BCR091
Anthanthrene
BCR®, certified reference material
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About This Item
Empirical Formula (Hill Notation):
C22H12
CAS Number:
Molecular Weight:
276.33
Beilstein:
2052392
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
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
Related Categories
Analysis Note
For more information please see:
BCR091
BCR091
Legal Information
BCR is a registered trademark of European Commission
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Irrit. 2
WGK
WGK 3
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[Accelerated development of an induced soft tissue sarcoma in hypokinesia].
M A Makarov et al.
Voprosy onkologii, 29(2), 96-99 (1983-01-01)
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
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.
Baiping Han et al.
The Journal of chemical physics, 130(24), 244502-244502 (2009-07-02)
In this paper, we investigate the properties of photon emission statistics of single molecule in solid matrix. The influences of solid matrix surroundings on photon emission of single molecule system under the laser field and rf field for several examples
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
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