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45484

Fenarimol

PESTANAL®, analytical standard

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250 mg
Please contact Customer Service for Availability
CZK 3,420.00

About This Item

Empirical Formula (Hill Notation):
C17H12Cl2N2O
CAS Number:
Molecular Weight:
331.20
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
262-095-7
Beilstein/REAXYS Number:
5972869
MDL number:

CZK 3,420.00


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grade

analytical standard

Quality Segment

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

OC(c1ccc(Cl)cc1)(c2cncnc2)c3ccccc3Cl

InChI

1S/C17H12Cl2N2O/c18-14-7-5-12(6-8-14)17(22,13-9-20-11-21-10-13)15-3-1-2-4-16(15)19/h1-11,22H

InChI key

NHOWDZOIZKMVAI-UHFFFAOYSA-N

General description

Fenarimol belongs to the pyrimidine class of compounds.

Application

Fenarimol may be used as an analytical reference standard for the determination of fenarimol in:
  • Honeys, honeybees and pollens by QuEChERS extraction followed by analysis using liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-LC-MS/MS) combined with multiple reaction monitoring (MRM) detection.
  • Grapes by ethyl acetate extraction, dispersive solid phase extraction (d-SPE) clean-up and LC-ESI-MS/MS with MRM detection.
  • Fruit-based baby food samples by programmed temperature vaporizer injection-low pressure gas chromatography coupled with high resolution time-of-flight mass spectrometry (PTV-LP-GC-HR-TOF-MS).[1]
  • Foodstuffs by capillary GC-MS equipped with electron impact (EI) mode of ionization.
  • Soya grain samples by LC-ESI-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

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application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

grade

analytical standard

grade

analytical standard

grade

analytical standard

grade

analytical standard

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

product line

PESTANAL®

product line

PESTANAL®

product line

PESTANAL®

product line

PESTANAL®


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pictograms

Health hazardEnvironment

signalword

Warning

Hazard Classifications

Aquatic Chronic 2 - Lact. - Repr. 2

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

212.0 °F - closed cup

flash_point_c

100 °C - closed cup

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges



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G Janer et al.
Aquatic toxicology (Amsterdam, Netherlands), 71(3), 273-282 (2005-01-27)
Testosterone conjugation activities, microsomal acyltransferases and cytosolic sulfotransferases, were investigated in three invertebrate species, the gastropod Marisa cornuarietis, the amphipod Hyalella azteca, and the echinoderm Paracentrotus lividus. The goals of the study were to characterize steroid conjugation pathways in different
Martine Keenan et al.
Journal of medicinal chemistry, 56(24), 10158-10170 (2013-12-07)
Chagas disease, caused by the protozoan parasite Trypanosoma cruzi (T. cruzi), is an increasing threat to global health. Available medicines were introduced over 40 years ago, have undesirable side effects, and give equivocal results of cure in the chronic stage
Helle Raun Andersen et al.
Toxicology letters, 163(2), 142-152 (2005-12-06)
The fungicide fenarimol has the potential to induce endocrine disrupting effects via several mechanisms since it possesses both estrogenic and antiandrogenic activity and inhibits aromatase activity in cell culture studies. Hence, the integrated response of fenarimol in vivo is not



Global Trade Item Number

SKUGTIN
45484-250MG04061832340715

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