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Merck

33855

Supelco

Mesotrione

PESTANAL®, analytical standard

Sinónimos:

2-(4-Mesyl-2-nitrobenzoyl)-1,3-cyclohexanedione

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About This Item

Fórmula empírica (notación de Hill):
C14H13NO7S
Número de CAS:
Peso molecular:
339.32
Beilstein/REAXYS Number:
8999656
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

CS(=O)(=O)c1ccc(C(=O)C2C(=O)CCCC2=O)c(c1)[N+]([O-])=O

InChI

1S/C14H13NO7S/c1-23(21,22)8-5-6-9(10(7-8)15(19)20)14(18)13-11(16)3-2-4-12(13)17/h5-7,13H,2-4H2,1H3

InChI key

KPUREKXXPHOJQT-UHFFFAOYSA-N

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General description

Mesotrione is a callistemone herbicide, chemically derived from the natural phytotoxin, which is obtained from Callistemon citrinus, a californian bottlebrush plant. It finds applications in weed management for use in maize crop.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

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

pictograms

Health hazardEnvironment

signalword

Warning

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2 - STOT RE 2

target_organs

Eyes,Nervous system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Gloves


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Los clientes también vieron

Zhaojie Chen et al.
International journal of phytoremediation, 21(6), 583-589 (2019-01-17)
This study aimed to investigate the potential use of water hyacinth (Eichhornia crassipes) in removing two herbicides (mesotrione and fomesafen) with long degradation cycles in water. The relative growth rate (RGR) of water hyacinth in the presence of 100-mg/L mesotrione
Response of soil microbial communities to the herbicide mesotrione: a dose-effect microcosm approach
Crouzet O, et al.
Soil Biology and Biochemistry, 42, 193-202 (2010)
Agata Jabłońska-Trypuć et al.
Nutrients, 12(5) (2020-05-14)
The interaction of different food ingredients is now a very important and often emerging topic of research. Pesticides and their breakdown products, which may be carcinogenic, are one of the frequently occurring food contaminants. Compounds like traumatic acid (TA), which
Chun Liu et al.
Pest management science, 73(2), 462-474 (2016-05-14)
Simulation models are useful tools for predicting and comparing the risk of herbicide resistance in weed populations under different management strategies. Most existing models assume a monogenic mechanism governing herbicide resistance evolution. However, growing evidence suggests that herbicide resistance is
Sridevi Nakka et al.
Frontiers in plant science, 8, 555-555 (2017-04-27)
Herbicides that inhibit hydroxyphenylpyruvate dioxygenase (HPPD) such as mesotrione are widely used to control a broad spectrum of weeds in agriculture.

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