V900593
Diethyl succinate
Vetec™, reagent grade, 98%
Synonym(s):
1,4-Diethyl butanedioate, Diethyl butanedioate
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About This Item
Linear Formula:
C2H5OCOCH2CH2COOC2H5
CAS Number:
Molecular Weight:
174.19
EC Number:
204-612-0
UNSPSC Code:
12162002
PubChem Substance ID:
Beilstein/REAXYS Number:
907645
MDL number:
InChI key
DKMROQRQHGEIOW-UHFFFAOYSA-N
InChI
1S/C8H14O4/c1-3-11-7(9)5-6-8(10)12-4-2/h3-6H2,1-2H3
SMILES string
CCOC(=O)CCC(=O)OCC
grade
reagent grade
vapor density
6 (vs air)
product line
Vetec™
assay
98%
refractive index
n20/D 1.42 (lit.)
bp
218 °C (lit.)
mp
−20 °C (lit.)
density
1.047 g/mL at 25 °C (lit.)
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Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
208.4 °F - closed cup
flash_point_c
98 °C - closed cup
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Wenhu Xu et al.
Journal of texture studies, 52(1), 124-136 (2020-11-14)
Drinking tastes and lubrication properties of Chinese rice wine (CRW) under different heating temperatures were studied by tribology tests, gas chromatography-mass spectrometry (GC-MS) and sensory evaluations. CRW's drinking tastes were evaluated by taste panelists. Flavor compounds were detected by GC-MS.
Florian Diot-Néant et al.
ChemSusChem, 13(10), 2613-2620 (2020-04-03)
The already-reported, low-yielding, and non-sustainable Et3 N-mediated homocoupling of levoglucosenone (LGO) into the corresponding LGO-CyreneTM diketone has been revisited and greened-up. The use of methanol as both a renewable solvent and catalyst and K2 CO3 as a safe inorganic base
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
M B Ashour et al.
Biochemical pharmacology, 36(12), 1869-1879 (1987-06-15)
A series of substituted trifluoroketones were tested as inhibitors of mammalian liver microsomal carboxylesterase(s) hydrolyzing a variety of substrates including malathion, diethylsuccinate (DES) and p-nitrophenyl acetate (p-NpAc). The trifluoroketones used were very potent "transition state" inhibitors of crude mouse and
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