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Acetonitrile acn

Manufactured by RCI Labscan
Sourced in Germany, Thailand

Acetonitrile (ACN) is a colorless, volatile liquid used as a solvent in various analytical and chemical processes. It is a polar aprotic solvent with a low boiling point. Acetonitrile is commonly used in high-performance liquid chromatography (HPLC) and other analytical techniques for the separation and purification of compounds.

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6 protocols using acetonitrile acn

1

Arsenic Speciation Using Poly(MIA) Sorbent

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All used reagents and solvents were of analytical reagent-grade. In order to prepare the poly(MIA) sorbent, glycidyl methacrylate (GMA), trimethylolpropane trimethacrylate (TMPTMA), 2,2′-azobisisobutyronitrile (AIBN), 1-methylimidazole (MIA) (Merck, Darmstadt, Germany), and acetonitrile (ACN) (Labscan, Dublin, Ireland) were used.
High-purity deionized water (DW) produced by the Millipore Milli-Q system (Millipore Corp., Milford, MA, USA) was used to prepare the aqueous solutions for the sorption/desorption experiments. The stock standard solutions of As were: 1000 mg/L As(III) (Fluka, Munich, Germany); 1000 mg/L As(V) (Merck, Darmstadt, Germany); 1000 mg/L monomethylarsonate (MMAs), prepared by dissolving disodium methylarsonate hexahydrate (CH3 AsO(ONa)2·6H2O) (Carlo Erba, Milan, Italy); 1000 mg/L dimethylarsinate (DMAs), prepared by dissolving of sodium cacodylate trihydrate ((CH3)2 As(O)ONa·3H2O) (Sigma Aldrich, St. Louis, MO, USA) in DW. The working standard solutions were prepared weekly and kept refrigerated at 4 °C.
AQUA-1, a drinking water certified reference material (CRM) from the National Research Council Canada (NRC) was used.
The pH of the sample solutions was adjusted with nitric acid or sodium hydroxide solution (Merck, Darmstadt, Germany). The elution solutions were prepared with acetic acid and hydrochloric acid (Merck, Darmstadt, Germany).
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2

U(VI) Ion-Imprinted Polymer Sorbents

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The stock standard solutions of U(VI) were CPAchem, solution of Uranium 10.00 g/L in 5% nitric acid (Stara Zagora, Bulgaria). Working standard solutions were daily prepared by appropriate dilution with deionized water (DW) (Millipore Corp., Milford, MA, USA). All reagents were of analytical-reagent grade.
Methacrylic acid (MAA), trimethylolpropane trimethacrylate (TMPTMA), 2,2′-azobisisobutyronitrile (AIBN), 4-(2-Pyridylazo)resorcinol (PAR, as Na salt), uranyl acetate (UO2(CH3COO)2·6H2O) (Merck, Darmstadt, Germany), and acetonitrile (ACN) (Labscan, Dublin, Ireland) were used to prepare the U(VI) ion-imprinted and non-imprinted polymer sorbents. Hydrochloric acid (Fisher Chemical™, Waltham, MA, USA) was used for uranium desorption. The pH value of water samples was adjusted with NH3 or HNO3.
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3

Metformin-based Cell Viability Assay

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Metformin (1,1-dimethylbiguanide
hydrochloride),
triethylammonium bicarbonate buffer (TEABC), thiazolyl blue tetrazolium
bromide (MTT), tris(2-carboxyethyl) phosphine hydrochloride (TCEP), S-methylmethanethiosulfonate, Tween 20, and Triton X-100
were purchased from Sigma-Aldrich (St. Louis, MO, USA). Acetonitrile
(ACN) was purchased from Lab-Scan. Sequencing grade modified trypsin
was purchased from Promega (Madison, WI, USA). Dimethyl sulfoxide
was purchased from Scharlau Chemie (Barcelona, Spain).
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4

Analytical Standards for Compound Analysis

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The standard compounds of umbelliferone, scopoletin, and celecoxib were purchased from Biomart Biotechnology Ltd. (Beijing, China). Acetonitrile (ACN) and methanol of chromatography grade were purchased from Lab-scan (Bangkok, Thailand). All aqueous solutions were prepared using ultra-pure water with a Milli-Q water purification system from Millipore (MA, United States). All chemicals not otherwise mentioned were purchased from Sigma-Aldrich (MO, United States) and were used without further purification.
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5

UHPLC-MS and NMR Analysis of Compounds

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Two different ultra-performance liquid chromatography-mass spectrometers were used: Agilent 1290 Infinity UHPLC system coupled to an Agilent 6530 Accurate-Mass Quadrupole Time-of-Flight Mass Spectrometer with Dual Electrospray Ionization Source (Agilent, CA, United States); and Waters ACQUITY UPLC I-Class PLUS System coupled to a Waters SQ Detector 2 with Electrospray Ionization Source (Waters, MA, United States). The Nuclear Magnetic Resonance (NMR) spectra were performed using a Bruker AVANCE-500 (Bruker Corporation, Germany), and the chemical shifts were referenced to tetramethylsilane (TMS). Column chromatography (CC) was run on silica gel 60 (230–400 mesh, Merck, Germany), and Sephadex LH-20 (GE Healthcare Bio-Sciences AB, Sweden). Thin layer chromatography (TLC) analysis was carried out using silica gel 60 F254 (TLC) plates (Merck, Germany). MS-grade methanol (MeOH) and acetonitrile (ACN) were obtained from RCI Labscan, Ltd. (Bangkok, Thailand). Formic acid was purchased from Thermo scientific, Inc. (Rockford, IL, United States). Ultrapure water was prepared with a Milli-Q system (Millipore, France).
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6

Crystallization of Organic Compounds

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The objects of the study: benzamide (BZA, C7H7NO, 99%), 4-hydroxybenzamide (4-OH-BZA, C7H7NO2, 98%), were obtained from Sigma–Aldrich. Carbamazepine (CBZ, C15H12N2O, 98%) and isonicotinamide (INAM, C6H6N2O, 99%) were purchased from Acros Organics.
The solvent, acetonitrile (ACN), was from RCI Labscan and used as received without further purification. All solvents used for the crystallization experiments were of analytical grade.
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