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12 protocols using n propylamine

1

Functionalized Nanomaterials Synthesis Protocols

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Tetraethyl orthosilicate (TEOS, 98%), (3-aminopropyl) triethoxysilane (APTES, 99%), and octadecyltrichlorosilane (OTS, ≥ 90%) were purchased from Sigma-Aldrich (NSW, Australia). Acetone, ethanol (EtOH), methanol (MeOH), acetonitrile (ACN), carbonyldiimidazole, chloroform (CHCl3), cyclohexane, toluene, beta-cyclodextrin (β-CD), cetyltrimethylammonium bromide (CTAB), dimethylformamide (DMF), sodium dodecyl sulfate (SDS), polyvinylpyrrolidone (PVP), n-propylamine, ammonium bicarbonate (NH4HCO3), ammonium hydroxide solution (28–30% NH3), formic acid (FA, ≥ 95%), n-propylamine, TRIS hydrochloride (Tris–HCl), DL-dithiothreitol (DDT), polystyrene sulfonate (PSS), poly(diallyldimethylammonium chloride) (PDDAC), trypsin, bovine serum albumin (BSA, ≥ 98%), and indole-3-acetic acid sodium salt (IAA, ≥ 98%) were obtained from Sigma-Aldrich. Unless otherwise stated, all reagents used were at least of analytical reagent grade. Ultrapure Milli-Q water (MQW) was supplied by a Milli-Q purification system (Millipore, Bedford, MA, USA). Stock standard solutions (2000 µg mL−1) of phenones (butyrophenone, valerophenone, and hexanophenone), non-steroidal anti-inflammatory drugs (NSAIDs) including ketoprofen, ibuprofen, and fenbufen, and racemic analytes (dichlorprop) were prepared in methanol.
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2

Synthesis and Characterization of Dental Composites

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Bisphenol A glycidyl dimethacrylate (Bis-GMA) and triethylene glycol dimethacrylate (TEGDMA) were obtained from Esstech (Essington, PA, USA) and used as received. N,N-dihydroxy ethyl-p-toluidine (DHEPT), ethylene-maleic anhydride (EMA), ammonium chloride, resorcinol, formaldehyde, bovine serum albumin (BSA), camphorquinone (CQ), ethyl 4-(diamethylamino) benzoate (4E), 2-Methacryloylothelxyethyl-phosphorylcholine (MPC), 3 methacryloxypropyltrimethoxysilane, and N-propylamine purchased from Sigma-Aldrich (Saint Louis, MO, USA) were used without further purification. Barium boroaluminosilicate glass particles were obtained from Caulk/ Dentsply (Milford, DE, USA).
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3

Facile Synthesis of CuO Nanoparticles

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CuO NPs were synthesized using copper acetate hydrate [Cu(CH3•COO)2•H2O], n-propyl amine [CH3–(CH2)2–NH2], and sodium hydroxide (NaOH), purchased from Sigma-Aldrich and used as received. In a typical experiment, 0.3 M of copper acetate hydrate and 20 mL of n-propyl amine were mixed in 100 mL of MeOH with constant stirring, after which the solution turned blue. NaOH (0.1 M) was mixed into the solution in steps and shaken each time to ensure complete mixing. After adding the NaOH, the pH of the solution, checked via a pH meter (Cole Parmer), was 12.01 because of the increased basicity of the solution. The solution was transferred to a double-necked refluxing pot and refluxed at ~90°C for 6 h. As the temperature of the solution increased, the color changed from blue to dark brown to black. After the reaction was complete, the product was centrifuged at 3,000 rpm for 3 min and washed repeatedly with MeOH, EtOH, and acetone to remove the intermediate by-products. The material was dried at room temperature in a glass Petri dish and utilized for further chemical, morphological, and biological studies.
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4

Synthesis and Characterization of Thermoresponsive Polymers

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N-isopropylacrylamide (NIPAM; Sigma-Aldrich Chemie GmbH Munich, Germany; purity 97%) and N-isopropylmethacrylamide (NIPMAM; Sigma-Aldrich, Chemie GmbH, Munich, Germany; purity 97%) were purified by recrystallisation from hexane. The cross-linker N,N’-methylenebisacrylamide (BIS; Sigma-Aldrich Chemie GmbH, Munich, Germany; purity 99%), the initiator ammonium persulfate (APS; Sigma-Aldrich Chemie GmbH, Munich, Germany; purity ≥ 98%) and pyrene (Sigma-Aldrich Chemie GmbH, Munich, Germany; purity ≥ 99%) were used without further purification. For all experiments, purified water from an Arium®pro VF system (Sartorius AG, Göttingen, Germany) was used.
N-n-propylacrylamide (NNPAM) was synthesized via a Schotten–Baumann reaction published by Hirano et al. [21 ]. For this reaction, acryloylchloride (Sigma-Aldrich Chemie GmbH, Munich, Germany; purity 98%), n-propylamine (Fluka, Sigma-Aldrich Chemie GmbH, Munich, Germany; purity 99%), triethylamine (Grüssing GmbH Analytika, Filsum, Germany; purity 99%) and methylenchloride (p.a.) were used as received. The obtained monomer NNPAM was washed with NaHCO 3 (10 wt %) and dried over MgSO 4 . After filtration, the solvent was evaporated and the product was distilled in vacuum (115 ° C, 10 mbar).
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Synthesis of Metal Oxide Nanoparticles

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KNO3 (Vekton, St Petersburg, Russia, 99.9%), Bi2O3 (Vekton, St Petersburg, Russia, 99.9%), and TiO2 (Vekton, St Petersburg, Russia, 99.9%) were dried at 200, 600, and 1000 °C, respectively. Methylamine (MeNH2, 38% solution in water, Chemical line, St Petersburg, Russia,), ethylamine (EtNH2, 70% solution in water, Merck, Darmstadt, Germany), n-propylamine (PrNH2, Sigma-Aldrich, St Louis, MI, USA, 98%), n-butylamine (BuNH2, 99.9%, Chemical line, St Petersburg, Russia,), n-hexylamine (HxNH2, Sigma-Aldrich, St Louis, MI, USA, 99.9%), n-heptane (ECOS, Moscow, Russia, 99.9%), TBAOH (40 wt. % solution in water, Acros Organics, NJ, USA); polyethyleneimine (PEI, approx. M.N. 60,000, branched, 50 wt. % solution in water, Acros Organics, NJ, USA) were used as received.
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6

Preparation of Arsenic Sulfide Solutions

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As2S3 solutions were prepared by dissolving amorphous As2S3 powder (Alfa Aesar 99.999%) in n-propylamine (Sigma-Aldrich 99.9%) at ten concentrations: 0.01, 0.04, 0.07, 0.1, 0.2, 0.3, 0.4, 0.7, 0.8, and 1.0 moles per liter solvent (mol Lsolv−1). Subsets of these concentrations were used for each kind of measurement, depending on restrictions of the technique. Solutions were prepared in a nitrogen atmosphere glovebox to avoid oxidation and humidity. Each was left for a week to dissolve and passed through a 0.1 μm millipore filter prior to characterization.
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7

Synthesis and Characterization of Siloxane-Based Antimicrobials

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The polymeric siloxane precursor—poly(vinylmethylsiloxane) terminated with trimethyl-silyl groups (VMS-T11; MnGPC = 1800 g/mol, MnNMR = 1000 g/mol, PDI = 1.3)—was purchased from Gelest (Morrisville, PA, USA). Other reagents: thioglyclic acid (≥99%); cysteamine (95%); n-propylamine ((≥99%); 2,2-dimethoxy-2-phenylacetophenone (DMPA, 99%) and silica (high-purity grade, pore size 60 Å, 70–230 mesh) were purchased from Sigma Aldrich (St. Louis, MO, USA) and used as received. Solvents (toluene (Chempur, Karlsruhe, Germany, pure p.a.) and tetrahydrofuran (THF, Chempur, pure p.a.)), were purified according to the literature procedures [62 ].
Trimethylvinylsilane (Me3SiVi, 97%), used for the in vitro tests of antimicrobial activity and for the synthesis of Me3SiCH2CH2SCH2COOH, was purchased from Sigma Aldrich and used as received. Poly(vinylsilsesquioxane) terminated with trimethylsilyl groups (LPSQ) was obtained as previously reported [50 (link)].
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8

Silver Nanoparticle Synthesis Protocol

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All the reagents and solvents were used without further purification. Silver nitrate (AgNO3, 99.99%), sodium citrate, ammonia, tetraethyl orthosilicate (TEOS), 3-(aminopropyl)trimethoxysilane, (APTMS, 97%), toluene, diethyl ether, dichloromethane, dansyl chloride (5-(dimethylamino)naphthalene-1-sulfonyl chloride, DNS-Cl), triethanolamine, n-propylamine, methylene chloride, triethylamine were purchased from Sigma-Aldrich (Poznan, Poland). All the samples were prepared using deionized water. Silver mirrors were purchased from Thin Metals Films Ltd. (Basingstoke, UK).
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9

Synthesis of Semiconductor Nanocrystals

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Di-n-octylamine (+98%), di-n-pentylamine
(99%), di-n-propylamine (99%), diethylamine (>99.5%),
phenethylamine
(≥99%), n-dodecylamine (≥99%), n-octylamine (+99%), n-pentylamine (+99%), n-propylamine (+98%), Cd(OAc)2·2H2O (>98%), trin-octylphosphine (TOP) (97%), and
oleylamine
(or cis-9-octadecenylamine, technical grade, 70%) were obtained from
Sigma-Aldrich. Selenourea (99.9%, metal basis) was obtained from Alpha
Aesar. All were used as received and stored under N2. Toluene
was obtained from Sigma-Aldrich (CHROMASOLV for HPLC, ≥99.9%).
Transmission electron microscopy (TEM) sample grids (Cu with holey
carbon film) were obtained from Ted Pella, Inc.
All synthetic
procedures were conducted under dry N2, except the final
washing steps, which were conducted in the ambient atmosphere. The
reaction mixtures were not stirred. The synthetic products were generally
stored as reaction mixtures, after addition of TOP (see below).
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10

Electrode Material Synthesis and Characterization

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Nb2O5, K2CO3, n-Propylamine, dopamine (DA), N-methyl-2-pyrrolidone (NMP), poly-vinylidene fluoride (PVDF), and conductive carbon black were purchased from Sigma-Aldrich. A liquid electrolyte consisting of 1 M LiPF6 in ethylene carbonate/dimethyl carbonate/ethyl methyl carbonate (1/1/1, weight ratio) with the addition of 1 wt% vinylene varbonate was provided by Shenzhen Kejingstar Technology Ltd. (Shenzhen, China). Deionized water was used in all experiments, and all of the chemicals were used without being further purified.
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