30317
Iodosulfuron-methyl-sodium
PESTANAL®, analytical standard
Sinónimos:
Methyl 4-iodo-2-[3-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)ureidosulfonyl]benzoate sodium salt
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Acerca de este artículo
Fórmula empírica (notación de Hill):
C14H13IN5NaO6S
Número CAS:
Peso molecular:
529.24
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
COC(=O)c1ccc(I)cc1S(=O)(=O)N([Na])C(=O)Nc2nc(C)nc(OC)n2
InChI
1S/C14H14IN5O6S.Na/c1-7-16-12(19-14(17-7)26-3)18-13(22)20-27(23,24)10-6-8(15)4-5-9(10)11(21)25-2;/h4-6H,1-3H3,(H2,16,17,18,19,20,22);/q;+1/p-1
InChI key
JUJFQMPKBJPSFZ-UHFFFAOYSA-M
General description
Iodosulfuron-methyl-sodium is a systemic sulfonylurea herbicide that affects the activity of acetolactate synthase (ALS) enzyme causing plant deformation, growth retardation, chlorosis and eventually death. It is absorbed by above-ground parts of weeds. This herbicide can also penetrate surface and groundwater as it has high mobility in environment.
Application
Iodosulfuron-methyl-sodium may have been used as stock reference standard in Liquid chromatography tandem-mass spectrometry (LC-MS) analysis done for the determination of sulfonylurea herbicides in tap and leaching water.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
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
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
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María Paz Castro Tapia et al.
Frontiers in plant science, 11, 951-951 (2020-07-17)
Seed treatments with antagonistic bacteria could reduce the severity of crown and root rot diseases in wheat crops. The objective of this study was to evaluate the potential antagonistic activity of a bacterial consortium of three Chilean strains of Pseudomonas
José G Vázquez-García et al.
Frontiers in plant science, 11, 553948-553948 (2020-11-17)
Different Lolium species, common weeds in cereal fields and fruit orchards in Chile, were reported showing isolated resistance to the acetyl CoA carboxylase (ACCase), acetolactate synthase (ALS) and 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) inhibiting herbicides in the late 1990s. The first case
Ana Zabalza et al.
Plants (Basel, Switzerland), 9(9) (2020-09-20)
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