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经验公式(希尔记法):
C21H11ClF6N2O3
化学文摘社编号:
分子量:
488.77
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
417-680-3
Beilstein/REAXYS Number:
8398323
MDL number:
产品名称
氟虫脲, PESTANAL®, analytical standard
InChI key
RYLHNOVXKPXDIP-UHFFFAOYSA-N
InChI
1S/C21H11ClF6N2O3/c22-12-8-10(21(26,27)28)4-7-17(12)33-11-5-6-16(15(25)9-11)29-20(32)30-19(31)18-13(23)2-1-3-14(18)24/h1-9H,(H2,29,30,31,32)
SMILES string
Fc1cc(Oc2ccc(cc2Cl)C(F)(F)F)ccc1NC(=O)NC(=O)c3c(F)cccc3F
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
Flufenoxuron may have been used as working standard in the determination of flufenoxuron residue in grapes using HPLC.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
General description
Flufenoxuron is an acylurea compound mostly used as an insecticide. It inhibits chitin synthesis in pests making it a slow acting growth regulator.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Lact.
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
农药列管产品
此项目有
Jinwoo Jeong et al.
Clinical toxicology (Philadelphia, Pa.), 48(1), 87-89 (2010-01-15)
Flufenoxuron is a recently introduced insecticide. The compound is known to exert its insecticidal activity by inhibiting chitin synthesis in insects. However, its toxic effects on humans are unknown. A 72-year-old woman was brought to the emergency department by ambulance.
S Wang et al.
Journal of agricultural and food chemistry, 47(8), 3416-3424 (1999-12-20)
This study describes immunochemical approaches for the compound-specific detection of flufenoxuron and class-specific detection of benzoylphenylurea (BPU) insecticides. With the aim of developing a highly specific immunoassay for flufenoxuron, a hapten was synthesized by introducing a spacer arm at the
Analysis of the pesticide flufenoxuron in apples and kiwifruit by high-performance liquid chromatography.
W A Hopkins et al.
Journal of chromatography, 516(2), 442-445 (1990-09-21)
Sinue I Morales et al.
Chemosphere, 235, 76-83 (2019-07-01)
A greenhouse study was conducted to investigate the degradation kinetics of spinosad, flufenoxuron, dimethoate and imidacloprid in tomato (Solanum lycopersicum L.) foliage and their residual toxicity on Engytatus varians (Distant) (Hemiptera: Miridae), a predator of the tomato psyllid Bactericera cockerelli
A I Valenzuela et al.
Rapid communications in mass spectrometry : RCM, 14(7), 572-577 (2000-04-25)
A liquid chromatography (LC) method for the quantitative determination of three benzoylurea insecticide residues (diflubenzuron, flufenoxuron and hexaflumuron) in citrus fruits is described. Residues were successfully separated on a C18 column by methanol/water gradient elution. Detection was by negative-ion, selected-ion
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