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Sigma-Aldrich 517135 Diethyl carbonate anhydrous, ≥99% CAS No.: 105-58-8 100 mL
Category
Brand
Stock Code
LB.SA.517135-100ML
Kısa Bilgi
Linear Formula: (C2H5O)2CO CAS Number: 105-58-8 Molecular Weight: 118.13 Beilstein: 956591 EC Number: 203-311-1 MDL number: MFCD00009107 PubChem Substance ID: 24873944 NACRES: NA.22
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Sigma-Aldrich 517135 Diethyl carbonate anhydrous, ≥99% 100 mL
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Linear Formula: (C2H5O)2CO
CAS Number: 105-58-8
Molecular Weight: 118.13
Beilstein: 956591
EC Number: 203-311-1
MDL number: MFCD00009107
PubChem Substance ID: 24873944
NACRES: NA.22
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PROPERTIES
grade anhydrous
Quality Level 100
vapor density 4.1 (vs air)
vapor pressure 10 mmHg ( 23.8 °C) 59 mmHg ( 37.8 °C)
Assay ≥99%
greener alternative product characteristics
Less Hazardous Chemical Syntheses
Safer Solvents and Auxiliaries
Design for Degradation
Learn more about the Principles of Green Chemistry.
impurities <0.002% water <0.005% water (100 mL)
refractive index n20/D 1.384 (lit.)
bp 126-128 °C (lit.)
mp −43 °C (lit.)
solubility water: insoluble
density 0.975 g/mL at 25 °C (lit.)
greener alternative category Aligned
SMILES string O=C(OCC)OCC
InChI 1S/C5H10O3/c1-3-7-5(6)8-4-2/h3-4H2,1-2H3
InChI key OIFBSDVPJOWBCH-UHFFFAOYSA-N
DESCRIPTION
General description
Diethyl carbonate is an dialkylcarbonate.[1] The synthesis of diethyl carbonate (DEC) from urea and ethanol has been investigated.[2] We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product is used as a greener reagent.
Application
Diethyl carbonate may be used in the following studies:
Synthesis of β-enamino esters.[3]
Synthesis of carbamates and unsymmetrical alkyl carbonates, via reaction with aliphatic amines or alcohols by using a hybrid organic-inorganic material prepared by anchoring TBD to MCM-41 silica.[4]
As solvent in ruthenium catalyzed direct functionalisation of arene C-H bonds by aryl halides.[5]
To compose the commercial liquid electrolyte for lithium ion batteries.[6]
Homogeneous alkoxycarbonylation of cellulose.[1]
Features and Benefits
Greener chemical
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