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Mesotrione

PESTANAL®, analytical standard

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C14H13NO7S
CAS Number:
104206-82-8
Molecular Weight:
339.32
Beilstein:
8999656
MDL number:
MFCD04112617
UNSPSC Code:
41116107
PubChem Substance ID:
329754672
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

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
GHS08,GHS09

Signal Word

Warning

Hazard Statements

H361d,H373,H410

Hazard Classifications

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

Target Organs

Eyes,Nervous system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ5224
BCCJ7155
BCCD6166
BCBT8608
BCBT4375

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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
Amelie Schmolke et al.
Environmental toxicology and chemistry, 37(6), 1545-1555 (2018-01-18)
Extrapolating from organism-level endpoints, as generated from standard pesticide toxicity tests, to populations is an important step in threatened and endangered species risk assessments. We apply a population model for a threatened herbaceous plant species, Boltonia decurrens, to estimate the
Laura Carretta et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 53(10), 661-668 (2018-05-31)
This study evaluates the dissipation of terbuthylazine, metolachlor, and mesotrione at different depths in soils with contrasting texture. The field trial was conducted at the Padua University Experimental Farm, north-east Italy. The persistence of three herbicides was studied in three
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)
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
View All Related Papers

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