Fludioxonil

Name: Fludioxonil
Brand: SIGMA
Price: 390 PLN

PESTANAL^®, analytical standard

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100 MG

390,00 zł

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Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):

C₁₂H₆F₂N₂O₂

Numer CAS:

131341-86-1

Masa cząsteczkowa:

248.19

UNSPSC Code:

41116107

NACRES:

NA.24

PubChem Substance ID:

329756604

MDL number:

MFCD01631158

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

100

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Ta pozycja	32343	68367	45684
Supelco 46102 Fludioxonil	Supelco 32343 Caspofungin diacetate	Supelco 68367 Prochloraz-(ethylene-d₄)	Supelco 45684 Thiabendazole
format neat	format neat	format neat	format neat
grade analytical standard	grade analytical standard	grade analytical standard	grade analytical standard
product line PESTANAL^®	product line -	product line PESTANAL^®	product line PESTANAL^®
shelf life limited shelf life, expiry date on the label	shelf life limited shelf life, expiry date on the label	shelf life limited shelf life, expiry date on the label	shelf life limited shelf life, expiry date on the label
application(s) agriculture environmental	application(s) forensics and toxicology veterinary	application(s) agriculture	application(s) agriculture cleaning products cosmetics environmental food and beverages personal care
Quality Level 100	Quality Level 100	Quality Level 100	Quality Level 100

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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pictograms

GHS09

signalword

Warning

hcodes

H410

pcodes

P273 - P391 - P501

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Klasa składowania

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

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Certyfikaty analizy (CoA)

Lot/Batch Number

BCCG9045

BCBZ1825

BCBV2209

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Field trial for evaluating the effects on honeybees of corn sown using Cruiser and Celest xl treated seeds.

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

Detection and fitness comparison of target-based highly fludioxonil-resistant isolates of Botrytis cinerea from strawberry and cucumber in China.

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

The group III two-component histidine kinase of filamentous fungi is involved in the fungicidal activity of the bacterial polyketide ambruticin.

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

Turgor and net ion flux responses to activation of the osmotic MAP kinase cascade by fludioxonil in the filamentous fungus Neurospora crassa.

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

Fungal fludioxonil sensitivity is diminished by a constitutively active form of the group III histidine kinase.

Kentaro Furukawa et al.

FEBS letters, 586(16), 2417-2422 (2012-06-13)

The fungicide fludioxonil is used to control plant-pathogenic fungi by causing improper activation of the Hog1-type MAPK. However, the appearance of fludioxonil resistant mutants, mostly caused by mutations in the group III histidine kinases, poses a serious problem. Moreover, such

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