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Supelco

Amidosulfuron

PESTANAL®, analytical standard

Sinonimo/i:

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

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100 MG
CHF 233.00

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Spedizione prevista il31 maggio 2025


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100 MG
CHF 233.00

About This Item

Formula empirica (notazione di Hill):
C9H15N5O7S2
Numero CAS:
Peso molecolare:
369.37
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

CHF 233.00


Spedizione prevista il31 maggio 2025


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Grado

analytical standard

Livello qualitativo

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

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)
CTTHWASMBLQOFR-UHFFFAOYSA-N

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Descrizione generale

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 [1]

Applicazioni

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).[1]
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Note legali

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

Pittogrammi

Environment

Avvertenze

Warning

Indicazioni di pericolo

Consigli di prudenza

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves


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Certificati d'analisi (COA)

Lot/Batch Number

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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
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
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
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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