The largest database of trusted experimental protocols

Chem station rev b 02 01 sr1 260

Manufactured by Agilent Technologies
Sourced in Germany

The Chem Station Rev. B. 02–01-SR1 (260) is a software application designed for data acquisition, analysis, and reporting in analytical chemistry laboratories. It provides essential functionalities for managing and processing data obtained from various analytical instruments.

Automatically generated - may contain errors

2 protocols using chem station rev b 02 01 sr1 260

1

Quantification of Ajugarin I in A. bracteosa

Check if the same lab product or an alternative is used in the 5 most similar protocols
A solution of 20 mg/ml A. bracteosa and 100 μg/ml Ajugarin I was prepared by dissolving substances in HPLC-grade methanol, sonicated, centrifuged, and filtered through Sartolon polyamide membrane filters. Samples were eluted at the flow rate of 1 ml/min with injection volume, 50 μL by the means of Agilent Chem Station Rev. B. 02–01-SR1 (260) and Agilent 1,200 series binary gradient pump, accompanied by diode array detector (DAD) (Agilent technologies, Germany). Reversed-phase column chromatography was conducted using a Zorbax-C8 analytical column (4.6 × 250 mm, 5 µm particle size) from Agilent Technologies, Germany. The separation process involved a gradient of concentrations, specifically 10% methanol in water (designated as mobile phase A) and 100% methanol (designated as mobile phase B). A gradient volume of pure methanol (mobile phase B) in 0–20 min was 0%–100%, 100% in 20–23 min, and 0% for the last 23–27 min. Chromatogram was obtained at 220 nm. The concentration of standard was 100 ppm in methanol. The amount of Ajugarin I quantified per mg A. bracteosa was observed in µg of DW. The standard and sample were compared using retention time and comparative chromatograms.
+ Open protocol
+ Expand
2

HPLC-Based Compound Identification

Check if the same lab product or an alternative is used in the 5 most similar protocols
The chromatographic analysis was carried out using HPLC Agilent 1100 integrated system equipped with a G1313A automated injector, a G1311A pump and G1315B multiwave-length diode-array detector (Agilent, Santa Clara, CA, USA). The chromatographic separation of the compounds was achieved with a reversed phase columns, ZORBAX SB-C18 (3.0 mm × 250 mm, 5 μm) from Agilent and (ODS-hypersil 2.1 mm × 100 mm 3 μm) from Thermo Fisher (Waltham, MA, USA) as well as normal phase ZORBAX-RX Sil 4.6 mm × 250 mm 5 μm and Polaris 5 Si 4.6 mm × 100 mm columns from Agilent, operating at constant room temperature (20°C). The chromatographic data were analyzed using Agilent Chemstation Rev. B.02.01-SR1 (260). The compounds under study were identified by their retention times and their UV spectral characteristics.
+ 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!