Capsaicin - chemistry
The
chemicals that cause the burning sensation in pepper come from a family of compounds
called the capsaicinoids, this family all have the same functional groups, only
varying by the length of the hydrocarbon chain. Of all the capsaicinoids,
only two compounds are responsible for 80-90% content of pepper, these are capsaicin
and dihydrocapsaicin. Different concentrations of capsaicinoids give different
pungencies and this therefore is the reason why some peppers are hotter than
others. Capsaicinoids come from a larger family of chemicals called the
vanilloids, compounds that contain the vanillyl group shown right.

Capsaicin - structure
The line drawing above shows the structure of capsaicin, below is a ball and stick models showing the arrangement of the atoms in space.

Capsaicin - facts
| Common name: | Capsaicin |
| Systematic name: | N-(4-hydroxy-3-methoxybenzyl)-
8-methylnon-trans-6-enamide |
| Molecular formula: | C18H27NO3 |
| Molecular weight: | 305.42 |
| Melting Point: | 65oC |
| Boiling Point: | 210-220oC at 0.01 torr pressure |
| Solubility: | freely soluble in ethanol, ether, benzene, chloroform; slightly soluble in carbon disulfide; insoluble in water |
Capsaicin - stereochemistry
Capsaicin contains cis/trans isomerism because the double bond prevents internal
rotation. Capsaicin is always found in the trans isomer because in cis,
the -CH(CH3)2 and the longer chain on the other side of
the double bond will be close together causing them to repel each other slightly,
this steric hindrance does not exist in the trans isomer. This additional
strain imposed causes the cis isomer to be of a less stable arrangement than
the trans isomer.
How hot?
It is the presence of capsaicinoids
that gives peppers their pungent flavour. The flavour of peppers varies
with harvest time as the quantity of capsaicinoids increases during maturation.
The amount of capsaicinoids also varies with species. Wilbur Scoville devised
a means of measuring pepper ‘hotness’. He found some ‘mad’ volunteers
to taste chilli powders on their own. The powders were then diluted down
using sugar and water until they no longer burned the taster’s mouths. The more
sugar that had to be added, the hotter the pepper. For example bell peppers
were measured to be about 100 Scoville units, whilst the hottest known pepper
was 577,000. Pure capsaicin has a value of 16 million Sc.units.
Capsaicin is soluble in fats and oils but not in water. Therefore milk,
ice cream and peanut butter can calm the pepper whilst water will spread the
flames!
Cancer Fighters?
The capsaicinoids are phyto chemicals, which means that they have medicinal benefits. Capsaicin helps the metabolism of epoxide aromatic hydrocarbons, which interferes with their ability of bind to DNA (causing mutations). Other uses have been suggested such as preventing ulcers, but it is not know what doses are required (for example, whether an excess of the chemical can be harmful.)
Links
The following links were used in compiling this site:
http://edgein.home.mindspring.com/science/majorcap.html
http://chileheads.netimages.com
http://micro.magnet.fsu.edu/micro/gallery/phytochemicals/phytochemical.html
http://wwwchem.uwimona.edu.jm:1104/lectures/peppers.html
This web page was brought to you by Jeni Tod and Nikki Catt, Keble College, Oxford