If you know the half-life or shelf life t₁ at a temperature T₁, you can estimate how long it will last at a different temperature T₂ – or at what temperature you will achieve a desired shelf life. The calculator uses the Arrhenius equation with the activation energy Ea and solves for t₁, T₁, t₂, T₂, or Ea. This is useful for storage temperatures, cold chains, or aging processes.
Do you want to calculate the rate constant k directly instead? Use our Arrhenius Calculator.
Almost all decay, degradation, and aging processes run faster at higher temperatures – a common rule of thumb states that the rate roughly doubles or triples for every 10 °C increase in temperature (RGT rule / Q10 temperature coefficient). This can be calculated more precisely using the Arrhenius equation.
If you know the shelf life at one temperature, you can convert it to any other temperature – without needing to know the pre-exponential factor A, as it cancels out when building the ratio.
Basic Formula
$$ t_2 = t_1 \cdot e^{\frac{E_a}{R}\left(\frac{1}{T_2} - \frac{1}{T_1}\right)} $$
Reference Values (t₁, T₁)
t₁ is a known half-life or shelf life, measured or specified at the temperature T₁ (e.g., manufacturer's specification: 2 years at 25 °C).
Target Values (t₂, T₂)
t₂ and T₂ describe the new scenario – either you want to know how long a product lasts at a new temperature T₂ (t₂ is unknown), or at what temperature a desired shelf life t₂ is achieved (T₂ is unknown).
Activation Energy (Ea)
Ea describes how sensitively the underlying process responds to temperature changes. The larger Ea is, the greater the impact of a temperature change on the shelf life.
Where Does the Formula Come From?
For first-order processes, t₁/₂ = ln(2)/k. Substituting k = A·e^(−Ea/(R·T)) for both temperatures and forming the ratio t₂/t₁, both ln(2) and A cancel out – leaving the formula above, which only contains Ea, T₁, and T₂.
Depending on which variable is being solved for, the formula is rearranged accordingly. The exact formulas are displayed directly in the results, but here is the general approach:
Solving for t₂ or t₁
Direct substitution into the basic formula or its inverse – the three remaining variables (T₁, T₂, Ea) must be known.
Solving for T₂ or T₁
Solve for 1/T first, then invert. It must be verified that the calculated temperature remains positive – otherwise, there is no physically meaningful solution.
Solving for Ea
Requires two different temperatures T₁ ≠ T₂ with known shelf lives t₁ and t₂ – for example, from two separate stability tests.
Two real-world examples demonstrate how to calculate depending on the variable you are solving for.
A medication has a shelf life of 2 years (t₁) at 25 °C (T₁), with Ea = 80 kJ/mol. How long will it keep in the refrigerator at 5 °C (T₂)?
Given
t₁ = 2 years, T₁ = 298.15 K, T₂ = 278.15 K, Ea = 80000 J/mol
Solution
t₂ = 2 · e^[(80000/8.314)·(1/278.15 − 1/298.15)] = 2 · e^(2.32) ≈ 20.4 years
t₂ ≈ 20.4 years → in the refrigerator, it keeps significantly longer.
A product lasts only 3 months (t₁) at 40 °C (T₁), with Ea = 95 kJ/mol. At what temperature T₂ will it keep for 24 months (t₂)?
Given
t₁ = 3 months, T₁ = 313.15 K, t₂ = 24 months, Ea = 95000 J/mol
Solution
1/T₂ = (R/Ea)·ln(t₂/t₁) + 1/T₁ = (8.314/95000)·ln(8) + 1/313.15 ≈ 0.003375 → T₂ ≈ 296.3 K
T₂ ≈ 296.3 K ≈ 23.2 °C
Reaction Order is Not 1st Order
The derivation assumes a first-order reaction (t₁/₂ is independent of concentration). For other reaction orders, while the fundamental temperature dependency via Ea remains, the exact half-life formula looks different.
Estimated or Uncertain Ea Value
Minor errors in Ea have a massive impact over large temperature differences (since Ea is in the exponent). For reliable predictions, Ea should be derived from actual measurements at two or more temperatures rather than guessed.
This type of extrapolation is widely used in practice: