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Ethylhexyl Triazone

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CAS:88122-99-0
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Products Intro: Product Name:ETHYLHEXY TRIAZONE For The UV Filter In Cosmetics And Sunscreens
CAS:88122-99-0
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Ethylhexyl Triazone manufacturers

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  • CAS:88122-99-0
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Ethylhexyl Triazone Basic information
Product Name:Ethylhexyl Triazone
Synonyms:Octyl lriazone;2,4,6-Trianilino(p-carbo-2-ethylhexyloxy)-1,3,5-triazine;Ethylhexyl Triazone (200 mg);4,4',4''-[s-Triazine-2,4,6-triyltris(imino)]tris[benzoic acid 2-ethylhexyl] ester;4,4',4''-(1,3,5-Triazine-2,4,6-triyltriimino)trisbenzoic acid tris(2-ethylhexyl) ester;EthylhexylTriazone(UV-T-150);Tris(2-ethylhexyl) 4,4′,4?″-(1,3,5-triazine-2,4,6-triyltriimino)trisbenzoate;UV Absorber 150
CAS:88122-99-0
MF:C48H66N6O6
MW:823.07
EINECS:402-070-1
Product Categories:88122-99-0
Mol File:88122-99-0.mol
Ethylhexyl Triazone Structure
Ethylhexyl Triazone Chemical Properties
Melting point 128°
Boiling point 869.5±75.0 °C(Predicted)
density 1.129±0.06 g/cm3(Predicted)
vapor pressure 0Pa at 20℃
Fp 307℃
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility DMSO : 30 mg/mL (36.45 mM)
form Solid
pka1.22±0.10(Predicted)
color White to Light yellow
Water Solubility 5-7μg/L at 25℃
λmax314nm(lit.)
Merck 14,3809
BRN 11001015
LogP7 at 25℃
Safety Information
Risk Statements 53
Safety Statements 61-24/25
WGK Germany 1
HS Code 29336990
MSDS Information
Ethylhexyl Triazone Usage And Synthesis
DescriptionAs a new type of triazine UV absorber, ethylhexyl triazone has a large molecular structure and high UV absorption efficiency, has a broad-spectrum sunscreen effect, is the most powerful oil-soluble UV-B absorber on the market today, has high photostability and prevents UV-B-induced immunosuppression. It has strong water resistance and a good affinity for skin keratin.
UsesEthylhexyl Triazone is used in sunscreen formulations as a UV filter to block out harmful ultraviolet light.
Usesethylhexyl triazone is the InCI name for octyltriazone. It is a uV filter and absorber. Clinical studies show high photostability and very high uVB-absorption capacity, particularly when compared to other popular uV filters. Studies also indicate that even low concentrations of ethylhexyltriazone in a sun care preparation can contribute significantly to the final product’s SPF. It appears to perform particularly well in synergy with zinc oxide.
DefinitionEthylhexyl triazone (octyl triazone; a derivative of PABA): Not authorized in the USA. Increases the effectiveness of other filters. Free radicals are released in sunlight. Very little data. Prudence (EWG 1 None)[1].
SynthesisTo the reactor was added 2000 mL of toluene, Sodium methoxide 103.6g and 1210mL isooctanol, heated and dissolved to dissolve, And heated to 110 ~ 115 °C, containing 1036g slowly added dropwise Methyl triazone 1500mL toluene solution was added dropwise, insulation reaction 8-10h, the reaction was continuously distilled to remove the methanol produced. The reaction is completed, and the solvent is distilled off. After the solvent is evaporated to dryness, 2500 mL of absolute ethanol is added. Crystallization of octyl triazone (UVT-150) product, filtration, Washed with anhydrous ethanol and water to obtain a UV absorber (UVT-150; Ethylhexyl Triazone)Product 1549g.
References [1] Sonia Santander Ballestín, M. J. Luesma Bartolomé. “Toxicity of Different Chemical Components in Sun Cream Filters and Their Impact on Human Health: A Review.” Applied Sciences-Basel (2023).
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