect to aquatic species.
- Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. pp. 79, 128. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
- Simond, M. R. (2012). "Dissociation Constants of Protonated Amines in Water at Temperatures from 293.15 K to 343.15 K". Journal of Solution Chemistry. 41: 130. doi:10.1007/s10953-011-9790-3.
- Budavari, Susan, ed. (2001), The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (13th ed.), Merck, ISBN 0911910131
- Frauenkron, Matthias; Melder, Johann-Peter; Ruider, Günther; Rossbacher, Roland; Höke, Hartmut, "Ethanolamines and Propanolamines", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH, doi:10.1002/14356007.a10_001
- Weissermel, Klaus; Arpe, Hans-Jürgen; Lindley, Charlet R.; Hawkins, Stephen (2003). "Chapter 7. Oxidation Products of Ethylene". Industrial Organic Chemistry. Wiley-VCH. pp. 159–161. ISBN 3-527-30578-5.
- Ashford, Robert D. (2011). Ashford’s Dictionary of Industrial Chemicals (3rd ed.). Saltash, Cornwall: Wavelength Publications. p. 9252. ISBN 978-0-9522674-3-0.
- Sohoni, S.; Sridhar, R.; Mandal, G. (1991). "Effect of grinding aids on the fine grinding of limestone, quartz and portland cement clinker". Powder Technology. 67 (3): 277–286. doi:10.1016/0032-5910(91)80109-V.
- "Holoforum.org". Holoforum.org. Retrieved 2016-07-16.
- Hamilton, T. K.; Zug, K. A. (1996). "Triethanolamine allergy inadvertently discovered from a fluorescent marking pen". Am. J. Contact Dermat. 7 (3): 164–5. doi:10.1016/S1046-199X(96)90006-8. PMID 8957332.
- Chu, C. Y.; Sun, C. C. (2001). "Allergic contact dermatitis from triethanolamine in a sunscreen". Contact Dermatitis. 44 (1): 41–2. doi:10.1034/j.1600-0536.2001.440107-8.x. PMID 11156016.
- Schmutz, J. L.; Barbaud, A.; Tréchot, P. (2007). "Contact allergy to triethanolamine in ear drops and shampoo". Ann. Dermatol. Venereol. 134 (1): 105. PMID 17384563.
- Gamer, A. O.; Rossbacher, R.; Kaufmann, W.; van Ravenzwaay, B. (2008). "The inhalation toxicity of di- and triethanolamine upon repeated exposure". Food Chem. Toxicol. 46 (6): 2173–2183. doi:10.1016/j.fct.2008.02.020. PMID 18420328.
- Lessmann, H.; Uter, W.; Schnuch, A.; Geier, J. (2009). "Skin sensitizing properties of the ethanolamines mono-, di-, and triethanolamine. Data analysis of a multicentre surveillance network (IVDK*) and review of the literature". Contact Dermatitis. 60 (5): 243–255. doi:10.1111/j.1600-0536.2009.01506.x. PMID 19397616.
- Stott, W. T.; Radtke, B. J.; Linscombe, V. A.; Mar, M. H.; Zeisel, S. H. (2004). "Evaluation of the potential of triethanolamine to alter hepatic choline levels in female B6C3F1 mice". Toxicol. Sci. 79 (2): 242–7. doi:10.1093/toxsci/kfh115. PMC 1592523. PMID 15056812.
- Libralato, G.; Volpi Ghirardini, A.; Avezzù, F. (2009). "Seawater ecotoxicity of monoethanolamine, diethanolamine and triethanolamine". J. Hazard. Mater. 176 (1–3): 535–9. doi:10.1016/j.jhazmat.2009.11.062. PMID 20022426.