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About This Item
Empirical Formula (Hill Notation):
C17H12Cl2N2O
CAS Number:
Molecular Weight:
331.20
Beilstein:
5972869
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
Recommended Products
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
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
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 2 - Lact. - Repr. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
212.0 °F - closed cup
Flash Point(C)
100 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Validation and uncertainty analysis of a multi-residue method for pesticides in grapes using ethyl acetate extraction and liquid chromatography-tandem mass spectrometry.
Banerjee K, et al.
Journal of Chromatography A, 1173(1-2), 98-109 (2007)
Xueyan Mu et al.
Environmental toxicology and chemistry, 23(4), 1085-1091 (2004-04-21)
Endocrine toxicants can interfere with hormone signaling through various mechanisms. Some of these mechanisms are interrelated in a manner that might result in synergistic interactions. Here we tested the hypothesis that combined exposure to chemicals that inhibit hormone synthesis and
Anne Marie Vinggaard et al.
Toxicology, 207(1), 21-34 (2004-12-14)
The fungicide fenarimol has estrogenic and antiandrogenic activity and inhibits aromatase activity in vitro. We tested, whether fenarimol had antiandrogenic effects in vivo. In a Hershberger assay, fenarimol given orally to castrated testosterone-treated male rats caused markedly reduced weights of
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
Karen L Thorpe et al.
Aquatic toxicology (Amsterdam, Netherlands), 85(3), 176-183 (2007-10-19)
Mechanism specific biomarkers are used in ecotoxicology to identify classes of chemicals and to inform on their presence in the environment, but their use in signalling for adverse effects has been limited by a poor understanding of their associated links
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