Database/Skin Conditioning Agent/Caprylyl Glycol
Route-dependent · ISO 16128

Is Caprylyl Glycol natural?

It depends. Caprylyl glycol is made either from coconut caprylic acid (natural origin 1.0) or from petrochemical 1-octene via epoxidation (0.0); both routes are commercial.

INCI nameCaprylyl Glycol
CAS1117-86-8
FormulaC8H18O2 · 146.23 Da
FunctionSkin Conditioning Agent · Humectant
FeedstockPlant route: reduction of coconut caprylic acid and…

Why the score varies

This ingredient is made commercially by more than one route, and ISO 16128 scores the feedstock actually used. Without a supplier certificate of origin the value cannot be claimed.

RouteFeedstockNOIShareNotes
OleochemicalCoconut caprylic acid1.00Common for natural-positioned gradesNatural origin
Petrochemical1-Octene from ethylene0.00CommonFully synthetic
Ask your supplier. A batch-specific certificate of origin or bio-based carbon test (ASTM D6866) settles which route applies.

How we scored it

What counts. ISO 16128-2 scores the atoms that remain in the final ingredient. Reagents, solvents, catalysts and protecting groups used during manufacture leave no mass behind and are not counted.

How it’s made

Epoxidation (peracid), then acid hydrolysis. Each curved arrow moves one electron pair, and the film ends on the score above.

Where it comes from

Plant route: reduction of coconut caprylic acid and hydroxylation. Petrochemical route: epoxidation and hydrolysis of 1-octene.

The industrial synthesis of caprylyl glycol (2-ethylhexyl-1,3-hexanediol) typically involves a multi-step process starting from petrochemical feedstocks. A common route begins with the aldol condensation of butyraldehyde, which is derived from propylene via hydroformylation (oxo process). This condensation yields 2-ethylhexenal.

Subsequently, 2-ethylhexenal undergoes hydrogenation. This hydrogenation step can be carried out in two stages or a single stage depending on the desired product and process. Initially, the aldehyde group is reduced to an alcohol, forming 2-ethylhexanol. Further reaction or a different pathway involving the unsaturated aldehyde can lead to the diol structure. Alternatively, caprylic acid (octanoic acid), which can be sourced from both natural fats and oils (like coconut oil) or petrochemical routes, can be reduced to capryl alcohol, and then further processed. However, the dominant commercial route for cosmetic grade caprylyl glycol is the petrochemical pathway.

The hydrogenation is typically performed using heterogeneous catalysts, such as nickel-based catalysts (e.g., Raney nickel) or precious metal catalysts (e.g., palladium or platinum on carbon), under elevated temperatures (e.g., 100-200 °C) and pressures (e.g., 50-200 bar) in the presence of hydrogen gas. The reaction is usually carried out in a liquid phase or gas phase reactor. Following the reaction, the crude product is purified through distillation to remove unreacted starting materials, byproducts, and catalyst residues, ensuring the high purity required for cosmetic applications.

In plain English

Caprylyl glycol is a versatile ingredient often found in skincare and cosmetic products. It's a synthetic compound that acts as a multi-functional agent, helping to improve the feel of products on your skin and keeping them stable. Think of it as a helper ingredient that enhances the overall performance and texture of your favorite creams, lotions, and serums.

Its primary role is to condition the skin, making it feel smoother and softer. It also has humectant properties, meaning it can help attract and retain moisture, contributing to skin hydration. Additionally, caprylyl glycol is known to boost the effectiveness of traditional preservatives, allowing formulators to use less of them while still ensuring the product remains safe and free from microbial contamination. This makes it a valuable component in modern cosmetic formulations.

CosIng definition: Caprylyl Glycol is the diol that conforms to the formula

Natural alternatives with the same function

Structure

2D structure of Caprylyl Glycol

octane-1,2-diol

PubChem CID 14231 ↗

References

  1. 1ISO 16128-1:2016 and ISO 16128-2:2017 — Guidelines on technical definitions and criteria for natural and organic cosmetic ingredients and products. ISO, Geneva.
  2. 2Caprylyl Glycol. PubChem CID 14231. National Center for Biotechnology Information. pubchem.ncbi.nlm.nih.gov ↗
  3. 3CAPRYLYL GLYCOL. CosIng — European Commission cosmetic ingredient database. ec.europa.eu/cosing ↗
  4. 4CAPRYLYL GLYCOL. CosIng u2014 European Commission database for information on cosmetic substances and ingredients. https://ec.europa.eu/growth/tools-databases/cosing/search?search=CAPRYLYL%20GLYCOL