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Merck

30317

Supelco

Iodosulfuron-methyl-Natrium

PESTANAL®, analytical standard

Synonym(e):

4-Iod-2-[3-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-ureidosulfonyl]-benzoesäure-methylester Natriumsalz

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About This Item

Empirische Formel (Hill-System):
C14H13IN5NaO6S
CAS-Nummer:
Molekulargewicht:
529.24
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

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

InChIKey

JUJFQMPKBJPSFZ-UHFFFAOYSA-M

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Allgemeine Beschreibung

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.

Anwendung

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.

Empfohlene Produkte

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.

Rechtliche Hinweise

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

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Piktogramme

Environment

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Aquatic Acute 1 - Aquatic Chronic 1

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves


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Analysenzertifikate (COA)

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Kunden haben sich ebenfalls angesehen

Microbial and enzymatic activity of soil contaminated with a mixture of diflufenican + mesosulfuron-methyl + iodosulfuron-methyl-sodium.
Bacmaga M
Environmental Science and Pollution Research International, 22(1), 643-656 (2015)
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
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
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
Trace analysis of sulfonylurea herbicides in water samples by solid-phase extraction and liquid chromatography-tandem mass spectrometry.
Fenoll J
Talanta, 101, 273-282 (2012)

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