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
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
265-268-5
Beilstein/REAXYS Number:
577255
MDL number:
Product Name
Chlorosulfuron, PESTANAL®, analytical standard
InChI key
VJYIFXVZLXQVHO-UHFFFAOYSA-N
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)
SMILES string
COc1nc(C)nc(NC(=O)NS(=O)(=O)c2ccccc2Cl)n1
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
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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.
General description
Chlorsulfuron belongs to the class of sulfonylurea herbicides.
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
pcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Regulatory Information
农药列管产品
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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)
Xiang Wen-Sheng et al.
Protein expression and purification, 45(1), 54-59 (2005-08-27)
To investigate the properties of wheat cytochrome P450 and the characteristics of herbicide metabolism by cytochrome P450 in vitro, deeply understand the mechanisms of herbicide selectivity, recombinant wheat cytochrome P450 monooxygenase (CYP71Cv1) heterologously expressed in yeast was purified by DE-52
Susana Gaston et al.
Plant physiology, 133(3), 1351-1359 (2003-10-25)
The adaptation of the respiratory metabolism in roots of soybean (Glycine max L. Merr. cv Ransom) treated with herbicides that inhibit the enzyme acetolactate synthase (ALS) was analyzed. A new gas phase dual-inlet mass spectrometry system for simultaneous measurement of
Jian-Guo Wang et al.
The FEBS journal, 276(5), 1282-1290 (2009-02-04)
Acetohydroxyacid synthase (AHAS; EC 2.2.1.6) is the first enzyme in the biosynthetic pathway of the branched-chain amino acids. It catalyzes the conversion of two molecules of pyruvate into 2-acetolactate or one molecule of pyruvate and one molecule of 2-ketobutyrate into
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