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Tetrahydrofuran thf

Manufactured by Thermo Fisher Scientific
Sourced in United States, United Kingdom, Belgium, Germany, Canada

Tetrahydrofuran (THF) is a colorless, volatile, and flammable liquid. It is a versatile organic solvent commonly used in various industrial and laboratory applications. THF has a cyclic ether structure and is miscible with water and many other organic solvents. It is a widely used solvent for a variety of chemical reactions and processes.

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63 protocols using tetrahydrofuran thf

1

Synthesis and Characterization of Cobalt Ferrite Nanoparticles

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Cobalt chloride (II) hexahydrate (ACS reagent, 98%), iron chloride (III) hexahydrate (ACS reagent, 97%), oleic acid (90%), hexane (ACS reagent, ≥98.5%), diethyl ether (anhydrous, ACS reagent, ≥99%), toluene (ACS reagent, ≥99.5%), and chloroform (for high-performance liquid chromatography, gas chromatography, and residue analysis, ≥99.9%) were purchased from Sigma-Aldrich. 1-Octadecene (90%) was purchased from Acros Organics, and sodium oleate (>97%) was purchased from TCI America. PEG, 5 kDa for ligand exchange, was procured from Sigma-Aldrich, and block copolymer polyethylene glycol-b-poly(lactic acid) PEG4.9kDa-b-PLA6.0kDa was purchased from Evonik Industries. Tetrahydrofuran (THF; 99.9% Acros Organics) was dried using sodium sulfate before use in Flash Nanoprecipitation (FNP). HA sodium salt from Streptococcus equi was purchased from Sigma-Aldrich. Bovine synovial fluid was obtained from Animal Technologies. Water was used from Milli-Q grade (Millipore, Bedford, MA).
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2

Synthesis and Characterization of Tamoxifen Analogues

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4-Bromophenol (97 %), triphenylphosphine (99 %), tris(dibenzylideneacetone)dipalladium(0) (97 %), extra dry on molecular sieves tetrahydrofuran (THF) (99.5 %), 2,2′-azobis(2-methylpropionitrile) (99 %) (AIBN), extra dry on molecular sieves dichloromethane (DCM) (99.8 %) and ethyl acetate (99 %) were all purchased from Acros Organic (Geel, Belgium). Dimethyl acetylenedicarboxylate 98 %, triphenyl arsine (98 %) and tributyl(vinyl)tin (96 %) were all purchased from Alfa Aesar (Karlsruhe, Germany). Magnesium sulphate (98 %), ethanol (99.5 %), sodium hydroxide and concentrated hydrochloric acid (37 %) were supplied by Carlo Erba (Val de Reuil, France.). Sodium fluoride (99 %), sodium chloride (98 %), methacrylic acid (MMA) (99 %), clomiphene citrate (analytical standard 42 % cis and 58 % trans), 4-hydroxy tamoxifen (>70 %) and EGDMA (98 %) were purchased from Sigma Aldrich (France and UK). Tamoxifen citrate (99 %) was purchased from LKT lab Inc. Acetonitrile (99.9 %) (ACN) was obtained from Fischer Chemicals; acetic acid (99.7 %) and methanol (99.9 %) were all HPLC grade and supplied by Carlo Erba (Val de Reuil, France). AIBN was recrystallised from methanol before use. Clomiphene and tamoxifen were isolated from their corresponding citrate salts using sodium bicarbonate (10 mM) and extracted with DCM. Falcon 96-microplates were purchased from SLS.
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3

Optimized Organic Solar Cell Fabrication

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PBDB-T-2F (Mn = 37.0 kDa, Mw = 101.6 kDa, PDI = 2.74), IT-4F, ITIC, and [6,6]-Phenyl-C71-butyric acid methyl ester (PC71BM) were purchased from Solarmer Inc (China). Y6 was received from Prof. Zou Yingping and used without further purification. Diethyl zinc, 1.5 M solution in toluene, and tetrahydrofuran (THF) was purchased from Acros. MoO3, 1-chloronaphthalene (CN), and chloroform (CF) were purchased from Sigma-Aldrich. C60-SAM was purchased from 1-Material Inc. All other materials were purchased and used as received.
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4

In-Situ Silica-Reinforced SSBR Composites

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Solution styrene butadiene rubber (SSBR) BUNA 2525-2 VSL HM containing 25% vinyl content and 25% styrene content was supplied by Lanxess, Cologne, Germany. Tetrahydrofuran (THF), N-butyl amine, sulfur, zinc oxide, and stearic acid were acquired from Acros Organics, Germany. The vulcanizing accelerators N-cyclohexyl 2-benzothioazolesulfonamide (CBS-Vulkacit CZ) and diphenyl guanidine (DPG) were delivered by Lanxess, Germany. The precursor for the in-situ silica generation tetraethoxyorthosilicate (TEOS) was obtained from Sigma Aldrich (Munich, Germany) with a purity of 90%. The precipitated silica (Ultrasil VN-3) exhibiting a BET surface of 175 m2/g and a purity of 99% and the silane coupling agent bis[3-(triethoxysilyl)propyl]tetrasulfide (TESPT) were kindly provided by Evonik Industries, Essen, Germany.
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5

Synthesis and Characterization of Functionalized PNiPAAm

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Poly (glycidyl methacrylate) (PGMA, Mn = 10–20,000 g/mol) was purchased from Sigma-Aldrich (Darmstadt, Germany). Absolute ethanol (EtOH, 99.8%) was acquired from Merck (Darmstadt, Germany). Tetrahydrofuran (THF, 99.98%) and chloroform (CHCl3, ≥99%) were purchased from Acros Organics (Darmstadt, Germany). Purified water (H2O) was used from a Milli-Q Direct-8 system from Merck Millipore (Darmstadt, Germany). All chemicals were used as received, if not otherwise specifically noted. Highly polished single-crystal silicon wafers of {100} orientation (Si-Mat Silicon Materials, Kaufering, Germany) were used as a substrate. End-functionalized PNiPAAm polymers (Mn = 50,200 g/mol, Mw/Mn = 1.28, monomer number of every chain is about 443) with a terminal (tert-butyl protected) carboxy group were synthesized and characterized as described previously [31 (link)].
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6

Synthesis of ZnS/Chitosan-Folic Acid Nanocomposite

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Low molecular weight chitosan (50–190 kDa) with the degree of deacetylation 75–85%, zinc chloride (reagent grade, ≥ 98%) and thiourea (ACS grade, 99%) were purchased from Sigma-Aldrich, USA (St-Louis, MO). Potassium persulfate (99.9% trace metals) and tetrahydrofuran (THF) (99.8%) were purchased from Acros Organics (New Jersey, USA). Ethanol and glacial acetic acid were purchased from Fisher Scientific (Hampton, NH). The proposed synthesis scheme is shown in Fig. 1.

Proposed schematic diagram of the preparation of ZnS/Chitosan-Folic acid.

Fig. 1
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7

Synthesis and Characterization of Ionic Crosslinkers

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Acryloyl chloride (96%, Alfa Aesar), 3-chloro-1-propanol (98%, Sigma Aldrich), 6-chloro-1-hexanol (96%, TCI), 8-chloro-1-octanol (98%, Sigma Aldrich), 1-butylimidazole (99%, abcr), 1-hexylimidazole (>98%, IoLiTec), tetrahydrofuran (THF, 99.5%, Acros Organics, stored over molecular sieve 0.3 nm), triethylamine (≥99.5%, TEA, Sigma Aldrich), diethyl ether (99.5%, ChemSolute), ethyl acetate (≥99.8%, fisher scientific), magnesium sulfate (anhydrous, Alfa Aesar) were used for the synthesis and purification of the monomers. The non-ionic crosslinker N,N’-diethyl-1,3-bis(acrylamido)propane (BAAP) was provided by Ivoclar Vivadent AG (Schaan, FL). The photoinitiator diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (97%, TPO, Sigma Aldrich), the conducting salts tetrabutylammonium chloride (TBACl, 98%, TCI), zinc perchlorate hexahydrate (99.997%, Thermo Fisher Scientific), and 1-hexyl-3-methylimidazolium chloride (>98%, IoLiTec) were used as received. Milli-Q water was used as a swelling agent. Zinc electrodes (99.995%, thickness 0.1 mm, Alfa Aesar), separator Celgard 2500 (thickness 25 µm, CELGARD, North Carolina, U.S.A.), ethylene carbonate (anhydrous, ≥99%, EC, Sigma Aldrich), dimethyl carbonate (anhydrous, 99%, DMC, Sigma Aldrich) and p(TEMPO-methacrylate) (p(TEMPO-MA)) electrodes were prepared in the Jena group according to former work [25 (link)].
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8

Fabrication of Organic Photovoltaic Devices

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Indium tin oxide (ITO) glass substrates were purchased from South China Science & Technology Company Limited (Shenzhen, China). Anhydrous bismuth triiodide (BiI3, >98.0%, anhydrous) was purchased from Tci (Shanghai, China). Copper(I) thiocyanate (CuSCN, 99%) was purchased from Aladdin (Shanghai, China). [6 (link),6 (link)]-phenyl-C71-butyric acid methyl ester (PC71BM) was purchased from Organtec Ltd (Beijing, China). Diethyl sulfide (DES, 97%+) was purchased from Adamas (Shanghai, China). Tetrahydrofuran (THF, 99.5%, extra dry), dimethyl sulfoxide (DMSO, 99.7+%, extra dry), trichloromethane (CF), and chlorobenzene (CB, 99.8%, extra dry) were purchased from Acros (Geel, Belgium). All of the materials were used as received without further purification.
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9

Synthesis and Characterization of Ionic Compounds

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All commercial reagents and solvents were
purchased from either Acros Organics or Sigma-Aldrich and used as
received. Tetrahydrofuran (THF) (99.9%) and N,N-dimethylformamide (DMF) (99.9%) were purchased as anhydrous
from Acros Organics and used as received. Ultrapure water having a
resistivity of 18 MΩ cm was produced using an ELGA Purelab Ultra
filtration device. A JEOL-ECS 400 MHz spectrometer was utilized to
obtain 1H and 13C NMR spectra, and chemical
shift values reported are referenced to residual solvent signals (CDCl3: 1H, 7.24 ppm; 13C, 77.16 ppm; DMSO-d6: 1H, 2.50 ppm; 13C,
39.52 ppm). Elemental analyses were completed by Atlantic Microlab,
Inc. The syntheses of 1-acetoacetoxy-6-bromohexane 4,19 (link) 1,4-bis(6′-acetoacetoxyhexyl)-1,2,4-triazolium
bis(trifluoromethylsulfonyl)imide 10,19 (link) and 1,4-bis(6′-acetoacetoxyhexyl)-imidazolium bis(trifluoromethylsulfonyl)imide 11(17 (link)) have been previously reported.
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10

Polycaprolactone Blends with Starch for Interfacial Agents

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Polycaprolactone (PCL, CAPA 6503, Mw = 50,000) from Solvay Caprolactones, Warrington, UK, was used for the blends and the preparation of the interfacial agents without further purification or drying. Glycidyl methacrylate (GMA, purity of 97%, Aldrich, Zwijndrecht, The Netherlands) as grafting monomer was also used without further purification. Azobisisobutyronitrile (AIBN, purity of 98%, Acros Organics, Landsmeer, The Netherlands) and benzoyl peroxide (BPO, 75% purity, from Merck, Darmstadt, Germany) were used as radical initiators. Carbon dioxide (Linde Schiedam, CO2) and nitrogen (Linde Schiedam, N2) were used during the grafting reaction. Tetrahydrofuran (THF, >99% purity from Acros, Geel, Belgium) and methanol (99.8% purity from Labscan, Dublin, Ireland) were used during the purification process. Potato starch (with 75% amylopectin and 25% amylose) from Avebe, Veendam, The Netherlands, was used in PCL/starch blends after being dried under vacuum for 24 h (110 °C).
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