Welcome to LookChem.com Sign In|Join Free
  • or
BIS(3,5-DI-T-BUTYL-4-HYDROXYBENZYL) SULFIDE is a phenolic antioxidant chemical compound known for its high thermal stability and compatibility with a wide range of substrates. It serves as an effective free radical scavenger, inhibiting oxidation and protecting materials from degradation caused by exposure to air and light.

1620-93-5

Post Buying Request

1620-93-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1620-93-5 Usage

Uses

Used in Plastics Industry:
BIS(3,5-DI-T-BUTYL-4-HYDROXYBENZYL) SULFIDE is used as an additive in the production of plastics to enhance their durability and performance by preventing degradation and extending the lifespan of the materials.
Used in Rubber Industry:
In the rubber industry, BIS(3,5-DI-T-BUTYL-4-HYDROXYBENZYL) SULFIDE is utilized as a stabilizer to protect rubber products from deterioration caused by exposure to air and light, ensuring their longevity and maintaining their properties.
Used in Adhesives Industry:
BIS(3,5-DI-T-BUTYL-4-HYDROXYBENZYL) SULFIDE is employed as a component in the formulation of adhesives to improve their resistance to oxidation and extend their shelf life, ensuring consistent performance over time.

Check Digit Verification of cas no

The CAS Registry Mumber 1620-93-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1620-93:
(6*1)+(5*6)+(4*2)+(3*0)+(2*9)+(1*3)=65
65 % 10 = 5
So 1620-93-5 is a valid CAS Registry Number.

1620-93-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-ditert-butyl-4-[(3,5-ditert-butyl-4-hydroxyphenyl)methylsulfanylmethyl]phenol

1.2 Other means of identification

Product number -
Other names di-(3,5-di-tert.-butyl-4-hydroxybenzyl)-sulfide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:1620-93-5 SDS

1620-93-5Upstream product

1620-93-5Downstream Products

1620-93-5Relevant academic research and scientific papers

4-Formyl amino-n-methylpiperidine derivatives, the use thereof as stabilisers and organic material stabilised therewith

-

, (2008/06/13)

The present invention relates to 4-formylamino-N-methylpiperidine derivatives of the formula (I) where the variables are as defined in the Description, to a process for preparing these piperidine derivatives, to the use of these piperidine derivatives of the invention, or prepared according to the invention, for stabilizing organic material, in particular for stabilizing plastics or coating materials, and also to the use of these piperidine derivatives of the invention, or prepared according to the invention, as light stabilizers or stabilizers for wood surfaces. The present invention further relates to stabilized organic material which comprises these piperidine derivatives of the invention or prepared according to the invention.

Thioether substituted hydroxybenzophenones and stabilized compositions

-

, (2008/06/13)

2-Hydroxybenzophenone derivatives substituted in the 4′-position by a thioether moiety exhibit enhanced absorption in the UV at longer wavelength. Compositions comprising organic material subject to actinic degradation are beneficially stabilized with such derivatives.

2-(2′-hydroxyphenyl)benzotriazoles used as U.V. stabilizers

-

, (2008/06/13)

2-(2′-hydroxyphenyl)benzotriazoles having general formula (I). The above 2-(2′-hydroxyphenyl)benzotriazoles are useful as light stabilizers for organic polymers.

2-(2′-hydroxyphenyl) benzotriazoles containing a 2,4-imidazolidinedione group and process for their preparation

-

, (2008/06/13)

2-(2′-hydroxyphenyl)benzotriazoles having general formula (I). The above 2-(2′-hydroyzphenyl)benzotriazoles having general formula (I) are useful as heat, oxygen and light stabilizers for organic polymers. In particular they are useful as UV stabilizers for organic polymers.

2-(2'Hydroxyphenyl) benzotriazoles and process for their preparation

-

, (2008/06/13)

2-(2'-hydroxyphenyl)benzotriazoles having general formula (I): The above 2-(2'-hydroxyphenyl)benzotriazoles can be used as light stabilizers for organic polymers.

2-(2'Hydroxyphenyl) benzotriazoles and their use as light stabilizers for organic polymers

-

, (2008/06/13)

2-(2'-hydroxyphenyl)benzotriazoles having general formula (I): The above 2-(2'-hydroxyphenyl)benzotriazoles can be used as light stabilizers for organic polymers.

Amorphous modification of 1,1',1"-nitrilo(tri-2-propyl-tris-[2,2'-ethylidene-bis(4,6-di-tert-butylphenyl] phosphite)

-

, (2008/06/13)

The new amorphous modification of 1,1',1"-nitrilo{tri-2-propyl-tris-[2,2'-ethylidene-bis(4,6-di-tert-butylphenyl)]phosphite } is obtained by cooling rapidly said compound from the melt to ambient temperature. This amorphous form is an effective process stabilizer for polyolefins, particularly polypropylene.

Beta crystalline modification of 2,2',2"-nitrilo[triethyl-tris-(3,3',5,5'-tetra-tert-butyl-1,1'-biphenyl-2,2'-diyl) phosphite]

-

, (2008/06/13)

The beta crystalline modification of 2,2',2"-nitrilo[triethyl-tris-(3,3',5,5'-tetra-tert-butyl-1,1'-biphenyl-2,2'-diyl) phosphite] is obtained by crystallizing said compound from the melt at elevated temperatures. The beta crystalline form is an effective process stabilizer for polyolefins, particularly polypropylene.

3,9-carbohydrate substituted 2,4,8,10-tetraoxa-3,9-diphosphaspiro(5.5)undecane phosphite stabilizers

-

, (2008/06/13)

Carbohydrate substituted phosphites of Formula I STR1 where A is a carbohydrate residue are effective stabilizers for polymers processed at elevated temperatures and subject to thermal or oxidative degradation.

Non-migrating 1-hydrocarbyloxy hindered amine derivatives as polymer stabilizers

-

, (2008/06/13)

1-Hydrocarbyloxy substituted hindered amine compounds which also contain a reactive functional group such as hydroxy, amino, oxirane or carboxyl can be chemically attached to selected polymer substrates by condensation reactions to give polymers containing a chemically-bonded, non-migrating stabilizer having excellent stabilization efficacy for protecting said polymer substrate from the adverse effects of actinic light.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1620-93-5