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Sigma-Aldrich

DBE-4 dibasic ester

98%

Synonym(s):

Dimethyl succinate, Succinic acid dimethyl ester

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About This Item

Linear Formula:
CH3OCOCH2CH2COOCH3
CAS Number:
106-65-0
Molecular Weight:
146.14
Beilstein/REAXYS Number:
956776
EC Number:
203-419-9
MDL number:
MFCD00008466
UNSPSC Code:
12352100
PubChem Substance ID:
24847113
NACRES:
NA.22

vapor pressure

0.3 mmHg ( 20 °C)

assay

98%

autoignition temp.

689 °F

expl. lim.

8.5 %

refractive index

n20/D 1.419 (lit.)

bp

200 °C (lit.)

mp

16-19 °C (lit.)

density

1.117 g/mL at 25 °C (lit.)

SMILES string

COC(=O)CCC(=O)OC

InChI

1S/C6H10O4/c1-9-5(7)3-4-6(8)10-2/h3-4H2,1-2H3

InChI key

MUXOBHXGJLMRAB-UHFFFAOYSA-N

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General description

Dimethyl succinate (DBE-4 dibasic ester ) is obtained by the oxidation of 1,4-butanediol and butyrolactone by using supported gold, palladium and gold-palladium nanoparticles.

DBE-4 can be used as an intermediate in the preparation of 1,4-butanediol, γ-butyrolactone, tetrahydrofuran and itaconic acid.

Legal Information

DuPont product

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

201.2 °F - closed cup

flash_point_c

94 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Determination and correlation of ternary isobaric vapour-liquid equilibrium data of (dimethyl succinate+ dimethyl glutarate+ dimethyl adipate) at 2, 5 and 8 kPa
Zhi C, et al.
The Journal of Chemical Thermodynamics, 143, 106047-106047 (2020)
Gemma L Brett et al.
ChemSusChem, 6(10), 1952-1958 (2013-10-10)
The oxidation of 1,4-butanediol and butyrolactone have been investigated by using supported gold, palladium and gold-palladium nanoparticles. The products of such reactions are valuable chemical intermediates and, for example, can present a viable pathway for the sustainable production of polymers.
J A García-Martínez et al.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme, 32(8), 306-309 (2000-09-13)
The insulinotropic action of GLP-1 is modulated by the nutritional environment of islet B-cells. This study explores whether an ester of succinic acid could be used to potentiate the insulin secretory response to GLP-1 in vivo. Fed anaesthetized male rats
V Leclercq-Meyer et al.
Life sciences, 58(14), 1195-1199 (1996-01-01)
The glucagon-like peptide 1 (7-36) amide (GLP-1, 1.0 nM) was administered to isolated rat pancreases perfused either in the absence of exogenous nutrient or presence of 10 mM succinic acid dimethyl ester (SAD). In the absence of any exogenous nutrient
L Ladrière et al.
Metabolism: clinical and experimental, 48(1), 102-106 (1999-01-27)
The metabolism of [2,3-13C]succinic acid dimethyl ester ([2,3-13C]-SAD) 10 mmol/L was examined in hepatocytes from overnight-fasted normal rats, 3-day starved rats, and overnight-fasted hereditarily diabetic Goto-Kakizaki (GK) rats. The amount of 13C-labeled succinate, fumarate, malate, lactate, alanine, and aspartate released
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