Chemistry:2-Ethyl-1-butanol
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| Names | |
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| Preferred IUPAC name
2-Ethylbutan-1-ol | |
| Other names
2-Ethyl-1-butanol
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| Identifiers | |
3D model (JSmol)
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| 1731254 | |
| ChemSpider | |
| EC Number |
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PubChem CID
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| RTECS number |
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| UNII | |
| UN number | 2275 |
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| Properties | |
| C6H14O | |
| Molar mass | 102.177 g·mol−1 |
| Appearance | Colorless liquid |
| Density | 830 mg mL−1 |
| Melting point | −114.40 °C; −173.92 °F; 158.75 K |
| Boiling point | 145 to 151 °C; 293 to 304 °F; 418 to 424 K |
| 10 g L−1 | |
| Vapor pressure | 206 Pa |
Refractive index (nD)
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1.422 |
| Thermochemistry | |
Heat capacity (C)
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246.65 J K−1 mol−1 |
| Hazards | |
| GHS pictograms | 
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| GHS Signal word | WARNING |
| H302, H312 | |
| P280 | |
| Flash point | 58 °C (136 °F; 331 K) |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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1.85 g kg−1 (oral, rat) |
| Related compounds | |
Related compounds
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
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 forms an azeotrope that otherwise limits the maximum ethanol concentration.[2]
Reactions
2-Ethyl-1-butanol is manufactured industrially by the aldol condensation of acetaldehyde and butyraldehyde, followed by hydrogenation.[3] It may also be prepared by the Guerbet reaction.
Properties and applications
The branching in 2-ethyl-1-butanol makes it harder to crystallize due to packing disruption, which results in a very low freezing point. Esters of 2-ethyl-1-butanol are similarly effected and it therefore finds application as a feedstock in the production of plasticizers and lubricants, where its presence helps reduce viscosity and lower freezing points.
See also
References
- ↑ Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.), Boca Raton, Florida: CRC Press, pp. 3–262, 8–106, 15–20, ISBN 978-0-8493-0594-8
- ↑ Roddy, James W. (1981). "Distribution of ethanol-water mixtures to organic liquids". Ind. Eng. Chem. Proc. Des. Dev. 20 (1): 104–108. doi:10.1021/i200012a016.
- ↑ McKetta, John J.; Cunningham, William Aaron (1994), Encyclopedia of Chemical Processing and Design, 47, Boca Raton, Florida: CRC Press, pp. 117, ISBN 978-0-8247-2451-1, https://books.google.com/books?id=iwSU5G5VzO0C&pg=PA279, retrieved 2010-01-25
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