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metacresol

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Also known as meta-Cresol, 3-Cresol, m-Cresylic acid, 1-Hydroxy-3-methylbenzene, 3-Hydroxytoluene, 3-Methyl phenol, m-methylphenol, 3-methylphenol

'''meta-Cresol, also 3-methylphenol', is an organic compound with the formula CH3C6H4(OH). It is a colourless, viscous liquid that is used as an intermediate in the production of other chemicals. It is a derivative of phenol and is an isomer of p-cresol and o''-cresol.

In the Vinony graph

Vinony's link graph records 30 inbound references to metacresol, and connects out to propylene, International Standard Book Number and ethanol.

It is catalogued under topics including 3-Tolyl compounds, Chembox having GHS data and Chembox image size set.

Vinony links it to 16 Wikipedia language editions.

Wikidata facts

Mass
108.058
Show 14 more facts
chemical formula
C₇H₈O
boiling point
202.27
canonical SMILES
CC1=CC(=CC=C1)O
NIOSH Pocket Guide ID
0155
density
1.03
immediately dangerous to life or health
1107.5
melting point
11.8
vapor pressure
0.14
flash point
187
solubility
2
lower flammable limit
1.1
ionization energy
8.29
time-weighted average exposure limit
10
Commons category
M-Cresol
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Encyclopedic overview

6 sections
Contents
  • Production
  • Applications
  • Natural occurrences
  • See also
  • References
  • External links

'''meta-Cresol, also 3-methylphenol', is an organic compound with the formula CH3C6H4(OH). It is a colourless, viscous liquid that is used as an intermediate in the production of other chemicals. It is a derivative of phenol and is an isomer of p-cresol and o-cresol.

==Production== Together with many other compounds, m-cresol is traditionally extracted from coal tar, the volatile materials obtained in the production of coke from (bituminous) coal. This residue contains a few percent by weight of phenol and isomeric cresols. In the cymene–cresol process, toluene is alkylated with propylene to give isomers of cymene, which can be oxidatively dealkylated analogous to the cumene process. Another method, involves carbonylation of a mixture of methallyl chloride and acetylene in the presence of nickel carbonyl.

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

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