P33429
4-Phenylpyridine
97%
Synonym(s):
γ-Phenylpyridine, 1-Benzylhydrazine dihydrochloride, p-Phenylpyridine
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About This Item
Empirical Formula (Hill Notation):
C11H9N
CAS Number:
Molecular Weight:
155.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-357-4
Beilstein/REAXYS Number:
110490
MDL number:
Assay:
97%
Form:
crystals
InChI
1S/C11H9N/c1-2-4-10(5-3-1)11-6-8-12-9-7-11/h1-9H
InChI key
JVZRCNQLWOELDU-UHFFFAOYSA-N
SMILES string
c1ccc(cc1)-c2ccncc2
assay
97%
form
crystals
bp
274-275 °C (lit.)
Quality Level
Gene Information
human ... MMP3(4314)
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
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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L A Carr et al.
Life sciences, 48(12), 1173-1177 (1991-01-01)
Exposure to cigarette smoke has been found to attenuate the reduction in striatal dopamine levels caused by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) in mice and to inhibit monoamine oxidase (MAO) activity in brain tissue. To confirm whether specific smoke constituents which have been
M R Gluck et al.
The Journal of biological chemistry, 269(5), 3167-3174 (1994-02-04)
We have investigated the mechanism of the inhibition of membrane-bound NADH dehydrogenase by 1-methyl-4-phenylpyridinium (MPP+) and a series of its 4'-alkyl-substituted analogs of increasing hydrophobicity, as well as their neutral, desmethyl congeners. Comparison of hydrophobicity, as measured by partition coefficients
C C Huang et al.
Brain research, 753(1), 27-35 (1997-04-04)
The effects of L-deprenyl (selegiline), a highly selective monoamine oxidase type B (MAO-B) inhibitor, on cell excitability of rat hippocampal CA1 neurons were examined in slice preparations using intracellular recording techniques. Superfusion of L-deprenyl (10 and 20 microM) reversibly limited
Camilla C Golfeto et al.
Journal of inorganic biochemistry, 104(5), 489-495 (2010-02-02)
The synthesis and characterization of ruthenium compounds of the type [RuCl(2)(NO)(dppp)(L)]PF(6) [dppp=1,3-bis(diphenylphosphino)propane; L=pyridine, 4-methylpyridine, 4-phenylpyridine and dimethyl sulfoxide] are described. The complexes were characterized by elemental analysis, UV/Vis and infrared spectroscopy, cyclic voltammetry, and X-ray crystallography for the complexes with
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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