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tyrosol

Structure via PubChem · Public domain (PubChem)

EntityQ402607· pop 18· linked from 85 articles

Also known as 4-Hydroxybenzeneethanol, p-Hydroxyphenethyl alcohol, 4-(2-hydroxyethyl)phenol, 4-Hydroxyphenylethyl alcohol, beta-(4-Hydroxyphenyl)ethanol, 2-(p-Hydroxyphenyl)ethanol, b-(p-Hydroxyphenyl)ethanol, 4-Hydroxyphenethyl alcohol

Tyrosol is an organic compound with the formula . Classified as a phenylethanoid, a derivative of phenethyl alcohol, it is found in a variety of natural sources. The compound is colorless solid. The principal source in the human diet is olive oil.

Chemical data

Formula
C8H10O2
Molecular weight
138.16 g/mol
IUPAC name
4-(2-hydroxyethyl)phenol
SMILES
C1=CC(=CC=C1CCO)O
InChIKey
YCCILVSKPBXVIP-UHFFFAOYSA-N
XLogP
0.4
Polar surface area
40.5 Ų
H-bond donors
2
H-bond acceptors
2
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Mass
138.068
Show 6 more facts
found in taxon
Vitis vinifera
chemical formula
C₈H₁₀O₂
subject has role
antiarrhythmic agent
canonical SMILES
C1=CC(=CC=C1CCO)O
melting point
91
Commons category
Tyrosol
Sources (3)

via Wikidata · CC0

~1 min read

Encyclopedic overview

3 sections
Contents
  • Research
  • See also
  • References

Tyrosol is an organic compound with the formula . Classified as a phenylethanoid, a derivative of phenethyl alcohol, it is found in a variety of natural sources. The compound is colorless solid. The principal source in the human diet is olive oil.

== Research == As an antioxidant, tyrosol may protect cells against injury due to oxidation in vitro. Although it is not as potent as other antioxidants present in olive oil (e.g., hydroxytyrosol), its higher concentration and good bioavailability indicate that it may have an important overall effect.

Excerpted from Wikipedia’s “tyrosol” article, available under the CC BY-SA 4.0 licence.