H57009
3-Hydroxypyridine
98%
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:
105699
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
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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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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G S M Kiruba et al.
The Journal of organic chemistry, 68(7), 2874-2881 (2003-03-29)
The tautomeric equilibria of a series of 3-hydroxypyridine derivatives including pyridoxal-5'-phosphate (PLP), the active form of vitamin B(6), have been studied using density functional calculations (B3LYP/6-311+G//B3LYP/6-31G) in the gas phase and in different solvents. Three different approaches, namely continuum, discrete
Zhongfa Liu et al.
Chemical research in toxicology, 16(2), 232-241 (2003-02-18)
2-hydroxyaldehydes have been previously identified as products of lipid peroxidation, and although they represent the simplest reducing sugars, their potential for modification of proteins under physiological conditions has not been investigated. Here, 2-hydroxyaldehydes were found to condense with amines in
Fazlul Huq et al.
European journal of medicinal chemistry, 39(8), 691-697 (2004-07-28)
Four trans-planaramineplatinum(II) complexes code named YH9, YH10, YH11 and YH12, each of the form trans-PtL(NH(3))Cl(2) where L = 2-hydroxypyridine and 3-hydroxypyridine, imidazole, and imidazo(1,2-alpha)pyridine for YH9, YH10, YH11 and YH12, respectively. All of the compounds have significant anticancer activity against
L D Lukyanova et al.
Bulletin of experimental biology and medicine, 148(4), 587-591 (2010-04-17)
Succinate-containing derivatives of 3-hydroxypyridine, mexidol and proxypin, serve as succinate donors for the respiratory chain and contribute to activation of the succinate oxidase pathway of oxidation. Under conditions of hypoxia, these changes promote recovery of aerobic energy production, normalization of
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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