Columbia University's institutional laboratory manual, Experiment 1, Glassware Calibration, Primary and Secondary Standards, and Manual Titrations, Part 3, specifies two weighed – portions of potassium hydrogen phthalate, transferred completely into separate Erlenmeyer flasks. Dissolve each in approximately distilled water; any warmed sample cools to room temperature before titration. Add two or three drops of phenolphthalein. Rinse and condition a clamped burette with the diluted sodium hydroxide, then titrate while swirling to faint pink lasting about seconds. Calculate concentration from each portion's own mass and delivered titre; repeat if results scatter. Part 1 identifies a Mettler balance, and Part 2 includes paired weighings of exposed sodium hydroxide and potassium hydrogen phthalate. These are prescribed procedures, not reported measurements.[ref]
The same manual directs keeping the diluted sodium hydroxide covered and limiting air exposure after titrant standardization.[ref] The MIT handout explains the associated carbon dioxide problem: carbonate contamination of sodium hydroxide is controlled during preparation, bottles are promptly capped, and atmospheric carbon dioxide makes the pink phenolphthalein endpoint fade.[ref] Consequently, a standardized concentration applies to the stored chemical solution under its handling conditions; continued uptake of carbon dioxide can change the reacting inventory per delivered volume.
The color is the readout, and stoichiometry supplies the inference. Phenolphthalein indicates a pH range, so its first reproducible pale pink is an operational titration endpoint, rather than a direct observation of equal reacting inventories. A potentiometric titration can locate an endpoint from a pH versus volume curve, but glass electrode calibration alone still does not determine sodium hydroxide concentration. Repeat portions test scatter; incomplete dissolution, an unmatched titration blank, or a shared endpoint error can bias all repeats together.