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Merck
CN

45677

Supelco

特丁净

PESTANAL®, analytical standard

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About This Item

经验公式(希尔记法):
C10H19N5S
CAS号:
分子量:
241.36
Beilstein:
611817
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
environmental

包装形式

neat

SMILES字符串

CCNc1nc(NC(C)(C)C)nc(SC)n1

InChI

1S/C10H19N5S/c1-6-11-7-12-8(15-10(2,3)4)14-9(13-7)16-5/h6H2,1-5H3,(H2,11,12,13,14,15)

InChI key

IROINLKCQGIITA-UHFFFAOYSA-N

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一般描述

Terbutryn is primarily used to control a wide variety of annual grass and broadleaf weed species. This preemergence and postemergence s-triazine herbicide inhibits root development by interrupting mitosis.

应用

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Terbutryn may be used as a reference standard for the determination of terbutryn in wastewater and soil by micellar liquid chromatography.

法律信息

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

象形图

Environment

警示用语:

Warning

危险声明

预防措施声明

危险分类

Aquatic Acute 1 - Aquatic Chronic 1

储存分类代码

11 - Combustible Solids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

农药列管产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Determination of diuron, terbuthylazine, and terbutryn in wastewater and soil by micellar liquid chromatography.
Pitarch-Andres S, et al.
Analytical and Bioanalytical Chemistry, 409(8), 2037-2049 (2017)
In vitro testing for genotoxicity of the herbicide terbutryn: cytogenetic and primary DNA damage.
Moretti M, et al.
Toxicology in vitro, 16(1), 81-88 (2002)
Effect of Pendimethalin, Trifluralin and Terbutryn on Lolium multiflorum growing with barley during pre-emergence stage.
Alshallash KS.
Annals of Agricultural Science, 59(2), 239-242 (2014)
Kristin Quednow et al.
Environmental science and pollution research international, 16(6), 630-640 (2009-05-23)
The present study focuses on the temporal concentration changes of four common organic pollutants in small freshwater streams of Hesse, Germany. The substances (tris(2-chloroethyl)phosphate (TCEP), the technical isomer mixture of 4-nonylphenol (NP), 2-(t-butylamino)-4-(ethylamino)-6-(methylthio)-s-triazine (terbutryn), and N,N-diethyl-m-toluamide (DEET)) are subject to
Matthias Broser et al.
The Journal of biological chemistry, 286(18), 15964-15972 (2011-03-04)
Herbicides that target photosystem II (PSII) compete with the native electron acceptor plastoquinone for binding at the Q(B) site in the D1 subunit and thus block the electron transfer from Q(A) to Q(B). Here, we present the first crystal structure

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