Basic information Description Uses Safety Supplier Related
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UV absorber-928

Basic information Description Uses Safety Supplier Related

UV absorber-928 Basic information

Product Name:
UV absorber-928
Synonyms:
  • 2-(2H-benzotriazol-2-yl)-6-(1-methyl-1-phenylethy)-4-(1,1,3,3-tetramethylbutyl)-Phenol
  • TINUVIN 928
  • 2-[2-HYDROXY-3-DIMETHYLBENZYLPHENYL-5-(1,1,3,3-TETRAMETHYLBUTYL)]-2H-BENZOTRIAZOLE
  • 2-6(2H-Benzotriazol-2-yl)-6-(1,1,3,3-tetramethylbutyl)Phenol
  • 2-(2H-BENZOTRIAZOL-2-YL)-6-(1-METHYL-1-PHENYLETHYL)-4-(1,1,3,3-TETRAMETHYLBUTYL)PHENOL
  • UV ABSORBER-928
  • Phenol, 2-(2H-benzotriazol-2-yl)-6-(1-methyl-1-phenylethyl)-4-(1,1,3,3-tetramethylbutyl)-
  • 2-[2-Hydroxy-3-dimethylbenzylphenyl-5-(1,1,3,3-tetramethylbutyl)]-2H-benzotriazol
CAS:
73936-91-1
MF:
C29H35N3O
MW:
441.61
EINECS:
422-600-5
Mol File:
73936-91-1.mol
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UV absorber-928 Chemical Properties

Melting point:
112 °C
Boiling point:
555.5±60.0 °C(Predicted)
Density 
1.07
solubility 
soluble in Toluene
form 
powder to crystal
pka
8.05±0.50(Predicted)
color 
White to Orange to Green
InChI
InChI=1S/C29H35N3O/c1-27(2,3)19-28(4,5)21-17-22(29(6,7)20-13-9-8-10-14-20)26(33)25(18-21)32-30-23-15-11-12-16-24(23)31-32/h8-18,33H,19H2,1-7H3
InChIKey
UZUNCLSDTUBVCN-UHFFFAOYSA-N
SMILES
C1(O)=C(C(C)(C2=CC=CC=C2)C)C=C(C(C)(C)CC(C)(C)C)C=C1N1N=C2C=CC=CC2=N1
EPA Substance Registry System
Phenol, 2-(2H-benzotriazol-2-yl)-6-(1-methyl-1-phenylethyl)-4-(1,1,3,3-tetramethylbutyl)- (73936-91-1)
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Safety Information

HS Code 
2933.99.8290
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UV absorber-928 Usage And Synthesis

Description

UV absorber-928(C29H35N3O) is a hydroxyphenyl benzotriazole UV absorber specially designed for high performance coating applications. UV absorber-928 provides efficiency to coating and light sensitive substrates due to its characteristic broad band absorption. With excellent solubility and high thermal and environmental performance, UV absorber-928 is particularly suitable for coatings exposed to high temperature curing processes, such as powder and coil coatings, or high environmental stress.

Uses

UV absorber-928 has broad absorption properties which can effectively protect coating and other photosensitive materials. UV absorber-928 has high solubility, high temperature resistant and good environmental durability and so on. UV absorber-928 is suitable for high performance coatings, especially suitable for powder coating and industrial and automotive coatings. UV absorber-928 can be enhanced when used in combination with a HALS stabilizer such as UV-292 or UV-123.

Chemical Properties

light yellow crystalline powder

Application

UV absorber-928(Tinuvin 928) is a UV absorber of the hydroxyphenyl benzotriazole class developed specially for high performance coating applications. Its characteristic broadband absorption provides efficient protection to coatings and light sensitive substrates. Its excellent solubility and high thermal and environmental permanence makes it particularly suitable for coatings exposed to high temperature curing processes, such as powder and coil coatings, or high environmental stress. Tinuvin 928 is recommended for applications such as:
automotive coatings
powder and coil coatings
hot melt adhesives
exterior construction coatings (roofing, etc.)
construction adhesives and sealants

Application

UV-928 has broad absorption properties which can effectively protect coating and other photosensitive materials.The product has high solubility, high temperature resistant and good environmental durability and so on..It is suitable for high performance coatings, especially suitable for powder coating and industrial and automotive coatings. UV-928 can be enhanced when used in combination with a HALS stabilizer such as UV-292 or UV-123.

Flammability and Explosibility

Not classified

Synthesis


In a dry argon atmosphere 0.150 g of oxime 5, 0.070 g of 1,2-phenylene diamine 1 and 0.150 ml triethyl-borate are dissolved in 4 ml dry THF and heated for 24 h at 60°C. After a TLC shows consumption of starting oxime the mixture is evaporated to dryness and the resulting residue purified by column chromatography (eluent: hexane - ethyl acetate: 10-1 vol/vol) to give 0.171 g (92 %) of the diazo-amine intermediate 6. Replacing the B(OEt)3 by 2.5 g of basic AI2O3 and the THF by 2 ml of xylene and heating this mixture to 140°C for 48 h gives after the usual work-up 0.089 mg of diazo compound 6 and 0.300 g of starting oxime 5. According the procedure given for the preparation of compound 4 in example 1, triazole 7 is obtained from 0.007 g (0.016 mmol) of intermediate amine 6 and 0.020 g (0.122 mmol) CuSO4 in 100% (0.007 g). In this comparative example, 7.73 equivalents of copper salt are used.

UV absorber-928Supplier

FUJIAN DISHENG TECHNOLOGY CO.,LTD. Gold
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