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Supelco

Fenbuconazol

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C19H17ClN4
CAS Number:
Molecular Weight:
336.82
Beilstein:
8333667
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

Clc1ccc(CCC(Cn2cncn2)(C#N)c3ccccc3)cc1

InChI

1S/C19H17ClN4/c20-18-8-6-16(7-9-18)10-11-19(12-21,13-24-15-22-14-23-24)17-4-2-1-3-5-17/h1-9,14-15H,10-11,13H2

InChI key

RQDJADAKIFFEKQ-UHFFFAOYSA-N

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General description

Fenbuconazol is a triazole fungicide intended to control leaf spot, yellow and brown rust, powdery mildew and net blotch on wheat and barley. The mode of action of fenbuconazol involves inhibition of biosynthesis of sterol (a component of fungal cell membrane).

Application

Fenbuconazol may be used as a reference standard for the determination of the analyte:
  • In soil and water samples by using chiral liquid chromatography coupled with tandem mass spectrometry.
  • In fruits, vegetables and cereals by supercritical fluid chromatography–tandem mass spectrometry (SFC-MS/MS) method.

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

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 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Simultaneous enantioselective determination of fenbuconazole and its main metabolites in soil and water by chiral liquid chromatography/tandem mass spectrometry.
Li Y, et al.
Journal of Chromatography A, 1218(38), 6667- 6674 (2011)
Determination of genotoxic effects of chlorfenvinphos and fenbuconazole in Allium cepa root cells by mitotic activity, chromosome aberration, DNA content, and comet assay.
Turko?lu, S
Pesticide Biochemistry and Physiology, 103(3), 224- 230 (2012)
Supercritical fluid chromatography--tandem mass spectrometry-assisted methodology for rapid enantiomeric analysis of fenbuconazole and its chiral metabolites in fruits, vegetables, cereals, and soil.
Tao Y, et al.
Food Chemistry, 241(3) (2018)

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