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BCR265

二苯并[a,e]荧蒽

BCR®, certified reference material

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About This Item

經驗公式（希爾表示法）:
C24H14
CAS號碼:
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

相關類別

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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O Perin-Roussel et al.
Cancer letters, 22(3), 289-298 (1984-04-01)
Dibenzo[a,e]fluoranthene ( DBF ), a non- alternant carcinogenic polycyclic aromatic hydrocarbon (PAH), binds covalently to DNA. The main adducts were characterized as covalent additions of its bay-region and pseudo-bay-region diol-epoxides. The structure of these 2 adducts was analyzed by mass
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
O Perin-Roussel et al.
Chemico-biological interactions, 37(1-2), 109-122 (1981-10-01)
The effects of norharman (NH) on the metabolism of dibenzo[a,e]-fluoranthene (DBF) and on its fixation on DNA, RNA and proteins have been studied in vitro by incubation with S-9 and microsomes from rats and mice. NH causes a decrease of
S Saguem et al.
Carcinogenesis, 4(7), 827-835 (1983-01-01)
The metabolism of the polycyclic hydrocarbon dibenzo[a,e]fluoranthene (DBF) has been investigated. Two new primary metabolites have been identified by proton n.m.r. as the trans diaxial dihydrodiols of the bay and of the pseudo bay regions of DBF. In addition, twelve
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
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