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Methyl 3-[3-tert-butyl-4-hydroxy-5-(5-chloro-2H-benzotriazol-2-yl)phenyl]propionate is a chemical compound that belongs to the benzotriazole family, known for its light stabilizing and UV-absorbing properties. This specific compound is characterized by its tert-butyl and chloro substituents, which enhance its ability to absorb UV radiation. It is also a derivative of propionic acid, commonly used as a food preservative. methyl 3-[3-tert-butyl-4-hydroxy-5-(5-chloro-2H-benzotriazol-2-yl)phenyl]propionate plays a crucial role in sun protection products and other applications requiring UV absorption.

83044-91-1

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83044-91-1 Usage

Uses

Used in Sunscreen and Cosmetic Products:
Methyl 3-[3-tert-butyl-4-hydroxy-5-(5-chloro-2H-benzotriazol-2-yl)phenyl]propionate is used as a UV-absorber in sunscreens and other cosmetic products to protect the skin from harmful UV radiation. Its ability to absorb and dissipate the sun's rays makes it an essential component in these products.
Used in Light Stabilizers:
methyl 3-[3-tert-butyl-4-hydroxy-5-(5-chloro-2H-benzotriazol-2-yl)phenyl]propionate is also used in light stabilizers, which are additives in various materials to prevent degradation caused by exposure to sunlight or other light sources. Its UV-absorbing capabilities help in maintaining the integrity and appearance of materials over time.
Used in Food Preservation:
As a derivative of propionic acid, methyl 3-[3-tert-butyl-4-hydroxy-5-(5-chloro-2H-benzotriazol-2-yl)phenyl]propionate can be used in food preservation to extend the shelf life of certain products by inhibiting the growth of mold and bacteria.

Check Digit Verification of cas no

The CAS Registry Mumber 83044-91-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,4 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 83044-91:
(7*8)+(6*3)+(5*0)+(4*4)+(3*4)+(2*9)+(1*1)=121
121 % 10 = 1
So 83044-91-1 is a valid CAS Registry Number.
InChI:InChI=1/C20H22ClN3O3/c1-20(2,3)14-9-12(5-8-18(25)27-4)10-17(19(14)26)24-22-15-7-6-13(21)11-16(15)23-24/h6-7,9-11,26H,5,8H2,1-4H3

83044-91-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-[3-tert-butyl-5-(5-chlorobenzotriazol-2-yl)-4-hydroxyphenyl]propanoate

1.2 Other means of identification

Product number -
Other names EINECS 280-173-9

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:83044-91-1 SDS

83044-91-1Relevant academic research and scientific papers

Composition comprising pesticide and benzotriazole UV absorbers

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Page/Page column 9, (2012/03/26)

The present invention relates to an agrochemical composition comprising pesticide and UV absorber. The invention furthermore relates to UV-absorbers and to the use thereof in agrochemical compositions. It moreover relates to a method of controlling phytopathogenic fungi and/or undesirable plant growth and/or undesirable insect or mite infestation and/or of regulating plant growth.

Processes for the preparation of benzotriazole UV absorbers

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, (2008/06/13)

Provided is a process for preparing 2H-benzotriazole UV absorbers containing a perfluoroalkyl moiety at the 5-position of the benzo ring, for example a trifluoromethyl group, which involves diazotizing the perfluoroalkyl substituted o-nitroaniline using concentrated sulfuric acid plus sodium nitrite or nitrosylsulfuric acid to form the corresponding monoazobenzene intermediate via the diazonium salt intermediate which is reduced to the corresponding 5-perfluoroalkyl substituted 2H-benzotriazole UV absorber compound by conventional reduction means. Also provided is a novel one-pot, multiphase reaction for the preparation of 2(2-nitrophenylazo) substituted phenols, which are precursors for 2H-benzotriazole UV absorbers.

One-pot process for the preparation of 5-sulfonyl-substituted benzotriazoles UV absorbers

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, (2008/06/13)

5-Sulfonyl substituted benzotriazole UV absorbers are prepared from the corresponding 5-chlorobenzotriazole in a two step, but one-pot process where the second step involves the oxidation of the non-isolated 5-thio substituted benzotriazole using sodium tungstate, hydrogen peroxide and formic acid. The 5-sulfonyl substituted benzotriazoles exhibit enhanced absorption in the near-visible range (over 350 nm) thus providing effective protection to substrates in this critical area of the spectrum.

Isocyanuric acid derivative useful as a light stabilizer

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, (2008/06/13)

Tris[2-hydroxy-3-(2,2,6,6-tetramethyl-4-piperidylamino)propyl] isocyanurate is useful as a light stabilizer for organic materials. A composition comprising an organic material and the isocyanurate is stable against light and also excellent in heat resistance. The isocyanurate can be produced by the reaction between tris(2,3-epoxypropyl) isocyanurate and 4-amino-2,2,6,6-tetramethylpiperidine.

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