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Pack fa

Manufactured by YMC
Sourced in Japan

YMC-Pack FA is a column packing material designed for flash chromatography. It is composed of spherical silica particles with a high surface area and uniform pore size distribution. The material is suitable for the purification and separation of a wide range of organic compounds.

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3 protocols using pack fa

1

Dissolution Analysis of Mg-St Content and Tablet Hardness

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The content ratio of Mg-St and the tablet hardness were measured in typical poor dissolution samples, A044, A048, A049, A131, B038, B057, B086, and B113 (Table 1). All of these samples were deemed unacceptable in the dissolution test according to Japanese Pharmacopoeia. In these measurements, a sample comprising three tablets were tested per measurement and analyzed using PCA.
The Mg-St determination was carried out by HPLC according to the application data provided by YMC Co., Ltd. (Kyoto, Japan). Using a fatty acid analysis kit, the carboxyl group of Mg-St was converted to 2-nitrophenylhydrazine, enabling highly sensitive detection in the ultraviolet (UV) and visible regions. HPLC analysis was conducted using a YMC-Pack FA (4.6 mm × 250 mm, YMC Co., Ltd., Kyoto, Japan) linked to an HPLC system (Alliance 2695, Waters Corporation, MA, USA) with a UV detector (2487, Waters Corporation, MA, USA). The column oven was kept at 35 °C. The mobile phase was a mixture of dilute hydrochloric acid solution (pH 4–5) and acetonitrile (15:85, v/v). The injection volume was 30 μL. The flow rate was 1.2 mL/min, and the detection wavelength for labeled Mg-St was 230 nm. Margaric acid was added as an internal standard. The analyses were performed in triplicate.
The hardness of the tablets was measured using a digital hardness tester (KHT-40, Fujiwara Scientific Co., Ltd., Tokyo, Japan).
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2

Automated SCFA and Ammonia Analysis in SHIME System

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The SHIME software (Prodigest, ver. 4.2.2) allowed online monitoring of the acid (0.5 M HCl) and base (0.5 M NaOH) consumption that was required to control the pH within the desired interval (6.6–6.9). Subsequently, 10 μL of each supernatant of sampled culture broth was immediately used for ammonia analysis using a Fuji Dri-chem Slide NH3-PII (Fujifilm Wako Pure Chemical Corporation) with Fuji Dri-chem (Fujifilm Wako Pure Chemical Corporation). Next, 200 μL of each supernatant was used for SCFA analysis with YMC-Pack FA (YMC Co., Ltd., Kyoto, Japan). The combined isocratic HPLC UV detector (400 nm) was operated with acetonitrile/methanol/water = 30/16/54 as the mobile phase at a flow rate of 1.2 mL/min at a temperature of 50 °C. After encoding the standard curve, each peak was integrated with the LCsolution software (Shimadzu Corporation, Kyoto, Japan, ver. 3.50).
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3

Efficient Synthesis and Characterization of Vanillin Derivatives

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General. In the following examples, the structures of the synthesized compounds were identified by nuclear magnetic resonance spectroscopy (Bruker AVANCE400 (400 MHz)). GC-MS were measured using 5890SERIESII, 5972SERIES, and 7673CON-TROLLER, all from Hewlett Packard (USA). Vanillin (7) was purchased from Rhodia (France) (now Solvay Aroma Performance, Belgium). Immobilized food-grade lipase preparation of Novozym 435 FG (renamed Lipozyme 435) was purchased from Novozymes (Denmark). All other reagents were obtained from commercial sources and were of the highest purity. The content of MNA (12) in DCT (2) was calculated from the peak Notes: Reactions were carried out at 47 °C in a 50 mol scale under reduced pressure (9.2 kPa) (Table 2, Entry 7).
integral value of the nuclear magnetic resonance spectrum or analyzed using a YMC fatty acid analysis kit (YMC-Pack FA, YMC Co. Ltd, Japan).
Analytical conditions 1. HPLC measurement conditions for VOH (8)
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