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"4,4',4''-[nitrilotris(methylene)]tris[2,6-bis(1,1-dimethylethyl)phenol]" is a complex organic compound, often referred to as a tris-phenol derivative. It is characterized by a central nitrilotrimethylene chain that connects three 2,6-bis(1,1-dimethylethyl)phenol units. This structure endows the compound with unique properties, such as high thermal stability and antioxidant activity. It is commonly used as an antioxidant in industrial applications, particularly in the rubber and plastics industries, to prevent degradation caused by heat, light, and oxygen exposure. The compound's molecular formula is C42H66N2O6, reflecting its composition of carbon, hydrogen, nitrogen, and oxygen atoms. Its chemical structure and properties make it a valuable additive for enhancing the longevity and performance of various materials.

752-60-3

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752-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 752-60-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,5 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 752-60:
(5*7)+(4*5)+(3*2)+(2*6)+(1*0)=73
73 % 10 = 3
So 752-60-3 is a valid CAS Registry Number.

752-60-3SDS

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 4-[[bis[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]amino]methyl]-2,6-ditert-butylphenol

1.2 Other means of identification

Product number -
Other names EINECS 212-035-0

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:752-60-3 SDS

752-60-3Relevant 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.

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.

Process for the preparation of diphosphonate derivatives

-

, (2008/06/13)

A process for the preparation of a compound of formula I, STR1 wherein R1 and R2 are independently C1-6 alkyl, R3 is hydroxy and R4 and R5 are independently C1-6 alkyl is disclosed. The process comprises reacting a compound of formula II, STR2 wherein R1, R2 and R3 are defined as in formula I and X is a leaving group, with a compound of formula III, STR3 wherein R4 and R5 are independently C1-6 alkyl, in the presence of a base.

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.

Reaction of 3,5-Di-tert-butyl-4-hydroxybenzyl Acetate with Amines

Bukharov,Nugumanova,Mukmeneva

, p. 1605 - 1608 (2007/10/03)

3,5-Di-tert-butyl-4-hydroxybenzyl acetate reacts with primary and secondary amines to give mainly the corresponding benzylamines. Base-catalyzed transformation of 3,5-di-tert-butyl-4-hydroxybenzyl acetate into 2,6-di-tert-butyl-4-methylene-2,5-cyclohexadienone occurs to a small extent. The major product of the reaction of 3,5-di-tert-butyl-4-hydroxybenzyl acetate with aqueous ammonia is bis(3,5-di-tert-butyl-4-hydroxybenzyl) ether which is formed by the action of ammonium acetate liberated during the process.

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.

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