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decane

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EntityQ150717· pop 52· linked from 172 articles

Also known as n-decane

Decane is an alkane hydrocarbon with the chemical formula C10H22. Although 75 structural isomers are possible for decane, the term usually refers to the normal-decane ("n-decane"), with the formula CH3(CH2)8CH3. All isomers, however, exhibit similar properties and little attention is paid to the composition. These isomers are flammable liquids. Decane is present in small quantities (less than 1%) in gasoline (petrol) and kerosene. Like other alkanes, it is a nonpolar solvent, and does not dissolve in water, and is readily combustible. Although it is a component of fuels, it is of little import

Chemical data

Formula
C10H22
Molecular weight
142.28 g/mol
IUPAC name
decane
SMILES
CCCCCCCCCC
InChIKey
DIOQZVSQGTUSAI-UHFFFAOYSA-N
XLogP
5
Polar surface area
0 Ų
H-bond donors
0
H-bond acceptors
0
Formal charge
0

via PubChem

~1 min read

Encyclopedic overview

5 sections
Contents
  • Reactions
  • Physical properties
  • See also
  • References
  • External links

Decane is an alkane hydrocarbon with the chemical formula C10H22. Although 75 structural isomers are possible for decane, the term usually refers to the normal-decane ("n-decane"), with the formula CH3(CH2)8CH3. All isomers, however, exhibit similar properties and little attention is paid to the composition. These isomers are flammable liquids. Decane is present in small quantities (less than 1%) in gasoline (petrol) and kerosene. Like other alkanes, it is a nonpolar solvent, and does not dissolve in water, and is readily combustible. Although it is a component of fuels, it is of little importance as a chemical feedstock, unlike a handful of other alkanes.

==Reactions== Decane undergoes combustion, just like other alkanes. In the presence of sufficient oxygen, it burns to form water and carbon dioxide. 2 C10H22 + 31 O2 → 20 CO2 + 22 H2O With insufficient oxygen, carbon monoxide is also formed.

Excerpted from Wikipedia’s “decane” article, available under the CC BY-SA 4.0 licence.

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