Merck
CN
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文件

安全信息

33588

Supelco

酰嘧磺隆

PESTANAL®, analytical standard

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别名:
1-(4,6-二甲氧基-2-嘧啶基)-3-(N-甲基甲磺酰胺磺酰基)脲
经验公式（希尔记法）:
C9H15N5O7S2
CAS号:
120923-37-7
分子量:
369.37
MDL编号:
MFCD01310639
PubChem化学物质编号:
329754592
NACRES:
NA.24

等级

analytical standard

质量水平

100

产品线

PESTANAL®

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

agriculture
environmental

格式

neat

SMILES字符串

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

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相关类别

一般描述

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

应用

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.

法律信息

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

象形图

Environment
GHS09

警示用语：

Warning

危险声明

H410

预防措施声明

P273

危险分类

Aquatic Acute 1 - Aquatic Chronic 1

储存分类代码

11 - Combustible Solids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves

法规信息

农药列管产品

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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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