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Contents

   



(Top)
 


1 Reactions  





2 See also  





3 References  














2-Pentanol






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From Wikipedia, the free encyclopedia
 

(Redirected from Pentan-2-ol)

2-Pentanol[1]
Names
Preferred IUPAC name

Pentan-2-ol

Other names

2-Pentanol
sec-amyl alcohol

Identifiers

CAS Number

  • 31087-44-2 (R) checkY
  • 26184-62-3 (S) checkY
  • 3D model (JSmol)

    ChEBI
    ChEMBL
    ChemSpider
    ECHA InfoCard 100.025.370 Edit this at Wikidata

    PubChem CID

    UNII

    CompTox Dashboard (EPA)

    • InChI=1S/C5H12O/c1-3-4-5(2)6/h5-6H,3-4H2,1-2H3 checkY

      Key: JYVLIDXNZAXMDK-UHFFFAOYSA-N checkY

    • InChI=1/C5H12O/c1-3-4-5(2)6/h5-6H,3-4H2,1-2H3

      Key: JYVLIDXNZAXMDK-UHFFFAOYAY

    • OC(C)CCC

    Properties

    Chemical formula

    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)

    Solubility in water

    45 g/L
    Solubility soluble in ethanol, diethyl ether, carbon tetrachloride, chloroform
    Vapor pressure 0.804 kPa

    Magnetic susceptibility (χ)

    -69.1·10−6cm3/mol
    Viscosity 3.470 mPa·s
    Thermochemistry

    Heat capacity (C)

    2.716 J·g−1·K−1 (liquid)

    Std enthalpy of
    formation
    fH298)

    -365.2 kJ·mol−1 (liquid)
    -311.0 kJ·mol−1 (gas)
    Hazards
    Flash point 34 °C (93 °F; 307 K)

    Autoignition
    temperature

    343 °C (649 °F; 616 K)
    Explosive limits 1.2–9%
    Related compounds

    Related compounds

    Amyl alcohol

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    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 bananasbygas chromatography–mass spectrometry, at an abundance of 14.26±2.63 ppm.[2]

    Reactions

    [edit]

    2-Pentanol can be manufactured by hydrationofpentene.[3]

    See also

    [edit]

    References

    [edit]
    1. ^ 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

  • t
  • e

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=2-Pentanol&oldid=1216882116"

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