P66807
3-Pyridinemethanol
98%
Synonym(s):
ω-Hydroxy-3-picoline, 3-(Hydroxymethyl)pyridine, 3-Pyridyl carbinol
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About This Item
Empirical Formula (Hill Notation):
C6H7NO
CAS Number:
Molecular Weight:
109.13
Beilstein:
107851
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
98%
refractive index
n20/D 1.545 (lit.)
bp
154 °C/28 mmHg (lit.)
density
1.124 g/mL at 25 °C (lit.)
SMILES string
OCc1cccnc1
InChI
1S/C6H7NO/c8-5-6-2-1-3-7-4-6/h1-4,8H,5H2
InChI key
MVQVNTPHUGQQHK-UHFFFAOYSA-N
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General description
3-Pyridinemethanol, an aromatic primary alcohol, is the key moiety of many bio-active and industrially important compounds.
Application
3-Pyridinemethanol can undergo aerobic photo-oxidation in the presence of catalytic amount of hydrobromic acid to form nicotinic acid.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
275.0 °F - closed cup
Flash Point(C)
135 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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)
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
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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