Date published: 2025-11-2

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Diethyl carbonate (CAS 105-58-8)

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Alternate Names:
DEC
Application:
Diethyl carbonate is used in the synthesis of 2-oxooxazolidines as antibacterials.
CAS Number:
105-58-8
Molecular Weight:
118.13
Molecular Formula:
C5H10O3
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Diethyl carbonate has garnered significant interest in scientific research due to its versatile applications and unique chemical properties. One of its primary uses is as a green solvent in various organic synthesis processes, offering an environmentally friendly alternative to traditional solvents. Additionally, diethyl carbonate has emerged as a promising electrolyte additive in lithium-ion batteries, where it contributes to enhanced battery performance and stability. Research suggests that diethyl carbonate acts as a film-forming additive on the surface of the lithium electrode, forming a stable solid-electrolyte interface (SEI) layer that improves battery cycling efficiency and prevents capacity degradation. Furthermore, studies have explored its potential as a reagent in organic transformations, particularly in the synthesis of cyclic carbonates and carbamates, which are valuable building blocks in pharmaceutical and polymer chemistry. Moreover, diethyl carbonate has been investigated for its role as a fuel additive in the production of biodiesel, aiming to improve fuel properties and reduce emissions. Overall, the diverse research applications of diethyl carbonate highlight its significance in advancing various fields of science and technology, ranging from sustainable chemistry to energy storage and beyond.


Diethyl carbonate (CAS 105-58-8) References

  1. FTIR spectroscopic studies of lithium tetrafluoroborate in propylene carbonate+diethyl carbonate mixtures.  |  Zhang, B., et al. 2014. Spectrochim Acta A Mol Biomol Spectrosc. 122: 59-64. PMID: 24295777
  2. Degradation of an Ethylene Carbonate/Diethyl Carbonate Mixture by Using Ionizing Radiation.  |  Wang, F., et al. 2017. Chemphyschem. 18: 2799-2806. PMID: 28419652
  3. Interfacial Reactions Between Graphite and Diethyl Carbonate Solutions Containing Different Concentrations of Li.  |  Jeong, SK. 2018. J Nanosci Nanotechnol. 18: 7023-7026. PMID: 29954526
  4. Atmospheric Photo-oxidation of Diethyl Carbonate: Kinetics, Products, and Reaction Mechanism.  |  Rimondino, GN., et al. 2020. J Phys Chem A. 124: 56-62. PMID: 31800246
  5. Sustainable Catalytic Synthesis of Diethyl Carbonate.  |  Putro, WS., et al. 2021. ChemSusChem. 14: 842-846. PMID: 33230917
  6. Environment-friendly synthesis of diethyl carbonate via ethyl carbamate alcoholysis over cerium oxide catalyst.  |  Ma, Y., et al. 2019. J Environ Manage. 232: 952-956. PMID: 33395763
  7. Studies of Ozone-Sensitized Low- and High-Temperature Oxidations of Diethyl Carbonate.  |  Zhao, H., et al. 2021. J Phys Chem A. 125: 1760-1765. PMID: 33525870
  8. Solvation Structure around Li+ Ions in Organic Carbonate Electrolytes: Spacer-Free Thin Cell IR Spectroscopy.  |  Lim, C., et al. 2021. Anal Chem. 93: 12594-12601. PMID: 34491717
  9. Readily-fabricated supported MgO catalysts for efficient and green synthesis of diethyl carbonate from ethyl carbamate and ethanol.  |  Li, F., et al. 2021. RSC Adv. 11: 15477-15485. PMID: 35424079
  10. Sustainable Synthesis of Dimethyl- and Diethyl Carbonate from CO2 in Batch and Continuous Flow-Lessons from Thermodynamics and the Importance of Catalyst Stability.  |  O'Neill, MF., et al. 2022. ACS Sustain Chem Eng. 10: 5243-5257. PMID: 35493694

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Diethyl carbonate, 500 ml

sc-234655
500 ml
$2462.00