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About This Item
Empirical Formula (Hill Notation):
C3H4O3
CAS Number:
Molecular Weight:
88.06
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-510-0
Beilstein/REAXYS Number:
106249
MDL number:
Assay:
98%
vapor density
3.04 (vs air)
Quality Level
vapor pressure
0.02 mmHg ( 36.4 °C)
assay
98%
bp
243-244 °C/740 mmHg (lit.)
mp
35-38 °C (lit.)
density
1.321 g/mL at 25 °C (lit.)
SMILES string
O=C1OCCO1
InChI
1S/C3H4O3/c4-3-5-1-2-6-3/h1-2H2
InChI key
KMTRUDSVKNLOMY-UHFFFAOYSA-N
Application
Ethylene carbonate has been used:
- In the synthesis of aliphatic polyurethanes using diamines and diols.
- As a precursor for ring-opening polymerization using KOH as initiator.
- As a reactant in the preparation of dimethyl carbonate, glycerol carbonate by transesterification reaction.
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - STOT RE 2 Oral
target_organs
Kidney
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
289.4 °F - closed cup
flash_point_c
143 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Articles
Solid-state lithium fast-ion conductors are crucial for safer, high-energy-density all-solid-state batteries, addressing conventional battery limitations.
Ring-opening polymerization of ethylene carbonate and depolymerization of poly (ethylene oxide-co-ethylene carbonate).
Lee J-C and Litt MH
Macromolecules, 33(5), 1618-1627 (2000)
Synthesis of dimethyl carbonate from transesterification of ethylene carbonate with methanol using immobilized ionic liquid on commercial silica.
Kim K-H, et al.
Korean Journal of Chemical Engineering, 27(5), 1441-1445 (2010)
Kinetics of the production of glycerol carbonate by transesterification of glycerol with dimethyl and ethylene carbonate using potassium methoxide, a highly active catalyst.
Esteban J, et al.
Fuel Processing Technology, 138(5), 243-251 (2015)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| E26258-100G | 04061833602782 |
| E26258-3KG | 04061832489926 |
| E26258-500G | 04061833602799 |

