CAS 202-33-5
:Benz[j]aceanthrylene
Description:
Benz[j]aceanthrylene is a polycyclic aromatic hydrocarbon (PAH) characterized by its complex fused ring structure, which consists of five interconnected aromatic rings. This compound is known for its planar geometry and high stability due to the delocalization of π-electrons across the aromatic system. Benz[j]aceanthrylene exhibits strong fluorescence properties, making it of interest in various applications, including organic electronics and photonics. It is typically insoluble in water but soluble in organic solvents, which is a common trait among PAHs. The compound is also recognized for its potential environmental persistence and toxicity, raising concerns regarding its impact on human health and ecosystems. As with many PAHs, it can be formed through incomplete combustion processes and is often found in fossil fuels and urban air pollution. Due to its structural characteristics, benz[j]aceanthrylene may also serve as a model compound for studying the behavior of larger PAHs in biological systems and their interactions with cellular components.
Formula:C20H12
InChI:InChI=1S/C20H12/c1-2-7-16-13(4-1)8-10-17-18-11-9-14-5-3-6-15(20(14)18)12-19(16)17/h1-12H
InChI key:InChIKey=OSKRAISUPBTHCP-UHFFFAOYSA-N
SMILES:C12=C3C=4C(C=C1C=CC=C2C=C3)=C5C(=CC4)C=CC=C5
Synonyms:- Benz[7,8]aceanthrylene
- Benz[J]Aceanthrylene
- Cholanthrylene
- Naphth[2,1-d]acenaphthylene
- Cyclopenta[ij]tetraphene
Sort by
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Found 5 products.
Benz[j]aceanthrylene and Benz[e]aceanthrylene (70:30 Mixture)
CAS:Controlled Product<p>Applications Polycyclic aromatic hydrocarbons (PAHs) and their PAH-DNA adducts in lung tissues, and their ability to mutate the Ki-ras oncogene in PAH-induced tumors. Seven PAHs were studied: cyclopenta[cd]pyrene (CPP), benzo[a]pyrene (B[a]P), benzo[b]fluoranthene (B[b]F), dibenz[a,h]anthracene (DBA), 5-methylchrysene (5MC), benz[j]aceanthrylene (B[j]A), and dibenzo[a,l]pyrene (DB[a,l]P).<br>References Nesnow, S., et al.: Cancer Lett., 73, 73 (1993), Herzog, C., et al.: Cancer Res., 54, 4007 (1994), Prahalad, A., et al.: Carcinogenesis, 18, 1955 (1997),<br></p>Formula:C20H12Color and Shape:Dark OrangeMolecular weight:252.31Benz[j]aceanthrylene
CAS:Controlled ProductFormula:C20H12Color and Shape:NeatMolecular weight:252.309Benz[j]aceanthrylene and Benz[e]aceanthrylene (70:30 Mixture)
CAS:<p>Benz[j]aceanthrylene and Benz[e]aceanthrylene (70:30 Mixture) are polycyclic aromatic hydrocarbons that have been shown to cause cancer in animals. They can be metabolized to covalent adducts with nucleic acids, proteins, and lipids. These adducts have been found in the liver cells of rats treated with these compounds. The hl-60 cells were also found to be sensitive to these compounds, which may be due to their ability to induce tumour suppressor protein p53. In addition, benz[j]aceanthrylene and benz[e]aceanthrylene (70:30 Mixture) are genotoxic chemicals that can damage DNA by causing mutations or inhibiting replication of DNA strands. Benz[j]aceanthrylene and benz[e]aceanthrylene (70:30 Mixture) also react readily with rat liver microsomes. This reaction leads</p>Formula:C20H12Purity:Min. 95 Area-%Color and Shape:PowderMolecular weight:252.31 g/mol



