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Iron 3 chloride hexahydrate

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Iron(III) chloride hexahydrate is a chemical compound with the formula FeCl3·6H2O. It is a crystalline solid that is soluble in water and other polar solvents. The compound is commonly used in various laboratory applications, serving as a source of iron(III) ions and as a flocculating agent.

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437 protocols using iron 3 chloride hexahydrate

1

Evaluation of Antioxidant and α-Glucosidase Inhibitory Activities

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Standards of the determined substances: acarbose, chlorogenic acid, epicatechin, quercetin, kaempferol, and rutin, were obtained from Sigma-Aldrich (St. Louis, MO, USA).
The reagents used in the conducted studies are as follows: α-D-glucopyranoside (pNPG), α-glucosidase, acarbose, 2,2-Diphenyl-1-picrylhydrazyl, TPTZ (2,4,6-tripyridyl-S-triazine) and Iron (III) chloride hexahydrate (FeCl3x6H2O), Folin–Ciocalteu’s phenol reagent, sodium carbonate, 2,4,6-tris(2-pyridyl)-1,3,5-triazine (TPTZ, C18H12N6), iron(III) chloride hexahydrate (FeCl3·6H2O), Trolox, α-cyclodextrin (α-CD), β-cyclodextrin (β-CD), and γ-cyclodextrin (γ-CD) were supplied by Sigma-Aldrich, St. Louis, MO, USA. Methanol, isopropanol, and acetone (Super Purity Solvent, Methanol 215 SPS) were supplied by ROMIL Ltd., Cambridge, England.
High-quality pure and ultra-high-quality pure water were prepared using a Direct-Q 3 UV Merck Millipore (Burlington, MA, USA) purification system.
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2

Heterogeneous Iron-Catalyzed Degradation Reactions

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Ciprofloxacin (CIP) and acetaminophen (ACE) were provided by Laproff laboratories (Medellín, Colombia). Acetonitrile, hydrochloric acid, Iron (III) chloride hexahydrate, Iron (II) sulfate heptahydrate, methyl orange (MO), and nutrient agar were purchased from Merk (Darmstadt, Germany). Formic acid was obtained from Carlo Erba (Barcelona, Spain). Peptone and yeast extract powders were purchased from Oxoid (Basingstoke, UK). All the culture media and broths were sterilized at 121 °C using an autoclave. All solutions were prepared using distilled water.
As the heterogeneous iron source, a natural mineral was used. This material was obtained from an iron mine in Colombia (Duitama, Boyacá). It was used without any pretreatment. The specific surface area was estimated at 19.79 m2 g−1 by the Brunauer–Emmett–Teller (BET) theory, and N2 physisorption measurements on a Micromeritics 3Flex apparatus were used for the measurements. The natural mineral contained 81.3% by mass of iron (as iron oxides, mainly hematite with traces of siderite, see Figure S2b) [19 (link)].
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3

Wheat Flour and Chlorella Characterization

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Wheat flour for breadmaking (12.07% of protein (N × 5.7), 12.9% moisture) was purchased from Harinera la Meta S.A. (Valencia, Spain) . Commercial Chlorella vulgaris microalga flour was purchased from Allmicroalgae (Lisbon, Portugal). The DPPH (2,2-diphenyl-1-picrylhydrazyl) was from Sigma Aldrich, USA, whereas TPTZ (2,4,6-tripyridyl-s-triazine) was obtained from Alfa Aesar, GmbH & Go KG, Karlsruhe, Germany. ABTS (2,2'-azinobis(3-ethylbenzothiazoline-6-sulfonic acid), Trolox ((S)-(-)-6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid), and gallic acid were from J&K Scientific GmbH, Pforzheim, Germany. Folin-Ciocalteu reagent, and methanol (HPLC grade) were obtained from Chem-Lab NV, Zedelgem, Belgium. Iron (III) chloride hexahydrate was from Merk, KGaA, Darmstadt, Germany. All the other chemicals used were of analytical grade.
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4

Synthesis and Characterization of Iron-Based Nanoparticles

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Iron (II) chloride tetrahydrate (FeCl 2 .4H 2 O), iron (III) chloride hexahydrate (FeCl 3 .6H 2 O), sodium hydroxide (NaOH), hydrochloric acid (HCl 37%), nitric acid (HNO 3 69%), meso-2,3-dimercaptosuccinic acid (DMSA), methoxy-PEG (molecular weight 550, 2000 and 5000 g.mol -1 ), 3-isocyanatopropyltriethoxysilane (ICPTS), dibutyltin dilaurate (DBTL), n-hexane and tetrahydrofuran (THF) were purchased from Aldrich and used without any further purification. THF was distilled over sodium metal and benzophenone just before use.
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5

Synthesis of Iron Oxide Nanoparticles

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Chemicals were purchased at the highest commercially available purity and were used without further treatment. Iron(III) chloride hexahydrate (97%, FeCl3∙6H2O), sodium borohydride (NaBH4), ammonia solution (35% in water) were obtained from Aldrich (Sigma-Aldrich, Italy).
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6

Magnetic Nanoparticle Synthesis and Separation

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Chemicals were purchased at the highest commercially available purity and were used without further treatments. Iron(III) chloride hexahydrate (97%), sodium borohydride (NaBH4), ammonia solution (35% w/w), hydrogen peroxide (H2O2), uric acid and xanthine were obtained from Aldrich (Sigma-Aldrich, Milan, Italy). A series of Nd-Fe-B magnets (N35, 263–287 kJ/m3 BH, 1200mT flux density by Powermagnet—Mannheim, Germany) was used for the magnetic control of nanoparticles (magnetic driving and separations).
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7

Magnetically-Controlled Microenvironment for Cellular Studies

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Iron(II) chloride tetrahydrate (FeCl2∙4H2O, 99.0%, Aldrich), iron(III) chloride hexahydrate (FeCl3∙6H2O, 99.0%, Aldrich), sodium hydroxide (NaOH, Daejung), poly(diallyldimethylammonium chloride) (PDADMAC, MW: 100,000–200,000, 20 wt%, in H2O, Aldrich), tetramethyl orthosilicate (TMOS, 99%, Aldrich), sodium phosphate dibasic (Na2HPO4, 99%, Aldrich), sodium dihydrogen phosphate (NaH2PO4, 99%, Aldrich), sodium chloride (NaCl, 99%, Jin Chemical), 11-mercaptoundecanoic acid (MUA, 95%, Aldrich), sulfuric acid (H2SO4, 95%, Junsei), hydrogen peroxide (H2O2, 30–35%, Junsei), hydrochloric acid (HCl, 35%, Junsei), fluorescein diacetate (FDA, Aldrich), Cell TrackerTM Green CMFDA (Invitrogen), Cell TrackerTM Violet BMQC (Invitrogen), Cell TrackerTM Orange CMRA (Invitrogen), yeast-extract-peptone-dextrose broth (YPD broth, Duchefa Biochemistry), yeast-extract-peptone-dextrose agar (YPD agar, Duchefa Biochemistry), absolute ethanol (99.8%, Merck), and acetone (99.8%, Merck) were used as received. Ultrapure water (18.3 MΩ∙cm) from the Human Ultrapure System (Human Corp.) was used. Permanent neodymium magnets (110 mT (15 × 10 × 1 mm), 270 mT (15 × 10 × 4 mm), and 320 mT (D30 × 10 mm), Umagnet) were used.
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8

Synthesis of Gadolinium-Labeled Dextran Nanoparticles

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All chemicals and solvents were of reagent grade and were used without additional purification unless stated otherwise. The Milli-Q water was produced from a Millipore system Milli-Q ≥ 18 MΩcm (with a Millipak membrane filter of 0.22 μm). Iron(III) chloride hexahydrate (FeCl3·6H2O), iron(II) chloride tetrahydrate (FeCl2·4H2O), sodium sulfite (NaSO3), ammonia solution (NH3 aqua, 25%), hydrochloric acid (HCl, 37%), sodium hydroxide in pellets (NaOH), tetrachloroauric(III) acid trihydrate 99% (HAuCl4·3H2O), sodium borohydride (NaBH4), gadolinium(III) chloride (GdCl3·6H2O), and dextran (Dx) from Leuconostoc mesenteroides (average mol wt. 9.000–11.000) were commercially acquired from Aldrich Chemical ( St. Louis, MO, USA).
The ligand 2-[4,7-bis(carboxymethyl)-10-[2-(3-sulfanylpropanoylamino)ethyl]-1,4,7,10-tetrazacyclododec1-yl]acetic acid (TDOTA) was synthesized as previously reported.16
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9

Salmonella Antibody Detection Assay

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Sodium citrate, polyacrylamide, Iron(III) chloride hexahydrate, urea, 3-amino-propyltriethoxysilane (APTES), glutaraldehyde, and Tween 20 were purchased from Aldrich (St. Louis, Missouri) and were used without further purification. Deionized water (18.3 MΩ cm−1) was obtained using a reverse osmosis water purification system and was used to prepare the phosphate buffer (PB) solution. Monoclonal Salmonella antibody and goat anti-mouse IgG antibody were purchased from Abcam Inc. (Cambridge, Massachusetts).
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10

Synthesis of Surfactant-Coated Magnetite Nanoparticles

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For the synthesis of surfactant coated magnetite nanoparticles, iron(iii)chloride hexahydrate (FeCl3·6H2O), iron(ii)chloride tetrahydrate (FeCl2·4H2O), citric acid (C6H8O7), and oleic acid (C18H34O2) are purchased from Aldrich Chemicals and ammonium hydroxide (NH4OH i.e. 30% NH3), acetone (C3H6O), and toluene (C7H8) are purchased from Merck Chemicals and used as received without any further purification. Distilled water was used throughout the synthesis procedure.
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