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Merck
CN

H57009

Sigma-Aldrich

3-羟基吡啶

98%

别名:

3-吡啶酚, 3-吡啶酮

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关于此项目

经验公式(希尔记法):
C5H5NO
化学文摘社编号:
分子量:
95.10
Beilstein:
105699
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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质量水平

方案

98%

mp

125-128 °C (lit.)

SMILES字符串

Oc1cccnc1

InChI

1S/C5H5NO/c7-5-2-1-3-6-4-5/h1-4,7H

InChI key

GRFNBEZIAWKNCO-UHFFFAOYSA-N

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象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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Michael M Iba et al.
Archives of biochemistry and biophysics, 404(2), 326-334 (2002-07-31)
Pyridine and its metabolites have been shown in previous studies to induce cytochrome P4501A1 (CYP1A1) expression in vivo in the rat and in vitro in cultured human lung explants. In this study, we assessed the role of the metabolites in
E Kindt et al.
Analytical biochemistry, 283(1), 71-76 (2000-08-10)
Preclinical efficacy testing commonly involves studies that require considerable resources and time. One valuable tool in this endeavor is the characterization of relevant biomarkers. A method has been developed for the simultaneous determination of collagen biomarker candidates as an instrument
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Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life, 41(4), 317-330 (2011-03-23)
The thermal condensation of formamide in the presence of mineral borates is reported. The products afforded are precursors of nucleic acids, amino acids derivatives and carboxylic acids. The efficiency and the selectivity of the reaction was studied in relation to
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Journal of medicinal chemistry, 48(22), 6787-6789 (2005-10-28)
Because alpha-tocopherol (alpha-TOH) mediates the peroxidation of cholesterol-esterified lipids in human low-density lipoprotein (LDL) in vitro and has displayed disappointing results against the onset and development of atherosclerosis, it may not be appropriate for use as a therapeutic in the
Stefica Horvat et al.
Chemical biology & drug design, 70(1), 30-39 (2007-07-17)
The kinetics of formation and identity of the reaction products of the glucuronic acid with three representative opioid peptides were investigated in vitro. Peptides were conjugated with glucuronic acid either in solution or under dry-heating conditions. From the incubations performed

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