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E44205

4-Ethylphenol

Name: 4-Ethylphenol
Brand: ALDRICH

99%

Synonym(s):

(4-Hydroxyphenyl)ethane, (p-Hydroxyphenyl)ethane, 1-Ethyl-4-hydroxybenzene, 4-Ethylphenol, p-Ethylphenol, p-Hydroxyethylbenzene

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About This Item

Linear Formula:

C₂H₅C₆H₄OH

CAS Number:

123-07-9

Molecular Weight:

122.16

NACRES:

NA.22

PubChem Substance ID:

24894555

eCl@ss:

39023356

UNSPSC Code:

12352100

EC Number:

204-598-6

MDL number:

MFCD00002393

Beilstein/REAXYS Number:

1363317

Assay:

99%

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Properties

vapor density

4.2 (vs air)

Quality Level

100

vapor pressure

0.13 mmHg ( 20 °C)

assay

99%

bp

218-219 °C (lit.)

mp

40-42 °C (lit.)

SMILES string

CCc1ccc(O)cc1

InChI

1S/C8H10O/c1-2-7-3-5-8(9)6-4-7/h3-6,9H,2H2,1H3

InChI key

HXDOZKJGKXYMEW-UHFFFAOYSA-N

Description

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pictograms

GHS05

signalword

Danger

hcodes

H318

pcodes

P280 - P305 + P351 + P338

Hazard Classifications

Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

212.0 °F - closed cup

flash_point_c

100 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Minimization of ethylphenol precursors in red wines via the formation of pyranoanthocyanins by selected yeasts.

S Benito et al.

International journal of food microbiology, 132(2-3), 145-152 (2009-05-15)

Different strains of Saccharomyces with different hydroxycinnamate decarboxylase (HCDC) activities, estimated by a bioconversion assay, were used for the fermentation of musts enriched with p-coumaric acid and grape anthocyanins, with the aim of favouring the formation of vinylphenolic pyranoanthocyanins, colour

Rapid screening and characterization of drug metabolites using multiple ion monitoring dependent product ion scan and postacquisition data mining on a hybrid triple quadrupole-linear ion trap mass spectrometer.

Ming Yao et al.

Rapid communications in mass spectrometry : RCM, 23(11), 1683-1693 (2009-05-07)

Multiple ion monitoring (MIM)-dependent acquisition with a triple quadrupole-linear ion trap mass spectrometer (Q-trap) was previously developed for drug metabolite profiling. In the analysis, multiple predicted metabolite ions are monitored in both Q1 and Q3 regardless of their fragmentations. The

The influence of hydroquinone on tyrosinase kinetics.

Michael R L Stratford et al.

Bioorganic & medicinal chemistry, 20(14), 4364-4370 (2012-06-16)

In vitro studies, using combined spectrophotometry and oximetry together with hplc/ms examination of the products of tyrosinase action demonstrate that hydroquinone is not a primary substrate for the enzyme but is vicariously oxidised by a redox exchange mechanism in the

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Global Trade Item Number

SKU	GTIN
E44205-5G	04061832284286
E44205-100G	04061833603765