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578576

Sigma-Aldrich

1,2-Epoxy-3-phenoxypropane

technical grade

Synonym(s):

2,3-Epoxypropyl phenyl ether, Glycidyl phenyl ether, Phenyl glycidyl ether

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100 G
$67.26

About This Item

Empirical Formula (Hill Notation):
C9H10O2
CAS Number:
Molecular Weight:
150.17
Beilstein/REAXYS Number:
2744
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

$67.26

List Price$70.80
Web-Only Promotion

Available to ship onMay 01, 2025Details


Request a Bulk Order

grade

technical grade

vapor density

5.2 (vs air)

vapor pressure

0.03 mmHg ( 20 °C)

refractive index

n20/D 1.53 (lit.)
n20/D 1.530 (lit.)

bp

245 °C (lit.)

mp

3.5 °C (lit.)

density

1.109 g/mL at 25 °C (lit.)

SMILES string

C1OC1COc2ccccc2

InChI

1S/C9H10O2/c1-2-4-8(5-3-1)10-6-9-7-11-9/h1-5,9H,6-7H2

InChI key

FQYUMYWMJTYZTK-UHFFFAOYSA-N

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pictograms

Health hazardExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Carc. 1B - Muta. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

237.2 °F - closed cup

flash_point_c

114 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Ida B Niklasson et al.
Chemical research in toxicology, 24(4), 542-548 (2011-03-05)
Epoxy resins are among the most common causes of occupational contact dermatitis. They are normally used in so-called epoxy resin systems (ERS). These commercial products are combinations of epoxy resins, curing agents, modifiers, and reactive diluents. The most frequently used
D L Deforce et al.
Analytical biochemistry, 258(2), 331-338 (1998-05-08)
The in vitro adduct formation between phenyl glycidyl ether (PGE) and calf thymus DNA was investigated. Agarose slab gel electrophoresis of DNA incubated with PGE revealed that nearly all high-molecular-weight species were degraded after 10 h of incubation. After DNA
F Lemière et al.
Journal of mass spectrometry : JMS, 34(8), 820-834 (1999-07-29)
The reaction between phenylglycidyl ether and 2'-deoxyguanosine or 2'-deoxyguanosine-5'-monophosphate yields a variety of different nucleoside and nucleotide adducts. The corresponding mixtures were analyzed by liquid chromatography/electrospray tandem mass spectrometry and the product ion spectra of the different isomers are discussed
Tamara Delaine et al.
Chemical research in toxicology, 24(8), 1312-1318 (2011-07-15)
Because of regulatory constraints and ethical considerations, research on alternatives to animal testing to predict the skin sensitization potential of novel chemicals has become a high priority. Ideally, these alternatives should not only predict the hazard of novel chemicals but
E van den Eeckhout et al.
Journal of chromatography, 541(1-2), 317-331 (1991-03-22)
2'-Deoxycitidine (dCyd) and 2'-deoxyguanosine (dGuo) were subjected to reaction with phenylglycidyl ether (PGE) in methanol in order to study the formation of the corresponding 2'-deoxynucleoside adducts. Separation methods were developed on analytical and semi-preparative scales using high-performance liquid chromatography with

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