This is an Application Brief and does not contain a detailed Experimental section.
This application brief demonstrates the gradient separation of histidine dipeptides on ACQUITY UPLC BEH HILIC Columns.
The compounds used in this study are:
Column: |
ACQUITY UPLC BEH HILIC, 2.1 x 50 mm, 1.7 μm |
Part Number: |
186003460 |
Mobile Phase A: |
50/50 ACN/10 mM ammonium formate, w/ 0.125% HCOOH, pH 3.0 |
Mobile Phase B: |
95/5 ACN/10 mM ammonium formate, w/ 0.125% HCOOH, pH 3.0 |
Flow Rate: |
0.5 mL/min |
Injection Volume: |
5.0 μL |
Sample Diluent: |
75:25 ACN:MeOH |
Sample Concentration: |
Creatinine 1μg/mL; Carnosine 5 μg/mL; Anserine 5 μg/mL; Creatine 5 μg/mL |
Column Temperature: |
30 °C |
Weak Needle Wash: |
ACN/H2O 95/5 |
Instrument: |
Waters ACQUITY UPLC with ACQUITY SQD |
Time (min) |
Profile |
|
---|---|---|
%A |
%B |
|
0.00 |
0.1 |
99.9 |
5.00 |
99.9 |
0.1 |
5.01 |
0.1 |
99.9 |
6.00 |
0.1 |
99.9 |
Ionization Mode: |
ES+ |
Capillary: |
2.5 kV |
Cone: |
20 V (Carnosine; Creatinine, Anserine); 25 V (Creatine) |
Source Temperature: |
120 °C |
Desolvation Temperature: |
400 °C |
Desolvation Gas Flow: |
800 L/Hr |
Cone gas Flow: |
5 L/Hr |
SIR m/z: |
227.1 m/z (Carnosine); 132.1 m/z (Creatine); 114.05 m/z (Creatinine); 241.1 m/z (Anserine) |
Dwell Time: |
0.1 s |
WA60139, August 2009