B9009
Benzo[ghi]perylene
98%
Synonym(s):
1,12-Benzoperylene
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About This Item
Empirical Formula (Hill Notation):
C22H12
CAS Number:
Molecular Weight:
276.33
Beilstein:
1913029
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23
Assay
98%
form
solid
bp
>500 °C (lit.)
mp
277-279 °C (lit.)
SMILES string
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
InChI key
GYFAGKUZYNFMBN-UHFFFAOYSA-N
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Related Categories
Application
An n-channel organic semiconductor.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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J R Van Gurp et al.
Cancer research, 43(12 Pt 1), 6031-6038 (1983-12-01)
The development of a selection procedure is described which utilizes the fact that certain polycyclic aromatic hydrocarbons are rendered highly cytotoxic when illuminated with near-ultraviolet light. Twenty polycyclic aromatic hydrocarbons were screened for phototoxicity and toxicity in the absence of
N C Hughes et al.
Carcinogenesis, 14(1), 127-133 (1993-01-01)
Benzo[ghi]perylene (B[ghi]P) is a polycyclic aromatic hydrocarbon (PAH), present in complex combustion products, and evidence for its carcinogenic activity in experimental animals is equivocal, and yet it has demonstrable mutagenic activity in vitro. In order to investigate the possible DNA
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
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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