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46318

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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:
99105-77-8
Molecular Weight:
328.77
Beilstein:
8155739
MDL number:
MFCD01632349
UNSPSC Code:
41116107
PubChem Substance ID:
329757134
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(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

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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.

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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

Signal Word

Warning

Hazard Statements

H317,H361d,H373,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2 - Skin Sens. 1A - STOT RE 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

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
BCCK2261
BCBZ6817
SZBE036XV
SZBB055XV
SZE6079X

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Sulcotrione soil metabolism in summer corn crops.
J Rouchaud et al.
Bulletin of environmental contamination and toxicology, 61(5), 669-676 (1998-12-05)
Soil dissipation of the post-emergence herbicide sulcotrione in maize crops treated with organic fertilizers.
J Rouchaud et al.
Bulletin of environmental contamination and toxicology, 57(3), 398-405 (1996-09-01)
Hanene Chaabane et al.
Journal of agricultural and food chemistry, 53(10), 4091-4095 (2005-05-12)
The retention process of sulcotrione and its two hydrolysis products, 1,3-cyclohexanedione (CHD) and 2-chloro-4-methylsulfonylbenzoic acid (CMBA), were studied in four different soils (Belgium, Landes, Perpignan, and Martinique) under laboratory conditions. Adsorption isotherms were well fitted by a Freundlich relationship. The
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
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
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