UV Absorber 329


  • Product Name
  • CasNo
  • MF
  • MW
  • Content
  • Appearance
  • Packing
  • Apply
  • UV Absorber 329
  • 3147-75-9
  • C20H25N3O
  • 323.438
  • Slightly yellowish powder
Inquiry

Factory supply good quality UV Absorber 329 3147-75-9 with stock

  • Molecular Formula:C20H25N3O
  • Molecular Weight:323.438
  • Appearance/Colour:Slightly yellowish powder 
  • Vapor Pressure:1.58E-09mmHg at 25°C 
  • Melting Point:101-108 °C 
  • Refractive Index:1.584 
  • Boiling Point:471.8 °C at 760 mmHg 
  • PKA:8.07±0.45(Predicted) 
  • Flash Point:239.2 °C 
  • PSA:50.94000 
  • Density:1.1 g/cm3 
  • LogP:4.83990 

Octrizole(Cas 3147-75-9) Usage

Characterization

UV-329 is an ultraviolet light absorber (UVA) of the hydroxyphenyl benzotriazole class, which is used as a light stabilizer for plastics and other organic substrates.

Applications

UV-329 is an effective light stabilizer for a variety of plastics and other organic substrates.

Features/benefits

UV-329 protects polymers from UV radiation, helping to preserve the original appearance and physical integrity of molded articles, films, sheets, and fibers during outdoor weathering.

Product forms

UV-329??? Slightly yellow powder UV-329 FL???? Slightly yellow, rodlike granules

Guidelines for use

The use levels of UV-329 range between 0.1 and 1.0 %, depending on substrate and performance requirements of the final application. The product can be used alone or in combination with other additives such as light stabilizers (hindered amines), antioxidants (hindered phenols, phosphites, thiosynergists, hydroxylamines), and other functional stabilizers and additives. The use of UV-329 in combination with hindered amine light stabilizers is particularly noteworthy in that a synergistic performance is often observed. Performance data of UV-329 alone or in combination with other additives are available in selected substrates.

Handling & Safety

UV-329 exhibits a very low order of oral toxicity and does not present any abnormal problems in its handling or general use. Detailed information on handling and any precautions to be observed in the use of the product(s) described in this leaflet can be found in our relevant health and safety information sheet.

Definition

An UV light absorber.

Flammability and Explosibility

Notclassified

InChI:InChI=1/C20H25N3O/c1-19(2,3)13-20(4,5)14-10-11-18(24)17(12-14)23-21-15-8-6-7-9-16(15)22-23/h6-12,24H,13H2,1-5H3

3147-75-9 Relevant articles

ANTI-BLUE LIGHT COMPOUND, PREPARATION METHOD AND APPLICATION THEREOF

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Paragraph 0105; 0107, (2021/07/30)

Disclosed is a blue light absorbing comp...

Reduction method of substituted phenol coupling compound

-

Paragraph 0018-0021, (2020/12/30)

The invention relates to a reduction met...

Novel polycyclic compound

-

Paragraph 0165; 0169-0170, (2020/07/06)

The invention provides a novel polycycli...

Preparation method of ultraviolet absorbent UV - 329 (by machine translation)

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Paragraph 0032; 0038; 0039; 0045; 0046; 0052, (2019/08/26)

The invention provides a preparation met...

3147-75-9 Process route

2-(2'-hydroxy-5'-tert-octylphenyl)nitrodiazobenzene
51656-57-6

2-(2'-hydroxy-5'-tert-octylphenyl)nitrodiazobenzene

Cyasorb UV 5411
3147-75-9,52188-76-8

Cyasorb UV 5411

Conditions
Conditions Yield
With methanol; Aminoiminomethanesulfinic acid; sodium hydroxide; In toluene; at 50 - 80 ℃; for 0.5h; Reagent/catalyst; Solvent; Temperature;
96.4%
With sodium hydroxide; zinc; In water; Petroleum ether; at 50 ℃; for 5h;
With sodium hydroxide; zinc; In water; Petroleum ether; at 50 ℃; for 5h;
C<sub>20</sub>H<sub>25</sub>N<sub>3</sub>O<sub>2</sub>

C20H25N3O2

Cyasorb UV 5411
3147-75-9,52188-76-8

Cyasorb UV 5411

Conditions
Conditions Yield
With hydrogenchloride; In water; toluene; at 70 ℃; for 2h; Concentration; Temperature; Reagent/catalyst;
89.5%
With hydrogenchloride; zinc; In toluene; Reflux;
88.2%

3147-75-9 Upstream products

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    51656-57-6

    2-(2-Nitro-phenylazo)-4-(1,1,3,3-tetramethyl-butyl)-phenol

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    52184-19-7

    2-Nitro-2'-hydroxy-3',5'-di-tert-pentyl-azobenzene

  • 486-25-9
    486-25-9

    9-fluorenone

  • 27959-42-8
    27959-42-8

    2-nitro-2'-hydroxy-5'-tert-butylazobenzene

3147-75-9 Downstream products

  • 10096-91-0
    10096-91-0

    2-(2-Hydroxyphenyl)-2H-benzotriazole

  • 116043-76-6
    116043-76-6

    6-allyl-2-(2H-1,2,3-benzotriazol-2-yl)-4-(t-octyl)phenol

  • 185155-06-0
    185155-06-0

    2,2'-dihydroxy-3-(2H-benzotriazol-2-yl)-3'-(4,6-diphenyl-s-triazin-2-yl)-5-tert-octyl-6'-hexyloxy-diphenylmethane

  • 943024-15-5
    943024-15-5

    trifluoromethanesulfonic acid 2-benzotriazol-2-yl-4-(1,1,3,3-tetramethylbutyl)phenyl ester

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