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Supelco

Amidosulfuron

PESTANAL®, analytical standard

Sinônimo(s):

1-(4,6-Dimethoxypyrimidin-2-yl)-3-(N-mesyl-N-methylsulfamoyl)urea

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About This Item

Fórmula empírica (Notação de Hill):
C9H15N5O7S2
Número CAS:
120923-37-7
Peso molecular:
369.37
Número MDL:
MFCD01310639
Código UNSPSC:
41116107
ID de substância PubChem:
329754592
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

linha de produto

PESTANAL®

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

agriculture
environmental

formato

neat

cadeia de caracteres SMILES

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)

chave InChI

CTTHWASMBLQOFR-UHFFFAOYSA-N

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Descrição geral

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

Aplicação

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.

Informações legais

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

Pictogramas

Environment
GHS09

Palavra indicadora

Warning

Frases de perigo

H410

Declarações de precaução

P273

Classificações de perigo

Aquatic Acute 1 - Aquatic Chronic 1

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves

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Certificados de análise (COA)

Lot/Batch Number
BCCH7808
BCCG1881
BCBW2031
SZBE017XV
SZBC031XV

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Laura R Davies et al.
Pest management science, 76(7), 2473-2482 (2020-02-16)
Anisantha and Bromus spp. are widespread and difficult to control, potentially due to the evolution of herbicide resistance. In this study, UK populations of four brome species have been tested for the early development of resistance to acetolactate synthase (ALS)-inhibiting
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
A Gimeno et al.
Journal of applied microbiology, 129(3), 680-694 (2020-03-17)
To evaluate biological control agents (BCAs) against Fusarium graminearum on infected maize stalks as a means to reduce Fusarium head blight (FHB) in subsequently grown wheat. In the laboratory, BCAs were applied against F. graminearum on maize stalk pieces. Clonostachys
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
HPLC-UV and HPLC-MSn multiresidue determination of amidosulfuron, azimsulfuron, nicosulfuron, rimsulfuron, thifensulfuron methyl, tribenuron methyl and azoxystrobin in surface waters.
Polati S, et al.
Analytica Chimica Acta, 579(2), 146-151 (2006)

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