Skip to content

Why is nitroglycerine so explosive and how is it used in medicine?

4 min read

Synthesized in 1846 by Ascanio Sobrero, nitroglycerine was immediately recognized as an extraordinarily unstable and dangerous liquid, so much so that its discoverer was terrified by his own creation. The same inherent chemical properties that made pure nitroglycerine so explosive also, paradoxically, paved the way for its eventual use in modern medicine.

Quick Summary

Nitroglycerine is highly explosive due to its unstable molecular structure, containing both a fuel source and an internal oxidizer, which enables a rapid, exothermic decomposition into a large volume of hot gas. Dilution and stabilization make it a safe medication.

Key Points

  • Internal Oxidizer: Nitroglycerine contains both its own fuel and oxygen within the same molecule, allowing for extremely rapid combustion without relying on external atmospheric oxygen.

  • Unstable Bonds: The covalent bonds within the nitrate groups ($- ext{ONO}_2$) are weak and break easily, leading to a low activation energy for the explosive decomposition.

  • Rapid Gas Expansion: The explosive decomposition reaction produces a large volume of hot gas ($N_2$, $CO_2$, $H_2O$) almost instantaneously, creating a destructive blast wave.

  • Medical Stabilization: For medicinal purposes, nitroglycerine is heavily diluted or mixed with inert binders, rendering it safe and non-explosive for treating conditions like angina.

  • Historical Context: Alfred Nobel made nitroglycerine usable as a safer explosive by mixing it with diatomaceous earth to create dynamite, a process that informed later pharmaceutical stabilization techniques.

  • Therapeutic Action: Medically, nitroglycerine works by converting to nitric oxide (NO) in the body, which relaxes blood vessels and improves blood flow to the heart.

In This Article

The Chemical Anatomy of an Explosive

At its core, the explosiveness of nitroglycerine (chemical formula $C_3H_5N_3O_9$) is rooted in its unique molecular structure. Unlike standard combustion, which requires an external source of oxygen to fuel a reaction, the nitroglycerine molecule is a self-contained explosive device. It possesses a glycerol backbone, which acts as the fuel (containing carbon and hydrogen atoms), and three nitrate groups ($- ext{ONO}_2$), which serve as powerful internal oxidizers. The oxygen atoms are already part of the molecule, bound within the nitrate groups, positioned close to the fuel atoms. This intimate contact between fuel and oxidizer is the first key ingredient for a rapid, explosive reaction.

The Instability of the Nitrate Bonds

The bonds within the nitrate groups are relatively weak and unstable. A small amount of energy—from heat, shock, friction, or even a chemical impurity—is all that is needed to initiate their rupture. This low activation energy is why pure nitroglycerine is notoriously sensitive and unpredictable. Once the reaction begins, it becomes a runaway process, as the energy released from the initial decomposition propagates rapidly through the rest of the material.

The Violent Detonation Reaction

The decomposition of nitroglycerine is a highly exothermic (heat-releasing) reaction that occurs at a blistering speed, creating a supersonic shock wave known as a detonation. The overall reaction is represented as:

$4C_3H_5(ONO_2)_3 o 12CO_2 + 10H_2O + 6N_2 + O_2$

Several factors contribute to the immense power of this reaction:

  • Massive Gas Production: Four molecules of nitroglycerine produce an astonishing 35 molecules of gas. This rapid increase in molecular volume is the primary source of the explosive force.
  • Intense Heat: The reaction generates extreme heat, with temperatures reaching up to 5,000 °C. This heat causes the newly formed gases ($CO_2$, $N_2$, $H_2O$) to expand violently and instantaneously, leading to the destructive blast wave.
  • Speed of Detonation: The supersonic speed of the detonation wave, approximately 7,700 meters per second, is what gives nitroglycerine its destructive 'brisance', or shattering capability.

Taming the Volatile Molecule: From Explosive to Medicine

For years, the volatility of pure nitroglycerine made it too dangerous for practical use. The breakthrough came with Swedish chemist Alfred Nobel, who discovered in 1867 that mixing nitroglycerine with an inert, porous substance like diatomaceous earth (kieselguhr) created a stable paste. This paste, which he patented as dynamite, could be safely handled and transported, and its detonation could be controlled with a blasting cap. This stabilization process was a critical step that later informed its medical application.

The Journey to Pharmacology

Nearly 130 years ago, physicians discovered that tiny, stabilized doses of nitroglycerine could be used to treat angina pectoris, or chest pain caused by reduced blood flow to the heart. In the body, nitroglycerine is metabolized into nitric oxide (NO). This molecule acts as a potent vasodilator, relaxing the smooth muscle in the blood vessel walls. This action widens the blood vessels, particularly the coronary arteries, which increases blood and oxygen supply to the heart muscle, relieving angina symptoms.

Stabilizing Nitroglycerine for Medical Use

Medical-grade nitroglycerine is vastly different from its explosive counterpart. In pharmaceutical forms—such as sublingual tablets, sprays, or transdermal patches—nitroglycerine is either heavily diluted with inert carriers like lactose or propylene glycol, or it is absorbed into binding agents. The concentration is so low that it is completely non-explosive and safe for human consumption.

Comparison of Explosive vs. Medical Grade Nitroglycerine

Feature Explosive-Grade Nitroglycerine Medical-Grade Nitroglycerine
Purity Pure, highly concentrated oily liquid Heavily diluted with inert substances
Stability Highly unstable, sensitive to shock and heat Stable and safe for storage and handling
Concentration Very high, 100% pure Very low, typically a small percentage
Form Liquid, or absorbed into a solid carrier (dynamite) Tablets, sprays, or patches
Purpose Detonation, blasting, propulsion Vasodilation to treat angina

The Elements of Nitroglycerine's Explosiveness

Here are the key chemical factors contributing to nitroglycerine's explosive power:

  • Built-in Oxidizer: The molecule contains its own oxygen supply in the form of nitrate groups, eliminating the need for atmospheric oxygen.
  • Energy-Rich Bonds: The chemical bonds in the molecule are less stable than the bonds in the reaction products (like $N_2$ and $CO_2$), meaning more energy is stored in the initial molecule.
  • High-Volume Gas Release: The rapid decomposition produces a significantly larger volume of gas than the original liquid, creating enormous pressure.
  • Extreme Exothermic Reaction: The decomposition releases a massive amount of heat, further expanding the gas volume and increasing the destructive force.
  • Low Activation Energy: A minimal amount of external energy, such as a bump or heat, can trigger the violent decomposition.

Conclusion

The paradoxical nature of nitroglycerine lies in the fact that the same chemical properties that make it a powerful, and notoriously unstable, high explosive are also responsible for its life-saving therapeutic effects in medicine. Its volatility stems from a chemically unstable structure with internal oxidizers, leading to a rapid, high-energy, gas-expanding detonation upon disturbance. The brilliant discovery by Alfred Nobel to stabilize this volatile substance led to dynamite, a safer explosive, and critically, enabled pharmacists to formulate it into the highly diluted, stable medication we know today. This transformation from a terrifying discovery into a powerful, controlled medicine is a remarkable chapter in the history of chemistry and pharmacology. You can learn more about its molecular properties at the Imperial College London Department of Chemistry.

Frequently Asked Questions

The primary reason for nitroglycerine's explosiveness is its unstable chemical structure. It contains both fuel (carbon and hydrogen) and its own internal oxygen supply (in nitrate groups) within the same molecule. This allows for an extremely rapid, self-contained, and highly exothermic decomposition reaction, producing a massive volume of hot gas instantly.

In medicine, nitroglycerine is used in extremely small, heavily diluted doses, rendering it completely non-explosive. The low concentration and stabilization with inert carriers in tablets, sprays, or patches make it safe for therapeutic use as a vasodilator for angina.

No, Alfred Nobel did not discover nitroglycerine. It was first synthesized by Italian chemist Ascanio Sobrero in 1846. However, Nobel's significant contribution was developing dynamite by mixing nitroglycerine with an absorbent material to make it a more stable and usable explosive.

When administered, medicinal nitroglycerine is converted into nitric oxide (NO) inside the body. Nitric oxide relaxes the smooth muscle in blood vessel walls, causing them to widen (a process called vasodilation) and improving blood flow to the heart.

Nitroglycerine is the highly unstable, pure liquid explosive. Dynamite is a stabilized version of nitroglycerine, created by Alfred Nobel, where the liquid is absorbed into an inert, porous substance like diatomaceous earth. This makes it much safer to handle and transport.

Yes, even in its diluted form, medicinal nitroglycerine can cause side effects. The most common one is a headache, caused by the vasodilation of blood vessels in the brain. Other side effects can include dizziness, lightheadedness, or flushing.

No, medical nitroglycerine tablets cannot explode. The concentration of nitroglycerine is far too low, and it is safely bound within an inert substance, removing any explosive risk under normal handling and storage conditions.

References

  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7
  8. 8
  9. 9

Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.