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N8141

Sigma-Aldrich

4-Nitroquinoline N-oxide

≥98%

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Synonym(s):
4-NQO, 4-Nitroquinoline 1-oxide
Empirical Formula (Hill Notation):
C9H6N2O3
CAS Number:
Molecular Weight:
190.16
Beilstein:
165756
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

≥98%

color

yellow to brown

mp

154-156 °C (lit.)

solubility

acetone: soluble, clear to hazy

storage temp.

−20°C

SMILES string

[O-][N+](=O)c1cc[n+]([O-])c2ccccc12

InChI

1S/C9H6N2O3/c12-10-6-5-9(11(13)14)7-3-1-2-4-8(7)10/h1-6H

InChI key

YHQDZJICGQWFHK-UHFFFAOYSA-N

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General description

4-Nitroquinoline N-oxide is a quinoline derivative widely used in chemical research and development.

Application

4-Nitroquinoline N-oxide has been used as a model compound to study its carcinogenic effects.

Biochem/physiol Actions

Skin and lung tumor initiator under experimental conditions.

Pictograms

Health hazard

Signal Word

Danger

Hazard Statements

Hazard Classifications

Carc. 1B

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Interplay of DNA repair, homologous recombination, and DNA polymerases in resistance to the DNA damaging agent 4-nitroquinoline-1-oxide in Escherichia coli.
Williams AB, et al.
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Antitumor activity of ficus deltoidea extract on oral cancer: An in vivo study
Al-Koshab M, et al.
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The antimutagenic effect of monoterpenes against UV-irradiation-, 4NQO-and t-BOOH-induced mutagenesis in coli.
Nikolic B, et al.
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Yeasts isolated from Italian beverages and foods (wine and cheeses) were identified as Saccharomyces cerevisiae and Debaryomyces hansenii by sequencing the D1/D2 domain of the 26S rRNA gene and differentiated, at strain level, by microsatellite PCR fingerprinting and RAPD-PCR. All

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