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Merck

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:
99105-77-8
Molecular Weight:
328.77
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329757134
MDL number:
MFCD01632349
Beilstein/REAXYS Number:
8155739

Key Documents

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Product Name

Sulcotrione, PESTANAL®, analytical standard

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

SMILES string

CS(=O)(=O)c1ccc(c(Cl)c1)C(=O)C2C(=O)CCCC2=O

InChI key

PQTBTIFWAXVEPB-UHFFFAOYSA-N

grade

analytical standard

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

Quality Level

100

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Legal Information

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

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.

General description

Sulcotrione is a herbicide belonging to the triketone class, commonly used in corn production.

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.

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Warning

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCK2261
BCBZ6817

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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
Sulcotrione soil metabolism in summer corn crops.
J Rouchaud et al.
Bulletin of environmental contamination and toxicology, 61(5), 669-676 (1998-12-05)
Alexandra Ter Halle et al.
Environmental science & technology, 40(9), 2989-2995 (2006-05-25)
Vegetation plays a key role in environmental cycling and the fate of many organic pollutants. This is especially the case for pesticides because plant leaves are their first reaction environment after application. It is commonly accepted that photochemical reactions of
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
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