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Merck
CN

142433

Sigma-Aldrich

苯乙二醛 水合物

97%

别名:

2,2-二羟基苯乙酮

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About This Item

线性分子式:
C6H5COCHO · xH2O
CAS号:
分子量:
134.13 (anhydrous basis)
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

97%

形式

powder

bp

142 °C/125 mmHg (lit.)

mp

76-79 °C (lit.)

溶解性

95% ethanol: soluble 5%, clear to very slightly hazy, colorless to light yellow

SMILES字符串

[H]O[H].[H]C(=O)C(=O)c1ccccc1

InChI

1S/C8H6O2.H2O/c9-6-8(10)7-4-2-1-3-5-7;/h1-6H;1H2

InChI key

YQBLQKZERMAVDO-UHFFFAOYSA-N

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应用

苯乙二醛水合物用于:
  • 改良猪肌肉碳酸酐酶 Ⅲ
  • 作为精氨酸基团的特异性试剂
  • 制备吡咯烷酮 和呋喃 衍生物
  • 作为化学发光试剂测定嘌呤

生化/生理作用

苯乙酮醛是一种强效的线粒体乙醛脱氢酶抑制剂 。它与纯化的 Hageman 因子(HF,凝血因子 XII)中的精氨酸残基发生反应,并抑制其凝血特性

象形图

Exclamation mark

警示用语:

Warning

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Analytica Chimica Acta, 278, 275-275 (1993)
William A Irwin et al.
Biochemical and biophysical research communications, 291(2), 215-219 (2002-02-16)
Fructose has been shown to protect hepatocyte viability during hypoxia or exposure to mitochondrial electron transport inhibitors. We report here that the fructose metabolite D-glyceraldehyde (D-GA) is a good inhibitor of the mitochondrial permeability transition pore (PTP) in isolated rat
Synthesis, 783-783 (1993)
O D Radnoff et al.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.), 148(1), 177-182 (1975-01-01)
Exposure of purified Hageman factor (HF, Factor XII) to phenylglyoxal hydrate (PHG), an agent reacting with arginine residues in protein, inhibited its coagulant properties upon subsequent exposure of negatively charged agents. Once HF had been exposed to kaolin or ellagic
L M Pullan et al.
Biochemistry, 24(3), 635-640 (1985-01-29)
Mammalian carbonic anhydrase III has previously been shown to catalyze the hydrolysis of p-nitrophenyl phosphate in addition to possessing the conventional CO2 hydratase and p-nitrophenylacetate esterase activities. Modification of pig muscle carbonic anhydrase III with the arginine reagent phenylglyoxal yielded

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