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Merck
CN

BCR091

蒽嵌蒽

BCR®, certified reference material

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经验公式(希尔记法):
C22H12
化学文摘社编号:
分子量:
276.33
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
205-884-3
Beilstein/REAXYS Number:
2052392
MDL number:
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InChI key

YFIJJNAKSZUOLT-UHFFFAOYSA-N

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

SMILES string

c1cc2ccc3cc4cccc5ccc6cc(c1)c2c3c6c45

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

format

neat

storage temp.

2-8°C

Analysis Note

For more information please see:
BCR091

Legal Information

BCR is a registered trademark of European Commission

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Skin Irrit. 2

存储类别

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)
Anthanthrene.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 32, 95-104 (1983-12-01)
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

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