Skip to Content
Merck
All Photos(1)

Documents

46102

Supelco

Fludioxonil

PESTANAL®, analytical standard

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C12H6F2N2O2
CAS Number:
Molecular Weight:
248.19
Beilstein:
8393936
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

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

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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
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
Allison McCormick et al.
PloS one, 7(6), e38262-e38262 (2012-06-08)
Two-component signaling systems are widespread in bacteria, but also found in fungi. In this study, we have characterized TcsC, the only Group III two-component sensor kinase of Aspergillus fumigatus. TcsC is required for growth under hyperosmotic stress, but dispensable for

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service