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Merck

46102

Fludioxonil

PESTANAL®, analytical standard

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Fórmula empírica (notación de Hill):
C12H6F2N2O2
Número CAS:
Peso molecular:
248.19
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
8393936
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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

SMILES string

FC1(F)Oc2cccc(c2O1)-c3c[nH]cc3C#N

InChI key

MUJOIMFVNIBMKC-UHFFFAOYSA-N

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

application(s)

agriculture
environmental

format

neat

Quality Level

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Categorías relacionadas

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

pictograms

Environment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves


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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
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
Jennifer N Apell et al.
Environmental science & technology, 53(19), 11240-11250 (2019-09-06)
Fludioxonil is a pyrrole-containing pesticide whose registration as a plant protection product is currently under review in the United States and Europe. There are concerns over its potential persistence and toxicity in the aquatic environment; however, the pyrrole moiety represents
José Francisco Díaz Nájera et al.
The plant pathology journal, 34(3), 171-181 (2018-06-12)
Fruit rot is the principal phytopathological problem of pipiana pumpkin (Cucurbita argyrosperma Huber) in the state of Guerrero. The aims of this research were to 1) identify the causal agent of southern blight on pumpkin fruits by morphological, pathogenic, and
Roger R Lew
Fungal genetics and biology : FG & B, 47(8), 721-726 (2010-06-16)
The internal hydrostatic pressure (turgor) of the filamentous fungus Neurospora crassa is regulated at about 400-500 kiloPascals, primarily by an osmotic MAP kinase cascade which activates ion uptake from the extracellular medium and glycerol synthesis. In the absence of hyperosmotic

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