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Supelco

Flusilazole

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C16H15F2N3Si
CAS Number:
85509-19-9
Molecular Weight:
315.39
Beilstein/REAXYS Number:
5824097
MDL number:
MFCD01076615
UNSPSC Code:
41116107
PubChem Substance ID:
329756936
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

C[Si](Cn1cncn1)(c2ccc(F)cc2)c3ccc(F)cc3

InChI

1S/C16H15F2N3Si/c1-22(12-21-11-19-10-20-21,15-6-2-13(17)3-7-15)16-8-4-14(18)5-9-16/h2-11H,12H2,1H3

InChI key

FQKUGOMFVDPBIZ-UHFFFAOYSA-N

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General description

Flusilazole is an organosilicon fungicide, which belongs to the class of sterol demethylation inhibitors. Its mode of action involves the inhibition of lanosterol 1,4-α-demethylation in fungal sterol biosynthesis.

Application

Flusilazole may be used as a reference standard for the determination of flusilazole in water samples using solid-phase extraction (SPE) method using multi-walled carbon nanotubes as adsorbent coupled with high-performance liquid chromatography (HPLC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

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

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 2 - Repr. 1B

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG3244
BCBZ0782
BCBV0143
SZBC320XV
SZB8294XV

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Determination of pyrazole and pyrrole pesticides in environmental water samples by solid-phase extraction using multi-walled carbon nanotubes as adsorbent coupled with high-performance liquid chromatography.
Ma J, et al.
Journal of Chromatographic Science, 53(2), 380-384 (2014)
Sensitivity of Venturia inaequalis isolates from British Columbia to flusilazole and myclobutanil.
Sholberg LP and Haag DP
Canadian Journal of Plant Pathology, 15(2), 102-106 (1993)
J M Trzaskos et al.
Antimicrobial agents and chemotherapy, 33(8), 1228-1231 (1989-08-01)
Flusilazole inhibits the 14 alpha-demethylation of [24,25-3H-2]dihydrolanosterol by yeast and rat liver cell-free preparations. The 50% inhibitory concentration of demethylation shows that the yeast system is 100 times more sensitive than the rat system. Purified rat liver P-45014DM is about
Chen Wang et al.
Environmental monitoring and assessment, 185(11), 9169-9176 (2013-05-10)
In this paper, dissipation dynamic and terminal residue of flusilazole in mandarin and soil, as well as residue distribution of flusilazole in mandarin, were studied at three sites in China. Mandarin peel, mandarin pulp, whole mandarin, and soil samples were
Dorien A M van Dartel et al.
Toxicology and applied pharmacology, 251(2), 110-118 (2011-01-05)
The murine embryonic stem cell test (EST) is designed to evaluate developmental toxicity based on compound-induced inhibition of embryonic stem cell (ESC) differentiation into cardiomyocytes. The addition of transcriptomic evaluation within the EST may result in enhanced predictability and improved
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