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BCR049

Benzo[j]fluoranthene

BCR®, certified reference material

Synonym(s):

Benzo[j]fluoranthene (purity)

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About This Item

Empirical Formula (Hill Notation):
C20H12
CAS Number:
205-82-3
Molecular Weight:
252.31
MDL number:
MFCD00152264
UNSPSC Code:
41116107
PubChem Substance ID:
329774202

grade

certified reference material

agency

BCR®

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care
pharmaceutical (small molecule)

format

neat

Storage temp.

2-8°C

SMILES string

c1ccc2c-3c(ccc2c1)-c4cccc5cccc-3c45

InChI

1S/C20H12/c1-2-8-15-13(5-1)11-12-17-16-9-3-6-14-7-4-10-18(19(14)16)20(15)17/h1-12H

Inchi Key

KHNYNFUTFKJLDD-UHFFFAOYSA-N

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Analysis Note

For more information please see:
BCR049

Legal Information

BCR is a registered trademark of European Commission

Pictograms

Health hazardEnvironment
GHS08,GHS09

signalword

Danger

hcodes

H350,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

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Etienne Bourgart et al.
Archives of toxicology, 93(8), 2165-2184 (2019-07-10)
Combined exposure to complex mixtures of polycyclic aromatic hydrocarbons (PAHs) and ultraviolet radiation (UVR) is suspected to enhance PAH skin permeability and skin cancer risk depending on PAH bioactivation. The impact of PAH mixtures (exposure dose, composition, and complexity) and
Carmela Lestingi et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 34(7), 1140-1152 (2017-05-18)
A gas-chromatographic single-quadrupole analytical method for the analysis of the 16 priority European Union (EU) polycyclic aromatic hydrocarbons (PAHs) in food is presented. The method fulfils the request of Regulation EU 836/2011 for an analytical procedure to be used for
Miyuki Fukai et al.
Journal of natural products, 75(1), 22-25 (2011-12-14)
Four novel benzo[j]fluoranthene derivatives, hypoxylonols C (3), D (4), E (5), and F (6), have been isolated from the mushroom Hypoxylon truncatum, together with two known benzo[j]fluoranthene derivatives, hypoxylonols A (1) and B (2). The structures were established by analysis
E J LaVoie et al.
Cancer research, 54(4), 962-968 (1994-02-15)
Benzo[j]fluoranthene (B[j]F), trans-4,5-dihydro-4,5-dihydroxy-B[j]F, and trans-9,10-dihydro-9,10-dihydroxy-B[j]F were evaluated for tumorigenic activity in newborn CD1 mice. These dihydrodiols were assayed at doses of 1.10 and 0.275 mumol/mouse. B[j]F and the syn- and anti-diol epoxides derived from these dihydrodiols were evaluated at doses
E H Weyand et al.
Chemico-biological interactions, 84(1), 37-53 (1992-09-14)
The metabolism and mutagenic activity of 4-fluorobenzo[j]fluoranthene (4F-B[j]F) and 10-fluorobenzo[j]fluoranthene (10F-B[j]F) were evaluated and compared with benzo[j]fluoranthene (B[j]F) using an identical rat liver homogenate preparation. Previous studies have shown that the major genotoxic metabolites of B[j]F are the 4,5- and
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