46028
Thifensulfuron-methyl
PESTANAL®, analytical standard
Synonym(s):
Harmony
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About This Item
Empirical Formula (Hill Notation):
C12H13N5O6S2
CAS Number:
Molecular Weight:
387.39
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
7448062
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
COC(=O)c1sccc1S(=O)(=O)NC(=O)Nc2nc(C)nc(OC)n2
InChI
1S/C12H13N5O6S2/c1-6-13-10(16-12(14-6)23-3)15-11(19)17-25(20,21)7-4-5-24-8(7)9(18)22-2/h4-5H,1-3H3,(H2,13,14,15,16,17,19)
InChI key
AHTPATJNIAFOLR-UHFFFAOYSA-N
General description
Thifensulfuron-methyl belongs to the class of sulfonylurea pesticides, generally employed for controlling many grasses and broadleaved weed species, affecting cultivation of crops such as corn, potatoes, tomatoes, citrus, vines and rice.
Application
Thifensulfuron-methyl may be used as an analytical reference standard for the quantification of the analyte in environmental matrices using various chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
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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
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Determination of sulfonylurea degradation products in soil by liquid chromatography-ultraviolet detection followed by confirmatory liquid chromatography-tandem mass spectrometry
Bossi R, et al.
Journal of Chromatography A, 855(2), 575-582 (1999)
Christine A Riedy et al.
BMC oral health, 8, 5-5 (2008-02-13)
Xylitol chewing gum has been shown to reduce Streptococcus mutans levels and decay. Two studies examined the presence and time course of salivary xylitol concentrations delivered via xylitol-containing pellet gum and compared them to other xylitol-containing products. A within-subjects design
Cheng-gen Xie et al.
Luminescence : the journal of biological and chemical luminescence, 26(4), 271-279 (2010-07-16)
Uniform molecular imprinting microspheres were prepared using precipitation polymerization with thifensulfuron-methyl (TFM) as template, acrylamide as functional monomer and ethylene glycol dimethacrylate as cross-linker. TFM could be selectively adsorbed on the molecularly imprinted polymers (MIPs) matrix through the hydrogen bonding