Retention time and peak area
reversed-phase, normal-phase, ion-pair, HILIC, or chiral HPLC
Material Analysis · Chromatography & Diagnostics
Characterise retention time and peak area, purity and component profile, and target concentration with calibration using a scope agreed around your sample and decision.
Why this service
High-Performance Liquid Chromatography is selected when the project needs defensible information on retention time and peak area, purity and component profile, or target concentration with calibration.…
reversed-phase, normal-phase, ion-pair, HILIC, or chiral HPLC
UV/DAD, fluorescence, RI, CAD, or ELSD detection
UHPLC method development or transfer
Choose the scope
The method, preparation route and reporting depth depend on what you need to decide.
retention time and peak area
purity and component profile
target concentration with calibration
Common outputs
Fields, conditions, processing and file formats are confirmed before work begins.
Chromatogram reported with the agreed units, sample reference and measurement conditions.
Peak identity/purity table supplied in a labelled format suitable for direct sample or condition comparison.
Quantitative results and system-suitability data provided with the processing basis and quality checks agreed during technical review.
Processed chromatogram or spectrum included when selected in the confirmed reporting scope.
Sample requirements
Provide representative, clearly labelled samples and identify the decision, feature or comparison that matters.
| Suitable sample | Submission requirement | Planning note |
|---|---|---|
| Liquid / solution | Provide a sealed, compatible container labelled with composition, concentration and solvent. | Declare volatility, corrosivity, suspended solids and any storage or temperature requirement. |
| Device / assembly | Provide a complete labelled device or assembly with drawings, interfaces and operating limits. | Confirm power, connections, operating state, access restrictions and permitted disassembly. |
| Solid / component | Provide a clean, stable and clearly labelled specimen with the target face or region identified. | Confirm dimensions, cutting permission and whether the original geometry must be preserved. |
Objective: state the decision, comparison or acceptance criterion the work must support.
Handling and access: declare hazards, instability, confidentiality, file constraints or special logistics before dispatch or transfer.
Questions and answers
Short answers to issues that can change preparation, scope, timing or interpretation.
Provide liquid / solution, device / assembly, solid / component as applicable. Exact quantity, dimensions and preparation are confirmed during technical review.
The final method, preparation and reporting scope are confirmed after the sample and project objective have been reviewed.
Typical turnaround is 8 working days after sample acceptance and method confirmation.
A detector responds only to compatible compounds. Co-elution and sample instability require method development or orthogonal confirmation.
Configure the service