| Weight | 102.177 g/mol |
|---|---|
| Formula | C6H14O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
2-Ethyl-1-butanol (97-95-0)
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- Sigma-Aldrich - 2-Ethyl-1-butanol28.80 - 103.00 USD
- Fisher Scientific - Search for 2-Ethyl-1-butanol
- TCI - 2-Ethyl-1-butanol16.00 - 144.00 USD
- Selective synthesis of 2-ethyl-1-hexanol from n-butanol through the Guerbet reaction by using bifunctional catalysts based on copper or palladium precursors and sodium butoxide (Journal of Molecular Catalysis A-chemical, 2004)
- Solubility of Genistein in Water, Methanol, Ethanol, Propan-2-ol, 1-Butanol, and Ethyl Acetate from (280 to 333) K (Journal of Chemical & Engineering Data, 2010)
- Density, refractive index and speed of sound for mixtures of ethyl acetate with 2-butanol and 3-methyl-1-butanol: Vaporliquid equilibrium of the ethyl acetate + 3-methyl-1-butanol system (Fluid Phase Equilibria, 2004)
- Volumetric properties of ternary (IL + 2-propanol or 1-butanol or 2-butanol + ethyl acetate) systems and binary (IL + 2-propanol or 1-butanol or 2-butanol) and (1-butanol or 2-butanol + ethyl acetate) systems (The Journal of Chemical Thermodynamics, 2012)
- Densities and volumetric properties of ethyl acrylate + 1-butanol, or 2-butanol, or 2-methyl-1-propanol, or 2-methyl-2-propanol binary mixtures at temperatures from 288.15 to 318.15 K (Journal of Molecular Liquids, 2009)
- Estimation of VLE of binary systems (tert-butanol + 2-ethyl-1-hexanol) and (n-butanol + 2-ethyl-1-hexanol) using GMDH-type neural network (The Journal of Chemical Thermodynamics, 2010)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 -
SMILESCCC(CC)CO
-
InChIKeyTZYRSLHNPKPEFV-UHFFFAOYSA-N
- Pubchem - 2-Ethyl-1-butanol
- Wikipedia - 2-ethylbutanol
2-Ethyl-1-butanol (IUPAC name: 2-ethylbutan-1-ol) is an organic chemical compound. It can be used to facilitate the separation of ethanol from water, which form an azeotrope that otherwise limits the maximum ethanol concentration.
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