The largest database of trusted experimental protocols

Cp chirasil dex cb capillary column

Manufactured by Agilent Technologies
Sourced in United States

The CP-Chirasil-Dex CB capillary column is a chromatographic column used for the separation and analysis of chiral compounds. It features a stationary phase consisting of a cyclodextrin derivative, which enables the resolution of enantiomers. The column is designed for use in gas chromatography applications.

Automatically generated - may contain errors

Lab products found in correlation

2 protocols using cp chirasil dex cb capillary column

1

Chromatographic Analysis of Ketone Conversions

Check if the same lab product or an alternative is used in the 5 most similar protocols
Samples were taken and prepared as in the Section 3.7.1 and the conversion was calculated in the same way.
The conversion of 4-phenyl-2-butanone was monitored by chromatography with flame ionization detector (GC-FID, Agilent 7890B, Santa Clara, CA, USA) with CP-Chirasil-Dex CB capillary column (Agilent J&W, 25 m × 0.25 mm × 0.25 µm) and hydrogen (H2) as the carrier gas with a flow of 1.15 mL/min. The injection volume was 1 µL with a 50:1 split. The oven temperature was initially 80 °C, then increased to 200 °C with a gradient of 5 °C/min, and was held for 3 min.
The conversion of 3′-hydroxyacetophenone was monitored by chromatography with flame ionization detector (GC-FID, Agilent 7890B, Santa Clara, CA, USA) with CP-Chirasil-Dex CB capillary column (Agilent J&W, 25 m × 0.25 mm × 0.25 µm) and hydrogen (H2) as the carrier gas with a flow of 1.15 mL/min. The injection volume was 1 µL with a 100:1 split. The oven temperature was initially 90 °C, then increased to 150 °C with a gradient of 30 °C/min, and was held for 15 min. Then increased to 200 °C with a gradient of 30 °C/min, and was held for 2 min.
+ Open protocol
+ Expand
2

Chiral GC-MS Analysis of Methylated Diketide Acids

Check if the same lab product or an alternative is used in the 5 most similar protocols
The concentrated organic extracts of the above-described enzymatic incubations were dissolved in 200 μL of methanol and then treated with 5 μL of TMS-diazomethane (2 M in hexane) for 10 min at room temperature. The derived reduced 2-methyl-diketide acid methyl esters were directly analyzed by chiral GC-MS.13 (link) GC-MS spectra were recorded on a GC-MS Agilent 5977A Series GC-MSD instrument, 70 eV EI in positive ion mode, using a Varian CP-Chirasil-DEX CB capillary column (0.25 mm inside diameter × 25 m length × 0.25 mm film, Agilent Technologies) and a temperature program of (1) initial temp 60 °C for 1 min, (2) increase at rate 0.3 °C/min up to 75 °C, (3) 5 °C/min up to 90 °C, and then 20 °C/min to final temp 200 °C. The extracted ion current (XIC) of the chromatogram was analyzed set on the base peak at m/z 88 for 2-methyl-3-hydroxypentanoic acid methyl ester. All assays were conducted in duplicate. The products were compared directly with authentic standards, as previously described (Figures S11-S15).13 (link)
+ 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!