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Merck

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號碼:
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

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 密鑰

IROINLKCQGIITA-UHFFFAOYSA-N

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相关类别

一般說明

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.

應用

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.

法律資訊

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

象形圖

Environment

訊號詞

Warning

危險聲明

防範說明

危險分類

Aquatic Acute 1 - Aquatic Chronic 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

Lot/Batch Number

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其他客户在看

Slide 1 of 5

1 of 5

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)
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
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

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