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2 hydroxy 2 methylpropiophenone

Manufactured by Merck Group
Sourced in United States, Germany, Italy

2-hydroxy-2-methylpropiophenone is a chemical compound used as an intermediate in the synthesis of various pharmaceutical and other products. It is a colorless crystalline solid with a mild odor. The compound is soluble in common organic solvents. Its primary function is as a building block in chemical reactions and formulations, but no further details on its intended use can be provided in an unbiased and factual manner.

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74 protocols using 2 hydroxy 2 methylpropiophenone

1

Photocurable Microcapsule Synthesis

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Both the inner and outer water phases were 5 wt% poly (vinyl alcohol) solution, while the middle oil phase was the mixture of photoinitiator 2-hydroxy-2-methylpropiophenone, photosensitive monomer ethoxylate trimethylolpropane triacrylate, fluorescent red pigment, and silica nanoparticle-loaded xylene solution, in which the poly (vinyl alcohol), trimethoxy (octadecyl) silane, 2-hydroxy-2-methylpropiophenone, and ethoxylated trimethylolpropane triacrylate were provided by Sigma-Aldrich. The silica nanoparticle-loaded xylene solution was purchased from Jingcai Chemical Co., Guangzhou, China, and the red pigment was bought from Aladdin, Shanghai, China. The deionized water was prepared using the Millipore Milli-Q system, Saint Louis, MO, USA.
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2

Fabrication of Hydrogel Optical Fibers

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Platinum-cured silicone tubes (Cole Parmer) with inner diameters of 250–1000 μm were used as a mold for the core. Precursor solution composed of 80% wt vol−1 PEGDA (700 Da; Sigma Aldrich), 5% wt vol−1 2-hydroxy-2-methyl-propiophenone (Sigma Aldrich) in distilled water was injected in the tube through a syringe adapted with a syringe filter with 0.45 μm pore. The PEG hydrogel was formed by photocrosslinking the solution with exposure to UV (365 nm, 5 mW cm−2; Spectroline) for 5 min. The tube with the crosslinked core was immersed in dichloromethane for 30 min, and then the core was isolated from the swollen tube. The core was immersed in distilled water at least for 1 hour to remove unreacted chemicals. To form the clad layer, the core was immersed in alginate solution (2 % wt vol−1; Sigma Aldrich) and then in calcium chloride solution (100 mM; Sigma Aldrich). This procedure was repeated to form a multi-layer clad. Successful fabrication of the core-clad fiber was checked by phase-contrast microscopy (Olympus).
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3

Fluorescent Carbon Dot Hydrogel Waveguides

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Fluorescent carbon dots were synthesized from citric acid with hydrothermal method following previously reported procedures31 (link), 32 (link) and the obtained solution was used for waveguide fabrication. To fabricate the fluorescent waveguide, the hydrogel precursor was synthesized by mixing degassed aqueous solution of 40% w/v PEGDA (700 Da, Sigma-Aldrich), cardon dots (0–12 × 10−5 % w/v) and 2% w/v 2-hydroxy-2-methyl-propiophenone (Sigma-Aldrich) in deionized water. Afterwards, the precursor was injected in a rectangular glass mold through a syringe and polymerized under UV irradiation (365 nm, 5 mW cm−2) for 5 min. The waveguide was then taken out after removing the cover slide of the mold. For light coupling, a silica multimode fiber (core/clad: 200/215 μm) was pigtailed to the waveguide by embedding a short section (~5 mm) of the fiber tip into the precursor and aligned to its center before photo-crosslinking. Additional epoxy resin was used to reinforce the joint. Optical losses of the waveguides at various thicknesses were measured by integrating the intensity at the width direction from the scattering pattern. To measure the refractive index of the carbon dots incorporated hydrogel, 300 μL of the precursor solution were placed on the prism of a digital refractometer (Atago) and the refractive index was measured after photo-crosslinking.
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4

Thermally Responsive Chiral Liquid Crystal Emulsions

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A temperature-insensitive CLC solution was prepared by mixing nematic LC (E7, Merck) with 2.64% (w/w) of a right-handed chiral dopant (R5011, HCCH). A temperature-responsive CLC solution was formulated by mixing the LC with two right-handed chiral dopants of 19.8% (w/w) of R811 (Merck) and 0.68% (w/w) of R5011. As a gain medium, 0.5% (w/w) of fluorescent dye of PM597 [1,3,5,7,8-pentamethyl-2,6-di-t-butylpyrromethene-difluoroborate complex (TCI)] was doped into the CLC mixtures. The aqueous alignment shell was an aqueous solution of 12% (w/w) of PVA (Mw, 13,000 to 23,000; 87 to 89% hydrolyzed; Sigma-Aldrich) and 7% (w/w) of glycerol (Sigma-Aldrich). The continuous phase was an aqueous solution of 10% (w/w) of PVA. The outer-shell phase was silicone methacrylate monomer (SB4722, Evonik Industries) containing 1% (w/w) of photoinitiator (2-hydroxy-2-methylpropiophenone, Sigma-Aldrich).
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5

Fabrication of Vertical Synaptic Devices

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Processing solvents such as acetone, chloroform, and 2-propanol were purchased from Sigma-Aldrich. P3HT (regioregular, average Mn: 54,000 to 75,000), For photo-patternable ion gel, poly(ethylene glycol)diacrylate monomer and 2-hydroxy-2-methylpropiophenone were also purchased from Sigma-Aldrich. 1-Ethyl-3-methylimidazolium bis(trifluoromethyl sulfonyl)imide ionic liquid was purchased from TCI Chemicals. The azide cross-linker 2Bx was synthesized and confirmed by the nuclear magnetic resonance spectroscopy as previously reported (42 (link), 46 (link)–48 (link)). The electrical properties of the vertical synaptic device and logic gates were measured using a Keithley 4200 electrometer.
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6

Fabrication of Hybrid Nanostructures

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Si wafers (p-type, 100) were purchased from Hissan (South Korea), and AZ GXR-601 (46 cps) photoresist (PR) was purchased from Merck (Germany). Polybutadiene-b-polyethyleneoxide (PBd-PEO; Mn: 1200 for PBd and 600 for PEO) and rhodamine-terminated PBd-PEO were purchased from Polymer Source (Canada), and 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[carboxy(polyethylene glycol)-2000] (DSPE-PEG2000-COOH) was purchased from Avanti Polar Lipids (USA). Polydimethylsiloxane (PDMS) was purchased from Dow Corning (USA) and used by mixing the base and curing agent at a ratio of 10:1. Hexamethyldisilazane (HMDS), perfluorooctyltrichlorosilane (PFOTS), perfluorodecyltrichlorosilane (PFDTS), perfluorododecyltrichlorosilane (PFDDTS), poly(ethylene glycol) diacrylate (PEGDMA; Mn: 1000), 2-hydroxy-2-methyl-propiophenone, poly(ethylene glycol)-block-poly(propylene glycol)-block-poly(ethylene glycol) (Poloxamer 188) solution, 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC), fluorodeoxyglucose (FDG), sucrose, isopropyl β-D-1-thiogalactopyranoside (IPTG), sarkosyl, β-mercaptoethanol, glycerol, imidazole, fluorescein isothiocyanate (FITC), β-galactosidase (β-ga), and all solvents were purchased from Sigma-Aldrich (USA) and used as received.
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7

Magnetic Cellulose Nanocomposite Synthesis

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3-dimethyl (methacryloyloxyethyl) ammonium propanesulfonate (DMAPS, 95%), 2-Hydroxy-2-methylpropiophenone (97%), Iron(II) chloride (FeCl2, 98%), Iron(III) chloride (FeCl3, 97%), Hydrochloric acid (HCl, 37%), Sodium hydroxide pellets (NaOH, 97%), Ammonium hydroxide solution (NH4OH, 30%), Ethanol ( > 98%), N,N′-Methylenebis(acrylamide) (BIS, 99%) and Methacrylic acid (MAA, 99%) were purchased from Sigma-Aldrich Co., Canada. Cellulose nanocrystal (CNC, 94%) was acquired from CelluForce Inc., Canada. Deionized water (DI water, > 16 MΩ cm resistivity) was used in all of the experiments. All the chemicals were used without further purification.
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8

Synthesis and Purification of Mechanofluorescent Probe

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EA, 1,4-butanediol diacrylate (BDA) and 2-hydroxy-2-methylpropiophenone (HMP) were purchased from Sigma-Aldrich. EA and BDA were eluted over activated alumina, whereas HMP was used as received. The mechanofluorescent π-extended anthracene maleimide probe, a Diels-Alder cross-linker (DACL), was synthesized and purified according to previously established procedures (17 (link)). All reagents were sparged with N2 for 45 min and transferred to a N2-filled glovebox.
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9

Preparation of Ionic Hydrogel Sensors

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The ionic hydrogel consisted of 10.45 wt.% acrylamide (Sigma-Aldrich, Inc., St. Louis, MO, USA) as the monomer, 22.66% wt. lithium chloride (Sigma-Aldrich, Inc., St. Louis, MO, USA) for ion induction, 0.007 wt.% N,N′-Methylenebisacrylamide (Sigma-Aldrich, Inc., St. Louis, MO, USA) as the crosslinking agent, 0.06 wt.% 2-Hydroxy-2-methylpropiophenone (Sigma-Aldrich, Inc., St. Louis, MO, USA) as the photoinitiator, and 66.82 wt.% ultra-pure water as the solvent. After thorough mixing, the resulting hydrogel precursor was cast in the sensor mold and crosslinked via exposure to UV light (wavelength 320–500 nm, OmniCure Model S1500, Excelitas Technologies Corp., Waltham, MA, USA). The silicone material was prepared by mixing parts A and B of Ecoflex 00-30 (Smooth-On, Inc., Macungie, PA, USA) with a ratio of 1:1. The mixture was crosslinked at room temperature for four hours to form the silicone encapsulation.
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10

Synthesis of Crosslinked PDMS-PEGDA Hydrogels

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Hydroxy-terminated poly(dimethylsiloxane) (PDMS, viscosity of 65 cSt), acryloyl chloride (≥97% purity), poly(ethylene glycol) diacrylate (PEGDA, Mn = 575), trimethilolpropane ethoxylate triacrylate (ETPTA, Mn ~428), trichloromethane (CHCl3, ≥99.5% purity), dichloromethane (CH2Cl2, anhydrous, ≥99.8% purity) tetrahydrofuran (THF, anhydrous, ≥99.9% purity), triethylamine (Et3N, ≥99.0% purity), K2CO3 (anhydrous, ≥99.0% purity), MgSO4 (anhydrous, 99.5% purity), 4-Dimethylaminopyridine (DMAP, ≥99%), 2-hydroxy-2-methylpropiophenone (HMPP, ≥97% purity), and lithium bis(trifluoromethane)sulfonimide (LiTFSI, 99.95%) were purchased from Sigma-Aldrich (Taufkirchen, Germany city, state country) and used as received.
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