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Merck

BCR271

Benzo[a]anthracene

BCR®, certified reference material

Sinónimos:

1,2-Benzanthracene, Tetraphene

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Fórmula empírica (notación de Hill):
C18H12
Número CAS:
Peso molecular:
228.29
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
200-280-6
Beilstein/REAXYS Number:
1909298
MDL number:
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InChI

1S/C18H12/c1-2-7-15-12-18-16(11-14(15)6-1)10-9-13-5-3-4-8-17(13)18/h1-12H

InChI key

DXBHBZVCASKNBY-UHFFFAOYSA-N

SMILES string

c1ccc2cc3c(ccc4ccccc34)cc2c1

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

bp

437.6 °C (lit.)

mp

157-159 °C (lit.)

format

neat

storage temp.

2-8°C

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General description

This compound is listed in the SVHC (Substances of very high concern) candidate list of ECHA (European Chemicals Agency)

Analysis Note

For more information please see:
BCR271

Legal Information

BCR is a registered trademark of European Commission

pictograms

Health hazardEnvironment

signalword

Danger

Clase de almacenamiento

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B - PBT - vPvB


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Denise Fernandes et al.
Aquatic toxicology (Amsterdam, Netherlands), 85(4), 258-266 (2007-11-06)
The metabolism of 17alpha-hydroxyprogesterone (17P(4)) was investigated in different subcellular fractions isolated from male gonads of sea bass (Dicentrarchus labrax L). The existence of CYP17 (C17,20-lyase activity) and CYP11B (11beta-hydroxylase) catalyzed reactions was demonstrated in the mitochondrial fraction, where 17P(4)
M Teresa Alcántara et al.
Journal of hazardous materials, 166(1), 462-468 (2009-01-06)
The presence of carcinogenic polycyclic aromatic hydrocarbons (PAHs) in soils poses a potential threat to human health if exposure levels are too high. Nevertheless, the removal of these contaminants presents a challenge to scientists and engineers. The high hydrophobic nature
Kwang Hwa Jung et al.
Environmental science & technology, 45(1), 300-306 (2010-12-08)
Whole blood is one of the most easily accessible biofluids, and circulating leukocytes would include informative transcripts as a first line of immune defense for many disease processes. To demonstrate that transcriptomic responses of circulating blood cells reflect the exposure
Sona Marvanová et al.
Chemical research in toxicology, 21(2), 503-512 (2008-01-22)
Monomethylated benz[ a]anthracenes (MeBaAs) are an important group of methylated derivatives of polycyclic aromatic hydrocarbons (PAHs). Although the methyl substitution reportedly affects their mutagenicity and tumor-initiating activity, little is known about the impact of methylation on the effects associated with
E Rosales et al.
Bioprocess and biosystems engineering, 35(5), 851-855 (2011-12-16)
In the present work, several samples from lab waste containers polluted with polycyclic aromatic hydrocarbons (PAHs) and heavy metals were investigated as potential sources of PAH-degrading microorganisms. After isolating, two fungal strains were selected as the best degrading microorganisms. Genetic

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