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Key Documents

W237701

Sigma-Aldrich

Diethyl succinate

≥99%, FCC, FG

Sinônimo(s):

Diethyl butanedioate

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About This Item

Fórmula linear:
C2H5OCOCH2CH2COOC2H5
Número CAS:
Peso molecular:
174.19
Número FEMA:
2377
Beilstein:
907645
Número CE:
Conselho da Europa nº:
438
Número MDL:
Código UNSPSC:
12164502
eCl@ss:
39022839
ID de substância PubChem:
Número de Flavis:
9.444
NACRES:
NA.21

fonte biológica

synthetic

Nível de qualidade

grau

FG
Fragrance grade
Halal
Kosher

Agency

follows IFRA guidelines
meets purity specifications of JECFA

conformidade reg.

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

densidade de vapor

6 (vs air)

Ensaio

≥99%

índice de refração

n20/D 1.42 (lit.)

pb

218 °C (lit.)

pf

−20 °C (lit.)

densidade

1.047 g/mL at 25 °C (lit.)

aplicação(ões)

flavors and fragrances

Documentação

see Safety & Documentation for available documents

alérgeno alimentar

no known allergens

alérgeno de fragrância

no known allergens

Organoléptico

apple; grape; fruity; waxy; floral

cadeia de caracteres SMILES

CCOC(=O)CCC(=O)OCC

InChI

1S/C8H14O4/c1-3-11-7(9)5-6-8(10)12-4-2/h3-6H2,1-2H3

chave InChI

DKMROQRQHGEIOW-UHFFFAOYSA-N

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Descrição geral

Diethyl succinate can be used as a flavoring agent in the food industry.
Natural occurrence: Apple, cocoa, grape, brandy, whiskey and wine.

Aplicação


  • 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).

Ações bioquímicas/fisiológicas

Taste at 10-100 ppm

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

208.4 °F - closed cup

Ponto de fulgor (°C)

98 °C - closed cup

Equipamento de proteção individual

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


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

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