V900526
3-吡啶甲醇
Vetec™, reagent grade, 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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经验公式（希尔记法）:
C6H7NO
化学文摘社编号:
分子量:
109.13
EC Number:
202-864-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
107851
MDL number:
InChI key
MVQVNTPHUGQQHK-UHFFFAOYSA-N
InChI
1S/C6H7NO/c8-5-6-2-1-3-7-4-6/h1-4,8H,5H2
SMILES string
OCc1cccnc1
grade
reagent grade
product line
Vetec™
assay
98%
bp
154 °C/28 mmHg (lit.)
density
1.124 g/mL at 25 °C (lit.)
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Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
T B Gelhard et al.
Journal de biologie buccale, 16(2), 95-99 (1988-06-01)
The F- uptake in vivo in sound human enamel from fluoridated toothpastes is described. Ten participants brushed for about 1 min twice a day, four enamel specimens in a dental appliance over three week periods. The enamel specimens were prepared
M Went
Zeitschrift fur die gesamte innere Medizin und ihre Grenzgebiete, 42(11), 313-316 (1987-06-01)
In 30 patients with organic disturbances of the arterial blood supply of the lower extremities the caudal epidural combination injection (one per cent procaine and radecol comp.) in comparison to the caudal epidural sympathetic blocking one per cent procaine) was
J Manzanares et al.
Thrombosis research, 49(6), 501-508 (1988-03-15)
We studied the anti-platelet aggregation activity of beta-pyridyl-carbinol (b-PC) (Ronicol, Roche). This compound has a chemical structure similar to nicotinic acid and is therapeutically indicated in functional and organic circulatory processes. We determined the in vitro antiaggregation activity induced by
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
The active site of liver alcohol dehydrogenase mechanistic inferences from the binding and turnover of 2-, 3-, and 4-pyridylcarbinols.
Y Pocker et al.
Progress in clinical and biological research, 232, 179-187 (1987-01-01)
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