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[3,5-bis(2H-benzotrizol-2-yl)-2,4-dihydroxyphenyl]phenyl-Methanone is a chemical compound belonging to the class of benzotriazole compounds. It is characterized by its ability to absorb and dissipate UV radiation, which makes it a valuable component in protecting materials from degradation due to sunlight exposure. [3,5-bis(2H-benzotrizol-2-yl)-2,4-dihydroxyphenyl]phenyl-Methanone is structurally similar to other UV stabilizers such as benzophenone and benzotriazole, and it functions by effectively converting absorbed UV light into harmless thermal energy. This process helps to prevent photo-oxidation and degradation of materials, thereby extending their lifespan and maintaining their integrity in outdoor and high UV exposure environments.

86936-87-0

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86936-87-0 Usage

Uses

Used in Polymer Industry:
[3,5-bis(2H-benzotrizol-2-yl)-2,4-dihydroxyphenyl]phenyl-Methanone is used as a UV light stabilizer and absorber for polymers to protect them from degradation caused by sunlight exposure. Its ability to absorb UV radiation and convert it into thermal energy helps to prevent photo-oxidation and degradation, ensuring the longevity and stability of polymers used in various applications.
Used in Coatings Industry:
In the coatings industry, [3,5-bis(2H-benzotrizol-2-yl)-2,4-dihydroxyphenyl]phenyl-Methanone is used as a UV stabilizer to protect coatings from the harmful effects of UV radiation. By absorbing and dissipating UV light, [3,5-bis(2H-benzotrizol-2-yl)-2,4-dihydroxyphenyl]phenyl-Methanone helps to maintain the color, appearance, and structural integrity of coatings, especially those exposed to outdoor environments with high levels of UV radiation.
Used in Other Materials:
[3,5-bis(2H-benzotrizol-2-yl)-2,4-dihydroxyphenyl]phenyl-Methanone is also used in other materials that require protection from UV degradation, such as adhesives, sealants, and elastomers. Its UV stabilizing properties help to extend the service life of these materials and maintain their performance in environments with significant UV exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 86936-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,3 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 86936-87:
(7*8)+(6*6)+(5*9)+(4*3)+(3*6)+(2*8)+(1*7)=190
190 % 10 = 0
So 86936-87-0 is a valid CAS Registry Number.

86936-87-0Downstream Products

86936-87-0Relevant academic research and scientific papers

Ultraviolet light absorbers having two different chromophors in the same molecule

-

, (2008/06/13)

Ultraviolet light absorbing compounds having two different chromophors in the same molecule, particularly the benzotriazole chromophor and either the dihydroxybenzophenone or dihydroxyacetophenone chromophor; specifically, the two compounds 3,5-[di(2H-benzotriazole-2-yl)]-2,4-dihydroxyacetophenone and 3,5-[di(2H-benzotriazole-2-yl)]2,4-dihydroxybenzophenone.

Functional Polymers, XL. Syntheses of Mono- and Di(4-methoxy)benzotriazole-Substituted 2,4-Dihydroxyaceto(or benzo)phenones

Fu, Shoukuan,Li, Shanjun,Vogl, Otto

, p. 805 - 820 (2007/10/02)

Eight benzotriazoles and (4-methoxy)benzotriazoles, mono- or di-substituted derivatives of 2,4-dihydroxyaceto(or benzo)phenone were synthesized by azo coupling of (4-methoxy)2-nitrobenzenediazonium chloride with 2,4-dihydroxyaceto(or benzo)phenone followed by reductive cyclization.Pure monosubstituted compounds were very difficult to prepare.Careful selection of the pH for the azo coupling and selection of the proper reagents for the reductive cyclization were essential.All compounds were characterized by their ultraviolet, infrared, 1H and 13C NMR spectra and theirelemental analysis.These compounds have both the 2(2-hydroxyphenyl)2H-benzotriazole unit and a 2-hydroxyaceto(or benzo)phenone unit in the same molecule and are effective and useful ultraviolet absorbers. - Keywords: Functional polymers; 2(2-Hydroxyphenyl)2H-benzotriazoles; 2-Hydroxyphenylaceto(benzo)phenones; Azo coupling; Reductive cyclization; Ultraviolet stabilizers

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