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Agilent 5975c inert msd

Manufactured by Agilent Technologies
Sourced in United States

The Agilent 5975C inert MSD is a high-performance gas chromatography-mass spectrometry (GC-MS) system designed for sensitive and reliable analytical measurements. It features an inert ion source and vacuum system, providing enhanced performance and extended maintenance intervals.

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6 protocols using agilent 5975c inert msd

1

Synthesis and Characterization of Benzothiazole Derivatives

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Chemicals and solvents were obtained from Sigma-Aldrich (USA) and Samchun chemical companies (South Korea). Solvents were dried and purified by standard procedures. Melting points (mp) were determined in Thermo Fisher scientific IA9200 apparatus (USA). Infra-red (IR) spectra were measured on Perkin Elmer spectrophotometer (USA) with potassium bromide (KBr) as diluent. 1H-NMR and 13C- NMR spectra were recorded on a Bruker Avance 400 MHz spectrometer (USA) in deuterated-dimethyl sulfoxide (DMSO-d6) solvent with tetramethylsilane (TMS) as the internal standard. Chemical shifts δ were reported in ppm downfield to TMS and coupling constants values (J) were estimated in Hertz (Hz). Mass spectra were recorded on Agilent 5975c-inert MSD with the Triple-Axis Detector spectrometer. Reactions were monitored using thin-layer chromatography (TLC) on pre-coated silica gel 60F254 TLC plates obtained from Merck Chemicals (Germany). The procedure for the synthesis of 4-((benzo[d]thiazol-2-ylimino)methyl)phenol derivatives (4a-e) is provided in Scheme 1.
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2

Volatile Compound Analysis of Tenax Traps

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The Tenax traps were analysed for volatile compounds with an Agilent 7890A gas chromatograph connected to an Agilent 5975C inert MSD with Triple Axis detector mass spectrometer (Agilent, Santa Clara CA, United States). The GC system was fitted with GERSTEL Multi-Purpose Sampler (MPS: Gerstel GmbH & Co. KG, Mülheim an der Ruhr, Germany). The GC capillary column (30 m, 250 µm internal diameter and 0.25 µm film thickness) was Agilent’s HP-5MS (5% phenyl and 95% dimethyl polysiloxane). Prior to analysis one microliter heptyl actetate (3.16 ng / µl) was added to the Tenax trap in a GERSTEL thermal desorption unit (TDU) followed by thermal desorption of the trap in splitless mode at initial temperature 40 °C and then increased by 120 °C / min to 270 °C, this end temperature was held for 5 min. The desorbed volatiles were focused on a tenax liner in a GERSTEL CIS inlet at 10 °C. The CIS inlet, which operated in splitless mode, was then heated at a rate of 12 °C/s to 280 °C during which the volatiles were transferred to the column. The GC oven temperature was initially held at 40 °C for 1 min and then increased by 4 °C / min to 280 °C which was held for 3 min. The carrier gas was helium at a pressure of 34 psi. The MS was at full scan and identified mass ranges from 30–400 m/z with electron ionization at 70 eV and ion source temperature at 230 °C.
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3

GC-MS Analysis of Essential Oils

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EOs were analyzed with GC-MS using an Agilent 7890 A gas chromatograph interfaced to an Agilent 5975 C inert MSD with Triple-Axis Detector (Agilent Technologies, Santa Clara, CA, United States). A NIST library was used for identifying the components. EO of 0.5 μL was injected into a HP-5 MS capillary column (30 m × 0.25 mm, 0.32 μm, i.d.) using a helium as gas carrier at 1 mL/min flow rate. Mass spectra were recorded from 30 to 650 m/z. Individual components were identified by matching their 70 eV mass spectra with those of the spectrometer database as well as by comparison of the fragmentation pattern with those reported in the literature.
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4

Nitric Oxide and Nitrous Oxide Analysis

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Nitric oxide and nitrous oxide (NO and N2O) were analyzed on an Agilent series 6890 gas chromatograph (Agilent, USA) equipped with a Porapak Q and a Molecular sieve column, coupled to a thermal conductivity detector and a mass spectrometer (MS; Agilent 5975 Cinert MSD; Agilent, USA) as described before (Ettwig et al., 2008 (link)). For all gas analyses, 100 μl gas samples were injected into the gas chromatograph. Furthermore, nitric oxide production was monitored directly from the gas outlet of the reactors using a nitric oxide analyzer (NOA 280i, GE) with a suction rate of 11.6 ml.min−1.
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5

Glucose Extraction, Derivatization, and GC-MS Analysis

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Extraction of glucose from the filter paper blood spots, derivatization of the extracted glucose, and gas chromatography–mass spectrometry (GC-MS) measurements of the glucose derivatives were done according to the analytical procedure described before (23 (link)). In short, a disk was punched out of the blood spots, glucose was extracted from the disk by incubating it in ethanol/water (10:1 v/v), and glucose was derivatized to its pentaacetate ester. Samples were analyzed by GC-MS (Agilent 5975C inert MSD, Agilent Technologies, Amstelveen, Netherlands) with separation of derivatives on 30-m × 0.25-mm interior diameter (0.25-µm film thickness) capillary columns (ZB-1701, Phenomenex, Utrecht, Netherlands) and with positive-ion chemical ionization with methane. Measured by GC-MS, the fractional isotopomer distribution (M0 to M6) was corrected for the fractional distribution due to natural abundance of 13C by multiple linear regression as described by Lee et al. (24 (link)) to obtain the excess fractional distribution of mass isotopomers (M0 to M6) due to the dilution of administered [U-13C6]-d-glucose; that is, M6 represents the fractional contribution of the administered tracer and was used in the calculations of blood glucose kinetics.
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6

GC-MS Analysis of UKM8-ME

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The UKM8-ME (500 µg/mL) was sent for compound analysis to Makmal Pencirian Struktur Molekul (MPSM), Center for Research and Instrumentation Management (CRIM), Universiti Kebangsaan Malaysia. The sample was analysed on Agilent 7890A gas chromatograph (GC) (USA) directly coupled to the mass spectrophotometer system (MS) of Agilent 5975C inert MSD with a triple-axis detector.
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