Skip to Content
MilliporeSigma
All Photos(4)

Key Documents

View All Documentation

E26258

Sigma-Aldrich

Ethylene carbonate

98%

Synonym(s):

1,3-Dioxolan-2-one

Sign Into View Organizational & Contract Pricing
All Photos(4)

About This Item

Empirical Formula (Hill Notation):
C3H4O3
CAS Number:
96-49-1
Molecular Weight:
88.06
Beilstein/REAXYS Number:
106249
EC Number:
202-510-0
MDL number:
MFCD00005382
UNSPSC Code:
12352100
PubChem Substance ID:
24894476
NACRES:
NA.22

vapor density

3.04 (vs air)

Quality Level

200

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

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.

related product

Product No.
Description
Pricing

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - STOT RE 2 Oral

target_organs

Kidney

Storage Class

11 - Combustible Solids

wgk_germany

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBK5809
STBK4270
MKCP9196
STBJ9878
STBJ6515

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
A new route to polyurethanes from ethylene carbonate, diamines and diols.
Rokicki G and Piotrowska A
Polymer, 43(10), 2927-2935 (2002)
Synthesis of dimethyl carbonate by transesterification of ethylene carbonate over activated dawsonites.
Georgiana Stoica et al.
ChemSusChem, 2(4), 301-304 (2009-02-07)
View All Related Papers

Articles

Complex Hydrides: A New Category of Solid-state Lithium Fast-ion Conductors

Research and development of solid-state lithium fast-ion conductors is crucial because they can be potentially used as solid electrolytes in all-solid-state batteries, which may solve the safety and energy-density related issues of conventional lithium-ion batteries that use liquid (farmable organic) electrolytes.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service