130133
5-Nitroacenaphthene
85%
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About This Item
Empirical Formula (Hill Notation):
C12H9NO2
CAS Number:
Molecular Weight:
199.21
UNSPSC Code:
12171500
PubChem Substance ID:
EC Number:
210-025-0
MDL number:
assay
85%
mp
100-101 °C (lit.)
SMILES string
[O-][N+](=O)c1ccc2CCc3cccc1c23
InChI
1S/C12H9NO2/c14-13(15)11-7-6-9-5-4-8-2-1-3-10(11)12(8)9/h1-3,6-7H,4-5H2
InChI key
CUARLQDWYSRQDF-UHFFFAOYSA-N
Other Notes
Contains 3-nitroacenaphthene
signalword
Danger
hcodes
Hazard Classifications
Carc. 1B
Storage Class
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
ppe
Eyeshields, Gloves, type P2 (EN 143) respirator cartridges
Regulatory Information
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E C McCoy et al.
Environmental mutagenesis, 5(1), 17-22 (1983-01-01)
The direct-acting mutagenicity of 5-nitroacenaphthene for Salmonella typhimurium is dependent upon the reduction of the nitro function as evidenced by the significant decrease in mutagenicity seen with nitroreductase-deficient Salmonella strains. Addition of microsomal preparations results in a significant increase in
K EL-Bayoumy et al.
Cancer research, 42(4), 1243-1248 (1982-04-01)
The metabolism of the mutagen and carcinogen, 5-nitroacenaphthene, by the 9000 x g supernatant from the livers of Aroclor-pretreated rats was studied. The major primary metabolites were 1-hydroxy-5-nitroacenaphthene and 2-hydroxy-5-nitroacenaphthene. These metabolites were oxidized to 1-oxo-5-nitroacenaphthene and 2-oxo-5-nitroacenaphthene, hydroxylated to
Angel Belles et al.
Chemosphere, 164, 347-354 (2016-09-07)
In this paper, a method for evaluating the in-situ degradation of nitro polycyclic aromatic hydrocarbons (nitro-PAH) in sediments is presented. The methodology is adapted from the passive sampler technique, which commonly uses the dissipation rate of labeled compounds loaded in