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46102

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Fludioxonil

PESTANAL®, analytical standard

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About This Item

Formula empirica (notazione di Hill):
C12H6F2N2O2
Numero CAS:
131341-86-1
Peso molecolare:
248.19
Beilstein:
8393936
Numero MDL:
MFCD01631158
Codice UNSPSC:
41116107
ID PubChem:
329756604
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

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
MUJOIMFVNIBMKC-UHFFFAOYSA-N

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Categorie correlate

Applicazioni

  • 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).

Note legali

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

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Pittogrammi

Environment
GHS09

Avvertenze

Warning

Indicazioni di pericolo

H410

Consigli di prudenza

P273 - P391 - P501

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG9045
BCBZ1825
BCBV2209

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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
Anita Dongo et al.
Applied and environmental microbiology, 75(1), 127-134 (2008-11-18)
We have shown that the plant pathogen Alternaria brassicicola exhibited very high susceptibility to ambruticin VS4 and to a lesser extent to the phenylpyrrole fungicide fludioxonil. These compounds are both derived from natural bacterial metabolites with antifungal properties and are
Chengwei Sang et al.
Pesticide biochemistry and physiology, 147, 110-118 (2018-06-24)
Botrytis cinerea has a high risk of developing resistance to fungicides. Fludioxonil, belonging to phenylpyrroles, has been used for more than three decades, however, only few cases of field resistance against phenylpyrroles have been reported. In this study, the highly
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
Gun-Hwi Lee et al.
Biomolecules, 9(9) (2019-09-22)
Fludioxonil is fungicide used in agriculture, which is present in fruits and vegetables. In this study, the effects of fludioxonil on human immune cell viability, apoptosis, cell cycle arrest, and mitochondrial membrane potential were examined in human immune cells, such
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