Chemistry:Hexanal

From HandWiki
Hexanal[1][2][3]
Hexanal.png
Names
Preferred IUPAC name
Hexanal
Other names
Hexanaldehyde
Aldehyde C-6
Caproic aldehyde
Capronaldehyde
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
UNII
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).
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Infobox references

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] It occurs naturally, and contributes to a hay-like "off-note" flavor in green peas.[7]

The first synthesis of hexanal was published in 1907 by P. Bagard.[8]

References

  1. "MSDS for hexanal, from Physical & Theoretical Chemistry Laboratory". Oxford University. http://ptcl.chem.ox.ac.uk/MSDS/HE/hexanal.html. 
  2. Hexanal, SAFETY DATA SHEET, 2010-2015
  3. "CAS: Hexanal". http://www.cas.org/motw/hexanal. 
  4. Hexanal Product Data Sheet 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. http://www.cbc.ca/news/canada/kitchener-waterloo/guelph-fruit-spray-extends-shelf-life-1.3647271. Retrieved 21 August 2017. 
  7. Roland, Wibke S. U.; Pouvreau, Laurice; Curran, Julianne; van de Velde, Fred; de Kok, Peter M. T. (5 October 2016). "Flavor Aspects of Pulse Ingredients". Cereal Chemistry 94 (1): 58–65. doi:10.1094/CCHEM-06-16-0161-FI. 
  8. Molecule of the Week: Hexanal / American Chemical Society