CAS 2380-91-8
:1-(4-Hydroxyphenyl)ethanol
Description:
1-(4-Hydroxyphenyl)ethanol, also known as p-hydroxyphenyl ethanol, is an organic compound characterized by a hydroxyl group (-OH) attached to a phenyl ring, which is further connected to an ethanol moiety. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in water and organic solvents, making it versatile for various applications. The presence of the hydroxyl group contributes to its reactivity, allowing it to participate in hydrogen bonding and making it a potential antioxidant. This compound is often studied for its biological activities, including potential antimicrobial and anti-inflammatory properties. Additionally, it can serve as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Safety data indicates that, like many phenolic compounds, it should be handled with care due to potential irritant effects on skin and eyes. Overall, 1-(4-Hydroxyphenyl)ethanol is a significant compound in both industrial and research contexts.
Formula:C8H10O2
InChI:InChI=1S/C8H10O2/c1-6(9)7-2-4-8(10)5-3-7/h2-6,9-10H,1H3
InChI key:InChIKey=PMRFBLQVGJNGLU-UHFFFAOYSA-N
SMILES:C(C)(O)C1=CC=C(O)C=C1
Synonyms:- (RS)-1-(4-Hydroxyphenyl)ethanol
- 1-(4-Hydroxyphenyl)-1-ethanol
- 1-(4-Hydroxyphenyl)Ethanol
- 1-(4-Hydroxyphenyl)ethyl alcohol
- 1-(p-Hydroxyphenyl)ethanol
- 4-(1-Hydroxyethyl)Phenol
- 4-Hydroxy-α-methylbenzenemethanol
- 4-Hydroxyphenylmethylcarbinol
- Benzenemethanol, 4-hydroxy-α-methyl-
- Benzyl alcohol, p-hydroxy-α-methyl-
- p-(1-Hydroxyethyl)phenol
- p-Hydroxy-α-methylbenzyl alcohol
- See more synonyms
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Found 5 products.
4-(1-Hydroxyethyl)phenol
CAS:Formula:C8H10O2Purity:>98.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:138.171-(P-HYDROXYPHENYL) ETHANOL
CAS:Formula:C8H10O2Purity:97%Color and Shape:SolidMolecular weight:138.16384-(1-Hydroxyethyl)phenol
CAS:<p>4-(1-Hydroxyethyl)phenol is a biochemical that has been shown to have a redox potential. It is a dehydrogenase, which catalyzes the oxidation of 4-hydroxyphenylacetaldehyde to acetaldehyde. This enzyme belongs to the class of hydroxylases, which catalyze the conversion of an alcohol and an acceptor to an organic acid and water. The enzyme also has catalysis activity on subunits. There are two enantiomers of 4-(1-Hydroxyethyl)phenol: S and R. The S form is more active than the R form in catalysing reactions with acetaldehyde as substrate. This chemical can be synthetically produced by reacting phenol with ethanol in the presence of acid catalyst, such as sulfuric acid or hydrochloric acid.</p>Formula:C8H10O2Purity:Min. 95%Color and Shape:PowderMolecular weight:138.16 g/mol




