| Weight | 130.255 g/mol |
|---|---|
| Formula | C8H20N+ |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
Tetraethylammonium (66-40-0)
Score:
#1240 in Physics
,
#2860 in Biology
,
#3580 in Chemistry
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- Interaction of Tetraethylammonium Ion Derivatives with the Potassium Channels of Giant Axons (The Journal of General Physiology, 1971)
- The Selective Inhibition of Delayed Potassium Currents in Nerve by Tetraethylammonium Ion (The Journal of General Physiology, 1967)
- Tetraethylammonium blockade distinguishes two inactivation mechanisms in voltage-activated K+ channels. (Proceedings of the National Academy of Sciences of the United States of America, 1991)
- The aromatic binding site for tetraethylammonium ion on potassium channels. (Neuron, 1992)
- ANOMALOUS RECTIFICATION IN THE SQUID GIANT AXON INJECTED WITH TETRAETHYLAMMONIUM CHLORIDE. (The Journal of General Physiology, 1965)
- The effects of 4aminopyridine and tetraethylammonium ions on normal and demyelinated mammalian nerve fibres. (The Journal of Physiology, 1981)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC[N+](CC)(CC)CC
-
InChIKeyCBXCPBUEXACCNR-UHFFFAOYSA-N
- Pubchem - Tetraethylammonium
- Wikipedia - tetraethylammonium
Tetraethylammonium (TEA), (NEt4+) or (Et4N+) is a quaternary ammonium cation consisting of four ethyl groups attached to a central nitrogen atom, and is positively charged. It is a counterion used in the research laboratory to prepare lipophilic salts of inorganic anions. It is used similarly to tetrabutylammonium, the difference being that its salts are less lipophilic and more easily crystallized.
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