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45484

Supelco

Fenarimol

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C17H12Cl2N2O
Número de CAS:
60168-88-9
Peso molecular:
331.20
Beilstein/REAXYS Number:
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

signalword

Warning

Hazard Classifications

Aquatic Chronic 2 - Lact. - Repr. 2

Storage Class

11 - Combustible Solids

wgk_germany

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

Choose from one of the most recent versions:

Certificados de análisis (COA)

Lot/Batch Number
BCCJ8056
BCCH6825
BCBW4607
SZBD071XV
SZB8042XV

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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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
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
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
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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