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BCR138

Dibenz[a,h]anthracene

BCR®, certified reference material

Sinónimos:

1,2:5,6-Dibenzanthracene

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About This Item

Fórmula empírica (notación de Hill):
C22H14
Número de CAS:
53-70-3
Peso molecular:
278.35
Beilstein/REAXYS Number:
1912416
EC Number:
200-181-8
MDL number:
MFCD00003708
UNSPSC Code:
41116107
PubChem Substance ID:
329774227
NACRES:
NA.24

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

524 °C (lit.)

mp

262-265 °C (lit.)

format

neat

storage temp.

2-8°C

SMILES string

c1ccc2c(c1)ccc3cc4c(ccc5ccccc45)cc23

InChI

1S/C22H14/c1-3-7-19-15(5-1)9-11-17-14-22-18(13-21(17)19)12-10-16-6-2-4-8-20(16)22/h1-14H

InChI key

LHRCREOYAASXPZ-UHFFFAOYSA-N

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Analysis Note

For more information please see:
BCR138

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

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificados de análisis (COA)

Lot/Batch Number

Lo sentimos, en este momento no disponemos de COAs para este producto en línea.

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Santiago A Bortolato et al.
Analytical chemistry, 80(21), 8276-8286 (2008-10-02)
This work presents a novel approach for the simultaneous ultratrace determination of benzo[ a]pyrene and dibenzo[ a,h]anthracene, the two most carcinogenic polycyclic aromatic hydrocarbons (PAHs), in a very interfering environment, combining the recently discovered ability of the nylon membrane to
M F Kirby et al.
Aquatic toxicology (Amsterdam, Netherlands), 81(3), 233-244 (2007-01-24)
The extent to which biological systems interact in fish from multi-contaminant areas needs to be understood for full interpretation of monitoring data. This study investigates the interaction between two biomarkers, ethoxyresorufin-O-deethylase (EROD) activity and plasma vitellogenin (VTG) in the European
Katarzyna Skupinska et al.
Toxicology in vitro : an international journal published in association with BIBRA, 23(5), 763-771 (2009-04-14)
Polycyclic aromatic hydrocarbons (PAHs)--environmental carcinogens--are metabolized by CYP1A1 and CYP1A2 enzymes to oxy-derivatives, which are able to bind to DNA and initiate carcinogenesis. PAHs induce CYP1A1 and CYP1A2 activity, which increases the risk of development of carcinogenesis. Isothiocyanates (ITCs), naturally
Sander Delahaye et al.
Journal of chromatography. A, 1258, 152-160 (2012-09-04)
Supercritical fluid chromatography (SFC) is attributed many advantages over high performance liquid chromatography (HPLC). Next to the fact that SFC is greener than HPLC, which is especially important for preparative separations, SFC is claimed to be able to deliver faster
Zhi-Xin Yuan et al.
Chemical research in toxicology, 16(12), 1581-1588 (2003-12-19)
Benzo[b]phenanthro[2,3-d]thiophene (BPT), a thia analogue of dibenz[a,h]anthracene (DBA), is a carcinogenic environmental pollutant. We have examined the metabolism of BPT by rodent liver microsomes to investigate the mechanism by which BPT produces mutagenic and carcinogenic effects. Both rat and mouse
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