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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

Formule empirique (notation de Hill):

C₂₀H₁₂

Numéro CAS:

205-99-2

Poids moléculaire :

252.31

Numéro Beilstein :

1872553

Numéro MDL:

MFCD00010582

Code UNSPSC :

41116107

ID de substance PubChem :

329755553

Nomenclature NACRES :

NA.24

Qualité

analytical standard

Durée de conservation

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

Température de stockage

2-8°C

Chaîne SMILES

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

Clé InChI

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.

Pictogrammes

GHS02,GHS08,GHS07,GHS09

Mention d'avertissement

Danger

Mentions de danger

H225,H304,H315,H336,H410

Conseils de prudence

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

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

-0.4 °F

Point d'éclair (°C)

-18 °C

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Certificats d'analyse (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

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

Amounts and proportion of administered pyrene dose excreted as urinary 1-hydroxypyrene after dietary exposure to polycyclic aromatic hydrocarbons.

Yeh-Chung Chien et al.

Archives of toxicology, 84(10), 767-776 (2010-06-24)

Although urinary 1-hydroxypyrene (1-OHP) is the most relevant parameter for assessing exposure to polycyclic aromatic hydrocarbons, the inability to further elucidate the intra- and inter-individual variability, specificity and kinetics makes it difficult to enhance its value as an exposure predictor.

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