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Merck

31652

Supelco

Tebufenozid

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C22H28N2O2
Número de CAS:
Peso molecular:
352.47
Beilstein/REAXYS Number:
7822297
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

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)

InChI key

QYPNKSZPJQQLRK-UHFFFAOYSA-N

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General description

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).

Legal Information

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

pictograms

Environment

hcodes

Hazard Classifications

Aquatic Chronic 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Certificados de análisis (COA)

Lot/Batch Number

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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
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
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
Wenping Xu et al.
Environmental toxicology and pharmacology, 49, 89-96 (2016-12-14)
Tebufenozide is a non-steroidal insect growth regulator and is extensively used to control pests, although it is considered to be safe for mammals and environmentally friendly. However, previous studies have found that tebufenozide is cytotoxic to man, although the exact

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