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Indium nitrate hydrate

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Indium nitrate hydrate is a chemical compound that consists of indium, nitrogen, and water. It is a crystalline solid that is used as a precursor in the manufacturing of various electronic and optoelectronic devices.

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Lab products found in correlation

Gallium nitrate hydrate, by Merck Group (5 mentions) Zinc nitrate hydrate, by Merck Group (3 mentions) Hydrochloric acid (hcl), by Merck Group (2 mentions) 1 dodecanethiol, by Merck Group (2 mentions) Oleic acid, by Merck Group (2 mentions) Oleylamine, by Merck Group (2 mentions) Anhydrous toluene, by Merck Group (2 mentions) Copper 1 iodide, by Merck Group (2 mentions) Methanol, by Merck Group (2 mentions) Sodium hydroxide (naoh), by Merck Group (2 mentions) Streptomycin sulfate, by Thermo Fisher Scientific (1 mentions) Carboxymethylcellulose sodium salt, by Merck Group (1 mentions) Penicillin g sodium, by Thermo Fisher Scientific (1 mentions) 3 4 5 dimethylthiazol 2 yl 2 5 diphenyltetrazolium bromide, by Merck Group (1 mentions) Amphotericin b, by Thermo Fisher Scientific (1 mentions) Paraformaldehyde (pfa), by Merck Group (1 mentions) Sodium dodecyl sulfate (sds), by Merck Group (1 mentions) Triton x 100, by Merck Group (1 mentions) Hek293t, by American Type Culture Collection (1 mentions) Aluminum nitrate nonahydrate, by Merck Group (1 mentions)

Spelling variants of this product

Indium (III) nitrate hydrate (12 citations) Indium nitrate (5 citations)

11 protocols using indium nitrate hydrate

1

Synthesis of Silver Nanoparticles

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Zinc nitrate hydrate (Zn(NO3)2·6H2O, >99%), indium nitrate hydrate (In(NO3)3·xH2O, In = 28.5% wt), carboxymethylcellulose sodium salt (CMC, degree of substitution: 0.7; average molecular mass = 90,000 Da; medium viscosity: 180 cps, 4% in H2O at 25°C), 3-(4,5-dimethylthiazol-2yl) 2,5-diphenyltetrazolium bromide (MTT, >98%), Triton™ X-100, sodium dodecyl sulfate (SDS, ≥99.0%), paraformaldehyde (95%), and hydrochloric acid (HCl, 37%) were purchased from Sigma-Aldrich (USA). Silver nitrate (AgNO3, 99.9%) and sodium sulfide hydrate (Na2S·9H2O, >98%) were purchased from Synth (Brazil). Dulbecco's Modified Eagle Medium (DMEM), fetal bovine serum (FBS), phosphate buffered saline (PBS), penicillin G sodium, streptomycin sulfate, and amphotericin-b were supplied by Gibco BRL (USA). Hydromount was purchased from Fisher Scientific Ltd. (UK). Human embryonic kidney (HEK 293T, American Type Culture Collection, ATCC® CRL-1573™) cells were kindly provided by Professor M.F Leite (Department of Physiology and Biophysics, UFMG). Malignant glioma (U-87 MG) cells were purchased from Rio de Janeiro Cell Bank (ATCC® HTB-14™).
Aforementioned chemicals were used without further purification, deionized water (DI water, Millipore Simplicity™) with a resistivity of 18 MΩ cm was used to prepare the solutions, and the procedures were performed at room temperature (RT, 23 ± 2°C), unless specified otherwise.
Mansur A.A., Mansur H.S., Carvalho S.M, & Caires A.J. (2017). One-Pot Aqueous Synthesis of Fluorescent Ag-In-Zn-S Quantum Dot/Polymer Bioconjugates for Multiplex Optical Bioimaging of Glioblastoma Cells. Contrast Media & Molecular Imaging, 2017, 3896107.
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2

Fabrication of Flexible IGZO-TFTs

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The IGZO solution (0.125 M) was prepared by dissolving indium nitrate hydrate (In(NO3)3 • xH2O), gallium nitrate hydrate (Ga(NO3)3 • xH2O) and zinc nitrate hydrate (Zn(NO3)2 • xH2O) powders (Sigma Aldrich) in 2-methoxyethanol (2-ME) as a solvent (anhydrous, Sigma Aldrich). The Al2O3 solution (0.8 M) was also prepared by dissolving aluminum nitrate nonahydrate (Al(NO3)3 • 9H2O) (Sigma Aldrich) powder in 2-ME as a solvent (anhydrous, Sigma Aldrich). The molar concentration of the Al2O3 solution used to construct flexible IGZO-TFTs was optimized to 0.15 M, which enables the device to operate at 1 V. The IGZO and Al2O3 solutions were magnetically stirred at 70 °C for 12 h at an ambient atmosphere.
Yu B.S., Jeon J.Y., Kang B.C., Lee W., Kim Y.H, & Ha T.J. (2019). Wearable 1 V operating thin-film transistors with solution-processed metal-oxide semiconductor and dielectric films fabricated by deep ultra-violet photo annealing at low temperature. Scientific Reports, 9, 8416.
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3

Synthesis of IGZO and IZO Solutions

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The IGZO solution was composed of indium nitrate hydrate (In(NO3)2·xH2O, Sigma Aldrich), gallium nitrate hydrate (Ga(NO3)2·xH2O, Sigma Aldrich, St. Louis, MO, USA), and zinc nitrate hexahydrate (Zn(NO3)2·6H2O, Sigma Aldrich) with a molar ratio of 6:1:2, dissolved in ethylene glycol monomethyl ether (Daejung, Siheung, Republic of Korea). The IZO solution was synthesized by blending In(NO3)2·xH2O and Zn(NO3)2·6H2O with ethylene glycol monomethyl ether (Daejung). For the division of ratios, IZO solutions were prepared by mixing the In precursor solution and Zn precursor solution in proportions of 8:2, 5:5, and 2:8. These processes resulted in a 0.1 M solution of IGZO and a 0.1 M solution of IZO. After stirring, they were stored in a humidity desiccator for more than a day before usage.
Kim Y.B., Jeong J.H., Park M.H., Yun J.M., Ma J.H., Ha H.J., Kang S.J, & Kang S.J. (2024). Low-Power Phototransistor with Enhanced Visible-Light Photoresponse and Electrical Performances Using an IGZO/IZO Heterostructure. Materials, 17(3), 677.
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4

Synthesis of Highly Luminescent Colloidal Nanocrystals

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Copper(I) acetate (CuOAc, 97%), indium nitrate
hydrate (In(NO3)3·H2O, 99.99%),
1-dodecanethiol (DDT, 98%), trioctylphosphine oxide (TOPO, 99%), 1-octadecene
(ODE, 90%), trioctylphosphine (TOP, 90%), zinc acetate (Zn(OAc)2, 99.99%), oleic acid (OA, 90%), hexadecylamine (HDA, 90%),
oleylamine (OLAM, 70%), trioctylamine (TOA, 98%), sulfur (S, 99.998%),
nitric acid (HNO3, 69.5%), anhydrous toluene, methanol
and butanol were purchased from Sigma-Aldrich. Lumogen red 305 (Article
No.: 94720) was from Kremer Pigmente GmbH & Co. KG. TOPO, ODE,
OA, HDA, OLAM and TOA were degassed at 120 °C for overnight prior
to synthesis. Other reagents were used as received. The chemicals
were weighted and handled inside a glovebox.
Xia C., Winckelmans N., Prins P.T., Bals S., Gerritsen H.C, & de Mello Donegá C. (2018). Near-Infrared-Emitting CuInS2/ZnS Dot-in-Rod Colloidal Heteronanorods by Seeded Growth. Journal of the American Chemical Society, 140(17), 5755-5763.
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5

Synthesis of Indium-Tin Oxide Nanoparticles

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The chemicals used in this study were indium
nitrate hydrate (In(NO3)3·xH2O, 99.99%, Sigma-Aldrich), tin chloride dihydrate (SnCl2·2H2O, ≥98%, Sigma-Aldrich), ethylenediaminetetraacetic
acid (H4EDTA, ≥99%, Sigma-Aldrich), polyethylenimine
(PEI, branched, Mw = ∼25,000, Sigma-Aldrich),
and ammonia solution (25.0–30.0%, Samchun). Deionized water
(DI water) was obtained using an 18.2 MΩ (VIVAGEN EXL3) system.
Park G., Kim D., Kim G, & Jeong U. (2022). High-Performance Indium–Tin Oxide (ITO) Electrode Enabled by a Counteranion-Free Metal–Polymer Complex. ACS Nanoscience Au, 2(6), 527-538.
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6

Synthesis of Perovskite Thin Films via Solution Processing

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Indium nitrate hydrate (In(NO3)3·xH2O, 99.999%) powder, N,N-dimethylacetamide (DMAC, 99.5%) were purchased from Sigma-Aldrich. 2-methoxyethanol (2-ME, 99.3%), acetylacetone (AcAc, 99%) and ammonium hydroxide (NH3·H2O, 28%) were obtained from Alfa Aesar. Formamidinium iodide (FAI, >98.0%), Methylammonium iodide (MAI, >99.0%), Cesium iodide (CsI, >99.0%), Lead (II) iodide (PbI2, 99.99%), Methylammonium bromide (MABr, >99.0%) and Lead(II) bromide (PbBr2, 99.99%) were purchased from Tokyo Chemical Industry Co. Ltd (TCI). Temozolomide (DMSO, 99%), N,N-Dimethylformamide (DMF, 98%) and chlorobenzene (CB, 99.8%) were purchased from J&K Scientific. Dichloromethane (DCM) was obtained from Innochem Science & Technology Co., Ltd. Colorless polyimide (CPI) powder was from Zhejiang OCAs New Materials Co. Ltd. Silicon wafer with 100 nm thick SiO2 layer was obtained from Silicon Valley Microelectronics, Inc. Isopropyl alcohol (AR, 99.7%), acetone (AR, 99.5%) and hydrochloric acid (HCl; AR, 36–38%) were provided by China National Medicines Co. Ltd. (Shanghai, China). Poly(perfluoroalkyl vinyl ether) (CYTOP) was purchased from Asahi glass company (Japan) and consisted of CTL-809M (solute) and CT-Solv.180 (solvent). Polymethyl methacrylate (PMMA, 495 K A2) was purchased from Kayaku Advanced Materials.
Tang Y., Jin P., Wang Y., Li D., Chen Y., Ran P., Fan W., Liang K., Ren H., Xu X., Wang R., Yang Y.(, & Zhu B. (2023). Enabling low-drift flexible perovskite photodetectors by electrical modulation for wearable health monitoring and weak light imaging. Nature Communications, 14, 4961.
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7

One-pot Synthesis of Ternary Metal Oxide

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Indium nitrate hydrate (In(NO3)3·x(H2O)), gallium nitrate hydrate (Ga(NO3)3·x(H2O)), and zinc acetate dehydrate (Zn(CH3COO)2·2(H2O)) were purchased from Sigma-Aldrich. All precursors were dissolved in a 2-methoxyethanol solvent with molar concentrations of 0.085:0.0125:0.0275 for indium, gallium, and zinc precursors. The solution was vigorously stirred for 12 h at 75 °C before use.
Park S., Lee S., Kim C.H., Lee I., Lee W.J., Kim S., Lee B.G., Jang J.H, & Yoon M.H. (2015). Sub-0.5 V Highly Stable Aqueous Salt Gated Metal Oxide Electronics. Scientific Reports, 5, 13088.
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8

Synthesis of Copper Nanostructures

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Indium nitrate hydrate
(In(NO3)3·xH2O, 99.9%), copper(I)
acetate (CuOAc, 97%), copper acetylacetonate (Cu(acac)2, 97%), copper(I) iodide (CuI, 98%), copper(I) bromide (CuBr, 98%),
copper(I) chloride (CuCl, 99%), 1-dodecanethiol (1-DDT, ≥98%),
oleic acid (OA, 90%), oleylamine (OLAM, 70%), anhydrous toluene, methanol,
butanol, and ethanol were purchased from Sigma-Aldrich and used as
received.
Xia C., van Oversteeg C.H., Bogaards V.C., Spanjersberg T.H., Visser N.L., Berends A.C., Meeldijk J.D., de Jongh P.E, & de Mello Donega C. (2021). Synthesis and Formation Mechanism of Colloidal Janus-Type Cu2–xS/CuInS2 Heteronanorods via Seeded Injection. ACS Nano, 15(6), 9987-9999.
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9

Zeolite Synthesis Protocols

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The following reagents were
used for zeolite synthesis as purchased from Sigma-Aldrich without
further purification: LUDOX AS-40 colloidal silica (40 wt % suspension
in water), sodium aluminate (anhydrous), sodium hydroxide (98% pellets),
zinc nitrate hydrate (98%), gallium nitrate hydrate (99.9%), indium
nitrate hydrate (99.9%), germanium oxide (99.99%), boric acid (99.5%),
magnesium hydroxide (95%), calcium hydroxide (95%), strontium hydroxide
octahydrate (95%), barium hydroxide octahydrate (95%), and zinc oxide
(99.9%). Deionized (DI) water was produced with an Aqua Solutions
purification system.
Mallette A.J., Hong S., Freeman E.E., Saslow S.A., Mergelsberg S., Motkuri R.K., Neeway J.J., Mpourmpakis G, & Rimer J.D. (2022). Heteroatom Manipulation of Zeolite Crystallization: Stabilizing Zn-FAU against Interzeolite Transformation. JACS Au, 2(10), 2295-2306.
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10

Synthesis and Characterization of Thiosemicarbazone Metal Complexes

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All common laboratory chemicals were purchased from commercial sources and used without further purification: 8-hydroxy-2-quinolinecarboxaldehyde, ≥96% (Sigma-Aldrich, St. Louis, MO, USA); thiosemicarbazide, ≥99.9% (Fluka, Buchs, Switzerland); 4-methyl-3-thiosemicarbazide, 97% (Fluorochem, Hadfield, UK); 4,4-dimethyl-3-thiosemicarbazide, ≥98.0% (TCI, Tokyo, Japan); 4-phenyl-3-thiosemicarbazide, 99% (Sigma-Aldrich); gallium nitrate hydrate, 99.9% (Sigma-Aldrich); indium nitrate hydrate, 99.9% (Sigma-Aldrich). NMR was recorded on a Bruker Anova spectrometer at 400 MHz (Billerica, MA, USA), with chemical shift reported in δ units (ppm). NMR spectra were referenced relative to residual NMR solvent peaks. The solvent used in the spectra’s acquisitions is DMSO-d6. The FT-IR measurements were recorded on Nicolet 5PC FT-IR (Rodano, MI, Italy) in the 4000–400 cm−1 range, equipped with the ATR accessory. Elemental analyses were performed using the Thermofisher Scientific Flashsmart CHNS Elemental Analyzer (Rodano, MI, Italy). ESI-MS were recorded on a Waters Acquity Ultraperformance ESI-MS spectrometer with a Single Quadrupole Detector (Sesto San Giovanni, MI, Italy). UV/Vis spectra were collected using a Thermofisher Scientific Evolution 260 Bio Spectrophotometer (Rodano, MI, Italy), using quartz cuvettes of 1 cm path length.
Verderi L., Scaccaglia M., Rega M., Bacci C., Pinelli S., Pelosi G, & Bisceglie F. (2024). New Stable Gallium(III) and Indium(III) Complexes with Thiosemicarbazone Ligands: A Biological Evaluation. Molecules, 29(2), 497.
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