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W239607

Sigma-Aldrich

Dimethyl succinate

98%, FG

Synonyma:

Dimethyl butanedioate, Succinic acid dimethyl ester

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About This Item

Lineární vzorec:
CH3OCOCH2CH2COOCH3
Číslo CAS:
106-65-0
Molekulová hmotnost:
146.14
FEMA Number:
2396
Beilstein/REAXYS Number:
956776
EC Number:
203-419-9
Council of Europe no.:
439
MDL number:
MFCD00008466
UNSPSC Code:
12164502
PubChem Substance ID:
24901044
Flavis number:
9.445
NACRES:
NA.21
organoleptic:
green; fruity; floral; sweet
grade:
FG
Halal
Kosher
biological source:
synthetic
food allergen:
no known allergens

biological source

synthetic

Quality Level

400

grade

FG
Halal
Kosher

reg. compliance

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

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.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

green; fruity; floral; sweet

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 can be used as a flavoring agent in the food industry.

Application


  • Metabolic Bypass Rescues Aberrant S-nitrosylation-Induced TCA Cycle Inhibition and Synapse Loss in Alzheimer′s Disease Human Neurons.: This research discusses the role of metabolic intermediates like Dimethyl succinate in bypassing biochemical blocks in Alzheimer′s disease, offering potential therapeutic avenues (Andreyev et al., 2024).

  • Update to RIFM fragrance ingredient safety assessment, dimethyl succinate, CAS Registry Number 106-65-0.: A comprehensive safety assessment of Dimethyl succinate as a fragrance ingredient, highlighting its toxicological profile and safe usage parameters (Api et al., 2023).

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

Vyberte jednu z posledních verzí:

Osvědčení o analýze (COA)

Lot/Batch Number
SHBS2029
SHBP3136
SHBP7100
SHBN8044
SHBN8042

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Diethyl succinate ≥99%, FCC, FG

Sigma-Aldrich

W237701

Diethyl succinate

Dimethyl methylsuccinate 98%

Sigma-Aldrich

178799

Dimethyl methylsuccinate

Diethyl succinate natural, ≥99%, FG

Sigma-Aldrich

W237712

Diethyl succinate

Dimethyl succinate-2,2,3,3-d4 98 atom % D

Sigma-Aldrich

492248

Dimethyl succinate-2,2,3,3-d4

Burdock, GA
Encyclopedia of Food and Color Additives, 1, 878-879 (1997)
Dushyant Shekhawat et al.
Bioresource technology, 97(2), 342-347 (2005-09-21)
A complete process model and economic analysis has been developed for itaconic acid production via catalytic condensation of dimethyl succinate and formaldehyde. The process model is based on experimental yields and selectivities obtained for the condensation reaction and on recovery
W J Malaisse et al.
Nutrition (Burbank, Los Angeles County, Calif.), 13(4), 330-341 (1997-04-01)
In rats injected with bacterial lipopolysaccharide (LPS; 5 gamma mg/g body weight [BWT]), the toxin provokes death within 24 h in 23% of the animals and, in surviving rats, causes a decrease in BWT, hyperlactacidemia, hyperlipacidemia, and hyperketonemia, as well
V Leclercq-Meyer et al.
Biochemical and molecular medicine, 59(1), 87-90 (1996-10-01)
Glucagon-like peptide 1 (GLP-1) is often referred to as a glucose-dependent insulinotropic agent and is currently under investigation as a tool in the treatment of noninsulin-dependent diabetes. This report shows that, in the absence of glucose, a nonglucidic nutrient, namely
Shohei Hamada et al.
Bioorganic & medicinal chemistry letters, 19(10), 2852-2855 (2009-04-11)
N-Oxalylglycine (NOG) derivatives were synthesized, and their inhibitory effect on histone lysine demethylase activity was evaluated. NOG and compound 1 inhibited histone lysine demethylases JMJD2A, 2C and 2D in enzyme assays, and their dimethyl ester prodrugs DMOG and 21 exerted
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