InChI
1S/C24H14/c1-3-7-19-15(5-1)13-17-9-12-22-20-8-4-2-6-16(20)14-18-10-11-21(19)23(17)24(18)22/h1-14H
SMILES string
c1ccc2c(c1)cc3ccc4c5ccccc5cc6ccc2c3c46
InChI key
RXUSYFJGDZFVND-UHFFFAOYSA-N
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:
BCR159
BCR159
Legal Information
BCR is a registered trademark of European Commission
signalword
Danger
hcodes
Hazard Classifications
Carc. 1B - Muta. 2
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
A W Wood et al.
Cancer research, 41(7), 2589-2597 (1981-07-01)
The mutagenic activities of dibenzo(a,h)(pyrene, dibenzo(a,i)pyrene, and a total of 11 of their benzo-ring derivatives were evaluated in bacterial and mammalian cells in the absence or presence of a mammalian metabolic activation system. trans-1,2-Dihydroxy-1,2-dihydrodibenzo(a,h)pyrene and trans-3,4-dihydroxy-3,4-dihydrodibenzo(a,i)pyrene, the expected dihydrodiol precursors
Dibenzo[a,h]pyrene.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 32, 331-335 (1983-12-01)
Tumorigenicity of bay-region diol-epoxides and other benzo-ring derivatives of dibenzo(a,h)pyrene and dibenzo(a,i)pyrene on mouse skin and in newborn mice.
R L Chang et al.
Cancer research, 42(1), 25-29 (1982-01-01)
G A Marsch et al.
Chemical research in toxicology, 5(6), 765-772 (1992-11-01)
The in vivo formation of dibenzo[a,h]pyrene-DNA adducts in mouse skin was assessed by laser-excited fluorescence spectroscopy at 77 and 4.2 K. Two adducts were identified with fluorescence origin bands at approximately 383.5 and 407.2 nm, and these were shown to
B S Hass et al.
Cancer research, 42(5), 1646-1649 (1982-05-01)
The polycyclic aromatic hydrocarbons dibenzo(a,i)pyrene and dibenzo(a,h)pyrene, each of which possesses two bay regions, and their bay-region difluorinated derivatives were tested for mutagenicity for ouabain and 6-thioguanine resistance in Chinese hamster V79 cells. Since V79 cells do not metabolize polycyclic
商品
This application note describes the fast and efficient separation of the EU’s list of 15 + 1 polynuclear aromatic hydrocarbons (PAHs) using Ascentis® Express PAH HPLC column.
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