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Hexamethylene bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate] is an antioxidant and stabilizer with a complex chemical structure that provides significant benefits in various applications. It is characterized by its ability to prevent oxidation and degradation in materials, thereby extending their lifespan and maintaining their quality. Hexamethylene bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate] is also known for its protective properties against heat and light-induced degradation, making it a valuable ingredient in a wide range of industrial and consumer products. Its relatively non-toxic and non-irritating nature further enhances its suitability for use in diverse applications.

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  • 3,5-Bis-(1,1-dimethylethyl)-4-hydroxybenzenepropanoic acid 1,6-hexanediyl ester

    Cas No: 35074-77-2

  • USD $ 1.2-5.0 / Kiloliter

  • 5 Kiloliter

  • 3000 Metric Ton/Month

  • Chemwill Asia Co., Ltd.
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  • 35074-77-2 Structure
  • Basic information

    1. Product Name: Hexamethylene bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate]
    2. Synonyms: Hexamethylene bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate];IRGANOX 259;3,5-bis(1,1-dimethylethyl)-4-hydroxy-benzenepropanoic acid 1,6-hexanediyl ester;1,6-hexamethylenebis(3,5-tert-butyl-4-hydroxyhydrocinnamate);1,6-hexanediyl3,5-bis(1,1-dimethylethyl)-4-hydroxybenzenepropanoate;benzenepropanoicacid,3,5-bis(1,1-dimethylethyl)-4-hydroxy-,1,6-hexanediyles;Benzenepropanoicacid,3,5-bis(1,1-dimethylethyl)-4-hydroxy-,1,6-hexanediylester;Hexamethylenebis(3,5-di-tert-butyl-4-hydroxyhydrocinnamate)
    3. CAS NO:35074-77-2
    4. Molecular Formula: C40H62O6
    5. Molecular Weight: 638.92
    6. EINECS: 252-346-9
    7. Product Categories: Organics
    8. Mol File: 35074-77-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 648.1 °C at 760 mmHg
    3. Flash Point: 180.7 °C
    4. Appearance: /
    5. Density: 1.033 g/cm3
    6. Vapor Pressure: 2.13E-17mmHg at 25°C
    7. Refractive Index: 1.518
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: Chloroform (Slightly), Methanol (Slightly)
    10. PKA: 12.03±0.40(Predicted)
    11. CAS DataBase Reference: Hexamethylene bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate](CAS DataBase Reference)
    12. NIST Chemistry Reference: Hexamethylene bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate](35074-77-2)
    13. EPA Substance Registry System: Hexamethylene bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate](35074-77-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 35074-77-2(Hazardous Substances Data)

35074-77-2 Usage

Uses

Used in Plastics Industry:
Hexamethylene bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate] is used as an antioxidant and stabilizer for plastics to prevent oxidation and degradation, thereby extending the lifespan and maintaining the quality of the plastic products.
Used in Adhesives Industry:
In the adhesives industry, Hexamethylene bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate] serves as an essential component to enhance the stability and performance of adhesives by preventing oxidation and degradation, ensuring a longer-lasting bond.
Used in Coatings Industry:
Hexamethylene bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate] is used as a stabilizer in coatings to protect against heat and light-induced degradation, ensuring the durability and appearance of coated surfaces over time.
Used in Industrial Applications:
Hexamethylene bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate] is utilized in various industrial applications as an antioxidant and stabilizer to enhance the performance and longevity of materials exposed to harsh conditions, such as high temperatures and UV radiation.
Used in Consumer Applications:
Hexamethylene bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate] is employed in consumer products to provide protection against oxidation and degradation, ensuring the quality and longevity of everyday items. Its non-toxic and non-irritating properties make it a safe choice for use in products that come into contact with the skin or are used in household settings.

Check Digit Verification of cas no

The CAS Registry Mumber 35074-77-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,7 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35074-77:
(7*3)+(6*5)+(5*0)+(4*7)+(3*4)+(2*7)+(1*7)=112
112 % 10 = 2
So 35074-77-2 is a valid CAS Registry Number.
InChI:InChI=1/C40H62O6/c1-37(2,3)29-23-27(24-30(35(29)43)38(4,5)6)17-19-33(41)45-21-15-13-14-16-22-46-34(42)20-18-28-25-31(39(7,8)9)36(44)32(26-28)40(10,11)12/h23-26,43-44H,13-22H2,1-12H3

35074-77-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]hexyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate

1.2 Other means of identification

Product number -
Other names Irganox 249

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Lubricants and lubricant additives,Oxidizing/reducing agents
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:35074-77-2 SDS

35074-77-2Upstream product

35074-77-2Downstream Products

35074-77-2Relevant articles and documents

Process for the production of hydroxyalkylphenyl derivatives

-

, (2008/06/13)

An improved process for the production of hydroxyalkylphenyl derivatives, especially esters and amides containing hydroxyalkylphenyl groups is disclosed, which process comprises gradually adding methyl acrylate, in the presence of an alkaline catalyst, to the alkyl substituted phenolic compound, and adding to the resultant reaction mixture a suitable alcohol or amine, optionally in the presence of a second catalyst which is different from the first catalyst. The improved process results in good yields and in a reduction of undesirable by-products while avoiding isolation of the intermediates.

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