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Tebufenozide

PESTANAL®, analytical standard

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About This Item

Formule empirique (notation de Hill):
C22H28N2O2
Numéro CAS:
112410-23-8
Poids moléculaire :
352.47
Numéro Beilstein :
7822297
Numéro CE :
412-850-3
Numéro MDL:
MFCD00467963
Code UNSPSC :
41116107
ID de substance PubChem :
329753866
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

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 

CCc1ccc(cc1)C(=O)NN(C(=O)c2cc(C)cc(C)c2)C(C)(C)C

InChI

1S/C22H28N2O2/c1-7-17-8-10-18(11-9-17)20(25)23-24(22(4,5)6)21(26)19-13-15(2)12-16(3)14-19/h8-14H,7H2,1-6H3,(H,23,25)

Clé InChI

QYPNKSZPJQQLRK-UHFFFAOYSA-N

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Catégories apparentées

Description générale

Tebufenozide is an insecticide very specific to lepidopteran pests.1

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Tebufenozide may have been used as analytical reference standard in the determination of insecticide residues in fruits and vegetables using ultra-performance liquid chromatography coupled with tandem mass spectrometry (UPLC-MS/MS).

Informations légales

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

Pictogrammes

Environment
GHS09

Mentions de danger

H411

Conseils de prudence

P273 - P391 - P501

Classification des risques

Aquatic Chronic 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number
BCCM3544
BCCH1296
BCBV7492
SZBC342XV
SZBB091XV

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Miwa Uchibori-Asano et al.
Scientific reports, 9(1), 4203-4203 (2019-03-14)
The smaller tea tortrix, Adoxophyes honmai, has developed strong resistance to tebufenozide, a diacylhydrazine-type (DAH) insecticide. Here, we investigated its mechanism by identifying genes responsible for the tebufenozide resistance using various next generation sequencing techniques. First, double-digest restriction site-associated DNA
Jiwan Kim et al.
Comparative biochemistry and physiology. Part A, Molecular & integrative physiology, 166(1), 60-69 (2013-05-09)
Parasitization by an endoparasitoid wasp, Cotesia plutellae, inhibits a larva-to-pupa metamorphosis of the diamondback moth, Plutella xylostella. This study tested an inhibitory effect of C. plutellae bracovirus (CpBV) on the metamorphosis of P. xylostella. Parasitized P. xylostella exhibited significantly reduced
Steven A Titus et al.
Current chemical genomics, 6, 79-86 (2013-01-25)
A hallmark of Huntington's disease is the presence of a large polyglutamine expansion in the first exon of the Huntingtin protein and the propensity of protein aggregation by the mutant proteins. Aberrant protein aggregation also occurs in other polyglutamine expansion
Xiaoshuang Luo et al.
Journal of the science of food and agriculture, 100(3), 1230-1237 (2019-11-07)
Ensuring the yield, quality, and profitability of okra by preventing and controlling pests with the application of insecticides has increased in the last decade. Some insecticide residues might remain in edible parts of okra (fruits) and lead to several potential
Ana R Cabrera et al.
PloS one, 12(4), e0176097-e0176097 (2017-04-28)
A novel feeding protocol for delivery of bio-active agents to Varroa mites was developed by providing mites with honey bee larva hemolymph supplemented with cultured insect cells and selected materials delivered on a fibrous cotton substrate. Mites were starved, fed
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