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8 protocols using butyl alcohol

1

Copper Complexation and Characterization

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Copper (II) acetate (GR for analysis, “Mikhailovsky Plant of Chemical Reagents”, Barnaul, Russia), copper (II) sulfate (GR for analysis, LLC “Khimsnab-2000”, Rostov-on-Don, Russia), copper (II) chloride (CP, LLC Formula, St. Petersburg, Russia), gelatin (Grade P-140, LLC TD-holding, Krasnodar, Russia), sodium hydroxide (GR for analysis, LLC Povolzhye, Dzerzhinsk, Russia), ethyl alcohol (CP, Merck, Germany), propyl alcohol (CP, Merck, Germany), butyl alcohol (CP, Merck, Germany), isobutyl alcohol (CP, Merck, Germany), isopropyl alcohol (CP, Acros Organics, Belgium), phosphoric acid (CP, AO LenReaktiv, Russia), acetic acid (CP, AO LenReaktiv, Russia), boric acid (CP, AO LenReaktiv, Russia), sodium chloride (CP, AO LenReaktiv, Russia), calcium chloride (GR for analysis, AO LenReaktiv, Russia), sodium sulfate (GR for analysis, ORT Khimreaktivy, Russia), phenolphthalein (CP, AO LenReaktiv, Russia), trilon B (CP, AO LenReaktiv, Russia), sodium diethyldithiocarbamate (CP, Chemical Line, Rusia), chloroform (CP, AO LenReaktiv, Russia).
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2

Zebrafish Toxicology Protocol with Analytical Standards

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Soman (98% purity) was obtained from the Chinese Laboratory of Analytical Chemistry (Beijing, China). Pinacolyl methylphosphonate acid (PMPA, >97% purity) and isopropyl methylphosphonate acid (IMPA, internal standard, >97% purity) were purchased from Aldrich (Milwaukee, WI, USA). The structures of those standards are shown in Fig. S1. 2-[(Dimethylamino)methyl]phenol (2-DMAMP, containing phenol, >70% purity), ammonium formate (98% purity), and methyl tert-butyl ether (MTBE, 99.9% purity) were obtained from Sigma-Aldrich (St. Louis, MO, USA). Chromatographic-grade acetonitrile and butyl alcohol were obtained from Merck (Darmstadt, Germany). Ultrapure water (18.2 MΩ cm resistivity) was generated in-house using a Milli-Q System from Millipore (Bedford, MA, USA). The other reagents were obtained from commercial sources and were analytical grade.
Zebrafish (Danio rerio) were purchased from a local aquarium (Huamao Longchang Aquarium Business Department) in Beijing, P. R. China, with a body weight from 0.25 to 0.55 g. They were allowed to acclimate to the laboratory conditions in glass aquaria filled with dechlorinated water for 2 weeks prior to the toxicity or exposure experiments. All the zebrafish feeding and experiments were conducted following the OECD Test Guideline 305 (OECD TG305).31
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3

Characterization of Polysaccharide Mixtures

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Maltodextrin (MD) was provided by Tate & Lyle Ingredients Americas, Decatur, IL (Corn syrup solids: STARDRI DE20). Solvents included ACS/USP-grade 100% ethanol (Pharmco Aaper, Shelbyville, KT) and deionized (DI) water (18.2Ω) produced using a Millipore Direct-Q 5 UV-R water purification system. Microcrystalline cellulose (Avicel PH 101) was purchased from FMC Corp. (Philadelphia, PA) and potato starch (Bob’s Red Mill, Milwaukie, OR) was purchased from a supermarket.
Thin layer chromatography (TLC) silica gel 60 plates were purchased from EMD Millipore (Billerica, MA). Carbohydrate standards for high performance liquid chromatography (HPLC) were purchased from the following vendors: glucose and maltose from Sigma Aldrich Corporation (St. Louis, MO); maltotriose and maltotetraose from Carbosynth Limited, (UK); maltopentaose, maltohexaose, and maltoheptaose from TCI America (Portland, OR). 1-napthol (ReagentPlus ≥99%) and butyl alcohol (≥99%, FCC, FG) were from Sigma-Aldrich (St. Louis, MO); sulfuric acid (ACS-grade anthrone, 99%) from Alfa Aesar (Ward Hill, MA); bicinchoninic acid sodium salt (BCA) from Pierce Chemical Co. (Rockford, IL); and deuterium oxide (99.96%) from Cambridge Isotope Laboratories (Tewksbury, MA).
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4

Cell Morphology Analysis by Microscopy

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The cell morphology experiment was conducted by staining at precise time points according to previous studies.28 (link) Cell morphology on different samples were confirmed by fluorescence microscopy (FM) and FE-SEMS-4800 (Hitachi). As for fluorescence microcopy observation, cells on samples were fixed by 4% paraformaldehyde (Sigma, USA) for an hour after three days of cell culture and then stained by phalloidin (Beyotime, China) for an hour and DAPI (Beyotime, China) for 15 min respectively. Accordingly, the cell morphology was detected by FM (Olympus IX71, Japan) after washing three times for background staining elimination. The cell areas and cell aspects ratio were analyzed by Image J (1.51).
The SEM observation of cells on different samples was also performed. Briefly, after three days of cell culture, the cells on specimens were fixed by 2.5% glutaraldehyde (Solarbio, China) for six hours, washed with PBS and gradient dehydration by 30%, 50%, 70%, 90%, and 100% alcohol respectively. Next, the 100% alcohol was replaced by Butyl alcohol (Sigma, USA) for 10 min, dried at room temperature and observed by field-emission scanning electron microscopy (FE-SEMS-4800 (Hitachi) after gold sputtering.
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5

Lipid Peroxidation and Hydrogen Peroxide Assay

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OVA-albumin from chicken egg white (>98%, grade V), (±)-a-lipoic acid synthetic (>99%), acetovanillone, ferric chloride, 2,3,5-triphenyltetrazolium chloride, acetate buffer (pH = 3,6), hydrochloric acid, thiobarbituric acid, trichloroacetic acid, butylated hydroxytoluene, butyl alcohol, sulfuric acid and other chemical reagents were purchased from Sigma-Aldrich-Poland. A lipid peroxidation (4-HNE) Assay Kit (Item No. ab238538) and a Hydrogen Peroxide Assay Kit (Item No. ab102500) were obtained from ABCAM. An 8-Isoprostane ELISA Kit (Item No. 516351) was obtained from Cayman Chemical Company, Ann Arbor, MI.
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6

Perovskite Solar Cell Fabrication

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Titanium diisopropoxide
bis(acetylacetone) (75 wt % in isopropanol, Sigma-Aldrich), butyl
alcohol (99%, Sigma-Aldrich), TiO2 (Dyesol NT-18, Dyesol,
Australia), absolute alcohol (≥99.5%, Sigma-Aldrich), lead(II)
iodide (99.999% trace metals basic, Sigma-Aldrich), N,N-dimethylformamide (DMF, 99.8%, Sigma-Aldrich),
dimethyl sulfoxide (DMSO, ≥99.9%, Sigma-Aldrich), trimesic
acid (TMA; benzene-1,3,5-tricarboxylic acid, 95%, Sigma-Aldrich),
formamidinium iodide (FAI, greatcellsolar, Australia), methylammonium
bromide (MABr, Sigma-Aldrich), methylammonium hydrochloride (MACl,
Sigma-Aldrich), 2-propanol (anhydrous, 99.5%, Sigma-Aldrich), chlorobenzene
(99.8%, Sigma-Aldrich), acetonitrile (99.93%, Sigma-Aldrich), and
2,2′,7,7′-tetrakis[N,N-di(4-methoxyphenyl)amino]-9,9′-spirobifluorene (spiro-OMeTAD,
99%, Sigma-Aldrich), 4-tert-butylpyridine (98%, Sigma-Aldrich),
bis(trifluoromethane)sulfonimide lithium salt (Li-TSFI; ≥99.0%,
Sigma-Aldrich) were used. All reagents were used as received without
any further purification.
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7

Fabrication of Perovskite Solar Cells

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Firstly, a cleaned FTO glass substrate was treated in TiCl4 (40 mM) at 70 °C for 30 min and washed with deionized water. Next, TiO2 mesoporous scaffold has been prepared from the mixed TiO2 precursor solution including Titanium(IV) ethoxide (Sigma-Aldrich, 12.7 g), concentrated HCl (Merck, 9.7 g), Pluronic P123 (Sigma-Aldrich, 4.0 g), and butyl alcohol (Sigma-Aldrich, 36.3 g). The solution has been dip-coated on the substrate (withdrawing speed; 30 mm/min) and has been subsequently annealed at 450 °C for 1 h. Then, the prepared PbI2 solution (1.4 M) via solving PbI2 in DMSO/DMF (1:9) has been spin-coated on TiO2 mesoporous coated substrate at 2000 rpm for 20 s (during the process, the temperature is kept at 80 °C). To convert the PbI2 film to CH3NH3PbI3, CH3NH3I solution (1 mg mL−1) was prepared in a mixed solvent of isopropanol/cyclohexane (1:9), and then, PbI2 films were immersed into the CH3NH3I solution for 12 h, and the as-prepared methylammonium lead triiodide (MAPbI3) films have been heated at 100 °C for 15 min36 ,37 (link). Finally, a commercial carbon paste composed of carbon black and graphite has been used for preparing the carbon back electrode. The carbon paste has been painted on the perovskite film followed by spraying an ethanol solution of 1H, 1H,2H,2H-perfluouorodecyltriethoxysilane (Sigma-Aldrich, 5% v/v) on the paste and heating at 100 °C for 1 h7 (link).
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8

Synthesis of 1-Butylimidazole from Imidazole

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Imidazole (Him), methyl Imidazole (mim), butyl bromide, 1,4butanesultone, sodium ethoxide, p-nitrophenyl acetate, sulfuric acid (97-98%), and sodium bisulfate used as precursors or reactants were from Sigma-Aldrich. Methanol, sulfuric ether, ethyl acetate, hexane, acetone, butyl alcohol, and dichloromethane used as solvents or eluents were from Sigma-Aldrich. 1-ButylImidazole (bim) was synthesized by reaction of Imidazole with butyl bromide through an aliphatic nucleophilic substitution, following a previously reported method that employs sodium ethoxide for deprotonating the Imidazole, 27, 28 as it described in the ESI. †
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