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P33429

Sigma-Aldrich

4-Phenylpyridine

97%

Sinonimo/i:

γ-Phenylpyridine, 1-Benzylhydrazine dihydrochloride, p-Phenylpyridine

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About This Item

Formula empirica (notazione di Hill):
C11H9N
Numero CAS:
939-23-1
Peso molecolare:
155.20
Beilstein:
110490
Numero CE:
213-357-4
Numero MDL:
MFCD00006420
Codice UNSPSC:
12352100
ID PubChem:
24898403
NACRES:
NA.22

Saggio

97%

Forma fisica

crystals

P. eboll.

274-275 °C (lit.)

Punto di fusione

69-73 °C (lit.)

Stringa SMILE

c1ccc(cc1)-c2ccncc2

InChI

1S/C11H9N/c1-2-4-10(5-3-1)11-6-8-12-9-7-11/h1-9H
JVZRCNQLWOELDU-UHFFFAOYSA-N

Informazioni sul gene

human ... MMP3(4314)

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Categorie correlate

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

Eye Irrit. 2 - 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

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Certificati d'analisi (COA)

Lot/Batch Number
MKCP8457
MKCL8729
MKCD9974
MKCG5135
MKCF4284

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Sigma-Aldrich

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Sigma-Aldrich

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4-Methoxypyridine 97%

Sigma-Aldrich

460621

4-Methoxypyridine

4-Methylpyridine 98%

Sigma-Aldrich

131490

4-Methylpyridine

4,4′-Bipyridine for synthesis

Sigma-Aldrich

8.20158

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Sigma-Aldrich

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1,2-Di(4-pyridyl)ethylene

R R Ramsay et al.
Biochemical and biophysical research communications, 146(1), 53-60 (1987-07-15)
The neurotoxicity of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, an impurity in an illicit drug, is expressed after its oxidation to 1-methyl-4-phenylpyridinium by monoamine oxidase. The pyridinium is concentrated by carrier-mediated transport into the mitochondria where it inhibits NADH dehydrogenase and, hence, ATP synthesis. Some
I Irwin et al.
Life sciences, 40(8), 731-740 (1987-02-23)
Because of the chemical and structural similarity between 4-phenylpyridine (4PP) and 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), the effects of 4PP alone and in combination with MPTP on striatal dopamine (DA) concentrations were studied in mice. 4PP did not deplete striatal DA, even when
K S Hsu et al.
The Journal of pharmacology and experimental therapeutics, 279(2), 740-747 (1996-11-01)
The effect of L-deprenyl (selegiline) on the excitatory synaptic transmission was characterized in the CA1 neurons of rat hippocampal slices by using a intracellular recording technique. Superfusion of L-deprenyl (0.1-10 microM) reversibly decreased the EPSP, which was evoked by orthodromic
Behavioral and biochemical effects of 4-phenylpyridine, 2-phenylpyridine, and 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine in rodents.
M N Hassan et al.
Advances in neurology, 53, 219-223 (1990-01-01)
Germano Giuliani et al.
Bioorganic & medicinal chemistry, 19(7), 2242-2251 (2011-03-23)
The quinoline nucleus of the previously described 4-phenylquinoline-3-carboxamides NK(1) receptor ligands 7 has been transformed into either substituted or azole-(i.e., triazole or tetrazole) fused pyridine moieties of compounds 9 and 10, respectively, in order to obtain NK(1) receptor ligands showing
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