Diethyl succinate, 98%, Thermo Scientific Chemicals
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Diethyl succinate, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Diethyl succinate, 98%, Thermo Scientific Chemicals

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Catalog number A15777.36
also known as A15777-36
Price (USD)/ Each
38.65
Online exclusive
42.70 
Save 4.05 (9%)
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Quantity:
500 g
Request bulk or custom format
Price (USD)/ Each
38.65
Online exclusive
42.70 
Save 4.05 (9%)
Add to cart
Diethyl succinate, 98%, Thermo Scientific Chemicals
Catalog numberA15777.36
Price (USD)/ Each
38.65
Online exclusive
42.70 
Save 4.05 (9%)
-
Add to cart
Chemical Identifiers
CAS123-25-1
IUPAC Name1,4-diethyl butanedioate
Molecular FormulaC8H14O4
InChI KeyDKMROQRQHGEIOW-UHFFFAOYSA-N
SMILESCCOC(=O)CCC(=O)OCC
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless
Assay (GC)≥97.5%
Refractive Index1.4180-1.4220 @ 20?C
FormLiquid
It is employed as emollients, masking agents, plasticisers and solvents.

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
It is employed as emollients, masking agents, plasticisers and solvents.

Solubility
Slightly soluble in water.

Notes
Store at room temperature. Keep away from oxidizing agents.
RUO – Research Use Only

General References:

  1. Tejraj M. Aminabhavi.; Hemant T. S. Phayde.; Rajashekhar S. Khinnavar.; Bindu Gopalakrishna.; Keith C. Hansen. Densities, refractive indices, speeds of sound, and shear viscosities of diethylene glycol dimethyl ether with ethyl acetate, methyl benzoate, ethyl benzoate, and diethyl succinate in the temperature range from 298.15 to 318.15 K.J. Chem. Eng. Data. 1994, 39 (2),251-260 .
  2. Niki M. Zacharias.; Henry R. Chan.; Napapon Sailasuta.; Brian D. Ross.; Pratip Bhattacharya. Real-Time Molecular Imaging of Tricarboxylic Acid Cycle Metabolism in Vivo by Hyperpolarized 1-13C Diethyl Succinate.J. Am. Chem. Soc. 2012, 134 (2),934-943 .
  3. Undergoes the Stobbe condensation with carbonyl compounds to give alkylidene derivatives; review: Org. React., 6, 1 (1951). For the Stobbe condensation with benzophenone to give the monoester of the product, see: Org. Synth. Coll., 4, 132 (1963).
  4. For an example of the acyloin condensation under silylating conditions to give 2-hydroxycyclobutanone, see: Org. Synth. Coll., 6, 167 (1988). An alternative work-up with bromine leads directly to 1,2-cyclobutanedione: Org. Synth. Coll., 7, 112 (1990):