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UV-320

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Company Name: Guangdong Wengjiang Chemical Reagent Co., Ltd.  Gold
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UV-320 manufacturers

  • uv absorber 320
  • uv absorber 320 pictures
  • 2026-06-02
  • CAS:3846-71-7
  • Min. Order: 25KG
  • Purity: 98%
  • Supply Ability: 20 tons
  • UV absorber UV-320
  • UV absorber UV-320 pictures
  • $10.00
  • 2026-05-28
  • CAS:3846-71-7
  • Min. Order: 10KG
  • Purity: 99%
  • Supply Ability: 10000kg
  • UV-320
  • UV-320 pictures
  • 2025-06-27
  • CAS:3846-71-7
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 500000kg
UV-320 Basic information
Product Name:UV-320
Synonyms:4,6-Di-tert-butyl-2-(2H-benzotriazole-2-yl)phenol;2-Benzotriazole-2-yl-4;6-di-tert-butylphenol;3,5-Dibutylhy-2-droxyphenylbenzotriazole;2-(3,5-Di-t-butyl-2-hydroxyphenyl)benzotriazole;2-(2H-Benzo[d][1,2,3]triazol-2-yl)-4,6-di-tert-butylphenol;uv absorber uv-320;2-(2'-Hydroxy-3',5'-di-t-butylphenyl)benzotriazole
CAS:3846-71-7
MF:C20H25N3O
MW:323.43
EINECS:223-346-6
Product Categories:
Mol File:3846-71-7.mol
UV-320 Structure
UV-320 Chemical Properties
Melting point 152-154°C
Boiling point 444.0±55.0 °C(Predicted)
density 1.10±0.1 g/cm3(Predicted)
Fp 215°C
storage temp. 2-8°C
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
pka9.41±0.48(Predicted)
color White to Off-White
InChIInChI=1S/C20H25N3O/c1-19(2,3)13-11-14(20(4,5)6)18(24)17(12-13)23-21-15-9-7-8-10-16(15)22-23/h7-12,24H,1-6H3
InChIKeyLHPPDQUVECZQSW-UHFFFAOYSA-N
SMILESC1(O)=C(C(C)(C)C)C=C(C(C)(C)C)C=C1N1N=C2C=CC=CC2=N1
CAS DataBase Reference3846-71-7(CAS DataBase Reference)
EPA Substance Registry SystemPhenol, 2-(2H-benzotriazol-2-yl)-4,6-bis(1,1-dimethylethyl)- (3846-71-7)
Safety Information
Risk Statements 48/22-52/53
Safety Statements 26-36/37/39
RIDADR 3077
TSCA TSCA listed
MSDS Information
ProviderLanguage
UV-320 English
ALFA English
UV-320 Usage And Synthesis
UsesUV-320 is a benzotriazole UV stabilizer, which is used to increase product stability and to prevent discolouration in various consumer and industrial goods such as plastics. Benzotriazole UV stabilizers are a pollutant for the aquatic environment and have been implicated as a potential stable and toxic ligands for aryl hydrocarbon receptor in human.
Synthesis
NSC 373428

84755-44-2

UV-320

3846-71-7

The general procedure for the synthesis of 2-(2H-3,5-di-tert-butyl-2-hydroxyphenyl)benzotriazole from 2-(2'-hydroxy-3',5'-di-tert-butylphenyl)benzotriazole N-oxide is as follows: Example 3: 10 g (0.03 mol) of 2-(2'-hydroxy-3',5'-di-tert-butylphenyl)benzotriazole-N-oxide, 100 mg of palladium-carbon catalyst, 100 ml of solvent mixture of toluene and water (4:1 ratio by volume), and 3 g of 50% dimethylamine solution were added to a 500 ml autoclave equipped with a stirrer. After replacing the air in the autoclave with hydrogen, the hydrogen pressure was set to 10 kg/cm2. The temperature was raised to 50 °C with stirring, and the reaction was maintained at this temperature until no more hydrogen was absorbed by the mixture. After completion of the reaction, the autoclave was cooled and the catalyst was removed by filtration. A portion of the filtrate was quantitatively analyzed by GC and the yield of 2-(2'-hydroxy-3',5'-di-tert-butylphenyl)benzotriazole was measured to be 85.6%. After removing the solvent from the filtrate by distillation, the residual solid was crystallized with ethanol and subsequently washed with ethanol to give 7.1 g of 2-(2'-hydroxy-3',5'-di-tert-butylphenyl)benzotriazole (71% yield; melting point 152-155 °C).

References[1] Tetrahedron Letters, 1997, vol. 38, # 48, p. 8303 - 8306
[2] Tetrahedron Letters, 1997, vol. 38, # 5, p. 845 - 848
[3] Journal of Organic Chemistry, 1995, vol. 60, p. 5683 - 5685
[4] Australian Journal of Chemistry, 1982, vol. 35, # 10, p. 2089 - 2093
[5] Patent: US5104992, 1992, A
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