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H57009

Sigma-Aldrich

3-Hydroxypyridin

98%

Synonym(e):

3(2H)-Pyridon, 3-Pyridinol

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About This Item

Empirische Formel (Hill-System):
C5H5NO
CAS-Nummer:
109-00-2
Molekulargewicht:
95.10
Beilstein:
105699
EG-Nummer:
203-637-4
MDL-Nummer:
MFCD00006378
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24895705
NACRES:
NA.22

Assay

98%

mp (Schmelzpunkt)

125-128 °C (lit.)

SMILES String

Oc1cccnc1

InChI

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

InChIKey

GRFNBEZIAWKNCO-UHFFFAOYSA-N

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Verwandte Kategorien

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

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(R)-1-Boc-3-Hydroxypiperidin 95%

Sigma-Aldrich

687278

(R)-1-Boc-3-Hydroxypiperidin

N-Methyl-2-Pyridon ≥99%

Sigma-Aldrich

M78259

N-Methyl-2-Pyridon

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
E Kindt et al.
Analytical biochemistry, 283(1), 71-76 (2000-08-10)
Preclinical efficacy testing commonly involves studies that require considerable resources and time. One valuable tool in this endeavor is the characterization of relevant biomarkers. A method has been developed for the simultaneous determination of collagen biomarker candidates as an instrument
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