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Merck

112402

Sigma-Aldrich

Succinato de dietilo

ReagentPlus®, 99%

Sinónimos:

1,4-Diethyl butanedioate, Diethyl butanedioate, Ethyl succinate

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About This Item

Fórmula lineal:
C2H5OCOCH2CH2COOC2H5
Número de CAS:
Peso molecular:
174.19
Beilstein/REAXYS Number:
907645
EC Number:
MDL number:
UNSPSC Code:
12162002
eCl@ss:
39022839
PubChem Substance ID:
NACRES:
NA.23

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

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

208.4 °F - closed cup

flash_point_c

98 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Performance and emission characteristics of green diesel blends containing diethyl-succinate and 1-octanol.
Phoon LY, et al.
Journal of Cleaner Production, 161, 1192-1202 (2017)
Diethyl succinate synthesis by reactive distillation
Orjuela A, et al.
Separation and Purification Technology, 88, 151-162 (2012)
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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