Skip to Content
Merck

578576

1,2-Epoxy-3-phenoxypropane

technical grade

Synonym(s):

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

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C9H10O2
CAS Number:
122-60-1
Molecular Weight:
150.17
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
24880937
EC Number:
204-557-2
Beilstein/REAXYS Number:
2744
MDL number:
MFCD00005133

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

FQYUMYWMJTYZTK-UHFFFAOYSA-N

InChI

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

SMILES string

C1OC1COc2ccccc2

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.)

Looking for similar products? Visit Product Comparison Guide

Related Categories

pictograms

Health hazardExclamation mark
GHS08,GHS07

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

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
04726HA

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

D L Deforce et al.
Carcinogenesis, 19(6), 1077-1086 (1998-07-17)
Calf thymus DNA was reacted in vitro with phenyl glycidyl ether (PGE) and was hydrolysed enzymatically, to the 5'-monophosphate nucleotides using deoxyribonuclease I (DNA-ase I) and nuclease P1. The adducts were concentrated using solid phase extraction (SPE), on a polystyrene
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
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
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
The inhalation toxicity of phenylglycidyl ether: reproduction, mutagenic, teratogenic, and cytogenic studies.
J B Terrill et al.
Toxicology and applied pharmacology, 64(2), 204-212 (1982-06-30)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service