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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)

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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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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCD4554
BCBW5156
BCBT4155
BCBR1953V
BCBN6286V

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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
Manfred T Reetz et al.
Organic letters, 6(2), 177-180 (2004-01-16)
[reaction: see text] The epoxide hydrolase (EH) from Aspergillus niger, which shows a selectivity factor of only E = 4.6 in the hydrolytic kinetic resolution of glycidyl phenyl ether, has been subjected to directed evolution for the purpose of enhancing
Ann Pontén et al.
Contact dermatitis, 60(2), 79-84 (2009-02-12)
Simultaneous contact allergies to the reactive diluent phenyl glycidyl ether (PGE) and epoxy resins based on diglycidyl ether of bisphenol A (DGEBA) or epoxy resins of the bisphenol F-type have been reported. The latter epoxy resins contain three isomers of
M S Larrechi et al.
Applied spectroscopy, 58(1), 47-53 (2004-01-20)
When applied to near-infrared (NIR) data, multivariate curve resolution methods, in particular alternating least squares (ALS), make it possible to calculate the concentration profiles and the spectra of all species involved in the reaction of curing epoxy resins. In this
Jung-Hee Woo et al.
Journal of bioscience and bioengineering, 109(6), 539-544 (2010-05-18)
As a continuous effort of developing highly enantioselective epoxide hydrolase from marine microorganisms, it was found that Maritimibacter alkaliphilus KCCM 42376 [corrected] was highly enantioselective toward racemic glycidyl phenyl ether (GPE). An open reading frame (ORF) encoding a putative epoxide
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