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Merck
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Documentos

31116

Supelco

Nuarimol

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C17H12ClFN2O
Número de CAS:
63284-71-9
Peso molecular:
314.74
Beilstein/REAXYS Number:
6223667
EC Number:
264-071-1
MDL number:
MFCD00078677
UNSPSC Code:
41116107
PubChem Substance ID:
329753654
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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
GHS07

signalword

Warning

hcodes

H302,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCJ6275
BCBW8830
SZBD119XV
SZB8092XV
SZE8092X

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Simón Navarro et al.
Journal of agricultural and food chemistry, 53(22), 8572-8579 (2005-10-27)
Over a 4 month brewing process, the fate of three fungicides, myclobutanil, propiconazole, and nuarimol, was studied in the spent grain, brewer wort, and final beer product. Only the residual level of myclobutanil after the mashing step was higher than
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)
G Kostka et al.
Journal of applied toxicology : JAT, 14(5), 337-342 (1994-09-01)
It is commonly believed that in short-term tests hepatic cytochrome P-450b inducers stimulate liver enlargement and mitogenesis in the absence of overt hepatotoxic effects. In this investigation male Wistar rats received naurimol (an organochlorine pesticide) in one, three and five
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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