Names | |
---|---|
IUPAC name
Triethylammonium acetate | |
Other names
teaa, triethylamine/acetate buffer | |
Identifiers | |
3D model (JSmol) |
|
ChemSpider | |
ECHA InfoCard | 100.023.632 |
PubChem CID |
|
CompTox Dashboard (EPA) |
|
| |
| |
Properties | |
(CH3CH2)3NHOCOCH3 | |
Molar mass | 161.24 g/mol |
Boiling point | 164.5 °C (328.1 °F; 437.6 K) |
Soluble | |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards |
Corrosive, harmful |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references |
Triethylammonium acetate is a volatile salt, which is often used as an ion-pairing reagent in high-performance liquid chromatography separations of oligonucleotides.[1][2][3][4] Since unadjusted triethylammonium acetate salt solutions contain neither conjugate acid nor conjugate base, they are not buffers.
References
- ↑ "Triethylammonium Acetate, 1 M Solution - CAS 5204-74-0 - Calbiochem 625718". Sigma-Aldrich. Retrieved 2020-07-25.
- ↑ PubChem. "Triethylammonium acetate". pubchem.ncbi.nlm.nih.gov. Retrieved 2020-07-25.
- ↑ Berton, Paula; Kelley, Steven P.; Wang, Hui; Rogers, Robin D. (2018-11-01). "Elucidating the triethylammonium acetate system: Is it molecular or is it ionic?". Journal of Molecular Liquids. 269: 126–131. doi:10.1016/j.molliq.2018.08.006. ISSN 0167-7322. S2CID 106116704.
- ↑ "Solution Preparation". www.chem.uci.edu. Retrieved 2020-07-25.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.