2-Ethoxyphenol

2-Ethoxyphenol
  • CAS No.:94-71-3
Other grades of this product :
2-Ethoxyphenol Basic information
Product Name:2-Ethoxyphenol
Synonyms:Catechol Monoethyl Ether Guethol Pyrocatechol Monoethyl Ether;PYROCATECHOL MONOETHYL ETHER FOR SYNTHES;Ethylvanillin DesforMyl IMpurity;Pyrocatechol monoethyl ethe;Pyrocatechol monoethyl ether for synthesis;Tamsulosin Impurity 3;2-Ethoxyphenol (Guaethol);2-ethoxy-pheno
CAS:94-71-3
MF:C8H10O2
MW:138.16
EINECS:202-358-5
Product Categories:Indazoles;Phenol&Thiophenol&Mercaptan;Phenetole
Mol File:94-71-3.mol
2-Ethoxyphenol Chemical Properties
Melting point 20-25 °C (lit.)
Boiling point 216-217 °C (lit.)
density 1.09 g/mL at 25 °C (lit.)
vapor pressure 1 hPa (45 °C)
refractive index n20/D 1.529(lit.)
Fp 91 °C
storage temp. Store below +30°C.
solubility 9g/l
form Liquid
pkapK1:10.109 (25°C)
color Clear colorless to yellow
Water Solubility 8.414g/L(24.99 ºC)
BRN 1100453
CAS DataBase Reference94-71-3(CAS DataBase Reference)
NIST Chemistry ReferencePhenol, 2-ethoxy-(94-71-3)
EPA Substance Registry SystemPhenol, 2-ethoxy- (94-71-3)
Safety Information
Hazard Codes Xn
Risk Statements 22-37/38-41
Safety Statements 26-36/37/39-37/39
WGK Germany 3
TSCA Yes
HS Code 29095090
ToxicityLD50 orally in Rabbit: > 2000 mg/kg
MSDS Information
ProviderLanguage
Pyrocatechol monoethyl ether English
SigmaAldrich English
ACROS English
ALFA English
2-Ethoxyphenol Usage And Synthesis
Chemical Propertiesclear colorless to yellow liquid
Uses2-Ethoxyphenol is used in the studies on the inhibition of oral bacteria by phenolic compounds. Studies on the prostagladins cyclooxygenase inhibition by phenolic compounds. Reagent for the stereoselective preparation of (arylthiomethyl)morpholines as selective norepinephrine reuptake inhibitors and dual serotonin/norepinephrine reuptake inhibitors.
Uses2-Ethoxyphenol has been used as carbon and energy supplement in the growth medium of red-pigmented coryneform bacterium, Rhodococcus rhodochrous strain 116.
General Description2-Ethoxyphenol is a smoke flavour compound and forms complexes with iron (III).

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