Date published: 2025-11-2

1-800-457-3801

SCBT Portrait Logo
Seach Input

2-(Ethylamino)ethanol (CAS 110-73-6)

0.0(0)
Write a reviewAsk a question

Alternate Names:
N-Ethylethanolamine
Application:
2-(Ethylamino)ethanol is A basic amino alcohol compound used for biochemical research
CAS Number:
110-73-6
Purity:
≥97%
Molecular Weight:
89.14
Molecular Formula:
C4H11NO
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

2-(ethylamino)ethanol, also known as Ethanolamine, is a versatile organic compound widely utilized in scientific and industrial research. In scientific research, 2-(ethylamino)ethanol finds extensive use as a reagent, solvent, and buffering agent within laboratory applications. Researchers employ 2-(ethylamino)ethanol to synthesize a diverse range of compounds, such as surfactants, detergents, and other amines. Additionally, it plays a role in the preparation of salts like sodium ethylenediaminetetraacetate (EDTA). Functionally, 2-(ethylamino)ethanol operates as a primary amine, exhibiting its ability to act as a base and accept protons from other compounds. This attribute allows it to function as a buffering agent, effectively stabilizing the pH of a solution. Furthermore, 2-(ethylamino)ethanol acts as a nucleophile, readily donating electrons to other molecules. This reactivity enables its participation in various reactions, including the synthesis of surfactants and other amines.


2-(Ethylamino)ethanol (CAS 110-73-6) References

  1. Biochemical characterization of the initial steps of the Kennedy pathway in Trypanosoma brucei: the ethanolamine and choline kinases.  |  Gibellini, F., et al. 2008. Biochem J. 415: 135-44. PMID: 18489261
  2. A NEW CLASS OF THIN FILM HYDROGELS PRODUCED BY PLASMA POLYMERIZATION.  |  Bhattacharyya, D., et al. 2007. Chem Mater. 19: 2222-2228. PMID: 19079730
  3. Chemical thermodynamics of ultrasound speed in solutions and liquid mixtures.  |  Reis, JC., et al. 2010. Chemphyschem. 11: 508-16. PMID: 20017181
  4. Head-group specificity for feedback regulation of CTP:phosphocholine cytidylyltransferase.  |  Jamil, H. and Vance, DE. 1990. Biochem J. 270: 749-54. PMID: 2173550
  5. A Comparative Study of the CO2 Absorption in Some Solvent-Free Alkanolamines and in Aqueous Monoethanolamine (MEA).  |  Barzagli, F., et al. 2016. Environ Sci Technol. 50: 7239-46. PMID: 27294832
  6. Microwave-Assisted Kabachnik⁻Fields Reaction with Amino Alcohols as the Amine Component.  |  Tajti, Á., et al. 2019. Molecules. 24: PMID: 31027303
  7. The CO2 absorption and desorption analysis of tri-solvent MEA + EAE + AMP compared with MEA + BEA + AMP along with 'coordination effects' evaluation.  |  Shi, H., et al. 2022. Environ Sci Pollut Res Int. 29: 40686-40700. PMID: 35083697
  8. Efficient Protocol for the Synthesis of 'N-Coded' Oligo- and Poly(N-Substituted Urethanes).  |  Mondal, T., et al. 2019. ACS Macro Lett. 8: 1002-1005. PMID: 35619476
  9. Sequential acid/reduction response of triblock copolymeric nanomicelles to release camptothecin and toll-like receptor 7/8 agonist for orchestrated chemoimmunotherapy.  |  Ge, X., et al. 2022. J Nanobiotechnology. 20: 369. PMID: 35953798
  10. Effects of analogles of ethanolamine and choline on phospholipid metabolism in rat hepatocytes.  |  Akesson, B. 1977. Biochem J. 168: 401-8. PMID: 606244

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-(Ethylamino)ethanol, 100 ml

sc-237870
100 ml
$15.00

2-(Ethylamino)ethanol, 500 ml

sc-237870A
500 ml
$34.00