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Squalane

MolecularEntity Emollient

Squalane is a 30-carbon saturated triterpene produced by the complete hydrogenation of – a process that eliminates all six of squalene’s double bonds, converting an oxidatively vulnerable molecule into one with no sites available for peroxidative attack. The result is chemically inert in the context of : squalane does not generate reactive aldehydes, does not peroxidise under UV or ambient oxygen exposure, and has a substantially longer shelf life than its precursor. It is produced commercially from olive oil squalene, sugarcane-derived squalene via fermentation, or – historically and now largely phased out on ethical grounds – from shark liver oil. [1]

Despite its structural simplicity, squalane integrates readily into the lipid environment, spreading easily across the surface and penetrating into the upper epidermal layers without the heaviness or occlusive density of wax- or -based formulations. Its comedogenicity rating is low, making it suitable for -prone presentations where heavier occlusive may not be appropriate. It provides emolliency – reducing friction at the skin surface and improving texture – without contributing oxidation products to a surface environment already managing UV-generated peroxidative stress.

The practical distinction from squalene is worth stating plainly: squalene is the endogenous component with antioxidant function that becomes a comedogenic liability under UV overload; squalane is the stable topical ingredient that delivers compatible emolliency without that liability. They are related molecules with different risk profiles, and the confusion between them in client-facing content and product marketing is common enough to warrant the distinction being made explicitly.

Published
Updated
References
  1. Makrantonaki E, Ganceviciene R, Zouboulis C (2011). An update on the role of the sebaceous gland in the pathogenesis of acne. Dermatoendocrinol, 3(1), 41-9 .

Molecular Structure

2D Molecular Structure of Squalane
Formula
C₃₀H₆₂
Weight
422.80 g/mol
IUPAC
2,6,10,15,19,23-hexamethyltetracosane
Computational Identifiers
Chemical Identifiers
InChI InChI=1S/C30H62/c1-25(2)15-11-19-29(7)23-13-21-27(5)17-9-10-18-28(6)22-14-24-30(8)20-12-16-26(3)4/h25-30H,9-24H2,1-8H3
InChIKeyPRAKJMSDJKAYCZ-UHFFFAOYSA-N
Canonical SMILESCC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C
Data sourced from: PubChem (NCBI) ↗

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