45681
胺菊酯
PESTANAL®, analytical standard
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关于此项目
经验公式（希尔记法）:
C19H25NO4
化学文摘社编号:
分子量:
331.41
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
231-711-6
Beilstein/REAXYS Number:
8807938
MDL number:
InChI key
CXBMCYHAMVGWJQ-UHFFFAOYSA-N
InChI
1S/C19H25NO4/c1-11(2)9-14-15(19(14,3)4)18(23)24-10-20-16(21)12-7-5-6-8-13(12)17(20)22/h9,14-15H,5-8,10H2,1-4H3
SMILES string
C\C(C)=C\C1C(C(=O)OCN2C(=O)C3=C(CCCC3)C2=O)C1(C)C
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
format
neat
Quality Level
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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
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - STOT SE 2 Inhalation
target_organs
Nervous system
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 2
ppe
Gloves
法规信息
农药列管产品
此项目有
Y Tomigahara et al.
Xenobiotica; the fate of foreign compounds in biological systems, 24(12), 1205-1214 (1994-12-01)
1. To examine the metabolic fate of (1RS, trans)- or (1RS, cis)-tetramethrin [3, 4, 5, 6-tetrahydrophthalimidomethyl (1RS, trans)- or (1RS, cis)-chrysanthemate], rat was administered a single oral dose of trans- or cis-[alcohol-14C]tetramethrin at dose levels of 2 or 250 mg/kg.
S Kalsner
Cardiovascular research, 28(12), 1843-1853 (1994-12-01)
The aim was to describe a novel form of non-neurogenic coronary artery contraction. Superfused cattle coronary artery preparations in vitro were placed between platinum electrodes and stimulated. The preparations responded to exceedingly brief transmural stimulation (a single ten thousandth of
Aklesso Kadala et al.
Neurotoxicology, 32(3), 320-330 (2011-03-08)
We studied the mode of action of type I pyrethroids on the voltage-dependent sodium current from honeybee olfactory receptor neurons (ORNs), whose proper function in antenna is crucial for interindividual communication in this species. Under voltage-clamp, tetramethrin and permethrin induce
Oguzhan Yavuz et al.
Cutaneous and ocular toxicology, 29(1), 16-25 (2009-12-02)
The aim of this study was to evaluate the repeated-dose 14-day dermal toxicity of different combinations of some synthetic pyrethroid insecticides, piperonyl butoxide, and tetramethrin in rats. A total of 70 adult Wistar rats were randomly divided into 7 (6
R G Abou el-Ela et al.
Journal of the Egyptian Society of Parasitology, 30(1), 51-58 (2000-04-29)
Four pediculicides were tested against head lice in-vitro. The LT50 for Licid ranged between 10.75 (at conc. 50%) to 25.08 (at conc. 1%). All lice died with conc. 100% within 5 minutes. With Malathion, the LT50 ranged between 4.23 to
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