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About This Item
Linear Formula:
CH3COOCH2CH2OCOCH3
CAS Number:
Molecular Weight:
146.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-881-1
Beilstein/REAXYS Number:
1762308
MDL number:
Assay:
99%
InChI key
JTXMVXSTHSMVQF-UHFFFAOYSA-N
InChI
1S/C6H10O4/c1-5(7)9-3-4-10-6(2)8/h3-4H2,1-2H3
SMILES string
CC(=O)OCCOC(C)=O
vapor density
5.04 (vs air)
vapor pressure
0.2 mmHg ( 20 °C)
assay
99%
autoignition temp.
899 °F
expl. lim.
1.6 %, 135 °F, 8.4 %, 154 °F
Quality Level
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.)
functional group
ester
Related Categories
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).
Storage Class
10 - Combustible liquids
wgk
WGK 1
flash_point_f
181.4 °F - closed cup
flash_point_c
83 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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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)
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)
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
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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