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45677

Supelco

Terbutryn

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C10H19N5S
CAS Number:
886-50-0
Molecular Weight:
241.36
Beilstein/REAXYS Number:
611817
EC Number:
212-950-5
MDL number:
MFCD00128025
UNSPSC Code:
41116107
PubChem Substance ID:
329756891
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

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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General description

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.

Application

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.

Legal Information

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

pictograms

Environment
GHS09

signalword

Warning

hcodes

H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ8003
BCCJ5958
BCBX4710
BCBW2096
SZEA166XV

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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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