The largest database of trusted experimental protocols

Hp 5ms

Manufactured by Shimadzu
Sourced in United States, Japan

The HP-5MS is a gas chromatography column designed for separation and analysis of a wide range of organic compounds. It features a 5% phenyl, 95% dimethylpolysiloxane stationary phase and is suitable for a variety of applications including environmental analysis, food testing, and pharmaceutical research.

Automatically generated - may contain errors

4 protocols using hp 5ms

1

GC-MS Analysis of Chemical Compounds

Check if the same lab product or an alternative is used in the 5 most similar protocols
A total of 1.0 µL of the sample solution was used in a Shimadzu GC-2010 gas chromatograph (Shimadzu Scientific Instrument, Inc., Columbia, MD, USA).
The GC-MS system was equipped with an HP-5ms (30 m × 250 µm × 0.25 µm) chromatographic column, made of (5%-phenyl)-methylpolysiloxane.
In the heating procedure, the initial temperature was set at 40 °C for 2 min, increased at 5 °C/min to 230 °C and held at 230 °C for 2 min, then increased to 250 °C at 20 °C/min and held at 250 °C for another 2 min. Samples were injected in splitless mode; Injection time was 1.00 min. The carrier gas was helium with a flow rate of one mL/min. The temperature of the GC injector was 250 °C.
The GC MS-QP2010 SE mass spectrometer was operated in EI mode at 70 eV of electron energy; ion source temperature was equal to 230 °C, and the interface temperature was equal to 250 °C. The solvent delay time was 1.00 min; The scan interval was 0.30 s with a 2,000 amu/s scan speed, and the scan Mas range was 50∼550 m/z. The maximum length of retention time was 43.00 min. All measurements were repeated three times.
+ Open protocol
+ Expand
2

GC-MS Analysis of Ocimum gratissimum Extracts

Check if the same lab product or an alternative is used in the 5 most similar protocols
The GC-MS (GCMS-QP2010 SE, Shimadzu, Japan) was used to analyse the biochemical constituents of the O. gratissimum EOs and methanolic extracts as prescribed by Gasparetto et al, with few modifications.3 The qualitative analysis was performed with a fused silica capillary column (HP-5Ms, 30×0.25, 0.25 µm, film thickness) using helium (flow-rate, 1 mL min−1). The oven temperature was set at 40 °C and held for 5 mins, then increased to reach 270 °C at a rate of 3 °C/min with a split ratio of 60:1. A temperature of 180 °C was set for the ion sources and connection parts, and the MS was operated using an interface temperature of 240 °C. Electron impact (EI) mode and 70 eV ionisation energy were used. The delay time for MS prior to scanning was 5 mins. Samples were run fully at a range of 50 to 650 m/z. OGEO and OG-MeOH component identification were performed by comparing retention indices and matching the recorded mass spectra of each compound with the Willey MS libraries and NIST 14 mass spectral library of chemicals.
+ Open protocol
+ Expand
3

GC-MS Analysis of Propofol Degradation

Check if the same lab product or an alternative is used in the 5 most similar protocols
GC-MS was used to analyze the degradation products of propofol as well, which was performed on a Shimadzu 2020 with an HP-5MS (30 m*0.25 mm*0.25 μm) instrument. The split injection separation ratio was set to 10, and the volume was 1 μL. The gas flow of the column was set to 1 mL min−1. The retention time was set to 1 min. The m/z scanning range was set as 25–200. The working temperature of the column was set to 280 °C.
+ Open protocol
+ Expand
4

Crude Oil Fractionation and GC-MS Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
The crude oils were dissolved
in excess n-hexane
to remove asphaltenes, and the remainder was separated into saturates,
aromatics, and resins by liquid chromatography on a column filled
with silica/alumina (2:1 v/v). The saturates, aromatics, and resins
were stepwise eluted with n-hexane, n-hexane/dichloromethane (DCM; 2:1 v/v), and DCM/methanol (1:1 v/v),
using a column filled with silica/alumina (2:1 v/v).
Gas chromatography–mass
spectrometry (GC-MS) analyses of the saturates and aromatic fractions
were performed on a Shimadzu QP2010 Ultra GC-MS instrument equipped
with an HP-5MS (30 m × 0.25 mm i.d., 0.25 μm film thickness).
Helium was used as the carrier gas at a constant flow rate of 1.0
mL/min. The temperature of GC oven was programmed to reach 200 °C
from 50 °C and held for 2 min at 50 °C, then heated to 310
°C and held for 10 min at 310 °C. The electron ionization
mode of MS was operated at 70 eV, and the ion-source temperature is
230 °C. The selective ion monitoring (SIM) and full-scan detection
were combined, and the scan range is 50–550 Da. The selected
ions included m/z 191, 217, and
218.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!