112402
Diethyl succinate
ReagentPlus®, 99%
Synonym(s):
1,4-Diethyl butanedioate, Diethyl butanedioate, Ethyl succinate
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About This Item
Linear Formula:
C2H5OCOCH2CH2COOC2H5
CAS Number:
Molecular Weight:
174.19
Beilstein:
907645
EC Number:
MDL number:
UNSPSC Code:
12162002
eCl@ss:
39022839
PubChem Substance ID:
NACRES:
NA.23
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vapor density
6 (vs air)
Quality Level
product line
ReagentPlus®
Assay
99%
form
liquid
refractive index
n20/D 1.42 (lit.)
bp
218 °C (lit.)
mp
−20 °C (lit.)
density
1.047 g/mL at 25 °C (lit.)
SMILES string
CCOC(=O)CCC(=O)OCC
InChI
1S/C8H14O4/c1-3-11-7(9)5-6-8(10)12-4-2/h3-6H2,1-2H3
InChI key
DKMROQRQHGEIOW-UHFFFAOYSA-N
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General description
Diethyl succinate(DES) is a diethyl ester with succinate molecules. It has two ester groups and is majorly used in fragrances. It produced by the esterification of succinic acid with ethanol.
Application
DES and 1-octanol can be blended with B5 palm oil biodiesel to improve the oxygen content and achieve a greener emission of combustion gases. It may also be used as a novel and highly efficient solvent to capture carbon dioxide(CO2) which can be potentially used as a technique to reduce carbon emission.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
208.4 °F - closed cup
Flash Point(C)
98 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Diethyl succinate synthesis by reactive distillation
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Separation and Purification Technology, 88, 151-162 (2012)
Performance and emission characteristics of green diesel blends containing diethyl-succinate and 1-octanol.
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Performance evaluation of CO2 capture with diethyl succinate.
Li H, et al.
Applied Energy, 200, 119-131 (2017)
Niki M Zacharias et al.
Journal of the American Chemical Society, 134(2), 934-943 (2011-12-08)
The Krebs tricarboxylic acid cycle (TCA) is central to metabolic energy production and is known to be altered in many disease states. Real-time molecular imaging of the TCA cycle in vivo will be important in understanding the metabolic basis of
M B Ashour et al.
Toxicology and applied pharmacology, 89(3), 361-369 (1987-07-01)
Treatment with 0.5% (w/w) dietary clofibrate, a peroxisome proliferator, for 14 days induced microsomal carboxylesterase activities for five substrates including malathion, clofibrate, diethylsuccinate, diethylphthalate, and p-nitrophenylacetate in liver and kidney of male Swiss-Webster mice and Sprague-Dawley rats. The induction was
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