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BCR310

3-Nitrofluoranthene

BCR®, certified reference material

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About This Item

Formula empirica (notazione di Hill):
C16H9NO2
Numero CAS:
892-21-7
Peso molecolare:
247.25
Beilstein:
2216474
Numero MDL:
MFCD00085494
Codice UNSPSC:
41116107
ID PubChem:
329773819
NACRES:
NA.24

165,00 €

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Grado

certified reference material

agenzia

BCR®

Produttore/marchio commerciale

JRC

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Punto di fusione

157-159 °C (lit.)

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

[O-][N+](=O)c1ccc2-c3ccccc3-c4cccc1c24

InChI

1S/C16H9NO2/c18-17(19)15-9-8-13-11-5-2-1-4-10(11)12-6-3-7-14(15)16(12)13/h1-9H
PIHGQKMEAMSUNA-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

3-Nitrofluoranthene, belonging to the class of nitrated-polycyclic aromatic hydrocarbons, is persistent in the environment. It is produced from direct sources such as diesel, gasoline exhaust and gas-phase reactions of polycyclic aromatic hydrocarbons (PAHs) with oxides of nitrogen.[1]

Risultati analitici

For more information please see:
BCR310

Note legali

BCR is a registered trademark of European Commission

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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J V Pothuluri et al.
Journal of toxicology and environmental health. Part A, 53(2), 153-174 (1998-01-28)
Metabolism of 2-nitrofluoranthene (2-NFA), one of the most abundant and genotoxic environmental pollutants in air, and of a mixture of 2-nitrofluoranthene and 3-nitrofluoranthene (3-NFA) was studied using (1) the fungus Cunninghamella elegans ATCC 36112 and (2) rat liver microsomes. The
K Horikawa et al.
Carcinogenesis, 12(6), 1003-1007 (1991-06-01)
3,9- and 3,7-Dinitrofluoranthene (3,9- and 3,7-DNF), 3-nitrofluoranthene (3-NF) and benzo[a]pyrene (B[a]P) were tested for pulmonary carcinogenicity by intrapulmonary implantation of the compounds into rat lung. These chemicals were given in various doses as suspensions in beeswax-trycaprylin and the animals were
R Edenharder et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 35(3-4), 357-372 (1997-03-01)
When 56 flavonoids, 32 coumarins, five naphthoquinones, 12 anthraquinones and five structurally-related compounds were tested for their antimutagenic potencies with respect to mutagenicities induced by 2-nitrofluorene (2-NF), 3-nitrofluoranthene (3-NFA) and 1-nitropyrene (1-NP) in Salmonella typhimurium TA98 distinct structure-activity relationships were
J V Pothuluri et al.
Journal of toxicology and environmental health, 42(2), 209-218 (1994-06-01)
We investigated the metabolism of 3-nitrofluoranthene by filamentous fungus, Cunninghamella elegans ATCC 36112. Cunninghamella elegans metabolized about 72% of the 3-nitro[3,4-14C]fluoranthene added during 144 h of incubation to 2 major metabolites. These metabolites were separated by reversed-phase high-performance liquid chromatography
F E Evans et al.
Chemical research in toxicology, 7(3), 352-357 (1994-05-01)
The structures of selected phenolic metabolites of 2- and 3-nitrofluoranthene have been analyzed. 1H NMR spectral analysis at 500 MHz using one- and two-dimensional methods proves that the site of hydroxy substitution in two metabolites previously reported as 3-nitrofluoranthen-8-ol and
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