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Merck
CN

31662

Lufenuron

PESTANAL®, analytical standard

Synonym(s):

1-[2,5-Dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)phenyl]-3-(2,6-difluorobenzoyl)urea

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About This Item

Empirical Formula (Hill Notation):
C17H8Cl2F8N2O3
CAS Number:
Molecular Weight:
511.15
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
410-690-9
Beilstein/REAXYS Number:
8398291
MDL number:
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Product Name

Lufenuron, PESTANAL®, analytical standard

InChI key

PWPJGUXAGUPAHP-UHFFFAOYSA-N

InChI

1S/C17H8Cl2F8N2O3/c18-6-5-11(32-17(26,27)14(22)16(23,24)25)7(19)4-10(6)28-15(31)29-13(30)12-8(20)2-1-3-9(12)21/h1-5,14H,(H2,28,29,30,31)

SMILES string

FC(C(F)(F)F)C(F)(F)Oc1cc(Cl)c(NC(=O)NC(=O)c2c(F)cccc2F)cc1Cl

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

format

neat

Quality Level

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Application

Lufenuron may be used as a reference standard in the determination of lufenuron in wheat flour using gas chromatography coupled with mass spectrometry (GC-MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

General description

Lufenuron is an insect growth regulator belonging to the benzoylphenylurea class of insecticide. It is used in controlling Ctenocephalides felis (cat flea) in cats.

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation markEnvironment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

>338.0 °F - (External MSDS)

flash_point_c

> 170 °C - (External MSDS)

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Regulatory Information

农药列管产品
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Development and application of a method for analysis of lufenuron in wheat flour by gas chromatography--mass spectrometry and confirmation of bio-efficacy against Tribolium castaneum (Herbst)(Coleoptera: Tenebrionidae)
Ahire.CK, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 861(1), 16-21 (2008)
Cyp12a4 confers lufenuron resistance in a natural population of Drosophila melanogaster
Bogwitz R M, et al.
Proceedings of the National Academy of Sciences of the USA, 102(36), 12807-12812 (2005)
Comparison of flea control strategies using imidacloprid or lufenuron on cats in controlled simulated home environment.
EDJ, et al.
American Journal of Veterinary Research, 58(11), 1260-1262 (1997)
Pilar Moya et al.
Pest management science, 66(6), 657-663 (2010-02-17)
Chemosterilisation with lufenuron bait stations is a recently developed technique that is being implemented for Ceratitis capitata Wiedemann control. The aim of this work was to evaluate the chemosterilising effect of lufenuron against four economically important Latin American fruit flies
Theo C M Brock et al.
Environmental toxicology and chemistry, 29(9), 1994-2008 (2010-09-08)
Under typical agricultural use of an insecticide, it is likely that only part of an edge-of-field drainage ditch will be directly contaminated by spray drift. The response, including recovery, of aquatic macroinvertebrates in sprayed ditch sections may be affected by

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