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106990-43-6

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  • Factory Supply N,N',N'',N'''-tetrakis(4,6-bis(butyl-(N-methyl-2,2,6,6-tetramethylpiperidin-4-yl)amino)triazin-2-yl)-4,7-diazadecane-1,10-diamine

    Cas No: 106990-43-6

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  • 1,5,8,12-Tetrakis-[4,6-bis-(N-butyl-N-1,2,2,6,6-pentamethyl-4-piperidylamino)-1,3,5-triazin-2-yl]-1,5,8,12-tetraazadodecane

    Cas No: 106990-43-6

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106990-43-6 Usage

Description

Chimassorb 119, also known as 1,5,8,12-Tetrakis[4,6-bis(N-butyl-N-1,2,2,6,6-pentamethyl-4-piperidylamino)-1,3,5-triazin-2-yl]-1,5,8,12-tetraazadodecane, is an off-white solid that functions as a light and thermal stabilizer. It is specifically designed for use in olefin polymers that come into contact with food, ensuring the preservation of product quality and safety.

Uses

Used in Food Packaging Industry:
Chimassorb 119 is used as a light/thermal stabilizer for olefin polymers in the food packaging industry. It helps maintain the quality and safety of food products by preventing degradation caused by exposure to light and heat, thereby extending the shelf life and ensuring the integrity of the packaged food.
Used in Plastics and Polymers Industry:
Chimassorb 119 is used as a light/thermal stabilizer in olefin polymers within the plastics and polymers industry. Its application ensures that these polymers maintain their structural and functional properties when used in various applications, including those that involve contact with food. This contributes to the overall performance and durability of the end products.

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 106990-43-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,9,9 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 106990-43:
(8*1)+(7*0)+(6*6)+(5*9)+(4*9)+(3*0)+(2*4)+(1*3)=136
136 % 10 = 6
So 106990-43-6 is a valid CAS Registry Number.

106990-43-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Chimassorb 119

1.2 Other means of identification

Product number -
Other names Chimassorb 944

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:106990-43-6 SDS

106990-43-6Downstream Products

106990-43-6Relevant articles and documents

Preparation method of hindered amine light stabilizer 119

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Paragraph 0036; 0047-0051; 0062-0066; 0077-0081; 0092-0095, (2021/08/28)

The invention provides a preparation method of a hindered amine light stabilizer 119, and particularly relates to the field of chemical processes. The preparation method comprises the following steps: preparation of an intermediate (I): adding a reactant, namely cyanuric chloride and a reaction solvent, then adding N-n-butyl-N-2,2,6,6-tetramethyl piperidylamine, then adding alkali, continuing reacting for 12 hours, and splitting phases after the reaction is finished so as to finally obtain the intermediate (I); preparation of an intermediate II: adding a catalyst Pd/C, a reaction solvent, and reactants, namely paraformaldehyde and the intermediate I in a molar ratio of 1: (2.1-2.9), then introducing hydrogen with a pressure of 0.5-2 MPa, and performing reacting for 6-9 hours at a temperature of 40-90 DEG C so as to finally obtain the intermediate II; and preparation of a target product, namely a compond (III): firstly, adding a reaction solvent, reactants consisting of the intermediate II and N,N'-bis(3-aminopropyl)ethylenediamine in a molar ratio of (4.1-4.9): 1 and alkali into a reaction container, then replacing air in a reaction system with nitrogen, and carrying out a reflux reaction at 90-120 DEG C for 5-8 hours so as to obtain the target product, namely the compound (III) after the reaction is finished. The preparation method has the advantages of simplicity, high preparation efficiency, high yield, small pollution and the like.

Preparation method of hindered amine light stabilizer

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Paragraph 0048-0056, (2020/04/06)

The invention relates to a preparation method of a hindered amine light stabilizer. The method comprises the following steps: reacting cyanuric chloride with N,N'-bis(3-aminopropyl)ethylenediamine toobtain an intermediate I; reacting the intermediate I with N-butyl-2,2,6,6-tetramethyl-4-piperidylamine to obtain an intermediate II; and adding paraformaldehyde or formaldehyde and formic acid, and carrying out a methylation reaction to obtain the target product. The method adopting the above new synthetic route has the advantages of avoiding of high-temperature or high-pressure reaction conditions in preparation, improvement of the density of hindered amine functional groups of the product, high purity, avoiding of the step of possibly generating hydrolysis byproducts, and great reduction ofthe industrial production cost of the product.

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