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P66807

Sigma-Aldrich

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:
100-55-0
Molecular Weight:
109.13
Beilstein:
107851
EC Number:
202-864-6
MDL number:
MFCD00006407
UNSPSC Code:
12352100
PubChem Substance ID:
24898789
NACRES:
NA.22

Quality Level

200

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319

Hazard Classifications

Eye Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

275.0 °F

Flash Point(C)

135 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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
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
D J Wise et al.
Archives of biochemistry and biophysics, 344(1), 176-183 (1997-08-01)
Haemophilus parasuis malate dehydrogenase ((S)-malate:NAD+ oxidoreductase; EC 1.1.1.37) isolated from cell sonicates was purified 584-fold to electrophoretic homogeneity with a 19% recovery and a specific activity of 222 units/mg protein. SDS-polyacrylamide gel electrophoresis and molecular exclusion chromatography indicated the purified
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