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31116

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Nuarimol

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C17H12ClFN2O
CAS Number:
Molecular Weight:
314.74
Beilstein:
6223667
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

OC(c1ccc(F)cc1)(c2cncnc2)c3ccccc3Cl

InChI

1S/C17H12ClFN2O/c18-16-4-2-1-3-15(16)17(22,13-9-20-11-21-10-13)12-5-7-14(19)8-6-12/h1-11,22H

InChI key

SAPGTCDSBGMXCD-UHFFFAOYSA-N

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Application

Nuarimol may be used as a reference standard for the determination of the analyte:
  • In fresh vegetables by gas chromatography-tandem mass spectrometry (GC-MS-MS).
  • In paprika by a modified Quick Easy Cheap Effective Rugged Safe (QuEChERS) method coupled with liquid chromatography-tandem mass spectrometry (LC–MS/MS).

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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E Tyrkiel et al.
Roczniki Panstwowego Zakladu Higieny, 47(2), 151-158 (1996-01-01)
The frequency of micronuclei was assessed in polychromatic erythrocytes of bone marrow and normochromatic erythrocytes in peripheral blood of mice following exposure to fenarimol (50, 100, 200 mg/kg b.w.) and nuarimol (100, 200, 400 mg/kg b.w.) for 21 days. Mitomycin
E Tyrkiel et al.
Roczniki Panstwowego Zakladu Higieny, 49(1), 55-66 (1998-09-12)
Nuarimol, the structural analogue of DDT, similarly to other polychlorinated aromatic hydrocarbons, induces monoxygenase activity. N-nitrosodimethylamine (NDMA) and 2-acetylaminofluorene (2-AAF) belong to chemical compounds exhibiting strong mutagenic and carcinogenic properties followed the metabolic activation. Genotoxic activity of promutagens, including NDMA
E Tyrkiel et al.
Roczniki Panstwowego Zakladu Higieny, 43(3-4), 325-331 (1992-01-01)
The clastogenic potential of the two DDT analogues: fenarimol and nuarimol was investigated, and the usefulness of the mouse spleen cells for this purpose was evaluated. Nuarimol and fenarimol were administered per o to 8-10 weeks old male mice (Swiss)
D T Cooke et al.
Biochimica et biophysica acta, 1061(2), 156-162 (1991-01-30)
Oat and rye plants were treated with either tetcyclacis (an experimental plant growth regulator), nuarimol (a fungicide) or gamma-ketotriazole (an experimental herbicide). These treatments reduced shoot growth and changed the lipid composition of the shoot plasma membranes. In oat, both
B Wiadrowska et al.
Roczniki Panstwowego Zakladu Higieny, 43(3-4), 281-287 (1992-01-01)
The effect of simultaneous administration of N-diethylnitrosamine (NDEA) and Nuarimol on the activity of gamma-GTPase, G-6-Pase ans APase in the liver and serum of Wistar rats was investigated in the 2-weeks experiment. The two-stage hepato-cancerogenesis model was used with NDEA

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