1-Pentanol
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| Names | |
|---|---|
| IUPAC name
Pentan-1-ol[1] | |
| Identifiers | |
71-41-0  | |
| 3D model (Jmol) | Interactive image |
| 1730975 | |
| ChEBI | CHEBI:44884 |
| ChEMBL | ChEMBL14568 |
| ChemSpider | 6040 |
| ECHA InfoCard | 100.000.684 |
| EC Number | 200-752-1 |
| 25922 | |
| KEGG | C16834  |
| MeSH | n-Pentanol |
| PubChem | 6276 |
| RTECS number | SB9800000 |
| UNII | M9L931X26Y |
| UN number | 1105 |
| |
| |
| Properties | |
| C5H12O | |
| Molar mass | 88.15 g·mol−1 |
| Density | 0.811 g cm−3 |
| Melting point | −78 °C; −109 °F; 195 K |
| Boiling point | 137 to 139 °C; 278 to 282 °F; 410 to 412 K |
| 22 g L−1 | |
| log P | 1.348 |
| Vapor pressure | 200 Pa (at 20 °C) |
| Refractive index (nD) |
1.409 |
| Thermochemistry | |
| 207.45 J K−1 mol−1 | |
| Std molar entropy (S |
258.9 J K−1 mol−1 |
| Std enthalpy of formation (ΔfH |
−351.90–−351.34 kJ mol−1 |
| Std enthalpy of combustion (ΔcH |
−3331.19–−3330.63 kJ mol−1 |
| Hazards | |
| GHS pictograms |   |
| GHS signal word | WARNING |
| H226, H315, H332, H335 | |
| P261 | |
| EU classification (DSD) |
 Xn |
| R-phrases | R10, R20, R37, R66 |
| S-phrases | (S1/2), S46 |
| NFPA 704 | |
| Flash point | 49 °C (120 °F; 322 K) |
| 300 °C (572 °F; 573 K) | |
| Related compounds | |
| Related compounds |
Hexane |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| verify (what is ?) | |
| Infobox references | |
1-Pentanol, (or n-pentanol, pentan-1-ol), is an alcohol with five carbon atoms and the molecular formula C5H11OH.[2] 1-Pentanol is a colorless liquid with an unpleasant aroma. It is the straight-chain form of amyl alcohol, one of 8 isomers with that formula.
The hydroxyl group (OH) is the active site of many reactions. The ester formed from 1-pentanol and butyric acid is pentyl butyrate, which smells like apricot. The ester formed from 1-pentanol and acetic acid is amyl acetate (also called pentyl acetate), which smells like banana.
Pentanol can be used as a solvent for coating CDs and DVDs. Pentanol has all the properties necessary to replace gasoline as an internal combustion fuel.
Pentanol can be prepared by fractional distillation of fusel oil. To reduce the use of fossil fuels, research is underway to develop cost-effective methods of producing (chemically identical) bio-pentanol with fermentation.
References
- ↑ "n-pentanol - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 26 March 2005. Identification and Related Records. Retrieved 10 October 2011.
- ↑ CRC Handbook of Chemistry and Physics 65Th Ed.