The largest database of trusted experimental protocols

Dinotefuran

Manufactured by Merck Group
Sourced in United States

Dinotefuran is a chemical compound used as an active ingredient in various lab equipment and instruments. It functions as an insecticide, targeting certain pest species. The core purpose of Dinotefuran is to provide effective pest control in laboratory environments, ensuring the integrity and safety of research samples and experiments.

Automatically generated - may contain errors

4 protocols using dinotefuran

1

Insecticide Efficacy Evaluation Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
All chemical agents tested were of analytical standard grade. Chlorogenic acid (Chemical Abstracts Service [CAS] #327-97-9), abamectin (CAS #71751-41-2), flupyradifurone (CAS #951659-40-8), cyantraniliprole (CAS #736994-63-1), imidacloprid (CAS #138261-41-3), thiamethoxam (CAS #153719-23-4), flonicamid (CAS #158062-67-0), acetamiprid (CAS #160430-64-8), clothianidin (CAS #210880-92-5), nitenpyram (CAS #150824-47-8), and dinotefuran (CAS #165252-70-0) were purchased from Sigma Aldrich (Shanghai, China). Afidopyropen (CAS #915972-17-7) and sulfoxaflor (CAS #946578-00-3) were purchased from Dr. Ehrenstorfer (Augsburg, Germany).
+ Open protocol
+ Expand
2

Cultivating Common Duckweed for Neonicotinoid Experiments

Check if the same lab product or an alternative is used in the 5 most similar protocols
Standards and chemicals of dinotefuran, thiacloprid, and imidaclothiz were purchased from Sigma-Aldrich (United States). The chemical structures of the three NEOs are displayed in Table 1. Methanol (HPLC grade) was purchased from Merck (Germany). The remaining reagents, which were at least of analytical grade, were purchased from Aladdin Reagent (China).
Common duckweed (L. aequinoctialis DKLe0261)1 was obtained from the China Culture Collection of Aquatic Plants (Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China). L. aequinoctialis was surface-sterilized by soaking in 75% ethanol for 3 min followed by treatment with 0.5% sodium hypochlorite for 5 min. Plant sterility was ascertained by incubating the plant tissues on Luria Bertani (LB) agar (yeast extract, 5 g L−1; tryptone, 10 g L−1; NaCl, 10 g L−1) at 30°C for 48 h and checking for the absence of bacterial contamination. The sterilized plants were successively cultured in flasks containing sterile Hoagland medium in a growth chamber (8,000 lux; 16:8 h light–dark cycle) at 24°C. Hoagland medium contained 293 mg L−1 K2SO4, 36.1 mg L−1 KNO3, 103 mg L−1 MgSO4·7H2O, 147 mg L−1 CaCl2·2 H2O, 5.03 mg L−1 NaH2PO4·2H2O, 0.95 mg L−1 H3BO3, 3.33 mg L−1 FeSO4·7H2O, 0.08 mg L−1 ZnSO4·7 H2O, 0.39 mg L−1 MnCl2·4H2O, 0.03 mg L−1 CuSO4·5H2O, 0.39 mg L−1 MnCl2·4 H2O, and 0.23 mg L−1 H2MoO4.
+ Open protocol
+ Expand
3

Honey Bee Toxicity Assay for Dinotefuran

Check if the same lab product or an alternative is used in the 5 most similar protocols
A dinotefuran (Sigma–Aldrich, St Louis, MO) stock solution (1,000 ng a.i./l) was prepared using 50% sucrose:water solution as the solvent. Six concentrations ranging from 1,000 to 0.01 ng a.i./l were prepared directly in a sucrose:water (1:1, w:v) diet after the pretest. In total, 30 newly emerged honey bees from each treatment group were divided into three cages of 10 honey bees, and a control group was set. The bees were fasted for 2 h, and then a plastic container filled with a diet (average of 10 µl diet/bee) and a cotton swab soaked in distilled water were placed at the cage bottom (Oliveira et al. 2014 (link)). After 48 h, the number of dead bees in each treatment group was recorded, and the LC10 and LC50 were determined by Data Processing System (DPS) software 18.01 (Tang and Zhang 2013 (link)).
+ Open protocol
+ Expand
4

Sublethal Dinotefuran Exposure in Honey Bees

Check if the same lab product or an alternative is used in the 5 most similar protocols
The residues of dinotefuran recorded in pollen, honey or syrup range from 0.03 ng/g to 147 ng/g [11 (link), 64 (link)–66 (link)]. On this basis, a field-realistic level of dinotefuran of 0.01 mg/L was selected as the sublethal concentration in this study. A dinotefuran (> 99% purity, Sigma-Aldrich, St Louis, MO, USA) stock solution (1000 ng a.i./L) was prepared using a 50% sucrose:water solution as the solvent. The bees were treated with 2 mL of 0.01 mg/L dinotefuran solution in the experimental group (DT). Fifteen honey bees were collected on the 1st day (DT_1d), 5th day (DT_5d) and 10th day (DT_10d). The bees in the control group were fed 2 mL of a 50% sucrose: water solution, and samples were collected at the same time on the 1st day (C_1d), 5th day (C_5d) and 10th day (C_10d). The honey bees were fed ad libitum. Dead bees were removed and both treatment solution and untreated sucrose solution were replaced daily throughout the experiment. The bee samples were preserved in liquid nitrogen and stored at − 80 °C until brain dissection. The in vivo portion of the study was carried out at 34 °C ± 1 °C under 60 ± 10% RH in darkness.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!