W239607
丁二酸二甲酯
98%, FG
别名:
丁二酸二甲酯, 琥珀酸二甲酯
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关于此项目
线性分子式:
CH3OCOCH2CH2COOCH3
CAS Number:
分子量:
146.14
FEMA编号:
2396
Beilstein:
956776
EC 号:
欧洲委员会编号:
439
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
9.445
NACRES:
NA.21
生物来源
synthetic
等级
FG
Halal
Kosher
管理合规性
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117
FDA 21 CFR 172.515
蒸汽压
0.3 mmHg ( 20 °C)
方案
98%
自燃温度
689 °F
expl. lim.
8.5 %
折射率
n20/D 1.419 (lit.)
沸点
200 °C (lit.)
mp
16-19 °C (lit.)
密度
1.117 g/mL at 25 °C (lit.)
应用
flavors and fragrances
文件
see Safety & Documentation for available documents
食品过敏原
no known allergens
性状检查
green; fruity; floral; sweet
SMILES字符串
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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一般描述
丁二酸二甲酯可作为调味剂用于食品工业。
应用
- 代谢旁路挽救了阿尔茨海默病患者神经元中异常S-亚硝基化诱导的TCA循环抑制和突触损失。: 这项研究讨论了琥珀酸二甲酯之类的代谢中间体在规避阿尔茨海默病生化阻滞中的作用，提供了潜在的治疗途径（Andreyev et al., 2024）。
- RIFM香精成分安全性评估更新，丁二酸二甲酯，CAS等级号码106-65-0。: 作为香精成分的丁二酸二甲酯的全面安全评估，强调了其毒理学特征和安全使用参数（Api et al., 2023）。
警示用语：
Warning
危险声明
预防措施声明
危险分类
Eye Irrit. 2
储存分类代码
10 - Combustible liquids
WGK
WGK 1
闪点(°F)
201.2 °F - closed cup
闪点(°C)
94 °C - closed cup
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Burdock, GA
Encyclopedia of Food and Color Additives, 1, 878-879 (1997)
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
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
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
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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