pH Calculator
Free pH calculator. Calculate pH from hydrogen ion concentration, find pOH, solve buffer pH with Henderson-Hasselbalch equation. 40+ chemical presets, temperature-adjusted Kw, and step-by-step solutions.
pH of an acid at given concentration
CH₃COOH · pKa = 4.74
Affects Kw (water ion product). Default 25°C.
Calculated pH
2.8753
pH Scale
Your result mapped against common substances
Similar to Cola
strongly acidic · 10,000× more H⁺ than water
Detailed Results
Ion concentrations at 25°C
Step-by-Step Solution
Ka = [H⁺]²/(C − [H⁺])
- 1Acetic Acid (CH₃COOH) is a weak acid
- 2Ka = 1.80e-5, pKa = 4.74
- 3C = 0.1 M
- 4Solve: x² + Ka·x − Ka·C = 0
- 5[H⁺] = (−Ka + √(Ka² + 4·Ka·C)) / 2
- 6[H⁺] = 1.3327e-3 M
- 7pH = 2.8753
Real-World Context
What your pH result means in practice
A pH of 2.88 is strongly acidic. This is closest in acidity to Cola. Each pH unit lower means 10× more hydrogen ions — so pH 2 is 10,000× more acidic than pure water.
How to Calculate pH
Core formulas for every solution type
pH measures how acidic or basic a solution is on a logarithmic scale. The fundamental relationship is pH = −log₁₀([H⁺]), where [H⁺] is the hydrogen ion concentration in mol/L. This calculator supports six different calculation modes to handle any solution type.
Strong Acid
pH = −log₁₀(C)
Full dissociation
Weak Acid (Ka)
Ka = x² / (C − x)
Equilibrium expression
Strong Base
pH = pKw + log₁₀(C)
Via pOH conversion
Buffer (H-H)
pH = pKa + log₁₀([A⁻]/[HA])
Henderson-Hasselbalch
Example — 0.1 M Acetic Acid (Ka = 1.8 × 10⁻⁵)
Concentration
0.1
CH₃COOH
M
Ka
1.8×10⁻⁵
Dissociation
[H⁺]
1.34×10⁻³
Quadratic soln.
M
pH
2.87
−log₁₀([H⁺])
What Is pH?
Understanding the hydrogen ion scale
pH (potential of hydrogen) quantifies the acidity or basicity of an aqueous solution. Introduced by Danish chemist S. P. L. Sørensen in 1909, it is defined as the negative logarithm of the hydrogen ion activity. In dilute solutions, activity approximates concentration, giving the practical formula pH = −log₁₀([H⁺]).
Because the scale is logarithmic, each whole-number pH change represents a 10-fold change in hydrogen ion concentration. A solution at pH 3 has 10× more H⁺ than one at pH 4, and 100× more than pH 5.
pH vs. pOH vs. pKa vs. pKb
Understanding the “p” quantities in acid-base chemistry
| Quantity | Formula | Measures | Neutral Value |
|---|---|---|---|
| pH | −log₁₀([H⁺]) | Acidity of a solution | 7.00 at 25°C |
| pOH | −log₁₀([OH⁻]) | Basicity of a solution | 7.00 at 25°C |
| pKa | −log₁₀(Ka) | Acid strength (lower = stronger) | N/A |
| pKb | −log₁₀(Kb) | Base strength (lower = stronger) | N/A |
| pKw | −log₁₀(Kw) | Water ion product | 14.00 at 25°C |
Temperature & pH
How Kw changes with temperature
The ion product of water (Kw) increases with temperature because the dissociation of water is endothermic. This means neutral pH shifts below 7 at higher temperatures — the water is still neutral, just with more ions.
| Temperature | Kw | pKw | Neutral pH |
|---|---|---|---|
| 0°C | 0.114 × 10⁻¹⁴ | 14.94 | 7.47 |
| 25°C | 1.01 × 10⁻¹⁴ | 14.00 | 7.00 |
| 37°C | 2.42 × 10⁻¹⁴ | 13.62 | 6.81 |
| 50°C | 5.47 × 10⁻¹⁴ | 13.26 | 6.63 |
| 100°C | 51.3 × 10⁻¹⁴ | 12.29 | 6.14 |
pH of Common Substances
Real-world reference values for everyday materials
Common Mistakes to Avoid
Frequent errors in pH calculations
Using pH = −log(C) for weak acids
This shortcut only works for strong acids that fully dissociate. Weak acids like acetic acid require the Ka equilibrium expression and quadratic formula. At 0.1 M, acetic acid has pH 2.87 — not 1.0.
Forgetting temperature effects on Kw
pH + pOH = 14 only holds at 25°C. At body temperature (37°C), pKw ≈ 13.6 and neutral pH is about 6.8 — not 7.0. Always specify or assume a temperature.
Confusing pKa with Ka
pKa = −log₁₀(Ka). A lower pKa means a stronger acid (larger Ka). Hydrochloric acid (pKa ≈ −7) is far stronger than acetic acid (pKa = 4.74). The relationship is inverse.
Assuming pH stays between 0 and 14
Concentrated strong acids can have pH below 0 (e.g., 10 M HCl → pH ≈ −1) and concentrated bases can exceed pH 14. The 0–14 range is practical, not theoretical.
Ignoring polyprotic acid steps
Acids like H₂SO₄ and H₃PO₄ donate multiple protons. The first dissociation may be complete, but subsequent ones have their own Ka values and must be calculated separately.
Using Henderson-Hasselbalch outside its range
The H-H equation gives accurate results only when [A⁻]/[HA] is between 0.1 and 10. Outside this range the approximation breaks down and the full equilibrium must be solved.
Common Acid & Base Reference
Ka, pKa, and classification of frequently used chemicals
| Name | Formula | Type | pKa / pKb | pH at 0.1 M |
|---|---|---|---|---|
| Hydrochloric Acid | HCl | Strong acid | ≈ −7 | 1.00 |
| Sulfuric Acid | H₂SO₄ | Strong acid | ≈ −3 | 1.00 |
| Phosphoric Acid | H₃PO₄ | Weak acid | 2.12 | 1.62 |
| Acetic Acid | CH₃COOH | Weak acid | 4.74 | 2.87 |
| Carbonic Acid | H₂CO₃ | Weak acid | 6.37 | 3.68 |
| Boric Acid | H₃BO₃ | Weak acid | 9.24 | 5.12 |
| Ammonia | NH₃ | Weak base | 4.74 | 11.13 |
| Sodium Hydroxide | NaOH | Strong base | — | 13.00 |
Frequently Asked Questions
Common questions and detailed answers
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Last updated Apr 9, 2026