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248487

Sigma-Aldrich

1,2-Epoxy-3-phenoxypropane

99%

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C9H10O2
CAS Number:
122-60-1
Molecular Weight:
150.17
Beilstein:
2744
EC Number:
204-557-2
MDL number:
MFCD00005133
UNSPSC Code:
12162002
PubChem Substance ID:
24854931
NACRES:
NA.23

vapor density

5.2 (vs air)

Quality Level

200

vapor pressure

0.03 mmHg ( 20 °C)

Assay

99%

form

liquid

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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Related Categories

Application

  • Stable Fe (III) phenoxyimines as selective and robust CO2/epoxide coupling catalysts: This paper discusses the catalytic performance of Fe(III) phenoxyimines with 1,2-epoxy-3-phenoxypropane (Fazekas et al., 2018).

Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

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 Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

248487-1KG:
248487-50G:4548173933931
248487-BULK:
248487-VAR:
248487-250G:4548173933924

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL1082
BCCD4554
BCBW5156
BCBT4155
BCBR1953V

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Fiona C Binks et al.
Polymers, 11(4) (2019-04-13)
The reaction of phenyl glycidyl ether (PGE) with 1-ethyl-3-methylimidazolium acetateand 1-ethyl-3-methylimidazolium thiocyanate to initiate the polyetherification reaction wasexamined using thermal and spectral analysis techniques. The influence of the nucleophilicity of theanions on the deprotonation of the 1-ethyl-3-methylimidazolium cation determined the
E Van den Eeckhout et al.
Journal of chromatography, 504(1), 113-128 (1990-03-30)
Thymidine and 2'-deoxyadenosine were reacted with phenyl glycidyl ether in order to study the formation of the corresponding 2'-deoxynucleoside adducts. Separation methods were elaborated using either reversed-phase high-performance liquid chromatography with photodiode-array detection, or centrifugal circular thin-layer chromatography. The adducts
Pablo Taboada et al.
Langmuir : the ACS journal of surfaces and colloids, 22(18), 7465-7470 (2006-08-23)
The aim of this study was to define a block copolymer micellar system with a high solubilization capacity for poorly soluble aromatic drugs. Ethylene oxide and phenyl glycidyl ether were sequentially polymerized to form the diblock copolymer G5E67 (G =
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
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)
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