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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
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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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)
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)


