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Copper sulphate pentahydrate cuso4.5h2o

Manufactured by Merck Group
Sourced in Germany, Portugal

Copper sulphate pentahydrate (CuSO4.5H2O) is a crystalline compound that consists of copper, sulfur, and water. It is a commonly used inorganic chemical in various laboratory applications.

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4 protocols using copper sulphate pentahydrate cuso4.5h2o

1

Synthesis of Amorphous Silica Nanoparticles

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Amorphous silica NPs ~20 nm in diameter were prepared using rice husk ash as per the procedure of Sankar et al. [29 (link)] with a few modifications. The detail of the synthesis of the SiO2 NPs was described in our previous report [30 (link)]. Other chemicals, including copper sulphate pentahydrate (CuSO4.5H2O, 98%) and hydrazine mono hydrate (N2H4.H2O, 80%), were purchased from Merck (Darmstadt, Hesse, Germany). Carboxymethyl cellulose (CMC) and ammonium hydroxide (NH4OH, 25%) were purchased from Xilong Scientific Company (Shantou, Guangdong, China). The P. capsici was supplied by the Pepper Research and Development Centre, Western Highland Agriculture and Forestry Science Institute (Buon Ma Thuot City, Dak Lak, Vietnam).
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2

Copper Sulfate-Ascorbic Acid Synthesis

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All the chemicals and reagents used in the experiment were of analytical grade. Copper sulphate pentahydrate CuSO4,5H2O, Ascorbic acid C6H8O6 and Sodium hydroxide NaOH were purchased from Merck and Gum Arabic sample was received from ICAR-CAZRI, Jodhpur and used as received without further purification. De-ionized water was used for all the experiments.
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3

Zebrafish Embryo Exposure to Copper, Anesthetic, and Bioactive Compounds

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E3 medium (0.5 mM NaCl, 0.017 mM KCl, 0.033 mM CaCl2, 0.033 mM MgSO4, pH 7.0–7.4) was used to prepare all solutions. Copper sulphate pentahydrate (CuSO4.5H2O) (Merck, S.A., Algés, Portugal) was used as the source of copper and a stock solution of 4 mM (1000 mg/L) was prepared in ultra-pure water and further diluted in E3 medium to 10 µM (2.5 mg/L) [27 (link)]. Tricaine methanesulfonate (MS-222) (Sigma Aldrich, Lisboa, Portugal) stock solution of 5.74 mM (1500 mg/L) was prepared in buffered water, pH was adjusted to 7.4 and diluted in E3 medium to 574 µM (150 mg/L), according to [28 (link),29 (link)]. Diclofenac (DIC) sodium salt (Alfa Aesar, Kandel, Germany) stock solution was prepared in E3 medium at 2 mM (636 mg/L) and diluted to 1.5 µM (4.75 mg/L) [26 (link)]. THY (5-methyl-2-propan-2-ylphenol) (Sigma Aldrich) stock solution was prepared in ultra-pure water containing 10% ethanol and diluted in E3 medium of 430 µM (64.5 mg/L) and further diluted to 20 µM (3 mg/L). A 20 µM (9.6 mg/L) stock solution of 24-EPI (Sigma Aldrich, Lisboa, Portugal) was prepared in ultra-pure water containing 5% ethanol and diluted to 5 µM (2.4 mg/L) in E3 medium. All other reagents used were purchased from Sigma Aldrich (Lisboa, Portugal) or of the highest commercially available grade.
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4

Biogenic Copper Oxide Nanostructures

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Copper sulphate pentahydrate (CuSO4.5H2O) of analytical grade was purchased from Merck. The solution of copper sulphate pentahydrate was used as the source for the CuO and the leaf extract as the reducing agent, capping agent and source of carbon. In double distilled water 0.01 M copper sulphate solution was made and added to the supernatant solution of leaf extract in 5:4 volume ratio followed by constant stirring and in a nitrogen atmosphere. The experiment was repeated for different volume ratios. But the maximum yield was obtained in the ratio 5:4. So the ratio was fixed to 5:4. The reaction mixture was continued to be stirred for half an hour. Then a cloudy cluster of particles was formed. The formation of nanostructures was observed with a notable colour change [22 ]. The pH of the precursor solution, plant extract and the mixture solution were noted during the experiment. Then the nanocomposite solution was incubated for 24 h to complete the reaction and the residue obtained was cleaned five times with deionized water and centrifuged. The purified particles were air-dried and used for further study.
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