188255
2-(4-Hydroxyphenyl)ethanol
98%
Synonym(s):
4-Hydroxyphenethyl alcohol, Tyrosol, p-HPEA
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About This Item
Linear Formula:
HOC6H4CH2CH2OH
CAS Number:
Molecular Weight:
138.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-930-8
Beilstein/REAXYS Number:
1859884
MDL number:
Product Name
2-(4-Hydroxyphenyl)ethanol, 98%
InChI key
YCCILVSKPBXVIP-UHFFFAOYSA-N
InChI
1S/C8H10O2/c9-6-5-7-1-3-8(10)4-2-7/h1-4,9-10H,5-6H2
SMILES string
OCCc1ccc(O)cc1
assay
98%
mp
89-92 °C (lit.)
functional group
hydroxyl
Quality Level
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Related Categories
Application
2-(4-Hydroxyphenyl)ethanol was used in chelated zero valent iron catalyzed oxidation of organic acids present in olive mill wastewater
Biochem/physiol Actions
Antioxidant found in olive oil.
General description
2-(4-Hydroxyphenyl)ethanol is a phenolic alcohol commonly present in olive mill wastewater.
2-(4-Hydroxyphenyl)ethanol is a polyphenolic building block used in the synthesis of monobenzoxazine resin.
2-(4-Hydroxyphenyl)ethanol is a polyphenolic building block used in the synthesis of monobenzoxazine resin.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Development of Low-Viscosity and High-Performance Biobased Monobenzoxazine from Tyrosol and Furfurylamine
Zhibin W et al.
MATERIALS, 14, 440-440 (2021)
Synthesis of New Tyrosol-Based Phosphodiester Derivatives: Effect on Amyloid $\beta$ Aggregation and Metal Chelation Ability
Valeria R et al.
ChemMedChem, 16, 1172-1183 (2021)
Irama Sanchez et al.
Journal of hazardous materials, 199-200, 328-335 (2011-11-29)
The aim of this study was to investigate the effect of a chelated zero valent iron as catalyst on the oxidation of six organic acids that are generally found in olive mill wastewater. The reaction was carried out in a
Yasuharu Satoh et al.
Journal of agricultural and food chemistry, 60(4), 979-984 (2012-01-10)
Metabolic engineering was applied to the development of Escherichia coli capable of synthesizing tyrosol (2-(4-hydroxyphenyl)ethanol), an attractive phenolic compound with great industrial value, from glucose, a renewable carbon source. In this strain, tyrosine, which was supplied not only from the
Mark W Sumarah et al.
Journal of natural products, 71(8), 1393-1398 (2008-07-19)
A collection of 250 foliar endophytes of Picea glauca (white spruce) yielded several isolates that produced metabolites toxic to Choristoneura fumiferana (spruce budworm). Three of these strains were selected for further study based on their ability to be cultured and
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