N22959
1-Nitropyrene
≥95%
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About This Item
Empirical Formula (Hill Notation):
C16H9NO2
CAS Number:
Molecular Weight:
247.25
UNSPSC Code:
41116107
NACRES:
NA.25
PubChem Substance ID:
EC Number:
226-868-2
Beilstein/REAXYS Number:
1882811
MDL number:
Quality Level
assay
≥95%
form
powder
mp
153-155 °C (lit.)
SMILES string
[O-][N+](=O)c1ccc2ccc3cccc4ccc1c2c34
InChI
1S/C16H9NO2/c18-17(19)14-9-7-12-5-4-10-2-1-3-11-6-8-13(14)16(12)15(10)11/h1-9H
InChI key
ALRLPDGCPYIVHP-UHFFFAOYSA-N
Biochem/physiol Actions
Potent mutagen, carcinogen, environmental pollutant.
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Ning Tang et al.
Chemosphere, 107, 324-330 (2014-02-11)
Airborne particulates were collected at a background site (Wajima Air Monitoring Station; WAMS) on the Noto Peninsula, Japan from January 2006 to December 2007. 1-, 2-nitropyrenes (1-, 2-NPs) and 2-nitrofluoranthene (2-NFR), in the particulates were determined with a sensitive HPLC
Jyan-Gwo J Su et al.
Toxicology, 244(2-3), 257-270 (2008-01-22)
It is reported that diesel exhaust particles contain more 1-nitropyrene (1-NP) than benzo[a]pyrene (B[a]P), both of which are potent carcinogenic compounds. In this study, we show that 1-NP is more potent in reducing cell viability than B[a]P, pyrene, nitrobenzene, and
Takayuki Kameda et al.
Environmental science & technology, 45(8), 3325-3332 (2011-03-17)
The formation of hydroxynitropyrene (OHNP) via a photochemical reaction of 1-nitropyrene (1-NP) was demonstrated using a UV irradiation system. The photoreaction of 1-NP in methanol gave products that were hydroxy-substituted at position 1 and mononitro-substituted at positions 2, 3, 5