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224111

Sigma-Aldrich

Ethylene glycol diethyl ether

98%

Synonym(s):

1,2-Diethoxyethane

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About This Item

Linear Formula:
CH3CH2OCH2CH2OCH2CH3
CAS Number:
629-14-1
Molecular Weight:
118.17
Beilstein/REAXYS Number:
1732917
EC Number:
211-076-1
MDL number:
MFCD00009253
UNSPSC Code:
12352112
PubChem Substance ID:
329752316
NACRES:
NA.21

vapor pressure

9.4 mmHg ( 20 °C)

assay

98%

form

liquid

refractive index

n20/D 1.3923 (lit.)

bp

121 °C (lit.)

mp

−74 °C (lit.)

density

0.842 g/mL at 25 °C (lit.)

SMILES string

CCOCCOCC

InChI

1S/C6H14O2/c1-3-7-5-6-8-4-2/h3-6H2,1-2H3

InChI key

LZDKZFUFMNSQCJ-UHFFFAOYSA-N

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Application


  • Correlation between urinary methoxyacetic acid and exposure of ethylene glycol dimethyl ether in a lithium battery plant.: This research investigates the exposure levels of ethylene glycol diethyl ether within a lithium battery manufacturing environment. By analyzing the correlation between urinary biomarkers and chemical exposure, the study provides insights into occupational health and safety measures required in industrial settings where such chemicals are used (Yokota et al., 2007).

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Repr. 1A

supp_hazards

EUH019

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

71.6 °F - closed cup

flash_point_c

22 °C - closed cup

Certificates of Analysis (COA)

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Fabrication and performance of membrane electrode assembly prepared by a catalyst-coated membrane method: effect of solvents used in a catalyst ink mixture
Therdthianwong A, et al.
Energy & Fuels, 24(2), 1191-1196 (2010)
Copper (I)-mediated living radical polymerization in the presence of oxyethylene groups: Online 1H NMR spectroscopy to investigate solvent effects
Haddleton DM, et al.
Macromolecules, 33(22), 8246-8251 (2000)
Solvate structures and computational/spectroscopic characterization of LiBF4 electrolytes
Seo DM, et al.
The Journal of Physical Chemistry C, 118(32), 18377-18386 (2014)
The bonding of fluorinated and hydrogenated diethers to Ru (001).
Walczak MM and Thiel PA.
Surface Science, 224(1), 425-450 (1989)
Fabio Marchetti et al.
Chemical communications (Cambridge, England), (31)(31), 3651-3653 (2008-07-31)
The formation of 1,4-dioxanes and alkyl chlorides from the reactions of polyethers (dme, diglyme, 1,2-diethoxyethane, 1,2-dimethoxypropane) with NbCl(5) at room temperature is described; as far as dme is concerned, the reaction mainly occurs in two steps, consisting of (i) cleavage
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