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Dry toluene

Manufactured by Merck Group
Sourced in Germany, France

Dry toluene is a refined aromatic hydrocarbon solvent. It is a clear, colorless liquid with a distinct, sweet odor. Dry toluene is commonly used as a laboratory reagent and in various industrial applications that require a high-purity solvent.

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8 protocols using dry toluene

1

Multifunctional Silica Nanoparticle Synthesis and Characterization

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Hexadecyltrimethylammonium bromide (CTAB), Tetraethyl orthosilicate (TEOS), and dry Toluene were purchased from Sigma-Aldrich. Ammonium hydroxide (NH4OH, 28–30%) from Fluka; (3-aminopropyl)triethoxysilane (APTES), TESPSA, and Fluorescein isothiocyanate, isomer I (FITC) were purchased from Abcr; Absolute Ethanol from Panreac; DBCO-PEG-NH2, and (R)-2-Amino-3-azidopropanoic acid hydrochloride (azide-D-alanine) were purchased from Jena Bioscience Gmbh. N,N'-Diisopropylcarbodiimide (DIC), N-Hydroxysuccinimide (NHS), TAMRA-Azide, Ammonium nitrate (NH4NO3), and Dibenzocyclooctyne-PEG4-Fluor 545 (TAMRA-DBCO) from Sigma-Aldrich.
DMEM, Luria-Bertani (LB) medium, Trypsin, FBS, and Antibiotic-Antimycotic (Anti-Anti) 100x from GIBCO. Rat tail Collagen (type I) Life Technologies S.A.; 10X PBS Buffer solution pH = 7.4 from Ambion. Sodium hydroxide (NaOH), Dimethyl sulfoxide (DMSO), Paraformaldehyde, Phalloidin-Atto 565, 4',6-diamidino-2-phenylindole (DAPI), and Doxorubicin hydrochloride (Dox) from Sigma-Aldrich; Alamar blue solution from Invitrogen. E. coli strain Seattle 1946 (ATCC 25 922) was used as a model of Gram negative bacteria. HT1080 human fibrosarcome cell line was obtained from ATCC (ATCC CCL-121).
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2

Synthesis of Styrene-based Copolymers

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The materials used were the following: styrene-d8, tris[2-(dimethylamino)ethyl]amine (Me6TREN), 2-hydroxyethyl 2-bromoisobutyrate, CuBr2, stannous 2-ethylhexanoate, Al2O3 (Brockmann l, activated, basic), dry toluene, tetrahydrofuran (THF) (all from Sigma-Aldrich), ε-caprolactone (Sigma-Aldrich), trimethylene carbonate (Boehringer Ingelheim), dry tetrahydrofuran (Acros Organics), dry toluene (Acros Organics), methanol (Fisher Scientific), and CDCl3 (Larodan Fine Chemicals). Solvents were used without further purification. Lithium bis(trifluoromethane)sulfonimide (LiTFSI, Purolyte, Ferro Corporation) was dried at 120 °C for 24 h before use. Lithium iron phosphate (LFP, Phostech Lithium), super P carbon black (Erachem), poly(vinylidene fluoride) (PVdF, Kynar Flex 2801-00, Arkema), NMC cathode (MTI), graphite anode (MTI), and aluminium and copper foil were used as received.
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3

Synthesis of Dapsone-Loaded Silica Nanoparticles

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Dapsone, sodium azide, petroleum ether 40–60 °C, absolute methanol, N,N-dimethylformamide dimethyl acetal (DMF-DMA) and dry toluene were procured from Sigma-Aldrich. Tetraethyl orthosilicate (TEOS) and Pluronic F-68 were purchased from Loba Chemie Pvt, Ltd, Mumbai, India. All chemicals and solvents were used without further purification.
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4

Mass Spectrometry Reagent Preparation

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Potassium chloride (KCl, 99.5%) was from AnalaR, Australia. Ethanol (99.5%) was from Asia Pacific Specialty, Australia. Alphacyano-4-hydroxycinnamic acid (CHCA, 99%), acetonitrile (ACN, 99.9%), and trifluoroacetic acid (TFA, 99.8%) were purchased from Merck. Triblock copolymer EO 20 PO 70 EO 20 (denoted P 123 , where EO is poly(ethylene oxide) and PO is poly(propylene oxide)), ammonium bicarbonate (98%), dry toluene, 3-aminopropyltriethoxysilane (APTS, 97%), tetramethylorthosilicate (TMOS, 99%), Trypsin (from bovine pancreas), myoglobin (from horse heart), bovine serum albumin (BSA), beta-casein (from bovine milk), cytochrome C (cyt C, from horse heart), 4-(2-hydroxyerhyl) piperazine-1-erhaesulfonic acid (HEPES, 99.5%), dithiothreitol (DTT, 99.0%), and IAA (iodoacetamide, 98%) were all obtained from Sigma-Aldrich (Schnelldorf, Germany). All buffer and protein solutions were prepared with deionized water from a milli-Q system (Millipore, Bedford, MA, USA).
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5

Synthesis and Characterization of Polymer Nanocomposites

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Polycarbonate (PC, Lexan-143R with MFI of 11 g/10 min) was procured from Sabic (India). PVDF (Kynar-761, with M w of 440 000 g mol -1 ) was kindly provided by Arkema. Nickel ferrite, (NF, NiFe 2 O 4 ) nanoparticles (with average diameter of 50 nm), barium titanate (BT, BaTiO 3 ) (with an average particle size of 100 nm), 3,4,9,10-perylenetetracarboxylic dianhydride (PTCD), imidazole, 4,4′-methylenedianiline (MDA), 3-aminopropyltriethoxysilane (APTS), H 2 O 2 (30% in water), N,N′dicyclohexylcarbodiimide (DCC) and dry toluene were procured from Sigma-Aldrich. N,N-Dimethylformamide, chloroform, and tetrahydrofuran were obtained from commercial sources. Pristine MWNTs (with an average diameter and length of 9.5 nm and 1.5 μm, respectively) were procured from Nanocyl SA (Belgium).
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6

Synthesis of Perfluorinated Polymer Nanoparticles

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D,L-lactide was purchased from Polysciences (Germany) and perfluorohexane (purity>98%) was acquired from Alfa Aesar (Germany). 1-hexanol from Acros Organics (Belgium), 2,2,3,3,4,4-heptafluoro-1-butanol, 1H,1H perfluoro-1-heptanol, 1H,1H perfluoro-1-nonanol, 1H,1H perfluoro-1-dodecanol and 1H,1H perfluoro-1-tetradecanol were acquired from Fluorochem (United Kingdom). Acetone, tetrahydrofuran (THF) and dichloromethane were purchased from Carlo Erba Reactifs (France), chloroform and diethyl ether from VWR (France). Stannous octoate, dry toluene, D 2 O, sodium cholate, trifluoroacetic acid (TFA) and polyvinyl alcohol (PVA, 30-70kDa, 87-90% hydrolyzed) were provided by Sigma-Aldrich (France). Deuterated solvents (CDCl3 and acetone-d) were purchased from Eurisotop (France), Cell culture reagents such as DMEM (Dulbecco's modified Eagle's medium), RPMI 1640 (Roswell Park Memorial Institute medium), FBS (Fetal Bovine Serum), trypsin-EDTA solution and PBS (Ca 2+ and Mg 2+ free phosphate buffer) were purchased from Sigma Aldrich (France). The ultrapure water was produced by a Millipore Synergy 185 apparatus coupled with a RiOs5 TM (Millipore, France) with a resistivity of 18.2 MΩ.cm. The NMR sample tubes and coaxial inserts were obtained from CortecNet (France).
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7

Copper-Catalyzed Silane Surface Functionalization

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Silicon wafers (boron doped, 0–100 Ω cm, and (100) orientation) were purchased from Prolog Semicor (Ukraine). Copper(I) chloride (99.999%), copper(II) bromide (99.999%), [11-(2-bromo-2-methyl)propionyloxy]undecyl trichlorosilane, dry toluene (99.8%), 2-(dimethyl amino)ethyl methacrylate (C8H15NO2), KCl (99%), KI (99%), and KBr (99%) were all purchased from Aldrich and used as received. HPLC-grade acetone and methanol were purchased from Fisher Scientific, and 2,2′-dipyridyl (99%) was purchased from Acros. Non-conductive silicon nitride triangular probes (MLCT, from Brucker) with nominal spring constant 0.065 Nm−1 and radius 20 nm were used for the FFM experiments.
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8

Amino-Functionalization of Mesoporous Silica

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SBA-15 (8 nm pore size) was purchased from Sigma-Aldrich and used without further purification. SBA-15 functionalization was carried out with amino-organosilanes; APTES (purity > 98%) and 3-DEAPTES (96%) were acquired from Sigma-Aldrich. It is worth mentioning that the dryness conditions of the reaction media and material are of paramount importance to prevent extension of lateral silane polymerization within the materials and to allow efficient silane functionalization. To achieve this, typically 2 g of SBA-15 was introduced in a closed reflux apparatus connected to a vacuum line and heated to 150 °C for 2 h. After cooling, nitrogen was introduced into the system prior to the opening of the reflux apparatus, and SBA-15 was refluxed with 100 cm3 of dry toluene (Aldrich, 99.8%) containing 9 mmol of the amino-organosilane for 24 h in a nitrogen atmosphere. The resulting material was purified by Soxhlet extraction with dry toluene, to remove the unreacted amino-organosilanes, and finally dried under vacuum at 120 °C for 24 h. Functionalized materials were named APTES@SBA-15 and DEAPTES@SBA-15.
The thermogravimetric, differential scanning calorimetry experiments, elemental analysis as well as the porous texture characterization of the materials (via N2 adsorption at −196 °C) were performed using the same protocol as described in our previous work46 (link) (details in the ESI).
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