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BCR310

3-Nitrofluoranthen

BCR®, certified reference material

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About This Item

Empirische Formel (Hill-System):
C16H9NO2
CAS-Nummer:
892-21-7
Molekulargewicht:
247.25
Beilstein:
2216474
MDL-Nummer:
MFCD00085494
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329773819
NACRES:
NA.24
Preise und Verfügbarkeit sind derzeit nicht verfügbar.

Qualität

certified reference material

Agentur

BCR®

Hersteller/Markenname

JRC

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

mp (Schmelzpunkt)

157-159 °C (lit.)

Format

neat

Lagertemp.

2-8°C

SMILES String

[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

InChIKey

PIHGQKMEAMSUNA-UHFFFAOYSA-N

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Allgemeine Beschreibung

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]

Hinweis zur Analyse

For more information please see:
BCR310

Rechtliche Hinweise

BCR is a registered trademark of European Commission

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

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Analysenzertifikate (COA)

Lot/Batch Number

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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
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
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
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
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
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