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Fórmula empírica (notación de Hill):
C9H15N5O7S2
Número CAS:
Peso molecular:
369.37
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
MDL number:
Servicio técnico
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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
COc1cc(OC)nc(NC(=O)NS(=O)(=O)N(C)S(C)(=O)=O)n1
InChI
1S/C9H15N5O7S2/c1-14(22(4,16)17)23(18,19)13-9(15)12-8-10-6(20-2)5-7(11-8)21-3/h5H,1-4H3,(H2,10,11,12,13,15)
InChI key
CTTHWASMBLQOFR-UHFFFAOYSA-N
General description
Amidosulfuron is a selective, sulfonylurea herbicide employed for the control of many grasses and broadleaf weeds in crop protection of vines, rice, citrus, corn, potatoes and tomatoes
Application
Amidosulfuron may be used as a reference standard for the determination of the analyte in surface waters using high-performance liquid chromatography with ultraviolet detection (HPLC-UV) and mass spectrometry (MS).
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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Quinate (1,3,4,5-tetrahydroxycyclohexanecarboxylate) is a compound synthesized in plants through a side-branch of the shikimate biosynthesis pathway, which is accumulated after glyphosate and acetolactate synthase inhibiting herbicides (ALS-inhibitors) and has phytotoxic potential. The objective of this study was to evaluate the
Petr Vítek et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 170, 234-241 (2016-07-28)
The effects of herbicides from three mode-of-action groups - inhibitors of protoporphyrinogen oxidase (carfentrazone-ethyl), inhibitors of carotenoid biosynthesis (mesotrione, clomazone, and diflufenican), and inhibitors of acetolactate synthase (amidosulfuron) - were studied in sunflower plants (Helianthus annuus). Raman spectroscopy, chlorophyll fluorescence
