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Key Documents

112755

Sigma-Aldrich

DBE-4 dibasic ester

98%

Sinonimo/i:

Dimethyl succinate, Succinic acid dimethyl ester

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About This Item

Formula condensata:
CH3OCOCH2CH2COOCH3
Numero CAS:
Peso molecolare:
146.14
Beilstein:
956776
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22

Tensione di vapore

0.3 mmHg ( 20 °C)

Livello qualitativo

Saggio

98%

Temp. autoaccensione

689 °F

Limite di esplosione

8.5 %

Indice di rifrazione

n20/D 1.419 (lit.)

P. eboll.

200 °C (lit.)

Punto di fusione

16-19 °C (lit.)

Densità

1.117 g/mL at 25 °C (lit.)

Stringa SMILE

COC(=O)CCC(=O)OC

InChI

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

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Descrizione generale

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.

Note legali

DuPont product

Pittogrammi

Exclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Eye Irrit. 2

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

201.2 °F - closed cup

Punto d’infiammabilità (°C)

94 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Certificati d'analisi (COA)

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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.
L Ladriere et al.
JPEN. Journal of parenteral and enteral nutrition, 20(4), 251-256 (1996-07-01)
Succinic acid dimethyl ester (SAD) is efficiently metabolized in several cell types as pancreatic islet cells, hepatocytes, and colonocytes. The purpose of this study was to assess the overall nutritional value of SAD in the whole organism. SAD was infused
André Mukala-Nsengu et al.
Biochemical pharmacology, 67(5), 981-988 (2004-04-24)
The relative contribution of glycolysis vs. oxidative metabolism to the stimulus secretion coupling mechanism of beta-cells was investigated in isolated islets. For that purpose, the secretory and intracellular calcium responses of islets to both glucose and succinic acid dimethyl ester
Lili Yang et al.
The Journal of biological chemistry, 283(32), 21978-21987 (2008-06-12)
We conducted a study coupling metabolomics and mass isotopomer analysis of liver gluconeogenesis and citric acid cycle. Rat livers were perfused with lactate or pyruvate +/- aminooxyacetate or mercaptopicolinate in the presence of 40% enriched NaH(13)CO(3). Other livers were perfused
J Cancelas et al.
International journal of molecular medicine, 8(3), 269-271 (2001-08-09)
It was recently proposed that suitable succinic acid esters could be used to potentiate the insulinotropic action of glucagon-like peptide 1 (GLP-1) in the treatment of type-2 diabetes mellitus. In such a perspective, the present study aimed mainly at investigating

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