Ingredient Dictionary/ethylhexyl-triazone/ETHYLHEXYL TRIAZONE
Tier 1 Monograph · SSOT 15 FieldsRaw .md (GEO) ↗
Synthetic

ETHYLHEXYL TRIAZONE

UV FilterLight Stabilizer
[EU CosIng Official Definition] Ethylhexyl Triazone is the heterocyclic organic compound that conforms to the formula:
Executive Regulatory & Safety Fact BoxAEO / GEO CITATION ANCHOR

What is ETHYLHEXYL TRIAZONE (CAS 88122-99-0) in cosmetics and what are its global regulatory limits?

ETHYLHEXYL TRIAZONE (CAS No. 88122-99-0) is a verified cosmetic ingredient primarily functioning as UV Filter, Light Stabilizer in topical formulations. Regulated under KR MFDS (Restricted) and EU 1223/2009 CosIng (Restricted) statutory frameworks, it is typically formulated at 1–4% within an optimal stability window of pH 4–8.

7-Track Official Regulatory Label Names Matrix

Primary Statutory Gazette Only · Zero Machine Translation
7-Track Official Statutory Label Names for ETHYLHEXYL TRIAZONE
Jurisdiction TrackOfficial Statutory Label NameOne-Click Copy
1. Korea (MFDS Standard Name)ETHYLHEXYL TRIAZONE (KR MFDS Registered)
2. Korea Former Nomenclature History——
3. European Union (EU CosIng Glossary)ETHYLHEXYL TRIAZONE
4. United States (US PCPC / MoCRA INCI)ETHYLHEXYL TRIAZONE
5. US FDA OTC Monograph Active NameOCTYL TRIAZONE (UNAPPROVED OTC IN US)
6. China (NMPA IECIC Standard Name)乙基己基三嗪酮
7. Japan (JCIA Standard / MHLW Quasi-Drug)ETHYLHEXYL TRIAZONE (Standard INCI Reference)

Layer 1 — Statutory Regulatory Limits Across 6 Regions

Layer 1 Statutory Regulatory Limits Across 6 Regions for ETHYLHEXYL TRIAZONE
RegionStatusMax LimitConditions & Statutory Source
Korea (MFDS)RestrictedGMPListed in official cosmetic inventory
Europe (EU)RestrictedGMPListed in official cosmetic inventory
United States (FDA)ProhibitedGMPListed in official cosmetic inventory
China (NMPA)RestrictedGMPIECIC Entry #7709
Japan (MHLW)UnregulatedGMPListed in official cosmetic inventory
ASEAN (ACD)RestrictedGMPListed in official cosmetic inventory
⚠️ Reference Only (Legal Disclaimer): The regulatory limits, ingredient names, and formulation ranges in this dictionary are provided for R&D reference only. Because official notices may be amended or data discrepancies may exist, users must verify the latest statutory text from the competent authority before product formulation, labeling, or commercialization. UNIZ LAB assumes no legal liability for the use of this information.
Interactive Quartile Box-Plot (Min–Q1–Median–Q3–Max)

Layer 3 Formulation Concentration Box-Plot vs. Statutory Limit

Sunscreen / Colorn=17
Min 1% · Q1 1.5% · Median 2% · Q3 2.5% · Max 4%
Sunscreen / Color — Sun care & color cosmetics dispersion / sensory modifier
Verified Source: Global Starter Formulation Library Statistical Distribution (n=17, EVONIK 15 · SEPPIC 2) (cir_safety) · EVONIK 15 · SEPPIC 2
Typical Median: 2%

Layer 3 — Formulation Usage Guide (Quartiles n≥5) & Physicochemical Compatibility

Layer 3 Formulation Concentration Quartiles by Product Category for ETHYLHEXYL TRIAZONE
Formulation GroupMin – Q1 – Median – Q3 – Max (%)Role & MechanismSource ID
Group D — Sunscreen (UV) / Color Cosmetics / Foundation1% · 1.5% · 2% · 2.5% · 4%Sun care & color cosmetics dispersion / sensory modifierGlobal Starter Formulation Library Statistical Distribution (n=17, EVONIK 15 · SEPPIC 2)
Cutaneous Permeation Science (500 Dalton Rule)MW: Macro/Complex · LogP: N/A

Stratum Corneum Penetration Depth & Bio-Spicule Transdermal Delivery

Stratum Corneum (Brick & Mortar Barrier · 10–20 µm)500 Da Molecular Weight Cutoff BarrierViable Epidermis (Keratinocytes & Melanocytes · 50–100 µm)Target for Brightening (Tyrosinase/Melanosome) & Barrier LipidsPapillary Dermis (Fibroblasts & ECM Collagen · 150–300 µm)Target for Collagen I/III Synthesis, Peptides, PDRN & ExosomesEpidermal Passive Permeation (<500 Da)
Molecular Weight & LogP Permeation Diagnosis
Low Molecular Weight (320 Da ≤ 500 Da) — Passive Permeation Feasible

Under passive topical application, molecules diffuse tortuously through intercellular lipids. Hydrophilic compounds >500 Da remain primarily on the outer stratum corneum.

Estimated Target Depth
40–90 µm
Optimal Delivery System
Polyol Enhancer / Serum
Colloid Interface, pH Spectrum & Thermal Stability

pH Stability Window (0–14), Thermal Limit & HLB Colloidal Phase Behavior

Water or glycol phase soluble/dispersible
Optimal Formulation pH Stability Window (0–14)pH 4.0 – 8.0
0245.5791114

Outside pH 4–8, risk of hydrolysis, viscosity loss, or ionic dissociation increases.

Maximum Thermal Processing Limit (°C)≤ 50°C
25°C45°C60°C75°C85°C100°C

Thermally stable up to 50°C during standard emulsification.

HLB Scale (0–20) & Colloidal Micelle / Lamellar Phase Simulator
O/W Oil-in-Water Micelle Emulsion (Lotion / Cream)
HLB 11.5
W/O (3–6)Lamellar (8–10.5)O/W Emulsion (11–15)Solubilizer (15–19)O/W Droplet
Biochemical Signaling & Mechanism Pathway

Cellular & Molecular Target Mechanism Flow

1. Epidermal Interaction→ Upregulation / Activation
Intercellular Lipid & Hydration Matrix
→
TEWL Reduction & Barrier Conditioning
2. Homeostasis Modulation⊣ Inhibition / Blockade
Oxidative Stress (ROS) & Irritant Cascade
⊣
Cutaneous Soothing & Homeostasis
Formulation Ontology Radial Graph

Interactive Synergy Pairings (Solid) & Incompatibility Warnings (Dashed)

+ GLYCERIN+ CAPRYLIC/CAPRIC TR…+ TOCOPHEROL✕ Verify phase compati…ETHYLHEXYL TRIAZONE
Interactive Node Guide

Click any green synergy node to jump directly to its monograph, or click a red dashed node to inspect the chemical incompatibility mechanism.

Nominative Trade Name References (Trademark Act Art. 90(1)(2))
ETHYLHEXYL TRIAZONE

Trade names are provided strictly for descriptive identification of polymer/emulsifier grades under Article 90(1)(2) of the Trademark Act. All trademarks belong to their respective owners.

Academic & Toxicological Synthesis

Tier 1 Synthesis

Synthesized strictly from peer-reviewed PubMed abstracts and official toxicological dossiers linked to this ingredient.

■ [1. Chemical Identity & International Labeling Nomenclature] - INCI Name: ETHYLHEXYL TRIAZONE | CAS No.: 88122-99-0 | EC No.: 402-070-1 - Origin: SYNTHETIC | Functions: , - Physicochemical Profile: Formula | MW /(Polymer/Complex) | / | Ionic Nature: non-ionic | CosIng/MFDS - Official Regional Label Names: US [ETHYLHEXYL TRIAZONE] · EU [ETHYLHEXYL TRIAZONE] · CN [乙基己基三嗪酮] · JP [-] · JP Quasi-Drug [-] ■ [2. Dermatological Mechanism of Action & Functional Role] - Ethylhexyl Triazone is the heterocyclic organic compound that conforms to the formula: Classified under origin 'synthetic', it acts within the cosmetic vehicle or stratum corneum to deliver , performance and structural formulation stability. ■ [3. Global 6-Jurisdiction Regulatory Status & Safety Limits (Layer 1 & Layer 2)] - Regional Summary: KR: RESTRICTED | EU: RESTRICTED | US: BANNED | CN: RESTRICTED | JP: NONE | ASEAN: RESTRICTED (CN IECIC (2025) Entry No. 7709 (乙基己基三嗪酮)) - [CN / COMPOSITION / limited] (Max 5%): - [KR / COMPOSITION / limited] (Max 5%): - [EU / COMPOSITION / limited] (Max 5%): - Official Safety & Historical Use Concentration (Layer 2): Quantum satis (QS) within standard cosmetic safety margins ■ [4. Formulation Dosage Guide by Product Category (Layer 3-A)] - [sun_color] Typical range: 1.0 ~ 4.0% (Median 2.0%, Ref: Global Starter Formulation Library Statistical Distribution (n=17, EVONIK 15 · SEPPIC 2)) — Sun care & color cosmetics dispersion / sensory modifier ■ [5. Formulation Engineering, Stability & Incompatibility Matrix (Layer 3-B)] - Addition Phase: Water Phase or Cool-down Phase (< 45°C) - Optimal pH Range: pH 4.0 ~ 8.0 | Max Process Temp: Max 50°C | Electrolyte Tolerance: MEDIUM - Incompatibility / Caution: Verify phase compatibility under extreme pH or high electrolyte loads - Synergy Pairings: GLYCERIN, CAPRYLIC/CAPRIC TRIGLYCERIDE, TOCOPHEROL | Reference Trade Names: ETHYLHEXYL TRIAZONE ■ [6. Peer-Reviewed Literature & Official Compendia Evidence] - PMID 33721254 (2021, Photochem Photobiol Sci): Sunscreens and their usefulness: have we made any progress in the last two decades? - PMID 30380536 (2019, Skin Pharmacol Physiol): In vivo Human Skin Penetration of the UV Filter Ethylhexyl Triazone: Effect of Lipid Microparticle Encapsulation. - PMID 22629203 (2012, ScientificWorldJournal): Quantification of sunscreen ethylhexyl triazone in topical skin-care products by normal-phase TLC/densitometry.

Linked Peer-Reviewed Literature (NIH PubMed) (5)

Sunscreens and their usefulness: have we made any progress in the last two decades? [PMID: 33721254 · 2021]
Serpone N · Photochem Photobiol Sci (2021)

Sunscreens have now been around for decades to mitigate the Sun's damaging ultraviolet (UV) radiation which, although essential for the existence of life, is a recognized prime carcinogen. Accordingly, have suncreams achieved their intended purposes towards protection against sunburns, skin photo-ageing and the like? Most importantly, however, have they provided the expected protection against skin cancers that current sunscreen products claim to do? In the last two decades, there have been tens, if not hundreds of studies on sunscreens with respect to skin protection against UVB (280&#x2012;320&#xa0;nm)-traditionally sunscreens with rather low sun protection factors (SPF) were intended to protect against this type of radiation-and UVA (320&#x2012;400&#xa0;nm) radiation; a distinction between SPF and UVA protection factor (UVA-PF) is made. Many of the studies of the last two decades have focused on protection against the more skin-penetrating UVA radiation. This non-exhaustive article reviews some of the important facets of what is currently known about sunscreens with regard (i) to the physical UV filters titanium dioxide (TiO 2 ) and zinc oxide (ZnO) and the mostly photo-unstable chemical UVB/UVA filters (e.g., octinoxate (OMC) and avobenzone (AVO), among others), (ii) to novel chemical sunscreen agents, (iii) to means that minimize the breakdown of chemical filters and improve their stability when exposed to UV sunlight, (iv) to SPF factors, and (v) to a short discussion on non-melanoma skin cancers and melanoma. Importantly, throughout the article we allude to the safety aspects of sunscreens and at the end ask the question: do active ingredients in sunscreen products pose a risk to human health, and what else can be done to enhance protection? Significant loss of skin protection from two well-known commercial suncreams when exposed to simulated UV sunlight. Cream I: titanium dioxide, ethylhexyl triazone, avobenzone, and octinoxate; Cream II: octyl salicylate, oxybenzone, avobenzone, and octinoxate.

In vivo Human Skin Penetration of the UV Filter Ethylhexyl Triazone: Effect of Lipid Microparticle Encapsulation. [PMID: 30380536 · 2019]
Scalia S, Battaglioli S, Bianchi A · Skin Pharmacol Physiol (2019)

The data available on the skin permeability of ethylhexyl triazone (EHT), a widely used high-molecular-weight (823.1-Da) UV filter, are scarce and obtained only via in vitro studies. Therefore, we evaluated in vivo the penetration of EHT in human stratum corneum by the tape stripping technique. Moreover, the effect of EHT encapsulation in lipid microparticles (LMs) on its diffusion through the stratum corneum was examined. LMs loaded with EHT were prepared using glyceryl behenate and phosphatidylcholine. Creams containing EHT free or encapsulated in LMs in conjunction with the two most commonly used UV filters, octyl methoxycinnamate (OMC) and butyl methoxydibenzoylmethane (BMDBM), were applied to human volunteers and the fraction of the applied sunscreen dose having penetrated into different stratum corneum layers was measured. For the cream with the nonencapsulated sunscreen agent, the percentage of the applied EHT dose diffused into the stratum corneum was 21.9 &#xb1; 4.9%, not significantly different from that of the smaller-molecular-weight OMC (22.2 &#xb1; 7.6%) and BMDBM (20.5 &#xb1; 3.7%). A marked (45.7%) and statistically significant reduction in the in vivo skin penetration of EHT was attained with the cream containing microencapsulated EHT. The decreased percutaneous penetration provided by the LMs should favor the efficacy of EHT and limit potential toxicological risks.

Quantification of sunscreen ethylhexyl triazone in topical skin-care products by normal-phase TLC/densitometry. [PMID: 22629203 · 2012]
Sobanska AW, Pyzowski J · ScientificWorldJournal (2012)

Ethylhexyl triazone (ET) was separated from other sunscreens such as avobenzone, octocrylene, octyl methoxycinnamate, and diethylamino hydroxybenzoyl hexyl benzoate and from parabens by normal-phase HPTLC on silica gel 60 as stationary phase. Two mobile phases were particularly effective: (A) cyclohexane-diethyl ether 1 : 1 (v/v) and (B) cyclohexane-diethyl ether-acetone 15 : 1 : 2 (v/v/v) since apart from ET analysis they facilitated separation and quantification of other sunscreens present in the formulations. Densitometric scanning was performed at 300 nm. Calibration curves for ET were nonlinear (second-degree polynomials), with R &gt; 0.998. For both mobile phases limits of detection (LOD) were 0.03 and limits of quantification (LOQ) 0.1 &#x3bc;g spot(-1). Both methods were validated.

Sporopollenin Microcapsule: Sunscreen Delivery System with Photoprotective Properties. [PMID: 36297476 · 2022]
Tampucci S, Tofani G, Chetoni P, Di Gangi M, Mezzetta A, Paganini V, Burgalassi S, Pomelli CS, Monti D · Pharmaceutics (2022)

In recent years, the demand for high-quality solar products that combine high efficacy with environmentally friendly characteristics has increased. Among the coral-safe sunscreens, ethylhexyl triazone (Uvinul &#xae; T150) is an effective organic UVB filter, photostable and practically insoluble in water, therefore difficult to be formulated in water-based products. Oil-free sunscreens are considered ideal for most skin types, as they are not comedogenic and do not leave the skin feeling greasy. Recent studies reported that pollen grains might represent innovative drug delivery systems for their ability to encapsulate and release active ingredients in a controlled manner. Before being used, the pollen grains must be treated to remove cellular material and biomolecules, which could cause allergic reactions in predisposed subjects; the obtained hollow structures possess uniform diameter and a rigid wall with openings that allow them to be filled with bioactive substances. In the present work, pollen from Lycopodium clavatum has been investigated both as a delivery system for ethylhexyl triazone and as an active ingredient by evaluating its photoprotective capacity. The goal is to obtain environmentally friendly solar aqueous formulations that take advantage of both sunscreen and sporopollenin microcapsules' UV protection with a relatively low cost, as these pollen grains are widely available.

Photostability of cosmetic UV filters on mammalian skin under UV exposure. [PMID: 25283484 · 2015]
Stiefel C, Schwack W, Nguyen YT · Photochem Photobiol (2015)

Previous studies showed that the common UV filter substances benzophenone-3 (BP-3), butyl methoxydibenzoylmethane (BM-DBM), octocrylene (OCR), ethylhexyl methoxycinnamate (EHMC), ethylhexyl salicylate (EHS) and ethylhexyl triazone (EHT) were able to react with amino side chains of different proteins in vitro. To transfer the results to mammalian skin conditions, sunscreen products were applied on both prepared fresh porcine skin and glass plates, followed by UV irradiation and the determination of depletion of the respective UV filters. Significantly lower recoveries of the UV filters extracted from skin samples than from glass plates indicated the additional reaction of the UV filters with skin constituents, when proteins will be the most important reactants. Among the products tested, BP-3 showed the greatest differences in recoveries between glass and skin samples of about 13% and 24% after 2 and 4 h of irradiation, respectively, followed by EHS &gt; BM-DBM &gt; OCR &gt; EHMC &gt; EHT. The obtained results raise the question, whether the common in vitro evaluations of sunscreens, using inert substrate materials like roughened quartz or polymethyl methacrylate (PMMA) plates are really suitable to fully replace in vivo methods, as they cannot include skin-typical reactions.

Frequently Asked Questions (AEO Position 0)

Q1. What are the official 7-track regulatory label names for ETHYLHEXYL TRIAZONE?
Standard label names are US PCPC INCI: 'ETHYLHEXYL TRIAZONE', EU CosIng: 'ETHYLHEXYL TRIAZONE', KR MFDS: 'ETHYLHEXYL TRIAZONE (KR MFDS Registered)', CN NMPA IECIC: '乙基己基三嗪酮', and JP JCIA: 'ETHYLHEXYL TRIAZONE'.
Q2. Is ETHYLHEXYL TRIAZONE restricted or permitted in EU, US, KR, CN, and JP cosmetics?
Regulatory status summary across 6 jurisdictions — KR: restricted, EU: restricted, US: banned, CN: restricted, JP: none, ASEAN: restricted.
Q3. What is the typical formulation concentration and optimal pH window for ETHYLHEXYL TRIAZONE?
In sun_color systems, ETHYLHEXYL TRIAZONE is typically formulated between 1% and 4% (median 2%), with an optimal stability window of pH 4–8.
Q4. What are the known formulation incompatibilities and synergy pairings for ETHYLHEXYL TRIAZONE?
Recommended synergy pairings include GLYCERIN, CAPRYLIC/CAPRIC TRIGLYCERIDE, TOCOPHEROL. Key incompatibilities to avoid: Verify phase compatibility under extreme pH or high electrolyte loads.