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31662

Supelco

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:
103055-07-8
Molecular Weight:
511.15
Beilstein:
8398291
EC Number:
410-690-9
MDL number:
MFCD00867616
UNSPSC Code:
41116107
PubChem Substance ID:
329753870
NACRES:
NA.24

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

format

neat

SMILES string

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

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)

InChI key

PWPJGUXAGUPAHP-UHFFFAOYSA-N

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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.

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.

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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
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H317,H410

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

>338.0 °F - (External MSDS)

Flash Point(C)

> 170 °C - (External MSDS)

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCH4412
BCBV9237
SZB9315XV
SZE5210X
5210X

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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)
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)
Vicente Navarro-Llopis et al.
Pest management science, 66(5), 511-519 (2010-01-27)
The chemosterilisation technique has been demonstrated to reduce the population and fruit damage of the Mediterranean fruit fly, Ceratitis capitata (Wiedemann), in citrus orchards. Field trials showed efficacy by reducing the fruit fly population, which was progressively achieved by continuous
V Navarro-Llopis et al.
Journal of economic entomology, 104(5), 1647-1655 (2011-11-10)
During 2008 and 2009, the efficacy of the combination of two Mediterranean fruit fly, Ceratitis capitata (Wiedemann) (Diptera: Tephritidae), control techniques, sterile insect technique (SIT) and a chemosterilant bait station system (Adress), was tested in three crops: citrus (Citrus spp.)
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