46102
Fludioxonil
PESTANAL®, analytical standard
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About This Item
Empirical Formula (Hill Notation):
C12H6F2N2O2
CAS Number:
Molecular Weight:
248.19
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
8393936
grade
analytical standard
Quality Level
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
application(s)
agriculture
environmental
format
neat
SMILES string
FC1(F)Oc2cccc(c2O1)-c3c[nH]cc3C#N
InChI
1S/C12H6F2N2O2/c13-12(14)17-10-3-1-2-8(11(10)18-12)9-6-16-5-7(9)4-15/h1-3,5-6,16H
InChI key
MUJOIMFVNIBMKC-UHFFFAOYSA-N
Application
- Fludioxonil fungicide in agricultural biotech: Fludioxonil′s effectiveness against the two-component histidine kinase Bos1 in Botrytis cinerea was explored, revealing its binding mode and molecular mechanism. This research underscores its critical role as a fungicide in agricultural biotechnology, providing insights that could lead to improved crop protection strategies (Yin et al., 2024).
- Fludioxonil biochemical research for pathogen resistance: The study on Fusarium species causing soybean root rot examined the genetic basis of differing sensitivities to DMI fungicides, including fludioxonil. This contributes to a deeper understanding of fungal resistance mechanisms, enhancing the development of more effective fungicidal treatments (Zhang et al., 2024).
- Fludioxonil antifungal properties in plant disease control: Research characterized fludioxonil and phenamacril dual resistant mutants of Fusarium graminearum, highlighting fludioxonil′s critical role in managing resistance in pathogens and its ongoing relevance in managing crop diseases (Wen et al., 2024).
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
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signalword
Warning
hcodes
pcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Regulatory Information
农药列管产品
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Paolo Tremolada et al.
Bulletin of environmental contamination and toxicology, 85(3), 229-234 (2010-07-27)
A first field study was conducted to investigate the possible adverse effects that seeds dressed with neonicotinoid insecticides pose to honeybees during sowing. It was observed that in the exposure hives bee mortality increased on the day of sowing and
Daisuke Hagiwara et al.
Fungal genetics and biology : FG & B, 46(11), 868-878 (2009-07-15)
In filamentous fungi, the His-Asp phosphorelay signaling system and HOG pathway are involved in the action of the fungicides, fludioxonil, and iprodione, as well as osmotic and oxidative stress responses. Aspergillusnidulans response regulators (RRs), SskA and SrrA, and histidine kinase
José Fenoll et al.
Chemosphere, 85(8), 1262-1268 (2011-08-16)
The efficiency of ZnO and TiO(2) suspensions in the photocatalytic degradation of two fungicides (cyprodinil and fludioxonil) in leaching water was investigated. The experiments were carried out at pilot plant scale using compound parabolic collectors under natural sunlight. The blank
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 46102-100MG-R | 04061835560721 |