P66807
3-吡啶甲醇
98%
别名:
ω-羟基-3-皮考啉, 3-(羟甲基)吡啶, 吡啶-3-甲醇
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关于此项目
经验公式（希尔记法）:
C6H7NO
化学文摘社编号:
分子量:
109.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-864-6
Beilstein/REAXYS Number:
107851
MDL number:
Assay:
98%
InChI key
MVQVNTPHUGQQHK-UHFFFAOYSA-N
InChI
1S/C6H7NO/c8-5-6-2-1-3-7-4-6/h1-4,8H,5H2
SMILES string
OCc1cccnc1
assay
98%
Quality Level
bp
154 °C/28 mmHg (lit.)
density
1.124 g/mL at 25 °C (lit.)
General description
3-吡啶甲醇是一种芳香族伯醇，是许多具有生物活性和工业重要性的化合物的关键成分。
Application
3-吡啶甲醇在催化量的氢溴酸存在下可发生好氧光氧化，从而形成烟酸。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
275.0 °F - closed cup
flash_point_c
135 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Conformational stability, molecular structure, vibrational, electronic, 1H and 13C spectral analysis of 3-pyridinemethanol using ab-initio/DFT method.
Sivaranjani T
Journal of Molecular Structure, 1108, 398-410 (2016)
Aerobic photo-oxidation of alcohols in the presence of a catalytic inorganic bromo source.
Hirashima S
Tetrahedron, 62(33), 7887-7891 (2006)
C Keller et al.
Klinische Wochenschrift, 66(14), 647-650 (1988-07-15)
We report two cases of unusual hepatic lesions following years of monotherapy with pyridylcarbinol (timespan) in a daily dose of 1.35 to 1.5 g for familial hypercholesterolemia. Mild elevations of liver enzymes correlated to a large tumor-like mass in the
T Fazekas et al.
Acta physiologica Hungarica, 74(2), 169-174 (1989-01-01)
The antilipolytic, nicotinic acid analogue beta-pyridylcarbinol (Ronicol) has previously been reported to decrease the free fatty acid (FFA) concentration of the arteria-blood, and to moderate the FFA-uptake and O2-consumption of the myocardium; on this basis, the drug may be expected
N Zöllner
International journal for vitamin and nutrition research. Supplement = Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Supplement, 30, 114-119 (1989-01-01)
The clinical use of nicotinic acid, nicotinamide, and pyridylcarbinol as drugs against hypercholesterolemia is critically reviewed. Though several questions remain open as to the mode of action of these compounds, it is concluded that they indeed belong to the most
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