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 a conjugate acid nor a conjugate base, they are not buffers.
Names | |
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IUPAC name
Triethylammonium acetate
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Other names
teaa, triethylamine/acetate buffer
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.023.632 |
PubChem CID
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CompTox Dashboard (EPA)
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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
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Corrosive, harmful |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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References
edit- ^ "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.