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关于此项目
经验公式（希尔记法）:
C13H18O5S
化学文摘社编号:
分子量:
286.34
EC Number:
247-525-3
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
5759730
MDL number:
format
neat
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
SMILES string
CCOC1Oc2ccc(OS(C)(=O)=O)cc2C1(C)C
grade
analytical standard
packaging
ampule of 1 g
manufacturer/tradename
Chem Service, Inc. PS-1045
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
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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.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
212.0 °F - closed cup
flash_point_c
100 °C - closed cup
法规信息
新产品
此项目有
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
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
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
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