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Lux i cellulose 5 column

Manufactured by Phenomenex
Sourced in United Kingdom, Germany

The Lux® i-Cellulose-5 column is a high-performance liquid chromatography (HPLC) column designed for the separation and analysis of a wide range of organic compounds. The column features a cellulose-based stationary phase that provides efficient separation and excellent peak shape. The column dimensions and properties are optimized for use in HPLC systems.

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2 protocols using lux i cellulose 5 column

1

Chiral Screening and Optimization of SCRAs

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Initial chiral column screening was carried out using an Agilent Infinity II HPLC system with photodiode array detection (PDA). The selectivity of Lux® Amylose-1, Lux® Cellulose-1-4 columns (all 5 μm, 4.6 × 100 mm) and a Lux® i-Cellulose-5 column (5 μm, 4.6 × 150 mm column) from Phenomenex, UK, were assessed by triplicate 5μL injections of a 0.2mg/mL SCRA racemic mixture standards using 50:50 MilliQ H2O (A) : ACN (B) with a flow rate of 1.0 mL/min. The two most selective chiral stationary phases (CSPs) were identified and optimized column formats selected (Lux® Amylose-1, 3 μm, 2.1 × 150 mm and Lux® i-Cellulose-5, 3 μm, 2.1 × 150 mm). To assess their chromatographic performance in more detail, triplicate 1 μL injections of a 200 μg/mL reference standard solution in both acetonitrile and methanol were made in isocratic mode at 45:55, 50:50, and 55:45 (A:B) with a flow rate of 0.2 mL/min. After optimization and after assessing the SCRAs known to be present in the seized samples to be analyzed, the Lux® Amylose-1 column was used for the analysis of seized samples.
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2

Enantioseparation of Sulfoxide Compounds

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HPLC for obtaining the sulfoxide enantiomers was performed on a Shimadzu instrument composed of LC-10AT and LC-10AS pumps, a SPD-10A UV-VIS detector, a SIL-10A auto injector, a DGU-20A3R degassing unit, a CTO-20AC temperature controller and a SCL-10A system controller (Duisburg, Germany). The LCsolution software was used for instrument control and data acquisition. A Lux i-Cellulose 5 column (150 × 4.6 mm, 5 µm, Phenomenex, Aschaffenburg, Germany) containing cellulose tris(3,5-dichlorophenylcarabamate) as chiral selector in combination with methanol as mobile phase was used. The flow rate was 1.0 mL/min, the temperature was set at 20 °C and detection was carried out at 254 nm. 50 µL of the solutions of the sulfoxides prepared at a concentration of 1,2 mg/mL in methanol, were injected. A minimum of 20 runs were performed for each sulfoxide and the eluate containing the respective enantiomers were pooled followed by evaporation of the solvent under reduced pressure. The compounds were obtained as amorphous off-white to yellow solids. The purity of the isolated enantiomers was estimated by HPLC analysis using the same experimental set-up. The optical rotation of the purified enantiomers was determined in ethanol using a P2000 polarimeter from Jasco (Pfungstadt, Germany).
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