PQS
HPLC FULL INSTRUMENT TRAINING SIMULATORInteractive startup, method setup, system suitability and sample analysis
Realistic virtual instrument

Operate the HPLC like an actual bench instrument

This simulator reproduces a full startup and routine-use workflow: solvent check, priming, column installation, method parameters, baseline equilibration, system-suitability injection, sample run and scientific review. The strongest outcome is not simply “getting peaks”; it is producing defensible analytical evidence.

Flow rate
Pressure0 bar
Wavelength
BaselineOffline
Column not installed
DEGASSER
Status: OFF
Lines: Disconnected
PUMP
Flow: 0.00 mL/min
Pressure: 0 bar
Prime: Not done
AUTOSAMPLER
Vial set: Not loaded
Injection: Idle
Needle wash: Ready
COLUMN OVEN
Column: Not installed
Temp: 25 °C
Status: Idle
UV DETECTOR
Wavelength: 0 nm
Baseline: Offline
Signal: 0.0000 AU

Immediate instrument actions

Scientific note

What makes this realistic: the simulator can produce acceptable or poor chromatographic behavior depending on what you did before injection. Skipping priming, choosing the wrong wavelength or running without equilibration will affect the instrument evidence, not just the final answer text.
Method control

Approved method parameters

Choose values that support the intended assay. The method is fictional, but the control logic is realistic: mobile-phase program, flow rate, wavelength, injection volume and oven temperature must be deliberately set and scientifically consistent.

Method entry panel

Expected method intent

ParameterExpected training valueReason
Flow rate1.00 mL/minReference instrument flow for the assay
Wavelength230 nmTraining analyte absorbance maximum
Oven temperature30 °CControlled retention / reproducibility
Injection volume10 µLBalances response and peak shape
Mobile phaseA:B 60:40Produces target retention / resolution in this scenario
The instrument will still “run” with incorrect settings, but the chromatographic evidence and system suitability can fail. That is intentional.
Live detector output

Chromatogram & run evidence

The traces below update after standard and sample injections. The standard injection determines whether the system is fit for use; the sample should only be interpreted if the run conditions are analytically defendable.

Time (min) Detector response Current run Reference
RunRetention time 1Retention time 2ResolutionTailingStatus
StandardNot run
SampleNot run
Troubleshooting & interpretation

Recognize causes, not just symptoms

A realistic analyst does more than notice a bad chromatogram. The analyst connects the symptom to instrument state, method settings and preparatory steps to identify the most likely cause and the correct next action.

Unstable baseline

Often linked to poor equilibration, bubbles or solvent mixing inconsistency.

High pressure

Can arise from blocked frits, column issues or excessive flow / viscosity.

Poor resolution

May result from wrong mobile phase, flow rate, wrong column conditions or column deterioration.

Training trap: if the standard run fails, the correct response is not to interpret the sample anyway. This simulator expects scientifically defensible run control.