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BCR265

二苯并[a,e]荧蒽

BCR®, certified reference material

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About This Item

经验公式（希尔记法）:
C24H14
CAS号:
5385-75-1
分子量:
302.37
Beilstein:
2120920
MDL號碼:
MFCD00215892
分類程式碼代碼:
41116107
PubChem物質ID:
329773799
NACRES:
NA.24

等級

certified reference material

agency

BCR®

製造商／商標名

JRC

技術

HPLC: suitable
gas chromatography (GC): suitable

格式

neat

儲存溫度

2-8°C

SMILES 字串

c1ccc-2c(c1)-c3cc4ccccc4c5cc6ccccc6c-2c35

InChI

1S/C24H14/c1-3-9-17-15(7-1)13-22-19-11-5-6-12-20(19)23-18-10-4-2-8-16(18)14-21(17)24(22)23/h1-14H

InChI 密鑰

JHOWUOKQHJHGMU-UHFFFAOYSA-N

分析報告

For more information please see:
BCR265

法律資訊

BCR is a registered trademark of European Commission

象形圖

Health hazard
GHS08

訊號詞

Warning

危險聲明

H351

防範說明

P201 - P308 + P313

危險分類

Carc. 2

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

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分析证书(COA)

Lot/Batch Number

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Dibenzo[a,e]fluoranthene.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 32, 321-325 (1983-12-01)
O Périn-Roussel et al.
Carcinogenesis, 6(12), 1791-1796 (1985-12-01)
In vivo binding of dibenzo[a,e]fluoranthene (DBF) to mouse embryo fibroblast DNA was compared with that observed previously in vitro on calf thymus DNA incubated with mouse liver microsomes. The h.p.l.c. elution patterns of the adducts formed by DBF metabolites with
O Périn-Roussel et al.
Carcinogenesis, 13(4), 723-725 (1992-04-01)
Quantitative and qualitative changes in the inhibition of DNA adduct formation in the presence of increasing concentrations of norharman (NH) were investigated in vivo in mouse fibroblasts treated with dibenzo[a,e]fluoranthene (DBF), a potent carcinogen in mice. The nuclease P1 modification
O Périn-Roussel et al.
Carcinogenesis, 9(8), 1383-1388 (1988-08-01)
The three-dimensional distribution of nuclear DNA damage induced by dibenzo(a,e)fluoranthene (DBF), a potent carcinogen for mouse fibroblasts, has been examined. The intact supercoiled nuclear DNA obtained from nucleoids of mouse fibroblasts incubated with DBF was fractionated into loop DNA attached
O Périn-Roussel et al.
Carcinogenesis, 11(2), 301-306 (1990-02-01)
The formation of DNA adducts was investigated in mouse fibroblasts treated with dibenzo[a,e]fluoranthene (DBF), using the nuclease P1 modification of the 32P-post-labeling method. In order to separate the poorly soluble, bulky DNA adducts of this potent sarcomogenic, six-ring polycyclic aromatic
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