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Retention time (revision 4)

Old revision·15:42, 18 Sep 2024·GroupBuyGalen

This is an old revision of this page, as it stood at 15:42, 18 Sep 2024, saved by GroupBuyGalen with the summary state the mass accuracy in parts per million rather than daltons. It may differ substantially from the current revision, and any error it contains may since have been corrected.
Retention time
Symbolt_R
Depends onColumn, mobile phase, gradient, flow, temperature
Relative measureRelative retention time, against a reference peak
Topic infobox · conventions

Retention time is the interval between injection and the appearance of a component's peak maximum at the detector. Under fixed conditions it is characteristic of a substance and reproducible, which makes it the basis of chromatographic identification.[1]

It is not a property of the substance alone. Column chemistry and dimensions, mobile-phase composition, gradient profile, flow rate, temperature and even instrument dwell volume all change it, so a retention time is only meaningful alongside the conditions that produced it.[1]

What it can identify

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Matching a sample peak's retention to that of a reference standard run under identical conditions on the same day is the ordinary chromatographic identification. It is weak evidence on its own: many species can share a retention time on a given system.[2]

Co-injection strengthens it substantially. Spiking the sample with the standard should enlarge the existing peak without producing a shoulder; a shoulder indicates two species.

References

  1. ^ a b United States Pharmacopeia, General Chapter <621>, Chromatography.
  2. ^ United States Pharmacopeia, General Chapter <1503>, Quality Attributes of Synthetic Peptide Drug Substances.