2-Nonanol

2-Nonanol
Names
Preferred IUPAC name
Nonan-2-ol
Identifiers
CAS Number
  • 628-99-9 ☒N
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:78304 ☒N
ChEMBL
  • ChEMBL454517 checkY
ChemSpider
  • 11861 checkY
ECHA InfoCard 100.010.060 Edit this at Wikidata
PubChem CID
  • 12367
UNII
  • 292T5234DX checkY
CompTox Dashboard (EPA)
  • DTXSID60862323 Edit this at Wikidata
InChI
  • InChI=1S/C9H20O/c1-3-4-5-6-7-8-9(2)10/h9-10H,3-8H2,1-2H3 checkY
    Key: NGDNVOAEIVQRFH-UHFFFAOYSA-N checkY
  • InChI=1/C9H20O/c1-3-4-5-6-7-8-9(2)10/h9-10H,3-8H2,1-2H3
    Key: NGDNVOAEIVQRFH-UHFFFAOYAZ
  • OC(CCCCCCC)C
Properties
Chemical formula
C9H20O
Molar mass 144.2545
Density 0.827 g/mL
Melting point −36 – −35 °C (−33 – −31 °F; 237–238 K)
Boiling point 193–194 °C (379–381 °F; 466–467 K)
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 ?)
Infobox references
Chemical compound

2-Nonanol is a simple alcohol. It has the odor of cucumber, and has been identified in oysters.[1] It is used by several insects as pheromones.[2] It is commercially available.

References

  1. ^ Pennarun, Anne-Laure; Prost, Carole; Demaimay, Michel (2002). "Identification and origin of the character-impact compounds of raw oyster Crassostrea gigas". Journal of the Science of Food and Agriculture. 82 (14): 1652. doi:10.1002/jsfa.1236.
  2. ^ "Nonan-2-ol: Behavioral Function". Pherobase.
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  • 1-Triacontanol (melissyl / myricyl)
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