1-Pentanol
Names | |
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Preferred IUPAC name Pentan-1-ol[1] | |
Identifiers | |
CAS Number |
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3D model (JSmol) |
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Beilstein Reference | 1730975 |
ChEBI |
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ChEMBL |
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ChemSpider |
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ECHA InfoCard | 100.000.684 |
EC Number |
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Gmelin Reference | 25922 |
KEGG |
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MeSH | n-Pentanol |
PubChem CID |
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RTECS number |
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UNII |
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UN number | 1105 |
CompTox Dashboard (EPA) |
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InChI
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Properties | |
Chemical formula | C5H12O |
Molar mass | 88.150 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) |
-67.7·10−6 cm3/mol | |
Refractive index (nD) | 1.409 |
Thermochemistry | |
Heat capacity (C) | 207.45 J K−1 mol−1 |
Std molar entropy (S⦵298) | 258.9 J K−1 mol−1 |
Std enthalpy of formation (ΔfH⦵298) | −351.90–−351.34 kJ mol−1 |
Std enthalpy of combustion (ΔcH⦵298) | −3331.19–−3330.63 kJ mol−1 |
Hazards | |
GHS labelling: | |
Warning | |
H226, H315, H332, H335 | |
P261 | |
NFPA 704 (fire diamond) | 1 2 0 |
Flash point | 49 °C (120 °F; 322 K) |
Autoignition temperature | 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). N verify (what is YN ?) Infobox references |
1-Pentanol, (or n-pentanol, pentan-1-ol), is an organic compound with the formula CH3CH2CH2CH2CH2OH and is classified as a primary alcohol.[2] It is a colourless liquid with a distinctive aroma. It is one of 8 isomeric alcohols with the formula C5H11OH. It is used as a solvent, a biological drying agent and in the synthesis of some fragrance compounds. It is also a common component of fusel alcohols (fusel oils), the undesirable byproducts of alcoholic fermentation.
Preparation
1-Pentanol is prepared from 1-butene by hydroformylation followed by hydrogenation of the resulting pentanal.[3]
- CH3CH2CH=CH2 + CO + H2 → CH3CH2CH2CH2CHO
- CH3CH2CH2CH2CHO + H2 → CH3CH2CH2CH2CH2OH
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.[4][5]
Uses and occurrence
The hydroxyl group (OH) is the active site of many reactions. The ester formed from 1-pentanol and butyric acid is pentyl butyrate, which has an apricot-like odor. The ester formed from 1-pentanol and acetic acid is amyl acetate (also called pentyl acetate), which has a banana-like odor.
It is a precursor to dipentyl zinc dithiophosphates, which are used in froth flotation.[3]
In 2014, a study was conducted comparing the performance of diesel fuel blends with various proportions of pentanol as an additive. While gaseous emissions increased with higher concentrations of pentanol, particulate emissions decreased.[6]
Pentanol is often used as a solvent.
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.
- ^ a b Lappe, Peter; Hofmann, Thomas (2011). "Pentanols". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a19_049.pub2. ISBN 9783527303854.
- ^ Cann, Anthony F.; Liao, James C. (2010-01-01). "Pentanol isomer synthesis in engineered microorganisms". Applied Microbiology and Biotechnology. 85 (4): 893–899. doi:10.1007/s00253-009-2262-7. ISSN 1432-0614. PMC 2804790. PMID 19859707.
- ^ Tseng, Hsien-Chung (2011). Production of pentanol in metabolically engineered Escherichia coli (Thesis thesis). Massachusetts Institute of Technology. hdl:1721.1/65767.
- ^ Wei, Liangjie & Cheung, C.s & Huang, Zuohua. (2014). Effect of n-pentanol addition on the combustion, performance and emission characteristics of a direct-injection diesel engine. Energy. 70. 10.1016/j.energy.2014.03.106.
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Alcohols found in alcoholic drinks |
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Medical alcohol |
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Toxic alcohols |
alcohols (1°)
Methanol | |
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Ethanol |
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Butanol |
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Straight-chain saturated C1 — C9 |
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Straight-chain saturated C10 — C19 |
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Straight-chain saturated C20 — C29 |
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Straight-chain saturated C30 — C39 |
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Straight-chain saturated C40 — C49 |
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alcohols (2°)
alcohols (3°)
- 2-Methyl-2-pentanol
- 2-Methylheptan-2-ol
- 2-Methylhexan-2-ol
- 3-Methyl-3-pentanol
- 3-Methyloctan-3-ol
- Diacetone alcohol
- Ethchlorvynol
- Methylpentynol
- Nonafluoro-tert-butyl alcohol
- tert-Amyl alcohol
- tert-Butyl alcohol
- Triphenylethanol
- Triphenylmethanol
Monohydric alcohols |
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Dihydric alcohols | |
Trihydric alcohols | |
Polyhydric alcohols (sugar alcohols) |
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fatty alcohols
unsaturated
fatty alcohols
- 3-Methyl-3-pentanol
- Erucyl alcohol
- Linolenyl alcohol
- Linoleyl alcohol
- Oleyl alcohol
- Palmitoleyl alcohol
- tert-Amyl alcohol
- tert-Butyl alcohol
C1 — C7 |
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Deoxy sugar alcohols | |
Cyclic sugar alcohols | |
Glycylglycitols |
Monoterpene alcohols | |
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Sesquiterpene alcohols | |
Diterpene alcohols |
- 1,3-Difluoro-2-propanol
- 2,2,2-Trifluoroethanol
- 2-Fluoroethanol
- Nonafluoro-tert-butyl alcohol
- Trifluoromethanol
- Category