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Merck
CN

BCR091

蒽嵌蒽

BCR®, certified reference material

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About This Item

经验公式(希尔记法):
C22H12
CAS号:
分子量:
276.33
Beilstein:
2052392
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

等级

certified reference material

Agency

BCR®

制造商/商品名称

JRC

技术

HPLC: suitable
gas chromatography (GC): suitable

格式

neat

储存温度

2-8°C

SMILES字符串

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

分析说明

For more information please see:
BCR091

法律信息

BCR is a registered trademark of European Commission

象形图

Exclamation mark

警示用语:

Warning

危险声明

预防措施声明

危险分类

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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