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Merck

P8001

Sigma-Aldrich

苯丙酮酸钠

powder

别名:

2-氧代-3-苯基丙酸, 苯丙酮酸 钠盐

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About This Item

线性分子式:
C6H5CH2COCOONa
CAS号:
分子量:
186.14
Beilstein:
4770978
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

形狀

powder

顏色

white to off-white

mp

>300 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

[Na+].[O-]C(=O)C(=O)Cc1ccccc1

InChI

1S/C9H8O3.Na/c10-8(9(11)12)6-7-4-2-1-3-5-7;/h1-5H,6H2,(H,11,12);/q;+1/p-1

InChI 密鑰

MQGYVGKMCRDEAF-UHFFFAOYSA-M

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儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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Jun Wang et al.
Frontiers in microbiology, 10, 2357-2357 (2019-11-05)
Endogenous hydrogen sulfide (H2S), which is primarily generated by 3-mercaptopyruvate sulfurtransferase (3-MST) in Escherichia coli (E. coli) under aerobic conditions, renders bacteria highly resistant to oxidative stress. However, the biosynthetic pathway and physiological role of this gas under anaerobic conditions
William M Moe et al.
Environmental science & technology, 52(16), 9311-9319 (2018-07-26)
In situ bioremediation practices that include subsurface addition of fermentable electron donors to stimulate reductive dechlorination by anaerobic bacteria have become widely employed to combat chlorinated solvent contamination in groundwater. At a contaminated site located near Baton Rouge, Louisiana (USA)
Cristiana M L Di Giuro et al.
PloS one, 8(7), e68932-e68932 (2013-08-13)
(S)-Hydroxymandelate synthase (Hms) is a nonheme Fe(II) dependent dioxygenase that catalyzes the oxidation of 4-hydroxyphenylpyruvate to (S)-4-hydroxymandelate by molecular oxygen. In this work, the substrate promiscuity of Hms is characterized in order to assess its potential for the biosynthesis of
Faqing Tang et al.
Clinical biochemistry, 44(8-9), 711-718 (2011-03-16)
To search for markers of nasopharyngeal carcinoma (NPC) for diagnosis. Using gas chromatography and mass spectrometry, we evaluated 51 serum metabolites in 49 NPC, 37 throat cancer patients and 40 healthy controls. High metabolites were selected and confirmed in NPC
Sumit Chakraborty et al.
Biochemistry, 47(12), 3800-3809 (2008-03-05)
Direct spectroscopic observation of thiamin diphosphate-bound intermediates was achieved on the enzyme benzaldehyde lyase, which carries out reversible and highly enantiospecific conversion of ( R)-benzoin to benzaldehyde. The key enamine intermediate could be observed at lambda max 393 nm in

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