Skip to Content
Merck
CN

Key Documents

View All Documentation

258598

4-Ethoxyphenol

99%

Synonym(s):

Hydroquinone monoethyl ether

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
C2H5OC6H4OH
CAS Number:
622-62-8
Molecular Weight:
138.16
NACRES:
NA.22
PubChem Substance ID:
24855650
UNSPSC Code:
12352100
EC Number:
210-748-1
MDL number:
MFCD00002334
Assay:
99%
Form:
solid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Quality Level

200

assay

99%

form

solid

bp

121 °C/9 mmHg (lit.)

mp

64-67 °C (lit.)

SMILES string

CCOc1ccc(O)cc1

InChI

1S/C8H10O2/c1-2-10-8-5-3-7(9)4-6-8/h3-6,9H,2H2,1H3

InChI key

LKVFCSWBKOVHAH-UHFFFAOYSA-N

General description

4-Ethoxyphenol is the major dehalogenated product formed during H2O2-driven microperoxidase-8-catalyzed dehalogenation of 4-fluorophenol.

Application

4-Ethoxyphenol has been used as substrate to evaluate kinetic constant for the monophenolase activity of mushroom tyrosinase.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCN2071
BCCK7975
BCCC8931
BCCC6521
BCCB3327

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

J C Espín et al.
European journal of biochemistry, 267(5), 1270-1279 (2000-02-26)
This paper reports a quantitative study of the effect of ring substituents in the 1-position of the aromatic ring on the rate of monophenol hydroxylation and o-diphenol oxidation catalyzed by tyrosinase. A possible correlation between the electron density of the
A M Osman et al.
Proceedings of the National Academy of Sciences of the United States of America, 94(9), 4295-4299 (1997-04-29)
The results of this study report the H2O2-driven microperoxidase-8 (MP8)-catalyzed dehalogenation of halophenols such as 4-fluorophenol, 4-chlorophenol, 4-bromophenol, and 2-fluorophenol in alcoholic solvents. In methanol, the conversion of the para-halophenols and 2-fluorophenol to, respectively, 4-methoxyphenol and 2-methoxyphenol, as the major
Cynthia D Selassie et al.
Journal of medicinal chemistry, 48(23), 7234-7242 (2005-11-11)
In this comprehensive study on the caspase-mediated apoptosis-inducing effect of 51 substituted phenols in a murine leukemia cell line (L1210), we determined the concentrations needed to induce caspase activity by 50% (I50) and utilized these data to develop the following
View All Related Papers

Global Trade Item Number

SKUGTIN
258598-25G04061832880020
258598-5G04061826062128