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Names | |
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Preferred IUPAC name
Pentan-2-ol | |
Other names
2-Pentanol
sec-amyl alcohol | |
Identifiers | |
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3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.025.370 |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C5H12O | |
Molar mass | 88.150 g·mol−1 |
Appearance | Colorless liquid |
Density | 0.812 g/cm3 |
Melting point | −73 °C (−99 °F; 200 K) |
Boiling point | 119.3 °C (246.7 °F; 392.4 K) |
45 g/L | |
Solubility | soluble in ethanol, diethyl ether, carbon tetrachloride, chloroform |
Vapor pressure | 0.804 kPa |
-69.1·10−6 cm3/mol | |
Viscosity | 3.470 mPa·s |
Thermochemistry | |
Heat capacity (C)
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2.716 J·g−1·K−1 (liquid) |
Std enthalpy of
formation (ΔfH⦵298) |
-365.2 kJ·mol−1 (liquid) -311.0 kJ·mol−1 (gas) |
Hazards | |
Flash point | 34 °C (93 °F; 307 K) |
343 °C (649 °F; 616 K) | |
Explosive limits | 1.2–9% |
Related compounds | |
Related compounds
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Amyl alcohol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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2-Pentanol (IUPAC name: pentan-2-ol; also called sec-amyl alcohol) is an organic chemical compound. It is used as a solvent and an intermediate in the manufacturing of other chemicals. 2-Pentanol is a component of many mixtures of amyl alcohols sold industrially. 2-Pentanol is chiral and thus can be obtained as either of two stereoisomers designated as (R)-(−)-2-pentanol and (S)-(+)-2-pentanol.
2-Pentanol has been detected in fresh bananas by gas chromatography–mass spectrometry, at an abundance of 14.26±2.63 ppm.[2]
Reactions[edit]
2-Pentanol can be manufactured by hydration of pentene.[3]
See also[edit]
References[edit]
- ^ Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.), Boca Raton, Florida: CRC Press, pp. 3–454, 5–42, 6–188, 8–102, 15–23, ISBN 0-8493-0594-2
- ^ Jordán, María J.; Tandon, Kawaljit; Shaw, Philip E.; Goodner, Kevin L. (2001), "Aromatic Profile of Aqueous Banana Essence and Banana Fruit by Gas Chromatography−Mass Spectrometry (GC-MS) and Gas Chromatography−Olfactometry (GC-O)", Journal of Agricultural and Food Chemistry, 49 (10): 4813–4817, doi:10.1021/jf010471k, PMID 11600027
- ^ McKetta, John J.; Cunningham, William Aaron (1977), Encyclopedia of Chemical Processing and Design, vol. 3, Boca Raton, Florida: CRC Press, pp. 280–281, ISBN 978-0-8247-2480-1, retrieved 2010-01-17
Well, that’s interesting to know that Psilotum nudum are known as whisk ferns. Psilotum nudum is the commoner species of the two. While the P. flaccidum is a rare species and is found in the tropical islands. Both the species are usually epiphytic in habit and grow upon tree ferns. These species may also be terrestrial and grow in humus or in the crevices of the rocks.
View the detailed Guide of Psilotum nudum: Detailed Study Of Psilotum Nudum (Whisk Fern), Classification, Anatomy, Reproduction