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30958

Supelco

Benzo[b]fluoranthene

certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Synonym(s):

2,3-Benzfluoranthene, 3,4-Benz[e]acephenanthrylene, 3,4-Benzfluoranthene, 3,4-Benzofluoranthene, Benz[e]acephenanthrylene, Benzo[e]fluoranthene, NSC 89265

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About This Item

Empirical Formula (Hill Notation):
C20H12
CAS Number:
205-99-2
Molecular Weight:
252.31
EC Number:
205-911-9
MDL number:
MFCD00010582
UNSPSC Code:
41116107
PubChem Substance ID:
329753609
NACRES:
NA.24

grade

certified reference material
TraceCERT®

Quality Level

300

product line

TraceCERT®

shelf life

limited shelf life, expiry date on the label

manufacturer/tradename

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

163-165 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

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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General description

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.

Application

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

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Legal Information

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Health hazardEnvironment
GHS08,GHS09

signalword

Danger

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

flash_point_f

Not applicable

flash_point_c

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCH1849
BCCD0251
BCBS4402V
BCBL7088V
BCBD3109V

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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
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)
Thomas L Ter Laak et al.
Environmental science & technology, 43(19), 7212-7217 (2009-10-24)
In this study, the uptake of pyrene and benzo[b]fluoranthene by an aquatic worm (Lumbriculus variegatus) and a poly(dimethylsiloxane) coated glass fiber was studied at different humic acid concentrations. The accumulation of pyrene was not affected by the presence of the
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
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
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Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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