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Merck
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Documenti

120618

Sigma-Aldrich

4-Hydroxypyridine

95%

Sinonimo/i:

4-Pyridinol, 4-Pyridone

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About This Item

Formula empirica (notazione di Hill):
C5H5NO
Numero CAS:
626-64-2
Peso molecolare:
95.10
Beilstein:
105800
Numero CE:
210-958-3
Numero MDL:
MFCD00040458
Codice UNSPSC:
12352100
ID PubChem:
24847422
NACRES:
NA.22

Saggio

95%

P. eboll.

230-235 °C/12 mmHg (lit.)

Punto di fusione

150-151 °C (lit.)

Stringa SMILE

O=C1C=CNC=C1

InChI

1S/C5H5NO/c7-5-1-3-6-4-2-5/h1-4H,(H,6,7)
GCNTZFIIOFTKIY-UHFFFAOYSA-N

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Applicazioni

4-Hydroxypyridine was used in the synthesis of (Ag3MoO3F3) (Ag3MoO4)Cl by hydro(solvato)thermal methods. It was used as model compound to study the natural photodegradation of representative aquatic environmental contaminants.

Pittogrammi

CorrosionExclamation mark
GHS05,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H302,H315,H318,H335

Classi di pericolo

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

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G P Carlson
Toxicology letters, 85(3), 173-178 (1996-06-01)
In order to evaluate the possibility that the metabolism of pyridine may be important for its toxic actions, pyridine was compared with pyridine N-oxide, 2-hydroxypyridine, 3-hydroxypyridine, 4-hydroxypyridine and pyridinium methyliodide in rats given equal molar doses of the chemicals i.p.
Fazlul Huq et al.
Medicinal chemistry (Shariqah (United Arab Emirates)), 5(4), 372-381 (2009-08-20)
This paper describes the synthesis, characterization, cytotoxicity of a new trinuclear Pt-Pd-Pt complex code named TH8 containing two 4-hydroxypyridine ligands bound to the central metal ion. In addition to its activity against human ovarian cancer cell lines: A2780, A2780(cisR) and
Rodger F Henry
Journal of computer-aided molecular design, 24(6-7), 587-590 (2010-04-28)
Tautomerism is a phenomenon well know to most chemists but frequently forgotten when chemistry leaves the bench and enters the computational realm. Through the examination of several examples from the crystallographic literature it can be clearly demonstrated that the tautomeric
Tilman Lechel et al.
The Journal of organic chemistry, 75(3), 726-732 (2009-12-25)
A three-component reaction with lithiated alkoxyallenes, nitriles, and perfluorinated carboxylic acids as precursors led to a series of perfluoroalkyl- or perfluoroaryl-substituted 4-hydroxypyridine derivatives. These compounds were converted into 4-pyridyl nonaflates which can be employed as versatile building blocks for the
M M Iba et al.
Archives of biochemistry and biophysics, 378(2), 299-310 (2000-06-22)
We compared pyridine and five of its metabolites in terms of (i) in vivo induction of CYP1A1 expression in the lung, kidney, and liver in the rat and (ii) in vitro binding to, and activation of, the aryl hydrocarbon receptor
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