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4021-36-7

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4021-36-7 Usage

Description

2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine is a triazine derivative chemical compound known for its effectiveness as a UV stabilizer and antioxidant. It is characterized by its ability to protect materials from degradation caused by ultraviolet radiation, thereby extending their lifespan and enhancing their durability.

Uses

Used in Plastics Industry:
2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine is used as a UV stabilizer and antioxidant for plastics, ensuring their resistance to UV-induced degradation and improving their overall performance and longevity.
Used in Rubber Industry:
In the rubber industry, 2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine serves as a stabilizer, protecting rubber materials from the damaging effects of UV radiation and prolonging their service life.
Used in Adhesives Production:
2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine is used as a stabilizer in the production of adhesives to enhance their durability and resistance to UV degradation, ensuring stronger and longer-lasting bonds.
Used in Coatings Production:
As a stabilizer in coatings, 2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine helps to maintain the integrity and appearance of coated surfaces by protecting them from UV-induced damage.
Used in Film Production:
2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine is used in the production of films to provide UV stabilization, ensuring the films remain clear and undamaged over time.
Used in Packaging Materials:
In the packaging industry, 2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine is utilized as a stabilizer to protect packaging materials from UV degradation, thus preserving the quality and appearance of the packaged products.

Check Digit Verification of cas no

The CAS Registry Mumber 4021-36-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,2 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4021-36:
(6*4)+(5*0)+(4*2)+(3*1)+(2*3)+(1*6)=47
47 % 10 = 7
So 4021-36-7 is a valid CAS Registry Number.

4021-36-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine

1.2 Other means of identification

Product number -
Other names -

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:4021-36-7 SDS

4021-36-7Relevant articles and documents

Nickel-catalysed C–O bond reduction of 2,4,6-triaryloxy-1,3,5-triazines in 2-methyltetrahydrofuran

Wang, Yaoyao,Shen, Jun,Chen, Qun,Wang, Liang,He, Mingyang

, p. 409 - 412 (2019)

A nickel-catalysed reduction of phenol derivatives activated by 2,4,6-trichloro-1,3,5-triazine (TCT) in ecofriendly 2-methyltetrahydrofuran (2-MeTHF) is described. The phenol-TCT derivatives were readily prepared using grinding method in short time without further purification. This catalytic system allowed the facile C–O cleavage of phenol-TCT derivatives under mild reaction conditions with high efficiency and good functional group tolerance. Gram-scale reaction was also achieved. Particularly, sequential functionalization of phenol-TCT derivatives followed by C–O bond reduction could also be realized, affording the high value-added products in moderate to good yields.

Efficient Ni-catalyzed conversion of phenols protected with 2,4,6-trichloro-1,3,5-triazine (TCT) to olefins

Etemadi-Davan,Iranpoor

supporting information, p. 12794 - 12797 (2017/12/06)

An efficient Ni(COD)2/dppf catalyzed olefination of Ar-O-TCT as synthetic equivalents of aryl halides is described. Activation of C-O bonds in phenols as readily available compounds was achieved with 2,4,6-trichloro-1,3,5-triazine (TCT). This method provides practical access to 1,2-disubstituted olefins in high yields and high functional group compatibility.

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