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Al222
Al222 (25415 pt) 2026-Sep-11 19:35

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

CharacteristicValueNote
INCI nameTrihydroxystearincosmetic ingredient name
Chemical nameGlyceryl tris(12-hydroxystearate)glycerin triester
Systematic name1,2,3-Propanetriyl tris(12-hydroxyoctadecanoate)chemical denomination
Chemical categoryhydroxylated triglyceride / lipid esterlipophilic structuring agent
Molecular formulaC₅₇H₁₁₀O₉defined molecular substance
Molecular weight939.5 g/molindicative value
CAS139-44-6principal identifier
EC205-364-6European identifier
PubChem CID25100chemical identifier
CosIng reference38718cosmetic ingredient reference
Cosmetic functionsSkin Conditioning; Viscosity Controllingdocumented functions
Cosmetics Regulation provisionsno specific provision identifiedno specific Annex II–VI provision identified

Indicative physicochemical properties

CharacteristicIndicative valueNote
Physical statewaxy solidat room temperature
Appearancewhite/off-white powder, granules, or waxy massgrade-dependent
Melting pointapproximately 85–89 °Ctypical commercial range
Water solubilitypractically insolublestrongly lipophilic structure
Compatibility with oilshigh after suitable heating and dispersionmainly used in the oil phase
Compatibility with siliconespossible in many systemsshould be verified experimentally
Volatilitynegligiblehigh molecular weight
Rheological behaviorgelling / thixotropicforms networks in lipid phases
Thermal stabilitygood under normal cosmetic processing conditionsexcessive prolonged heating should be avoided
Oxidative stabilitygenerally goodpredominantly 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:

  1. disperse the material in the oil phase;

  2. heat sufficiently for proper incorporation;

  3. use adequate mixing;

  4. 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.