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PS379

Terbutryn

analytical standard

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About This Item

Formule empirique (notation de Hill) :
C10H19N5S
Numéro CAS:
886-50-0
Poids moléculaire :
241.36
Beilstein:
611817
Numéro CE :
212-950-5
Numéro MDL:
MFCD00128025
Code UNSPSC :
41116107
ID de substance PubChem :
24899199
Le tarif et la disponibilité ne sont pas disponibles actuellement.

Qualité

analytical standard

Conditionnement

ampule of 1000 mg

Fabricant/nom de marque

Chem Service, Inc. PS-379

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Chaîne SMILES 

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)

Clé InChI

IROINLKCQGIITA-UHFFFAOYSA-N

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Description générale

Terbutryn is a systemic herbicide used primarily for elimination of annual broadleaf weeds. It is a triazine compound and is known to inhibit photosynthesis. This selective herbicide is also used in controlling submerged and free-floating weeds, algae in reservoirs, and fish ponds.[1]

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 water samples by solid-phase extraction followed by high-performance liquid chromatography.[2]

Pictogrammes

Environment
GHS09

Mention d'avertissement

Warning

Mentions de danger

H410

Conseils de prudence

P273 - P391 - P501

Classification des risques

Aquatic Acute 1 - Aquatic Chronic 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number

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Consulter la Bibliothèque de documents

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
K Marja Talja et al.
Journal of agricultural and food chemistry, 56(24), 11962-11968 (2008-12-05)
The degradation of pesticides atrazine and terbutryn was investigated under aerobic and anaerobic conditions in the northern boreal region subsurface deposits and sterilized controls from the depths of 6.3-21.0 m below the surface and 1.2-16.9 m below the groundwater table.
O González-Barreiro et al.
Environmental pollution (Barking, Essex : 1987), 144(1), 266-271 (2006-02-21)
The uptake of the triazine herbicides, atrazine and terbutryn, was determined for two freshwater photosynthetic microorganisms, the green microalga Chlorella vulgaris and the cyanobacterium Synechococcus elongatus. An extremely rapid uptake of both pesticides was recorded, although uptake rate was lower
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