推荐产品
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
environmental
格式
neat
SMILES字符串
CCNc1nc(NC(C)C)nc(OC)n1
InChI
1S/C9H17N5O/c1-5-10-7-12-8(11-6(2)3)14-9(13-7)15-4/h6H,5H2,1-4H3,(H2,10,11,12,13,14)
InChI key
PXWUKZGIHQRDHL-UHFFFAOYSA-N
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一般描述
Atraton is a triazine herbicide intended to control weeds in a variety of crops. Triazines herbicides act by inhibiting photosynthesis in all organisms with oxygen-evolving photosystems.
应用
Atraton may be used as a reference standard for the determination of the analyte:
- In environmental water samples using liquid chromatography-electrospray ionization mass spectrometry (LC/ESI/MS).
- In fruits using an ultrasonic-assisted matrix solid-phase dispersion (UA-MSPD) method.
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
Ultrasonic-assisted matrix solid-phase dispersion as an improved methodology for the determination of pesticides in fruits.
Journal of Chromatography A, 1212(1-2), 145- 149 (2008)
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 836(1-2), 129-132 (2006-04-08)
Atrazine is an herbicide which has shown potential antimalarial effects both in vitro and in vivo in rats. In order to study the metabolism of atrazine in rat livers, we developed a sensitive LC/MS/MS method for the identification of atrazine
The mode of action of triazine herbicides in plants
The Triazine Herbicides (2011)
Determination of triazine pesticides and related compounds in environmental water by liquid chromatography-mass spectrometry.
Analytical Sciences, 20(1), 227- 230 (2004)
The Journal of biological chemistry, 285(40), 30606-30614 (2010-07-28)
Atrazine chlorohydrolase, TrzN (triazine hydrolase or atrazine chlorohydrolase 2), initiates bacterial metabolism of the herbicide atrazine by hydrolytic displacement of a chlorine substituent from the s-triazine ring. The present study describes crystal structures and reactivity of wild-type and active site
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