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502332

Supelco

Benzo[j]fluoranthen -Lösung

certified reference material, 2000 μg/mL in dichloromethane

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About This Item

Empirische Formel (Hill-System):
C20H12
CAS-Nummer:
205-82-3
Molekulargewicht:
252.31
MDL-Nummer:
MFCD00152264
UNSPSC-Code:
12000000

Qualität

certified reference material
TraceCERT®

Produktlinie

TraceCERT®

Analysenzertifikat (CofA)

current certificate can be downloaded

Verpackung

ampule of 1 mL

Konzentration

2000 μg/mL in dichloromethane

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

cleaning products
cosmetics
environmental
food and beverages
personal care

Format

single component solution

Lagertemp.

2-30°C

SMILES String

c21c3c4c(c2ccc5c1cccc5)cccc4ccc3

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

InChIKey

KHNYNFUTFKJLDD-UHFFFAOYSA-N

Allgemeine Beschreibung

Benzo[j]fluoranthene is a polycyclic aromatic hydrocarbon, which is carcinogenic in nature and can be generated into the environment via combustion of coal, coal tar and petroleum products.

Anwendung

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

Sonstige Hinweise

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Rechtliche Hinweise

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

Piktogramme

Health hazardExclamation mark
GHS08,GHS07

Signalwort

Danger

Gefahreneinstufungen

Aquatic Chronic 3 - Carc. 1B - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Central nervous system

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number

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Report on Carcinogens (12th Ed. ) (2011)
A Comprehensive Guide to the Hazardous Properties of Chemical Substances (2007)
J E Rice et al.
Cancer research, 47(23), 6166-6170 (1987-12-01)
The metabolism of benzo[j]fluoranthene (BjF) in vivo in mouse skin was investigated. trans-4,5-Dihydro-4,5-dihydroxybenzo[j]fluoranthene (BjF-4,5-diol) and trans-9,10-dihydro-9,10-dihydroxybenzo[j]fluoranthene (BjF-9,10-diol) have been identified as major metabolites. In addition, 4- and 10-hydroxybenzo[j]fluoranthene and benzo[j]fluoranthen-4,5-dione have been tentatively identified among the metabolites formed in vivo
E H Weyand et al.
Chemical research in toxicology, 6(1), 117-124 (1993-01-01)
Studies have demonstrated that the metabolic activation of benzo[j]fluoranthene (B[j]F) to a genotoxic agent proceeds through the formation of either the trans-4,5-dihydrodiol (B[j]F-4,5-diol) or the trans-9,10-dihydrodiol (B[j]F-9,10-diol) metabolite of B[j]F. Using 32P-postlabeling analysis, the profiles of DNA adducts formed in
J E Rice et al.
Chemico-biological interactions, 63(3), 227-237 (1987-01-01)
The metabolites of benzo[j]fluoranthene (BjF) as formed in vitro using the 9000 X g supernatant from Aroclor-pretreated rats have been identified. Two dihydrodiols, trans-4,5-dihydro-4,5-dihydroxyBjF and trans-9,10-dihydro-9,10-dihydroxyBjF have been identified as major metabolites by comparison of their spectral and chromatographic properties
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