Cyclohexane (C6H12)

This is our most popular Cyclohexane (C6H12) - Cyclohexane (General Use)

Cyclohexane (General Use)

Cyclohexane (General Use)

Bulk Discounts (applied at checkout)
1-3 4+
£25.43 £24.16

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Buy Your Cyclohexane Online Today

When you're buying online, you want to make sure you're getting the highest quality products at the best price. That's where we come in. ReAgent is one of the leading UK chemical suppliers and is supported by a catalogue of accreditations. From our ISO 9001 Quality Standard to our ISO 14001 Environmental Standard, we're suppliers you cant trust.

We supply cyclohexane (C6H12) in 2.5L containers and even offer discounts on bulk orders. We also offer many other options to suit your business needs, including customised labelling and non-standard pack sizes. All of our products are backed by a 100% quality guarantee and are usually shipped within 24 hours after purchase.

Cyclohexane Conformation

Also known as hexamethylene, cyclohexane (C6H12) is a cycloalkane that is mostly used in the industrial production of adipic acid and caprolactam. These are all precursors to nylon.

Theoretically, cyclohexane could form a simple and flat hexagon with 120° internal angles. In reality, the compound assumes a warped conformation to keep the angles closer to 109.5°, allowing for a lower strain energy than the flat structure. There are many 3D formations cyclohexane can assume and maintain the integrity of its bonds in. The most common formations are called boat, twist-boat, chair and half-chair. The compound can easily change from one conformation to another, and only chair and twist-boat can be isolated in their pure form.

Cyclohexane has been the object of study for many researchers, fascinated with this ability of cyclohexane to change conformation, known among chemists as conformational isomerism. Scientists are particularly curious about how this small change can influence its physical and chemical properties.

This idea was originally developed by Hermann Sachse who correctly identified two positions for cyclohexane in 1890. He understood that the oxygens could have different positions, but his ideas were never accepted among more established chemists. It wasn't until 1918 that Ernst Mohr used X-ray crystallography to confirm one of Sachse's conformations. Derek Barton and Odd Hassel later described many of the other possible conformations for cyclohexane and were awarded a Nobel Prize for their work.

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