Difference between revisions of "Pentanol"

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===Relevant Sciencemadness threads===
 
===Relevant Sciencemadness threads===
 
*[http://www.sciencemadness.org/talk/viewthread.php?tid=65422 n-amyl alcohol]
 
*[http://www.sciencemadness.org/talk/viewthread.php?tid=65422 n-amyl alcohol]
 +
*[http://www.sciencemadness.org/talk/viewthread.php?tid=75246 n-Pentane to n-Pentanol]
  
 
[[Category:Chemical compounds]]
 
[[Category:Chemical compounds]]

Revision as of 18:56, 14 July 2017

Pentanol
Names
IUPAC name
Pentan-1-ol
Other names
1-Pentanol
Amyl alcohol
n-Amyl alcohol
n-Pentanol
Properties
C5H12O
C5H11OH
Molar mass 88.15 g/mol
Appearance Colorless liquid
Odor Fusel-like
Density 0.818 g/cm3 (15 °C)
0.8146 g/cm3 (20 °C)
0.811 g/cm3 (25 °C)
Melting point −78 °C (−108 °F; 195 K)
Boiling point 137.5 °C (279.5 °F; 410.6 K)
2.2 g/100 ml (25 °C)
Solubility Miscible with acetone, diethyl ether, ethanol
Vapor pressure 2.2 mmHg at 25 °C
Thermochemistry
258.9 J·K−1·mol−1
−351.90–−351.34 kJ/mol
Hazards
Safety data sheet Sigma-Aldrich
Flash point 49 °C (120 °F; 322 K)
Lethal dose or concentration (LD, LC):
3,645 mg/kg (rat, oral)
Related compounds
Related compounds
Butanol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Pentanol, also known as n-pentanol, 1-pentanol or pentan-1-ol, is a higher chain alcohol, used in the manufacturing of various pleasant smelling esters. It has the chemical formula C5H12O or C5H11OH.

Properties

Chemical

Pentanol can be oxidized to pentanoic acid.

Physical

Pentanol is a colorless liquid, slightly soluble in water.

Availability

Amyl alcohol is sold by various chemical suppliers.

Pentanol can be obtained from the fractional distillation of fusel oil.

Preparation

n-Pentanol is cheaper to buy than synthesize it yourself.

Projects

  • Make esters

Handling

Safety

Like most higher-chain alcohols, n-pentanol has a high flash point, meaning it has low flammability.

Storage

In closed bottles.

Disposal

Can be safely destroyed by mixing it with a more flammable solvent and burned.

References

Relevant Sciencemadness threads