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Compounds · Phenols · Heat (Maillard reaction and pyrolysis)

Phenol

Also known as Carbolic acid · Acid phenic — an analysis may use any of these names

Antiseptic, asphalt, with a slight note of printing ink. Sharp and dry.

CAS
108-95-2
Formula
C6H6O
Molar mass
94.11
Odour threshold
5.9 ppmin water
Boiling point
≈ 182 °C at atmospheric pressure
Volatility
150 °C290 °C
Threshold
most potentleast potent

The two axes are 64 points apart. Volatility tells you whether the compound leaves a surface early or late; the threshold tells you how much of it the nose needs before it notices. When the two sit this far apart, they explain things the percentages on an analysis cannot explain on their own.

Where it comes from

Biosynthetic pathway: Heat (Maillard reaction and pyrolysis) — fire breaks large molecules into ones you can smell.

About the threshold figure

High. It needs a large concentration, and at that level it is already irritating.

Published thresholds differ by several orders of magnitude, because of differences in measuring method, sample purity and panel. The figure here is an order of magnitude for relative comparison, not a measurement. We give it only for compounds where the literature broadly agrees — 52 of the 106 compounds in the library. The rest are left blank rather than guessed.

Why it sits where it does

An aromatic ring with one hydroxyl group, forming strong hydrogen bonds, so it boils much higher than benzene of the same size.

Where else you meet it

Wood smoke, asphalt, and some island whiskies.

Regulatory note

Corrosive in pure form; in essential oils it is present only in trace amounts. This is a labelling requirement, not a warning about the product.