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chemistry

Nitroglycerin

Nitroglycerin is a chemistry topic covered in the lgStudy science library. This page brings together a partial reference excerpt, illustrations, worked examples, real-world applications and a short study plan, so you can understand Nitroglycerin rather than just read about it. In short: Nitroglycerin (NG, alternative spelling nitroglycerine), also known as trinitroglycerol (TNG), nitro, glyceryl trinitrate (GTN), or 1,2,3-trinitroxypropane, is a dense, colorless or pale yellow, oily, explosive liquid most commonly produced by nitrating glycerol with white fuming nitric acid under conditions appropriate to the formation of the nitric acid ester. Chemically, the substance is a nitrate ester rather th…

Nitroglycerin — main illustration
Nitroglycerin — illustration

Key takeaways

  • Nitroglycerin belongs to chemistry; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect Nitroglycerin to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of Nitroglycerin from memory before moving on to harder problems.

Reference excerpt

Nitroglycerin (NG, alternative spelling nitroglycerine), also known as trinitroglycerol (TNG), nitro, glyceryl trinitrate (GTN), or 1,2,3-trinitroxypropane, is a dense, colorless or pale yellow, oily, explosive liquid most commonly produced by nitrating glycerol with white fuming nitric acid under conditions appropriate to the formation of the nitric acid ester. Chemically, the substance is a nitrate ester rather than a nitro compound, but the traditional name is retained. Discovered in 1846 by Ascanio Sobrero, nitroglycerin has been used as an active ingredient in the manufacture of explosives, namely dynamite, and as such it is employed in the construction, demolition, and mining industries. It is combined with nitrocellulose to form double-based smokeless powder, used as a propellant in artillery and firearms since the 1880s. As is the case for many other explosives, nitroglycerin becomes more and more prone to exploding (i.e., spontaneous decomposition) as the temperature is increased. Upon exposure to heat above 218 °C at sea-level atmospheric pressure, nitroglycerin becomes extremely unstable and tends to explode. When placed in vacuum, it has an autoignition temperature of 270 °C instead. With a melting point of 12.8 °C, the chemical is almost always encountered as a thick and viscous fluid, changing to a crystalline solid when frozen. Although the pure compound itself is colorless, in practice the presence of nitric oxide impurities left over during production tends to give it a slight yellowish tint. Due to its high boiling point and consequently low vapor pressure (0.00026 mmHg at 20 °C), pure nitroglycerin has practically no odor at room temperature, with a sweet and burning taste when ingested. Unintentional detonation may ensue when dropped, shaken, lit on fire, rapidly heated, exposed to sunlight and ozone, subjected to sparks and electrical discharges, or roughly handled. Its sensitivity to exploding is responsible for numerous devastating industrial accidents throughout its history. The chemical's characteristic reactivity may be reduced through the addition of desensitizing agents, which makes it less likely to explode. Clay (diatomaceous earth) is an example of such an agent, forming dynamite, a much more easily handled composition. The addition of other desensitizing agents gives birth to the various formulations of dynamite. Nitroglycerin as a medication has been used since 1878 as a potent vasodilator (causing dilation of the vascular system) to treat heart conditions, such as angina pectoris and chronic heart failure. Though it was previously known that these beneficial effects are due to nitroglycerin being converted to nitric oxide, a potent vasodilator, the enzyme for this conversion was only discovered to be mitochondrial aldehyde dehydrogenase (ALDH2) in 2002. Nitroglycerin is available in sublingual tablets, sprays, ointments, and patches.

History

… excerpt ends here. Continue reading the full article.

Illustrations

Nitroglycerin: Skeletal formula of zwitterionic nitroglycerin
Skeletal formula of zwitterionic nitroglycerin
Nitroglycerin: Ball and stick model of nitroglycerin
Ball and stick model of nitroglycerin
Nitroglycerin: Spacefill model of nitroglycerin
Spacefill model of nitroglycerin
Nitroglycerin illustration
Nitroglycerin illustration

Worked examples

Example 1 — a first encounter with Nitroglycerin

Start with the simplest possible case. Write down what Nitroglycerin claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In chemistry, the smallest case is usually a single object, a single equation or a single measurement. Check that every symbol or term in your sentence has a meaning in that case.

Example 2 — changing one variable

Take the situation from Example 1 and change exactly one quantity: double it, halve it, or set it to zero. Predict what should happen to Nitroglycerin before you calculate. Comparing your prediction with the result is the fastest way to find out whether you understand the idea or only the words.

Example 3 — an exam-style question

Typical questions about Nitroglycerin ask you to (a) state it precisely, (b) apply it to given data, and (c) explain a limitation. Practise writing all three answers in under five minutes; the third part is what separates a full-mark answer from an average one.

Applications of Nitroglycerin

In research
Nitroglycerin appears in chemistry research whenever the underlying quantities have to be modelled precisely. Papers usually cite it as a starting assumption and then explore where it breaks down.
In technology and industry
Engineering practice reuses Nitroglycerin in design rules, simulations and safety margins. Knowing the idea lets you read a specification sheet and understand why the numbers look the way they do.
In the classroom
Nitroglycerin is common in secondary-school and first-year university syllabi. It links to neighbouring topics Aldehyde dehydrogenase inhibitors, Disulfiram-like drugs, Explosive chemicals, so understanding it makes those chapters shorter.
In everyday life
Look for Nitroglycerin outside the textbook — in sport, cooking, traffic, electronics or the sky above you. An example you found yourself is remembered far longer than one you were given.

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How to study Nitroglycerin in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what Nitroglycerin means in your own words.
  3. Compare your version with the excerpt and mark what you missed.
  4. Work through the three examples above with pen and paper.
  5. Explain Nitroglycerin out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is Nitroglycerin in simple terms?

Nitroglycerin (NG, alternative spelling nitroglycerine), also known as trinitroglycerol (TNG), nitro, glyceryl trinitrate (GTN), or 1,2,3-trinitroxypropane, is a dense, colorless or pale yellow, oily, explosive liquid most commonly produced by nitrating glycerol with white fuming nitric acid under…

Why does Nitroglycerin matter?

Because it connects several chemistry ideas at once: it gives you a definition you can apply, a quantity you can calculate, and a way to check whether a result is plausible.

How should I study Nitroglycerin?

Read the excerpt, restate it from memory, then work through the examples and applications listed on this page. The five-step study plan above takes about twenty minutes.

What does this page cover?

It gives you a compact reference excerpt plus original lgStudy explanations, examples, applications and study material on Nitroglycerin.

Tags

  • Aldehyde dehydrogenase inhibitors
  • Disulfiram-like drugs
  • Explosive chemicals
  • Glycerol esters
  • Italian inventions
  • Liquid explosives
  • Nitrate esters
  • Sugar alcohol explosives

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