This is an old revision of this page, as edited by Plasmic Physics (talk | contribs) at 10:53, 12 November 2011. The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.
Revision as of 10:53, 12 November 2011 by Plasmic Physics (talk | contribs)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)
| |
| |
| Names | |
|---|---|
| IUPAC name Pentan-1-ol | |
| Identifiers | |
| CAS Number | |
| 3D model (JSmol) | |
| Beilstein Reference | 1730975 |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.000.684 
|
| EC Number |
|
| Gmelin Reference | 25922 |
| KEGG | |
| MeSH | n-Pentanol |
| PubChem CID | |
| RTECS number |
|
| UNII | |
| UN number | 1105 |
| CompTox Dashboard (EPA) | |
InChI
| |
SMILES
| |
| Properties | |
| Chemical formula | C5H12O |
| Molar mass | 88.150 g·mol |
| Density | 814.4 mg cm |
| Melting point | −78 °C; −109 °F; 195 K |
| Solubility in water | 22 g dm |
| log P | 1.348 |
| Vapor pressure | 200 Pa (at 20 °C) |
| Refractive index (nD) | 1.409 |
| Thermochemistry | |
| Heat capacity (C) | 207.45 J K mol |
| Std molar entropy (S298) |
258.9 J K mol |
| Std enthalpy of formation (ΔfH298) |
−351.90–−351.34 kJ mol |
| Std enthalpy of combustion (ΔcH298) |
−3331.19–−3330.63 kJ mol |
| Hazards | |
| GHS labelling: | |
| Pictograms |  
|
| Signal word | Warning |
| Hazard statements | H226, H315, H332, H335 |
| Precautionary statements | P261 |
| NFPA 704 (fire diamond) |
 |
| Flash point | 49 °C |
| Related compounds | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
 Y verify (what is ?)
Infobox references
| |
1-Pentanol, (or n-pentanol, pentan-1-ol), is an alcohol with five carbon atoms and the molecular formula C5H12O. 1-Pentanol is a colorless liquid with an unpleasant aroma. There are 8 alcohols with this molecular formula (see amyl alcohol). The ester formed from butanoic acid and 1-pentanol, pentyl butyrate, smells like apricot. The ester formed from acetic acid and 1-pentanol, amyl acetate (pentyl acetate), smells like banana.
Pentanol can be prepared by fractional distillation of fusel oil. To reduce the use of fossil fuels, research is underway to discover cost effective methods of utilizing fermentation to produce Bio-Pentanol. Pentanol can be used as a solvent for coating CDs and DVDs. Another use is a replacement for gasoline.
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.
 | This article about an alcohol is a stub. You can help Misplaced Pages by expanding it. |