Basic information Safety Supplier Related

ETHYLENE GLYCOL MONO-P-TOLYL ETHER

Basic information Safety Supplier Related

ETHYLENE GLYCOL MONO-P-TOLYL ETHER Basic information

Product Name:
ETHYLENE GLYCOL MONO-P-TOLYL ETHER
Synonyms:
  • AI3-09181
  • p-Cresol 2-hydroxyethyl ether
  • Einecs 239-209-9
  • Ethanol, 2-(p-tolyloxy)- (8ci)
  • 2-(p-Methylphenoxy)ethylalcohol
  • beta-Hydroxyethyl p-methylphenyl ether
  • Ethanol, 2-(p-tolyloxy)-
  • Ethanol,2-(4-methylphenoxy)-
CAS:
15149-10-7
MF:
C9H12O2
MW:
152.19
EINECS:
239-209-9
Product Categories:
  • Ethylene Glycols & Monofunctional Ethylene Glycols
  • Monofunctional Ethylene Glycols
Mol File:
15149-10-7.mol
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ETHYLENE GLYCOL MONO-P-TOLYL ETHER Chemical Properties

Melting point:
45°C
Boiling point:
123°C 8mm
Density 
1.058±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
pka
14.30±0.10(Predicted)
color 
White to Almost white
Odor
at 100.00 %. floral jasmin animal
Odor Type
floral
LogP
1.686 (est)
EPA Substance Registry System
2-(4-Methylphenoxy)ethanol (15149-10-7)
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Safety Information

Risk Statements 
36/37/38-41
Safety Statements 
26-36-39
HS Code 
2909498090
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ETHYLENE GLYCOL MONO-P-TOLYL ETHER Usage And Synthesis

Synthesis

106-44-5

107-07-3

15149-10-7

The general procedure for synthesizing 2-(4-methylphenoxy)ethanol from p-toluol and 2-chloroethanol was as follows: referring to Example 2 step a; the experimental operation of Example 1a was repeated using 108 g (1 mol) of p-toluol in place of p-(α,α,γ,γ-tetramethylbutyl)phenol, and mixing with 345 g (2.5 mol) of potassium carbonate powder. All other components, dosages and reaction conditions were kept unchanged, and only the addition rate of 2-chloroethanol was adjusted to 1-2 hours. Upon completion of the reaction, 2-(4-methylphenoxy)ethanol was isolated and the product was a yellow to light brown oily residue. The yield of the crude product was 88-92% and the GC purity was 90-95%.

References

[1] Patent: EP1892235, 2008, A1. Location in patent: Page/Page column 4
[2] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 6, p. 1557 - 1561

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