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Homovanillyl alcohol

From Wikipedia, the free encyclopedia
Homovanillyl alcohol[1]
Names
Preferred IUPAC name
4-(2-Hydroxyethyl)-2-methoxyphenol
Other names
Homovanillic alcohol; MOPET; 3-Methoxy-4-hydroxyphenylethanol; 3-Methoxy-4-hydroxyphenethyl alcohol; 4-Hydroxy-3-methoxyphenethanol, 4-Hydroxy-3-methoxyphenethyl alcohol
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.017.433 Edit this at Wikidata
EC Number
  • 219-175-1
UNII
  • InChI=1S/C9H12O3/c1-12-9-6-7(4-5-10)2-3-8(9)11/h2-3,6,10-11H,4-5H2,1H3 ☒N
    Key: XHUBSJRBOQIZNI-UHFFFAOYSA-N ☒N
  • InChI=1/C9H12O3/c1-12-9-6-7(4-5-10)2-3-8(9)11/h2-3,6,10-11H,4-5H2,1H3
    Key: XHUBSJRBOQIZNI-UHFFFAOYAP
  • Oc1ccc(cc1OC)CCO
Properties
C9H12O3
Molar mass 168.19 g/mol
Melting point 40 to 42 °C (104 to 108 °F; 313 to 315 K)
Hazards
GHS labelling:[2]
GHS07: Exclamation mark
Warning
H315, H319, H335
P261, P264, P271, P280, P302 P352, P304 P340, P305 P351 P338, P312, P321, P332 P313, P337 P313, P362, P403 P233, P405, P501
Flash point 113 °C (235 °F; 386 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 ?)

Homovanillyl alcohol is a metabolite of hydroxytyrosol, which in turn is a metabolite of the neurotransmitter dopamine.

See also

[edit]

References

[edit]
  1. ^ Homovanillyl alcohol at Sigma-Aldrich
  2. ^ "Homovanillyl alcohol". pubchem.ncbi.nlm.nih.gov. Retrieved 13 December 2021.