34322
Chlorosulfuron
PESTANAL®, analytical standard
Synonym(s):
1-(2-Chlorophenylsulfonyl)-3-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-urea, Chlorsulfuron
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About This Item
Empirical Formula (Hill Notation):
C12H12ClN5O4S
CAS Number:
Molecular Weight:
357.77
Beilstein:
577255
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
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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
COc1nc(C)nc(NC(=O)NS(=O)(=O)c2ccccc2Cl)n1
InChI
1S/C12H12ClN5O4S/c1-7-14-10(17-12(15-7)22-2)16-11(19)18-23(20,21)9-6-4-3-5-8(9)13/h3-6H,1-2H3,(H2,14,15,16,17,18,19)
InChI key
VJYIFXVZLXQVHO-UHFFFAOYSA-N
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General description
Chlorsulfuron belongs to the class of sulfonylurea herbicides.
Application
Chlorosulfuron may be used as an analytical reference standard for the determination of chlorosulfuron in:
- Environmental water samples by magnetic solid phase extraction (MSPE) using multi-walled carbon nanotubes adsorbents combined with high performance liquid chromatography-diode-array-detection (HPLC-DAD).
- Soya milk samples by QuEChERS (quick, easy, cheap, effective, rugged and safe) extraction and HPLC-DAD as well as HPLC combined with triple quadrupole tandem mass spectrometry (QqQ-MS/MS).
- Honeybees by dispersive SPE followed by liquid and gas chromatography combined with tandem mass spectrometry (LC-MS/MS and GC-MS/MS) with electrospray ionization (ESI), and multiple reaction monitoring (MRM) detection.
- Fruits and vegetable samples by methanolic extraction and ultra-HPLC in conjunction with ESI-MS/MS and MRM detection.
- Cereals by QuEChERS extraction and HPLC coupled to ESI-MS/MS with selected reaction monitoring (SRM) detection.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
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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
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1
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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Simple, cost-effective and sensitive liquid chromatography diode array detector method for simultaneous determination of eight sulfonylurea herbicides in soya milk samples.
Rejczak T and Tuzimski T
Journal of Chromatography A, 1473, 56-65 (2016)
Analysis of four sulfonylurea herbicides in cereals using modified Quick, Easy, Cheap, Effective, Rugged, and Safe sample preparation method coupled with liquid chromatography-tandem mass spectrometry.
Ni Y, et al.
Journal of Chromatography A, 1537, 27-34 (2018)
Giovanna Boschin et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 38(6), 737-746 (2003-12-03)
Two sulfonylurea herbicides, chlorsulfuron and metsulfuron-methyl, were studied under laboratory conditions, in order to elucidate the biodegradation pathway operated by Aspergillus niger, a common soil fungus, which is often involved in the degradation of xenobiotics. HPLC-UV was used to study
Francisco Flores-Céspedes et al.
Journal of agricultural and food chemistry, 57(7), 2856-2861 (2009-04-02)
Controlled release formulations (CRFs) have been researched to reduce the water-polluting risk derived from the use of conventional formulations of chlorsulfuron. Coated chlorsulfuron granules were produced in a Wuster-type fluidized-bed equipment using two different amounts of ethylcellulose. The highest one
René Ruiter et al.
Plant molecular biology, 53(5), 675-689 (2004-03-11)
In this study we tested the performance of chimeraplasts, chimeric RNA/DNA oligonucleotides, for the creation of directed changes in chromosomal sequences in tobacco and oilseed rape. As target genes for chimeraplasty, the endogenous als gene and two transgenes, bar and
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