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Merck

32766

Supelco

环磺酮

PESTANAL®, analytical standard

别名:

2-{2-氯-4-(甲磺酰)-3-[(2,2,2-三氟乙氧基)甲基]苯甲酰基}-1,3-环己二酮, 2-{2-氯-4-甲磺酰基-3-[(2,2,2-三氟乙氧基)甲基]苯甲酰基}环己烷-1,3-二酮

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About This Item

经验公式(希尔记法):
C17H16ClF3O6S
分子量:
440.82
MDL號碼:
分類程式碼代碼:
41116107
PubChem物質ID:
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

CS(=O)(=O)c1ccc(c(Cl)c1COCC(F)(F)F)C(=O)C2C(=O)CCCC2=O

InChI

1S/C17H16ClF3O6S/c1-28(25,26)13-6-5-9(15(18)10(13)7-27-8-17(19,20)21)16(24)14-11(22)3-2-4-12(14)23/h5-6,14H,2-4,7-8H2,1H3

InChI 密鑰

IUQAXCIUEPFPSF-UHFFFAOYSA-N

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相关类别

一般說明

环磺酮是 β-三酮类除草剂,在字段玉米出苗后早期到中期用于控制草和阔叶杂草。

應用

有关合适仪器技术的更多信息,请参考产品分析证书。如需进一步支持,请联系技术服务部门。
通过快速、简便、廉价、有效、耐用且安全的 (QuEchERS) 提取方法和分散液-液微萃取 (DLLME) 后采用高效液相色谱 (HPLC) 二极管阵列检测器 (DAD) 进行分析, 蜜蜂采用改良 QuEchERS 萃取后采用 LC 和气相色谱 (GC) 结合串联质谱 (MS/MS) 进行分析, 食品样品采用超高效液相色谱 (UHPLC) 和四极杆飞行时间质谱 (QTOFMS) 结合电喷雾离子化 进行分析,植物组织以及水样采用 DLLME、基质固相分散 (MSPD) 和固相萃取 (SPE) 结合 HPLC-DAD 进行分析,环磺酮可作为引用番茄中环磺酮测定的参考标准。

法律資訊

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

訊號詞

Warning

危險分類

Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2 - Skin Sens. 1 - STOT RE 2

儲存類別代碼

13 - Non Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

No data available

閃點(°C)

No data available

個人防護裝備

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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分析证书(COA)

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Screening of over 600 pesticides, veterinary drugs, food-packaging contaminants, mycotoxins, and other chemicals in food by ultra-high performance liquid chromatography quadrupole time-of-flight mass spectrometry (UHPLC-QTOFMS).
Perez-Ortega P, et al.
Food Analytical Methods, 10(5), 1216-1244 (2017)
Extraction procedures for the study of phytotoxicity and degradation processes of selected triketones in a water ecosystem.
Barchanska H, et al.
Environmental Science and Pollution Research International, 21(6), 4751-4758 (2014)
Anita Küpper et al.
Pest management science, 74(10), 2325-2334 (2017-11-07)
Resistance to the 4-hydroxyphenylpyruvate dioxygenase (HPPD)-inhibiting herbicide tembotrione in an Amaranthus palmeri population from Nebraska (NER) has previously been confirmed to be attributable to enhanced metabolism. The objective of this study was to identify and quantify the metabolites formed in
Analysis of pesticides in tomato combining QuEChERS and dispersive liquid-liquid microextraction followed by high-performance liquid chromatography.
Melo A, et al.
Food Analytical Methods, 6(2), 559-568 (2013)
Monopersulfate photocatalysis under 365 nm radiation. Direct oxidation and monopersulfate promoted photocatalysis of the herbicide tembotrione.
Solis RR, et al.
Journal of Environmental Management, 181, 385-394 (2016)

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