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140287

Sigma-Aldrich

1,2-Diphenoxyethane

99%

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Synonym(s):
Ethylene glycol diphenyl ether
Linear Formula:
C6H5OCH2CH2OC6H5
CAS Number:
Molecular Weight:
214.26
Beilstein:
2052248
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

mp

94-96 °C (lit.)

SMILES string

C(COc1ccccc1)Oc2ccccc2

InChI

1S/C14H14O2/c1-3-7-13(8-4-1)15-11-12-16-14-9-5-2-6-10-14/h1-10H,11-12H2

InChI key

XCSGHNKDXGYELG-UHFFFAOYSA-N

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This Item
225800271020184497
1,2-Diphenoxyethane 99%

Sigma-Aldrich

140287

1,2-Diphenoxyethane

1,3-Dioxolane anhydrous, contains ~75 ppm BHT as inhibitor, 99.8%

Sigma-Aldrich

271020

1,3-Dioxolane

1,3-Dioxolane ReagentPlus®, contains ~75 ppm BHT as inhibitor, 99%

Sigma-Aldrich

184497

1,3-Dioxolane

mp

94-96 °C (lit.)

mp

-

mp

−95 °C (lit.)

mp

−95 °C (lit.)

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

General description

1,2-Diphenoxyethane is the intermediate formed during sonochemical oxidation of phenoxyacetic acid and chlorophenol.

Pictograms

Environment

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Chronic 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

341.2 °F

Flash Point(C)

171.8 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Yakov Yasman et al.
Ultrasonics sonochemistry, 13(3), 271-277 (2005-06-25)
The application of finely divided (black) Pd and Pd-Fe powder in the sono-electro-catalytic reduction of chlorophenoxy herbicides (2,4-D) and chlorophenols (2,4-DCP) in aqueous solutions allows for effective destruction of toxic chlorinated aromatic compounds. At 20 degrees C complete conversion of
Martin Eckardt et al.
Journal of chromatography. A, 1609, 460437-460437 (2019-08-15)
Thermal papers (e.g. point of sale receipts, adhesive labels, tickets) significantly contribute to contamination of paper material cycles and the environment with substances of (eco-) toxicological concern. In particular, they contain color developers like endocrine disrupting bisphenols in typical concentrations

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