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Merck
CN

31652

Tebufenozide

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C22H28N2O2
CAS Number:
112410-23-8
Molecular Weight:
352.47
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329753866
EC Number:
412-850-3
Beilstein/REAXYS Number:
7822297
MDL number:
MFCD00467963

Key Documents

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Product Name

Tebufenozide, PESTANAL®, analytical standard

InChI key

QYPNKSZPJQQLRK-UHFFFAOYSA-N

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)

SMILES string

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

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

100

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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).

General description

Tebufenozide is an insecticide very specific to lepidopteran pests.1

Legal Information

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

pictograms

Environment
GHS09

hcodes

H411

Hazard Classifications

Aquatic Chronic 2

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

农药列管产品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCN8332
BCCN8331
BCCN1895
BCCM3544
BCCH1296

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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
Residue analysis of four diacylhydrazine insecticides in fruits and vegetables by Quick, Easy, Cheap, Effective, Rugged, and Safe (QuEChERS) method using ultra-performance liquid chromatography coupled to tandem mass spectrometry.
Liu X
Analytical and Bioanalytical Chemistry, 401(3), 1051-1058 (2011)
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
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
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
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