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BCR271

Benz[a]anthracene

BCR®, certified reference material

Synonym(s):

1,2-Benzanthracene, Tetraphene

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About This Item

Empirical Formula (Hill Notation):
C18H12
CAS Number:
56-55-3
Molecular Weight:
228.29
Beilstein:
1909298
EC Number:
200-280-6
MDL number:
MFCD00003599
UNSPSC Code:
41116107
PubChem Substance ID:
329773804

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

SMILES string

c1ccc2cc3c(ccc4ccccc34)cc2c1

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

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Analysis Note

For more information please see:
BCR271

Legal Information

BCR is a registered trademark of European Commission

Pictograms

Health hazardEnvironment
GHS08,GHS09

Signal Word

Danger

Hazard Statements

H350 - H410

Hazard Classifications

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

Storage Class Code

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

EU REACH SVHC Candidate List

CAS No.

EU REACH Annex XVII (Restriction List)

CAS No.

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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
Yi-Rui Wu et al.
Bioresource technology, 101(24), 9666-9672 (2010-08-10)
An investigation was undertaken on the biodegradation of two kinds of polycyclic aromatic hydrocarbons (PAHs), anthracene (ANT) and benz[a]anthracene (BAA), by fungi isolated from PAH-contaminated mangrove sediments environment in Ma Wan, Hong Kong. ANT (50mg l(-1)) and BAA (20mg l(-1))
S D Yakan et al.
Marine pollution bulletin, 63(5-12), 471-476 (2011-03-25)
Polycyclic aromatic hydrocarbons (PAHs) are important environmental pollutants due to their persistence and bioaccumulation potential both in organisms and in sediments. In this study, bioaccumulation and depuration experiments were performed employing local Mediterranean mussel species, Mytilus galloprovincialis, with two biomarkers:
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)
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
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