36181
氧乐果
PESTANAL®, analytical standard
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关于此项目
经验公式（希尔记法）:
C5H12NO4PS
化学文摘社编号:
分子量:
213.19
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
214-197-8
Beilstein/REAXYS Number:
1785256
MDL number:
产品名称
氧乐果, PESTANAL®, analytical standard
format
neat
InChI key
PZXOQEXFMJCDPG-UHFFFAOYSA-N
InChI
1S/C5H12NO4PS/c1-6-5(7)4-12-11(8,9-2)10-3/h4H2,1-3H3,(H,6,7)
SMILES string
CNC(=O)CSP(=O)(OC)OC
grade
analytical standard
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
storage temp.
2-8°C
Quality Level
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Application
有关合适的仪器技术的更多信息，请参阅产品′的检验报告。想要获得更多支持，请联系技术服务部。
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Aquatic Acute 1
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
212.0 °F - closed cup
flash_point_c
100 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
农药列管产品
此项目有
Musa Isnas et al.
Toxicology and industrial health, 28(1), 27-34 (2011-10-26)
The study aimed mainly to assess effects of omethoate on certain oxidative stress biomarkers in various tissues of frogs (Rana ridibunda). Biomarkers selected for stress monitoring were malondialdehyde (MDA) and antioxidant defense system (ADS) constituent such as reduced glutathione (GSH)
Yanhong Bai et al.
Journal of agricultural and food chemistry, 57(14), 6238-6245 (2009-06-19)
A practical, inexpensive, and green chemical process is greatly needed for degrading pesticides in food and environmental water. In this work, the impact of O(2) plasma treatment on reduction of dichlorvos (DDVP) and omethoate in maize was determined by gas
Ozden Tacal et al.
Journal of applied toxicology : JAT, 30(5), 469-475 (2010-03-17)
Organophosphorus pesticides used most commonly in Turkey include methamidophos, dichlorvos, O-methoate and diazinon. These toxic chemicals or their metabolites make a covalent bond with the active site serine of butyrylcholinesterase. Our goal was to identify the adducts that result from
Eiji Ueno et al.
Shokuhin eiseigaku zasshi. Journal of the Food Hygienic Society of Japan, 51(3), 122-127 (2010-07-03)
We studied the simultaneous determination of acephate, methamidophos, and omethoate in animal and fishery products, their processed foods, and honey by means of liquid chromatography coupled with mass spectrometry (LC-MS). The sample was extracted with ethyl acetate in the presence
Ismail Celik et al.
Toxicology and industrial health, 27(4), 357-362 (2010-10-16)
The study was carried out to investigate the neurotoxic and immunotoxic effects of fenthion- and omethoate-used agricultural areas on frogs (Rana ridibunda) at acute exposure. The neurotoxic effects of the chemicals were evaluated by measuring the activities of acetylcholinesterase (AChE)
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