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45479

Supelco

Ethofumesate

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C13H18O5S
CAS Number:
26225-79-6
Molecular Weight:
286.34
Beilstein/REAXYS Number:
5759730
EC Number:
247-525-3
MDL number:
MFCD00055321
UNSPSC Code:
41116107
PubChem Substance ID:
329756771
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
environmental

format

neat

SMILES string

CCOC1Oc2ccc(OS(C)(=O)=O)cc2C1(C)C

InChI

1S/C13H18O5S/c1-5-16-12-13(2,3)10-8-9(18-19(4,14)15)6-7-11(10)17-12/h6-8,12H,5H2,1-4H3

InChI key

IRCMYGHHKLLGHV-UHFFFAOYSA-N

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Application

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
GHS07,GHS09

signalword

Warning

Hazard Classifications

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

wgk_germany

WGK 3

flash_point_f

212.0 °F

flash_point_c

100 °C

ppe

Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG3134
BCCB5795
BCBZ8303
SZBE090XV
SZBB091XV

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D S Gardner et al.
Journal of agricultural and food chemistry, 49(6), 2894-2898 (2001-06-21)
The effect of turfgrass cover on the leaching and dissipation of ethofumesate and halofenozide was studied. Sampling cylinders (20 cm diam. x 30 cm long) were placed vertically in plots of creeping bentgrass (Agrostis palustris Huds.), tall fescue (Festuca arundinaceae
Anne Chevillard et al.
Journal of hazardous materials, 205-206, 32-39 (2012-01-11)
The potential use of nanoclays for modulating transfer properties of active agents in bio-sourced polymers was explored. For this purpose, new pesticide formulations were designed by combining wheat gluten, ethofumesate (model pesticide) and three montmorillonites (MMT) using a bi-vis extrusion
Wentao Zhu et al.
Chirality, 19(8), 632-637 (2007-06-08)
The stereoselective toxicokinetics of ethofumesate enantiomers following a single intravenous (i.v.) administration at doses of 30 mg/kg were investigated in rabbits. Plasma concentrations of (+)- and (-)-ethofumesate were analyzed by a validated chiral HPLC method that involved extraction of plasma
W Zhu et al.
Xenobiotica; the fate of foreign compounds in biological systems, 39(9), 649-655 (2009-06-26)
1. The stereoselective metabolism of ethofumesate (ETO) and its enantiomers in rabbit and rat liver microsomes have been studied by chiral high-performance liquid chromatography (HPLC) method. Two metabolites were detected in both liver microsomes in the presence of beta-nicotinamide adenine
Peng Xu et al.
Chemosphere, 112, 163-169 (2014-07-23)
Earthworms represent an important food source for many vertebrates and as a result, predators may encounter toxic effects via the food chain from consumption of contaminated worms. Therefore, including an assessment of xenobiotic to worms in risk assessment procedures is
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