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Karl Fischer titration: difference between revisions

Diff·revision 8 → 9·07:04, 27 Sep 2024

Difference between revision 8 and revision 9 of Karl Fischer titration. 4 lines changed; the page grew by 308 bytes.

Revision 8 — 00:01, 11 Sep 2024
INN_Ingrid (talk)
state that ultraviolet response is not uniform across impurities
4,173 bytes +37
Revision 9 — 07:04, 27 Sep 2024
PBM_Perrin (talk)
add the forced-degradation conditions the claim rests on
4,481 bytes +308
1{{Infobox method1{{Infobox method
2| name = Karl Fischer titration2| name = Karl Fischer titration
+3| image = coa-sheet.svg
+4| caption = Water content appears on a certificate of analysis alongside purity and peptide content.
3| Measures = Water (moisture) content5| Measures = Water (moisture) content
4| Classification = Titrimetric, iodine-based6| Classification = Titrimetric, iodine-based
28* the endpoint is detectable amperometrically, because excess iodine depolarises a double-platinum indicator electrode;30* the endpoint is detectable amperometrically, because excess iodine depolarises a double-platinum indicator electrode;
29* one faraday of charge liberates one mole of iodine, so in the coulometric variant the ''charge passed'' is a direct measure of water — no titrant standardisation is required.31* one faraday of charge liberates one mole of iodine, so in the coulometric variant the ''charge passed'' is a direct measure of water — no titrant standardisation is required.
+32
+33Away from the buffered pH window the stoichiometry drifts, which is the reason strongly acidic or basic samples require a modified reagent rather than a correction factor.
3034
31== Volumetric and coulometric variants ==35== Volumetric and coulometric variants ==