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Merck

W237701

Sigma-Aldrich

Diethylsuccinat

≥99%, FCC, FG

Synonym(e):

Diethylbutanedioat

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About This Item

Lineare Formel:
C2H5OCOCH2CH2COOC2H5
CAS-Nummer:
Molekulargewicht:
174.19
FEMA-Nummer:
2377
Beilstein:
907645
EG-Nummer:
CoE-Nummer:
438
MDL-Nummer:
UNSPSC-Code:
12164502
eCl@ss:
39022839
PubChem Substanz-ID:
Flavis-Nummer:
9.444
NACRES:
NA.21

Biologische Quelle

synthetic

Qualitätsniveau

Qualität

FG
Fragrance grade
Halal
Kosher

Agentur

follows IFRA guidelines
meets purity specifications of JECFA

Einhaltung gesetzlicher Vorschriften

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 117
FDA 21 CFR 172.515

Dampfdichte

6 (vs air)

Assay

≥99%

Brechungsindex

n20/D 1.42 (lit.)

bp

218 °C (lit.)

mp (Schmelzpunkt)

−20 °C (lit.)

Dichte

1.047 g/mL at 25 °C (lit.)

Anwendung(en)

flavors and fragrances

Dokumentation

see Safety & Documentation for available documents

Nahrungsmittelallergen

no known allergens

Allergener Duftstoff

no known allergens

Organoleptisch

apple; grape; fruity; waxy; floral

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

InChIKey

DKMROQRQHGEIOW-UHFFFAOYSA-N

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Allgemeine Beschreibung

Diethylsuccinat kann als Aromastoff in der Lebensmittelindustrie eingesetzt werden.
Natürliches Vorkommen: Apfel, Kakao, Traube, Branntwein, Whiskey und Wein.

Anwendung


  • Impact of indigenous Oenococcus oeni and Lactiplantibacillus plantarum species co-culture on Cabernet Sauvignon wine malolactic fermentation: Kinetic parameters, color, and aroma.: This study explores the co-culture fermentation process in Cabernet Sauvignon wine, focusing on kinetic parameters, color, and aroma. Diethyl succinate was analyzed among the volatile compounds, contributing to the wine′s aroma profile. (Zhang et al., 2024).

  • Enhancement of ester biosynthesis in blueberry wines through co-fermentation via cell-cell contact between Torulaspora delbrueckii and Saccharomyces cerevisiae.: The research investigates the role of cell-cell contact in ester biosynthesis during the co-fermentation of blueberry wines. Diethyl succinate is one of the key esters produced, enhancing the aroma and flavor profile of the wine. (Wang et al., 2024).

  • Enhancing blueberry wine aroma: Insights from cultivar selection and berry sorting.: This article examines how different blueberry cultivars and sorting methods impact the aroma of blueberry wine, with a focus on the production of aromatic esters such as diethyl succinate. (Wang et al., 2023).

  • Comparative analysis of microbial communities and volatile flavor components in the brewing of Hongqu rice wines fermented with different starters.: The study provides a comparative analysis of microbial communities and their impact on volatile flavor components, including diethyl succinate, in Hongqu rice wines fermented with different starters. (Chen et al., 2023).

  • Update to RIFM fragrance ingredient safety assessment, diethyl succinate, CAS Registry Number 123-25-1.: This update focuses on the safety assessment of diethyl succinate as a fragrance ingredient, providing comprehensive toxicological data and usage guidelines. (Api et al., 2023).

Biochem./physiol. Wirkung

Geschmack bei 10–100 ppm

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 2

Flammpunkt (°F)

208.4 °F - closed cup

Flammpunkt (°C)

98 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


Analysenzertifikate (COA)

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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Burdock, GA
Encyclopedia of Food and Color Additives, 1, 822-823 (1997)
Burdock, GA
Encyclopedia of Food and Color Additives, 1, 822-823 (1997)
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.
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
Organoleptic Characteristics of Flavor Materials
Mosciano, G.
Perfumer & Flavorist, 30, 48-48 (2005)

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