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36955

Benzo[b]fluoranthene solution

Name: Benzo[b]fluoranthene solution
Brand: SIAL

100 μg/mL in cyclohexane, analytical standard

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About This Item

Fórmula empírica (notación de Hill):

C₂₀H₁₂

Número de CAS:

205-99-2

Peso molecular:

252.31

Beilstein/REAXYS Number:

1872553

MDL number:

MFCD00010582

UNSPSC Code:

41116107

PubChem Substance ID:

329755553

NACRES:

NA.24

grade

analytical standard

shelf life

limited shelf life, expiry date on the label

concentration

100 μg/mL in cyclohexane

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

single component solution

storage temp.

2-8°C

SMILES string

c1ccc-2c(c1)-c3cccc4c3c-2cc5ccccc45

InChI

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

InChI key

FTOVXSOBNPWTSH-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

GHS02,GHS08,GHS07,GHS09

signalword

Danger

hcodes

H225,H304,H315,H336,H410

pcodes

P210 - P233 - P273 - P301 + P310 - P303 + P361 + P353 - P331

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

-0.4 °F

flash_point_c

-18 °C

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Certificados de análisis (COA)

Lot/Batch Number

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Benzo[b]fluoranthene: tumorigenicity in strain A/J mouse lungs, DNA adducts and mutations in the Ki-ras oncogene.

M J Mass et al.

Carcinogenesis, 17(8), 1701-1704 (1996-08-01)

The polycyclic aromatic hydrocarbon benzo[b]fluoranthene (B[b]F) is a pervasive constituent of environmental combustion products. We sought to examine the lung tumorigenic activity of B[b]F in strain A/J mice, to study the relationship between formation and decay of B[b]F-DNA adducts and

Quantitative and temporal relationships between DNA adduct formation in target and surrogate tissues: implications for biomonitoring.

S Nesnow et al.

Environmental health perspectives, 101 Suppl 3, 37-42 (1993-10-01)

DNA-carcinogen adducts offer a potential dosimeter for environmental genotoxicants reaching the exposed individual. Because the target tissues for many chemical carcinogens are not readily accessible for monitoring adducts in humans, peripheral blood lymphocytes (PBLs) have served as surrogate sources of

Benzo[b]fluoranthene, a potential alternative to benzo[a]pyrene as an indicator of exposure to airborne PAHs in the vicinity of Söderberg aluminum smelters.

S Aubin et al.

Journal of the Air & Waste Management Association (1995), 50(12), 2093-2101 (2001-01-05)

Benzo[b]fluoranthene (B[b]F) was used in relative abundance ratios (RARs), a parameter obtained by dividing the concentration of individual polycyclic aromatic hydrocarbons (PAHs) found in a given sample by the concentration of B[b]F in the same sample. The B[b]F RARs were

Distributions and concentrations of PAHs in Hong Kong soils.

H B Zhang et al.

Environmental pollution (Barking, Essex : 1987), 141(1), 107-114 (2005-10-26)

Surface soil (0-10 cm) samples from 53 sampling sites including rural and urban areas of Hong Kong were collected and analyzed for 16 EPA priority polycyclic aromatic hydrocarbons (PAHs). Total PAH concentrations were in the range of 7.0-410 microg kg(-1)

The aryl hydrocarbon receptor-dependent deregulation of cell cycle control induced by polycyclic aromatic hydrocarbons in rat liver epithelial cells.

Zdenek Andrysík et al.

Mutation research, 615(1-2), 87-97 (2006-12-05)

Disruption of cell proliferation control by polycyclic aromatic hydrocarbons (PAHs) may contribute to their carcinogenicity. We investigated role of the aryl hydrocarbon receptor (AhR) in disruption of contact inhibition in rat liver epithelial WB-F344 'stem-like' cells, induced by the weakly

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