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Merck
CN

45484

Supelco

氯苯嘧啶醇

PESTANAL®, analytical standard

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About This Item

经验公式(希尔记法):
C17H12Cl2N2O
CAS号:
分子量:
331.20
Beilstein:
5972869
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

等级

analytical standard

质量水平

产品线

PESTANAL®

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

格式

neat

SMILES字符串

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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一般描述

Fenarimol belongs to the pyrimidine class of compounds.

应用

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.

法律信息

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

象形图

Health hazardEnvironment

警示用语:

Warning

危险声明

危险分类

Aquatic Chronic 2 - Lact. - Repr. 2

WGK

WGK 2

闪点(°F)

212.0 °F

闪点(°C)

100 °C

个人防护装备

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

农药列管产品

Choose from one of the most recent versions:

分析证书(COA)

Lot/Batch Number

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访问文档库

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)
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
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
Therese Jacobson et al.
Environmental toxicology and chemistry, 25(4), 1126-1131 (2006-04-25)
An endocrine disruptor, the fungicide fenarimol, was investigated regarding its effects on reproduction and hormone (ecdysteroid) levels in the deposit-feeding amphipod Monoporeia affinis. In addition, the influence of food shortage, both by itself and in combination with fenarimol, on reproduction
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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