D/L Amino Acids
Most important amino acids exist as stereoisomers. D- and L- forms of mirror image isomers, or enantiomers, are named according to their activity on polarized light. By using CROWNPAK CR-I(+) and CR-I(-) columns with chiral stationary phases, the D- and L-forms of amino acids can be analyzed separately. With CR-I(+) elution order is from D- to L-, and with CR-I(-) the elution order is reversed.
In Just Ten Minutes, Chiral Amino Acids Can Be Analyzed Simultaneously
With conventional chiral amino acid analysis, it is necessary to perform derivatization or use very long run times. With this method package, derivatization is not necessary, and high-sensitivity analysis can be performed in a short period of time, bringing efficiency to the chiral separations laboratory.
- Column : CROWNPAK CR-I(+)/(-) (3 mmI.D. × 150 mmL., 5 µm)
- Mobile Phase : Acetonitrile/Ethanol/Water/TFA = 80/15/5/0.5
- Flowrate : 0.6 mL/min
- Injection Volume : 1 µL
- Column Temp. : 25 °C
- Nebulizer Gas Flowrate : 3.0 L/min
- Drying Gas Flowrate : 15.0 L/min
- Heating Gas Flowrate : 5.0 L/min
- Interface Temp. : 250 °C
- DL Temp. : 250 °C
- Heat Block Temp : 300 °C
All D/L Amino Acids Can Be Quantified by Column Switching
The physicochemical properties of Glutamine and Lysine, Isoleucine and allo-Isoleucine, Threonine and allo-Threonine are extremely similar. They have virtually the same MS/MS fragmentation patterns, and share many of their MRM transitions. Chromatographic separation is therefore required to analyze them individually by LC-MS/MS. Even if there is coelution on the CR-I(+) column, confirmation can be made by automated switching to a secondary CR-I(-) column.
List of Registered Amino Acids
- D/L-Aspartic acid
- D/L-Glutamic acid