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Compound library · Biosynthetic pathways

Fatty acid derivatives

Enzymes cut fat chains into fragments you can smell

10 compounds in the library

When plant or animal tissue is damaged, enzymes immediately cut the fatty acids in the cell membranes into shorter fragments. The result is the group of six-carbon compounds we call green leaf volatiles.

This is the pathway of injury and of immediacy. Freshly cut grass, a crushed leaf, a fruit just cut open — all three trigger the same mechanism within seconds.

The same pathway, with longer chains, gives the eight- to twelve-carbon aldehydes of citrus peel, and the lactones that give a sense of fattiness in coconut and milk.

Compounds that follow this pathway

CompoundChemical familyBoiling pointThreshold
cis-3-Hexenol Alcohols 156 °C 70 ppb
3-Octanone Ketones 167 °C —
1-Octen-3-ol Alcohols 175 °C 1 ppb
1-Octen-3-one Ketones 175 °C 0.005 ppb
3-Octanol Alcohols 175 °C —
Decanal Aldehydes 208 °C 2 ppb
Dodecanal Aldehydes 238 °C 2 ppb
γ-Nonalactone Lactones 243 °C —
cis-Jasmone Ketones 248 °C —
δ-Decalactone Lactones 281 °C —

Three axes, three questions

This library classifies compounds along three axes, and each answers a different question.

Boiling point tells you when you smell a compound — early or late on the smelling strip. Chemical family tells you how it behaves — stable or fragile, and how to recognise it on an analysis. Biosynthetic pathway tells you where it comes from.

The third axis is the explanatory one. The other two describe how compounds cluster into groups; this one says why they cluster that way.