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Merck

45751

Supelco

Diflufenican

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C19H11F5N2O2
Número de CAS:
Peso molecular:
394.29
Beilstein/REAXYS Number:
4212494
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

Fc1ccc(NC(=O)c2cccnc2Oc3cccc(c3)C(F)(F)F)c(F)c1

InChI

1S/C19H11F5N2O2/c20-12-6-7-16(15(21)10-12)26-17(27)14-5-2-8-25-18(14)28-13-4-1-3-11(9-13)19(22,23)24/h1-10H,(H,26,27)

InChI key

WYEHFWKAOXOVJD-UHFFFAOYSA-N

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General description

Diflufenican is a pre- and early post-emergence herbicide used to control dicotyledonous weeds in winter cereals, including Galium aparine, Veronica hederifolia, Veronica persica and Viola arvensis, which are resistant to substituted urea herbicides.

Application

Diflufenican may be used as a reference standard in the determination of diflufenican in water samples using solid-phase microextraction followed by gas chromatography coupled with ion trap-tandem mass spectrometry (SPME-GC-ITD-MS/MS).
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

Exclamation markEnvironment

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves


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Los clientes también vieron

V Lecomte et al.
Journal of environmental quality, 30(6), 2113-2119 (2002-01-16)
Because soil surface structure has a considerable influence on infiltration rate, the sealing process is postulated to have a significant effect on herbicide loss through runoff. We evaluated the effect of degraded soil surface structures on herbicide loss in runoff
Umi S Ramli et al.
The New phytologist, 184(2), 330-339 (2009-08-07)
* Oil crops are a very important commodity. Although many genes and enzymes involved in lipid accumulation have been identified, much less is known of regulation of the overall process. To address the latter we have applied metabolic control analysis
Shuang Bai et al.
Pesticide biochemistry and physiology, 155, 8-14 (2019-03-13)
Myosoton aquaticum L., a widespread and competitive winter weed of wheat in China, has evolved resistance to many classes of herbicides. In one M. aquaticum population (AH03), collected from Anhui Province, where tribenuron-methyl and florasulam had been used to control
Gary D Bending et al.
Environmental pollution (Barking, Essex : 1987), 139(2), 279-287 (2005-07-27)
The extent of within field variability in the degradation rate of the pesticides isoproturon, azoxystrobin and diflufenican, and the role of intrinsic soil factors and technical errors in contributing to the variability, was investigated in sites on sandy-loam and clay-loam.
Analysis of trace levels of pesticides in rainwater using SPME and GC-tandem mass spectrometry.
Scheyer A, et al.
Analytical and Bioanalytical Chemistry, 384(2), 475-487 (2006)

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