45484
Fenarimol
PESTANAL®, analytical standard
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A propos de cet article
Formule empirique (notation de Hill) :
C17H12Cl2N2O
Numéro CAS:
Poids moléculaire :
331.20
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
262-095-7
Beilstein/REAXYS Number:
5972869
MDL number:
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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).
- 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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signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Lact. - Repr. 2
Classe de stockage
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
Numéro d'article de commerce international
| Référence | GTIN |
|---|---|
| 45484-250MG | 04061832340715 |