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About This Item
Empirical Formula (Hill Notation):
C4H8O3
CAS Number:
Molecular Weight:
104.10
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
26111700
MDL number:
Product Name
Ethyl methyl carbonate, 99%
InChI
1S/C4H8O3/c1-3-7-4(5)6-2/h3H2,1-2H3
SMILES string
CCOC(=O)OC
InChI key
JBTWLSYIZRCDFO-UHFFFAOYSA-N
assay
99%
form
liquid
greener alternative product characteristics
Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
refractive index
n20/D 1.378
bp
101 °C
mp
-55 °C
density
1.006 g/mL at 25 °C
application(s)
battery manufacturing
greener alternative category
, Enabling
Quality Level
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Application
EMC is majorly utilized as a co-solvent in the nonaqueous electrolyte. It enhances the energy density and discharge capacity of lithium-ion batteries.
General description
Ethyl methyl carbonate (EMC) is a low viscosity solvent, generally prepared by the esterification of chloroformate with ethanol. It can also be prepared by transesterification of dimethyl carbonate (DMC) with ethanol.
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signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
75.0 °F
flash_point_c
23.9 °C
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Zeolitic imidazolate framework as efficient heterogeneous catalyst for the synthesis of ethyl methyl carbonate
Zhou X, et al.
J. Mol. Catal. A: Chem., 366, 43-47 (2013)
Lithium difluoro (oxalato) borate/ethylene carbonate+ propylene carbonate+ ethyl (methyl) carbonate electrolyte for LiMn2O4 cathode
Fu MH, et al.
Journal of Power Sources, 195(3), 862-866 (2010)
Metal-organic frameworks as an acid catalyst for the synthesis of ethyl methyl carbonate via transesterification
Zhou Y, et al.
J. Mol. Catal. A: Chem., 308(1-2), 68-72 (2009)
Liu J, et al.
Electrochemical Communications, 13(3), 269-269 (2011)
McEwen A, et al.
Journal of the Electrochemical Society, 146(5), 1687-1687 (1999)
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