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V900285

Sigma-Aldrich

3-Hydroxypyridine

Vetec, reagent grade, 99%

Synonym(s):

3-Pyridinol, 3-Pyridone

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About This Item

Empirical Formula (Hill Notation):
C5H5NO
CAS Number:
Molecular Weight:
95.10
Beilstein/REAXYS Number:
105699
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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grade

reagent grade

product line

Vetec

assay

99%

mp

125-128 °C (lit.)

SMILES string

Oc1cccnc1

InChI

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

InChI key

GRFNBEZIAWKNCO-UHFFFAOYSA-N

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Legal Information

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Misaki Nakai et al.
Journal of inorganic biochemistry, 99(6), 1275-1282 (2005-05-27)
Metal complexes of 3-hydroxypyridine-2-carboxylic acid (H(2)hpic), [Co(Hhpic)(2)(H(2)O)(2)] (1), [Fe(Hhpic)(2)(H(2)O)(2)] (2), [Zn(Hhpic)(2)(H(2)O)(2)] (3), [Mn(Hhpic)(2)(H(2)O)(2)] (4), and [Cu(Hhpic)(2)] (5) have been synthesized and characterized by mass spectrometry, elemental analysis, magnetic susceptibility, infrared, electronic absorption and electron paramagnetic resonance (EPR) spectroscopies. The solid-state
N L Sakina et al.
Bulletin of experimental biology and medicine, 147(2), 193-195 (2009-06-11)
Photoprotective activity of heteroaromatic compounds (derivatives of 3-hydroxypyridine, amino-6-hydroxybenzothiazole, and 5-hydroxybenzimidazole) was studied in the system of UV-induced cardiolipin peroxidation. Although all three compounds had the antioxidant effect during free radical oxidation of luminol, only derivatives of amino-6-hydroxybenzothiazole and 5-hydroxybenzimidazole
Fazlul Huq et al.
Journal of molecular modeling, 8(3), 81-86 (2002-07-12)
Molecular mechanics and semiempirical calculations using HyperChem 5 were carried out to investigate whether the results obtained can explain why 2-hydroxypyridine is far more soluble in water than 3-hydroxypyridine. The results of molecular mechanics calculations show that in solution in
E B Watkins et al.
Bioorganic & medicinal chemistry letters, 11(16), 2099-2100 (2001-08-22)
Tyrosine phenol-lyase from Citrobacter freundii synthesizes 2-aza-L-tyrosine and 3-aza-L-tyrosine from 3-hydroxypyridine and 2-hydroxypyridine, respectively, and ammonium pyruvate.
Raffaele Saladino et al.
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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