45484
氯苯嘧啶醇
PESTANAL®, analytical standard
登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C17H12Cl2N2O
化学文摘社编号:
分子量:
331.20
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
262-095-7
Beilstein/REAXYS Number:
5972869
MDL number:
产品名称
氯苯嘧啶醇, PESTANAL®, analytical standard
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
正在寻找类似产品? 访问 产品对比指南
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.
General description
Fenarimol belongs to the pyrimidine class of compounds.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Lact. - Repr. 2
存储类别
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
法规信息
农药列管产品
此项目有
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
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
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
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持