88122-99-0

Basic information

• Product Name: UVT-150
• Synonyms: 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;Uvinul T 150;2,4,6-Trianilino(p-carbo-2-ethylhexyloxy)-1,3,5-triazine;Ethylhexyl Triazone (200 mg);Octyl lriazone;EthylhexylTriazone(UV-T-150);Tris(2-ethylhexyl) 4,4′,4?″-(1,3,5-triazine-2,4,6-triyltriimino)trisbenzoate
• CAS NO: 88122-99-0
• Molecular Formula: C₄₈H₆₆N₆O₆
• Molecular Weight: 823.07
• EINECS: 402-070-1
• Mol File: 88122-99-0.mol
• Article Data: 27

Chemical Properties

• Melting Point: 128°
• Boiling Point: 869.5 °C at 760 mmHg
• Flash Point: 307℃
• Appearance: /
• Density: 1.129 g/cm³
• Vapor Pressure: 0Pa at 20℃
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 1.22±0.10(Predicted)
• Water Solubility: 5-7μg/L at 25℃
• Merck: 14,3809
• BRN: 11001015
• CAS DataBase Reference: UVT-150(CAS DataBase Reference)
• NIST Chemistry Reference: UVT-150(88122-99-0)
• EPA Substance Registry System: UVT-150(88122-99-0)

Safety Data

• Statements: 53
• Safety Statements: 61-24/25
• WGK Germany: 1
• Hazardous Substances Data: 88122-99-0(Hazardous Substances Data)

Usage

Description

UVT-150, also known as Ethylhexyl Triazone, is a UV filter and absorber with high photostability and UVB-absorption capacity. It is particularly effective when used in combination with zinc oxide, making it a popular ingredient in sunscreen formulations.
Used in Sun Care Industry:
UVT-150 is used as a UV filter in sunscreen formulations for its ability to block out harmful ultraviolet light, providing protection against sunburn and reducing the risk of skin cancer and premature skin aging. Its high photostability and UVB-absorption capacity make it an effective ingredient in sun care products.
Used in Combination with Zinc Oxide:
UVT-150 is used in synergy with zinc oxide to enhance the overall effectiveness of sunscreen formulations. The combination of these two ingredients provides broad-spectrum protection against both UVA and UVB rays, ensuring comprehensive skin protection.

Upstream product

• 26218-04-2 2-ethylhexyl 4-aminobenzoate 
• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 104-76-7 2-Ethylhexyl alcohol 
• 96474-94-1 4,4',4''-(1,3,5-triazine-2,4,6-triyltriimino)trisbenzoic acid triethyl ester 
• 62-23-7 4-nitro-benzoic acid 
• 16397-70-9 4-nitro-benzoic acid, 2-ethylhexyl ester 
• 63557-10-8 4 ,4 ′,4 ″-((1,3,5-triazine-2,4,6-triyl)tris(azanediyl))tribenzoic acid 

Relevant articles and documents

Preparation method of sun-screening agent octyl triazinone

The invention discloses a preparation method of a sun-screening agent octyl triazinone, octyl triazinone prepared by the preparation method and an application of octyl triazinone, and the method comprises the following steps: step 1, carrying out esterification reaction on p-nitrobenzoic acid and isooctyl alcohol to obtain a product I, 2, carrying out a hydrogenation reaction on the product I in the presence of a catalyst, filtering after the reaction is completed, and carrying out reduced pressure distillation to obtain a product II, and step 3, adding a solvent into the product II, heating to reflux, adding the solution A, carrying out a reaction, and carrying out post-treatment to obtain octyltriazinone. Cheap and easily available p-nitrobenzoic acid is used as a raw material, the sun-screening agent octyl triazinone is efficiently prepared through esterification, hydrogenation and coupling, meanwhile, iso-octyl p-aminobenzoate is obtained, the obtained octyl triazinone is high in chromatographic purity and yield, and the method has the advantages of being few in three wastes, low in cost, green, environmentally friendly, easy to operate, easy to control and the like.Easy realization of industrial production.

An ultraviolet absorbent octyl triazone synthetic method

The invention relates to a synthetic method for an ultraviolet absorbent--octyl triazone. The method comprises the following steps: with sodium bisulfate as a catalyst, reacting p-nitrobenzoic acid with isooctanol under the action of toluene so as to prep