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6120 single quadrupole lc ms system

Manufactured by Agilent Technologies
Sourced in United States

The 6120 single quadrupole LC/MS system is an analytical instrument manufactured by Agilent Technologies. It is designed to perform liquid chromatography-mass spectrometry (LC/MS) analysis. The system combines a liquid chromatography component with a single quadrupole mass spectrometer, enabling the separation and detection of chemical compounds in complex samples.

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5 protocols using 6120 single quadrupole lc ms system

1

Liquid Chromatography-Mass Spectrometry of cGAMP

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Liquid chromatography-mass spectrometry (LC-MS) with an electrospray ionization (ESI) interface was used to verify the production of cGAMP. The Agilent Technologies 1260 Infinity II LC System was coupled to Agilent Technologies 6120 Single Quadrupole LC/MS System (Agilent Technologies Inc., Santa Clara, CA, USA) and further equipped with a Diode Array Detector (1260 DAD HS, Agilent Technologies Inc., Santa Clara, CA, USA), Multicolumn Thermostat (1260 MCT, Agilent Technologies Inc., Santa Clara, CA, USA), Degasser (1260 Degasser, Agilent Technologies Inc., Santa Clara, CA, USA), Multisampler (1260 Multisampler), Binary Pump (1260 Binary Pump, Agilent Technologies Inc., Santa Clara, CA, USA) and an Agilent Poroshell 120 EC-C18 (4.6 × 100 mm, 2.7 μm particle size) column. Sample volumes of 5 μL were injected and separated by a gradient of mobile phase A (0.1 % formic acid) and mobile phase B (acetonitrile) (0 min 5% A, 95% B; 7 min 95% A, 5% B; 9 min 5% A, 95% B; 14 min 5% A, 95% B). The flow rate was set to 1 mL min−1 at a column temperature of 40 °C and a detection wavelength of 254 nm. Measured masses ranged from 100 to 1000 m/z. The gas chamber was heated to 350 °C with a gas flow of 12 L min−1. The capillary voltage was set to 3 kV and the nebulizer pressure to 35 psi.
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2

Analytical Characterization of Metabolites

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UV/Vis spectra were obtained on an Agilent (USA) Cary 300 UV-visible spectrophotometer with a path length of 10 mm. 1H and 2D- (gCOSY, gHSQC, and gHMBC) NMR spectral data were measured on an Agilent (USA) 600 MHz NMR spectrometer equipped with a cold probe, and the chemical shifts were recorded as δ values (ppm). Low-resolution HPLC/MS data was measured using an Agilent 6120 single quadrupole LC/MS system. High-resolution ESI-MS data was obtained using an Agilent iFunnel 6550 Q-TOF instrument fitted with an electrospray ionization (ESI) source coupled to an Agilent (USA) 1290 Infinity HPLC system. Flash column chromatography was carried out on Waters Sep-Pak® Vac 35cc (10g) C18 or silica cartridges. The isolation of metabolites was performed using an Agilent (USA) Prepstar HPLC system with an Agilent (USA) Polaris C18-A 5 μm (21.2 × 250 mm) column, a Phenomenex (USA) Luna C18(2) (100Å) 10 μm (10.0 × 250 mm) column, and an Agilent (USA) Phenyl-Hexyl 5 μm (9.4 × 250 mm) column.
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3

Analytical Characterization of Metabolites

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UV/Vis spectra were obtained on an Agilent (USA) Cary 300 UV-visible spectrophotometer with a path length of 10 mm. 1H and 2D- (gCOSY, gHSQC, and gHMBC) NMR spectral data were measured on an Agilent (USA) 600 MHz NMR spectrometer equipped with a cold probe, and the chemical shifts were recorded as δ values (ppm). Low-resolution HPLC/MS data was measured using an Agilent 6120 single quadrupole LC/MS system. High-resolution ESI-MS data was obtained using an Agilent iFunnel 6550 Q-TOF instrument fitted with an electrospray ionization (ESI) source coupled to an Agilent (USA) 1290 Infinity HPLC system. Flash column chromatography was carried out on Waters Sep-Pak® Vac 35cc (10g) C18 or silica cartridges. The isolation of metabolites was performed using an Agilent (USA) Prepstar HPLC system with an Agilent (USA) Polaris C18-A 5 μm (21.2 × 250 mm) column, a Phenomenex (USA) Luna C18(2) (100Å) 10 μm (10.0 × 250 mm) column, and an Agilent (USA) Phenyl-Hexyl 5 μm (9.4 × 250 mm) column.
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4

Solid-Phase Peptide Synthesis and Characterization

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The peptide was synthesized in solid phase on chlorotrityl resin, using Fmoc protection and HBTU activation, followed by purification using reverse-phase HPLC, using standard procedures [20 (link)]. 1H-NMR spectra were recorded at 400 MHz on a Varian Innova Instrument with chemical shift reported as ppm (in DMSO or MeCN with tetramethylsilane as internal standard). ESI-MS spectra were recorded on an Agilent 6120 single quadrupole LC–MS system.
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5

Solid-Phase Peptide Synthesis: Reagent Inventory

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Materials and general methods 2-chlorotrityl resin, O-Benzotriazole-N,N,N,N'-tetramethyluronium-hexafluoro-phosphate (HBTU), and Fmoc protected amino acids were purchased from GL Biochem (Shanghai) Ltd. All solvents were purchased from Merck, at analytical grade. Piperidine, trifluoroacetic acid (TFA), N,N-diisopropyl ethylamine (DIPEA), triisopropyl silane (TIPS) were from Acros. Sodium dihydrogen phosphate and disodium hydrogen phosphate were from BDH AnalaR. High purity Milli-Q-water with a resistivity greater than 18 M Ω cm was obtained from an in-line Millipore RiOs/Origin system. 1 H-NMR and 13 C-NMR spectra were recorded at 400 MHz on a Varian Innova Instrument with chemical shift reported as ppm (in DMSO with tetramethylsilane as internal standard). ESI-MS spectra were recorded on an Agilent 6120 single quadrupole LC-MS system.
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