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BCR091

Anthanthrene

BCR®, certified reference material

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About This Item

Empirical Formula (Hill Notation):
C22H12
CAS Number:
191-26-4
Molecular Weight:
276.33
Beilstein:
2052392
EC Number:
205-884-3
MDL number:
MFCD00215887
UNSPSC Code:
41116107
PubChem Substance ID:
329774215
NACRES:
NA.24
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grade

certified reference material

Agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

format

neat

storage temp.

2-8°C

SMILES string

c1cc2ccc3cc4cccc5ccc6cc(c1)c2c3c6c45

InChI

1S/C22H12/c1-3-13-7-9-18-12-16-6-2-4-14-8-10-17-11-15(5-1)19(13)21(18)22(17)20(14)16/h1-12H

InChI key

YFIJJNAKSZUOLT-UHFFFAOYSA-N

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Analysis Note

For more information please see:
BCR091

Legal Information

BCR is a registered trademark of European Commission

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315

Precautionary Statements

P302 + P352

Hazard Classifications

Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

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E L Cavalieri et al.
Journal of cancer research and clinical oncology, 115(1), 67-72 (1989-01-01)
Comparative studies of tumor-initiating activity in mouse skin and carcinogenicity in rat mammary gland were conducted with several dibenzo[a]-pyrenes (DBPs). SENCAR mice were initiated with DB[a, e]P, DB[a, h]P, DB[a, i]P, DB[a, l]P and anthanthrene, and promoted with tetradecanoyl-phorbol acetate.
Shiqiang Zhao et al.
Science advances, 6(22), eaba6714-eaba6714 (2020-06-12)
Two-dimensional van der Waals heterojunctions (2D-vdWHs) stacked from atomically thick 2D materials are predicted to be a diverse class of electronic materials with unique electronic properties. These properties can be further tuned by sandwiching monolayers of planar organic molecules between
[Accelerated development of an induced soft tissue sarcoma in hypokinesia].
M A Makarov et al.
Voprosy onkologii, 29(2), 96-99 (1983-01-01)
Karl L Platt et al.
Chemical research in toxicology, 15(3), 332-342 (2002-03-19)
Metabolically formed dihydrodiol epoxides in the bay-region of polycyclic aromatic hydrocarbons are thought to be responsible for the genotoxic properties of these environmental pollutants. The hexacyclic aromatic hydrocarbon dibenzo[def,mno]chrysene (anthanthrene), although lacking this structural feature, was found to exhibit considerable
Anthanthrene.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 32, 95-104 (1983-12-01)
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