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525200

Sigma-Aldrich

Ethylene glycol diacetate

99%

Synonym(s):

1,2-Diacetoxyethane, Ethylene diacetate, Glycol diacetate

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About This Item

Linear Formula:
CH3COOCH2CH2OCOCH3
CAS Number:
111-55-7
Molecular Weight:
146.14
Beilstein/REAXYS Number:
1762308
EC Number:
203-881-1
MDL number:
MFCD00008718
UNSPSC Code:
12352100
PubChem Substance ID:
24874480
NACRES:
NA.22

vapor density

5.04 (vs air)

Quality Level

200

vapor pressure

0.2 mmHg ( 20 °C)

assay

99%

autoignition temp.

899 °F

expl. lim.

1.6 %, 135 °F
8.4 %, 154 °F

refractive index

n20/D 1.415 (lit.)

bp

186-187 °C (lit.)

mp

−41 °C (lit.)

density

1.104 g/mL at 20 °C (lit.)

SMILES string

CC(=O)OCCOC(C)=O

InChI

1S/C6H10O4/c1-5(7)9-3-4-10-6(2)8/h3-4H2,1-2H3

InChI key

JTXMVXSTHSMVQF-UHFFFAOYSA-N

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General description

Ethylene glycol diacetate (EGDA) is an acetic acid ester of ethylene glycol. It is widely used as a hardener for silicates. The predicted values of the torsion angles and bond angles are found to be in agreement with the crystal structure data on the benzoate derivatives of ethylene glycol. EGDA can be prepared from ethylene glycol and acetic acid, via esterification in the presence of supported ionic liquids (catalyst). It is a substitute of glyceryl triacetate for the industrial manufacture of tobacco.

Application

Ethylene glycol diacetate may be used as an acyl donor for the in situ generation of peracetic acid, during the chemoenzymatic synthesis of caprolactone. It may be employed as a precursor for the enzymatic synthesis of poly (ethylene glutarate).

wgk_germany

WGK 1

flash_point_f

closed cup

flash_point_c

closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Study on the esterification for ethylene glycol diacetate using supported ionic liquids as catalyst: Catalysts preparation, characterization, and reaction kinetics, process.
Yang J, et al.
Chemical Engineering Journal, 280, 147-157 (2015)
Xiaoman Zhao et al.
Ultrasonics sonochemistry, 31, 506-511 (2016-03-12)
The present work explores the best conditions for the enzymatic synthesis of poly (ethylene glutarate) for the first time. The start-up materials are the liquids; diethyl glutarate and ethylene glycol diacetate, without the need of addition of extra solvent. The
The toxic compounds and leaching characteristics of spent foundry sands.
Ji S, et al.
Water, Air, and Soil Pollution, 132(3-4), 347- 364 (2001)
Baeyer?Villiger Oxidation of Cyclohexanone in Aqueous Medium with In Situ Generation of Peracid Catalyzed by Perhydrolase CLEA.
Chavez G, et al.
Topics in Catalysis, 57(5), 349-355 (2014)
Conformational Studies on Oligomethylene Glycol Derivatives III. Ethylene Glycol Diacetate.
Sundararajan PR, et al.
Canadian Journal of Chemistry, 53(23), 3557-3562 (1975)
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