6659-92-3

Usage

Uses

Used in Plastics Industry:
2-(4-METHOXY-PHENYL)-2H-BENZOTRIAZOL-5-YLAMINE is used as a UV absorber and light stabilizer for protecting plastics from degradation and discoloration caused by exposure to sunlight.
Used in Coatings Industry:
In the coatings industry, 2-(4-METHOXY-PHENYL)-2H-BENZOTRIAZOL-5-YLAMINE serves as a UV stabilizer, ensuring the longevity and color retention of coated surfaces by shielding them from harmful UV rays.
Used in Cosmetics Industry:
2-(4-METHOXY-PHENYL)-2H-BENZOTRIAZOL-5-YLAMINE is utilized as a photostabilizer in cosmetics to protect sensitive ingredients such as dyes and pigments from UV-induced damage, thereby maintaining the product's efficacy and appearance.
Used in Preservation of Sensitive Materials:
2-(4-Methoxy-phenyl)-2H-benzotriazol-5-ylamine is used as a photostabilizer for the preservation of sensitive materials like dyes and pigments, preventing their degradation and ensuring their stability under exposure to light.

Upstream product

• 20311-41-5 (E)-4-(2-(4-methoxyphenyl)diazenyl)benzene-1,3-diamine 
• 17333-79-8 p-methoxybenzenediazonium 
• 541-69-5 m-phenylenediamine dihydrochloride 

Relevant academic research and scientific papers

TREATMENT OF DUCHENNE MUSCULAR DYSTROPHY

There are disclosed compound of Formula (I) or (II) wherein A1, A2, A3, A4and A5, which may be the same or different, represent N or CR1, R9 represents - L -R3, in whi

APPLICATION OF FLUORESCENT TRIAZOLES TO ANALYTICAL CHEMISTRY. III. FLUORESCENCE CHARACTERISTICS OF 2-PHENYLBENZOTRIAZOLYL-5-AMINE DERIVATIVES AS FLUORESCENT PROBES

2-Phenylbenzotriazole derivatives with a COCH3 or NH2 group on the 2-phenyl ring were synthesized and found to be applicable as fluorescent hydrophobic probes.The fluorescence intensities of these compounds, which were intense in non-polar solvents, were dramatically quenched in polar solvents.In particular, 2-(4-acetylphenyl)-2H-benzotriazolyl-5-amine (7) showed a much higher ratio of the fluorescence intensity in the organic solvent to that in water (Fo/Fw) than 8-anilino-1-naphthalenesulfonate (ANS): The Fo/Fw values of 7 were 470 for dioxane and 440 for acetone, while those of ANS were 100 for dioxane and 90 for acetone.We modified compound 7 to obtain water-soluble probes for use in drug-protein binding studies and examined the interaction of these probes with human serum albumin (HSA).All the compounds, which were practically non-fluorescent in the buffer solution, bound to HSA and fluoresced.Keywords: 2-phenylbenzotriazolyl-5-amine; fluorescence characteristies; solvent effect; fluorescent probe; protein binding