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30 m db 5 capillary column

Manufactured by Agilent Technologies
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The 30-m DB-5 capillary column is an analytical instrument used in gas chromatography. It is designed to separate and analyze various chemical compounds. The column features a 30-meter length and a DB-5 stationary phase, which is a commonly used phase in gas chromatography applications.

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6 protocols using 30 m db 5 capillary column

1

Gas Chromatographic Analysis of Diluted Oils

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Ten microliters of either oil was diluted in 4.990 ml of hexane and vortexed. Ten microliters of this solution were again mixed with 990 µl of hexane and vortexed: 1 µl samples of this mixture were analyzed by a Thermo Scientific ISQ QD mass selective detector interfaced with a Thermo Scientific Trace 1300 gas chromatography (Thermo Scientific, Waltham, MA). Inlet temperatures were maintained at 200°C and samples were injected in splitless mode. A 30-m DB-5 capillary column (0.25 mm I.D., 0.25 µm film thickness; Agilent Technologies, Santa Clara, CA) was employed. Helium, the carrier gas, was set at constant pressure (6 psi) and injector temperature was set at 280°C. Oven temperature was increased from 50 to 280°C at 10°C/min. The NIST mass spectral library on the MS data system was used for identification.
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2

Glycosyl Linkage Analysis of SCWP

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Glycosyl linkage analysis was performed according to a modification of the method of Ciucanu and Kerek [29 ] as described previously [12 (link)]. The resulting partially methylated alditol acetates (PMAA) were dissolved in dichloromethane and analyzed by GC-MS using a DB-1 or SP-2330 capillary column as described [12 (link), 30 (link)]. The carbohydrate compositions of the SCWP and derived fractions were determined by preparing the TMS-methyl glycosides with GC-MS (electron impact) analysis [31 (link), 32 ] using a 30-m DB-5 capillary column (J&W Scientific, (Agilent Technologies Inc.) Folsom, CA USA). The absolute configuration of glycosyl residues was determined by preparing the diastereomeric TMS-(α)-2-butyl glycoside derivatives [33 ], with GC-MS analysis on a DB-1 column with comparisons to authentic D-Gal, D-GlcNAc, and D-ManNAc derivatives.
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3

GC-MS Analysis of Essential Oils

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The chemical composition of the essential oils was analyzed by gas chromatography-mass spectrometry (GC-MS). A gas chromatograph 7890B (Agilent Technologies, USA) equipped with a 30 m DB-5 capillary column (0.25 mm inner diameter, 0.25 µm lm thickness) was used in combination with a mass spectrometer 5977A (Agilent Technologies, electron ionization detector). All injections were performed in split mode with auto sampler. Ten-microliter syringes were used to inject 1µl of samples. The injector temperature was set at 280°C and the ow rate was maintained at 1.0 ml/min using helium as the carrier gas. The initial oven temperature was set at 50°C for 5 min and ramped at 10°C /min to 280°C. The ion source and interface temperature were 230°C and 300°C, respectively. The MSD was used in the electron impact (EI) full scan monitoring mode with a solvent delay time of 5 min.
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4

Gland Extract Analysis by GC-FID and GC-MS

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Gland extract were analyzed by GC-FID and coupled GC-MS. Samples were injected in splitless mode using a Hewlett Packard 6890 GC, interfaced to a Hewlett Packard 5973 mass selective detector (electron impact, 70 eV). For gland extracts and chemical comparison analysis, a 30-m DB-5 capillary column (0.25-mm ID, 0.25-µm film thickness, J&W Scientific, Folsom, CA) was used. The temperature program was 50°C for 1 min, then rising to 280°C at 10°C/min and holding for 5 min at 280°C. The temperature of the inlet was 250°C, and the transfer line temperature was 280°C. The Wiley MS library (Wiley 2005 ) was installed on the data system. For the analysis of the weathered extracted septa, a 30-m Stabilwax capillary column (0.32-mm ID, 0.25-µm film thickness, Restek, Bellefonte, PA) was used. The temperature program was 100°C for 1 min, then rising to 240°C at 5°C/min and holding for 2 min at 240°C. The temperature of the inlet was 255°C, and FID detector temperature was 255°C. Due to extracted septa compounds unrelated to the Type I, Type II, and ISTDs, which interfered with the residue analysis on the DB-5 capillary column, the Stabilwax column was chosen for the residue analysis. All of the GC analyses used He as carrier gas at constant pressure (41.4 KPa).
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5

GC-ECD Analysis of Organic Compounds

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The method was performed in a GC 17A with a nickel-63 electron capture detector model ECD-2010 Exceed (Shimadzu, Kyoto, Japan). The gas chromatographic system was equipped with a 30 m DB-5 capillary column with stationary phase of trifluoropropyl methyl polysiloxane (J&W Scientific, Folsom, CA, USA) with an internal diameter of 0.25 mm and 0.25 µm film thickness. Helium with a purity of 99.999% (Linde, Brazil) was used as a gas carrier with a column head pressure of 12 p.s.i., split/splitless unit. Chromatographic data were collected and recorded using GC Analyst software (Shimadzu, Kyoto, Japan).
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6

GC and GC-MS Analysis of Volatile Compounds

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Volatile collections were analyzed by GC with flame-ionization detection (FID) and coupled GC-MS. Samples were injected in splitless mode using a Hewlett Packard 6890 GC, interfaced to a Hewlett Packard 5973 mass-selective detector (electron impact, 70 eV). For most analyses, a 30-m DB-5 capillary column (0.25 mm ID, 0.25-µm film thickness, J&W Scientific, Folsom, CA) was used. The temperature program was 50°C for 1 min, then rising to 280°C at 10°C per min, and holding for 5 min at 280°C. The temperature of the inlet was 250°C, and the transfer line temperature was 280°C. The Wiley MS library (Wiley 2005 ) was installed on the data system. All the GC analyses used He as carrier gas at constant pressure (41.4 KPa).
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