ArticleslgStudy

chemistry

Indole-3-butyric acid

Indole-3-butyric acid 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 Indole-3-butyric acid rather than just read about it. In short: Indole-3-butyric acid (1H-indole-3-butanoic acid, IBA) is a white to light-yellow crystalline solid, with the molecular formula C12H13NO2. It melts at 125°C in atmospheric pressure.

Indole-3-butyric acid — main illustration
Indole-3-butyric acid — illustration

Key takeaways

  • Indole-3-butyric acid belongs to chemistry; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect Indole-3-butyric acid to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of Indole-3-butyric acid from memory before moving on to harder problems.

Reference excerpt

Indole-3-butyric acid (1H-indole-3-butanoic acid, IBA) is a white to light-yellow crystalline solid, with the molecular formula C12H13NO2. It melts at 125°C in atmospheric pressure. IBA is a plant hormone in the auxin family and is an ingredient in many commercial horticultural plant rooting products.

Plant hormone Since IBA is not completely soluble in water, it is typically dissolved in 75% aqueous ethanol (aqua vitae) for use in plant rooting, making a solution of between 10,000 and 50,000 ppm. This alcohol solution is then diluted with distilled water to the desired concentration. IBA is also available as a alkali metal salt, which is soluble in water. The solution should be kept in a cool, dark place for best results. This compound had been thought to be strictly synthetic; however, it was reported that the compound was isolated from leaves and seeds of maize and other species. In maize, IBA has been shown to be biosynthesized in vivo from IAA and other compounds as precursors. This chemical may also be extracted from any of the Salix (Willow) genus.

Plant tissue culture In plant tissue culture, IBA and other auxins are used to initiate root formation in vitro in a procedure called micropropagation. Micropropagation of plants is the process of using small samples of plants called explants and causing them to undergo growth of differentiated or undifferentiated cells. In connection with cytokinins like kinetin, auxins like IBA can be used to cause the formation of masses of undifferentiated cells called callus. Callus formation is often used as a first step process in micropropagation where the callus cells are then caused to form other tissues such as roots by exposing them to certain hormones like auxins that produce roots. The process of callus to root formation is called indirect organogenesis whereas if roots are formed from the explant directly it is called direct organogenesis. In a study of Camellia sinensis, the effect of three different auxins, IBA, IAA and NAA were examined to determine the relative effect of each auxin on root formation. According to the result for the species, IBA was shown to produce a higher yield of roots compared to the other auxins. The effect of IBA is in concurrence with other studies where IBA is the most commonly used auxin for root formation.

Mechanism Although the exact method of how IBA works is still largely unknown, genetic evidence has been found that suggests that IBA may be converted into IAA through a similar process to β-oxidation of fatty acids. The conversion of IBA to IAA then suggests that IBA works as a storage sink for IAA in plants. There is other evidence that suggests that IBA is not converted to IAA but acts as an auxin on its own.

References

External links Media related to Indolebutyric acid at Wikimedia Commons

Illustrations

Indole-3-butyric acid illustration
Indole-3-butyric acid illustration
Indole-3-butyric acid illustration

Worked examples

Example 1 — a first encounter with Indole-3-butyric acid

Start with the simplest possible case. Write down what Indole-3-butyric acid 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 Indole-3-butyric acid 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 Indole-3-butyric acid 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 Indole-3-butyric acid

In research
Indole-3-butyric acid 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 Indole-3-butyric acid 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
Indole-3-butyric acid is common in secondary-school and first-year university syllabi. It links to neighbouring topics Auxins, Carboxylic acids, Indoles, so understanding it makes those chapters shorter.
In everyday life
Look for Indole-3-butyric acid 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.
Ask Teacher Smith questions about this articleOpens your AI tutor with a question about “Indole-3-butyric acid” →

Affiliate

Preply — study more efficiently by working with a personal tutor. 50% off.

How to study Indole-3-butyric acid in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what Indole-3-butyric acid 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 Indole-3-butyric acid out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is Indole-3-butyric acid in simple terms?

Indole-3-butyric acid (1H-indole-3-butanoic acid, IBA) is a white to light-yellow crystalline solid, with the molecular formula C12H13NO2. It melts at 125°C in atmospheric pressure.

Why does Indole-3-butyric acid 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 Indole-3-butyric acid?

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 Indole-3-butyric acid.

Tags

  • Auxins
  • Carboxylic acids
  • Indoles
  • Plant growth regulators

Keep exploring