Skip to content
2-octanone

Structure via PubChem · Public domain (PubChem)

EntityQ18611679· pop 5· linked from 7 articles

2-octanone

Sign in to save

Also known as octan-2-one, hexyl methyl ketone, methyl hexyl ketone

2-Octanone is an organic compound with the formula . It is a colorless volatile liquid that is produced commercially for use in the fragrance industry. It is produced by the condensation of acetone and pentanal followed by hydrogenation of the alkene. It can also be produced by selective oxidation of 1-octene. It is one of three octanones, the others being 3-octanone and 4-octanone. It is a common if trace component of many cooked foods.

In the Vinony graph

Vinony's link graph records 7 inbound references to 2-octanone, and connects out to International Standard Book Number, mass density and digital object identifier.

It sits within the topics Chembox having GHS data, ECHA InfoCard ID from Wikidata and Octanones.

Vinony links it to 5 Wikipedia language editions.

Chemical data

Formula
C8H16O
Molecular weight
128.21 g/mol
IUPAC name
octan-2-one
SMILES
CCCCCCC(=O)C
InChIKey
ZPVFWPFBNIEHGJ-UHFFFAOYSA-N
XLogP
2.4
Polar surface area
17.1 Ų
H-bond donors
0
H-bond acceptors
1
Formal charge
0

via PubChem

Wikidata facts

Mass
128.120115132
Show 5 more facts
canonical SMILES
CCCCCCC(=O)C
found in taxon
Eryngium foetidum
melting point
-16.0
chemical formula
C₈H₁₆O
has characteristic
bitterness
Sources (3)

via Wikidata · CC0

~1 min read

Encyclopedic overview

2 sections
Contents
  • See also
  • References

2-Octanone is an organic compound with the formula . It is a colorless volatile liquid that is produced commercially for use in the fragrance industry. It is produced by the condensation of acetone and pentanal followed by hydrogenation of the alkene. It can also be produced by selective oxidation of 1-octene. It is one of three octanones, the others being 3-octanone and 4-octanone. It is a common if trace component of many cooked foods.

==See also== Filbertone

Excerpted from Wikipedia’s “2-octanone” article, available under the CC BY-SA 4.0 licence.

Available in 5 languages

via Wikidata sitelinks · CC0

Connections

Categories