Octanal

Octanal
Names

IUPAC name Octanal
Other names Caprylic aldehyde Octanaldehyde Aldehyde C-8
Identifiers
CAS Number	124-13-0^Y
3D model (Jmol)	Interactive image
ChEBI	CHEBI:17935^N
ChemSpider	441^N
ECHA InfoCard	100.004.259
PubChem	454
UNII	XGE9999H19^Y
InChI InChI=1S/C8H16O/c1-2-3-4-5-6-7-8-9/h8H,2-7H2,1H3^N Key: NUJGJRNETVAIRJ-UHFFFAOYSA-N^N InChI=1/C8H16O/c1-2-3-4-5-6-7-8-9/h8H,2-7H2,1H3 Key: NUJGJRNETVAIRJ-UHFFFAOYAK
SMILES CCCCCCCC=O
Properties
Chemical formula	C₈H₁₆O
Molar mass	128.21204
Appearance	Colorless or lightly yellow liquid
Density	0.821 g/cm³
Melting point	12 to 15 °C (54 to 59 °F; 285 to 288 K)
Boiling point	171 °C (340 °F; 444 K)
Solubility in water	Slightly soluble
Hazards
Flash point	51 °C (124 °F; 324 K)
Related compounds
Related aldehydes	Heptanal Nonanal
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is ^YN ?)
Infobox references

Octanal is the organic compound, an aldehyde, with the chemical formula CH₃(CH₂)₆CHO. A colorless fragrant liquid with a fruit-like odor, it occurs naturally in citrus oils. It is used commercially as a component in perfumes and in flavor production for the food industry. It is usually produced by hydroformylation of heptene and the dehydrogenation of 1-octanol.^[1]

Octanal can also be referred to as caprylic aldehyde or aldehyde C-8.

References

Silberberg, 2006, Principles of Chemistry
Octanal

↑ Christian Kohlpaintner, Markus Schulte, Jürgen Falbe, Peter Lappe, Jürgen Weber (2005), "Aldehydes, Aliphatic", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH, doi:10.1002/14356007.a01_321.pub2

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