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2,4,6-Trimethylphenol

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2,4,6-Trimethylphenol Basic information

Product Name:
2,4,6-Trimethylphenol
Synonyms:
  • 2,4,6-TRIMETHYLPHENOL, 1000MG, NEAT
  • 2,4,6-TRIMETHYLPHENOL PESTANAL, 250 MG
  • 2,4,6-TRIMETHYLPHENOL / MESITOL
  • Benzene, 2-hydroxy-1,3,5-trimethyl
  • 2,4,6-Trimethylphenol,99%
  • Hydroxymesitylene Mesitol
  • 2-hydroxymesitylen
  • mesito
CAS:
527-60-6
MF:
C9H12O
MW:
136.19
EINECS:
208-419-2
Product Categories:
  • Aromatic Phenols
  • Building Blocks
  • C9 to C20+
  • Chemical Synthesis
  • Organic Building Blocks
  • Oxygen Compounds
  • Phenols
Mol File:
527-60-6.mol
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2,4,6-Trimethylphenol Chemical Properties

Melting point:
70-72 °C(lit.)
Boiling point:
220 °C(lit.)
Density 
0.9809 (estimate)
vapor pressure 
3.86Pa at 25℃
FEMA 
4329 | 2,4,6-TRIMETHYLPHENOL
refractive index 
1.5148 (estimate)
Flash point:
220-221°C
storage temp. 
under inert gas (argon)
form 
Crystalline Needles
pka
pK1:10.88 (25°C)
color 
Beige
Odor
at 0.10 % in propylene glycol. mild phenolic coffee grounds
Odor Type
phenolic
Water Solubility 
1.008g/L(25 ºC)
JECFA Number
2013
BRN 
1859675
LogP
2.73 at 25℃
CAS DataBase Reference
527-60-6(CAS DataBase Reference)
NIST Chemistry Reference
Phenol, 2,4,6-trimethyl-(527-60-6)
EPA Substance Registry System
2,4,6-Trimethylphenol (527-60-6)
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Safety Information

Hazard Codes 
C,N
Risk Statements 
34-51/53
Safety Statements 
26-36/37/39-45-24/25-61
RIDADR 
UN 2430 8/PG 3
WGK Germany 
2
RTECS 
OX6590000
TSCA 
Yes
HazardClass 
8
PackingGroup 
III
HS Code 
29071990
Hazardous Substances Data
527-60-6(Hazardous Substances Data)

MSDS

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2,4,6-Trimethylphenol Usage And Synthesis

Chemical Properties

BEIGE CRYSTALLINE NEEDLES

Production Methods

2,4,6-Trimethylphenol is the main product (more than 80%) of the gas phase alkylation of phenol with excess methanol (molar ratio 1 : 5) at 450 ℃ on magnesium oxide catalysts, which are doped with alkali or other metal oxides (e.g., V2O5, SrO). 2,6-Xylenol and 2,3,4,6-tetramethylphenol are the main byproducts.

Synthesis Reference(s)

Journal of the American Chemical Society, 107, p. 1060, 1985 DOI: 10.1021/ja00290a053
Synthetic Communications, 18, p. 1207, 1988 DOI: 10.1080/00397918808060912

Flammability and Explosibility

Not classified

Purification Methods

Crystallise the phenol from water and sublime it in vacuo. [Beilstein 6 IV 3253.]

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