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Metformin has acid dissociation constant values (pK a) of 2.8 and 11.5, so it exists very largely as the hydrophilic cationic species at physiological pH values. The metformin pK a values make it a stronger base than most other basic medications with less than 0.01% nonionized in blood.
The electron-withdrawing effect of the substituent makes ionisation easier, so successive pK a values decrease in the series 4.7, 2.8, 1.4, and 0.7 when 0, 1, 2, or 3 chlorine atoms are present. [49] The Hammett equation , provides a general expression for the effect of substituents.
Buffer capacity falls to 33% of the maximum value at pH = pK a ± 1, to 10% at pH = pK a ± 1.5 and to 1% at pH = pK a ± 2. For this reason the most useful range is approximately p K a ± 1. When choosing a buffer for use at a specific pH, it should have a p K a value as close as possible to that pH.
This compound causes rainfall pH to be around 5.0–5.5. When rainfall has a lower pH than natural levels, it can cause rapid acidification of soil. Sulfur dioxide and nitrogen oxides are precursors of stronger acids that can lead to acid rain production when they react with water in the atmosphere
Most water, including drinking water, has a neutral pH that exists between 6.5 and 8.5, but acid rain has a pH level lower than this and ranges from 4–5 on average. [1] [2] The more acidic the acid rain is, the lower its pH is. [2] Acid rain can have harmful effects on plants, aquatic animals, and infrastructure.
CO 2 from the atmosphere or the decomposition of organic matter affects freshwater acidity. [4] The CO 2 dissolved in water to form carbonic acid. This carbonic acid dissociated into hydrogen ions (H⁺) and bicarbonate (HCO₃⁻), which increases the H+ ions and leads to decrease in pH level. [5]
Whether you’re taking metformin for weight loss, type 2 diabetes, prediabetes, polycystic ovary syndrome (PCOS), or another medical condition entirely, you want to get the most out of your ...
From the titration of protonatable group, one can read the so-called pK a 1 ⁄ 2 which is equal to the pH value where the group is half-protonated (i.e. when 50% such groups would be protonated). The pK a 1 ⁄ 2 is equal to the Henderson–Hasselbalch pK a (pK HH a) if the titration curve follows the Henderson–Hasselbalch equation. [14]
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