Molecular structure of 2-(4-Hydroxyphenyl)ethanol, CAS Number: 501-94-0
2-(4-Hydroxyphenyl)ethanol (CAS 501-94-0)
See product citations (2)
Alternate Names:
Tyrosol
CAS Number:
501-94-0
Purity:
≥99%
Molecular Weight:
138.16
Molecular Formula:
C8H10O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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2-(4-Hydroxyphenyl)ethanol is found in various plants, including olive oil, and is also known as tyrosol. It is a phenylethanoid, a type of phenolic compound, and is derived from the amino acid tyrosine. 2-(4-Hydroxyphenyl)ethanol has antioxidant properties and has been studied for its potential health benefits. It has anti-inflammatory effects and may play a role in protecting cells from oxidative stress. 2-(4-Hydroxyphenyl)ethanol has potential cardiovascular benefits and neuroprotective effects.
2-(4-Hydroxyphenyl)ethanol (CAS 501-94-0) References
- Biotransformation of styrene in mice. Stereochemical aspects. | Linhart, I., et al. 2000. Chem Res Toxicol. 13: 36-44. PMID: 10649965
- A photoreactive analogue of the immunosuppressant FTY720. | Sun, C. and Bittman, R. 2006. J Org Chem. 71: 2200-2. PMID: 16497020
- Neuroprotective effect of tyrosol on transient focal cerebral ischemia in rats. | Bu, Y., et al. 2007. Neurosci Lett. 414: 218-21. PMID: 17316989
- Terpenoids and phenolics from Plectranthus strigosus, bioactivity screening. | Gaspar-Marques, C., et al. 2008. Nat Prod Res. 22: 167-77. PMID: 18075900
- Evaluation of the environmental fate of thymol and phenethyl propionate in the laboratory. | Hu, D. and Coats, J. 2008. Pest Manag Sci. 64: 775-9. PMID: 18381775
- Cytotoxic phenolic compounds from Chionanthus retusus. | Kwak, JH., et al. 2009. Arch Pharm Res. 32: 1681-7. PMID: 20162394
- Removal of phenols from aqueous solutions by emulsion liquid membranes. | Reis, MT., et al. 2011. J Hazard Mater. 192: 986-94. PMID: 21703759
- Production of aromatic compounds by metabolically engineered Escherichia coli with an expanded shikimate pathway. | Koma, D., et al. 2012. Appl Environ Microbiol. 78: 6203-16. PMID: 22752168
- Proteomics analysis in Caenorhabditis elegans to elucidate the response induced by tyrosol, an olive phenol that stimulates longevity and stress resistance. | Cañuelo, A. and Peragón, J. 2013. Proteomics. 13: 3064-75. PMID: 23929540
- Simultaneous determination of phenolic compounds in sesame oil using LC-MS/MS combined with magnetic carboxylated multi-walled carbon nanotubes. | Wu, R., et al. 2016. Food Chem. 204: 334-342. PMID: 26988510
- A new griseofulvin derivative from a soft coral-derived fungus Eupenicillium sp. SCSIO41208. | Li, Y., et al. 2020. Nat Prod Res. 34: 2971-2975. PMID: 30957549
- Spray-dried olive mill wastewater reduces Maillard reaction in cookies model system. | Troise, AD., et al. 2020. Food Chem. 323: 126793. PMID: 32334301
- Synthesis of Tyrosol 1,2,3-Triazole Derivatives and Their Phytotoxic Activity against Euphorbia heterophylla. | Franco, CA., et al. 2022. J Agric Food Chem. 70: 2806-2816. PMID: 35225607
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-(4-Hydroxyphenyl)ethanol, 5 g | sc-237860 | 5 g | $85.00 |