4-ethylphenol
Sign in to saveAlso known as p-Ethylphenol, 4-Hydroxyphenylethane
Ethylphenol (4-EP) is an organic compound with the formula C2H5C6H4OH. It is one of three isomeric ethylphenols. A white solid, it occurs as an impurity in xylenols and as such is used in the production of some commercial phenolic resins. It is also a precursor to 4-vinylphenol.
In the Vinony graph
Within Vinony's link graph, 4-ethylphenol is referenced by 19 other articles, and connects out to odor, (E)-p-coumaric acid and beer.
It sits within the topics 4-Hydroxyphenyl compounds, Alkylphenols and Chembox having GHS data.
Its subject is documented across 14 Wikipedia language editions.
Wikidata facts
- Mass
- 122.073
Show 5 more facts
- chemical formula
- C₈H₁₀O
- canonical SMILES
- CCC1=CC=C(C=C1)O
- melting point
- 45.08
- boiling point
- 217.98
- ionization energy
- 7.84
Sources (1)
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Encyclopedic overview
6 sectionsContents
- Production
- Natural occurrences
- Biochemistry
- See also
- References
- External links
Ethylphenol (4-EP) is an organic compound with the formula C2H5C6H4OH. It is one of three isomeric ethylphenols. A white solid, it occurs as an impurity in xylenols and as such is used in the production of some commercial phenolic resins. It is also a precursor to 4-vinylphenol.
==Production== 4-Ethylphenol is produced by careful sulfonation of ethylbenzene to 4-ethylphenylsulfonic acid. The sulfonic acid is subsequently subjected to alkaline fusion, the dissolution of the sulfonic acid in molten alkali metal base. The main steps in the synthesis are shown: (Et = ethyl)
Excerpted from Wikipedia’s “4-ethylphenol” article, available under the CC BY-SA 4.0 licence.