antioxidant 330


  • Product Name
  • CasNo
  • MF
  • MW
  • Content
  • Appearance
  • Packing
  • Apply
  • antioxidant 330
  • 1709-70-2
  • C54H78O3
  • 775.212
  • White crystalline powder
Inquiry

Manufacturer Sells Best Quality antioxidant 330 1709-70-2 with stock

  • Molecular Formula:C54H78O3
  • Molecular Weight:775.212
  • Appearance/Colour:White crystalline powder 
  • Vapor Pressure:5.02E-22mmHg at 25°C 
  • Melting Point:248-250 °C(lit.) 
  • Refractive Index:1.546 
  • Boiling Point:730 °C at 760 mmHg 
  • PKA:11.91±0.40(Predicted) 
  • Flash Point:240 °C 
  • PSA:60.69000 
  • Density:1.004 g/cm3 
  • LogP:14.28600 

1,3,5-Trimethyl-2,4,6-tris(3,5-di-tert-butyl-4-hydroxybenzyl)benzene(Cas 1709-70-2) Usage

Characterization

Antioxidant 1330 – a sterically hindered phenolic antioxidant – is as highly effective stabilizer for organic substrates such as polymers, synthetic fibers, elastomers, adhesives, waxes, oils and fats. It protects these substrates against thermo-oxidative degradation.

Applications

Antioxidant 1330 is used in polyolefins e.g. polyethylene, polypropylene, polybutene for the stabilization of pipes, molded articles, wires and cables, dielectric films, etc.. Furthermore, it is applied in other polymers such as engineering plastics like linear polyesters, polyamides, and styrene homoand copolymers. It may also be used in PVC, polyurethanes, elastomers, adhesives, and other organic substrates.

Features/benefits

Antioxidant 1330 has good compatibility with most substrates, high resistance to extraction and is odorless. It offers also excellent dielectrical properties. The product can be used in combination with other additives such as costabilizers (e.g. thioethers, phosphites, phosphonites), light stabilizers and other functional stabilizers. The effectiveness of the blends of Irganox 1330 with Irgafos 168 (Irganox B-blends) is particularly noteworthy. Irganox 1330 is particularly recommended for polyolefin applications requiring good water extraction resistance combined with low color development. Furthermore, Irganox 1330 reduces water carry-over in polypropylene tape extrusion.

Product forms

Antioxidant 1330 ? ? ? white, free-flowing powder Antioxidant 1330 FF??? white, free-flowing granules

Guidelines for use

In polyolefins, the concentration levels for Antioxidant 1330 range typically between 0.05 % and 0.3 % depending on substrate, processing conditions and long-term thermal stability requirements. The optimum level is application specific. Concentration levels of Antioxidant 1330 in hot melt adhesives range from 0.2 % to 1 %, in synthetic tackifier resins, Irganox 1330 concentration ranges between 0.1 % and 0.5 %. Extensive performance data of Irganox 1330 in various organic polymers and applications are available upon request.

Health & Safety

Antioxidant 1330 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.

General Description

1,3,5-Trimethyl-2,4,6-tris(3,5-di-tert-butyl-4-hydroxybenzyl)benzene(HEMA) is an antioxidant that can be used to prevent the oxidative degradation of plastics.

Flammability and Explosibility

Nonflammable

Safety Profile

Moderately toxic by ingestion. An experimental teratogen. When heated to decomposition it emits acrid smoke and irritating fumes.

InChI:InChI=1/C54H78O3/c1-31-37(22-34-25-40(49(4,5)6)46(55)41(26-34)50(7,8)9)32(2)39(24-36-29-44(53(16,17)18)48(57)45(30-36)54(19,20)21)33(3)38(31)23-35-27-42(51(10,11)12)47(56)43(28-35)52(13,14)15/h25-30,55-57H,22-24H2,1-21H3

1709-70-2 Relevant articles

Preparation method of antioxidant 330

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Paragraph 0027-0034, (2021/01/29)

The invention relates to the technical f...

Bifunctional compound and synthesis method thereof, and applications of bifunctional compound as antioxidant

-

, (2020/02/14)

The invention discloses a bifunctional c...

Novel method for synthesizing antioxidant 330 by catalyst

-

Page/Page column 12-18, (2018/09/28)

The invention aims at providing a method...

Method for synthesizing multi-hindered phenolic antioxidant 330

-

Paragraph 0022-0024, (2018/11/03)

The invention relates to a method for sy...

1709-70-2 Process route

3,5-di-tert-butyl-4-hydroxybenzyl acetate
14387-17-8

3,5-di-tert-butyl-4-hydroxybenzyl acetate

1,3,5-trimethyl-benzene
108-67-8

1,3,5-trimethyl-benzene

4,4'-Methylenebis(2,6-di-tert-butylphenol)
118-82-1

4,4'-Methylenebis(2,6-di-tert-butylphenol)

1,3,5-trimethyl-2,4,6-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)benzene
1709-70-2

1,3,5-trimethyl-2,4,6-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)benzene

1,3,5-trimethyl-2,4-di(3,5-di-tert-butyl-4-hydroxybenzyl)benzene
41642-52-8

1,3,5-trimethyl-2,4-di(3,5-di-tert-butyl-4-hydroxybenzyl)benzene

Conditions
Conditions Yield
With sulfuric acid; In acetic acid; at 20 - 60 ℃; for 27h; Inert atmosphere;
2,6-di-tert-butylphenol
128-39-2

2,6-di-tert-butylphenol

4,4'-Methylenebis(2,6-di-tert-butylphenol)
118-82-1

4,4'-Methylenebis(2,6-di-tert-butylphenol)

1,3,5-trimethyl-2,4,6-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)benzene
1709-70-2

1,3,5-trimethyl-2,4,6-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)benzene

1,3,5-trimethyl-2,4-di(3,5-di-tert-butyl-4-hydroxybenzyl)benzene
41642-52-8

1,3,5-trimethyl-2,4-di(3,5-di-tert-butyl-4-hydroxybenzyl)benzene

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: diethylamine / 11 h / Reflux
2: sulfuric acid / acetic acid / 27 h / 20 - 60 °C / Inert atmosphere
With sulfuric acid; diethylamine; In acetic acid;

1709-70-2 Upstream products

  • 149475-62-7
    149475-62-7

    1,3,5-tris(3,5-di-tert-butyl-4-hydroxybenzyl)-2,4,6-trimethylbenzene radical

  • 87-97-8
    87-97-8

    2,6-di-tert-butyl-4-methoxymethylene-phenol

  • 108-67-8
    108-67-8

    1,3,5-trimethyl-benzene

  • 128-39-2
    128-39-2

    2,6-di-tert-butylphenol

1709-70-2 Downstream products

  • 20357-51-1
    20357-51-1

    1.3.5-Trimethyl-2.4.6-tris-<3.5-bis-(tert.-butyl)-4-oxo-cyclohexadien-(2.5)-yliden-(1)-methyl>-benzol

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