B9009
Benzo[ghi]perylene
98%
Sinônimo(s):
1,12-Benzoperylene
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25 MG
R$ 783,00
100 MG
R$ 1.936,00
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25 MG
R$ 783,00
100 MG
R$ 1.936,00
About This Item
Fórmula empírica (Notação de Hill):
C22H12
Número CAS:
Peso molecular:
276.33
Beilstein:
1913029
Número CE:
Número MDL:
Código UNSPSC:
12352103
ID de substância PubChem:
NACRES:
NA.23
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Ensaio
98%
Formulário
solid
p.e.
>500 °C (lit.)
pf
277-279 °C (lit.)
cadeia de caracteres SMILES
c1cc2ccc3ccc4ccc5cccc6c(c1)c2c3c4c56
InChI
1S/C22H12/c1-3-13-7-9-15-11-12-16-10-8-14-4-2-6-18-17(5-1)19(13)21(15)22(16)20(14)18/h1-12H
chave InChI
GYFAGKUZYNFMBN-UHFFFAOYSA-N
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Categorias relacionadas
Aplicação
An n-channel organic semiconductor.[1]
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Aquatic Acute 1 - Aquatic Chronic 1
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 2
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
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Stepan Boitsov et al.
Marine environmental research, 68(5), 236-245 (2009-08-01)
Polycyclic aromatic hydrocarbons (PAH) were measured in sediment cores from 13 locations in South-Western Barents Sea as part of a detailed study of the Norwegian seabed under the MAREANO program. The generally low PAH levels found, an average around 200
Py and BPe solvent polarity scales: effect of temperature on pyrene and benzo[ghi]perylene fluorescence spectra.
R Waris et al.
The Analyst, 113(9), 1465-1467 (1988-09-01)
N Nijegorodov et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 57(13), 2673-2685 (2002-01-05)
Absorption. fluorescence and laser properties of perylene, benzo(ghi)perylene and coronene are studied experimentally (under the same conditions) and quantum chemically at room (293 K) and at low (77 and 4 K) temperatures and direct comparison is made between the results
Nobuyasu Itoh et al.
Analytica chimica acta, 615(1), 47-53 (2008-04-29)
Microwave-assisted extraction using 1M KOH/methanol (alkaline-MAE) in combination with solid-phase extraction treatment was developed and applied to polycyclic aromatic hydrocarbons (PAHs) in a sediment sample. Although various conditions were examined (100 or 150 degrees C for 10 or 30 min)
Karl L Platt et al.
Chemical research in toxicology, 18(4), 700-710 (2005-04-19)
Carcinogenic polycyclic aromatic hydrocarbons (PAH), e.g., benzo[a]pyrene (BaP), possess a bay region comprising an ortho-fused benzene ring. Benzo[ghi]perylene (BghiP) represents the group of PAHs lacking such a "classic" bay region and hence cannot be metabolically converted like BaP to bay
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