46318
Sulcotrione
PESTANAL®, analytical standard
Synonym(s):
2-[2-Chloro-4-(methylsulfonyl)benzoyl]-1,3-cyclohexanedione
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About This Item
Empirical Formula (Hill Notation):
C14H13ClO5S
CAS Number:
Molecular Weight:
328.77
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
8155739
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(Cl)c1)C(=O)C2C(=O)CCCC2=O
InChI
1S/C14H13ClO5S/c1-21(19,20)8-5-6-9(10(15)7-8)14(18)13-11(16)3-2-4-12(13)17/h5-7,13H,2-4H2,1H3
InChI key
PQTBTIFWAXVEPB-UHFFFAOYSA-N
Related Categories
General description
Sulcotrione is a herbicide belonging to the triketone class, commonly used in corn production.
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Sulcotrione may be used as an analytical reference standard for the quantification of the analyte in environmental samples using liquid chromatography coupled to tandem mass spectrometry.
Other Notes
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2 - Skin Sens. 1A - STOT RE 2
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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J L Bonnet et al.
Archives of environmental contamination and toxicology, 55(4), 576-583 (2008-03-07)
The potential toxicity of sulcotrione (2-[2-chloro-4-(methylsulfonyl)benzoyl]-1,3-cyclohexanedione) and mesotrione (2-[4-(methylsulfonyl)-2-nitrobenzoyl]-1,3-cyclohexanedione), two selective triketonic herbicides, was assessed using representative environmental microorganisms frequently used in ecotoxicology: the eukaryote Tetrahymena pyriformis and the prokaryote Vibrio fischeri. The aims were also to evaluate the toxicity
Jaroslaw Wiszniowski et al.
Chemosphere, 74(9), 1224-1230 (2008-12-30)
One of the strategies for decreasing the consumption of herbicides consists in improving their uptake and efficiency. It was suggested that the photodegradation of herbicides due to sunlight results in a greater demand of herbicides to be introduced into the
Sophia Keller et al.
PloS one, 6(10), e26604-e26604 (2011-11-03)
The opportunistic human pathogenic fungus Aspergillus fumigatus is able to produce the dark brown pigment pyomelanin by degradation of L-tyrosine. Pyomelanin was shown to protect the fungus against reactive oxygen intermediates as well as cell wall disturbing compounds and is
Christophe Calvayrac et al.
Pest management science, 68(3), 340-347 (2011-09-16)
The dissipation kinetics of the herbicide sulcotrione sprayed 4 times on a French soil was studied using a laboratory microcosm approach. An advanced cultivation-based method was then used to isolate the bacteria responsible for biotransformation of sulcotrione. Chromatographic methods were
P D Fraser et al.
The Plant journal : for cell and molecular biology, 24(4), 551-558 (2000-12-15)
The application of high-performance liquid chromatography (HPLC) using a C30 reverse-phase stationary matrix has enabled the simultaneous separation of carotenes, xanthophylls, ubiquinones, tocopherols and plastoquinones in a single chromatogram. Continuous photodiode array (PDA) detection ensured identification and quantification of compounds
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