Trihydroxystearin: properties, uses, pros, cons, safety
Trihydroxystearin is the triester of glycerin and 12-hydroxystearic acid, a waxy lipid used primarily to structure and thicken the oil phase of cosmetic formulations.
It is particularly effective as a gelling and rheology-modifying agent in anhydrous systems, oils, and some silicones. Hydroxyl groups on the lipid chains promote the formation of a three-dimensional network capable of partially immobilizing the liquid phase, thereby increasing consistency and stability.

Its documented cosmetic functions are Skin Conditioning and Viscosity Controlling.
No specific Cosmetics Regulation provisions are identified under Annexes II–VI of the EU Cosmetics Regulation.
Description
Chemically, Trihydroxystearin is glyceryl tri(12-hydroxystearate).
Its three long C18 chains and three secondary hydroxyl groups make it:
strongly lipophilic;
practically insoluble in water;
solid at room temperature;
capable of forming crystalline or semicrystalline structures;
particularly suitable for gelling oils.
Unlike a simple liquid emollient, its main role is structural.
When properly dispersed and heated in the lipid phase and subsequently cooled, it can form a network that gives the formulation thixotropic behavior: the product remains consistent at rest but becomes more fluid under pressure or shear.
Manufacturing process
Trihydroxystearin can be produced mainly by esterification of glycerin with 12-hydroxystearic acid.
Another industrial route is associated with castor oil, naturally rich in ricinoleic-acid triglycerides. Hydrogenation saturates the double bonds and generates materials rich in 12-hydroxystearate derivatives.
Processing may include:
hydrogenation of the lipid raw material;
esterification or transesterification;
removal of unreacted materials;
purification;
filtration;
melting-point control;
standardization;
micronization or preparation in the desired commercial form.
Chemically defined Trihydroxystearin should be distinguished from generic Hydrogenated Castor Oil, which may represent a more complex raw material and is not necessarily equivalent to pure Trihydroxystearin.
Identification data and specifications
| Characteristic | Value | Note |
|---|---|---|
| INCI name | Trihydroxystearin | cosmetic ingredient name |
| Chemical name | Glyceryl tris(12-hydroxystearate) | glycerin triester |
| Systematic name | 1,2,3-Propanetriyl tris(12-hydroxyoctadecanoate) | chemical denomination |
| Chemical category | hydroxylated triglyceride / lipid ester | lipophilic structuring agent |
| Molecular formula | C₅₇H₁₁₀O₉ | defined molecular substance |
| Molecular weight | 939.5 g/mol | indicative value |
| CAS | 139-44-6 | principal identifier |
| EC | 205-364-6 | European identifier |
| PubChem CID | 25100 | chemical identifier |
| CosIng reference | 38718 | cosmetic ingredient reference |
| Cosmetic functions | Skin Conditioning; Viscosity Controlling | documented functions |
| Cosmetics Regulation provisions | no specific provision identified | no specific Annex II–VI provision identified |
Indicative physicochemical properties
| Characteristic | Indicative value | Note |
|---|---|---|
| Physical state | waxy solid | at room temperature |
| Appearance | white/off-white powder, granules, or waxy mass | grade-dependent |
| Melting point | approximately 85–89 °C | typical commercial range |
| Water solubility | practically insoluble | strongly lipophilic structure |
| Compatibility with oils | high after suitable heating and dispersion | mainly used in the oil phase |
| Compatibility with silicones | possible in many systems | should be verified experimentally |
| Volatility | negligible | high molecular weight |
| Rheological behavior | gelling / thixotropic | forms networks in lipid phases |
| Thermal stability | good under normal cosmetic processing conditions | excessive prolonged heating should be avoided |
| Oxidative stability | generally good | predominantly saturated structure |
Cosmetics
Trihydroxystearin is particularly useful when consistency must be increased without introducing large amounts of hard waxes.
It may be used in:
lip balms;
lipsticks;
glosses;
sticks;
foundations;
concealers;
sunscreens;
cleansing balms;
gelled oils;
anhydrous creams;
deodorant sticks;
massage products;
formulations containing suspended pigments or particles.
Oil-phase gelation
Its technological behavior is based on the ability of molecules to associate through hydrogen bonding between –OH groups, forming a three-dimensional network during cooling.
This can help:
increase viscosity;
reduce oil separation;
stabilize anhydrous products;
suspend pigments and particles;
improve stick consistency;
create creamy or balm-like textures;
reduce sedimentation and migration of certain components.
Performance depends strongly on concentration, oil composition, and thermal processing.
Formulation process
To obtain a uniform structure, it is generally necessary to:
disperse the material in the oil phase;
heat sufficiently for proper incorporation;
use adequate mixing;
control the cooling stage.
Poor processing may result in:
graininess;
irregular crystallization;
non-uniform gels;
lower-than-expected viscosity;
oil separation.
The optimal use level should therefore be determined experimentally for each formulation.
Pros
Effective oil-phase gelling agent.
Can provide thixotropic behavior.
Improves consistency and stability of anhydrous formulations.
Helps keep pigments and particles suspended.
Particularly useful in sticks, balms, and make-up.
Generally good oxidative stability.
Can reduce the need for high levels of traditional waxes.
Contributes to a smooth, uniform sensory profile.
Has a favorable cosmetic safety assessment under evaluated conditions of use.
Cons
Practically insoluble in water.
Usually requires heating during processing.
Rheological performance depends strongly on the oil phase.
Incorrect dosage or cooling may cause graininess or undesirable crystallization.
Excessive use can make the texture too rigid.
It is not a primary emulsifier and does not automatically replace an emulsifying system.
It should not be confused with generic Hydrogenated Castor Oil.
Supplier performance claims should be verified in the actual formulation.
Safety and regulation
Trihydroxystearin has been evaluated within cosmetic safety assessments of triglyceride-based ingredients and is considered safe under the practices and concentrations of use evaluated.
Available data do not indicate a particular concern for:
acute toxicity;
significant irritation under normal cosmetic conditions;
relevant sensitization;
mutagenicity.
Its large molecular size and high lipophilicity also limit penetration through intact skin.
Hazard profile
Available regulatory information does not indicate a significant harmonized hazard classification for normal cosmetic handling conditions.
As with any raw material, assessment should nevertheless be based on the actual commercial grade, including possible impurities or additives.
EU Cosmetics Regulation provisions
No specific:
Cosmetics Regulation provisions
are identified for Trihydroxystearin under Annexes II–VI of Regulation (EC) No 1223/2009.
The absence of a specific Annex provision does not remove the requirement to assess the safety of the finished cosmetic product.
Raw-material control
For professional evaluation, it is advisable to obtain:
updated SDS;
Certificate of Analysis (COA);
technical data sheet;
assay/purity;
melting point;
acid value;
hydroxyl value;
free glycerol;
free 12-hydroxystearic acid;
residual starting materials;
residual catalyst metals where relevant;
residual solvents where applicable;
particle-size distribution for powder grades;
stability data;
origin of the lipid raw material;
storage conditions.
For grades intended specifically for oil gelation, it is also useful to obtain data on:
activation temperature;
recommended use level;
compatible oils;
gelling capacity;
thixotropic behavior;
cooling conditions.
Environment
Trihydroxystearin is a lipid ester that can be produced from plant-derived raw materials, often associated with the castor-oil supply chain.
Its environmental profile depends mainly on:
agricultural origin of the raw material;
castor cultivation;
hydrogenation process;
energy consumption;
catalysts;
purification;
transport;
management of production residues.
Its very low volatility limits atmospheric emissions during normal cosmetic use.
The ester bonds allow degradation pathways, although the actual environmental fate depends on exposure conditions and formulation type.
Conclusion
Trihydroxystearin is a hydroxylated triglyceride used mainly as a structuring and viscosity-controlling agent in oil phases.
Its ability to create a thixotropic network makes it particularly useful in balms, sticks, make-up, anhydrous products, and formulations containing pigments or suspended particles.
Its safety profile is favorable, and no specific Cosmetics Regulation provisions are identified in the European Union.
Trihydroxystearin can be considered a generally favorable and technologically useful cosmetic ingredient, with particular attention to purity, melting point, acid value, correct dispersion in the oil phase, processing temperature, and control of crystallization during cooling.