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Rtx 5

Manufactured by Shimadzu
Sourced in India, Japan

The RTX-5 is a high-performance gas chromatography (GC) column manufactured by Shimadzu. It is designed to provide efficient separation and analysis of a wide range of chemical compounds. The column features a proprietary stationary phase that offers excellent peak resolution and reproducibility, making it a reliable choice for various analytical applications.

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4 protocols using rtx 5

1

CO2 Fixation using Quaternary Ammonium Salts

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Chemicals including NEt3, NBu4Br, NBu4Cl, NBu4I, NBu4PF6, epoxides and CO2 are commercially available and used directly without further purification. Gas chromatography (GC) was performed on a Shimadzu GC-2014 equipped with a capillary column (RTX-5, 30 m × 0.25 μm) using a flame ionization detector.
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2

Fungal Metabolite Identification by GC-MS

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The most active fungal extracts were selected to undergo secondary metabolites identification using gas-chromatography mass spectrometry GCMS, (GC-MS TQ8050; Shimadzu, Johannesburg, South Africa) equipped with a Multifunctional Autosampler (AOC-6000), a capillary column (RTX-5, 60 m × 0.25 mm × 0.25 µm, New Delhi, India) as described by Sharma et al. [7 ]. The identities of the compounds were determined by searching known molecules in databases of NIST05; WILEY 8, and FFNSC1.3 libraries.
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3

Bioactive Compound Identification via GC-MS

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The compounds separated by TLC were identified using gas chromatograph. The purified methanolic crude extract was subjected to GC-MS analysis to identify the bioactive compounds. The GC–MS-MS analysis of the crude extracts was carried out in a Shimadzu GC-MS-QP 2010 Plus fitted with a RTX-5 (60 m × 0.25 mm × 0.25 µm) capillary column in JNU, New Delhi. The instrument was set to an initial temperature of 70 °C, and maintained at this temperature for 2 min. At the end of this period the oven temperature was rose up to 280 °C, at the rate of an increase of 5 °C/min, and maintained for 9 min. Injection port temperature was ensured as 260 °C and Helium flow rate as 1 mL/min. The ionization voltage was 70 eV. The samples were injected in split mode as 10:1. Mass spectral scan range was set at 45–450 (m/z). The identification of bioactive compounds present in the extracts was performed by comparing the mass spectra with data from NIST05 (National Institute of Standards and Technology, US), WILEY 8, and FFNSC1.3 (Flavour and Fragrance Natural and Synthetic Compounds) libraries. The name, molecular weight and structure of the components of the test material were ascertained.
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4

Methylation Analysis of Polysaccharides

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Before the methylation reaction, galacturonic acid in the sample was methyl-esterified, and reduced to (6,6-dideutero)galactose using NaBD 4 as described previously (11) . Methylation of the polysaccharide was performed according to the Ciucanu method using sodium hydroxide and CH 3 I ( 12). The methylated polysaccharide was then hydrolyzed, reduced, and acetylated before analysis by gas chromatography/mass spectroscopy (GLC-MS). The GLC-MS analysis was performed with a QP-2010 plus instrument (Shimadzu, Kyoto, Japan) fitted with a fused silica capillary column (Rtx-5, 30 m × 0.25 mm × 0.25 µm; Restek, Shimadzu).
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