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130133

Sigma-Aldrich

5-Nitroacenaphthene

85%

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About This Item

Empirical Formula (Hill Notation):
C12H9NO2
CAS Number:
Molecular Weight:
199.21
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:

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

pictograms

Health hazard

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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P2 (EN 143) respirator cartridges


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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
Tengxuan Tang et al.
Journal of fluorescence, 29(2), 445-450 (2019-02-03)
A new fluorescent sensor was designed and synthesized from 5-nitro-1,2-dihydroacenaphthylene, n-butyl amine and 1-(2-pyridyl)piperazine. In DMF/H2O (3:1, v/v), the sensor showed excellent selectivity and sensitivity to Fe3+ with fast fluorescence enhancement and good anti-interference ability. The maximal fluorescence intensity was
Jijie Kong et al.
Journal of chromatography. A, 1603, 92-101 (2019-07-10)
In this study, three kinds of Zeolite imidazolate framework-8 (ZIF-8), synthesized by solvothermal, stirring and ball-milling method, were fabricated on the stainless steel wire via sol-gel technique. These fibers were used as solid phase microextraction (SPME) coating materials and applied

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