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Mesitol information


Mesitol
Names
Preferred IUPAC name
2,4,6-Trimethylphenol
Other names
Hydroxymesitylene; Mesityl alcohol
Identifiers
CAS Number
  • 527-60-6
3D model (JSmol)
  • Interactive image
ChemSpider
  • 10248
ECHA InfoCard 100.007.655 Edit this at Wikidata
EC Number
  • 208-419-2
PubChem CID
  • 10698
UNII
  • FPZ32614N6
CompTox Dashboard (EPA)
  • DTXSID7022049 Edit this at Wikidata
InChI
  • InChI=1S/C9H12O/c1-6-4-7(2)9(10)8(3)5-6/h4-5,10H,1-3H3
    Key: BPRYUXCVCCNUFE-UHFFFAOYSA-N
SMILES
  • Cc1cc(c(c(c1)C)O)C
Properties
Chemical formula
 C9H12O
Molar mass 136.194 g·mol−1
Appearance white solid
Melting point 70–72 °C (158–162 °F; 343–345 K)[1]
Boiling point 220 °C (428 °F; 493 K)[1]
Solubility in water
 1.01 g/l
Hazards
GHS labelling:
Pictograms
 GHS05: CorrosiveGHS09: Environmental hazard
Signal word
 Danger
Hazard statements
 H314, H411
Precautionary statements
 P260, P264, P273, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P391, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Mesitol (2,4,6-trimethylphenol) is an organic compound with the formula (CH3)3C6H2OH. It is one of several isomers of trimethylphenol. The name and structure of mesitol derives from the combination of mesitylene and phenol.

  1. ^ a b "2,4,6-Trimethylphenol". Sigma-Aldrich.

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Mesitol

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Mesitol (2,4,6-trimethylphenol) is an organic compound with the formula (CH3)3C6H2OH. It is one of several isomers of trimethylphenol. The name and structure...

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C9H12O

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C9H12O (molar mass: 136.19 g/mol, exact mass: 136.0888 u) may refer to: Mesitol (2,4,6-trimethylphenol) 2-Phenyl-2-propanol 2,3,6-Trimethylphenol This...

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Mesitylene

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is formed. Mesitylene is oxidised by trifluoroperacetic acid to produce mesitol (2,4,6-trimethylphenol). Bromination occurs readily, giving mesityl bromide:...

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Peroxymonophosphoric acid

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for the hydroxylation of aromatic rings. The conversion of mesitylene to mesitol can be achieved at room temperature in less than four hours. The compound...

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Organolead chemistry

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p-methoxyphenyllead triacetate is displaced by carbon nucleophiles, such as the phenol mesitol, exclusively at the aromatic ortho position: The reaction requires the...

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Trifluoroperacetic acid

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Mesitylene, for example, reacts with trifluoroperacetic acid to form mesitol (2,4,6-trimethylphenol). Researchers attempting to form a lactone by Baeyer–Villiger...

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