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Flufenoxuron

PESTANAL®, analytical standard

Synonym(s):

N-{4-[2-Chloro-4-(trifluoromethyl)phenoxy]-2-fluorophenylaminocarbonyl}-2,6-difluoro-benzamide

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250 MG
R 2 399,04

R 2 399,04

List PriceR 2 448,00
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250 MG
R 2 399,04

About This Item

Empirical Formula (Hill Notation):
C21H11ClF6N2O3
CAS Number:
101463-69-8
Molecular Weight:
488.77
Beilstein:
8398323
EC Number:
417-680-3
MDL number:
MFCD00274597
UNSPSC Code:
41116107
PubChem Substance ID:
329753839
NACRES:
NA.24

R 2 399,04

List PriceR 2 448,00
Please contact Customer Service for Availability
Request a Bulk Order

grade

analytical standard

Quality Level

100

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

SMILES string

Fc1cc(Oc2ccc(cc2Cl)C(F)(F)F)ccc1NC(=O)NC(=O)c3c(F)cccc3F

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)

InChI key

RYLHNOVXKPXDIP-UHFFFAOYSA-N

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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.[1]

Application

Flufenoxuron may have been used as working standard in the determination of flufenoxuron residue in grapes using HPLC.[2]
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

Pictograms

Environment
GHS09

Signal Word

Warning

Hazard Statements

H362,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Lact.

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK4571
BCCH6654
BCBW5374

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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
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)
High-performance liquid chromatographic determination of benzoylurea insecticides residues in grapes and wine using liquid and solid-phase extraction.
Miliadis GE, Tsiropoulos NG, Aplada-Sarlis PG.
Journal of Chromatography A, 835(1-2), 113-120 (1999)
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
B L Reid et al.
Journal of economic entomology, 85(4), 1194-1200 (1992-08-01)
Laboratory and field studies on the benzoylphenyl urea (BPU) chitin synthetase inhibitor flufenoxuron (DPX EY-059) showed great potential for its use in suppressing infestations of German cockroach, Blattella germanica (L.). When fed continuously to fifth (last) instars, the LC50 of
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