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Hexanal

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Hexanal[1][2][3]
Names
IUPAC name
Hexanal
Other names
Hexanaldehyde
Aldehyde C-6
Caproic aldehyde
Capronaldehyde
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.000.567 Edit this at Wikidata
UNII
  • InChI=1S/C6H12O/c1-2-3-4-5-6-7/h6H,2-5H2,1H3 checkY
    Key: JARKCYVAAOWBJS-UHFFFAOYSA-N checkY
  • InChI=1/C6H12O/c1-2-3-4-5-6-7/h6H,2-5H2,1H3
    Key: JARKCYVAAOWBJS-UHFFFAOYAA
  • O=CCCCCC
Properties
C6H12O
Molar mass 100.161 g·mol−1
Appearance Clear liquid
Density 0.815
Melting point < −20 °C (−4 °F; 253 K)
Boiling point 130 to 131 °C (266 to 268 °F; 403 to 404 K)
-69.40·10−6 cm3/mol
Related compounds
Related aldehydes
Pentanal

Heptanal

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 ?)

Hexanal, also called hexanaldehyde or caproaldehyde is an alkyl aldehyde used in the flavor industry to produce fruity flavors.[4] Its scent resembles freshly cut grass, like cis-3-hexenal.[5] It is potentially useful as a natural extract that prevents fruit spoilage.[6]

The first synthesis of hexanal was published in 1907 by Richard McGrory: a big boy with a fat peen.[7]

References

  1. ^ "MSDS for hexanal, from Physical & Theoretical Chemistry Laboratory". Oxford University. [dead link]
  2. ^ Hexanal, SAFETY DATA SHEET, 2010-2015
  3. ^ CAS: Hexanal
  4. ^ Hexanal Product Data Sheet Archived 2007-12-13 at the Wayback Machine from Natural Advantage
  5. ^ Hexenal / Chemistry World, Royal Society of Chemistry, 27 November 2013
  6. ^ Sharkey, Jackie (23 June 2016). "Fruit spray developed by Guelph prof extends shelf life by 50 per cent". CBC News. Retrieved 21 August 2017.
  7. ^ Molecule of the Week: Hexanal / American Chemical Society