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Merck
모든 사진(3)

주요 문서

184497

Sigma-Aldrich

1,3-Dioxolane

ReagentPlus®, contains ~75 ppm BHT as inhibitor, 99%

동의어(들):

Ethylene glycol methylene ether, Formaldehyde ethylene acetal

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About This Item

실험식(Hill 표기법):
C3H6O2
CAS Number:
Molecular Weight:
74.08
Beilstein:
102453
EC Number:
MDL number:
UNSPSC 코드:
12352005
PubChem Substance ID:
NACRES:
NA.21
bp:
75-76 °C/1.013 hPa
vapor pressure:
70 mmHg ( 20 °C)

Grade

reagent

Quality Level

vapor density

2.6 (vs air)

vapor pressure

70 mmHg ( 20 °C)

제품 라인

ReagentPlus®

분석

99%

양식

liquid

autoignition temp.

525 °F

포함

~75 ppm BHT as inhibitor

expl. lim.

2.1-20.5 %

dilution

(for general lab use)

refractive index

n20/D 1.401 (lit.)

bp

75-76 °C/1.013 hPa

mp

−95 °C (lit.)

density

1.06 g/mL at 25 °C (lit.)

SMILES string

C1COCO1

InChI

1S/C3H6O2/c1-2-5-3-4-1/h1-3H2

InChI key

WNXJIVFYUVYPPR-UHFFFAOYSA-N

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일반 설명

1,3-Dioxolane (DOXL) is a cyclic ether. It is a green solvent. It undergoes reaction with C60 to afford an epoxide and 1,3-dioxolane derivative. Reaction has been reported to proceed via a diradical mechanism. A mixture of tetra(ethylene glycol) dimethyl ether (TEGDME) and DOXL has been used to compose the binary electrolyte for use in lithium-sulfur battery. Its efficacy as a solvent in a non-aqueous redox flow battery system has been tested.

애플리케이션

1,3-Dioxolane may be used in the fabrication of batteries and capacitors. It may be used as one of the co-solvent to prepare the electrolyte for lithium-sulfur batteries.

법적 정보

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

픽토그램

FlameHealth hazardExclamation mark

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Repr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point (°F)

26.6 °F - closed cup

Flash Point (°C)

-3 °C - closed cup


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문서 라이브러리 방문

Enhanced electrochemical performance of a crosslinked polyaniline-coated graphene oxide-sulfur composite for rechargeable lithium-sulfur batteries.
Moon S, et al.
Journal of Power Sources, 294, 386-392 (2015)
1, 3-Dioxolane, tetrahydrofuran, acetylacetone and dimethyl sulfoxide as solvents for non-aqueous vanadium acetylacetonate redox-flow-batteries.
Herr T, et al.
Electrochimica Acta, 113, 127-133 (2013)
Reaction of C60 with Dimethyldioxirane-Formation of an Epoxide and a 1, 3-Dioxolane Derivative.
Elemes Y, et al.
Angewandte Chemie (International Edition in English), 31(3), 351-353 (1992)
Binary electrolyte based on tetra (ethylene glycol) dimethyl ether and 1, 3-dioxolane for lithium-sulfur battery.
Chang DR, et al.
Journal of Power Sources, 112(2), 452-460 (2002)
1, 3-Dioxolane: A green solvent for the preparation of carbon nanotube-modified electrodes.
Moscoso R, et al.
Electrochemical Communications, 48, 69-72 (2014)

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