| Weight | 101.193 g/mol |
|---|---|
| Formula | C6H15N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
Triethylamine (121-44-8)
triethylamine hydrochloride · triethylammonium formate · triethylamine phosphate
Score:
#206 in Physics
,
#593 in Chemistry
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- Ruthenium(II)-Catalyzed Asymmetric Transfer Hydrogenation of Ketones Using a Formic AcidTriethylamine Mixture (Journal of the American Chemical Society, 1996)
- Palladium catalyzed reductions of halo- and nitroaromatic compounds with triethylammonium formate (Journal of Organic Chemistry, 1977)
- The Horner-Wadsworth-Emmons modification of the Wittig reaction using triethylamine and lithium or magnesium salts (Journal of Organic Chemistry, 1985)
- Palladium catalyzed triethylammonium formate reduction of aryl triflates. A selective method for the deoxygenation of phenols. (Tetrahedron Letters, 1986)
- Fabrication of Dye-Sensitized Solar Cells Using Triethylamine Hydrothiocyanate as a CuI Crystal Growth Inhibitor (Langmuir, 2002)
- Polymerization of m-chlorophenylacetylene initiated by (Rh(norbornadiene)Cl)2-triethylamine catalyst containing long-lived propagation species. (Polymer Journal, 1990)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H225: Highly Flammable liquid and vapor
Danger Flammable liquids - Category 2 - H311: Toxic in contact with skin
Danger Acute toxicity, dermal - Category 3 - H312: Harmful in contact with skin
Warning Acute toxicity, dermal - Category 4 - H318: Causes serious eye damage
Danger Serious eye damage/eye irritation - Category 1 - H332: Harmful if inhaled
Warning Acute toxicity, inhalation - Category 4 - H370: Causes damage to organs
Danger Specific target organ toxicity, single exposure - Category 1 - H401: Toxic to aquatic life
Hazardous to the aquatic environment, acute hazard - Category 2 - triethylamine hydrochloride
- triethylammonium formate
- triethylamine phosphate
- triethylamine acetate
- triethylamine hydrobromide
- triethylamine dinitrate
- triethylamine sulfite (1:1)
- triethylamine phosphonate (1:1)
- triethylamine phosphate (1:1)
- triethylamine sulfate
- triethylamine maleate (1:1)
- triethylamine sulfate (2:1)
- triethylamine sulfite (2:1)
-
SMILESCCN(CC)CC
-
InChIKeyZMANZCXQSJIPKH-UHFFFAOYSA-N
- Pubchem - Triethylamine
- Wikipedia - triethylamine
Triethylamine is the chemical compound with the formula N(CH2CH3)3, commonly abbreviated Et3N. It is also abbreviated TEA, yet this abbreviation must be used carefully to avoid confusion with triethanolamine or tetraethylammonium, for which TEA is also a common abbreviation. It is a colourless volatile liquid with a strong fishy odor reminiscent of ammonia and is also the smell of the hawthorn plant.
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Alternate Names
Estimated Properties
| Boiling Point | 85.24 C | EPA T.E.S.T. |
|---|---|---|
| Density | 0.77 g/cm3 | EPA T.E.S.T. |
| Flash Point | 5.11 C | EPA T.E.S.T. |
| Water Solubility | 100304 mg/L | EPA T.E.S.T. |
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Synthesis
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Triethylamine
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