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Supelco

Nuarimol

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C17H12ClFN2O
CAS Number:
63284-71-9
Molecular Weight:
314.74
Beilstein:
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

Signal Word

Warning

Hazard Statements

H302,H319

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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Certificates of Analysis (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)
Maria Amparo Martínez-Gómez et al.
Journal of separation science, 31(18), 3265-3271 (2008-09-24)
The present paper deals with the enantiomeric separation of nuarimol enantiomers by affinity EKC-partial filling technique using HSA as chiral selector. Firstly, a study of nuarimol interactions with HSA by CE-frontal analysis was performed. The binding parameters obtained for the
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
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
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