Pristine zinc oxide nanocrystals (ZnO NCs) were synthetized by a wet chemical method using zinc acetate dihydrate (Zn(CH3COO)2·H2O) and sodium hydroxide (NaOH) as precursors and methanol as a solvent. In detail, 0.818 g (3.73 mmol) of Zn(CH3COO)2·H2O was dissolved in 42 mL of methanol in a 100 mL round bottom flask and heated to 60 °C under vigorous stirring. When the temperature reached 60 °C, 318 μL of bi-distilled water (from a Direct Q3 system, Millipore) and a solution of 0.289 g (7.22 mmol) of NaOH in 23 mL of methanol were dropwise added to the zinc acetate solution. The resulting synthesis mixture was maintained, under continuous stirring, at 60 °C for 2.15 h and then washed two times with fresh ethanol using a repeated centrifugation–redispersion process.
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Zinc Acetate Dihydrate
Zinc Acetate Dihydrate
Zinc Acetate Dihydrate is a chemical compound with the formula Zn(CH3COO)2·2H2O.
It is a white crystalline solid that is soluble in water and commonly used in various applications, such as in the production of zinc-containing supplements, catalyst, and as a component in cosmetic and personal care products.
This compound has been extensively studied and documented in the scientific literature, and researchers can leverage the power of PubCompare.ai's AI-driven protocol optimization to streamline their Zinc Acetate Dihydrate research.
The platform helps locate the best protocols from literature, preprints, and patents, with intelligent comparisons to ensure reproducible and reliable results.
Researchers can trust PubCompare.ai as their partner in protocol optimization, as it helps them discover the true potential of their Zinc Acetate Dihydrate studies.
It is a white crystalline solid that is soluble in water and commonly used in various applications, such as in the production of zinc-containing supplements, catalyst, and as a component in cosmetic and personal care products.
This compound has been extensively studied and documented in the scientific literature, and researchers can leverage the power of PubCompare.ai's AI-driven protocol optimization to streamline their Zinc Acetate Dihydrate research.
The platform helps locate the best protocols from literature, preprints, and patents, with intelligent comparisons to ensure reproducible and reliable results.
Researchers can trust PubCompare.ai as their partner in protocol optimization, as it helps them discover the true potential of their Zinc Acetate Dihydrate studies.
Most cited protocols related to «Zinc Acetate Dihydrate»
Anabolism
Centrifugation
Ethanol
Methanol
ML 23
Sodium Hydroxide
Solvents
Suby's G solution
Zinc Acetate
Zinc Acetate Dihydrate
Zinc Oxide
Zinc oxide nanoparticles were
synthesized according to a previously described protocol with slight
modifications. Briefly, 6.0 g of zinc acetate dihydrate (Zn(NO3)2·2H2O) (Sigma-Aldrich) was added
to 100 mL of extract and kept on a magnetic stirrer at 60 °C
for 2 h. Once the reaction was complete, the mixture was allowed to
cool down at 25 °C and centrifuged (HERMLE Z326K) at 10 000
rpm for 10 min. The supernatant was discarded, and the remaining pellet
was washed thrice with distilled water, poured into a clean Petri
plate, and oven-dried at 90 °C. The dried material was then ground
into fine powder in a pestle and mortar and calcined for 2 h at 500
°C to remove any impurities. The annealed powder was stored in
an airtight glass vial, labeled as ZnO-NPs, and was further used for
physical characterizations and biological applications.28 (link)
synthesized according to a previously described protocol with slight
modifications. Briefly, 6.0 g of zinc acetate dihydrate (Zn(NO3)2·2H2O) (Sigma-Aldrich) was added
to 100 mL of extract and kept on a magnetic stirrer at 60 °C
for 2 h. Once the reaction was complete, the mixture was allowed to
cool down at 25 °C and centrifuged (HERMLE Z326K) at 10 000
rpm for 10 min. The supernatant was discarded, and the remaining pellet
was washed thrice with distilled water, poured into a clean Petri
plate, and oven-dried at 90 °C. The dried material was then ground
into fine powder in a pestle and mortar and calcined for 2 h at 500
°C to remove any impurities. The annealed powder was stored in
an airtight glass vial, labeled as ZnO-NPs, and was further used for
physical characterizations and biological applications.28 (link)
Biopharmaceuticals
Powder
Zinc Acetate Dihydrate
All the glassware were autoclaved before use. To prepare leaf extract, fresh leaves of C. fistula and M. azadarach were thoroughly washed with tap water followed by distilled water (d.H2O) to remove any contamination. The leaves were air dried for a week at room temperature (∼37°C). About 5 g of leaves from each of C. fistula and M. azadarach were ground to fine powder with the help of pestle and mortar. This powder was mixed in 500 mL of d.H2O and then heated at 70°C for 30 minutes. The mixture was filtered first by muslin cloth and then using Whatman filter paper No.1. As a result, pale yellow and red colored solutions were obtained as leaf extracts of C. fistula and M. azadarach respectively which were stored at 4 °C.
0.01 M zinc acetate dihydrate (Zn (C2H3O2)2.2H2O) solution was prepared in d.H2O. For synthesis of ZnO nanoparticles, 95 mL of 0.01 M zinc acetate dihydrate (Zn (C2H3O2)2.2H2O) solution was mixed separately with 5 mL plant extract of each of C. fistula and M. azadarach in individual 250 mL flasks. These mixtures were incubated at 70°C for 1 hour with continuous shaking at 150 rpm. This led to the settlement of bio-reduced salt at the bottom of the flask which appeared as white precipitate. The supernatant was decanted and powdery precipitate was transferred to 1.5 mL centrifuge tubes. Both the samples were subjected to washing with d.H2O by centrifugation at 3000 rpm for 30 minutes. Washing step was repeated thrice to ensure removal of impurities22 (link).
0.01 M zinc acetate dihydrate (Zn (C2H3O2)2.2H2O) solution was prepared in d.H2O. For synthesis of ZnO nanoparticles, 95 mL of 0.01 M zinc acetate dihydrate (Zn (C2H3O2)2.2H2O) solution was mixed separately with 5 mL plant extract of each of C. fistula and M. azadarach in individual 250 mL flasks. These mixtures were incubated at 70°C for 1 hour with continuous shaking at 150 rpm. This led to the settlement of bio-reduced salt at the bottom of the flask which appeared as white precipitate. The supernatant was decanted and powdery precipitate was transferred to 1.5 mL centrifuge tubes. Both the samples were subjected to washing with d.H2O by centrifugation at 3000 rpm for 30 minutes. Washing step was repeated thrice to ensure removal of impurities22 (link).
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Anabolism
Centrifugation
Fistula
Plant Extracts
Plant Leaves
Powder
Sodium Chloride
Strains
Zinc Acetate Dihydrate
ZnO NPs were obtained in accordance with the procedure described in our previous publications [12 (link),18 (link),19 (link)]. The solution (900 mL) of zinc acetate dihydrate (0.3037 mol/dm3) dissolved in ethylene glycol was prepared using a hot-plate magnetic stirrer (70 °C, 450 rpm, SLR, SI Analytics GmbH, Mainz, Germany). Upon the complete zinc acetate dissolution, the solution was immediately poured into a bottle (1000 mL, polypropylene), which was then sealed. The water (H2O) content test in the precursor was carried out once the solution temperature reached room temperature (RT). A properly calculated amount of H2O was added to the precursor such that the content was 1.5 wt. %, which was verified.
The synthesis reaction was carried out in a stop-flow microwave reactor, MSS2 model (3 kW, 2.45 GHz, IHPP PAS (Warsaw), ITeE-PIB (Radom), ERTEC (Wroclaw), Poland) [63 (link)]. The synthesis parameters are provided inTable 1 .
The reactions of ZnO NPs synthesis in ethylene glycol are described by the following general Equation (1):
After the synthesis, the obtained suspensions were sedimented and the supernatants were decanted. The sediments were rinsed three times with water and centrifuged (MPW-350, MPW Med Instruments, Warsaw, Poland). As a result of vigorous stirring of moist powders with water in 100 mL containers, water suspensions of ZnO NPs were obtained from these powders, and subsequently their concentration was determined. Half of the volume of ZnO NPs suspensions was frozen in liquid nitrogen and dried in a freeze dryer (Lyovac GT-2, SRK Systemtechnik GmbH, Riedstadt, Germany).
The synthesis reaction was carried out in a stop-flow microwave reactor, MSS2 model (3 kW, 2.45 GHz, IHPP PAS (Warsaw), ITeE-PIB (Radom), ERTEC (Wroclaw), Poland) [63 (link)]. The synthesis parameters are provided in
The reactions of ZnO NPs synthesis in ethylene glycol are described by the following general Equation (1):
After the synthesis, the obtained suspensions were sedimented and the supernatants were decanted. The sediments were rinsed three times with water and centrifuged (MPW-350, MPW Med Instruments, Warsaw, Poland). As a result of vigorous stirring of moist powders with water in 100 mL containers, water suspensions of ZnO NPs were obtained from these powders, and subsequently their concentration was determined. Half of the volume of ZnO NPs suspensions was frozen in liquid nitrogen and dried in a freeze dryer (Lyovac GT-2, SRK Systemtechnik GmbH, Riedstadt, Germany).
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Anabolism
Desiccation
Freezing
Glycol, Ethylene
Microwaves
Nitrogen
Polypropylenes
Powder
Zinc Acetate
Zinc Acetate Dihydrate
ZTO nanostructures were
synthesized via hydrothermal method, using a modified version of the
synthesis reported by Li et al.,12 (link) without
the use of a seed layer (in ref (12 (link)) a stainless steel mesh seed-layer is used).Figure S18a shows the schematic of the synthesis
where the precursor concentrations used were 0.020 M SnCl4·5H2O and 0.040 M Zn(CH3COO)2·2H2O. The precursors were separately dissolved in
7.5 mL of Millipore water and were then mixed together. Afterward,
7.5 mL of the surfactant ethylenediamine (EDA) were added, and
the mixture was left stirring for 30 min. Finally 0.240 M NaOH was
added. The precursors were smashed in a mortar before being added
to water to help dissolution. The reagents used were all commercially
available: zinc acetate dihydrate 99.0% (Zn(CH3COO)2·2H2O), sodium hydroxide ≥98% (NaOH),
and ethylenediamine 99% (EDA) from Sigma-Aldrich, tin(IV) chloride
5-hydrate (SnCl4·5H2O) extra pure from
Riedel-de Haën and zinc chloride 98% (ZnCl2) from
Merck.
To study the influence of the zinc precursor, zinc acetate
was replaced by zinc chloride, maintaining the same concentration
of zinc in the solution. Different Zn:Sn ratios (molar concentration)
were studied, namely, 2:1, 1:1, and 1:2. The ratio between H2O and EDA was varied (H2O:EDA, 15:0, 9:6, 8:7, 7.5:7.5,
7:8, 6:9, 0:15), as well as the concentration of NaOH (0.100 M, 0.175
M, 0.240, and 0.350 M). When the solution was ready, it was transferred
into a 45 mL Teflon-lined stainless-steel autoclave, filling 80% of
the total autoclave volume. The mixture was kept in an electric oven
(Thermo Scientific) at 200 °C for 24 h, with a heating ramp of
200 °C/h. The autoclave was cooled to ambient temperature naturally.
The resultant precipitate, comprising the nanostructures, was centrifuged
at 4000 rpm and washed several times with deionized water and isopropyl
alcohol, alternately. The nanostructures were finally dried at 60
°C,
in vacuum, for 2 h, as schematized inFigure S18b .
synthesized via hydrothermal method, using a modified version of the
synthesis reported by Li et al.,12 (link) without
the use of a seed layer (in ref (12 (link)) a stainless steel mesh seed-layer is used).
where the precursor concentrations used were 0.020 M SnCl4·5H2O and 0.040 M Zn(CH3COO)2·2H2O. The precursors were separately dissolved in
7.5 mL of Millipore water and were then mixed together. Afterward,
7.5 mL of the surfactant ethylenediamine (EDA) were added, and
the mixture was left stirring for 30 min. Finally 0.240 M NaOH was
added. The precursors were smashed in a mortar before being added
to water to help dissolution. The reagents used were all commercially
available: zinc acetate dihydrate 99.0% (Zn(CH3COO)2·2H2O), sodium hydroxide ≥98% (NaOH),
and ethylenediamine 99% (EDA) from Sigma-Aldrich, tin(IV) chloride
5-hydrate (SnCl4·5H2O) extra pure from
Riedel-de Haën and zinc chloride 98% (ZnCl2) from
Merck.
To study the influence of the zinc precursor, zinc acetate
was replaced by zinc chloride, maintaining the same concentration
of zinc in the solution. Different Zn:Sn ratios (molar concentration)
were studied, namely, 2:1, 1:1, and 1:2. The ratio between H2O and EDA was varied (H2O:EDA, 15:0, 9:6, 8:7, 7.5:7.5,
7:8, 6:9, 0:15), as well as the concentration of NaOH (0.100 M, 0.175
M, 0.240, and 0.350 M). When the solution was ready, it was transferred
into a 45 mL Teflon-lined stainless-steel autoclave, filling 80% of
the total autoclave volume. The mixture was kept in an electric oven
(Thermo Scientific) at 200 °C for 24 h, with a heating ramp of
200 °C/h. The autoclave was cooled to ambient temperature naturally.
The resultant precipitate, comprising the nanostructures, was centrifuged
at 4000 rpm and washed several times with deionized water and isopropyl
alcohol, alternately. The nanostructures were finally dried at 60
°C,
in vacuum, for 2 h, as schematized in
Electricity
ethylenediamine
Molar
Sodium Hydroxide
Stainless Steel
stannic chloride
Surface-Active Agents
Teflon
Vacuum
Zinc
Zinc Acetate Dihydrate
zinc chloride
Most recents protocols related to «Zinc Acetate Dihydrate»
Zinc acetate dihydrate (Zn(OAC)2·2H2O, 99.99%) and dopamine hydrochloride (AR, 98.0%,) were purchased from Aladdin Corp. Cetyltrimethylammonium bromide (CTAB, 99%) and triblock poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide) Pluronic F-127 (Mav = 12,600) were purchased from Sigma-Aldrich. Tris(hydroxymethyl)aminomethane (Tris, ≥99.5%), 2-methylimidazole (1-MeIM, AR, ≥98.0%), zinc nitrate hexahydrate (Zn(NO3)2·6H2O, AR, ≥99.0%), cobalt (II) nitrate hexahydrate (Co(NO3)2·2H2O, ≥ 98.5%,), 1,3,5-trimethylbenzene (TMB, ≥ 99.5%), hydrochloric acid (HCl, 36.0–38.0%), 2,3,6-trimethylphenol (TMP, 98.0%), methanol anhydrous (AR, ≥99.5%), hydrogen peroxide (30 wt.%), ammonium hydroxide solution (28 wt.% NH3 in H2O), polyvinylpyrrolidone K30 (GR), copper(II) chloride dihydrate(AR, ≥99.0%) and anhydrous ethanol (AR, ≥99.7%) were purchased from Sinopharm Chemical Reagent Co., Ltd. Disulfiram (97%) was purchased from Aladdin Reagent Co. Ltd. Fetal bovine serum (FBS), penicillin-streptomycin, trypsin, and RPMI 1640 medium were provided by Gibco Life Technologies Co. Cell Counting Kit-8 (CCK-8), calcein-AM/propidium iodide (PI) and annexin V-FITC Apoptosis Detection Kit were obtained from Beyotime Biotech (China).
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2-methylimidazole
Absolute Alcohol
Ammonium Hydroxide
Apoptosis
Cetrimonium Bromide
Chlorides
Cobalt
Copper
Disulfiram
Fetal Bovine Serum
FITC-annexin A5
fluorexon
Hydrochloric acid
Hydrochloride, Dopamine
Methanol
methylamine
Nitrates
Penicillins
PEO-PPO-PEO
Peroxide, Hydrogen
Pluronics
Povidone
Propidium Iodide
Streptomycin
Tromethamine
Trypsin
Zinc Acetate Dihydrate
zinc nitrate hexahydrate
An amount of 0.317 g (0.02 M) of zinc acetate dihydrate in 30 mL of methanol was taken and heated to 60 °C while being evenly stirred for 20 min. The temperature of the solution was kept constant at 60 °C, and it was stirred consistently for a period of two hours after the addition of a stabilizer that consisted of 1 mL of ethanolamine. After this period was finished, the solution was left out at room temperature for twenty-four hours so that the zinc oxide seed layer solution could be obtained. Then, using a spin coater, 40 L of zinc oxide seed layer solution was applied to the cleaned silicon substrates. A two-step spin coating was used for a uniform film coating. To achieve a homogenous ZnO seed layer, successive applications of 1000 rpm for 10 s and 1500 rpm for 40 s were used. After deposition, the substrates were heated at 120 °C for 20 min, and the procedure was repeated twice. Later, the substrates coated with the zinc oxide seed layer were placed in a tungsten boat and kept inside a furnace tube at a high temperature (500 °C) for annealing for 2 h. Furthermore, by fabricating multiple samples of ZnO NRs using the same process and comparing the diameters of the as-grown ZnO NRs on the Si substrates, the repeatability of the ZnO seed layer was confirmed. The uniformity of the diameter distribution across multiple samples was maintained. Through this method, seed layer thicknesses of around 23.41 ± 0.23 nm and diameters of the NRs of around 128.50 ± 0.66 were maintained constantly in all our samples. In the supporting information file, Section S1 , the SEM top view and cross-section view of the deposited ZnO seed layer, distribution of the seed layer thickness, and distribution of NR diameters are provided.
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Ethanolamine
Fever
Homozygote
Methanol
Silicon
Tungsten
Zinc Acetate Dihydrate
A stoichiometric ratio of zinc acetate dihydrate and cyclo-hexamethylenetetramine (HMTA) were taken in 90 mL of deionized water and stirred well for 30 min to complete the synthesis of the reaction solution of ZnO NRs. Then, the solution was transferred to the Teflon-lined autoclave and the substrates were kept inside the solution for the growth of the ZnO NRs. The autoclave was placed in an oven at a temperature of 80 °C for 4 h, and after being reduced to room temperature, the substrates were taken out and cleaned with deionized water. The decoration of the ZnO NRs with Ag nanoparticles was achieved using a simple vacuum sputtering technique under ambient conditions for 5 min, adopting the method followed by Yoon, J. et al. [26 (link)]. The pressure during the sputtering process was maintained at 20 Pa and the current was controlled at 2 mA. The calculated average diameter of the Ag NPs of 15.55 ± 3.71 nm was maintained using the above-mentioned sputtering conditions for all the samples fabricated in this study. The diameter distribution of the Ag NPs decorating the ZnO NRs is included in the supporting information file, Section S2 . After Ag decoration, 20 μL of the glucose solutions of different concentrations was filled with ZnO NRs and placed on a heating plate at 80 °C for 1 h and then used for the analysis. The schematic diagram of the synthesis of ZnO, Ag@ZnO, and glucose/Ag@ZnO is shown in Figure 1 .
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Anabolism
Glucose
Methenamine
Pressure
Teflon
Vacuum
Zinc Acetate Dihydrate
Zinc acetate dihydrate (99.9%, Pol-Aura, Morąg, Poland), citric acid monohydrate (99.9%, POCH, Gliwice, Poland), sodium hydroxide (≥98%, Stanlab, Lublin, Poland).
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Citric Acid Monohydrate
Sodium Hydroxide
Zinc Acetate Dihydrate
In the first step of zinc oxide synthesis, 30 g of zinc acetate dihydrate was added to 200 mL of distilled water and stirred until completely dissolved. Next, a 1 mol L−1 sodium hydroxide solution was prepared and dropped (at a rate of 20 drops/1 min) into the zinc acetate solution. The mixture was stirred vigorously. The pH value was controlled with a pH-meter. Using the same volume of alkali solution as in the temperature-optimized synthesis, a pH of ~13.5 was obtained. For subsequent reaction solutions, the pH was successively adjusted to 11.0, 9.0, 8.5, 8.0, and 7.5 by lowering the volume of the infused sodium hydroxide solution. All six solutions with different pH were transferred to Teflon-lined steel autoclaves and subjected to hydrothermal treatment at 160 °C for 12 h. The resulting products were filtered, washed with distilled water and ethanol, and then dried in an oven at 60 °C for 24 h. Referring to the adjusted pH values, the samples were designated accordingly: ZnO7.5, ZnO8.0, ZnO8.5, ZnO9.0, ZnO11.0, and ZnO13.5.
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Alkalies
Anabolism
Ethanol
Sodium Hydroxide
Steel
Teflon
Zinc Acetate
Zinc Acetate Dihydrate
Zinc Oxide
Top products related to «Zinc Acetate Dihydrate»
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Zinc acetate dihydrate is a chemical compound with the formula Zn(CH3COO)2·2H2O. It is a white crystalline solid that is soluble in water and other polar solvents. Zinc acetate dihydrate is commonly used as a laboratory reagent and in various industrial applications.
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Sodium hydroxide is a chemical compound with the formula NaOH. It is a white, odorless, crystalline solid that is highly soluble in water and is a strong base. It is commonly used in various laboratory applications as a reagent.
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Ethanol is a clear, colorless liquid chemical compound commonly used in laboratory settings. It is a key component in various scientific applications, serving as a solvent, disinfectant, and fuel source. Ethanol has a molecular formula of C2H6O and a range of industrial and research uses.
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Methanol is a clear, colorless, and flammable liquid that is widely used in various industrial and laboratory applications. It serves as a solvent, fuel, and chemical intermediate. Methanol has a simple chemical formula of CH3OH and a boiling point of 64.7°C. It is a versatile compound that is widely used in the production of other chemicals, as well as in the fuel industry.
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Hydrochloric acid is a commonly used laboratory reagent. It is a clear, colorless, and highly corrosive liquid with a pungent odor. Hydrochloric acid is an aqueous solution of hydrogen chloride gas.
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Ethanolamine is a chemical compound used in various laboratory applications. It serves as a key component in the production and analysis of organic compounds. Ethanolamine is a colorless, viscous liquid with a characteristic odor. Its primary function is to act as a chemical building block and buffer solution in various experimental and analytical procedures.
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Zinc acetate dihydrate is a chemical compound used in various laboratory and industrial applications. It is a white crystalline solid that is soluble in water and alcohol. Zinc acetate dihydrate is a common source of zinc ions and is used as a reagent in chemical reactions, as a catalyst, and in the production of other zinc compounds.
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DMSO is a versatile organic solvent commonly used in laboratory settings. It has a high boiling point, low viscosity, and the ability to dissolve a wide range of polar and non-polar compounds. DMSO's core function is as a solvent, allowing for the effective dissolution and handling of various chemical substances during research and experimentation.
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Zinc acetate dihydrate, Zn(CH3COO)2·2H2O, is a chemical compound that consists of zinc ions (Zn2+) and acetate ions (CH3COO-) with two molecules of water. It is a white crystalline solid that is soluble in water and organic solvents. Zinc acetate dihydrate is commonly used as a source of zinc ions in various applications.
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2-methoxyethanol is a colorless, volatile liquid used as a solvent in various industrial and laboratory applications. It has a molecular formula of CH₃OCH₂CH₂OH. The core function of 2-methoxyethanol is to serve as a solvent for a wide range of organic compounds, including paints, coatings, and cleaning products.
More about "Zinc Acetate Dihydrate"
Zinc acetate dihydrate is a chemical compound with the formula Zn(CH3COO)2·2H2O, also known as zinc diacetate dihydrate or zinc(II) acetate dihydrate.
It is a white crystalline solid that is soluble in water and commonly used in various applications, such as the production of zinc-containing supplements, catalysts, and as a component in cosmetic and personal care products.
This versatile compound has been extensively studied and documented in the scientific literature.
Researchers can leverage the power of PubCompare.ai's AI-driven protocol optimization to streamline their Zinc Acetate Dihydrate research.
The platform helps locate the best protocols from literature, preprints, and patents, with intelligent comparisons to ensure reproducible and reliable results.
Researchers can trust PubCompare.ai as their partner in protocol optimization, as it helps them discover the true potential of their Zinc Acetate Dihydrate studies.
In addition to Zinc Acetate Dihydrate, other related compounds and chemicals such as Sodium Hydroxide, Ethanol, Methanol, Hydrochloric Acid, Ethanolamine, DMSO, and 2-Methoxyethanol are often used in research and applications involving this versatile compound.
Researchers can leverage the insights and tools provided by PubCompare.ai to optimize their workflows and streamline their Zinc Acetate Dihydrate research, leading to more efficient and reliable results.
It is a white crystalline solid that is soluble in water and commonly used in various applications, such as the production of zinc-containing supplements, catalysts, and as a component in cosmetic and personal care products.
This versatile compound has been extensively studied and documented in the scientific literature.
Researchers can leverage the power of PubCompare.ai's AI-driven protocol optimization to streamline their Zinc Acetate Dihydrate research.
The platform helps locate the best protocols from literature, preprints, and patents, with intelligent comparisons to ensure reproducible and reliable results.
Researchers can trust PubCompare.ai as their partner in protocol optimization, as it helps them discover the true potential of their Zinc Acetate Dihydrate studies.
In addition to Zinc Acetate Dihydrate, other related compounds and chemicals such as Sodium Hydroxide, Ethanol, Methanol, Hydrochloric Acid, Ethanolamine, DMSO, and 2-Methoxyethanol are often used in research and applications involving this versatile compound.
Researchers can leverage the insights and tools provided by PubCompare.ai to optimize their workflows and streamline their Zinc Acetate Dihydrate research, leading to more efficient and reliable results.