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Merck
CN

N22959

1-硝基芘

≥95%

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关于此项目

经验公式(希尔记法):
C16H9NO2
化学文摘社编号:
分子量:
247.25
UNSPSC Code:
41116107
NACRES:
NA.25
PubChem Substance ID:
EC Number:
226-868-2
Beilstein/REAXYS Number:
1882811
MDL number:
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InChI key

ALRLPDGCPYIVHP-UHFFFAOYSA-N

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

SMILES string

[O-][N+](=O)c1ccc2ccc3cccc4ccc1c2c34

assay

≥95%

form

powder

mp

153-155 °C (lit.)

Quality Level

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Biochem/physiol Actions

强效诱变剂、致癌物、环境污染物。

pictograms

Health hazard

signalword

Warning

hcodes

pcodes

Hazard Classifications

Carc. 2

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
Wen-Cheng Chu et al.
Chemical research in toxicology, 22(12), 1938-1947 (2009-12-08)
Cytochrome P450 1a1 (Cyp1a1) is a phase I xenobiotic-metabolizing enzyme, the expression of which is mainly driven by the aryl hydrocarbon receptor (AhR). Cyp1a1 messenger (m)RNA is labile. Our study indicates that 1-nitropyrene (1-NP) highly induced Cyp1a1 protein expression, although
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
N Podechard et al.
Toxicology letters, 206(3), 289-299 (2011-08-30)
1-Nitropyrene (1-NP) is a nitro-polycyclic aromatic hydrocarbon (nitro-PAH) present in diesel exhaust and bound to particular matter in urban air. We show that 1-NP and the referent PAH benzo(a)pyrene (BP) induce apoptosis and a lipid accumulation dependent on cytochrome P450

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