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6 protocols using uv 1601pc spectrometer

1

Spectroscopic Analysis of Dopamine Chlorination

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UV-visible specta for dopamine were collected using a Shimadzu UV – 1601PC spectrometer and UVProbe software (Shimadzu Scientific Instruments Inc., Columbia, MD). All reactions were performed in quartz cuvettes and at 22 °C.
The loss of dopamine fluorescence due to chlorination by HOCl was monitored at an emission wavelength of 315 nm due to excitation at 270 nm (slit width for both wavelengths was 5 nm). These studies were carried out using a Photomultiplier Detection System 710 and the FelixGX software (Photon Technology International, Birmingham, NJ). The reactions were performed in quartz cuvettes and a volume of 2.5 mL at 22 °C.
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2

Comprehensive Leachate and Dust Analysis

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A leachate from LFW and dust samples were prepared in the ratio 1:10 (24 h) in accordance with PN–EN 12457–2: 2006. In leachates from waste and dust as well as in deionized water the following were determined: pH by potentiometric method (Elmetron CPC–501), electrical conductivity (EC) by the conductometric method (Elmetron CPC–501), sulfate(VI) concentration by the turbidimetry with barium chloride and the spectrophotometric method concentration of: chlorides with mercury thiocyanate, fluoride with SPADNS, formaldehyde with phenylhydrazine, phenol with phenyl hydrazine, cyanides with barbituric acid and pyridine, using UV–1601pc spectrometer (Shimadzu) according to Polish standards. Each sample was analyzed in triplicate.
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3

Characterization of Organic Compounds

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Optical rotations were measured on a Perkin-Elmer 343 polarimeter (Perkin Elmer, Waltham, MA, USA). UV spectra were recorded on a Shimadzu UV-1601PC spectrometer (Shimadzu Corporation, Kyoto, Japan) in methanol. CD spectra were measured with a Chirascan-Plus CD spectrometer (Leatherhead, UK) in methanol. NMR spectra were recorded on a Bruker DRX-700 spectrometer (Bruker BioSpin GmbH, Rheinstetten, Germany), using TMS as an internal standard. HRESIMS spectra were measured on a Maxis Impact mass spectrometer (Bruker Daltonics GmbH, Rheinstetten, Germany).
Low-pressure liquid column chromatography was performed using silica gel (50/100 μm, Imid Ltd., Krasnodar, Russia). Plates (5 × 10.0 cm) precoated with silica gel (5–17 μm, Imid Ltd., Krasnodar, Russia) were used for thin-layer chromatography. Preparative HPLC was carried out on a Shimadzu LC-20 chromatograph (Shimadzu USA Manufacturing, Canby, OR, USA) using a YMC ODS-AM (YMC Co., Ishikawa, Japan) (5 µm, 10 mm × 250 mm) column with a Shimadzu RID-20A refractometer (Shimadzu Corporation, Kyoto, Japan).
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4

Characterization of Natural Products

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Optical rotations were measured on a Perkin-Elmer 343 polarimeter (Perkin Elmer, Waltham, MA, USA). UV spectra were recorded on a Shimadzu UV-1601PC spectrometer (Shimadzu Corporation, Kyoto, Japan) in methanol. CD spectra were measured with a Chirascan-Plus CD Spectrometer (Leatherhead, UK) in methanol. NMR spectra were recorded in CD3OD and CDCl3, on a Bruker DPX-500 (Bruker BioSpin GmbH, Rheinstetten, Germany) and a Bruker DRX-700 (Bruker BioSpin GmbH, Rheinstetten, Germany) spectrometer, using TMS as an internal standard. HRESIMS spectra were measured on a Maxis impact mass spectrometer (Bruker Daltonics GmbH, Rheinstetten, Germany).
Low-pressure liquid column chromatography was performed using Si gel L (50/100 μm, Imid, Russia) and Gel ODS-A (12 nm, S – 75 um, YMC Co, Ishikawa, Japan). Plates precoated with Si gel (5–17 μm, 4.5 × 6.0 cm, Imid) and Si gel60 RP-18 F254S (20 × 20 cm, Merck KGaA, Germany) were used for thin-layer chromatography. Preparative HPLC was carried out on aAgilent 1100 chromatograph (Agilent Technologies, USA) using a YMC ODS-AM (YMC Co., Ishikawa, Japan) (5 µm, 10 × 250 mm), YMC ODS-A (YMC Co., Ishikawa, Japan) (5 µm, 4.6 × 250 mm) and Supelco Discovery C-18 (5 μm, 250 × 4.6 mm) columns with a Agilent 1100 refractometer (Agilent Technologies, Santa Clara, CA, USA).
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5

Spectroscopic Characterization of Organic Compounds

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Optical rotations were measured on a Perkin-Elmer 343 polarimeter in MeOH. UV spectra were recorded on a Shimadzu UV-1601PC spectrometer in MeOH. ECD spectra were measured on a Chirascan-Plus CD Spectrometer in MeOH. 1H and 13C NMR spectra were recorded in aceton-d6 on a Bruker Avance-300, Avance-500 and Avance III-700 spectrometers (Bruker BioSpin GmbH) operating at 300 and 75, 500 and 125 MHz and 700 and 176 MHz, respectively. HRESIMS spectra were obtained on a Bruker maXis Impact II mass spectrometer (Bruker Daltonics GmbH). Low-pressure liquid column chromatography was performed using C18-SiO2 Gel ODS-A (12 nm, S—75 um, YMC Co., Ishikawa, Japan) and a Buchi B-688 Chromatography Pump on a Buchi glass column using Si gel KSK (50/100 μm, Imid Ltd., Russia). Plates precoated with Si gel (5–17 μm, 4.5 × 6.0 cm, Imid Ltd., Russia) and Si gel 60 RP-18 F254S (20 × 20 cm, Merck KGaA, Germany) were used for thin-layer chromatography. Preparative HPLC was carried out on a Shimadzu LC-20 (Shimadzu, Kyoto, Japan) and Agilent 1100 (Agilent Technologies, Santa Clara, CA, USA) chromatographs using a Shimadzu RID-20A and Agilent 1100 refractometers and YMC ODS-AM (YMC Co, 5 μm, 250 × 10 mm), Ultrasphere Si (5 μm, 250 × 4.6 mm), and Hydro-RP (Phenomenex, 4 μm, 250 × 10 mm) columns.
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6

Comprehensive Analytical Methods for Natural Products

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Optical rotations were measured on a Perkin-Elmer 141polarimeter. UV spectra were recorded on a Shimadzu UV-1601PC spectrometer in MeOH. CD spectra were measured on a Chirascan-Plus CD spectrometer (United Kingdom) in MeOH and acetonitrile. 1 H and 13 C NMR spectra were recorded in DMSO-d6 on a Bruker DPX-500 (500.13/125.77 MHz) and Bruker DRX-700 (700.00/176.04 MHz) spectrometers, using TMS as an internal standard. HRESIMS spectra were measured on an Agilent 6510 Q-TOF LC mass spectrometer and Maxis impact mass spectrometer (Bruker Daltonics GmbH, Rheinstetten, Germany).
Low pressure liquid column chromatography was performed using silica gel (50-100 µm, Imid Ltd.).
Plates (4.5 x 6.0 cm) precoated silica gel (5-17 μ, Imid Ltd.) were used for thin layer chromatography.
Preparative HPLC was carried out on a Shimadzu LC-20 chromatograph with Shimadzu RID-20A
refractometer, using a YMC ODS-AM (5 µm, 10×250 mm, 1.5 ml/min) and YMC SIL (5 µm, 10×250 mm, 1.5 ml/min) columns.
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