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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:
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

Signal Word

Warning

Hazard Statements

H302 + H312,H410

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

212.0 °F - closed cup

Flash Point(C)

100 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCG3134
BCCB5795
BCBZ8303
SZBE090XV
SZBB091XV

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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
Tânia Vidal et al.
Environmental toxicology, 27(9), 537-548 (2011-03-05)
As a way to improve the efficacy to target organisms, new pesticide generation is based on technologically advanced coformulations of two or more active ingredients. One example is Betanal(®)Expert, a postemergence herbicide composed of an Advanced Micro Droplet coformulation of
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
View All Related Papers

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