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Ethylene carbonate
[CAS# 96-49-1]

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Complete supplier list of Ethylene carbonate
Identification
Classification Organic raw materials >> Inorganic acid ester
Name Ethylene carbonate
Synonyms 1,3-Dioxolan-2-one; Ethylene glycol carbonate
Molecular Structure CAS # 96-49-1, Ethylene carbonate, 1,3-Dioxolan-2-one, Ethylene glycol carbonate
Molecular Formula C3H4O3
Molecular Weight 88.06
CAS Registry Number 96-49-1
EC Number 202-510-0
SMILES C1COC(=O)O1
Properties
Density 1.3±0.1 g/cm3 Calc.*, 1.321 g/mL (Expl.)
Melting point 35 - 38 ºC (Expl.)
Boiling point 248.2 ºC 760 mmHg (Calc.)*, 244.3 - 245.3 ºC (Expl.)
Flash point 160.0 ºC (Calc.)*, 143 ºC (Expl.)
Solubility water: 214 g/L (20 ºC) (Expl.)
Index of refraction 1.424 (Calc.)*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol symbol   GHS07;GHS08 Warning    Details
Hazard Statements H302-H315-H319-H373    Details
Precautionary Statements P260-P264-P264+P265-P270-P280-P301+P317-P302+P352-P305+P351+P338-P319-P321-P330-P332+P317-P337+P317-P362+P364-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Eye irritationEye Irrit.2H319
Acute toxicityAcute Tox.4H302
Specific target organ toxicity - repeated exposureSTOT RE2H373
Skin irritationSkin Irrit.2H315
Serious eye damageEye Dam.1H318
Specific target organ toxicity - single exposureSTOT SE3H335
SDS Available
up Discovory and Applicatios
Ethylene carbonate is an organic carbonate with the molecular formula C3H4O3. Structurally, it is a five-membered cyclic carbonate consisting of a carbonyl group bonded to a ring containing two methylene units and an oxygen atom, forming a cyclic ester of carbonic acid. The compound is typically a colorless, odorless solid with a relatively high melting point and good thermal stability. It is highly polar and soluble in water as well as in a variety of organic solvents such as acetonitrile, dimethylformamide, and dimethyl sulfoxide.

Ethylene carbonate is primarily used as a solvent and electrolyte component in lithium-ion batteries. Its high dielectric constant, chemical stability, and ability to dissolve lithium salts make it a critical component in electrolytes, facilitating efficient ion transport and battery performance. It also contributes to the formation of stable solid-electrolyte interphases on electrode surfaces, which is essential for long-term cycling stability.

In addition to battery applications, ethylene carbonate is employed as a reactive intermediate in organic synthesis. Its cyclic carbonate functionality allows it to participate in ring-opening reactions to generate mono- or di-functionalized derivatives, which are useful in the synthesis of polycarbonates, pharmaceuticals, and fine chemicals. It can react with nucleophiles, such as amines and alcohols, to produce carbamates or hydroxyethyl derivatives.

Ethylene carbonate is typically produced by the reaction of ethylene oxide with carbon dioxide under catalytic conditions, a process that is both efficient and environmentally favorable due to the use of CO2 as a feedstock. Handling precautions include avoiding exposure to strong acids or bases, which can hydrolyze the carbonate ring, and using standard measures for high-purity solvents.

Overall, ethylene carbonate is a highly versatile cyclic carbonate with applications in energy storage, organic synthesis, and polymer production. Its polar, thermally stable structure and reactive carbonate ring make it valuable as both a solvent and a chemical intermediate in industrial and laboratory settings.

References

2013. Hydrothermal Synthesis of Nickel Oxide Nanosheets for Lithium-Ion Batteries and Supercapacitors with Excellent Performance. Chemistry � An Asian Journal, 8(10).
DOI: 10.1002/asia.201300708

2012. Polymers containing phosphorus groups and polyethers: from synthesis to application. Chemistry Central Journal, 6(1).
DOI: 10.1186/1752-153x-6-132
Market Analysis Reports
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