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Merck
CN

14075

Sigma-Aldrich

琥珀半醛 溶液

~15% in H2O (T)

别名:

4-Oxobutyric acid, 4-氧丁酸, Succinaldehydic acid, 琥珀半醛单体

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关于此项目

线性分子式:
HCOCH2CH2COOH
化学文摘社编号:
分子量:
102.09
Beilstein:
1745187
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
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浓度

~15% in H2O (T)

储存温度

2-8°C

SMILES字符串

OC(=O)CCC=O

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其他说明

与 DHAP 发生酶催化羟醛反应;琥珀半醛脱氢酶的底物

象形图

Exclamation mark

警示用语:

Warning

危险声明

预防措施声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2

储存分类代码

12 - Non Combustible Liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Kathryn M McCulloch et al.
Biochemistry, 49(6), 1226-1235 (2010-01-27)
The gene identification and kinetic characterization of (E)-2-(acetamidomethylene)succinate (E-2AMS) hydrolase has recently been described. This enzyme catalyzes the final reaction in the degradation of vitamin B(6) and produces succinic semialdehyde, acetate, ammonia, and carbon dioxide from E-2AMS. The structure of
Natsumi Saito et al.
The Journal of biological chemistry, 284(24), 16442-16451 (2009-04-18)
The search for novel enzymes and enzymatic activities is important to map out all metabolic activities and reveal cellular metabolic processes in a more exhaustive manner. Here we present biochemical and physiological evidence for the function of the uncharacterized protein
W.-D. Fessner et al.
Angewandte Chemie (International Edition in English), 103, 596-596 (1991)
Baiqiang Yuan et al.
Journal of nutritional science and vitaminology, 54(3), 185-190 (2008-07-19)
We have found for the first time that a chromosomal gene, mlr6787, in Mesorhizobium loti encodes the pyridoxine degradative enzyme alpha-(N-acetylaminomethylene)succinic acid (AAMS) amidohydrolase. The recombinant enzyme expressed in Escherichia coli cells was homogeneously purified and characterized. The enzyme consisted
C P O'Byrne et al.
Journal of microbiological methods, 84(1), 137-139 (2010-11-04)
The GABase assay is widely used to rapidly and accurately quantify levels of extracellular γ-aminobutyric acid (GABA). Here we demonstrate a modification of this assay that enables quantification of intracellular GABA in bacterial cells. Cells are lysed by boiling and

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