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Fenarimol

PESTANAL®, analytical standard

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Empirical Formula (Hill Notation):
C17H12Cl2N2O
CAS Number:
60168-88-9
Molecular Weight:
331.20
Beilstein:
5972869
EC Number:
262-095-7
MDL number:
MFCD00055325
UNSPSC Code:
41116107
PubChem Substance ID:
329756776
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
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

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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).
  • 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

Pictograms

Health hazardEnvironment
GHS08,GHS09

Signal Word

Warning

Hazard Statements

H361fd,H362,H411

Hazard Classifications

Aquatic Chronic 2 - Lact. - Repr. 2

WGK

WGK 2

Flash Point(F)

212.0 °F

Flash Point(C)

100 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

农药列管产品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Michela Sugni et al.
Ecotoxicology (London, England), 19(3), 538-554 (2009-11-26)
Two echinoderm species, the sea urchin Paracentrotus lividus and the feather star Antedon mediterranea, were exposed for 28 days to several EDCs: three putative androgenic compounds, triphenyltin (TPT), fenarimol (FEN), methyltestosterone (MET), and two putative antiandrogenic compounds, p,p'-DDE (DDE) and
Jin-Cheol Kim et al.
Pest management science, 60(8), 803-808 (2004-08-17)
Methanol extracts of fresh materials of 183 plants were screened for in vivo antifungal activity against Magnaporthe grisea, Corticium sasaki, Botrytis cinerea, Phytophthora infestans, Puccinia recondita and Erysiphe graminis f sp hordei. Among them, 33 plant extracts showed disease-control efficacy
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
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
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