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63812-63-5

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  • N-Butyl-4,6-dichloro-N-(2,2,6,6-tetramethyl-4-piperidyl)-1,3,5-triazin-2-amine

    Cas No: 63812-63-5

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63812-63-5 Usage

General Description

N-Butyl-4,6-dichloro-N-(2,2,6,6-tetramethyl-4-piperidyl)-1,3,5-triazin-2-amine is a chemical compound that belongs to the class of triazine-based UV stabilizers. It is commonly used in the production of various plastic and rubber products to protect them from degradation caused by exposure to ultraviolet (UV) radiation. N-Butyl-4,6-dichloro-N-(2,2,6,6-tetramethyl-4-piperidyl)-1,3,5-triazin-2-amine is known for its excellent UV absorption and light stabilization properties, making it a popular choice in the manufacturing of outdoor and long-term exposed applications such as automotive parts, agricultural films, and construction materials. Additionally, this chemical is also used in adhesives, coatings, and sealants as a light stabilizer to enhance the longevity and durability of the final products.

Check Digit Verification of cas no

The CAS Registry Mumber 63812-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,1 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63812-63:
(7*6)+(6*3)+(5*8)+(4*1)+(3*2)+(2*6)+(1*3)=125
125 % 10 = 5
So 63812-63-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H27Cl2N5/c1-6-7-8-23(14-20-12(17)19-13(18)21-14)11-9-15(2,3)22-16(4,5)10-11/h11,22H,6-10H2,1-5H3

63812-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-butyl-4,6-dichloro-N-(2,2,6,6-tetramethylpiperidin-4-yl)-1,3,5-triazin-2-amine

1.2 Other means of identification

Product number -
Other names EINECS 264-471-6

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:63812-63-5 SDS

63812-63-5Downstream Products

63812-63-5Relevant articles and documents

Low alkaline polymerization type hindered amine light stabilizer and preparation method thereof

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Paragraph 0028; 0039; 0042, (2019/07/08)

The invention provides a compound as shown in a formula I. The compound is used for preparing a low alkaline polymerization type hindered amine light stabilizer. The hindered amine light stabilizer isexcellent in light stabilizing effect, great in molecular weight, extraction-resistant, low in alkalinity, good in compatibility and wide in application range. The invention also provides a preparation method and an application of the low alkaline polymerization type hindered amine light stabilizer.

A low-alkaline hindered amine light stabilizer and its preparation method

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Paragraph 0038-0039; 0044-0045; 0049-0050; 0053-0054, (2018/11/22)

The invention discloses a low-alkalinity hindered amine light stabilizer of which the structure is disclosed as Formula I. The low-alkalinity hindered amine light stabilizer has the advantages of excellent stabilizing effect, favorable compatibility, extraction resistance and wide application range. The invention also discloses a preparation method of the light stabilizer, which comprises the following steps: reacting N-(2,2,6,6-tetramethyl-4-piperidyl)amine and cyanuric chloride to obtain an intermediate; and reacting the intermediate and N,N'-bis[N-(2,2,6,6-tetramethyl-4-piperidyl)]-1,6-hexamethylenediamine to obtain a polymer, and methylating to obtain the product. The synthesis method is simple to operate, and has the advantages of high product yield, narrow molecular weight distribution and the like.

OLIGOMERIC STERICALLY HINDERED AMINES AND THEIR USE AS POLYMER STABILISERS

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Page/Page column 6, (2009/10/31)

This invention relates to new polypiperidine compounds of general formula (I) which give different kinds of polymer materials, in particular polyolefins, high stability towards oxidative action and photodegradation. The invention also relates to the processes used to prepare the compounds of formula (I).

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