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Propylene carbonate

Selectophore, ≥99.0%

Synonym(s):

1,2-Propanediol cyclic carbonate, 4-Methyl-1,3-dioxolan-2-one

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About This Item

Empirical Formula (Hill Notation):
C4H6O3
CAS Number:
Molecular Weight:
102.09
Beilstein:
107913
EC Number:
MDL number:
UNSPSC Code:
26111700
PubChem Substance ID:
NACRES:
NB.61

grade

for ion-selective electrodes

Quality Level

vapor pressure

0.13 mmHg ( 20 °C)
0.98 mmHg ( 50 °C)

description

solvent for preparation of membranes

product line

Selectophore

Assay

≥99.0% (GC)
≥99.0%

form

liquid

autoignition temp.

851 °F

expl. lim.

14.3 %

refractive index

n20/D 1.421 (lit.)
n20/D 1.423

bp

240 °C (lit.)

mp

−55 °C (lit.)

density

1.204 g/mL at 25 °C (lit.)

SMILES string

CC1COC(=O)O1

InChI

1S/C4H6O3/c1-3-2-6-4(5)7-3/h3H,2H2,1H3

InChI key

RUOJZAUFBMNUDX-UHFFFAOYSA-N

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General description

Propylene carbonate (PC) is an organic amide compound generally used as solvent in organic electrochemistry. It is considered as a high-permittivity component of electrolytes.
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Application

It has been used to exfoliate graphite oxide by bath sonication. It has also been used to prepare 1M lithium perchlorate, which served as electrolyte in measurement of thin-film of orthorhombic Niobium pentoxide (Nb2O5).

Legal Information

Selectophore is a trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

269.6 °F - closed cup

Flash Point(C)

132 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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High-rate electrochemical energy storage through Li+ intercalation pseudocapacitance.
Augustyn, Veronica, et al.
Nature Materials, 12.6, 518-522 (2013)
Ole Hammerich, Henning Lund
Organic Electrochemistry, 1416-1416 (2000)
Exfoliation of graphite oxide in propylene carbonate and thermal reduction of the resulting graphene oxide platelets.
Zhu, Yanwu, et al.
ACS Nano, 4.2, 1227-1233 (2010)
Mussel-inspired polydopamine-treated polyethylene separators for high-power li-ion batteries.
Myung-Hyun Ryou et al.
Advanced materials (Deerfield Beach, Fla.), 23(27), 3066-3070 (2011-05-25)
Michael North et al.
Organic letters, 12(10), 2378-2381 (2010-04-20)
Proline-catalyzed aldol reactions between enolizable ketones and aromatic aldehydes can be carried out in propylene carbonate. When enantiomerically pure propylene carbonate is used, the combination of (R)-proline and (R)-propylene carbonate constitutes a matched pair, while (S)-proline and (R)-propylene carbonate constitutes

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