Fenarimol

Name: Fenarimol
Brand: SIAL
Price: 191 USD
Availability: InStock

PESTANAL^®, analytical standard

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250 MG

$191.00

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About This Item

Empirical Formula (Hill Notation):

C₁₇H₁₂Cl₂N₂O

CAS Number:

60168-88-9

Molecular Weight:

331.20

UNSPSC Code:

41116107

NACRES:

NA.24

PubChem Substance ID:

329756776

EC Number:

262-095-7

Beilstein/REAXYS Number:

5972869

MDL number:

MFCD00055325

Key Documents

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InChI key

NHOWDZOIZKMVAI-UHFFFAOYSA-N

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

SMILES string

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

grade

analytical standard

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

Quality Level

100

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Related Categories

Analytical Chemistry

Food & Cosmetic Component Standards

Pesticide Standards

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Show Differences

1 of 4

This Item	45753	45684	32057
Supelco 45484 Fenarimol	Supelco 45753 Flusilazole	Supelco 45684 Thiabendazole	Supelco 32057 Folpet
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
format neat	format neat	format neat	format neat
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^®

General description

Fenarimol belongs to the pyrimidine class of compounds.[1]

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.[1]
Grapes by ethyl acetate extraction, dispersive solid phase extraction (d-SPE) clean-up and LC-ESI-MS/MS with MRM detection.[2]
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).[3]
Foodstuffs by capillary GC-MS equipped with electron impact (EI) mode of ionization.[4]
Soya grain samples by LC-ESI-MS/MS.[5]

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

GHS08,GHS09

signalword

Warning

hcodes

H361fd,H362,H411

pcodes

P202 - P260 - P263 - P264 - P273 - P308 + P313

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

BCCJ8056

BCCH6825

BCBW4607

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Effects of two fungicides with multiple modes of action on reproductive endocrine function in the fathead minnow (Pimephales promelas).

Gerald T Ankley et al.

Toxicological sciences : an official journal of the Society of Toxicology, 86(2), 300-308 (2005-05-20)

Many chemicals that adversely affect reproduction and/or development do so through multiple pathways within the reproductive tract and hypothalamic-pituitary-gonadal axis. Notable in this regard are fungicides, such as prochloraz or fenarimol, which in mammals have the potential to impact endocrine

Daphnia magna and ecotoxicogenomics: gene expression profiles of the anti-ecdysteroidal fungicide fenarimol using energy-, molting- and life stage-related cDNA libraries.

Anneleen Soetaert et al.

Chemosphere, 67(1), 60-71 (2006-11-23)

In the present study, the existing life stage-specific cDNA library was extended with energy- and molting-related genes using Suppression Subtractive Hybridization PCR and a microarray for the aquatic test organism Daphnia magna was created. A gene set of 2455 fragments

Estrogenic effects in vitro and in vivo of the fungicide fenarimol.

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

Screening extracts of Achyranthes japonica and Rumex crispus for activity against various plant pathogenic fungi and control of powdery mildew.

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

Chemical fate and biological effects of several endocrine disrupters compounds in two echinoderm species.

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

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