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Peptide content: difference between revisions

Diff·revision 5 → 6·18:51, 25 Oct 2024

Difference between revision 5 and revision 6 of Peptide content. 6 lines changed; the page grew by 537 bytes.

Revision 5 — 18:31, 6 Oct 2024
FigureFerdinand (talk)
add the ionisation mode to the mass-spectrometry description
2,954 bytes +425
Revision 6 — 18:51, 25 Oct 2024
PeakShapePol (talk)
convert the method-comparison paragraph to a table
3,491 bytes +537
1{{Infobox method1{{Infobox method
2| name = Peptide content2| name = Peptide content
+3<!-- Definition -->
+4| Quantity = Mass of peptide ÷ mass of preparation
+5| Units = Per cent by mass
+6| Typical range = 70–90% for a lyophilised trifluoroacetate salt
3}}7}}
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21The acetonitrile carried over from preparative purification is the residual solvent that dominates in practice; it is classified for toxicity and given a concentration limit under the harmonised residual-solvent guideline, and it is determined by headspace gas chromatography rather than inferred.{{r|ichq3c}}25The acetonitrile carried over from preparative purification is the residual solvent that dominates in practice; it is classified for toxicity and given a concentration limit under the harmonised residual-solvent guideline, and it is determined by headspace gas chromatography rather than inferred.{{r|ichq3c}}
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+27The counterion share is the term that surprises people. Trifluoroacetic acid is used in the mobile phase of the purification, and a basic peptide leaves that step as its trifluoroacetate salt with one counterion per basic site. For a peptide with several basic residues and a modest molecular mass, the counterion can be a fifth of the dry weight.{{r|usp1503}}
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23== References ==29== References ==