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31662

Supelco

Lufenuron

PESTANAL®, analytical standard

Synonyme(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

Formule empirique (notation de Hill):
C17H8Cl2F8N2O3
Numéro CAS:
Poids moléculaire :
511.15
Numéro Beilstein :
8398291
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Format

neat

Chaîne SMILES 

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)

Clé InChI

PWPJGUXAGUPAHP-UHFFFAOYSA-N

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Catégories apparentées

Description générale

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.

Produits recommandés

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.

Informations légales

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

Pictogrammes

Exclamation markEnvironment

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

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

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

>338.0 °F - (External MSDS)

Point d'éclair (°C)

> 170 °C - (External MSDS)

Équipement de protection individuelle

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


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Certificats d'analyse (COA)

Lot/Batch Number

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Les clients ont également consulté

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)
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)
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)
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
Umesh Gangishetti et al.
European journal of cell biology, 88(3), 167-180 (2008-11-11)
Chitin is an essential constituent of the insect exoskeleton, the cuticle, which is an extracellular matrix (ECM) covering the animal. It is produced by the glycosyltransferase chitin synthase at the apical plasma membrane of epidermal and tracheal cells. To fulfil

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