跳转至内容
Merck
CN

31594

氟虫脲

PESTANAL®, analytical standard

别名:

N-{4-[2-氯-4-(三氟甲基)苯氧基]-2-氟苯基氨基羰基}-2,6-二氟-苯甲酰胺

登录 查看组织和合同定价。

选择尺寸


关于此项目

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:
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

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

正在寻找类似产品? 访问 产品对比指南

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

pictograms

Environment

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

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

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持