Diethyl carbonate, 99%, Thermo Scientific Chemicals
Diethyl carbonate, 99%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Diethyl carbonate, 99%, Thermo Scientific Chemicals

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Catalog number A12477.0D
also known as A12477-0D
Price (USD)/ Each
378.65
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420.00 
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Quantity:
10,000 mL
Request bulk or custom format
Price (USD)/ Each
378.65
Online exclusive
420.00 
Save 41.35 (10%)
Add to cart
Diethyl carbonate, 99%, Thermo Scientific Chemicals
Catalog numberA12477.0D
Price (USD)/ Each
378.65
Online exclusive
420.00 
Save 41.35 (10%)
-
Add to cart
Chemical Identifiers
CAS105-58-8
IUPAC Namediethyl carbonate
Molecular FormulaC5H10O3
InChI KeyOIFBSDVPJOWBCH-UHFFFAOYSA-N
SMILESCCOC(=O)OCC
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SpecificationsSpecification SheetSpecification Sheet
Assay (GC)≥99.0%
Refractive Index1.3835-1.3855 @ 20?C
Appearance (Color)Clear colorless
Identification (FTIR)Conforms
FormLiquid
Diethyl carbonate is esters, beta-enamino esters, carbamates and unsymmetrical alkyl carbonates. It is an active component of electrolytes used in lithium which is used as a solvent for cellulose ethers, nitro cellulose, natural and synthetic resin and in erythromycin intramuscular injections. It is also used in the synthesis of 3-ethyl-4-methyl-5-phenyl-3H-oxazol-2-one, phenobarbital, pyrethrum batteries.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Diethyl carbonate is esters, beta-enamino esters, carbamates and unsymmetrical alkyl carbonates. It is an active component of electrolytes used in lithium which is used as a solvent for cellulose ethers, nitro cellulose, natural and synthetic resin and in erythromycin intramuscular injections. It is also used in the synthesis of 3-ethyl-4-methyl-5-phenyl-3H-oxazol-2-one, phenobarbital, pyrethrum batteries.

Solubility
Miscible with diehtyl ether, ethanol and chloroform.Immiscible with water.

Notes
Store in cool place. Moisture sensitive. Incompatible with strong acids, oxidizing agents, strong bases and reducing agents.
RUO – Research Use Only

General References:

  1. Carboethoxylates carbanions derived from ketones, nitriles, esters, etc. For examples, see: Org. Synth. Coll., 4, 461 (1963); 5, 198 (1973); 6, 611 (1988). Arylacetic esters are converted to arylmalonic diesters: Org. Prep. Proced. Int., 6, 5 (1974). The dianions of carboxylic acids can be carboethoxylated with diethyl carbonate (or Ethyl chloroformate, L06311), to give monoesters of malonic acids: Tetrahedron Lett., 2721 (1974).
  2. For use as an alkylating agent for alcohols, phenols, thiols, etc., see Dimethyl carbonate, A13104.
  3. 1,3-Diols undergo dehydration to give oxetanes; see, e.g.: Tetrahedron Lett., 24, 5571 (1983):
  4. Srilakshmi, M.; Krishna, T. S.; Narendra, K.; Dey, R.; Ratnakar, A. Influence of alkyl group and temperature on excess thermodynamic properties of diethyl carbonate and their binary mixtures at 0.1 MPa. J. Mol. Liq. 2015, 211, 854-867.
  5. Li, F.; Li, H.; Wang, L.; He, P.; Cao, Y. Magnesium oxide nanosheets as effective catalysts for the synthesis of diethyl carbonate from ethyl carbamate and ethanol. Catal. Sci. Technol. 2015, 5 (2), 1021-1034.