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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-637-4
Beilstein/REAXYS Number:
105699
MDL number:
Assay:
98%
InChI key
GRFNBEZIAWKNCO-UHFFFAOYSA-N
InChI
1S/C5H5NO/c7-5-2-1-3-6-4-5/h1-4,7H
SMILES string
Oc1cccnc1
assay
98%
Quality Level
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Related Categories
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
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
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
Georg T Wondrak et al.
The Journal of biological chemistry, 279(29), 30009-30020 (2004-05-11)
Photocarcinogenesis and photoaging are established consequences of chronic exposure of human skin to solar irradiation. Accumulating evidence supports a causative involvement of UVA irradiation in skin photo-damage. UVA photodamage has been attributed to photosensitization by endogenous skin chromophores leading to
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
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
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