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Merck

BCR309

6-Nitrochrysene

BCR®, certified reference material

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About This Item

Fórmula empírica (notación de Hill):
C18H11NO2
Número de CAS:
Peso molecular:
273.29
Beilstein/REAXYS Number:
2134652
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

220 °C (dec.) (lit.)

format

neat

storage temp.

2-8°C

SMILES string

[O-][N+](=O)c1cc2c3ccccc3ccc2c4ccccc14

InChI

1S/C18H11NO2/c20-19(21)18-11-17-13-6-2-1-5-12(13)9-10-15(17)14-7-3-4-8-16(14)18/h1-11H

InChI key

UAWLTQJFZUYROA-UHFFFAOYSA-N

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Application

6-Nitrochrysene may be used as a certified reference material for the quantification of the analyte in air samples, standard reference material 1649a (urban dust), air and diesel particulate reference materials using gas chromatography-mass spectrometry with negative ion chemical ionization (GC/NICI-MS).

Analysis Note

For more information please see:
BCR309

Legal Information

BCR is a registered trademark of European Commission

pictograms

Health hazardExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 1B - Muta. 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 P3 (EN 143) respirator cartridges


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Certificados de análisis (COA)

Lot/Batch Number

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R M Chen et al.
Toxicology letters, 117(1-2), 69-77 (2000-10-18)
The present study has determined the effects of 6-nitrochrysene (6-NC) on human cytochrome P450-dependent monooxygenases in human hepatoma HepG2 cells. Treatment of HepG2 cells with 6-NC increased the activities of microsomal benzo[a]pyrene hydroxylase, 7-ethoxycoumarin and 7-ethoxyresorufin O-deethylases, cytosolic glutathione S-transferase
E A Carrasco-Flores et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 61(3), 509-514 (2004-12-08)
The infrared and Raman spectra of solids and thin solid films of 6-nitrochrysene, its electronic spectra, and resonance Raman scattering (RRS) obtained with UV-laser excitation at 325 nm are reported. The vibrational assignment is supported by ab initio computations at
Wanli Xing et al.
International journal of environmental research and public health, 17(3) (2020-02-06)
Polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs (NPAHs) in PM2.5 samples were collected at a roadside monitoring station in Kanazawa, Japan, in every season from 2017 to 2018. Nine PAHs and five NPAHs were determined using high-performance liquid chromatography with fluorescence
Jacek Krzeminski et al.
Chemical research in toxicology, 24(1), 65-72 (2010-12-01)
Ubiquitous environmental agents [e.g., polynuclear aromatic hydrocarbons (PAHs) and their nitrated derivatives (NO(2)-PAHs)] that are known to induce mammary cancer in rodents are regarded as potential human risk factors for inducing analogous human cancers. Although 6-nitrochrysene (6-NC) is less abundant
Karam El-Bayoumy et al.
Chemical research in toxicology, 17(12), 1591-1599 (2004-12-21)
The environmental pollutant 6-nitrochrysene (6-NC) is a potent carcinogen in several animal models including the rat mammary gland. 6-NC can be activated to intermediates that can damage DNA by simple nitroreduction, ring oxidation, or a combination of ring oxidation and

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