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2-(2'-Hydroxy-3'-sec-butyl-5'-tert-butylphenyl)benzotriazole, also known as 2-(2H-Benzotriazol-2-yl)-4-(tert-butyl)-6-(sec-butyl)phenol, is a chemical compound that belongs to the benzotriazole family. It is characterized by its ability to absorb ultraviolet (UV) radiation, making it a useful UV stabilizer in various applications.

36437-37-3

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36437-37-3 Usage

Uses

Used in Plastics Industry:
2-(2'-Hydroxy-3'-sec-butyl-5'-tert-butylphenyl)benzotriazole is used as a UV stabilizer for plastics to increase product stability and prevent discoloration. Its ability to absorb UV radiation helps protect plastics from degradation caused by exposure to sunlight or other UV sources, thereby extending their lifespan and maintaining their appearance.
Used in Aquatic Environment:
Although 2-(2'-Hydroxy-3'-sec-butyl-5'-tert-butylphenyl)benzotriazole is a pollutant for the aquatic environment, it has been implicated as a potential stable and toxic ligand for the aryl hydrocarbon receptor in humans. This suggests that further research is needed to understand its impact on both the environment and human health.

Check Digit Verification of cas no

The CAS Registry Mumber 36437-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,4,3 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 36437-37:
(7*3)+(6*6)+(5*4)+(4*3)+(3*7)+(2*3)+(1*7)=123
123 % 10 = 3
So 36437-37-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H25N3O/c1-6-13(2)15-11-14(20(3,4)5)12-18(19(15)24)23-21-16-9-7-8-10-17(16)22-23/h7-13,24H,6H2,1-5H3

36437-37-3Downstream Products

36437-37-3Relevant academic research and scientific papers

Process for the preparation of benzotriazoles

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Page 9, (2010/02/05)

A process for the preparation of compounds of formula (I): wherein the general symbols are as defined in claim 1, which comprises reacting a compound of formula (V): wherein R1, R2, R3, R4, R5, R6, R7, R8, R9 and R18 are as defined in claim 1, and R18 is especially nitro, chlorine or bromine, with an azide compound of formula (IX): wherein M and n are as defined in claim 1, especially with sodium azide.

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

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, (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

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, (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.

Preparation of Some 2-(2' H-Benzotriazol-2'-yl)phenol Ultraviolet Absorbers: Application of the Transalkylation Reaction

Rosevear, Judi,Wilshire, John F.K.

, p. 1163 - 1176 (2007/10/02)

When 2-(2' H-benzotriazol-2'-yl)phenols containing t-alkyl substituents are warmed in toluene solution with an aluminium chloride/nitromethane catalyst, the t-alkyl groups are transferred to the solvent (toluene).This transalkylation reaction has been used to prepare not readily accessible or previously inaccessible 2-(2' H-benzotriazol-2'-yl)phenols, a class of ultraviolet absorbers widely used in industry.

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