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Mesotrion

PESTANAL®, analytical standard

Synonym(e):

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

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About This Item

Empirische Formel (Hill-System):
C14H13NO7S
CAS-Nummer:
104206-82-8
Molekulargewicht:
339.32
Beilstein:
8999656
MDL-Nummer:
MFCD04112617
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329754672
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

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

InChIKey

KPUREKXXPHOJQT-UHFFFAOYSA-N

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Allgemeine Beschreibung

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.

Anwendung

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

Rechtliche Hinweise

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

Piktogramme

Health hazardEnvironment
GHS08,GHS09

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Eyes,Nervous system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Gloves

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
BCCJ5224
BCCJ7155
BCCD6166
BCBT8608
BCBT4375

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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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
Activity of mesotrione on resistant weeds in maize
Sutton P, et al.
Pest Management Science, 58, 981-984 (2002)
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
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)
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