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Absolute ethanol

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Absolute ethanol is a pure, anhydrous form of ethanol. It is a clear, colorless, volatile liquid with a characteristic odor. Absolute ethanol is used as a solvent, disinfectant, and as a raw material in various chemical and pharmaceutical applications.

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760 protocols using absolute ethanol

1

Synthesis and Modification of Nanoparticle-Silica

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All chemicals, except absolute ethanol, were obtained commercially from Sigma Aldrich (Munich, Germany) and used without further purification. absolute ethanol was purchased from Merck (Darmstadt, Germany).
NPSNPs were prepared by adding 3.16 g cetyltrimethylammonium bromide (CTAB) and 0.23 g diethanolamine (DEA) to a solution of 75 mL ultrapure water and 13.4 mL absolute ethanol. The mixture was heated to 40°C and stirred. After 30 min, 8.56 mL tetraethoxysilane (TEOS) were added and the reaction mixture was stirred for additional 2 h. The product was centrifuged (30 min at 18000 g) and washed twice with water and once with ethanol. Afterwards, the particles were dried overnight at 60°C. To remove the structure-directing agent, a calcination for 5 h at 550°C (heating rate: 1 K min-1) followed [58 ].
The amino modification of the silica surface was performed via post-grafting by dispersing 500 mg of NPSNPs in 20 mL toluene. To this dispersion 75 μL 1,8-diaza-bicyclo[5.4.0]undec-7-ene (DBU) and 95 μL 3-aminopropyltrimethoxysilane (APTMS) were added. Afterwards, the solution was stirred for 2 h at 80°C. The modified nanoparticles were collected by centrifugation, washed three times with ethanol and dried at 60°C [52 ].
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2

ORMOSIL Coatings Preparation Protocol

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In this paper, analytical grade chemicals were used such as absolute ethanol (Sigma-Aldrich, St. Louis, MO, USA), N-(2-aminoethyl)-3-(trimethyloxypyrite) propylamine (N-(2-Aminoethyl)-3-(trimethoxysilyl) propylamine, Ζ 6020, Sigma-Aldrich, St. Louis, MO, USA), epoxy resin (epoxy resin “Araldite GY 257”, GY 257, Ciba-Geigy, Basel, Switzerland), and 2,2′-diaminodyethylamine (2,2′-Diaminodiethylamine, HS 943, Sigma-Aldrich, St. Louis, MO, USA). In addition, the chemicals 5-amino-1, 3, 4-thiadiazole-2-thiol (5-ATDT), and Cerium(III) acetylacetonate were purchased by Acros-Organics, Morris Plains, NJ, USA.
The ORMOSIL coatings were produced by using absolute ethanol (Sigma-Aldrich, St. Louis, MO, USA), N-(2-aminoethyl)-3-(trimethyloxypyrite) propylamine, Ζ 6020, (Sigma-Aldrich, St. Louis, MO, USA), epoxy resin (epoxy resin “Araldite GY 257”, GY 257, Ciba-Geigy, Basel, Switzerland), 2,2′-Diaminodiethylamine, HΥ 943, (Sigma-Aldrich, St. Louis, MO, USA).
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3

Fabrication of a Microfluidic Circuit Board

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The FCB was fabricated as described previously [23 (link)]. Briefly, it was composed of two cast 10 mm and one 15 mm polymethylmethacrylate Poly (methyl methacrylate) (PMMA) plates (Altuglass, Saint-Avold, France), where all connecting channels and fittings for Luer-slip connectors were milled with a CNC micro mill (Datron Neo, Datron AG, Mühltal, Germany). The dimensions of fluidic circuit are shown in Table S2. After milling, the FCB was assembled as follows: both layers of the FCB were thoroughly cleaned using industrial cleaning wipes (Adolf Würth GmbH & Co, Duisburg, Germany), deionized water, absolute ethanol (Sigma-Aldrich, St. Louis, MO, USA) and propanol (Sigma-Aldrich). A solution of acetone (Sigma-Aldrich) in absolute ethanol at a volume ratio of 1:10 was added on top of the connection layer slab and the complementary channel layer slab was then pressed onto the connection layer slab and aligned using alignment pins (DIN 7-ISO 2338). The assembled FCB was then pressed at 1 kN at 55 °C using a hydraulic press (model 3889, Carver Inc., Miami, FL, USA).
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4

Synthesis and Characterization of PEGylated MIL-89

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MIL-89 was prepared as previously described.17 (link)26 (link, link, link, no link found, link, link, link, link, link) Briefly, iron(III) chloride hexahydrate (FeCl3.6H2O) (MW = 270.3; 1 mmol; Sigma Aldrich®, UK) and trans-trans muconic acid (MW = 142.1; 1 mmol; Sigma Aldrich®, UK) were mixed in 10 mL of absolute ethanol (99.5%; Sigma Aldrich®-UK), heated at 100℃ for 15 h in a Parr reactor and the precipitate recovered by centrifugation at 10,500 rpm for 15 min. The sample was purified by serial washes in deionized water and air dried to retrieve the brown precipitate of MIL-89 (10 mg), which was used in further studies.
The PEGylated form of MIL-89 (MIL-89 PEG) was prepared as above with the following modifications; FeCl3.6H2O (MW = 270.3; 1 mmol; Sigma Aldrich®, UK), trans-trans muconic acid (MW = 142.1; 1 mmol; Sigma Aldrich®, UK) and alpha-methoxy-omega-amino poly(ethylene glycol) (PEG-MW 5.000 Da; IRIS Biotech-Germany) were dissolved in 10 mL of absolute ethanol (99.5%; Sigma Aldrich®, UK), heated to 100℃ for 6 h and centrifuged to retrieve the creamy color precipitate. The sample was washed with deionized water, air-dried, and ground to a fine powder (50 mg) for use in further studies (see below).
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5

Orlistat Preparation and In Vivo Dosage

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For in vitro experiments, the 40 mM orlistat stock solution was obtained by dissolving a Xenical capsule in 6 ml absolute ethanol (Merck) and stored at −20 °C. For in vivo treatment, orlistat was dissolved in 33% absolute ethanol and 66% PEG400 (Sigma). The mice were treated with 240 mg/kg body weight/day24 (link).
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6

Antioxidant Assay of Fruit Waste

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Ascorbic acid, 2,2-diphenyl-1-picrylhydrazyl (DPPH) reagent powder and absolute ethanol were purchased from Merck (Germany), where the aqueous ethanol was prepared by mixing the absolute ethanol and distilled water at right composition (54%). Choline chloride was purchased from Sigma-Aldrich (Germany). All chemicals and reagents used were of analytical grade. The fresh fruits of M. pajang were collected from a retailer in Sarawak, Malaysia. The fruit wastes of the fruit (peels and kernels) were separated and dried at 60 for 24 hours. The dried fruit wastes were grounded into fine powders, kept in an air-tight container and stored in a freezer (-20 ) until further analysis (Abu Bakar et al., 2009) (link).
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7

Substrate Preparation for Surface Studies

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Gold-coated substrates (1 × 1 cm2), obtained from Instituto de Engenharia de Sistemas e Computadores–Microsistemas e Nanotecnologias, Portugal (INESC-MN), were prepared by the deposition of a thin layer of chromium (2.3 nm) and gold (37 nm) on silicon wafers as previously described [40 (link)]. Immediately before use, gold substrates were cleaned with fresh ‘‘piranha’’ solution [7 parts concentrated sulfuric acid (95 vol.%, BDH Prolabo, VWR- International), 3 parts hydrogen peroxide (30 vol.% Merck, Darmstadt, Germany)] for 5 min (caution: this solution reacts violently with many organic materials and should be handled with care). Gold-coated substrates were then rinsed sequentially with absolute ethanol (99.8%, Merck), Type II water (purified and deionized: Resistivity > 1 MΩ/cm; Conductivity < 1 µS/cm; Total organic carbons < 50 ppb) and absolute ethanol once again in an ultrasonic bath for 2 min, followed by drying with a gentle argon stream.
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8

Extraction and Purification of Bacterial sec-RNA

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The supernatant of bacteria cells grown at 37 °C to an OD600nm = 1.0 was obtained by centrifugation at 16,000× g for 3 min. The supernatant was sterile filtered using 0.22 µm filter (Merck, Darmstadt, Germany). Extraction of sec-RNA (secreted RNA) was done by adding 1:1 ethanol absolute (Sigma) to cell-free supernatant and overnight precipitation at −20 °C. RNA was collected by centrifugation at 4 °C for 45 min at 6000× g. The miRNeasy Mini Kit (Qiagen) was used for RNA isolation.
The SecA2/SecA1 protein solution was incubated with phenol/chloroform isoamylalcohol (Roth) for 5 min at RT. The aqueous phase, that contains the SecA2/SecA1-associated RNA, was separated by centrifugation at 16,000× g at 4 °C for 15 min and mixed with 3 M sodium acetate pH 4.8–5.2 (10%) and 1 volume cold ethanol absolute (Sigma) over night at −20 °C. SecA2/SecA1-associated RNA was collected by centrifugation, dried, and resuspended in RNase-free water and stored at −80 °C.
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9

Characterization of Essential Oil Compounds

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2-Hydroxypropyl-β-cyclodextrin (HP-β-CD) was supplied by Roquette (Lestrem, France), and hydrogenated soybean Phospholipon 90H was purchased from Lipoid GmbH (Ludwigshafen am Rhein, Germany). Eugenol (Eug), eugenyl acetate (Eug-Ac), thymol, absolute ethanol, cholesterol, and methanol-HPLC grade were purchased from Sigma–Aldrich (Darmstadt, Germany). CEO (essential oil from Syzygium aromaticum), having as the main compounds Eug (86.89%), Eu-Ac (2.91%), trans-caryophyllene (9.04%), α-caryophyllene (0.97%), and the butyl acetate (0.09 %), was bought from a clove essential oil producer located in Valença (BA, Brazil). LEO (essential oil from Lippia sidoides), having thymol (68.5%), p-cimeno (9.43%), trans-caryophyllene (7.72%), β-myrcene (2.84%), γ-terpinene (2.71%), α-terpinene (1.16%), and thymol methyl ether (0.97%) as the main compounds, was obtained from PRONAT (Produtos Naturais Ltd.a, Recife, PE, Brazil).
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10

Visualizing Fly Bristle Morphology via SEM

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Ore-R adult female flies within one week after eclosion were used for visualizing the external morphology of the bristle using SEM. Anesthetized flies of the desired genotypes were deprived of their wings and legs, washed in standard saline solution three times, and stored in absolute ethanol (99.8%, Sigma-Aldrich) at RT. Dehydrated samples were critical point dried (EM CPD300, Leica Microsystems) and mounted with their dorsal side up on a stub using carbon tape and silver paint. Samples were sputter coated (Q150RS Plus, Quorum Technologies) with platinum at approximately 3 nm thickness. Images were collected on a JCM-6000Plus (JEOL) SEM using the Everhart-Thornley secondary electron detector at 10 kV.
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