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Signaling PathwaysOthersOthersImidacloprid-urea
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Imidacloprid-urea

Imidacloprid-urea
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Purity:99.89%
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COA HPLC HNMR

Imidacloprid-urea

Catalog No. T72077Cas No. 120868-66-8
Imidacloprid-urea is a secondary metabolite of imidacloprid. Imidacloprid is a potent and widely used neonicotinoid with inhibitory effects on pests of cereals, vegetables, tea and cotton. imidacloprid-urea can occupy or block the adsorption sites of imidacloprid on the soil, which may affect the fate, transport and bioavailability of imidacloprid in the environment.
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
Pack SizePriceAvailabilityQuantity
10 mg$34In Stock
25 mg$72In Stock
50 mg$113In Stock
100 mg$172In Stock
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Product Introduction

Bioactivity
Description
Imidacloprid-urea is a secondary metabolite of imidacloprid. Imidacloprid is a potent and widely used neonicotinoid with inhibitory effects on pests of cereals, vegetables, tea and cotton. imidacloprid-urea can occupy or block the adsorption sites of imidacloprid on the soil, which may affect the fate, transport and bioavailability of imidacloprid in the environment.
In vitro
Imidacloprid (0, 10, and 20 μM ; 4-6 days) can reduce insulin-stimulated glucose uptake in adipocytes (3T3-L1), hepatocytes (HepG2), and myotubes (C2C12) cell culture models. Treatment with imidacloprid inhibits phosphorylation of protein kinase B (AKT) and ribosomal S6 kinase (S6K).[3]
In vivo
Imidacloprid(0, 5, 10, 20 mg/kg/day ; oral ; female rats) shows mild pathological changes in the brain, liver, and kidneys of rats.[4]
Chemical Properties
Molecular Weight211.65
FormulaC9H10ClN3O
Cas No.120868-66-8
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
H2O: 11.2 mg/mL (53.2 mM )
DMSO: 112.5 mg/mL (531.5 mM )
Solution Preparation Table
DMSO/H2O
1mg5mg10mg50mg
1 mM4.7248 mL23.6239 mL47.2478 mL236.2391 mL
5 mM0.9450 mL4.7248 mL9.4496 mL47.2478 mL
10 mM0.4725 mL2.3624 mL4.7248 mL23.6239 mL
20 mM0.2362 mL1.1812 mL2.3624 mL11.8120 mL
50 mM0.0945 mL0.4725 mL0.9450 mL4.7248 mL
DMSO
1mg5mg10mg50mg
100 mM0.0472 mL0.2362 mL0.4725 mL2.3624 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
1 Enter information below:
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