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Merck

32429

Supelco

丙硫咪唑脱硫

PESTANAL®, analytical standard

别名:

α-(1-氯环丙基)-α-[(2-氯苯基)甲基]-1H-1,2,4-三唑-1-乙醇

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About This Item

经验公式(希尔记法):
C14H15Cl2N3O
分子量:
312.19
Beilstein:
13200866
分類程式碼代碼:
41116107
NACRES:
NA.24

等級

analytical standard

品質等級

產品線

PESTANAL®

儲存期限

limited shelf life, expiry date on the label

技術

HPLC: suitable
gas chromatography (GC): suitable

應用

agriculture
environmental

格式

neat

SMILES 字串

OC(Cc1ccccc1Cl)(Cn2cncn2)C3(Cl)CC3

InChI

1S/C14H15Cl2N3O/c15-12-4-2-1-3-11(12)7-14(20,13(16)5-6-13)8-19-10-17-9-18-19/h1-4,9-10,20H,5-8H2

InChI 密鑰

HHUQPWODPBDTLI-UHFFFAOYSA-N

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相关类别

一般說明

脱硫丙硫菌唑是丙硫菌唑的主要手性代谢产物。

應用

有关合适的仪器技术的更多信息,请参阅产品的分析证书。如需进一步支持,请联系技术服务。
脱硫丙硫菌唑可用作分析参考标准品,用于测定以下样品中的分析物:
  • 通过气相色谱-电子捕获检测法 (GC-ECD) 测定菜籽油样品
  • 通过高效液相色谱-电喷雾串联质谱联用法 (HPLC-ESI-MS/MS) 测定动物性食品样品
  • 通过分散固相萃取(dSPE)结合液相色谱电子电离(EI)质谱(MS)联用法在多反应监控(MRM)模式下测定蜜蜂

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法律資訊

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

象形圖

Health hazardEnvironment

訊號詞

Warning

危險聲明

危險分類

Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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访问文档库

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An improved extraction method of rapeseed oil sample preparation for the subsequent determination in it of azole class fungicides by gas chromatography.
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Simultaneous enantioselective determination of the chiral fungicide Prothioconazole and its major chiral metabolite Prothioconazole-desthio in food and environmental samples by Ultraperformance liquid chromatography-tandem mass spectrometry.
Zhang Z, et al.
Journal of Agricultural and Food Chemistry, 65(37), 8241-8247 (2017)
Approach for pesticide residue analysis for metabolite prothioconazole-desthio in animal origin food.
Liu H, et al.
Journal of Agricultural and Food Chemistry, 65(11), 2481-2487 (2017)
Iza Matarashvili et al.
Journal of separation science, 38(24), 4173-4179 (2015-10-27)
The separation of the stereoisomers of 23 chiral basic agrochemicals was studied on six different polysaccharide-based chiral columns in high-performance liquid chromatography with various polar organic mobile phases. Along with the successful separation of analyte stereoisomers, emphasis was placed on

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